GO:0000003PHENOTYPE	reproduction phenotype
GO:0000028PHENOTYPE	ribosomal small subunit assembly phenotype
GO:0000045PHENOTYPE	autophagosome assembly phenotype
GO:0000050PHENOTYPE	urea cycle phenotype
GO:0000070PHENOTYPE	mitotic sister chromatid segregation phenotype
GO:0000077PHENOTYPE	DNA damage checkpoint phenotype
GO:0000082PHENOTYPE	G1/S transition of mitotic cell cycle phenotype
GO:0000122PHENOTYPE	negative regulation of transcription from RNA polymerase II promoter phenotype
GO:0000132PHENOTYPE	establishment of mitotic spindle orientation phenotype
GO:0000165PHENOTYPE	MAPK cascade phenotype
GO:0000184PHENOTYPE	nuclear-transcribed mRNA catabolic process, nonsense-mediated decay phenotype
GO:0000226PHENOTYPE	microtubule cytoskeleton organization phenotype
GO:0000244PHENOTYPE	spliceosomal tri-snRNP complex assembly phenotype
GO:0000245PHENOTYPE	spliceosomal complex assembly phenotype
GO:0000266PHENOTYPE	mitochondrial fission phenotype
GO:0000278PHENOTYPE	mitotic cell cycle phenotype
GO:0000280PHENOTYPE	nuclear division phenotype
GO:0000281PHENOTYPE	mitotic cytokinesis phenotype
GO:0000381PHENOTYPE	regulation of alternative mRNA splicing, via spliceosome phenotype
GO:0000387PHENOTYPE	spliceosomal snRNP assembly phenotype
GO:0000398PHENOTYPE	mRNA splicing, via spliceosome phenotype
GO:0000422PHENOTYPE	mitophagy phenotype
GO:0000448PHENOTYPE	cleavage in ITS2 between 5.8S rRNA and LSU-rRNA of tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA) phenotype
GO:0000467PHENOTYPE	exonucleolytic trimming to generate mature 3'-end of 5.8S rRNA from tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA) phenotype
GO:0000578PHENOTYPE	embryonic axis specification phenotype
GO:0000724PHENOTYPE	double-strand break repair via homologous recombination phenotype
GO:0000902PHENOTYPE	cell morphogenesis phenotype
GO:0000904PHENOTYPE	cell morphogenesis involved in differentiation phenotype
GO:0000956PHENOTYPE	nuclear-transcribed mRNA catabolic process phenotype
GO:0001501PHENOTYPE	skeletal system development phenotype
GO:0001502PHENOTYPE	cartilage condensation phenotype
GO:0001503PHENOTYPE	ossification phenotype
GO:0001525PHENOTYPE	angiogenesis phenotype
GO:0001541PHENOTYPE	ovarian follicle development phenotype
GO:0001556PHENOTYPE	oocyte maturation phenotype
GO:0001568PHENOTYPE	blood vessel development phenotype
GO:0001569PHENOTYPE	patterning of blood vessels phenotype
GO:0001570PHENOTYPE	vasculogenesis phenotype
GO:0001649PHENOTYPE	osteoblast differentiation phenotype
GO:0001654PHENOTYPE	eye development phenotype
GO:0001666PHENOTYPE	response to hypoxia phenotype
GO:0001667PHENOTYPE	ameboidal-type cell migration phenotype
GO:0001702PHENOTYPE	gastrulation with mouth forming second phenotype
GO:0001706PHENOTYPE	endoderm formation phenotype
GO:0001707PHENOTYPE	mesoderm formation phenotype
GO:0001708PHENOTYPE	cell fate specification phenotype
GO:0001709PHENOTYPE	cell fate determination phenotype
GO:0001714PHENOTYPE	endodermal cell fate specification phenotype
GO:0001736PHENOTYPE	establishment of planar polarity phenotype
GO:0001738PHENOTYPE	morphogenesis of a polarized epithelium phenotype
GO:0001743PHENOTYPE	optic placode formation phenotype
GO:0001754PHENOTYPE	eye photoreceptor cell differentiation phenotype
GO:0001755PHENOTYPE	neural crest cell migration phenotype
GO:0001756PHENOTYPE	somitogenesis phenotype
GO:0001757PHENOTYPE	somite specification phenotype
GO:0001764PHENOTYPE	neuron migration phenotype
GO:0001774PHENOTYPE	microglial cell activation phenotype
GO:0001775PHENOTYPE	cell activation phenotype
GO:0001779PHENOTYPE	natural killer cell differentiation phenotype
GO:0001780PHENOTYPE	neutrophil homeostasis phenotype
GO:0001822PHENOTYPE	kidney development phenotype
GO:0001837PHENOTYPE	epithelial to mesenchymal transition phenotype
GO:0001839PHENOTYPE	neural plate morphogenesis phenotype
GO:0001840PHENOTYPE	neural plate development phenotype
GO:0001841PHENOTYPE	neural tube formation phenotype
GO:0001843PHENOTYPE	neural tube closure phenotype
GO:0001845PHENOTYPE	phagolysosome assembly phenotype
GO:0001885PHENOTYPE	endothelial cell development phenotype
GO:0001889PHENOTYPE	liver development phenotype
GO:0001894PHENOTYPE	tissue homeostasis phenotype
GO:0001895PHENOTYPE	retina homeostasis phenotype
GO:0001935PHENOTYPE	endothelial cell proliferation phenotype
GO:0001944PHENOTYPE	vasculature development phenotype
GO:0001945PHENOTYPE	lymph vessel development phenotype
GO:0001946PHENOTYPE	lymphangiogenesis phenotype
GO:0001947PHENOTYPE	heart looping phenotype
GO:0001957PHENOTYPE	intramembranous ossification phenotype
GO:0001958PHENOTYPE	endochondral ossification phenotype
GO:0001964PHENOTYPE	startle response phenotype
GO:0001966PHENOTYPE	thigmotaxis phenotype
GO:0001974PHENOTYPE	blood vessel remodeling phenotype
GO:0001975PHENOTYPE	response to amphetamine phenotype
GO:0002009PHENOTYPE	morphogenesis of an epithelium phenotype
GO:0002011PHENOTYPE	morphogenesis of an epithelial sheet phenotype
GO:0002027PHENOTYPE	regulation of heart rate phenotype
GO:0002040PHENOTYPE	sprouting angiogenesis phenotype
GO:0002042PHENOTYPE	cell migration involved in sprouting angiogenesis phenotype
GO:0002043PHENOTYPE	blood vessel endothelial cell proliferation involved in sprouting angiogenesis phenotype
GO:0002062PHENOTYPE	chondrocyte differentiation phenotype
GO:0002063PHENOTYPE	chondrocyte development phenotype
GO:0002064PHENOTYPE	epithelial cell development phenotype
GO:0002072PHENOTYPE	optic cup morphogenesis involved in camera-type eye development phenotype
GO:0002088PHENOTYPE	lens development in camera-type eye phenotype
GO:0002089PHENOTYPE	lens morphogenesis in camera-type eye phenotype
GO:0002093PHENOTYPE	auditory receptor cell morphogenesis phenotype
GO:0002138PHENOTYPE	retinoic acid biosynthetic process phenotype
GO:0002159PHENOTYPE	desmosome assembly phenotype
GO:0002176PHENOTYPE	male germ cell proliferation phenotype
GO:0002218PHENOTYPE	activation of innate immune response phenotype
GO:0002232PHENOTYPE	leukocyte chemotaxis involved in inflammatory response phenotype
GO:0002233PHENOTYPE	leukocyte chemotaxis involved in immune response phenotype
GO:0002244PHENOTYPE	hematopoietic progenitor cell differentiation phenotype
GO:0002253PHENOTYPE	activation of immune response phenotype
GO:0002262PHENOTYPE	myeloid cell homeostasis phenotype
GO:0002283PHENOTYPE	neutrophil activation involved in immune response phenotype
GO:0002320PHENOTYPE	lymphoid progenitor cell differentiation phenotype
GO:0002446PHENOTYPE	neutrophil mediated immunity phenotype
GO:0002521PHENOTYPE	leukocyte differentiation phenotype
GO:0002522PHENOTYPE	leukocyte migration involved in immune response phenotype
GO:0002523PHENOTYPE	leukocyte migration involved in inflammatory response phenotype
GO:0002562PHENOTYPE	somatic diversification of immune receptors via germline recombination within a single locus phenotype
GO:0002573PHENOTYPE	myeloid leukocyte differentiation phenotype
GO:0002574PHENOTYPE	thrombocyte differentiation phenotype
GO:0002679PHENOTYPE	respiratory burst involved in defense response phenotype
GO:0002761PHENOTYPE	regulation of myeloid leukocyte differentiation phenotype
GO:0002934PHENOTYPE	desmosome organization phenotype
GO:0003007PHENOTYPE	heart morphogenesis phenotype
GO:0003009PHENOTYPE	skeletal muscle contraction phenotype
GO:0003014PHENOTYPE	renal system process phenotype
GO:0003015PHENOTYPE	heart process phenotype
GO:0003073PHENOTYPE	regulation of systemic arterial blood pressure phenotype
GO:0003093PHENOTYPE	regulation of glomerular filtration phenotype
GO:0003094PHENOTYPE	glomerular filtration phenotype
GO:0003128PHENOTYPE	heart field specification phenotype
GO:0003139PHENOTYPE	secondary heart field specification phenotype
GO:0003140PHENOTYPE	determination of left/right asymmetry in lateral mesoderm phenotype
GO:0003143PHENOTYPE	embryonic heart tube morphogenesis phenotype
GO:0003144PHENOTYPE	embryonic heart tube formation phenotype
GO:0003146PHENOTYPE	heart jogging phenotype
GO:0003147PHENOTYPE	neural crest cell migration involved in heart formation phenotype
GO:0003151PHENOTYPE	outflow tract morphogenesis phenotype
GO:0003157PHENOTYPE	endocardium development phenotype
GO:0003160PHENOTYPE	endocardium morphogenesis phenotype
GO:0003161PHENOTYPE	cardiac conduction system development phenotype
GO:0003170PHENOTYPE	heart valve development phenotype
GO:0003171PHENOTYPE	atrioventricular valve development phenotype
GO:0003179PHENOTYPE	heart valve morphogenesis phenotype
GO:0003181PHENOTYPE	atrioventricular valve morphogenesis phenotype
GO:0003188PHENOTYPE	heart valve formation phenotype
GO:0003190PHENOTYPE	atrioventricular valve formation phenotype
GO:0003197PHENOTYPE	endocardial cushion development phenotype
GO:0003203PHENOTYPE	endocardial cushion morphogenesis phenotype
GO:0003205PHENOTYPE	cardiac chamber development phenotype
GO:0003206PHENOTYPE	cardiac chamber morphogenesis phenotype
GO:0003208PHENOTYPE	cardiac ventricle morphogenesis phenotype
GO:0003209PHENOTYPE	cardiac atrium morphogenesis phenotype
GO:0003228PHENOTYPE	atrial cardiac muscle tissue development phenotype
GO:0003229PHENOTYPE	ventricular cardiac muscle tissue development phenotype
GO:0003230PHENOTYPE	cardiac atrium development phenotype
GO:0003231PHENOTYPE	cardiac ventricle development phenotype
GO:0003232PHENOTYPE	bulbus arteriosus development phenotype
GO:0003234PHENOTYPE	bulbus arteriosus formation phenotype
GO:0003242PHENOTYPE	cardiac chamber ballooning phenotype
GO:0003245PHENOTYPE	cardiac muscle tissue growth involved in heart morphogenesis phenotype
GO:0003261PHENOTYPE	cardiac muscle progenitor cell migration to the midline involved in heart field formation phenotype
GO:0003262PHENOTYPE	endocardial progenitor cell migration to the midline involved in heart field formation phenotype
GO:0003272PHENOTYPE	endocardial cushion formation phenotype
GO:0003294PHENOTYPE	atrial ventricular junction remodeling phenotype
GO:0003301PHENOTYPE	physiological cardiac muscle hypertrophy phenotype
GO:0003303PHENOTYPE	BMP signaling pathway involved in heart jogging phenotype
GO:0003305PHENOTYPE	cell migration involved in heart jogging phenotype
GO:0003309PHENOTYPE	type B pancreatic cell differentiation phenotype
GO:0003310PHENOTYPE	pancreatic A cell differentiation phenotype
GO:0003311PHENOTYPE	pancreatic D cell differentiation phenotype
GO:0003313PHENOTYPE	heart rudiment development phenotype
GO:0003314PHENOTYPE	heart rudiment morphogenesis phenotype
GO:0003315PHENOTYPE	heart rudiment formation phenotype
GO:0003317PHENOTYPE	cardioblast cell midline fusion phenotype
GO:0003318PHENOTYPE	cell migration to the midline involved in heart development phenotype
GO:0003319PHENOTYPE	cardioblast migration to the midline involved in heart rudiment formation phenotype
GO:0003323PHENOTYPE	type B pancreatic cell development phenotype
GO:0003330PHENOTYPE	regulation of extracellular matrix constituent secretion phenotype
GO:0003341PHENOTYPE	cilium movement phenotype
GO:0003351PHENOTYPE	epithelial cilium movement phenotype
GO:0003352PHENOTYPE	regulation of cilium movement phenotype
GO:0003355PHENOTYPE	cilium movement involved in otolith formation phenotype
GO:0003358PHENOTYPE	noradrenergic neuron development phenotype
GO:0003370PHENOTYPE	cell-cell adhesion involved in mesendodermal cell migration phenotype
GO:0003379PHENOTYPE	establishment of cell polarity involved in gastrulation cell migration phenotype
GO:0003381PHENOTYPE	epithelial cell morphogenesis involved in gastrulation phenotype
GO:0003401PHENOTYPE	axis elongation phenotype
GO:0003403PHENOTYPE	optic vesicle formation phenotype
GO:0003404PHENOTYPE	optic vesicle morphogenesis phenotype
GO:0003406PHENOTYPE	retinal pigment epithelium development phenotype
GO:0003407PHENOTYPE	neural retina development phenotype
GO:0003412PHENOTYPE	establishment of epithelial cell apical/basal polarity involved in camera-type eye morphogenesis phenotype
GO:0003417PHENOTYPE	growth plate cartilage development phenotype
GO:0003419PHENOTYPE	growth plate cartilage chondrocyte proliferation phenotype
GO:0003428PHENOTYPE	chondrocyte intercalation involved in growth plate cartilage morphogenesis phenotype
GO:0003720PHENOTYPE	telomerase activity phenotype
GO:0003990PHENOTYPE	acetylcholinesterase activity phenotype
GO:0004089PHENOTYPE	carbonate dehydratase activity phenotype
GO:0004097PHENOTYPE	catechol oxidase activity phenotype
GO:0004129PHENOTYPE	cytochrome-c oxidase activity phenotype
GO:0004345PHENOTYPE	glucose-6-phosphate dehydrogenase activity phenotype
GO:0004439PHENOTYPE	phosphatidylinositol-4,5-bisphosphate 5-phosphatase activity phenotype
GO:0004465PHENOTYPE	lipoprotein lipase activity phenotype
GO:0004683PHENOTYPE	calmodulin-dependent protein kinase activity phenotype
GO:0004693PHENOTYPE	cyclin-dependent protein serine/threonine kinase activity phenotype
GO:0004707PHENOTYPE	MAP kinase activity phenotype
GO:0004708PHENOTYPE	MAP kinase kinase activity phenotype
GO:0004984PHENOTYPE	olfactory receptor activity phenotype
GO:0005096PHENOTYPE	GTPase activator activity phenotype
GO:0005219PHENOTYPE	ryanodine-sensitive calcium-release channel activity phenotype
GO:0005245PHENOTYPE	voltage-gated calcium channel activity phenotype
GO:0005248PHENOTYPE	voltage-gated sodium channel activity phenotype
GO:0005262PHENOTYPE	calcium channel activity phenotype
GO:0005614PHENOTYPE	interstitial matrix phenotype
GO:0005634PHENOTYPE	nucleus phenotype
GO:0005737PHENOTYPE	cytoplasm phenotype
GO:0005746PHENOTYPE	mitochondrial respiratory chain phenotype
GO:0005840PHENOTYPE	ribosome phenotype
GO:0005861PHENOTYPE	troponin complex phenotype
GO:0005892PHENOTYPE	acetylcholine-gated channel complex phenotype
GO:0005911PHENOTYPE	cell-cell junction phenotype
GO:0005923PHENOTYPE	bicellular tight junction phenotype
GO:0006024PHENOTYPE	glycosaminoglycan biosynthetic process phenotype
GO:0006029PHENOTYPE	proteoglycan metabolic process phenotype
GO:0006090PHENOTYPE	pyruvate metabolic process phenotype
GO:0006094PHENOTYPE	gluconeogenesis phenotype
GO:0006096PHENOTYPE	glycolytic process phenotype
GO:0006120PHENOTYPE	mitochondrial electron transport, NADH to ubiquinone phenotype
GO:0006183PHENOTYPE	GTP biosynthetic process phenotype
GO:0006260PHENOTYPE	DNA replication phenotype
GO:0006303PHENOTYPE	double-strand break repair via nonhomologous end joining phenotype
GO:0006306PHENOTYPE	DNA methylation phenotype
GO:0006351PHENOTYPE	transcription, DNA-templated phenotype
GO:0006355PHENOTYPE	regulation of transcription, DNA-templated phenotype
GO:0006357PHENOTYPE	regulation of transcription from RNA polymerase II promoter phenotype
GO:0006364PHENOTYPE	rRNA processing phenotype
GO:0006366PHENOTYPE	transcription from RNA polymerase II promoter phenotype
GO:0006378PHENOTYPE	mRNA polyadenylation phenotype
GO:0006397PHENOTYPE	mRNA processing phenotype
GO:0006401PHENOTYPE	RNA catabolic process phenotype
GO:0006402PHENOTYPE	mRNA catabolic process phenotype
GO:0006406PHENOTYPE	mRNA export from nucleus phenotype
GO:0006412PHENOTYPE	translation phenotype
GO:0006417PHENOTYPE	regulation of translation phenotype
GO:0006468PHENOTYPE	protein phosphorylation phenotype
GO:0006486PHENOTYPE	protein glycosylation phenotype
GO:0006487PHENOTYPE	protein N-linked glycosylation phenotype
GO:0006497PHENOTYPE	protein lipidation phenotype
GO:0006555PHENOTYPE	methionine metabolic process phenotype
GO:0006582PHENOTYPE	melanin metabolic process phenotype
GO:0006585PHENOTYPE	dopamine biosynthetic process from tyrosine phenotype
GO:0006629PHENOTYPE	lipid metabolic process phenotype
GO:0006631PHENOTYPE	fatty acid metabolic process phenotype
GO:0006684PHENOTYPE	sphingomyelin metabolic process phenotype
GO:0006687PHENOTYPE	glycosphingolipid metabolic process phenotype
GO:0006688PHENOTYPE	glycosphingolipid biosynthetic process phenotype
GO:0006694PHENOTYPE	steroid biosynthetic process phenotype
GO:0006704PHENOTYPE	glucocorticoid biosynthetic process phenotype
GO:0006754PHENOTYPE	ATP biosynthetic process phenotype
GO:0006783PHENOTYPE	heme biosynthetic process phenotype
GO:0006809PHENOTYPE	nitric oxide biosynthetic process phenotype
GO:0006812PHENOTYPE	cation transport phenotype
GO:0006814PHENOTYPE	sodium ion transport phenotype
GO:0006816PHENOTYPE	calcium ion transport phenotype
GO:0006821PHENOTYPE	chloride transport phenotype
GO:0006826PHENOTYPE	iron ion transport phenotype
GO:0006874PHENOTYPE	cellular calcium ion homeostasis phenotype
GO:0006879PHENOTYPE	cellular iron ion homeostasis phenotype
GO:0006883PHENOTYPE	cellular sodium ion homeostasis phenotype
GO:0006885PHENOTYPE	regulation of pH phenotype
GO:0006888PHENOTYPE	ER to Golgi vesicle-mediated transport phenotype
GO:0006897PHENOTYPE	endocytosis phenotype
GO:0006898PHENOTYPE	receptor-mediated endocytosis phenotype
GO:0006909PHENOTYPE	phagocytosis phenotype
GO:0006911PHENOTYPE	phagocytosis, engulfment phenotype
GO:0006914PHENOTYPE	autophagy phenotype
GO:0006915PHENOTYPE	apoptotic process phenotype
GO:0006919PHENOTYPE	activation of cysteine-type endopeptidase activity involved in apoptotic process phenotype
GO:0006935PHENOTYPE	chemotaxis phenotype
GO:0006936PHENOTYPE	muscle contraction phenotype
GO:0006937PHENOTYPE	regulation of muscle contraction phenotype
GO:0006941PHENOTYPE	striated muscle contraction phenotype
GO:0006954PHENOTYPE	inflammatory response phenotype
GO:0006955PHENOTYPE	immune response phenotype
GO:0006970PHENOTYPE	response to osmotic stress phenotype
GO:0006974PHENOTYPE	cellular response to DNA damage stimulus phenotype
GO:0006979PHENOTYPE	response to oxidative stress phenotype
GO:0007004PHENOTYPE	telomere maintenance via telomerase phenotype
GO:0007005PHENOTYPE	mitochondrion organization phenotype
GO:0007006PHENOTYPE	mitochondrial membrane organization phenotype
GO:0007010PHENOTYPE	cytoskeleton organization phenotype
GO:0007015PHENOTYPE	actin filament organization phenotype
GO:0007018PHENOTYPE	microtubule-based movement phenotype
GO:0007030PHENOTYPE	Golgi organization phenotype
GO:0007033PHENOTYPE	vacuole organization phenotype
GO:0007040PHENOTYPE	lysosome organization phenotype
GO:0007043PHENOTYPE	cell-cell junction assembly phenotype
GO:0007052PHENOTYPE	mitotic spindle organization phenotype
GO:0007059PHENOTYPE	chromosome segregation phenotype
GO:0007060PHENOTYPE	male meiosis chromosome segregation phenotype
GO:0007062PHENOTYPE	sister chromatid cohesion phenotype
GO:0007064PHENOTYPE	mitotic sister chromatid cohesion phenotype
GO:0007080PHENOTYPE	mitotic metaphase plate congression phenotype
GO:0007088PHENOTYPE	regulation of mitotic nuclear division phenotype
GO:0007093PHENOTYPE	mitotic cell cycle checkpoint phenotype
GO:0007095PHENOTYPE	mitotic G2 DNA damage checkpoint phenotype
GO:0007097PHENOTYPE	nuclear migration phenotype
GO:0007098PHENOTYPE	centrosome cycle phenotype
GO:0007141PHENOTYPE	male meiosis I phenotype
GO:0007155PHENOTYPE	cell adhesion phenotype
GO:0007158PHENOTYPE	neuron cell-cell adhesion phenotype
GO:0007163PHENOTYPE	establishment or maintenance of cell polarity phenotype
GO:0007165PHENOTYPE	signal transduction phenotype
GO:0007179PHENOTYPE	transforming growth factor beta receptor signaling pathway phenotype
GO:0007219PHENOTYPE	Notch signaling pathway phenotype
GO:0007223PHENOTYPE	Wnt signaling pathway, calcium modulating pathway phenotype
GO:0007224PHENOTYPE	smoothened signaling pathway phenotype
GO:0007254PHENOTYPE	JNK cascade phenotype
GO:0007268PHENOTYPE	synaptic transmission phenotype
GO:0007274PHENOTYPE	neuromuscular synaptic transmission phenotype
GO:0007281PHENOTYPE	germ cell development phenotype
GO:0007283PHENOTYPE	spermatogenesis phenotype
GO:0007292PHENOTYPE	female gamete generation phenotype
GO:0007314PHENOTYPE	oocyte anterior/posterior axis specification phenotype
GO:0007315PHENOTYPE	pole plasm assembly phenotype
GO:0007343PHENOTYPE	egg activation phenotype
GO:0007344PHENOTYPE	pronuclear fusion phenotype
GO:0007346PHENOTYPE	regulation of mitotic cell cycle phenotype
GO:0007368PHENOTYPE	determination of left/right symmetry phenotype
GO:0007369PHENOTYPE	gastrulation phenotype
GO:0007398PHENOTYPE	ectoderm development phenotype
GO:0007399PHENOTYPE	nervous system development phenotype
GO:0007405PHENOTYPE	neuroblast proliferation phenotype
GO:0007409PHENOTYPE	axonogenesis phenotype
GO:0007411PHENOTYPE	axon guidance phenotype
GO:0007412PHENOTYPE	axon target recognition phenotype
GO:0007413PHENOTYPE	axonal fasciculation phenotype
GO:0007416PHENOTYPE	synapse assembly phenotype
GO:0007417PHENOTYPE	central nervous system development phenotype
GO:0007418PHENOTYPE	ventral midline development phenotype
GO:0007420PHENOTYPE	brain development phenotype
GO:0007422PHENOTYPE	peripheral nervous system development phenotype
GO:0007423PHENOTYPE	sensory organ development phenotype
GO:0007492PHENOTYPE	endoderm development phenotype
GO:0007498PHENOTYPE	mesoderm development phenotype
GO:0007502PHENOTYPE	digestive tract mesoderm development phenotype
GO:0007507PHENOTYPE	heart development phenotype
GO:0007509PHENOTYPE	mesoderm migration involved in gastrulation phenotype
GO:0007517PHENOTYPE	muscle organ development phenotype
GO:0007519PHENOTYPE	skeletal muscle tissue development phenotype
GO:0007520PHENOTYPE	myoblast fusion phenotype
GO:0007525PHENOTYPE	somatic muscle development phenotype
GO:0007528PHENOTYPE	neuromuscular junction development phenotype
GO:0007530PHENOTYPE	sex determination phenotype
GO:0007568PHENOTYPE	aging phenotype
GO:0007589PHENOTYPE	body fluid secretion phenotype
GO:0007596PHENOTYPE	blood coagulation phenotype
GO:0007599PHENOTYPE	hemostasis phenotype
GO:0007601PHENOTYPE	visual perception phenotype
GO:0007603PHENOTYPE	phototransduction, visible light phenotype
GO:0007605PHENOTYPE	sensory perception of sound phenotype
GO:0007606PHENOTYPE	sensory perception of chemical stimulus phenotype
GO:0007613PHENOTYPE	memory phenotype
GO:0007623PHENOTYPE	circadian rhythm phenotype
GO:0007626PHENOTYPE	locomotory behavior phenotype
GO:0007631PHENOTYPE	feeding behavior phenotype
GO:0007632PHENOTYPE	visual behavior phenotype
GO:0007634PHENOTYPE	optokinetic behavior phenotype
GO:0007635PHENOTYPE	chemosensory behavior phenotype
GO:0007638PHENOTYPE	mechanosensory behavior phenotype
GO:0008015PHENOTYPE	blood circulation phenotype
GO:0008016PHENOTYPE	regulation of heart contraction phenotype
GO:0008028PHENOTYPE	monocarboxylic acid transmembrane transporter activity phenotype
GO:0008045PHENOTYPE	motor neuron axon guidance phenotype
GO:0008057PHENOTYPE	eye pigment granule organization phenotype
GO:0008078PHENOTYPE	mesodermal cell migration phenotype
GO:0008090PHENOTYPE	retrograde axon cargo transport phenotype
GO:0008104PHENOTYPE	protein localization phenotype
GO:0008233PHENOTYPE	peptidase activity phenotype
GO:0008237PHENOTYPE	metallopeptidase activity phenotype
GO:0008283PHENOTYPE	cell proliferation phenotype
GO:0008285PHENOTYPE	negative regulation of cell proliferation phenotype
GO:0008298PHENOTYPE	intracellular mRNA localization phenotype
GO:0008331PHENOTYPE	high voltage-gated calcium channel activity phenotype
GO:0008345PHENOTYPE	larval locomotory behavior phenotype
GO:0008347PHENOTYPE	glial cell migration phenotype
GO:0008354PHENOTYPE	germ cell migration phenotype
GO:0008356PHENOTYPE	asymmetric cell division phenotype
GO:0008361PHENOTYPE	regulation of cell size phenotype
GO:0008380PHENOTYPE	RNA splicing phenotype
GO:0008417PHENOTYPE	fucosyltransferase activity phenotype
GO:0008543PHENOTYPE	fibroblast growth factor receptor signaling pathway phenotype
GO:0008544PHENOTYPE	epidermis development phenotype
GO:0008584PHENOTYPE	male gonad development phenotype
GO:0008585PHENOTYPE	female gonad development phenotype
GO:0008589PHENOTYPE	regulation of smoothened signaling pathway phenotype
GO:0008593PHENOTYPE	regulation of Notch signaling pathway phenotype
GO:0008594PHENOTYPE	photoreceptor cell morphogenesis phenotype
GO:0008595PHENOTYPE	anterior/posterior axis specification, embryo phenotype
GO:0009081PHENOTYPE	branched-chain amino acid metabolic process phenotype
GO:0009303PHENOTYPE	rRNA transcription phenotype
GO:0009304PHENOTYPE	tRNA transcription phenotype
GO:0009306PHENOTYPE	protein secretion phenotype
GO:0009408PHENOTYPE	response to heat phenotype
GO:0009410PHENOTYPE	response to xenobiotic stimulus phenotype
GO:0009411PHENOTYPE	response to UV phenotype
GO:0009416PHENOTYPE	response to light stimulus phenotype
GO:0009566PHENOTYPE	fertilization phenotype
GO:0009583PHENOTYPE	detection of light stimulus phenotype
GO:0009584PHENOTYPE	detection of visible light phenotype
GO:0009611PHENOTYPE	response to wounding phenotype
GO:0009612PHENOTYPE	response to mechanical stimulus phenotype
GO:0009615PHENOTYPE	response to virus phenotype
GO:0009617PHENOTYPE	response to bacterium phenotype
GO:0009636PHENOTYPE	response to toxic substance phenotype
GO:0009652PHENOTYPE	thigmotropism phenotype
GO:0009749PHENOTYPE	response to glucose phenotype
GO:0009792PHENOTYPE	embryo development ending in birth or egg hatching phenotype
GO:0009794PHENOTYPE	regulation of mitotic cell cycle, embryonic phenotype
GO:0009798PHENOTYPE	axis specification phenotype
GO:0009826PHENOTYPE	unidimensional cell growth phenotype
GO:0009880PHENOTYPE	embryonic pattern specification phenotype
GO:0009887PHENOTYPE	organ morphogenesis phenotype
GO:0009913PHENOTYPE	epidermal cell differentiation phenotype
GO:0009948PHENOTYPE	anterior/posterior axis specification phenotype
GO:0009950PHENOTYPE	dorsal/ventral axis specification phenotype
GO:0009952PHENOTYPE	anterior/posterior pattern specification phenotype
GO:0009953PHENOTYPE	dorsal/ventral pattern formation phenotype
GO:0009954PHENOTYPE	proximal/distal pattern formation phenotype
GO:0009957PHENOTYPE	epidermal cell fate specification phenotype
GO:0009968PHENOTYPE	negative regulation of signal transduction phenotype
GO:0010001PHENOTYPE	glial cell differentiation phenotype
GO:0010002PHENOTYPE	cardioblast differentiation phenotype
GO:0010155PHENOTYPE	regulation of proton transport phenotype
GO:0010165PHENOTYPE	response to X-ray phenotype
GO:0010171PHENOTYPE	body morphogenesis phenotype
GO:0010172PHENOTYPE	embryonic body morphogenesis phenotype
GO:0010212PHENOTYPE	response to ionizing radiation phenotype
GO:0010310PHENOTYPE	regulation of hydrogen peroxide metabolic process phenotype
GO:0010389PHENOTYPE	regulation of G2/M transition of mitotic cell cycle phenotype
GO:0010424PHENOTYPE	DNA methylation on cytosine within a CG sequence phenotype
GO:0010452PHENOTYPE	histone H3-K36 methylation phenotype
GO:0010459PHENOTYPE	negative regulation of heart rate phenotype
GO:0010467PHENOTYPE	gene expression phenotype
GO:0010468PHENOTYPE	regulation of gene expression phenotype
GO:0010470PHENOTYPE	regulation of gastrulation phenotype
GO:0010506PHENOTYPE	regulation of autophagy phenotype
GO:0010564PHENOTYPE	regulation of cell cycle process phenotype
GO:0010628PHENOTYPE	positive regulation of gene expression phenotype
GO:0010629PHENOTYPE	negative regulation of gene expression phenotype
GO:0010644PHENOTYPE	cell communication by electrical coupling phenotype
GO:0010669PHENOTYPE	epithelial structure maintenance phenotype
GO:0010717PHENOTYPE	regulation of epithelial to mesenchymal transition phenotype
GO:0010719PHENOTYPE	negative regulation of epithelial to mesenchymal transition phenotype
GO:0010842PHENOTYPE	retina layer formation phenotype
GO:0010882PHENOTYPE	regulation of cardiac muscle contraction by calcium ion signaling phenotype
GO:0010906PHENOTYPE	regulation of glucose metabolic process phenotype
GO:0010960PHENOTYPE	magnesium ion homeostasis phenotype
GO:0010975PHENOTYPE	regulation of neuron projection development phenotype
GO:0010996PHENOTYPE	response to auditory stimulus phenotype
GO:0014002PHENOTYPE	astrocyte development phenotype
GO:0014003PHENOTYPE	oligodendrocyte development phenotype
GO:0014004PHENOTYPE	microglia differentiation phenotype
GO:0014005PHENOTYPE	microglia development phenotype
GO:0014010PHENOTYPE	Schwann cell proliferation phenotype
GO:0014013PHENOTYPE	regulation of gliogenesis phenotype
GO:0014025PHENOTYPE	neural keel formation phenotype
GO:0014028PHENOTYPE	notochord formation phenotype
GO:0014029PHENOTYPE	neural crest formation phenotype
GO:0014032PHENOTYPE	neural crest cell development phenotype
GO:0014033PHENOTYPE	neural crest cell differentiation phenotype
GO:0014036PHENOTYPE	neural crest cell fate specification phenotype
GO:0014037PHENOTYPE	Schwann cell differentiation phenotype
GO:0014044PHENOTYPE	Schwann cell development phenotype
GO:0014045PHENOTYPE	establishment of endothelial blood-brain barrier phenotype
GO:0014065PHENOTYPE	phosphatidylinositol 3-kinase signaling phenotype
GO:0014066PHENOTYPE	regulation of phosphatidylinositol 3-kinase signaling phenotype
GO:0014704PHENOTYPE	intercalated disc phenotype
GO:0014706PHENOTYPE	striated muscle tissue development phenotype
GO:0014707PHENOTYPE	branchiomeric skeletal muscle development phenotype
GO:0014743PHENOTYPE	regulation of muscle hypertrophy phenotype
GO:0014812PHENOTYPE	muscle cell migration phenotype
GO:0014831PHENOTYPE	gastro-intestinal system smooth muscle contraction phenotype
GO:0014835PHENOTYPE	myoblast differentiation involved in skeletal muscle regeneration phenotype
GO:0014866PHENOTYPE	skeletal myofibril assembly phenotype
GO:0014881PHENOTYPE	regulation of myofibril size phenotype
GO:0015012PHENOTYPE	heparan sulfate proteoglycan biosynthetic process phenotype
GO:0015078PHENOTYPE	hydrogen ion transmembrane transporter activity phenotype
GO:0015562PHENOTYPE	efflux transmembrane transporter activity phenotype
GO:0015696PHENOTYPE	ammonium transport phenotype
GO:0015698PHENOTYPE	inorganic anion transport phenotype
GO:0015721PHENOTYPE	bile acid and bile salt transport phenotype
GO:0015840PHENOTYPE	urea transport phenotype
GO:0016055PHENOTYPE	Wnt signaling pathway phenotype
GO:0016075PHENOTYPE	rRNA catabolic process phenotype
GO:0016192PHENOTYPE	vesicle-mediated transport phenotype
GO:0016198PHENOTYPE	axon choice point recognition phenotype
GO:0016199PHENOTYPE	axon midline choice point recognition phenotype
GO:0016203PHENOTYPE	muscle attachment phenotype
GO:0016236PHENOTYPE	macroautophagy phenotype
GO:0016308PHENOTYPE	1-phosphatidylinositol-4-phosphate 5-kinase activity phenotype
GO:0016321PHENOTYPE	female meiosis chromosome segregation phenotype
GO:0016322PHENOTYPE	neuron remodeling phenotype
GO:0016331PHENOTYPE	morphogenesis of embryonic epithelium phenotype
GO:0016338PHENOTYPE	calcium-independent cell-cell adhesion via plasma membrane cell-adhesion molecules phenotype
GO:0016339PHENOTYPE	calcium-dependent cell-cell adhesion via plasma membrane cell adhesion molecules phenotype
GO:0016358PHENOTYPE	dendrite development phenotype
GO:0016477PHENOTYPE	cell migration phenotype
GO:0016525PHENOTYPE	negative regulation of angiogenesis phenotype
GO:0016925PHENOTYPE	protein sumoylation phenotype
GO:0016973PHENOTYPE	poly(A)+ mRNA export from nucleus phenotype
GO:0019216PHENOTYPE	regulation of lipid metabolic process phenotype
GO:0019222PHENOTYPE	regulation of metabolic process phenotype
GO:0019228PHENOTYPE	neuronal action potential phenotype
GO:0019722PHENOTYPE	calcium-mediated signaling phenotype
GO:0019725PHENOTYPE	cellular homeostasis phenotype
GO:0019827PHENOTYPE	stem cell population maintenance phenotype
GO:0019896PHENOTYPE	axon transport of mitochondrion phenotype
GO:0019915PHENOTYPE	lipid storage phenotype
GO:0020027PHENOTYPE	hemoglobin metabolic process phenotype
GO:0021501PHENOTYPE	prechordal plate formation phenotype
GO:0021508PHENOTYPE	floor plate formation phenotype
GO:0021509PHENOTYPE	roof plate formation phenotype
GO:0021510PHENOTYPE	spinal cord development phenotype
GO:0021511PHENOTYPE	spinal cord patterning phenotype
GO:0021512PHENOTYPE	spinal cord anterior/posterior patterning phenotype
GO:0021513PHENOTYPE	spinal cord dorsal/ventral patterning phenotype
GO:0021514PHENOTYPE	ventral spinal cord interneuron differentiation phenotype
GO:0021517PHENOTYPE	ventral spinal cord development phenotype
GO:0021520PHENOTYPE	spinal cord motor neuron cell fate specification phenotype
GO:0021521PHENOTYPE	ventral spinal cord interneuron specification phenotype
GO:0021522PHENOTYPE	spinal cord motor neuron differentiation phenotype
GO:0021529PHENOTYPE	spinal cord oligodendrocyte cell differentiation phenotype
GO:0021530PHENOTYPE	spinal cord oligodendrocyte cell fate specification phenotype
GO:0021532PHENOTYPE	neural tube patterning phenotype
GO:0021534PHENOTYPE	cell proliferation in hindbrain phenotype
GO:0021535PHENOTYPE	cell migration in hindbrain phenotype
GO:0021536PHENOTYPE	diencephalon development phenotype
GO:0021537PHENOTYPE	telencephalon development phenotype
GO:0021538PHENOTYPE	epithalamus development phenotype
GO:0021544PHENOTYPE	subpallium development phenotype
GO:0021545PHENOTYPE	cranial nerve development phenotype
GO:0021546PHENOTYPE	rhombomere development phenotype
GO:0021547PHENOTYPE	midbrain-hindbrain boundary initiation phenotype
GO:0021549PHENOTYPE	cerebellum development phenotype
GO:0021551PHENOTYPE	central nervous system morphogenesis phenotype
GO:0021552PHENOTYPE	midbrain-hindbrain boundary structural organization phenotype
GO:0021554PHENOTYPE	optic nerve development phenotype
GO:0021555PHENOTYPE	midbrain-hindbrain boundary morphogenesis phenotype
GO:0021557PHENOTYPE	oculomotor nerve development phenotype
GO:0021561PHENOTYPE	facial nerve development phenotype
GO:0021570PHENOTYPE	rhombomere 4 development phenotype
GO:0021571PHENOTYPE	rhombomere 5 development phenotype
GO:0021572PHENOTYPE	rhombomere 6 development phenotype
GO:0021575PHENOTYPE	hindbrain morphogenesis phenotype
GO:0021576PHENOTYPE	hindbrain formation phenotype
GO:0021577PHENOTYPE	hindbrain structural organization phenotype
GO:0021587PHENOTYPE	cerebellum morphogenesis phenotype
GO:0021588PHENOTYPE	cerebellum formation phenotype
GO:0021591PHENOTYPE	ventricular system development phenotype
GO:0021592PHENOTYPE	fourth ventricle development phenotype
GO:0021593PHENOTYPE	rhombomere morphogenesis phenotype
GO:0021594PHENOTYPE	rhombomere formation phenotype
GO:0021602PHENOTYPE	cranial nerve morphogenesis phenotype
GO:0021623PHENOTYPE	oculomotor nerve formation phenotype
GO:0021628PHENOTYPE	olfactory nerve formation phenotype
GO:0021634PHENOTYPE	optic nerve formation phenotype
GO:0021636PHENOTYPE	trigeminal nerve morphogenesis phenotype
GO:0021654PHENOTYPE	rhombomere boundary formation phenotype
GO:0021661PHENOTYPE	rhombomere 4 morphogenesis phenotype
GO:0021680PHENOTYPE	cerebellar Purkinje cell layer development phenotype
GO:0021692PHENOTYPE	cerebellar Purkinje cell layer morphogenesis phenotype
GO:0021702PHENOTYPE	cerebellar Purkinje cell differentiation phenotype
GO:0021703PHENOTYPE	locus ceruleus development phenotype
GO:0021707PHENOTYPE	cerebellar granule cell differentiation phenotype
GO:0021742PHENOTYPE	abducens nucleus development phenotype
GO:0021744PHENOTYPE	dorsal motor nucleus of vagus nerve development phenotype
GO:0021755PHENOTYPE	eurydendroid cell differentiation phenotype
GO:0021772PHENOTYPE	olfactory bulb development phenotype
GO:0021778PHENOTYPE	oligodendrocyte cell fate specification phenotype
GO:0021779PHENOTYPE	oligodendrocyte cell fate commitment phenotype
GO:0021782PHENOTYPE	glial cell development phenotype
GO:0021785PHENOTYPE	branchiomotor neuron axon guidance phenotype
GO:0021794PHENOTYPE	thalamus development phenotype
GO:0021797PHENOTYPE	forebrain anterior/posterior pattern specification phenotype
GO:0021798PHENOTYPE	forebrain dorsal/ventral pattern formation phenotype
GO:0021846PHENOTYPE	cell proliferation in forebrain phenotype
GO:0021854PHENOTYPE	hypothalamus development phenotype
GO:0021877PHENOTYPE	forebrain neuron fate commitment phenotype
GO:0021879PHENOTYPE	forebrain neuron differentiation phenotype
GO:0021884PHENOTYPE	forebrain neuron development phenotype
GO:0021885PHENOTYPE	forebrain cell migration phenotype
GO:0021898PHENOTYPE	commitment of multipotent stem cells to neuronal lineage in forebrain phenotype
GO:0021899PHENOTYPE	fibroblast growth factor receptor signaling pathway involved in forebrain neuron fate commitment phenotype
GO:0021903PHENOTYPE	rostrocaudal neural tube patterning phenotype
GO:0021906PHENOTYPE	hindbrain-spinal cord boundary formation phenotype
GO:0021910PHENOTYPE	smoothened signaling pathway involved in ventral spinal cord patterning phenotype
GO:0021915PHENOTYPE	neural tube development phenotype
GO:0021923PHENOTYPE	cell proliferation in hindbrain ventricular zone phenotype
GO:0021934PHENOTYPE	hindbrain tangential cell migration phenotype
GO:0021952PHENOTYPE	central nervous system projection neuron axonogenesis phenotype
GO:0021953PHENOTYPE	central nervous system neuron differentiation phenotype
GO:0021954PHENOTYPE	central nervous system neuron development phenotype
GO:0021955PHENOTYPE	central nervous system neuron axonogenesis phenotype
GO:0021960PHENOTYPE	anterior commissure morphogenesis phenotype
GO:0021961PHENOTYPE	posterior commissure morphogenesis phenotype
GO:0021979PHENOTYPE	hypothalamus cell differentiation phenotype
GO:0021982PHENOTYPE	pineal gland development phenotype
GO:0021983PHENOTYPE	pituitary gland development phenotype
GO:0021984PHENOTYPE	adenohypophysis development phenotype
GO:0021985PHENOTYPE	neurohypophysis development phenotype
GO:0021986PHENOTYPE	habenula development phenotype
GO:0021999PHENOTYPE	neural plate anterior/posterior regionalization phenotype
GO:0022008PHENOTYPE	neurogenesis phenotype
GO:0022010PHENOTYPE	central nervous system myelination phenotype
GO:0022011PHENOTYPE	myelination in peripheral nervous system phenotype
GO:0022027PHENOTYPE	interkinetic nuclear migration phenotype
GO:0022408PHENOTYPE	negative regulation of cell-cell adhesion phenotype
GO:0022604PHENOTYPE	regulation of cell morphogenesis phenotype
GO:0022857PHENOTYPE	transmembrane transporter activity phenotype
GO:0022904PHENOTYPE	respiratory electron transport chain phenotype
GO:0030030PHENOTYPE	cell projection organization phenotype
GO:0030031PHENOTYPE	cell projection assembly phenotype
GO:0030036PHENOTYPE	actin cytoskeleton organization phenotype
GO:0030041PHENOTYPE	actin filament polymerization phenotype
GO:0030097PHENOTYPE	hemopoiesis phenotype
GO:0030098PHENOTYPE	lymphocyte differentiation phenotype
GO:0030099PHENOTYPE	myeloid cell differentiation phenotype
GO:0030104PHENOTYPE	water homeostasis phenotype
GO:0030154PHENOTYPE	cell differentiation phenotype
GO:0030155PHENOTYPE	regulation of cell adhesion phenotype
GO:0030166PHENOTYPE	proteoglycan biosynthetic process phenotype
GO:0030168PHENOTYPE	platelet activation phenotype
GO:0030177PHENOTYPE	positive regulation of Wnt signaling pathway phenotype
GO:0030178PHENOTYPE	negative regulation of Wnt signaling pathway phenotype
GO:0030182PHENOTYPE	neuron differentiation phenotype
GO:0030183PHENOTYPE	B cell differentiation phenotype
GO:0030186PHENOTYPE	melatonin metabolic process phenotype
GO:0030193PHENOTYPE	regulation of blood coagulation phenotype
GO:0030198PHENOTYPE	extracellular matrix organization phenotype
GO:0030199PHENOTYPE	collagen fibril organization phenotype
GO:0030206PHENOTYPE	chondroitin sulfate biosynthetic process phenotype
GO:0030216PHENOTYPE	keratinocyte differentiation phenotype
GO:0030217PHENOTYPE	T cell differentiation phenotype
GO:0030218PHENOTYPE	erythrocyte differentiation phenotype
GO:0030220PHENOTYPE	platelet formation phenotype
GO:0030223PHENOTYPE	neutrophil differentiation phenotype
GO:0030224PHENOTYPE	monocyte differentiation phenotype
GO:0030225PHENOTYPE	macrophage differentiation phenotype
GO:0030237PHENOTYPE	female sex determination phenotype
GO:0030238PHENOTYPE	male sex determination phenotype
GO:0030239PHENOTYPE	myofibril assembly phenotype
GO:0030240PHENOTYPE	skeletal muscle thin filament assembly phenotype
GO:0030241PHENOTYPE	skeletal muscle myosin thick filament assembly phenotype
GO:0030278PHENOTYPE	regulation of ossification phenotype
GO:0030282PHENOTYPE	bone mineralization phenotype
GO:0030299PHENOTYPE	intestinal cholesterol absorption phenotype
GO:0030301PHENOTYPE	cholesterol transport phenotype
GO:0030317PHENOTYPE	sperm motility phenotype
GO:0030318PHENOTYPE	melanocyte differentiation phenotype
GO:0030325PHENOTYPE	adrenal gland development phenotype
GO:0030334PHENOTYPE	regulation of cell migration phenotype
GO:0030336PHENOTYPE	negative regulation of cell migration phenotype
GO:0030431PHENOTYPE	sleep phenotype
GO:0030432PHENOTYPE	peristalsis phenotype
GO:0030500PHENOTYPE	regulation of bone mineralization phenotype
GO:0030502PHENOTYPE	negative regulation of bone mineralization phenotype
GO:0030509PHENOTYPE	BMP signaling pathway phenotype
GO:0030510PHENOTYPE	regulation of BMP signaling pathway phenotype
GO:0030534PHENOTYPE	adult behavior phenotype
GO:0030576PHENOTYPE	Cajal body organization phenotype
GO:0030593PHENOTYPE	neutrophil chemotaxis phenotype
GO:0030595PHENOTYPE	leukocyte chemotaxis phenotype
GO:0030641PHENOTYPE	regulation of cellular pH phenotype
GO:0030728PHENOTYPE	ovulation phenotype
GO:0030851PHENOTYPE	granulocyte differentiation phenotype
GO:0030855PHENOTYPE	epithelial cell differentiation phenotype
GO:0030859PHENOTYPE	polarized epithelial cell differentiation phenotype
GO:0030866PHENOTYPE	cortical actin cytoskeleton organization phenotype
GO:0030878PHENOTYPE	thyroid gland development phenotype
GO:0030900PHENOTYPE	forebrain development phenotype
GO:0030901PHENOTYPE	midbrain development phenotype
GO:0030902PHENOTYPE	hindbrain development phenotype
GO:0030903PHENOTYPE	notochord development phenotype
GO:0030910PHENOTYPE	olfactory placode formation phenotype
GO:0030916PHENOTYPE	otic vesicle formation phenotype
GO:0030917PHENOTYPE	midbrain-hindbrain boundary development phenotype
GO:0030947PHENOTYPE	regulation of vascular endothelial growth factor receptor signaling pathway phenotype
GO:0030951PHENOTYPE	establishment or maintenance of microtubule cytoskeleton polarity phenotype
GO:0030953PHENOTYPE	astral microtubule organization phenotype
GO:0030968PHENOTYPE	endoplasmic reticulum unfolded protein response phenotype
GO:0031016PHENOTYPE	pancreas development phenotype
GO:0031017PHENOTYPE	exocrine pancreas development phenotype
GO:0031018PHENOTYPE	endocrine pancreas development phenotype
GO:0031032PHENOTYPE	actomyosin structure organization phenotype
GO:0031033PHENOTYPE	myosin filament organization phenotype
GO:0031054PHENOTYPE	pre-miRNA processing phenotype
GO:0031076PHENOTYPE	embryonic camera-type eye development phenotype
GO:0031099PHENOTYPE	regeneration phenotype
GO:0031100PHENOTYPE	organ regeneration phenotype
GO:0031101PHENOTYPE	fin regeneration phenotype
GO:0031102PHENOTYPE	neuron projection regeneration phenotype
GO:0031103PHENOTYPE	axon regeneration phenotype
GO:0031109PHENOTYPE	microtubule polymerization or depolymerization phenotype
GO:0031114PHENOTYPE	regulation of microtubule depolymerization phenotype
GO:0031122PHENOTYPE	cytoplasmic microtubule organization phenotype
GO:0031146PHENOTYPE	SCF-dependent proteasomal ubiquitin-dependent protein catabolic process phenotype
GO:0031175PHENOTYPE	neuron projection development phenotype
GO:0031290PHENOTYPE	retinal ganglion cell axon guidance phenotype
GO:0031413PHENOTYPE	regulation of buoyancy phenotype
GO:0031443PHENOTYPE	fast-twitch skeletal muscle fiber contraction phenotype
GO:0031444PHENOTYPE	slow-twitch skeletal muscle fiber contraction phenotype
GO:0031573PHENOTYPE	intra-S DNA damage checkpoint phenotype
GO:0031580PHENOTYPE	membrane raft distribution phenotype
GO:0031647PHENOTYPE	regulation of protein stability phenotype
GO:0031998PHENOTYPE	regulation of fatty acid beta-oxidation phenotype
GO:0032006PHENOTYPE	regulation of TOR signaling phenotype
GO:0032007PHENOTYPE	negative regulation of TOR signaling phenotype
GO:0032019PHENOTYPE	mitochondrial cloud phenotype
GO:0032060PHENOTYPE	bleb assembly phenotype
GO:0032077PHENOTYPE	positive regulation of deoxyribonuclease activity phenotype
GO:0032259PHENOTYPE	methylation phenotype
GO:0032287PHENOTYPE	peripheral nervous system myelin maintenance phenotype
GO:0032289PHENOTYPE	central nervous system myelin formation phenotype
GO:0032290PHENOTYPE	peripheral nervous system myelin formation phenotype
GO:0032330PHENOTYPE	regulation of chondrocyte differentiation phenotype
GO:0032400PHENOTYPE	melanosome localization phenotype
GO:0032402PHENOTYPE	melanosome transport phenotype
GO:0032434PHENOTYPE	regulation of proteasomal ubiquitin-dependent protein catabolic process phenotype
GO:0032438PHENOTYPE	melanosome organization phenotype
GO:0032456PHENOTYPE	endocytic recycling phenotype
GO:0032474PHENOTYPE	otolith morphogenesis phenotype
GO:0032475PHENOTYPE	otolith formation phenotype
GO:0032504PHENOTYPE	multicellular organism reproduction phenotype
GO:0032506PHENOTYPE	cytokinetic process phenotype
GO:0032525PHENOTYPE	somite rostral/caudal axis specification phenotype
GO:0032526PHENOTYPE	response to retinoic acid phenotype
GO:0032776PHENOTYPE	DNA methylation on cytosine phenotype
GO:0032782PHENOTYPE	bile acid secretion phenotype
GO:0032835PHENOTYPE	glomerulus development phenotype
GO:0032868PHENOTYPE	response to insulin phenotype
GO:0032880PHENOTYPE	regulation of protein localization phenotype
GO:0032922PHENOTYPE	circadian regulation of gene expression phenotype
GO:0032956PHENOTYPE	regulation of actin cytoskeleton organization phenotype
GO:0032964PHENOTYPE	collagen biosynthetic process phenotype
GO:0032965PHENOTYPE	regulation of collagen biosynthetic process phenotype
GO:0033077PHENOTYPE	T cell differentiation in thymus phenotype
GO:0033152PHENOTYPE	immunoglobulin V(D)J recombination phenotype
GO:0033153PHENOTYPE	T cell receptor V(D)J recombination phenotype
GO:0033278PHENOTYPE	cell proliferation in midbrain phenotype
GO:0033292PHENOTYPE	T-tubule organization phenotype
GO:0033333PHENOTYPE	fin development phenotype
GO:0033334PHENOTYPE	fin morphogenesis phenotype
GO:0033336PHENOTYPE	caudal fin development phenotype
GO:0033338PHENOTYPE	medial fin development phenotype
GO:0033339PHENOTYPE	pectoral fin development phenotype
GO:0033340PHENOTYPE	pelvic fin development phenotype
GO:0033504PHENOTYPE	floor plate development phenotype
GO:0033555PHENOTYPE	multicellular organismal response to stress phenotype
GO:0033564PHENOTYPE	anterior/posterior axon guidance phenotype
GO:0034101PHENOTYPE	erythrocyte homeostasis phenotype
GO:0034332PHENOTYPE	adherens junction organization phenotype
GO:0034334PHENOTYPE	adherens junction maintenance phenotype
GO:0034394PHENOTYPE	protein localization to cell surface phenotype
GO:0034505PHENOTYPE	tooth mineralization phenotype
GO:0034599PHENOTYPE	cellular response to oxidative stress phenotype
GO:0034613PHENOTYPE	cellular protein localization phenotype
GO:0034629PHENOTYPE	cellular protein complex localization phenotype
GO:0034644PHENOTYPE	cellular response to UV phenotype
GO:0034650PHENOTYPE	cortisol metabolic process phenotype
GO:0034651PHENOTYPE	cortisol biosynthetic process phenotype
GO:0034672PHENOTYPE	anterior/posterior pattern specification involved in pronephros development phenotype
GO:0034976PHENOTYPE	response to endoplasmic reticulum stress phenotype
GO:0035046PHENOTYPE	pronuclear migration phenotype
GO:0035050PHENOTYPE	embryonic heart tube development phenotype
GO:0035051PHENOTYPE	cardiocyte differentiation phenotype
GO:0035082PHENOTYPE	axoneme assembly phenotype
GO:0035088PHENOTYPE	establishment or maintenance of apical/basal cell polarity phenotype
GO:0035094PHENOTYPE	response to nicotine phenotype
GO:0035095PHENOTYPE	behavioral response to nicotine phenotype
GO:0035118PHENOTYPE	embryonic pectoral fin morphogenesis phenotype
GO:0035138PHENOTYPE	pectoral fin morphogenesis phenotype
GO:0035141PHENOTYPE	medial fin morphogenesis phenotype
GO:0035143PHENOTYPE	caudal fin morphogenesis phenotype
GO:0035148PHENOTYPE	tube formation phenotype
GO:0035162PHENOTYPE	embryonic hemopoiesis phenotype
GO:0035176PHENOTYPE	social behavior phenotype
GO:0035188PHENOTYPE	hatching phenotype
GO:0035195PHENOTYPE	gene silencing by miRNA phenotype
GO:0035196PHENOTYPE	production of miRNAs involved in gene silencing by miRNA phenotype
GO:0035264PHENOTYPE	multicellular organism growth phenotype
GO:0035265PHENOTYPE	organ growth phenotype
GO:0035270PHENOTYPE	endocrine system development phenotype
GO:0035282PHENOTYPE	segmentation phenotype
GO:0035284PHENOTYPE	brain segmentation phenotype
GO:0035315PHENOTYPE	hair cell differentiation phenotype
GO:0035418PHENOTYPE	protein localization to synapse phenotype
GO:0035462PHENOTYPE	determination of left/right asymmetry in diencephalon phenotype
GO:0035469PHENOTYPE	determination of pancreatic left/right asymmetry phenotype
GO:0035474PHENOTYPE	selective angioblast sprouting phenotype
GO:0035475PHENOTYPE	angioblast cell migration involved in selective angioblast sprouting phenotype
GO:0035476PHENOTYPE	angioblast cell migration phenotype
GO:0035479PHENOTYPE	angioblast cell migration from lateral mesoderm to midline phenotype
GO:0035622PHENOTYPE	intrahepatic bile duct development phenotype
GO:0035633PHENOTYPE	maintenance of blood-brain barrier phenotype
GO:0035641PHENOTYPE	locomotory exploration behavior phenotype
GO:0035675PHENOTYPE	neuromast hair cell development phenotype
GO:0035676PHENOTYPE	anterior lateral line neuromast hair cell development phenotype
GO:0035677PHENOTYPE	posterior lateral line neuromast hair cell development phenotype
GO:0035701PHENOTYPE	hematopoietic stem cell migration phenotype
GO:0035775PHENOTYPE	pronephric glomerulus morphogenesis phenotype
GO:0035776PHENOTYPE	pronephric proximal tubule development phenotype
GO:0035777PHENOTYPE	pronephric distal tubule development phenotype
GO:0035778PHENOTYPE	pronephric nephron tubule epithelial cell differentiation phenotype
GO:0035779PHENOTYPE	angioblast cell differentiation phenotype
GO:0035844PHENOTYPE	cloaca development phenotype
GO:0035845PHENOTYPE	photoreceptor cell outer segment organization phenotype
GO:0035850PHENOTYPE	epithelial cell differentiation involved in kidney development phenotype
GO:0035881PHENOTYPE	amacrine cell differentiation phenotype
GO:0035904PHENOTYPE	aorta development phenotype
GO:0035907PHENOTYPE	dorsal aorta development phenotype
GO:0035912PHENOTYPE	dorsal aorta morphogenesis phenotype
GO:0035914PHENOTYPE	skeletal muscle cell differentiation phenotype
GO:0035987PHENOTYPE	endodermal cell differentiation phenotype
GO:0035988PHENOTYPE	chondrocyte proliferation phenotype
GO:0035994PHENOTYPE	response to muscle stretch phenotype
GO:0036060PHENOTYPE	slit diaphragm assembly phenotype
GO:0036073PHENOTYPE	perichondral ossification phenotype
GO:0036099PHENOTYPE	female germ-line stem cell population maintenance phenotype
GO:0036135PHENOTYPE	Schwann cell migration phenotype
GO:0036158PHENOTYPE	outer dynein arm assembly phenotype
GO:0036159PHENOTYPE	inner dynein arm assembly phenotype
GO:0036268PHENOTYPE	swimming phenotype
GO:0036269PHENOTYPE	swimming behavior phenotype
GO:0036302PHENOTYPE	atrioventricular canal development phenotype
GO:0036303PHENOTYPE	lymph vessel morphogenesis phenotype
GO:0036342PHENOTYPE	post-anal tail morphogenesis phenotype
GO:0036367PHENOTYPE	light adaption phenotype
GO:0036368PHENOTYPE	cone photoresponse recovery phenotype
GO:0036372PHENOTYPE	opsin transport phenotype
GO:0036466PHENOTYPE	synaptic vesicle recycling via endosome phenotype
GO:0038092PHENOTYPE	nodal signaling pathway phenotype
GO:0039015PHENOTYPE	cell proliferation involved in pronephros development phenotype
GO:0039020PHENOTYPE	pronephric nephron tubule development phenotype
GO:0039021PHENOTYPE	pronephric glomerulus development phenotype
GO:0039022PHENOTYPE	pronephric duct development phenotype
GO:0039023PHENOTYPE	pronephric duct morphogenesis phenotype
GO:0040001PHENOTYPE	establishment of mitotic spindle localization phenotype
GO:0040011PHENOTYPE	locomotion phenotype
GO:0040016PHENOTYPE	embryonic cleavage phenotype
GO:0040036PHENOTYPE	regulation of fibroblast growth factor receptor signaling pathway phenotype
GO:0040040PHENOTYPE	thermosensory behavior phenotype
GO:0042044PHENOTYPE	fluid transport phenotype
GO:0042060PHENOTYPE	wound healing phenotype
GO:0042063PHENOTYPE	gliogenesis phenotype
GO:0042073PHENOTYPE	intraciliary transport phenotype
GO:0042074PHENOTYPE	cell migration involved in gastrulation phenotype
GO:0042098PHENOTYPE	T cell proliferation phenotype
GO:0042119PHENOTYPE	neutrophil activation phenotype
GO:0042127PHENOTYPE	regulation of cell proliferation phenotype
GO:0042166PHENOTYPE	acetylcholine binding phenotype
GO:0042168PHENOTYPE	heme metabolic process phenotype
GO:0042246PHENOTYPE	tissue regeneration phenotype
GO:0042254PHENOTYPE	ribosome biogenesis phenotype
GO:0042416PHENOTYPE	dopamine biosynthetic process phenotype
GO:0042423PHENOTYPE	catecholamine biosynthetic process phenotype
GO:0042427PHENOTYPE	serotonin biosynthetic process phenotype
GO:0042438PHENOTYPE	melanin biosynthetic process phenotype
GO:0042461PHENOTYPE	photoreceptor cell development phenotype
GO:0042462PHENOTYPE	eye photoreceptor cell development phenotype
GO:0042471PHENOTYPE	ear morphogenesis phenotype
GO:0042472PHENOTYPE	inner ear morphogenesis phenotype
GO:0042476PHENOTYPE	odontogenesis phenotype
GO:0042491PHENOTYPE	auditory receptor cell differentiation phenotype
GO:0042509PHENOTYPE	regulation of tyrosine phosphorylation of STAT protein phenotype
GO:0042541PHENOTYPE	hemoglobin biosynthetic process phenotype
GO:0042552PHENOTYPE	myelination phenotype
GO:0042572PHENOTYPE	retinol metabolic process phenotype
GO:0042573PHENOTYPE	retinoic acid metabolic process phenotype
GO:0042577PHENOTYPE	lipid phosphatase activity phenotype
GO:0042592PHENOTYPE	homeostatic process phenotype
GO:0042593PHENOTYPE	glucose homeostasis phenotype
GO:0042632PHENOTYPE	cholesterol homeostasis phenotype
GO:0042663PHENOTYPE	regulation of endodermal cell fate specification phenotype
GO:0042670PHENOTYPE	retinal cone cell differentiation phenotype
GO:0042692PHENOTYPE	muscle cell differentiation phenotype
GO:0042693PHENOTYPE	muscle cell fate commitment phenotype
GO:0042694PHENOTYPE	muscle cell fate specification phenotype
GO:0042742PHENOTYPE	defense response to bacterium phenotype
GO:0042752PHENOTYPE	regulation of circadian rhythm phenotype
GO:0042769PHENOTYPE	DNA damage response, detection of DNA damage phenotype
GO:0042771PHENOTYPE	intrinsic apoptotic signaling pathway in response to DNA damage by p53 class mediator phenotype
GO:0042981PHENOTYPE	regulation of apoptotic process phenotype
GO:0043005PHENOTYPE	neuron projection phenotype
GO:0043009PHENOTYPE	chordate embryonic development phenotype
GO:0043010PHENOTYPE	camera-type eye development phenotype
GO:0043049PHENOTYPE	otic placode formation phenotype
GO:0043060PHENOTYPE	meiotic metaphase I plate congression phenotype
GO:0043065PHENOTYPE	positive regulation of apoptotic process phenotype
GO:0043066PHENOTYPE	negative regulation of apoptotic process phenotype
GO:0043113PHENOTYPE	receptor clustering phenotype
GO:0043153PHENOTYPE	entrainment of circadian clock by photoperiod phenotype
GO:0043161PHENOTYPE	proteasome-mediated ubiquitin-dependent protein catabolic process phenotype
GO:0043249PHENOTYPE	erythrocyte maturation phenotype
GO:0043277PHENOTYPE	apoptotic cell clearance phenotype
GO:0043280PHENOTYPE	positive regulation of cysteine-type endopeptidase activity involved in apoptotic process phenotype
GO:0043281PHENOTYPE	regulation of cysteine-type endopeptidase activity involved in apoptotic process phenotype
GO:0043282PHENOTYPE	pharyngeal muscle development phenotype
GO:0043296PHENOTYPE	apical junction complex phenotype
GO:0043362PHENOTYPE	nucleate erythrocyte maturation phenotype
GO:0043363PHENOTYPE	nucleate erythrocyte differentiation phenotype
GO:0043473PHENOTYPE	pigmentation phenotype
GO:0043476PHENOTYPE	pigment accumulation phenotype
GO:0043484PHENOTYPE	regulation of RNA splicing phenotype
GO:0043487PHENOTYPE	regulation of RNA stability phenotype
GO:0043523PHENOTYPE	regulation of neuron apoptotic process phenotype
GO:0043534PHENOTYPE	blood vessel endothelial cell migration phenotype
GO:0043535PHENOTYPE	regulation of blood vessel endothelial cell migration phenotype
GO:0043570PHENOTYPE	maintenance of DNA repeat elements phenotype
GO:0043576PHENOTYPE	regulation of respiratory gaseous exchange phenotype
GO:0043583PHENOTYPE	ear development phenotype
GO:0043584PHENOTYPE	nose development phenotype
GO:0043588PHENOTYPE	skin development phenotype
GO:0043589PHENOTYPE	skin morphogenesis phenotype
GO:0043652PHENOTYPE	engulfment of apoptotic cell phenotype
GO:0043695PHENOTYPE	detection of pheromone phenotype
GO:0043697PHENOTYPE	cell dedifferentiation phenotype
GO:0043931PHENOTYPE	ossification involved in bone maturation phenotype
GO:0043985PHENOTYPE	histone H4-R3 methylation phenotype
GO:0044030PHENOTYPE	regulation of DNA methylation phenotype
GO:0044241PHENOTYPE	lipid digestion phenotype
GO:0044255PHENOTYPE	cellular lipid metabolic process phenotype
GO:0044332PHENOTYPE	Wnt signaling pathway involved in dorsal/ventral axis specification phenotype
GO:0044342PHENOTYPE	type B pancreatic cell proliferation phenotype
GO:0044381PHENOTYPE	glucose import in response to insulin stimulus phenotype
GO:0044458PHENOTYPE	motile cilium assembly phenotype
GO:0044772PHENOTYPE	mitotic cell cycle phase transition phenotype
GO:0044782PHENOTYPE	cilium organization phenotype
GO:0045002PHENOTYPE	double-strand break repair via single-strand annealing phenotype
GO:0045087PHENOTYPE	innate immune response phenotype
GO:0045088PHENOTYPE	regulation of innate immune response phenotype
GO:0045111PHENOTYPE	intermediate filament cytoskeleton phenotype
GO:0045132PHENOTYPE	meiotic chromosome segregation phenotype
GO:0045165PHENOTYPE	cell fate commitment phenotype
GO:0045176PHENOTYPE	apical protein localization phenotype
GO:0045187PHENOTYPE	regulation of circadian sleep/wake cycle, sleep phenotype
GO:0045197PHENOTYPE	establishment or maintenance of epithelial cell apical/basal polarity phenotype
GO:0045198PHENOTYPE	establishment of epithelial cell apical/basal polarity phenotype
GO:0045199PHENOTYPE	maintenance of epithelial cell apical/basal polarity phenotype
GO:0045214PHENOTYPE	sarcomere organization phenotype
GO:0045216PHENOTYPE	cell-cell junction organization phenotype
GO:0045217PHENOTYPE	cell-cell junction maintenance phenotype
GO:0045299PHENOTYPE	otolith mineralization phenotype
GO:0045333PHENOTYPE	cellular respiration phenotype
GO:0045444PHENOTYPE	fat cell differentiation phenotype
GO:0045445PHENOTYPE	myoblast differentiation phenotype
GO:0045471PHENOTYPE	response to ethanol phenotype
GO:0045475PHENOTYPE	locomotor rhythm phenotype
GO:0045494PHENOTYPE	photoreceptor cell maintenance phenotype
GO:0045620PHENOTYPE	negative regulation of lymphocyte differentiation phenotype
GO:0045637PHENOTYPE	regulation of myeloid cell differentiation phenotype
GO:0045664PHENOTYPE	regulation of neuron differentiation phenotype
GO:0045682PHENOTYPE	regulation of epidermis development phenotype
GO:0045730PHENOTYPE	respiratory burst phenotype
GO:0045746PHENOTYPE	negative regulation of Notch signaling pathway phenotype
GO:0045765PHENOTYPE	regulation of angiogenesis phenotype
GO:0045766PHENOTYPE	positive regulation of angiogenesis phenotype
GO:0045786PHENOTYPE	negative regulation of cell cycle phenotype
GO:0045787PHENOTYPE	positive regulation of cell cycle phenotype
GO:0045839PHENOTYPE	negative regulation of mitotic nuclear division phenotype
GO:0045859PHENOTYPE	regulation of protein kinase activity phenotype
GO:0045879PHENOTYPE	negative regulation of smoothened signaling pathway phenotype
GO:0045892PHENOTYPE	negative regulation of transcription, DNA-templated phenotype
GO:0045893PHENOTYPE	positive regulation of transcription, DNA-templated phenotype
GO:0045930PHENOTYPE	negative regulation of mitotic cell cycle phenotype
GO:0045932PHENOTYPE	negative regulation of muscle contraction phenotype
GO:0046154PHENOTYPE	rhodopsin metabolic process phenotype
GO:0046323PHENOTYPE	glucose import phenotype
GO:0046328PHENOTYPE	regulation of JNK cascade phenotype
GO:0046530PHENOTYPE	photoreceptor cell differentiation phenotype
GO:0046548PHENOTYPE	retinal rod cell development phenotype
GO:0046549PHENOTYPE	retinal cone cell development phenotype
GO:0046619PHENOTYPE	optic placode formation involved in camera-type eye formation phenotype
GO:0046660PHENOTYPE	female sex differentiation phenotype
GO:0046716PHENOTYPE	muscle cell cellular homeostasis phenotype
GO:0046777PHENOTYPE	protein autophosphorylation phenotype
GO:0046844PHENOTYPE	micropyle formation phenotype
GO:0046847PHENOTYPE	filopodium assembly phenotype
GO:0046849PHENOTYPE	bone remodeling phenotype
GO:0046850PHENOTYPE	regulation of bone remodeling phenotype
GO:0046856PHENOTYPE	phosphatidylinositol dephosphorylation phenotype
GO:0046907PHENOTYPE	intracellular transport phenotype
GO:0046921PHENOTYPE	alpha-(1->6)-fucosyltransferase activity phenotype
GO:0046959PHENOTYPE	habituation phenotype
GO:0046974PHENOTYPE	histone methyltransferase activity (H3-K9 specific) phenotype
GO:0047173PHENOTYPE	phosphatidylcholine-retinol O-acyltransferase activity phenotype
GO:0048048PHENOTYPE	embryonic eye morphogenesis phenotype
GO:0048066PHENOTYPE	developmental pigmentation phenotype
GO:0048069PHENOTYPE	eye pigmentation phenotype
GO:0048193PHENOTYPE	Golgi vesicle transport phenotype
GO:0048246PHENOTYPE	macrophage chemotaxis phenotype
GO:0048255PHENOTYPE	mRNA stabilization phenotype
GO:0048264PHENOTYPE	determination of ventral identity phenotype
GO:0048318PHENOTYPE	axial mesoderm development phenotype
GO:0048319PHENOTYPE	axial mesoderm morphogenesis phenotype
GO:0048320PHENOTYPE	axial mesoderm formation phenotype
GO:0048327PHENOTYPE	axial mesodermal cell fate specification phenotype
GO:0048331PHENOTYPE	axial mesoderm structural organization phenotype
GO:0048332PHENOTYPE	mesoderm morphogenesis phenotype
GO:0048339PHENOTYPE	paraxial mesoderm development phenotype
GO:0048342PHENOTYPE	paraxial mesodermal cell differentiation phenotype
GO:0048348PHENOTYPE	paraxial mesodermal cell fate specification phenotype
GO:0048368PHENOTYPE	lateral mesoderm development phenotype
GO:0048382PHENOTYPE	mesendoderm development phenotype
GO:0048384PHENOTYPE	retinoic acid receptor signaling pathway phenotype
GO:0048389PHENOTYPE	intermediate mesoderm development phenotype
GO:0048469PHENOTYPE	cell maturation phenotype
GO:0048484PHENOTYPE	enteric nervous system development phenotype
GO:0048485PHENOTYPE	sympathetic nervous system development phenotype
GO:0048512PHENOTYPE	circadian behavior phenotype
GO:0048513PHENOTYPE	organ development phenotype
GO:0048514PHENOTYPE	blood vessel morphogenesis phenotype
GO:0048534PHENOTYPE	hematopoietic or lymphoid organ development phenotype
GO:0048538PHENOTYPE	thymus development phenotype
GO:0048546PHENOTYPE	digestive tract morphogenesis phenotype
GO:0048557PHENOTYPE	embryonic digestive tract morphogenesis phenotype
GO:0048562PHENOTYPE	embryonic organ morphogenesis phenotype
GO:0048565PHENOTYPE	digestive tract development phenotype
GO:0048566PHENOTYPE	embryonic digestive tract development phenotype
GO:0048568PHENOTYPE	embryonic organ development phenotype
GO:0048570PHENOTYPE	notochord morphogenesis phenotype
GO:0048589PHENOTYPE	developmental growth phenotype
GO:0048592PHENOTYPE	eye morphogenesis phenotype
GO:0048593PHENOTYPE	camera-type eye morphogenesis phenotype
GO:0048596PHENOTYPE	embryonic camera-type eye morphogenesis phenotype
GO:0048598PHENOTYPE	embryonic morphogenesis phenotype
GO:0048599PHENOTYPE	oocyte development phenotype
GO:0048644PHENOTYPE	muscle organ morphogenesis phenotype
GO:0048663PHENOTYPE	neuron fate commitment phenotype
GO:0048665PHENOTYPE	neuron fate specification phenotype
GO:0048666PHENOTYPE	neuron development phenotype
GO:0048668PHENOTYPE	collateral sprouting phenotype
GO:0048670PHENOTYPE	regulation of collateral sprouting phenotype
GO:0048675PHENOTYPE	axon extension phenotype
GO:0048677PHENOTYPE	axon extension involved in regeneration phenotype
GO:0048696PHENOTYPE	regulation of collateral sprouting in absence of injury phenotype
GO:0048699PHENOTYPE	generation of neurons phenotype
GO:0048701PHENOTYPE	embryonic cranial skeleton morphogenesis phenotype
GO:0048702PHENOTYPE	embryonic neurocranium morphogenesis phenotype
GO:0048703PHENOTYPE	embryonic viscerocranium morphogenesis phenotype
GO:0048705PHENOTYPE	skeletal system morphogenesis phenotype
GO:0048706PHENOTYPE	embryonic skeletal system development phenotype
GO:0048708PHENOTYPE	astrocyte differentiation phenotype
GO:0048709PHENOTYPE	oligodendrocyte differentiation phenotype
GO:0048730PHENOTYPE	epidermis morphogenesis phenotype
GO:0048738PHENOTYPE	cardiac muscle tissue development phenotype
GO:0048741PHENOTYPE	skeletal muscle fiber development phenotype
GO:0048745PHENOTYPE	smooth muscle tissue development phenotype
GO:0048747PHENOTYPE	muscle fiber development phenotype
GO:0048752PHENOTYPE	semicircular canal morphogenesis phenotype
GO:0048753PHENOTYPE	pigment granule organization phenotype
GO:0048755PHENOTYPE	branching morphogenesis of a nerve phenotype
GO:0048757PHENOTYPE	pigment granule maturation phenotype
GO:0048769PHENOTYPE	sarcomerogenesis phenotype
GO:0048785PHENOTYPE	hatching gland development phenotype
GO:0048793PHENOTYPE	pronephros development phenotype
GO:0048794PHENOTYPE	swim bladder development phenotype
GO:0048795PHENOTYPE	swim bladder morphogenesis phenotype
GO:0048797PHENOTYPE	swim bladder formation phenotype
GO:0048798PHENOTYPE	swim bladder inflation phenotype
GO:0048812PHENOTYPE	neuron projection morphogenesis phenotype
GO:0048813PHENOTYPE	dendrite morphogenesis phenotype
GO:0048814PHENOTYPE	regulation of dendrite morphogenesis phenotype
GO:0048821PHENOTYPE	erythrocyte development phenotype
GO:0048823PHENOTYPE	nucleate erythrocyte development phenotype
GO:0048839PHENOTYPE	inner ear development phenotype
GO:0048840PHENOTYPE	otolith development phenotype
GO:0048844PHENOTYPE	artery morphogenesis phenotype
GO:0048845PHENOTYPE	venous blood vessel morphogenesis phenotype
GO:0048846PHENOTYPE	axon extension involved in axon guidance phenotype
GO:0048853PHENOTYPE	forebrain morphogenesis phenotype
GO:0048854PHENOTYPE	brain morphogenesis phenotype
GO:0048855PHENOTYPE	adenohypophysis morphogenesis phenotype
GO:0048859PHENOTYPE	formation of anatomical boundary phenotype
GO:0048865PHENOTYPE	stem cell fate commitment phenotype
GO:0048870PHENOTYPE	cell motility phenotype
GO:0048871PHENOTYPE	multicellular organismal homeostasis phenotype
GO:0048873PHENOTYPE	homeostasis of number of cells within a tissue phenotype
GO:0048881PHENOTYPE	mechanosensory lateral line system development phenotype
GO:0048882PHENOTYPE	lateral line development phenotype
GO:0048883PHENOTYPE	neuromast primordium migration phenotype
GO:0048884PHENOTYPE	neuromast development phenotype
GO:0048885PHENOTYPE	neuromast deposition phenotype
GO:0048886PHENOTYPE	neuromast hair cell differentiation phenotype
GO:0048892PHENOTYPE	lateral line nerve development phenotype
GO:0048899PHENOTYPE	anterior lateral line development phenotype
GO:0048901PHENOTYPE	anterior lateral line neuromast development phenotype
GO:0048903PHENOTYPE	anterior lateral line neuromast hair cell differentiation phenotype
GO:0048909PHENOTYPE	anterior lateral line nerve development phenotype
GO:0048914PHENOTYPE	myelination of anterior lateral line nerve axons phenotype
GO:0048915PHENOTYPE	posterior lateral line system development phenotype
GO:0048916PHENOTYPE	posterior lateral line development phenotype
GO:0048918PHENOTYPE	posterior lateral line nerve development phenotype
GO:0048919PHENOTYPE	posterior lateral line neuromast development phenotype
GO:0048920PHENOTYPE	posterior lateral line neuromast primordium migration phenotype
GO:0048922PHENOTYPE	posterior lateral line neuromast deposition phenotype
GO:0048923PHENOTYPE	posterior lateral line neuromast hair cell differentiation phenotype
GO:0048925PHENOTYPE	lateral line system development phenotype
GO:0048929PHENOTYPE	efferent axon development in posterior lateral line nerve phenotype
GO:0048932PHENOTYPE	myelination of posterior lateral line nerve axons phenotype
GO:0048933PHENOTYPE	afferent axon development in posterior lateral line nerve phenotype
GO:0048935PHENOTYPE	peripheral nervous system neuron development phenotype
GO:0048936PHENOTYPE	peripheral nervous system neuron axonogenesis phenotype
GO:0048937PHENOTYPE	lateral line nerve glial cell development phenotype
GO:0050650PHENOTYPE	chondroitin sulfate proteoglycan biosynthetic process phenotype
GO:0050665PHENOTYPE	hydrogen peroxide biosynthetic process phenotype
GO:0050670PHENOTYPE	regulation of lymphocyte proliferation phenotype
GO:0050673PHENOTYPE	epithelial cell proliferation phenotype
GO:0050678PHENOTYPE	regulation of epithelial cell proliferation phenotype
GO:0050680PHENOTYPE	negative regulation of epithelial cell proliferation phenotype
GO:0050688PHENOTYPE	regulation of defense response to virus phenotype
GO:0050727PHENOTYPE	regulation of inflammatory response phenotype
GO:0050728PHENOTYPE	negative regulation of inflammatory response phenotype
GO:0050767PHENOTYPE	regulation of neurogenesis phenotype
GO:0050768PHENOTYPE	negative regulation of neurogenesis phenotype
GO:0050801PHENOTYPE	ion homeostasis phenotype
GO:0050803PHENOTYPE	regulation of synapse structure or activity phenotype
GO:0050808PHENOTYPE	synapse organization phenotype
GO:0050832PHENOTYPE	defense response to fungus phenotype
GO:0050848PHENOTYPE	regulation of calcium-mediated signaling phenotype
GO:0050881PHENOTYPE	musculoskeletal movement phenotype
GO:0050885PHENOTYPE	neuromuscular process controlling balance phenotype
GO:0050890PHENOTYPE	cognition phenotype
GO:0050900PHENOTYPE	leukocyte migration phenotype
GO:0050905PHENOTYPE	neuromuscular process phenotype
GO:0050908PHENOTYPE	detection of light stimulus involved in visual perception phenotype
GO:0050910PHENOTYPE	detection of mechanical stimulus involved in sensory perception of sound phenotype
GO:0050931PHENOTYPE	pigment cell differentiation phenotype
GO:0050935PHENOTYPE	iridophore differentiation phenotype
GO:0050936PHENOTYPE	xanthophore differentiation phenotype
GO:0050953PHENOTYPE	sensory perception of light stimulus phenotype
GO:0050957PHENOTYPE	equilibrioception phenotype
GO:0050974PHENOTYPE	detection of mechanical stimulus involved in sensory perception phenotype
GO:0050976PHENOTYPE	detection of mechanical stimulus involved in sensory perception of touch phenotype
GO:0050996PHENOTYPE	positive regulation of lipid catabolic process phenotype
GO:0051026PHENOTYPE	chiasma assembly phenotype
GO:0051124PHENOTYPE	synaptic growth at neuromuscular junction phenotype
GO:0051146PHENOTYPE	striated muscle cell differentiation phenotype
GO:0051209PHENOTYPE	release of sequestered calcium ion into cytosol phenotype
GO:0051216PHENOTYPE	cartilage development phenotype
GO:0051225PHENOTYPE	spindle assembly phenotype
GO:0051236PHENOTYPE	establishment of RNA localization phenotype
GO:0051276PHENOTYPE	chromosome organization phenotype
GO:0051298PHENOTYPE	centrosome duplication phenotype
GO:0051301PHENOTYPE	cell division phenotype
GO:0051302PHENOTYPE	regulation of cell division phenotype
GO:0051311PHENOTYPE	meiotic metaphase plate congression phenotype
GO:0051402PHENOTYPE	neuron apoptotic process phenotype
GO:0051445PHENOTYPE	regulation of meiotic cell cycle phenotype
GO:0051453PHENOTYPE	regulation of intracellular pH phenotype
GO:0051480PHENOTYPE	cytosolic calcium ion homeostasis phenotype
GO:0051493PHENOTYPE	regulation of cytoskeleton organization phenotype
GO:0051560PHENOTYPE	mitochondrial calcium ion homeostasis phenotype
GO:0051567PHENOTYPE	histone H3-K9 methylation phenotype
GO:0051597PHENOTYPE	response to methylmercury phenotype
GO:0051607PHENOTYPE	defense response to virus phenotype
GO:0051648PHENOTYPE	vesicle localization phenotype
GO:0051726PHENOTYPE	regulation of cell cycle phenotype
GO:0051782PHENOTYPE	negative regulation of cell division phenotype
GO:0051875PHENOTYPE	pigment granule localization phenotype
GO:0051876PHENOTYPE	pigment granule dispersal phenotype
GO:0051877PHENOTYPE	pigment granule aggregation in cell center phenotype
GO:0051923PHENOTYPE	sulfation phenotype
GO:0051960PHENOTYPE	regulation of nervous system development phenotype
GO:0051966PHENOTYPE	regulation of synaptic transmission, glutamatergic phenotype
GO:0051969PHENOTYPE	regulation of transmission of nerve impulse phenotype
GO:0055001PHENOTYPE	muscle cell development phenotype
GO:0055002PHENOTYPE	striated muscle cell development phenotype
GO:0055003PHENOTYPE	cardiac myofibril assembly phenotype
GO:0055005PHENOTYPE	ventricular cardiac myofibril assembly phenotype
GO:0055007PHENOTYPE	cardiac muscle cell differentiation phenotype
GO:0055008PHENOTYPE	cardiac muscle tissue morphogenesis phenotype
GO:0055010PHENOTYPE	ventricular cardiac muscle tissue morphogenesis phenotype
GO:0055011PHENOTYPE	atrial cardiac muscle cell differentiation phenotype
GO:0055012PHENOTYPE	ventricular cardiac muscle cell differentiation phenotype
GO:0055013PHENOTYPE	cardiac muscle cell development phenotype
GO:0055015PHENOTYPE	ventricular cardiac muscle cell development phenotype
GO:0055016PHENOTYPE	hypochord development phenotype
GO:0055062PHENOTYPE	phosphate ion homeostasis phenotype
GO:0055064PHENOTYPE	chloride ion homeostasis phenotype
GO:0055069PHENOTYPE	zinc ion homeostasis phenotype
GO:0055072PHENOTYPE	iron ion homeostasis phenotype
GO:0055074PHENOTYPE	calcium ion homeostasis phenotype
GO:0055077PHENOTYPE	gap junction hemi-channel activity phenotype
GO:0055078PHENOTYPE	sodium ion homeostasis phenotype
GO:0055088PHENOTYPE	lipid homeostasis phenotype
GO:0055109PHENOTYPE	invagination involved in gastrulation with mouth forming second phenotype
GO:0055113PHENOTYPE	epiboly involved in gastrulation with mouth forming second phenotype
GO:0055117PHENOTYPE	regulation of cardiac muscle contraction phenotype
GO:0055123PHENOTYPE	digestive system development phenotype
GO:0060005PHENOTYPE	vestibular reflex phenotype
GO:0060021PHENOTYPE	palate development phenotype
GO:0060026PHENOTYPE	convergent extension phenotype
GO:0060027PHENOTYPE	convergent extension involved in gastrulation phenotype
GO:0060028PHENOTYPE	convergent extension involved in axis elongation phenotype
GO:0060030PHENOTYPE	dorsal convergence phenotype
GO:0060031PHENOTYPE	mediolateral intercalation phenotype
GO:0060034PHENOTYPE	notochord cell differentiation phenotype
GO:0060035PHENOTYPE	notochord cell development phenotype
GO:0060036PHENOTYPE	notochord cell vacuolation phenotype
GO:0060037PHENOTYPE	pharyngeal system development phenotype
GO:0060038PHENOTYPE	cardiac muscle cell proliferation phenotype
GO:0060041PHENOTYPE	retina development in camera-type eye phenotype
GO:0060042PHENOTYPE	retina morphogenesis in camera-type eye phenotype
GO:0060047PHENOTYPE	heart contraction phenotype
GO:0060048PHENOTYPE	cardiac muscle contraction phenotype
GO:0060055PHENOTYPE	angiogenesis involved in wound healing phenotype
GO:0060059PHENOTYPE	embryonic retina morphogenesis in camera-type eye phenotype
GO:0060070PHENOTYPE	canonical Wnt signaling pathway phenotype
GO:0060074PHENOTYPE	synapse maturation phenotype
GO:0060080PHENOTYPE	inhibitory postsynaptic potential phenotype
GO:0060092PHENOTYPE	regulation of synaptic transmission, glycinergic phenotype
GO:0060097PHENOTYPE	cytoskeletal rearrangement involved in phagocytosis, engulfment phenotype
GO:0060113PHENOTYPE	inner ear receptor cell differentiation phenotype
GO:0060117PHENOTYPE	auditory receptor cell development phenotype
GO:0060118PHENOTYPE	vestibular receptor cell development phenotype
GO:0060119PHENOTYPE	inner ear receptor cell development phenotype
GO:0060122PHENOTYPE	inner ear receptor stereocilium organization phenotype
GO:0060128PHENOTYPE	corticotropin hormone secreting cell differentiation phenotype
GO:0060173PHENOTYPE	limb development phenotype
GO:0060215PHENOTYPE	primitive hemopoiesis phenotype
GO:0060216PHENOTYPE	definitive hemopoiesis phenotype
GO:0060217PHENOTYPE	hemangioblast cell differentiation phenotype
GO:0060218PHENOTYPE	hematopoietic stem cell differentiation phenotype
GO:0060219PHENOTYPE	camera-type eye photoreceptor cell differentiation phenotype
GO:0060221PHENOTYPE	retinal rod cell differentiation phenotype
GO:0060242PHENOTYPE	contact inhibition phenotype
GO:0060249PHENOTYPE	anatomical structure homeostasis phenotype
GO:0060271PHENOTYPE	cilium morphogenesis phenotype
GO:0060272PHENOTYPE	embryonic skeletal joint morphogenesis phenotype
GO:0060285PHENOTYPE	cilium-dependent cell motility phenotype
GO:0060287PHENOTYPE	epithelial cilium movement involved in determination of left/right asymmetry phenotype
GO:0060293PHENOTYPE	germ plasm phenotype
GO:0060294PHENOTYPE	cilium movement involved in cell motility phenotype
GO:0060307PHENOTYPE	regulation of ventricular cardiac muscle cell membrane repolarization phenotype
GO:0060312PHENOTYPE	regulation of blood vessel remodeling phenotype
GO:0060319PHENOTYPE	primitive erythrocyte differentiation phenotype
GO:0060322PHENOTYPE	head development phenotype
GO:0060323PHENOTYPE	head morphogenesis phenotype
GO:0060324PHENOTYPE	face development phenotype
GO:0060325PHENOTYPE	face morphogenesis phenotype
GO:0060347PHENOTYPE	heart trabecula formation phenotype
GO:0060348PHENOTYPE	bone development phenotype
GO:0060349PHENOTYPE	bone morphogenesis phenotype
GO:0060351PHENOTYPE	cartilage development involved in endochondral bone morphogenesis phenotype
GO:0060363PHENOTYPE	cranial suture morphogenesis phenotype
GO:0060385PHENOTYPE	axonogenesis involved in innervation phenotype
GO:0060386PHENOTYPE	synapse assembly involved in innervation phenotype
GO:0060415PHENOTYPE	muscle tissue morphogenesis phenotype
GO:0060429PHENOTYPE	epithelium development phenotype
GO:0060471PHENOTYPE	cortical granule exocytosis phenotype
GO:0060491PHENOTYPE	regulation of cell projection assembly phenotype
GO:0060536PHENOTYPE	cartilage morphogenesis phenotype
GO:0060537PHENOTYPE	muscle tissue development phenotype
GO:0060538PHENOTYPE	skeletal muscle organ development phenotype
GO:0060541PHENOTYPE	respiratory system development phenotype
GO:0060548PHENOTYPE	negative regulation of cell death phenotype
GO:0060575PHENOTYPE	intestinal epithelial cell differentiation phenotype
GO:0060612PHENOTYPE	adipose tissue development phenotype
GO:0060729PHENOTYPE	intestinal epithelial structure maintenance phenotype
GO:0060784PHENOTYPE	regulation of cell proliferation involved in tissue homeostasis phenotype
GO:0060785PHENOTYPE	regulation of apoptosis involved in tissue homeostasis phenotype
GO:0060803PHENOTYPE	BMP signaling pathway involved in mesodermal cell fate specification phenotype
GO:0060809PHENOTYPE	mesodermal to mesenchymal transition involved in gastrulation phenotype
GO:0060823PHENOTYPE	canonical Wnt signaling pathway involved in neural plate anterior/posterior pattern formation phenotype
GO:0060828PHENOTYPE	regulation of canonical Wnt signaling pathway phenotype
GO:0060831PHENOTYPE	smoothened signaling pathway involved in dorsal/ventral neural tube patterning phenotype
GO:0060832PHENOTYPE	oocyte animal/vegetal axis specification phenotype
GO:0060836PHENOTYPE	lymphatic endothelial cell differentiation phenotype
GO:0060837PHENOTYPE	blood vessel endothelial cell differentiation phenotype
GO:0060840PHENOTYPE	artery development phenotype
GO:0060841PHENOTYPE	venous blood vessel development phenotype
GO:0060847PHENOTYPE	endothelial cell fate specification phenotype
GO:0060854PHENOTYPE	patterning of lymph vessels phenotype
GO:0060855PHENOTYPE	venous endothelial cell migration involved in lymph vessel development phenotype
GO:0060872PHENOTYPE	semicircular canal development phenotype
GO:0060875PHENOTYPE	lateral semicircular canal development phenotype
GO:0060876PHENOTYPE	semicircular canal formation phenotype
GO:0060879PHENOTYPE	semicircular canal fusion phenotype
GO:0060896PHENOTYPE	neural plate pattern specification phenotype
GO:0060898PHENOTYPE	eye field cell fate commitment involved in camera-type eye formation phenotype
GO:0060900PHENOTYPE	embryonic camera-type eye formation phenotype
GO:0060914PHENOTYPE	heart formation phenotype
GO:0060956PHENOTYPE	endocardial cell differentiation phenotype
GO:0060964PHENOTYPE	regulation of gene silencing by miRNA phenotype
GO:0060968PHENOTYPE	regulation of gene silencing phenotype
GO:0060971PHENOTYPE	embryonic heart tube left/right pattern formation phenotype
GO:0060972PHENOTYPE	left/right pattern formation phenotype
GO:0060973PHENOTYPE	cell migration involved in heart development phenotype
GO:0060974PHENOTYPE	cell migration involved in heart formation phenotype
GO:0060975PHENOTYPE	cardioblast migration to the midline involved in heart field formation phenotype
GO:0061007PHENOTYPE	hepaticobiliary system process phenotype
GO:0061008PHENOTYPE	hepaticobiliary system development phenotype
GO:0061009PHENOTYPE	common bile duct development phenotype
GO:0061010PHENOTYPE	gall bladder development phenotype
GO:0061011PHENOTYPE	hepatic duct development phenotype
GO:0061017PHENOTYPE	hepatoblast differentiation phenotype
GO:0061026PHENOTYPE	cardiac muscle tissue regeneration phenotype
GO:0061028PHENOTYPE	establishment of endothelial barrier phenotype
GO:0061031PHENOTYPE	endodermal digestive tract morphogenesis phenotype
GO:0061035PHENOTYPE	regulation of cartilage development phenotype
GO:0061041PHENOTYPE	regulation of wound healing phenotype
GO:0061053PHENOTYPE	somite development phenotype
GO:0061055PHENOTYPE	myotome development phenotype
GO:0061056PHENOTYPE	sclerotome development phenotype
GO:0061061PHENOTYPE	muscle structure development phenotype
GO:0061074PHENOTYPE	regulation of neural retina development phenotype
GO:0061195PHENOTYPE	taste bud formation phenotype
GO:0061298PHENOTYPE	retina vasculature development in camera-type eye phenotype
GO:0061299PHENOTYPE	retina vasculature morphogenesis in camera-type eye phenotype
GO:0061300PHENOTYPE	cerebellum vasculature development phenotype
GO:0061303PHENOTYPE	cornea development in camera-type eye phenotype
GO:0061304PHENOTYPE	retinal blood vessel morphogenesis phenotype
GO:0061312PHENOTYPE	BMP signaling pathway involved in heart development phenotype
GO:0061316PHENOTYPE	canonical Wnt signaling pathway involved in heart development phenotype
GO:0061326PHENOTYPE	renal tubule development phenotype
GO:0061337PHENOTYPE	cardiac conduction phenotype
GO:0061351PHENOTYPE	neural precursor cell proliferation phenotype
GO:0061355PHENOTYPE	Wnt protein secretion phenotype
GO:0061371PHENOTYPE	determination of heart left/right asymmetry phenotype
GO:0061386PHENOTYPE	closure of optic fissure phenotype
GO:0061472PHENOTYPE	karyomere membrane fusion phenotype
GO:0061484PHENOTYPE	hematopoietic stem cell homeostasis phenotype
GO:0061512PHENOTYPE	protein localization to cilium phenotype
GO:0061515PHENOTYPE	myeloid cell development phenotype
GO:0061549PHENOTYPE	sympathetic ganglion development phenotype
GO:0061550PHENOTYPE	cranial ganglion development phenotype
GO:0061564PHENOTYPE	axon development phenotype
GO:0061626PHENOTYPE	pharyngeal arch artery morphogenesis phenotype
GO:0065003PHENOTYPE	macromolecular complex assembly phenotype
GO:0070050PHENOTYPE	neuron cellular homeostasis phenotype
GO:0070054PHENOTYPE	mRNA splicing, via endonucleolytic cleavage and ligation phenotype
GO:0070059PHENOTYPE	intrinsic apoptotic signaling pathway in response to endoplasmic reticulum stress phenotype
GO:0070073PHENOTYPE	clustering of voltage-gated calcium channels phenotype
GO:0070121PHENOTYPE	Kupffer's vesicle development phenotype
GO:0070192PHENOTYPE	chromosome organization involved in meiosis phenotype
GO:0070278PHENOTYPE	extracellular matrix constituent secretion phenotype
GO:0070285PHENOTYPE	pigment cell development phenotype
GO:0070286PHENOTYPE	axonemal dynein complex assembly phenotype
GO:0070293PHENOTYPE	renal absorption phenotype
GO:0070306PHENOTYPE	lens fiber cell differentiation phenotype
GO:0070309PHENOTYPE	lens fiber cell morphogenesis phenotype
GO:0070365PHENOTYPE	hepatocyte differentiation phenotype
GO:0070374PHENOTYPE	positive regulation of ERK1 and ERK2 cascade phenotype
GO:0070444PHENOTYPE	oligodendrocyte progenitor proliferation phenotype
GO:0070445PHENOTYPE	regulation of oligodendrocyte progenitor proliferation phenotype
GO:0070509PHENOTYPE	calcium ion import phenotype
GO:0070527PHENOTYPE	platelet aggregation phenotype
GO:0070586PHENOTYPE	cell-cell adhesion involved in gastrulation phenotype
GO:0070650PHENOTYPE	actin filament bundle distribution phenotype
GO:0070654PHENOTYPE	sensory epithelium regeneration phenotype
GO:0070658PHENOTYPE	neuromast hair cell differentiation involved in neuromast regeneration phenotype
GO:0070738PHENOTYPE	tubulin-glycine ligase activity phenotype
GO:0070740PHENOTYPE	tubulin-glutamic acid ligase activity phenotype
GO:0070831PHENOTYPE	basement membrane assembly phenotype
GO:0070925PHENOTYPE	organelle assembly phenotype
GO:0070983PHENOTYPE	dendrite guidance phenotype
GO:0070986PHENOTYPE	left/right axis specification phenotype
GO:0070989PHENOTYPE	oxidative demethylation phenotype
GO:0071340PHENOTYPE	skeletal muscle acetylcholine-gated channel clustering phenotype
GO:0071407PHENOTYPE	cellular response to organic cyclic compound phenotype
GO:0071425PHENOTYPE	hematopoietic stem cell proliferation phenotype
GO:0071479PHENOTYPE	cellular response to ionizing radiation phenotype
GO:0071482PHENOTYPE	cellular response to light stimulus phenotype
GO:0071539PHENOTYPE	protein localization to centrosome phenotype
GO:0071542PHENOTYPE	dopaminergic neuron differentiation phenotype
GO:0071599PHENOTYPE	otic vesicle development phenotype
GO:0071600PHENOTYPE	otic vesicle morphogenesis phenotype
GO:0071632PHENOTYPE	optomotor response phenotype
GO:0071678PHENOTYPE	olfactory bulb axon guidance phenotype
GO:0071679PHENOTYPE	commissural neuron axon guidance phenotype
GO:0071688PHENOTYPE	striated muscle myosin thick filament assembly phenotype
GO:0071690PHENOTYPE	cardiac muscle myosin thick filament assembly phenotype
GO:0071696PHENOTYPE	ectodermal placode development phenotype
GO:0071698PHENOTYPE	olfactory placode development phenotype
GO:0071699PHENOTYPE	olfactory placode morphogenesis phenotype
GO:0071707PHENOTYPE	immunoglobulin heavy chain V-D-J recombination phenotype
GO:0071711PHENOTYPE	basement membrane organization phenotype
GO:0071733PHENOTYPE	transcriptional activation by promoter-enhancer looping phenotype
GO:0071871PHENOTYPE	response to epinephrine phenotype
GO:0071896PHENOTYPE	protein localization to adherens junction phenotype
GO:0071907PHENOTYPE	determination of digestive tract left/right asymmetry phenotype
GO:0071908PHENOTYPE	determination of intestine left/right asymmetry phenotype
GO:0071910PHENOTYPE	determination of liver left/right asymmetry phenotype
GO:0071911PHENOTYPE	synchronous neurotransmitter secretion phenotype
GO:0071929PHENOTYPE	alpha-tubulin acetylation phenotype
GO:0072015PHENOTYPE	glomerular visceral epithelial cell development phenotype
GO:0072019PHENOTYPE	proximal convoluted tubule development phenotype
GO:0072045PHENOTYPE	convergent extension involved in nephron morphogenesis phenotype
GO:0072046PHENOTYPE	establishment of planar polarity involved in nephron morphogenesis phenotype
GO:0072078PHENOTYPE	nephron tubule morphogenesis phenotype
GO:0072089PHENOTYPE	stem cell proliferation phenotype
GO:0072091PHENOTYPE	regulation of stem cell proliferation phenotype
GO:0072104PHENOTYPE	glomerular capillary formation phenotype
GO:0072112PHENOTYPE	glomerular visceral epithelial cell differentiation phenotype
GO:0072114PHENOTYPE	pronephros morphogenesis phenotype
GO:0072148PHENOTYPE	epithelial cell fate commitment phenotype
GO:0072175PHENOTYPE	epithelial tube formation phenotype
GO:0072196PHENOTYPE	proximal/distal pattern formation involved in pronephric nephron development phenotype
GO:0072332PHENOTYPE	intrinsic apoptotic signaling pathway by p53 class mediator phenotype
GO:0072359PHENOTYPE	circulatory system development phenotype
GO:0072378PHENOTYPE	blood coagulation, fibrin clot formation phenotype
GO:0072498PHENOTYPE	embryonic skeletal joint development phenotype
GO:0072507PHENOTYPE	divalent inorganic cation homeostasis phenotype
GO:0072554PHENOTYPE	blood vessel lumenization phenotype
GO:0072574PHENOTYPE	hepatocyte proliferation phenotype
GO:0072576PHENOTYPE	liver morphogenesis phenotype
GO:0072593PHENOTYPE	reactive oxygen species metabolic process phenotype
GO:0072659PHENOTYPE	protein localization to plasma membrane phenotype
GO:0072679PHENOTYPE	thymocyte migration phenotype
GO:0085029PHENOTYPE	extracellular matrix assembly phenotype
GO:0086001PHENOTYPE	cardiac muscle cell action potential phenotype
GO:0086004PHENOTYPE	regulation of cardiac muscle cell contraction phenotype
GO:0086009PHENOTYPE	membrane repolarization phenotype
GO:0086013PHENOTYPE	membrane repolarization during cardiac muscle cell action potential phenotype
GO:0086014PHENOTYPE	atrial cardiac muscle cell action potential phenotype
GO:0090017PHENOTYPE	anterior neural plate formation phenotype
GO:0090090PHENOTYPE	negative regulation of canonical Wnt signaling pathway phenotype
GO:0090104PHENOTYPE	pancreatic epsilon cell differentiation phenotype
GO:0090134PHENOTYPE	cell migration involved in mesendoderm migration phenotype
GO:0090150PHENOTYPE	establishment of protein localization to membrane phenotype
GO:0090162PHENOTYPE	establishment of epithelial cell polarity phenotype
GO:0090171PHENOTYPE	chondrocyte morphogenesis phenotype
GO:0090242PHENOTYPE	retinoic acid receptor signaling pathway involved in somitogenesis phenotype
GO:0090243PHENOTYPE	fibroblast growth factor receptor signaling pathway involved in somitogenesis phenotype
GO:0090245PHENOTYPE	axis elongation involved in somitogenesis phenotype
GO:0090248PHENOTYPE	cell migration involved in somitogenic axis elongation phenotype
GO:0090307PHENOTYPE	mitotic spindle assembly phenotype
GO:0090382PHENOTYPE	phagosome maturation phenotype
GO:0090387PHENOTYPE	phagolysosome assembly involved in apoptotic cell clearance phenotype
GO:0090398PHENOTYPE	cellular senescence phenotype
GO:0090504PHENOTYPE	epiboly phenotype
GO:0090594PHENOTYPE	inflammatory response to wounding phenotype
GO:0097009PHENOTYPE	energy homeostasis phenotype
GO:0097095PHENOTYPE	frontonasal suture morphogenesis phenotype
GO:0097150PHENOTYPE	neuronal stem cell population maintenance phenotype
GO:0097154PHENOTYPE	GABAergic neuron differentiation phenotype
GO:0097155PHENOTYPE	fasciculation of sensory neuron axon phenotype
GO:0097193PHENOTYPE	intrinsic apoptotic signaling pathway phenotype
GO:0097205PHENOTYPE	renal filtration phenotype
GO:0097272PHENOTYPE	ammonia homeostasis phenotype
GO:0097324PHENOTYPE	melanocyte migration phenotype
GO:0097325PHENOTYPE	melanocyte proliferation phenotype
GO:0097352PHENOTYPE	autophagosome maturation phenotype
GO:0097374PHENOTYPE	sensory neuron axon guidance phenotype
GO:0097435PHENOTYPE	fibril organization phenotype
GO:0097475PHENOTYPE	motor neuron migration phenotype
GO:0097535PHENOTYPE	lymphoid lineage cell migration into thymus phenotype
GO:0098508PHENOTYPE	endothelial to hematopoietic transition phenotype
GO:0098534PHENOTYPE	centriole assembly phenotype
GO:0098609PHENOTYPE	cell-cell adhesion phenotype
GO:0098727PHENOTYPE	maintenance of cell number phenotype
GO:0098742PHENOTYPE	cell-cell adhesion via plasma-membrane adhesion molecules phenotype
GO:0098749PHENOTYPE	cerebellar neuron development phenotype
GO:0098754PHENOTYPE	detoxification phenotype
GO:0098773PHENOTYPE	skin epidermis development phenotype
GO:0098856PHENOTYPE	intestinal lipid absorption phenotype
GO:0098900PHENOTYPE	regulation of action potential phenotype
GO:0098908PHENOTYPE	regulation of neuronal action potential phenotype
GO:1900107PHENOTYPE	regulation of nodal signaling pathway phenotype
GO:1900746PHENOTYPE	regulation of vascular endothelial growth factor signaling pathway phenotype
GO:1900748PHENOTYPE	positive regulation of vascular endothelial growth factor signaling pathway phenotype
GO:1901166PHENOTYPE	neural crest cell migration involved in autonomic nervous system development phenotype
GO:1901214PHENOTYPE	regulation of neuron death phenotype
GO:1901342PHENOTYPE	regulation of vasculature development phenotype
GO:1901343PHENOTYPE	negative regulation of vasculature development phenotype
GO:1902176PHENOTYPE	negative regulation of oxidative stress-induced intrinsic apoptotic signaling pathway phenotype
GO:1902262PHENOTYPE	apoptotic process involved in patterning of blood vessels phenotype
GO:1902354PHENOTYPE	blood vessel endothelial cell delamination involved in blood vessel lumen ensheathment phenotype
GO:1902355PHENOTYPE	endothelial tube lumen extension involved in blood vessel lumen ensheathment phenotype
GO:1902362PHENOTYPE	melanocyte apoptotic process phenotype
GO:1902414PHENOTYPE	protein localization to cell junction phenotype
GO:1902600PHENOTYPE	hydrogen ion transmembrane transport phenotype
GO:1902749PHENOTYPE	regulation of cell cycle G2/M phase transition phenotype
GO:1902866PHENOTYPE	regulation of retina development in camera-type eye phenotype
GO:1902882PHENOTYPE	regulation of response to oxidative stress phenotype
GO:1903041PHENOTYPE	regulation of chondrocyte hypertrophy phenotype
GO:1903045PHENOTYPE	neural crest cell migration involved in sympathetic nervous system development phenotype
GO:1903224PHENOTYPE	regulation of endodermal cell differentiation phenotype
GO:1903426PHENOTYPE	regulation of reactive oxygen species biosynthetic process phenotype
GO:1903706PHENOTYPE	regulation of hemopoiesis phenotype
GO:1903707PHENOTYPE	negative regulation of hemopoiesis phenotype
GO:1903798PHENOTYPE	regulation of production of miRNAs involved in gene silencing by miRNA phenotype
GO:1990126PHENOTYPE	retrograde transport, endosome to plasma membrane phenotype
GO:1990266PHENOTYPE	neutrophil migration phenotype
GO:1990523PHENOTYPE	bone regeneration phenotype
GO:2000145PHENOTYPE	regulation of cell motility phenotype
GO:2000252PHENOTYPE	negative regulation of feeding behavior phenotype
GO:2000310PHENOTYPE	regulation of N-methyl-D-aspartate selective glutamate receptor activity phenotype
GO:2000377PHENOTYPE	regulation of reactive oxygen species metabolic process phenotype
HP:0000504	Abnormality of vision
HP:0000505	Visual impairment
HP:0000618	Blindness
HP:0001508	Failure to thrive
HP:0001510	Growth delay
HP:0001511	Intrauterine growth retardation
HP:0001635	Congestive heart failure
HP:0002067	Bradykinesia
HP:0002269	Abnormality of neuronal migration
HP:0003130	Abnormal peripheral myelination
HP:0004359	Abnormal circulating fatty-acid concentration
HP:0004363	Abnormal circulating calcium concentration
HP:0010831	Impaired proprioception
HP:0010901	Abnormal circulating methionine concentration
HP:0011014	Abnormal glucose homeostasis
HP:0011018	Abnormality of the cell cycle
HP:0011028	Abnormality of blood circulation
HP:0011036	Abnormality of renal excretion
HP:0011400	Abnormal CNS myelination
HP:0011675	Arrhythmia
HP:0012347	Abnormal protein N-linked glycosylation
HP:0012358	Abnormal protein O-linked glycosylation
HP:0012447	Abnormal myelination
HP:0012535	Abnormal synaptic transmission
HP:0030895	Abnormal gastrointestinal motility
HP:0031377	Abnormal cell proliferation
HP:0100529	Abnormal blood phosphate concentration
MP:0000060	delayed bone ossification
MP:0000118	arrest of tooth development
MP:0001155	arrest of spermatogenesis
MP:0001633	poor circulation
MP:0002113	abnormal skeleton development
MP:0003416	premature bone ossification
MP:0003417	premature endochondral bone ossification
MP:0003786	premature aging
MP:0004022	abnormal cone electrophysiology
MP:0004251	failure of heart looping
MP:0005528	decreased renal glomerular filtration rate
MP:0005573	increased pulmonary respiratory rate
MP:0008261	arrest of male meiosis
MP:0012177	delayed head development
ZP:0000002	somitogenesis disrupted, abnormal
ZP:0000003	somite specification disrupted, abnormal
ZP:0000004	determination of left/right asymmetry in lateral mesoderm disrupted, abnormal
ZP:0000005	ectoderm development disrupted, abnormal
ZP:0000006	lateral mesoderm development disrupted, abnormal
ZP:0000007	blood vessel morphogenesis disrupted, abnormal
ZP:0000008	hematopoietic stem cell differentiation disrupted, abnormal
ZP:0000009	blood decreased amount, abnormal
ZP:0000010	somite border somite 5 amorphous, abnormal
ZP:0000011	somite quality, abnormal
ZP:0000012	somite morphology, abnormal
ZP:0000013	somite shape, abnormal
ZP:0000014	somite border somite 7 amorphous, abnormal
ZP:0000015	somite border somite 8 amorphous, abnormal
ZP:0000016	somite border somite 6 amorphous, abnormal
ZP:0000017	somite border somite 9 amorphous, abnormal
ZP:0000018	post-vent region quality, abnormal
ZP:0000019	intersegmental vessel malformed, abnormal
ZP:0000020	somite border irregular spatial pattern, abnormal
ZP:0000021	somite border deformed, abnormal
ZP:0000022	hematopoietic stem cell decreased amount, abnormal
ZP:0000023	hindbrain morphology, abnormal
ZP:0000024	motor neuron spinal cord decreased amount, abnormal
ZP:0000025	spinal cord interneuron decreased amount, abnormal
ZP:0000026	trunk decreased length, abnormal
ZP:0000027	post-vent region decreased length, abnormal
ZP:0000028	endoderm development disrupted, abnormal
ZP:0000029	retinal ganglion cell axon guidance disrupted, abnormal
ZP:0000030	skeletal muscle fiber development disrupted, abnormal
ZP:0000031	swim bladder inflation arrested, abnormal
ZP:0000032	brain quality, abnormal
ZP:0000033	endoderm morphology, abnormal
ZP:0000034	hindbrain quality, abnormal
ZP:0000035	midbrain hindbrain boundary malformed, abnormal
ZP:0000036	neural crest quality, abnormal
ZP:0000038	pericardium edematous, abnormal
ZP:0000039	swim bladder physical object quality, abnormal
ZP:0000040	yolk quality, abnormal
ZP:0000041	pharyngeal arch 3-7 skeleton quality, abnormal
ZP:0000042	cerebellum malformed, abnormal
ZP:0000043	eye decreased size, abnormal
ZP:0000044	heart quality, abnormal
ZP:0000045	liver mislocalised anteriorly, abnormal
ZP:0000046	pectoral fin bud aplastic, abnormal
ZP:0000047	retinal photoreceptor layer disorganized, abnormal
ZP:0000048	retina morphology, abnormal
ZP:0000049	surface structure quality, abnormal
ZP:0000050	optic tectum decreased size, abnormal
ZP:0000051	optic tectum disorganized, abnormal
ZP:0000053	RoL2 rhombomere 4 mislocalised, abnormal
ZP:0000054	head decreased size, abnormal
ZP:0000055	pectoral fin quality, abnormal
ZP:0000056	pectoral fin aplastic, abnormal
ZP:0000057	Meckel's cartilage decreased size, abnormal
ZP:0000058	Meckel's cartilage fused with ceratohyal cartilage, abnormal
ZP:0000059	exocrine pancreas mislocalised anteriorly, abnormal
ZP:0000060	endocrine pancreas mislocalised anteriorly, abnormal
ZP:0000061	fin bud aplastic, abnormal
ZP:0000062	palatoquadrate cartilage decreased size, abnormal
ZP:0000063	palatoquadrate cartilage fused with hyosymplectic cartilage, abnormal
ZP:0000064	ceratohyal cartilage decreased size, abnormal
ZP:0000065	hyosymplectic cartilage decreased size, abnormal
ZP:0000066	ceratobranchial cartilage absent, abnormal
ZP:0000067	RoL2 increased amount, abnormal
ZP:0000068	Mauthner neuron absent, abnormal
ZP:0000069	axon guidance disrupted, abnormal
ZP:0000070	olfactory bulb development disrupted, abnormal
ZP:0000071	neuromast primordium migration delayed, abnormal
ZP:0000072	posterior lateral line nerve development disrupted, abnormal
ZP:0000073	innervation disrupted, abnormal
ZP:0000074	fasciculation of sensory neuron axon disrupted, abnormal
ZP:0000075	olfactory placode disorganized, abnormal
ZP:0000076	posterior lateral line nerve decreased length, abnormal
ZP:0000077	glomerular layer aplastic, abnormal
ZP:0000078	olfactory bulb disorganized, abnormal
ZP:0000079	GABAergic neuron olfactory bulb decreased amount, abnormal
ZP:0000080	dopaminergic neuron olfactory bulb decreased amount, abnormal
ZP:0000081	olfactory epithelium disorganized, abnormal
ZP:0000082	olfactory epithelium split, abnormal
ZP:0000083	posterior lateral line neuromast malformed, abnormal
ZP:0000084	posterior lateral line neuromast decreased amount, abnormal
ZP:0000085	posterior lateral line primordium circular, abnormal
ZP:0000086	posterior lateral line primordium crescent-shaped, abnormal
ZP:0000087	anterior lateral line neuromast decreased amount, abnormal
ZP:0000088	olfactory receptor cell spatial pattern, abnormal
ZP:0000089	axon olfactory receptor cell decreased length, abnormal
ZP:0000090	axon olfactory receptor cell disorganized, abnormal
ZP:0000091	neuromast hair cell decreased amount, abnormal
ZP:0000092	uroporphyrinogen decarboxylase activity decreased rate, abnormal
ZP:0000093	porphyrin-containing compound metabolic process disrupted, abnormal
ZP:0000094	blood quality, abnormal
ZP:0000095	whole organism lethal (sensu genetics), abnormal
ZP:0000096	nucleate erythrocyte fluorescence, abnormal
ZP:0000097	endoderm formation process quality, abnormal
ZP:0000098	endodermal cell fate specification disrupted, abnormal
ZP:0000100	brain morphology, abnormal
ZP:0000101	endodermal cell endoderm decreased amount, abnormal
ZP:0000102	yolk increased size, abnormal
ZP:0000103	extension decreased length, abnormal
ZP:0000104	extension increased thickness, abnormal
ZP:0000105	fourth ventricle collapsed, abnormal
ZP:0000106	gut aplastic, abnormal
ZP:0000107	heart morphology, abnormal
ZP:0000108	heart cleft, abnormal
ZP:0000109	heart duplicated, abnormal
ZP:0000110	notochord aplastic, abnormal
ZP:0000111	somite fused with somite, abnormal
ZP:0000112	tectal ventricle collapsed, abnormal
ZP:0000113	heart tube duplicated, abnormal
ZP:0000114	heart tube bifurcated, abnormal
ZP:0000115	nervous system quality, abnormal
ZP:0000116	anterior-posterior axis whole organism curved ventral, abnormal
ZP:0000117	head hypoplastic, abnormal
ZP:0000118	forebrain ventricle collapsed, abnormal
ZP:0000119	endochondral ossification disrupted, abnormal
ZP:0000120	chondrocyte differentiation delayed, abnormal
ZP:0000121	eye mislocalised, abnormal
ZP:0000122	notochord undulate, abnormal
ZP:0000123	mouth absent, abnormal
ZP:0000124	head malformed, abnormal
ZP:0000125	Meckel's cartilage mislocalised, abnormal
ZP:0000126	Meckel's cartilage malformed, abnormal
ZP:0000127	ceratobranchial 5 bone composition, abnormal
ZP:0000128	pharyngeal arch aplastic, abnormal
ZP:0000129	neurocranial trabecula decreased size, abnormal
ZP:0000130	neurocranial trabecula malformed, abnormal
ZP:0000131	ceratohyal cartilage mislocalised, abnormal
ZP:0000132	ceratohyal cartilage malformed, abnormal
ZP:0000133	ethmoid cartilage decreased size, abnormal
ZP:0000134	cranial cartilage disorganized, abnormal
ZP:0000135	pharyngeal arch cartilage disorganized, abnormal
ZP:0000136	ceratobranchial cartilage decreased size, abnormal
ZP:0000137	perichordal connective tissue morphology, abnormal
ZP:0000138	chondrocyte disorganized, abnormal
ZP:0000139	gastrulation with mouth forming second quality, abnormal
ZP:0000140	gastrulation with mouth forming second disrupted, abnormal
ZP:0000141	dorsal/ventral pattern formation disrupted, abnormal
ZP:0000142	epidermal cell fate specification disrupted, abnormal
ZP:0000143	post-anal tail morphogenesis disrupted, abnormal
ZP:0000144	post-anal tail morphogenesis having extra processual parts post-anal tail morphogenesis, abnormal
ZP:0000145	tail bud mislocalised posteriorly, abnormal
ZP:0000146	heart rudiment unfused from heart rudiment, abnormal
ZP:0000147	notochord quality, abnormal
ZP:0000148	notochord increased width, abnormal
ZP:0000149	otic placode disorganized, abnormal
ZP:0000150	otic placode aplastic, abnormal
ZP:0000151	pronephric duct hypoplastic, abnormal
ZP:0000152	somite circular, abnormal
ZP:0000153	somite increased width, abnormal
ZP:0000154	paraxial mesoderm morphology, abnormal
ZP:0000155	paraxial mesoderm has extra parts of type adaxial cell, abnormal
ZP:0000156	anterior-posterior axis paraxial mesoderm decreased length, abnormal
ZP:0000157	rhombomere 5 fused with left side right side rhombomere 5, abnormal
ZP:0000158	rhombomere 3 increased length, abnormal
ZP:0000159	whole organism shape, abnormal
ZP:0000160	whole organism wholly dorsalized, abnormal
ZP:0000161	whole organism ovate, abnormal
ZP:0000162	whole organism has extra parts of type post-vent region, abnormal
ZP:0000163	trunk condensed, abnormal
ZP:0000164	trunk rotational curvature, abnormal
ZP:0000165	post-vent region aplastic, abnormal
ZP:0000166	post-vent region has extra parts of type tail bud, abnormal
ZP:0000167	post-vent region has extra parts of type notochord, abnormal
ZP:0000168	neural tube morphology, abnormal
ZP:0000169	pectoral fin mislocalised, abnormal
ZP:0000170	neuron spinal cord neural rod increased amount, abnormal
ZP:0000171	neuron spinal cord neural rod mislocalised laterally, abnormal
ZP:0000172	blood cell decreased amount, abnormal
ZP:0000173	erythroid lineage cell absent, abnormal
ZP:0000174	cell proliferation in hindbrain decreased occurrence, abnormal
ZP:0000175	fourth ventricle development disrupted, abnormal
ZP:0000176	hypothalamus development process quality, abnormal
ZP:0000177	hindbrain development disrupted, abnormal
ZP:0000178	retinoic acid catabolic process decreased rate, abnormal
ZP:0000179	forebrain morphogenesis process quality, abnormal
ZP:0000180	embryonic retina morphogenesis in camera-type eye process quality, abnormal
ZP:0000181	optic vesicle wholly ventralized, abnormal
ZP:0000182	diencephalon physical object quality, abnormal
ZP:0000183	forebrain physical object quality, abnormal
ZP:0000184	fourth ventricle structure, abnormal
ZP:0000185	optic stalk malformed, abnormal
ZP:0000186	retinal pigmented epithelium mislocalised, abnormal
ZP:0000187	retina malformed, abnormal
ZP:0000188	retina physical object quality, abnormal
ZP:0000189	optic cup physical object quality, abnormal
ZP:0000190	optic fissure closure incomplete, abnormal
ZP:0000191	embryonic heart tube morphogenesis decreased process quality, abnormal
ZP:0000192	endocardium morphogenesis decreased process quality, abnormal
ZP:0000194	cardiac muscle tissue morphogenesis decreased process quality, abnormal
ZP:0000195	cardioblast migration to the midline involved in heart field formation decreased process quality, abnormal
ZP:0000196	postoptic commissure increased width, abnormal
ZP:0000197	myocardium mislocalised, abnormal
ZP:0000198	endocardium mislocalised, abnormal
ZP:0000199	abnormal(ly) malformed endocardium cell
ZP:0000200	startle response disrupted, abnormal
ZP:0000201	optokinetic behavior disrupted, abnormal
ZP:0000202	larval locomotory behavior rhythm quality, abnormal
ZP:0000203	response to absence of light disrupted, abnormal
ZP:0000204	response to auditory stimulus disrupted, abnormal
ZP:0000205	axon midline choice point recognition disrupted, abnormal
ZP:0000206	musculoskeletal movement quality, abnormal
ZP:0000208	neuromuscular process controlling balance disrupted, abnormal
ZP:0000209	equilibrioception disrupted, abnormal
ZP:0000210	commissural neuron axon guidance disrupted, abnormal
ZP:0000211	postoptic commissure decreased width, abnormal
ZP:0000212	whole organism viability, abnormal
ZP:0000213	whole organism movement behavioral quality, abnormal
ZP:0000214	post-vent region movement quality, abnormal
ZP:0000215	hindbrain commissure disorganized, abnormal
ZP:0000216	axon Mauthner neuron mislocalised, abnormal
ZP:0000217	liver development disrupted, abnormal
ZP:0000218	yolk low brightness, abnormal
ZP:0000219	liver primordium duplicated, abnormal
ZP:0000220	post-vent region morphology, abnormal
ZP:0000221	fin regeneration disrupted, abnormal
ZP:0000222	heart looping disrupted, abnormal
ZP:0000223	heart development disrupted, abnormal
ZP:0000224	whole organism curvature, abnormal
ZP:0000225	head increased variability of size, abnormal
ZP:0000226	ossification involved in bone maturation delayed, abnormal
ZP:0000227	calcium ion import decreased process quality, abnormal
ZP:0000228	cAMP biosynthetic process decreased rate, abnormal
ZP:0000229	GTP biosynthetic process decreased rate, abnormal
ZP:0000231	heart composition, abnormal
ZP:0000232	heart decreased contractility, abnormal
ZP:0000233	heart decreased functionality, abnormal
ZP:0000234	splanchnocranium hypoplastic, abnormal
ZP:0000235	mandibular arch skeleton hypoplastic, abnormal
ZP:0000236	sarcomere organization disrupted, abnormal
ZP:0000237	striated muscle cell development disrupted, abnormal
ZP:0000238	actin filament bundle distribution disrupted, abnormal
ZP:0000239	whole organism immobile, abnormal
ZP:0000240	whole organism bent, abnormal
ZP:0000241	muscle trunk refractivity, abnormal
ZP:0000242	sarcomere skeletal muscle disorganized, abnormal
ZP:0000243	Z disc skeletal muscle disorganized, abnormal
ZP:0000246	actin filament fast muscle cell disorganized, abnormal
ZP:0000247	actin filament fast muscle cell distributed, abnormal
ZP:0000249	myofibril fast muscle cell degenerate, abnormal
ZP:0000250	myofibril fast muscle cell disorganized, abnormal
ZP:0000254	spinal cord motor neuron cell fate specification disrupted, abnormal
ZP:0000255	spinal cord oligodendrocyte cell fate specification disrupted, abnormal
ZP:0000256	glioblast (sensu Vertebrata) spinal cord absent, abnormal
ZP:0000257	glioblast (sensu Vertebrata) spinal cord decreased amount, abnormal
ZP:0000258	secondary motor neuron spinal cord decreased amount, abnormal
ZP:0000259	radial glial cell spinal cord disorganized, abnormal
ZP:0000260	radial glial cell spinal cord decreased amount, abnormal
ZP:0000261	dopaminergic neuron diencephalon increased amount, abnormal
ZP:0000262	lymphangiogenesis arrested, abnormal
ZP:0000263	thoracic duct hypoplastic, abnormal
ZP:0000264	vascular lymphangioblast hypoplastic, abnormal
ZP:0000265	lymphangiogenesis disrupted, abnormal
ZP:0000266	opercle curved, abnormal
ZP:0000267	opercle decreased width, abnormal
ZP:0000268	symplectic decreased size, abnormal
ZP:0000269	Meckel's cartilage morphology, abnormal
ZP:0000270	palatoquadrate cartilage truncated, abnormal
ZP:0000271	hyosymplectic cartilage elongated, abnormal
ZP:0000272	hyosymplectic cartilage deformed, abnormal
ZP:0000273	thoracic duct absent, abnormal
ZP:0000274	thoracic duct wholeness, abnormal
ZP:0000276	oligodendrocyte development arrested, abnormal
ZP:0000277	rhombomere boundary formation disrupted, abnormal
ZP:0000279	radial glial cell division in pallium increased occurrence, abnormal
ZP:0000280	cell differentiation involved in pronephros development disrupted, abnormal
ZP:0000282	central nervous system cellular quality, abnormal
ZP:0000283	hindbrain increased rate cell death, abnormal
ZP:0000284	epithelium hindbrain disorganized, abnormal
ZP:0000286	neuroepithelial cell hindbrain aggregated, abnormal
ZP:0000287	blood vessel telencephalon prominent, abnormal
ZP:0000288	blood vessel telencephalon dilated, abnormal
ZP:0000289	blood vessel telencephalon increased diameter, abnormal
ZP:0000290	neural plate morphology, abnormal
ZP:0000291	pronephros cellular quality, abnormal
ZP:0000292	capillary optic tectum decreased variability of size, abnormal
ZP:0000293	blood vessel optic tectum decreased variability of size, abnormal
ZP:0000294	dorsal telencephalon has extra parts of type ventricular zone radial glial cell, abnormal
ZP:0000295	radial glial cell dorsal telencephalon proliferative, abnormal
ZP:0000296	neuron posterior lateral line ganglion increased amount, abnormal
ZP:0000297	caudal fin blood vessel broken, abnormal
ZP:0000298	caudal fin blood vessel increased diameter, abnormal
ZP:0000299	caudal fin blood vessel hemorrhagic, abnormal
ZP:0000300	caudal fin blood vessel displaced, abnormal
ZP:0000301	peripheral neuron decreased length, abnormal
ZP:0000302	somitogenesis decreased functionality, abnormal
ZP:0000303	cell cycle arrested, abnormal
ZP:0000304	cell population proliferation decreased occurrence, abnormal
ZP:0000305	embryo development arrested, abnormal
ZP:0000306	whole organism dead, abnormal
ZP:0000307	post-vent region arrested segmentation, abnormal
ZP:0000308	portion of tissue necrotic, abnormal
ZP:0000309	pigment cell decreased amount, abnormal
ZP:0000310	spliceosomal snRNP assembly decreased process quality, abnormal
ZP:0000311	apoptotic process increased occurrence, abnormal
ZP:0000312	Cajal body organization decreased process quality, abnormal
ZP:0000313	mRNA cis splicing, via spliceosome decreased occurrence, abnormal
ZP:0000314	cell whole organism apoptotic, abnormal
ZP:0000315	cell whole organism dead, abnormal
ZP:0000316	Cajal body cell decreased amount, abnormal
ZP:0000317	small nuclear ribonucleoprotein complex cell dispersed, abnormal
ZP:0000318	neural crest cell development disrupted, abnormal
ZP:0000319	brain hydrocephalic, abnormal
ZP:0000320	hindbrain hydrocephalic, abnormal
ZP:0000321	fourth ventricle increased size, abnormal
ZP:0000322	midbrain hydrocephalic, abnormal
ZP:0000323	tectal ventricle increased size, abnormal
ZP:0000324	whole organism decreased size, abnormal
ZP:0000325	melanocyte trunk decreased amount, abnormal
ZP:0000326	melanocyte post-vent region decreased amount, abnormal
ZP:0000327	DoLA increased amount, abnormal
ZP:0000328	melanocyte spatial pattern, abnormal
ZP:0000329	melanocyte decreased amount, abnormal
ZP:0000330	neural crest cell decreased amount, abnormal
ZP:0000331	neuron increased amount, abnormal
ZP:0000332	heart morphogenesis disrupted, abnormal
ZP:0000333	determination of left/right symmetry disrupted, abnormal
ZP:0000334	heart development delayed, abnormal
ZP:0000335	blood circulation disrupted, abnormal
ZP:0000336	thalamus development process quality, abnormal
ZP:0000337	thalamus development decreased process quality, abnormal
ZP:0000338	Wnt-activated signaling pathway involved in forebrain neuron fate commitment disrupted, abnormal
ZP:0000339	forebrain development disrupted, abnormal
ZP:0000340	embryonic eye morphogenesis disrupted, abnormal
ZP:0000341	epithelial cell proliferation increased occurrence, abnormal
ZP:0000342	canonical Wnt signaling pathway increased occurrence, abnormal
ZP:0000343	cell migration in diencephalon delayed, abnormal
ZP:0000344	epiphysis increased size, abnormal
ZP:0000345	photoreceptor cell epiphysis increased amount, abnormal
ZP:0000346	neuron epiphysis increased amount, abnormal
ZP:0000347	floor plate quality, abnormal
ZP:0000348	peripheral olfactory organ absent, abnormal
ZP:0000349	olfactory placode aplastic, abnormal
ZP:0000350	optic vesicle absent, abnormal
ZP:0000351	postoptic commissure aplastic, abnormal
ZP:0000352	antero-lateral region prechordal plate decreased size, abnormal
ZP:0000353	telencephalon decreased size, abnormal
ZP:0000354	telencephalon aplastic, abnormal
ZP:0000355	eye quality, abnormal
ZP:0000356	eye absent, abnormal
ZP:0000357	eye aplastic, abnormal
ZP:0000358	forebrain quality, abnormal
ZP:0000359	forebrain decreased size, abnormal
ZP:0000360	heart linear, abnormal
ZP:0000362	cardiac muscle cell heart decreased amount, abnormal
ZP:0000364	trigeminal placode increased size, abnormal
ZP:0000365	sensory neuron trigeminal placode mislocalised anteriorly, abnormal
ZP:0000366	presumptive telencephalon aplastic, abnormal
ZP:0000367	presumptive diencephalon increased size, abnormal
ZP:0000368	dorsal thalamus cellular quality, abnormal
ZP:0000369	epithelial cell posterior intestine increased amount, abnormal
ZP:0000370	epithelial cell intestinal bulb increased amount, abnormal
ZP:0000372	anterior-posterior axis whole organism deformed, abnormal
ZP:0000373	anterior commissure aplastic, abnormal
ZP:0000374	head apoptotic, abnormal
ZP:0000375	head degenerate, abnormal
ZP:0000376	adenohypophysis decreased size, abnormal
ZP:0000377	endocardial cushion hyperplastic, abnormal
ZP:0000378	cardiac jelly increased volume, abnormal
ZP:0000379	intestine morphology, abnormal
ZP:0000380	intestine increased thickness, abnormal
ZP:0000381	parapineal organ position, abnormal
ZP:0000382	primary neuron tract of the postoptic commissure morphology, abnormal
ZP:0000383	intestinal bulb epithelium increased thickness, abnormal
ZP:0000384	intestinal bulb epithelium disorganized, abnormal
ZP:0000385	intestinal bulb epithelium cellular quality, abnormal
ZP:0000386	mid diencephalic organizer increased thickness, abnormal
ZP:0000387	mid diencephalic organizer cellular quality, abnormal
ZP:0000388	dorso-rostral cluster absent, abnormal
ZP:0000389	intestinal epithelial cell proliferative, abnormal
ZP:0000390	vasculature development disrupted, abnormal
ZP:0000391	swim bladder morphogenesis process quality, abnormal
ZP:0000392	swim bladder morphology, abnormal
ZP:0000393	neutrophil blood island decreased amount, abnormal
ZP:0000394	pancreas primordium physical object quality, abnormal
ZP:0000395	pharyngeal arch physical object quality, abnormal
ZP:0000396	nucleate erythrocyte decreased amount, abnormal
ZP:0000397	central nervous system necrotic, abnormal
ZP:0000398	whole organism necrotic, abnormal
ZP:0000399	head flat, abnormal
ZP:0000400	lens quality, abnormal
ZP:0000401	eye degenerate, abnormal
ZP:0000402	eye decreased pigmentation, abnormal
ZP:0000403	gut hypoplastic, abnormal
ZP:0000404	liver hypoplastic, abnormal
ZP:0000405	retinal pigmented epithelium degenerate, abnormal
ZP:0000406	sensory system quality, abnormal
ZP:0000407	head decreased width, abnormal
ZP:0000408	activation of cysteine-type endopeptidase activity involved in apoptotic process increased occurrence, abnormal
ZP:0000409	locomotion decreased process quality, abnormal
ZP:0000410	pericardium swollen, abnormal
ZP:0000411	swim bladder aplastic, abnormal
ZP:0000412	cranial nerve II aplastic, abnormal
ZP:0000413	ventricular system increased size, abnormal
ZP:0000414	ventral mandibular arch malformed, abnormal
ZP:0000415	lens development in camera-type eye disrupted, abnormal
ZP:0000416	endocardium development disrupted, abnormal
ZP:0000417	retina layer formation disrupted, abnormal
ZP:0000418	lens fiber cell development disrupted, abnormal
ZP:0000419	lens fiber cell morphogenesis disrupted, abnormal
ZP:0000420	lens morphology, abnormal
ZP:0000421	lens structure, abnormal
ZP:0000422	lens separated from retina, abnormal
ZP:0000423	nucleus lens increased amount, abnormal
ZP:0000424	cell lens loose, abnormal
ZP:0000425	fourth ventricle decreased size, abnormal
ZP:0000426	heart increased amount, abnormal
ZP:0000427	heart bifurcated, abnormal
ZP:0000428	midbrain quality, abnormal
ZP:0000429	midbrain morphology, abnormal
ZP:0000430	somite degenerate, abnormal
ZP:0000431	myotome increased size, abnormal
ZP:0000433	actin filament myotome increased length, abnormal
ZP:0000435	muscle tendon junction myotome morphology, abnormal
ZP:0000436	myosin filament myotome disorganized, abnormal
ZP:0000437	ventricular system collapsed, abnormal
ZP:0000438	somite border shape, abnormal
ZP:0000439	somite border aplastic, abnormal
ZP:0000440	corneal epithelium morphology, abnormal
ZP:0000441	corneal epithelium undulate, abnormal
ZP:0000442	cell death increased occurrence, abnormal
ZP:0000443	trigeminal ganglion malformed, abnormal
ZP:0000444	pharyngeal arch malformed, abnormal
ZP:0000445	ceratobranchial cartilage hypotrophic, abnormal
ZP:0000446	epibranchial ganglion malformed, abnormal
ZP:0000447	pharyngeal arch 2 morphology, abnormal
ZP:0000448	pharyngeal arch 1 morphology, abnormal
ZP:0000449	blood vessel development disrupted, abnormal
ZP:0000450	blood circulation arrested, abnormal
ZP:0000451	hemopoiesis disrupted, abnormal
ZP:0000452	heart contraction rhythm quality, abnormal
ZP:0000454	heart tube morphology, abnormal
ZP:0000455	intersegmental vessel aplastic, abnormal
ZP:0000456	trunk vasculature morphology, abnormal
ZP:0000457	vascular cord morphology, abnormal
ZP:0000458	heart jogging disrupted, abnormal
ZP:0000459	mRNA catabolic process disrupted, abnormal
ZP:0000460	embryonic heart tube left/right pattern formation disrupted, abnormal
ZP:0000461	somite asymmetrical, abnormal
ZP:0000462	heart looping delayed, abnormal
ZP:0000463	heart contraction arrested, abnormal
ZP:0000464	determination of digestive tract left/right asymmetry disrupted, abnormal
ZP:0000465	blood island decreased size, abnormal
ZP:0000466	heart orientation left-right axis whole organism, abnormal
ZP:0000467	heart aligned with central region whole organism, abnormal
ZP:0000468	heart tube aligned with central region whole organism, abnormal
ZP:0000469	ventral fin fold decreased size, abnormal
ZP:0000470	post-vent region decreased size, abnormal
ZP:0000471	intestine orientation left-right axis whole organism, abnormal
ZP:0000472	intersegmental vessel shortened, abnormal
ZP:0000473	whole organism decreased length, abnormal
ZP:0000474	neuron degenerate, abnormal
ZP:0000475	neural crest cell migration disrupted, abnormal
ZP:0000476	mesodermal cell migration disrupted, abnormal
ZP:0000477	thyroid gland development disrupted, abnormal
ZP:0000478	pectoral fin morphogenesis disrupted, abnormal
ZP:0000479	enteric nervous system development disrupted, abnormal
ZP:0000480	digestive tract development disrupted, abnormal
ZP:0000481	smooth muscle cell differentiation disrupted, abnormal
ZP:0000482	heart contraction disrupted, abnormal
ZP:0000483	heart contraction decreased intensity, abnormal
ZP:0000484	heart formation disrupted, abnormal
ZP:0000485	determination of intestine left/right asymmetry disrupted, abnormal
ZP:0000486	cardiac ventricle structure, abnormal
ZP:0000487	heart primordium unfused from heart primordium, abnormal
ZP:0000488	myocardial precursor heart primordium decreased amount, abnormal
ZP:0000489	fin quality, abnormal
ZP:0000490	heart malformed, abnormal
ZP:0000491	heart rudiment bifurcated, abnormal
ZP:0000492	lateral plate mesoderm decreased width, abnormal
ZP:0000493	liver duplicated, abnormal
ZP:0000494	pancreas duplicated, abnormal
ZP:0000495	pectoral fin bud decreased size, abnormal
ZP:0000496	dentary shape, abnormal
ZP:0000497	thyroid follicle decreased amount, abnormal
ZP:0000498	thyroid primordium decreased size, abnormal
ZP:0000499	neuron enteric nervous system decreased amount, abnormal
ZP:0000500	Meckel's cartilage decreased length, abnormal
ZP:0000501	smooth muscle cell intestine morphology, abnormal
ZP:0000502	neuron intestine decreased amount, abnormal
ZP:0000503	epicardium aplastic, abnormal
ZP:0000504	cardiac muscle cell organization quality, abnormal
ZP:0000505	retinal cone cell decreased amount, abnormal
ZP:0000506	embryonic hemopoiesis disrupted, abnormal
ZP:0000507	hemoglobin biosynthetic process disrupted, abnormal
ZP:0000508	pigmentation disrupted, abnormal
ZP:0000509	ventral fin fold kinked, abnormal
ZP:0000510	trunk decreased pigmentation, abnormal
ZP:0000511	intersegmental vessel decreased size, abnormal
ZP:0000512	dorsal longitudinal anastomotic vessel structure, abnormal
ZP:0000513	nucleate erythrocyte shape, abnormal
ZP:0000514	nucleate erythrocyte low saturation, abnormal
ZP:0000515	nucleate erythrocyte increased size, abnormal
ZP:0000516	nucleate erythrocyte immature, abnormal
ZP:0000517	nucleus nucleate erythrocyte morphology, abnormal
ZP:0000518	cranial ganglion neoplastic, abnormal
ZP:0000519	neuronal stem cell cranial ganglion increased amount, abnormal
ZP:0000520	neuron cranial ganglion proliferative, abnormal
ZP:0000521	esophagus inflamed, abnormal
ZP:0000522	cranial nerve neoplastic, abnormal
ZP:0000523	intestinal bulb inflamed, abnormal
ZP:0000524	whole organism neoplastic, invasive, abnormal
ZP:0000525	pigment cell irregular spatial pattern, abnormal
ZP:0000526	mitotic cell cycle duration, abnormal
ZP:0000527	brain hemorrhagic, abnormal
ZP:0000528	cardiac ventricle decreased size, abnormal
ZP:0000529	dorsal aorta closed, abnormal
ZP:0000530	dorsal aorta collapsed, abnormal
ZP:0000531	dorsal aorta aplastic, abnormal
ZP:0000532	heart increased size, abnormal
ZP:0000533	sarcomere heart increased size, abnormal
ZP:0000534	cardiac muscle cell heart increased size, abnormal
ZP:0000535	atrium increased size, abnormal
ZP:0000536	cranial vasculature broken, abnormal
ZP:0000537	intersegmental vessel collapsed, abnormal
ZP:0000538	cardiac muscle cell atrial myocardium increased amount, abnormal
ZP:0000539	cardiac muscle cell atrial myocardium decreased mass density, abnormal
ZP:0000540	subintestinal vein collapsed, abnormal
ZP:0000541	cardiac muscle cell ventricular myocardium increased amount, abnormal
ZP:0000542	cardiac muscle cell ventricular myocardium increased mass density, abnormal
ZP:0000543	myeloid cell differentiation process quality, abnormal
ZP:0000544	granulocyte differentiation decreased rate, abnormal
ZP:0000545	granulocyte differentiation decreased occurrence, abnormal
ZP:0000546	definitive hemopoiesis process quality, abnormal
ZP:0000547	definitive hemopoiesis disrupted, abnormal
ZP:0000548	myeloid cell blood island absent, abnormal
ZP:0000549	myeloid cell blood island decreased amount, abnormal
ZP:0000550	hematopoietic multipotent progenitor cell blood island absent, abnormal
ZP:0000551	cranium shape, abnormal
ZP:0000552	hematopoietic stem cell ventral wall of dorsal aorta decreased amount, abnormal
ZP:0000553	myeloid cell ventral wall of dorsal aorta absent, abnormal
ZP:0000554	myeloid cell ventral wall of dorsal aorta decreased amount, abnormal
ZP:0000555	neutrophil ventral wall of dorsal aorta decreased amount, abnormal
ZP:0000556	hematopoietic multipotent progenitor cell ventral wall of dorsal aorta absent, abnormal
ZP:0000557	hematopoietic stem cell aplastic, abnormal
ZP:0000558	erythroid progenitor cell absent, abnormal
ZP:0000559	macrophage increased amount, abnormal
ZP:0000560	lymphocyte decreased amount, abnormal
ZP:0000561	monocyte decreased amount, abnormal
ZP:0000562	thrombocyte decreased amount, abnormal
ZP:0000563	neutrophil decreased amount, abnormal
ZP:0000564	cranium decreased size, abnormal
ZP:0000565	somitogenesis delayed, abnormal
ZP:0000566	calcium-dependent cell-cell adhesion via plasma membrane cell adhesion molecules disrupted, abnormal
ZP:0000567	epiboly involved in gastrulation with mouth forming second delayed, abnormal
ZP:0000568	axis decreased length, abnormal
ZP:0000569	yolk circular, abnormal
ZP:0000570	gut quality, abnormal
ZP:0000571	liver quality, abnormal
ZP:0000572	palate decreased size, abnormal
ZP:0000573	palate fused with palate, abnormal
ZP:0000574	central nervous system development disrupted, abnormal
ZP:0000575	notochord development disrupted, abnormal
ZP:0000576	ball increased size, abnormal
ZP:0000577	central nervous system morphology, abnormal
ZP:0000578	central nervous system malformed, abnormal
ZP:0000581	cranium edematous, abnormal
ZP:0000582	myotome increased width, abnormal
ZP:0000583	caudal fin curled, abnormal
ZP:0000584	caudal fin decreased length, abnormal
ZP:0000585	whole organism shortened, abnormal
ZP:0000586	anterior-posterior axis whole organism decreased length, abnormal
ZP:0000588	central artery decreased length, abnormal
ZP:0000589	central artery decreased branchiness, abnormal
ZP:0000592	neural retina development disrupted, abnormal
ZP:0000593	cell population proliferation increased occurrence, abnormal
ZP:0000594	embryo development delayed, abnormal
ZP:0000595	head development disrupted, abnormal
ZP:0000596	retinal pigmented epithelium quality, abnormal
ZP:0000597	retinal pigmented epithelium decreased pigmentation, abnormal
ZP:0000598	head quality, abnormal
ZP:0000599	pigment granule melanocyte decreased amount, abnormal
ZP:0000600	pigment granule xanthophore decreased amount, abnormal
ZP:0000601	pigment granule iridophore decreased amount, abnormal
ZP:0000602	heart jogging arrested, abnormal
ZP:0000603	floor plate formation arrested, abnormal
ZP:0000604	floor plate formation disrupted, abnormal
ZP:0000605	neural plate anterior/posterior regionalization disrupted, abnormal
ZP:0000606	developmental process delayed, abnormal
ZP:0000607	cell migration involved in gastrulation disrupted, abnormal
ZP:0000608	axial mesodermal cell fate specification disrupted, abnormal
ZP:0000609	convergent extension disrupted, abnormal
ZP:0000610	ventral region central nervous system decreased size, abnormal
ZP:0000611	floor plate absent, abnormal
ZP:0000612	floor plate decreased size, abnormal
ZP:0000613	floor plate aplastic, abnormal
ZP:0000614	ventral region floor plate hypoplastic, abnormal
ZP:0000615	hypothalamus decreased size, abnormal
ZP:0000616	prechordal plate morphology, abnormal
ZP:0000617	spinal cord morphology, abnormal
ZP:0000618	axial chorda mesoderm morphology, abnormal
ZP:0000619	axial chorda mesoderm aplastic, abnormal
ZP:0000620	eye mislocalised medially, abnormal
ZP:0000621	eye decreased distance eye, abnormal
ZP:0000622	eye fused with eye, abnormal
ZP:0000623	anterior region fourth ventricle absent, abnormal
ZP:0000624	notochord morphology, abnormal
ZP:0000625	notochord structure, abnormal
ZP:0000626	notochord decreased size, abnormal
ZP:0000627	notochord bent, abnormal
ZP:0000628	notochord curved ventral, abnormal
ZP:0000629	nucleus notochord decreased amount, abnormal
ZP:0000630	cell notochord morphology, abnormal
ZP:0000631	heart tube centered, abnormal
ZP:0000632	medial longitudinal fasciculus fused with medial longitudinal fasciculus, abnormal
ZP:0000633	axon medial longitudinal fasciculus disorganized, abnormal
ZP:0000634	cranial nerve IV fused with cranial nerve IV, abnormal
ZP:0000635	central canal absent, abnormal
ZP:0000636	trunk curved ventral, abnormal
ZP:0000637	post-vent region curved, abnormal
ZP:0000638	post-vent region curved ventral, abnormal
ZP:0000639	neuroectoderm morphology, abnormal
ZP:0000640	neural tube quality, abnormal
ZP:0000641	cell presumptive floor plate decreased amount, abnormal
ZP:0000642	cell presumptive floor plate undifferentiated, abnormal
ZP:0000643	floor plate rhombomere region aplastic, abnormal
ZP:0000644	parachordal cartilage fused with parachordal cartilage, abnormal
ZP:0000645	chondrocranium morphology, abnormal
ZP:0000646	trabecula cranii fused with trabecula cranii, abnormal
ZP:0000647	anterior neural plate morphology, abnormal
ZP:0000648	cranial neural crest cell mislocalised ventrally, abnormal
ZP:0000649	axon secondary motor neuron decreased amount, abnormal
ZP:0000650	lens decreased size, abnormal
ZP:0000651	lens immature, abnormal
ZP:0000652	eye decreased diameter, abnormal
ZP:0000653	retina structure, abnormal
ZP:0000654	retina decreased size, abnormal
ZP:0000655	retina disorganized, abnormal
ZP:0000656	pupil decreased diameter, abnormal
ZP:0000657	retinal ganglion cell decreased amount, abnormal
ZP:0000658	skeletal muscle tissue development delayed, abnormal
ZP:0000659	skeletal muscle tissue development disrupted, abnormal
ZP:0000660	myofibril assembly disrupted, abnormal
ZP:0000661	embryonic cranial skeleton morphogenesis disrupted, abnormal
ZP:0000663	cephalic musculature decreased amount, abnormal
ZP:0000664	whole organism movement quality, abnormal
ZP:0000665	ceratohyal cartilage decreased length, abnormal
ZP:0000666	chondrocyte ceratohyal cartilage morphology, abnormal
ZP:0000667	chondrocyte ceratohyal cartilage decreased size, abnormal
ZP:0000669	muscle disorganized, abnormal
ZP:0000671	sarcomere muscle disorganized, abnormal
ZP:0000672	chondrocyte stacked, abnormal
ZP:0000674	fast muscle cell decreased process quality muscle fiber development, abnormal
ZP:0000675	heart morphogenesis decreased process quality, abnormal
ZP:0000676	cell population proliferation increased rate, abnormal
ZP:0000677	myeloid cell differentiation disrupted, abnormal
ZP:0000678	embryonic heart tube development disrupted, abnormal
ZP:0000679	cardioblast migration to the midline involved in heart field formation disrupted, abnormal
ZP:0000680	heart primordium unfused from left side right side heart primordium, abnormal
ZP:0000681	swim bladder non-functional, abnormal
ZP:0000682	gut immature, abnormal
ZP:0000683	gut deformed, abnormal
ZP:0000684	heart hypoplastic, abnormal
ZP:0000685	heart physical object quality, abnormal
ZP:0000686	heart tube malformed, abnormal
ZP:0000688	cardiac muscle cell decreased amount, abnormal
ZP:0000689	sprouting angiogenesis process quality, abnormal
ZP:0000690	hormone activity decreased occurrence, abnormal
ZP:0000691	nitric oxide biosynthetic process disrupted, abnormal
ZP:0000692	blood circulation absent, abnormal
ZP:0000693	regulation of cardiac muscle contraction by calcium ion signaling disrupted, abnormal
ZP:0000694	calcium-mediated signaling disrupted, abnormal
ZP:0000695	erythrocyte differentiation process quality, abnormal
ZP:0000697	embryonic hemopoiesis decreased process quality, abnormal
ZP:0000698	nucleate erythrocyte development disrupted, abnormal
ZP:0000699	artery morphogenesis delayed, abnormal
ZP:0000700	venous blood vessel morphogenesis disrupted, abnormal
ZP:0000701	regulation of cardiac muscle contraction disrupted, abnormal
ZP:0000702	heart contraction absent, abnormal
ZP:0000703	primitive hemopoiesis process quality, abnormal
ZP:0000704	distal tubule development arrested, abnormal
ZP:0000705	proximal convoluted tubule development arrested, abnormal
ZP:0000706	blood vessel lumenization disrupted, abnormal
ZP:0000707	blood flow rate, abnormal
ZP:0000708	blood increased accumulation caudal vein, abnormal
ZP:0000709	blood accumulation blood vasculature, abnormal
ZP:0000710	blood accumulation trunk, abnormal
ZP:0000711	brain decreased size, abnormal
ZP:0000712	cardiac ventricle conductivity, abnormal
ZP:0000713	cardiac ventricle decreased functionality, abnormal
ZP:0000714	cardiac ventricle decreased diameter, abnormal
ZP:0000715	dorsal aorta structure, abnormal
ZP:0000716	dorsal aorta unlumenized, abnormal
ZP:0000717	brain vasculature hemorrhagic, abnormal
ZP:0000718	fourth ventricle decreased diameter, abnormal
ZP:0000719	heart non-contractile, abnormal
ZP:0000720	liver decreased size, abnormal
ZP:0000721	basibranchial condensed, abnormal
ZP:0000722	blood vessel endothelial cell common cardinal vein decreased amount, abnormal
ZP:0000723	anterior cardinal vein unlumenized, abnormal
ZP:0000724	atrium dilated, abnormal
ZP:0000725	posterior cardinal vein unlumenized, abnormal
ZP:0000726	thymus decreased size, abnormal
ZP:0000727	hematopoietic multipotent progenitor cell thymus decreased amount, abnormal
ZP:0000728	trunk increased accumulation anterior side nucleate erythrocyte, abnormal
ZP:0000729	hematopoietic multipotent progenitor cell trunk decreased amount, abnormal
ZP:0000730	ventricular system decreased size, abnormal
ZP:0000731	cranial vasculature unlumenized, abnormal
ZP:0000732	palatoquadrate arch decreased length, abnormal
ZP:0000733	intersegmental vessel structure, abnormal
ZP:0000734	intersegmental vessel structure, cavities, abnormal
ZP:0000735	caudal vein plexus decreased size, abnormal
ZP:0000737	ceratohyal cartilage orientation ceratohyal cartilage, abnormal
ZP:0000738	simple columnar epithelium displaced, abnormal
ZP:0000739	simple cuboidal epithelium displaced, abnormal
ZP:0000740	ceratobranchial cartilage orientation ceratobranchial cartilage, abnormal
ZP:0000741	pronephric glomerulus unfused from pronephric glomerulus, abnormal
ZP:0000742	basilar artery decreased diameter, abnormal
ZP:0000743	central artery physical object quality, abnormal
ZP:0000744	central artery decreased diameter, abnormal
ZP:0000745	hematopoietic system decreased functionality, abnormal
ZP:0000746	trabecular layer aplastic, abnormal
ZP:0000747	sarcomere ventricular myocardium disorganized, abnormal
ZP:0000748	hepatic sinusoid aplastic, abnormal
ZP:0000749	blood vessel collapsed, abnormal
ZP:0000751	nucleate erythrocyte absent, abnormal
ZP:0000752	cardiac muscle cell increased amount, abnormal
ZP:0000753	cardiac muscle cell electric potential, abnormal
ZP:0000754	cardiac muscle cell decreased area, abnormal
ZP:0000755	abnormal(ly) disrupted  diencephalon development
ZP:0000756	Z disc cardiac muscle cell shape, abnormal
ZP:0000758	hematopoietic multipotent progenitor cell decreased amount, abnormal
ZP:0000759	midbrain hindbrain boundary aplastic, abnormal
ZP:0000760	cerebellum decreased thickness, abnormal
ZP:0000761	extension decreased thickness, abnormal
ZP:0000762	fin aplastic, abnormal
ZP:0000763	fourth ventricle opaque, abnormal
ZP:0000764	otic placode decreased size, abnormal
ZP:0000765	optic tectum increased size, abnormal
ZP:0000766	post-vent region bent, abnormal
ZP:0000767	RNA processing premature, abnormal
ZP:0000768	translational initiation premature, abnormal
ZP:0000769	gastrulation arrested, abnormal
ZP:0000770	nodal signaling pathway premature, abnormal
ZP:0000772	epiboly arrested, abnormal
ZP:0000774	nucleus yolk syncytial layer increased amount, abnormal
ZP:0000775	blastomere delayed RNA localization, abnormal
ZP:0000776	whole organism decreased life span, abnormal
ZP:0000777	neural crest cell migration decreased process quality, abnormal
ZP:0000778	regulation of smoothened signaling pathway disrupted, abnormal
ZP:0000779	regulation of mitotic cell cycle, embryonic process quality, abnormal
ZP:0000781	neural crest cell differentiation decreased process quality, abnormal
ZP:0000782	diencephalon development disrupted, abnormal
ZP:0000783	neurogenesis disrupted, abnormal
ZP:0000784	melanocyte differentiation decreased process quality, abnormal
ZP:0000785	forebrain development decreased process quality, abnormal
ZP:0000788	cell proliferation in midbrain disrupted, abnormal
ZP:0000789	negative regulation of transcription, DNA-templated disrupted, abnormal
ZP:0000790	embryonic neurocranium morphogenesis decreased process quality, abnormal
ZP:0000791	embryonic viscerocranium morphogenesis decreased process quality, abnormal
ZP:0000792	xanthophore differentiation decreased process quality, abnormal
ZP:0000793	melanocyte migration decreased process quality, abnormal
ZP:0000794	hindbrain malformed, abnormal
ZP:0000795	hypothalamus cellular quality, abnormal
ZP:0000796	retinal neural layer decreased size, abnormal
ZP:0000797	fourth ventricle malformed, abnormal
ZP:0000798	midbrain malformed, abnormal
ZP:0000799	tectal ventricle decreased size, abnormal
ZP:0000800	tectal ventricle malformed, abnormal
ZP:0000801	ventral thalamus decreased size, abnormal
ZP:0000802	ventral thalamus cellular quality, abnormal
ZP:0000803	head has fewer parts of type xanthoblast, abnormal
ZP:0000805	trunk has fewer parts of type xanthoblast, abnormal
ZP:0000806	trunk has fewer parts of type melanoblast, abnormal
ZP:0000807	neural tube malformed, abnormal
ZP:0000808	cranial neural crest mislocalised dorsally, abnormal
ZP:0000809	optic fissure malformed, abnormal
ZP:0000810	stomodeum decreased size, abnormal
ZP:0000811	pharyngeal arch cellular quality, abnormal
ZP:0000812	neurocranial trabecula shortened, abnormal
ZP:0000815	medial region ethmoid cartilage absent, abnormal
ZP:0000816	pharyngeal arch cartilage hypoplastic, abnormal
ZP:0000819	pharyngeal arch 2 decreased size, abnormal
ZP:0000820	pharyngeal arch 2 malformed, abnormal
ZP:0000821	pharyngeal arch 1 decreased size, abnormal
ZP:0000822	neural crest cell cellular quality, abnormal
ZP:0000823	melanoblast mislocalised, abnormal
ZP:0000824	melanoblast aggregated, abnormal
ZP:0000825	circadian regulation of gene expression process quality, abnormal
ZP:0000826	cardiac muscle cell atrium increased amount, abnormal
ZP:0000827	cardiac muscle myoblast presumptive atrium primitive heart tube increased amount, abnormal
ZP:0000829	thigmotaxis decreased occurrence, abnormal
ZP:0000830	voltage-gated sodium channel activity amplitude, abnormal
ZP:0000831	voltage-gated sodium channel activity decreased occurrence, abnormal
ZP:0000832	mechanosensory behavior disrupted, abnormal
ZP:0000833	larval locomotory behavior decreased occurrence, abnormal
ZP:0000834	neuron differentiation process quality, abnormal
ZP:0000835	sensory perception of touch decreased magnitude, abnormal
ZP:0000836	axon collateral dorsal root ganglion mislocalised laterally, abnormal
ZP:0000837	neuron neural crest derived dorsal root ganglion mislocalised ventrally, abnormal
ZP:0000838	neuron dorsal root ganglion mobile, abnormal
ZP:0000839	neuron dorsal root ganglion mislocalised ventrally, abnormal
ZP:0000840	voltage-gated sodium channel complex mechanoreceptor cell decreased functionality, abnormal
ZP:0000841	Rohon-Beard neuron present, abnormal
ZP:0000842	Rohon-Beard neuron membrane potential, abnormal
ZP:0000843	Rohon-Beard neuron increased life span, abnormal
ZP:0000844	Rohon-Beard neuron decreased functionality, abnormal
ZP:0000845	primary motor neuron decreased functionality, abnormal
ZP:0000846	axon secondary motor neuron misrouted, abnormal
ZP:0000850	nucleus yolk syncytial layer aggregated, abnormal
ZP:0000853	macula utricle has fewer parts of type hair cell, abnormal
ZP:0000854	semicircular canal malformed, abnormal
ZP:0000856	whole organism curved ventral, abnormal
ZP:0000857	pillar of the semicircular canal unfused from pillar of the semicircular canal, abnormal
ZP:0000858	macula saccule has fewer parts of type hair cell, abnormal
ZP:0000859	neuromast hair cell morphology, abnormal
ZP:0000860	cardiac ventricle dilated, abnormal
ZP:0000861	kidney increased size, abnormal
ZP:0000862	kidney hyperplastic, abnormal
ZP:0000863	kidney has extra parts of type erythroid progenitor cell, abnormal
ZP:0000864	nucleate erythrocyte binucleate, abnormal
ZP:0000865	nucleate erythrocyte spherical, abnormal
ZP:0000866	nucleate erythrocyte teardrop-shaped, abnormal
ZP:0000867	nucleus nucleate erythrocyte structure, abnormal
ZP:0000868	convergent extension involved in gastrulation disrupted, abnormal
ZP:0000869	anterior-posterior axis whole organism shortened, abnormal
ZP:0000870	ossification disrupted, abnormal
ZP:0000871	embryonic viscerocranium morphogenesis disrupted, abnormal
ZP:0000872	cartilage morphogenesis disrupted, abnormal
ZP:0000873	otic lateral line neuromast decreased amount, abnormal
ZP:0000874	cleithrum decreased length, abnormal
ZP:0000875	cleithrum malformed, abnormal
ZP:0000876	dentary malformed, abnormal
ZP:0000877	dentary curved caudal, abnormal
ZP:0000878	dentary fused with maxilla, abnormal
ZP:0000879	mandibular muscle wholly dorsalized, abnormal
ZP:0000880	opercle shape, abnormal
ZP:0000881	opercle size, abnormal
ZP:0000882	opercle increased size, abnormal
ZP:0000883	opercle decreased size, abnormal
ZP:0000884	opercle increased width, abnormal
ZP:0000885	opercle aplastic, abnormal
ZP:0000886	opercle increased variability of size, abnormal
ZP:0000887	cartilaginous joint opercle increased thickness, abnormal
ZP:0000888	cartilaginous joint opercle distended, abnormal
ZP:0000889	maxilla malformed, abnormal
ZP:0000890	maxilla curved caudal, abnormal
ZP:0000891	branchiostegal ray position, abnormal
ZP:0000892	branchiostegal ray decreased size, abnormal
ZP:0000893	branchiostegal ray malformed, abnormal
ZP:0000894	branchiostegal ray falciform, abnormal
ZP:0000895	mouth quality, abnormal
ZP:0000896	mouth concave 3-D shape, abnormal
ZP:0000897	symplectic absent, abnormal
ZP:0000898	infraorbital lateral line neuromast decreased amount, abnormal
ZP:0000899	opercular lateral line neuromast absent, abnormal
ZP:0000901	opercular lateral line neuromast mislocalised dorsally, abnormal
ZP:0000902	opercular lateral line neuromast decreased amount, abnormal
ZP:0000903	middle lateral line neuromast decreased amount, abnormal
ZP:0000904	Meckel's cartilage absent, abnormal
ZP:0000905	Meckel's cartilage bent, abnormal
ZP:0000906	Meckel's cartilage aplastic, abnormal
ZP:0000907	Meckel's cartilage protruding, abnormal
ZP:0000908	Meckel's cartilage mislocalised posteriorly, abnormal
ZP:0000909	Meckel's cartilage fused with palatoquadrate cartilage, abnormal
ZP:0000910	splanchnocranium quality, abnormal
ZP:0000911	joint mandibular arch skeleton absent, abnormal
ZP:0000912	pharyngeal arch 3 skeleton decreased length, abnormal
ZP:0000913	pharyngeal arch 4 skeleton decreased length, abnormal
ZP:0000914	ceratobranchial 5 bone decreased length, abnormal
ZP:0000915	ceratobranchial 5 bone malformed, abnormal
ZP:0000916	ventral mandibular arch decreased size, abnormal
ZP:0000917	ventral mandibular arch aplastic, abnormal
ZP:0000918	ventral mandibular arch orientation eye, abnormal
ZP:0000919	pharyngeal arch 2 skeleton decreased size, abnormal
ZP:0000920	palatoquadrate cartilage increased length, abnormal
ZP:0000921	ceratohyal cartilage morphology, abnormal
ZP:0000922	ceratohyal cartilage structure, abnormal
ZP:0000923	ceratohyal cartilage absent, abnormal
ZP:0000924	ceratohyal cartilage inverted, abnormal
ZP:0000925	ceratohyal cartilage aplastic, abnormal
ZP:0000926	ventral hyoid arch morphology, abnormal
ZP:0000927	hyosymplectic cartilage increased width, abnormal
ZP:0000928	anterior lateral line neuromast increased amount, abnormal
ZP:0000929	anterior lateral line neuromast mislocalised, abnormal
ZP:0000930	pharyngeal arch 2 position, abnormal
ZP:0000931	pharyngeal arch 1 position, abnormal
ZP:0000932	pharyngeal arch 1 malformed, abnormal
ZP:0000934	joint pharyngeal arch 1 physical object quality, abnormal
ZP:0000935	ceratohyal-branchiostegal ray joint morphology, abnormal
ZP:0000936	interhyal-epihyal joint absent, abnormal
ZP:0000937	melanosome localization disrupted, abnormal
ZP:0000938	swimming behavior decreased duration, abnormal
ZP:0000939	swimming behavior disrupted, abnormal
ZP:0000940	cellular pigment accumulation arrested, abnormal
ZP:0000941	retina development in camera-type eye disrupted, abnormal
ZP:0000942	optomotor response decreased process quality, abnormal
ZP:0000943	eye morphology, abnormal
ZP:0000944	photoreceptor cell retinal photoreceptor layer absent, abnormal
ZP:0000945	pigment cell quality, abnormal
ZP:0000946	melanocyte area, abnormal
ZP:0000947	melanosome melanocyte spatial pattern, abnormal
ZP:0000948	melanosome melanocyte dispersed, abnormal
ZP:0000949	retinal bipolar neuron increased amount, abnormal
ZP:0000950	heme biosynthetic process disrupted, abnormal
ZP:0000951	liver has extra parts of type erythroid lineage cell, abnormal
ZP:0000952	kidney has extra parts of type erythroid lineage cell, abnormal
ZP:0000953	hemoglobin complex nucleate erythrocyte composition, abnormal
ZP:0000954	determination of pancreatic left/right asymmetry disrupted, abnormal
ZP:0000955	determination of heart left/right asymmetry disrupted, abnormal
ZP:0000956	determination of liver left/right asymmetry disrupted, abnormal
ZP:0000958	heart mislocalised, abnormal
ZP:0000959	liver mislocalised, abnormal
ZP:0000960	pancreas mislocalised, abnormal
ZP:0000961	trunk bent, abnormal
ZP:0000962	axonal fasciculation disrupted, abnormal
ZP:0000963	synapse assembly increased occurrence, abnormal
ZP:0000965	retinal ganglion cell axon guidance quality, abnormal
ZP:0000966	retinal ganglion cell axon guidance process quality, abnormal
ZP:0000967	anterior/posterior axon guidance process quality, abnormal
ZP:0000968	anterior/posterior axon guidance disrupted, abnormal
ZP:0000969	collateral sprouting in absence of injury increased occurrence, abnormal
ZP:0000970	axon trigeminal ganglion increased branchiness, abnormal
ZP:0000971	axon collateral trigeminal ganglion increased length, abnormal
ZP:0000972	trigeminal ganglion has extra parts of type sensory neuron presynaptic active zone sensory neuron, abnormal
ZP:0000973	cranial nerve III mislocalised, abnormal
ZP:0000974	axon optic chiasm morphology, abnormal
ZP:0000975	supraoptic tract misrouted, abnormal
ZP:0000977	neuron projection dorso-rostral cluster mislocalised, abnormal
ZP:0000978	neuron projection dorso-rostral cluster misrouted, abnormal
ZP:0000980	axon dopaminergic neuron mislocalised medially, abnormal
ZP:0000981	dopaminergic neuron adjacent to axon anterior-posterior axis hindbrain, abnormal
ZP:0000982	dopaminergic neuron adjacent to axon anterior-posterior axis spinal cord, abnormal
ZP:0000983	dopaminergic neuron adjacent to axon axis spinal cord, abnormal
ZP:0000984	axon retinal ganglion cell mislocalised, abnormal
ZP:0000985	axon retinal ganglion cell misrouted, abnormal
ZP:0000986	retinal ganglion cell displaced to axon hindbrain, abnormal
ZP:0000987	retinal ganglion cell displaced to axon telencephalon, abnormal
ZP:0000988	retinal ganglion cell displaced to axon ventral region diencephalon, abnormal
ZP:0000989	retinal ganglion cell displaced to axon contralateral side eye, abnormal
ZP:0000990	vestibular reflex disrupted, abnormal
ZP:0000992	anterior macula fused with posterior macula, abnormal
ZP:0000993	inner ear decreased size, abnormal
ZP:0000995	semicircular canal decreased size, abnormal
ZP:0000996	lapillus mislocalised, abnormal
ZP:0000997	lapillus fused with sagitta, abnormal
ZP:0000998	hair cell anterior macula decreased amount, abnormal
ZP:0000999	posterior lateral line neuromast absent, abnormal
ZP:0001000	whole organism balance, abnormal
ZP:0001001	whole organism decreased coordination, abnormal
ZP:0001003	otolith fused with otolith, abnormal
ZP:0001004	vestibular reflex delayed, abnormal
ZP:0001005	hair cell macula utricle irregular spatial pattern, abnormal
ZP:0001006	utricle lacks parts or has fewer parts of type hair cell, abnormal
ZP:0001007	hair cell utricle morphology, abnormal
ZP:0001008	hair cell mislocalised, abnormal
ZP:0001009	hair cell apoptotic, abnormal
ZP:0001010	otic vesicle decreased size, abnormal
ZP:0001015	epibranchial ganglion decreased amount, abnormal
ZP:0001016	eye development disrupted, abnormal
ZP:0001017	lens morphogenesis in camera-type eye arrested, abnormal
ZP:0001018	lens morphogenesis in camera-type eye disrupted, abnormal
ZP:0001019	type B pancreatic cell differentiation disrupted, abnormal
ZP:0001020	embryo development paedomorphic growth, abnormal
ZP:0001021	anterior/posterior pattern specification disrupted, abnormal
ZP:0001022	lens elliptic, abnormal
ZP:0001023	lens aplastic, abnormal
ZP:0001024	lens protruding, abnormal
ZP:0001025	cornea mislocalised, abnormal
ZP:0001026	rhombomere condensed, abnormal
ZP:0001027	peptide hormone secreting cell endocrine pancreas increased amount, abnormal
ZP:0001028	pancreatic B cell absent, abnormal
ZP:0001029	pancreatic B cell decreased amount, abnormal
ZP:0001030	pancreatic A cell increased amount, abnormal
ZP:0001031	pancreatic A cell decreased amount, abnormal
ZP:0001032	D cell decreased amount, abnormal
ZP:0001033	larval locomotory behavior amplitude, abnormal
ZP:0001034	larval locomotory behavior increased frequency, abnormal
ZP:0001035	collateral sprouting increased occurrence, abnormal
ZP:0001036	whole organism increased speed, abnormal
ZP:0001037	motor neuron decreased amount, abnormal
ZP:0001038	axon collateral motor neuron increased amount, abnormal
ZP:0001039	cartilage development disrupted, abnormal
ZP:0001040	dentary decreased size, abnormal
ZP:0001041	maxilla decreased size, abnormal
ZP:0001042	coracoid absent, abnormal
ZP:0001043	retroarticular aplastic, abnormal
ZP:0001044	ceratobranchial bone decreased size, abnormal
ZP:0001045	ceratobranchial bone aplastic, abnormal
ZP:0001046	ceratohyal bone aplastic, abnormal
ZP:0001047	entopterygoid aplastic, abnormal
ZP:0001048	hyomandibula aplastic, abnormal
ZP:0001049	head circular, abnormal
ZP:0001050	pectoral fin decreased length, abnormal
ZP:0001051	pectoral fin decreased size, abnormal
ZP:0001052	mandibular arch skeleton morphology, abnormal
ZP:0001053	ceratobranchial 5 bone decreased size, abnormal
ZP:0001054	palatoquadrate arch quality, abnormal
ZP:0001055	neurocranial trabecula aplastic, abnormal
ZP:0001056	palatoquadrate cartilage aplastic, abnormal
ZP:0001057	ethmoid cartilage aplastic, abnormal
ZP:0001058	hyosymplectic cartilage aplastic, abnormal
ZP:0001059	parachordal cartilage aplastic, abnormal
ZP:0001060	basal plate cartilage aplastic, abnormal
ZP:0001061	scapulocoracoid decreased size, abnormal
ZP:0001062	scapulocoracoid aplastic, abnormal
ZP:0001063	cranial cartilage aplastic, abnormal
ZP:0001064	cranial cartilage decreased amount, abnormal
ZP:0001065	pharyngeal arch cartilage absent, abnormal
ZP:0001066	basihyal cartilage aplastic, abnormal
ZP:0001067	ceratobranchial cartilage aplastic, abnormal
ZP:0001068	neurocranium absent, abnormal
ZP:0001069	pharyngeal arch 3-7 decreased size, abnormal
ZP:0001070	type B pancreatic cell differentiation decreased process quality, abnormal
ZP:0001071	Notch signaling pathway disrupted, abnormal
ZP:0001072	exocrine pancreas development decreased process quality, abnormal
ZP:0001073	intrahepatic bile duct development disrupted, abnormal
ZP:0001074	intrahepatic bile duct development decreased process quality, abnormal
ZP:0001075	hepaticobiliary system development disrupted, abnormal
ZP:0001076	gall bladder development disrupted, abnormal
ZP:0001077	otic vesicle aplastic, abnormal
ZP:0001078	fin fold actinotrichium decreased amount, abnormal
ZP:0001079	liver green, abnormal
ZP:0001080	pancreas green, abnormal
ZP:0001081	acinar cell pancreas decreased amount, abnormal
ZP:0001082	cleithrum decreased size, abnormal
ZP:0001083	dentary aplastic, abnormal
ZP:0001084	dorsal root ganglion irregular spatial pattern, abnormal
ZP:0001085	dorsal root ganglion decreased amount, abnormal
ZP:0001086	gall bladder decreased size, abnormal
ZP:0001087	maxilla aplastic, abnormal
ZP:0001088	branchiostegal ray aplastic, abnormal
ZP:0001089	parasphenoid decreased size, abnormal
ZP:0001090	whole organism decreased thickness, abnormal
ZP:0001091	post-vent region increased curvature, abnormal
ZP:0001092	ceratobranchial 5 bone aplastic, abnormal
ZP:0001093	endocrine pancreas mislocalised, abnormal
ZP:0001094	endocrine pancreas lacks all parts of type secondary islet, abnormal
ZP:0001095	pancreatic duct morphology, abnormal
ZP:0001096	pancreatic duct malformed, abnormal
ZP:0001097	pancreatic duct dilated, abnormal
ZP:0001098	pancreatic duct decreased branchiness, abnormal
ZP:0001099	pancreatic duct has fewer parts of type cell, abnormal
ZP:0001100	basal plate cartilage decreased size, abnormal
ZP:0001101	pectoral fin endoskeletal disc decreased size, abnormal
ZP:0001102	occipital arch cartilage decreased size, abnormal
ZP:0001103	digestive system duct amorphous, abnormal
ZP:0001104	bile canaliculus decreased length, abnormal
ZP:0001105	bile canaliculus increased width, abnormal
ZP:0001106	intrahepatic bile duct morphology, abnormal
ZP:0001107	intrahepatic bile duct malformed, abnormal
ZP:0001108	primary islet decreased size, abnormal
ZP:0001109	melanocyte increased size, abnormal
ZP:0001110	hepatocyte organization quality, abnormal
ZP:0001111	iridophore decreased amount, abnormal
ZP:0001112	hypothalamus physical object quality, abnormal
ZP:0001113	hypothalamus has fewer parts of type neurosecretory neuron, abnormal
ZP:0001114	hypothalamus has fewer parts of type dopaminergic neuron, abnormal
ZP:0001115	dopaminergic neuron diencephalon decreased amount, abnormal
ZP:0001116	dopaminergic neuron forebrain decreased amount, abnormal
ZP:0001117	serotonergic neuron forebrain decreased amount, abnormal
ZP:0001119	preoptic area physical object quality, abnormal
ZP:0001120	caudal tuberculum physical object quality, abnormal
ZP:0001121	embryonic pattern specification disrupted, abnormal
ZP:0001122	pharyngeal system development disrupted, abnormal
ZP:0001123	canonical Wnt signaling pathway decreased occurrence, abnormal
ZP:0001124	cilium Kupffer's vesicle decreased length, abnormal
ZP:0001125	brain apoptotic, abnormal
ZP:0001126	brain malformed, abnormal
ZP:0001127	hindbrain disorganized, abnormal
ZP:0001129	tail bud morphology, abnormal
ZP:0001130	tail bud decreased length, abnormal
ZP:0001132	pharyngeal arch 3-7 skeleton decreased size, abnormal
ZP:0001133	cerebellum apoptotic, abnormal
ZP:0001135	midbrain apoptotic, abnormal
ZP:0001136	notochord truncated, abnormal
ZP:0001137	somite decreased amount, abnormal
ZP:0001140	central canal dilated, abnormal
ZP:0001141	primary neuron rhombomere crowded, abnormal
ZP:0001142	primary neuron rhombomere disorganized, abnormal
ZP:0001143	head increased size, abnormal
ZP:0001144	post-vent region truncated, abnormal
ZP:0001145	post-vent region kinked, abnormal
ZP:0001146	post-vent region has fewer parts of type somite, abnormal
ZP:0001147	mandibular arch skeleton aplastic, abnormal
ZP:0001149	pharyngeal arch 3-7 morphology, abnormal
ZP:0001150	neuron hindbrain commissure absent, abnormal
ZP:0001151	aortic arch morphology, abnormal
ZP:0001155	cell projection radial glial cell irregular spatial pattern, abnormal
ZP:0001157	neural retina development delayed, abnormal
ZP:0001158	neural retina development decreased process quality, abnormal
ZP:0001159	bone resorption decreased process quality, abnormal
ZP:0001160	macrophage chemotaxis decreased process quality, abnormal
ZP:0001161	brain lacks all parts of type microglial cell, abnormal
ZP:0001162	spinal cord protruding into central canal, abnormal
ZP:0001163	retina undifferentiated, abnormal
ZP:0001164	retina proliferative, abnormal
ZP:0001165	retina lacks all parts of type microglial cell, abnormal
ZP:0001166	retina decreased process quality neurogenesis, abnormal
ZP:0001167	retina delayed neuron differentiation, abnormal
ZP:0001168	retina decreased process quality neuron differentiation, abnormal
ZP:0001169	caudal vein mislocalised, abnormal
ZP:0001170	osteoclast hemal arch decreased amount, abnormal
ZP:0001171	central canal decreased diameter, abnormal
ZP:0001172	osteoclast neural arch decreased amount, abnormal
ZP:0001173	whole organism decreased pigmentation, abnormal
ZP:0001174	melanophore stripe trunk disorganized, abnormal
ZP:0001175	melanocyte hypodermis decreased amount, abnormal
ZP:0001176	xanthophore hypodermis absent, abnormal
ZP:0001177	vertebra decreased size, abnormal
ZP:0001178	microglial cell decreased amount, abnormal
ZP:0001179	melanocyte quality, abnormal
ZP:0001180	melanocyte irregular spatial pattern, abnormal
ZP:0001181	xanthophore quality, abnormal
ZP:0001182	retinal ganglion cell undifferentiated, abnormal
ZP:0001183	adaxial cell morphology, abnormal
ZP:0001184	myofibril muscle pioneer decreased length, abnormal
ZP:0001185	myofibril muscle pioneer decreased thickness, abnormal
ZP:0001186	slow muscle cell malformed, abnormal
ZP:0001187	myofibril slow muscle cell decreased length, abnormal
ZP:0001188	myofibril slow muscle cell decreased thickness, abnormal
ZP:0001189	fast muscle cell malformed, abnormal
ZP:0001190	fast muscle cell unfused from fast muscle cell, abnormal
ZP:0001191	myofibril fast muscle cell decreased length, abnormal
ZP:0001192	heart edematous, abnormal
ZP:0001193	inner ear quality, abnormal
ZP:0001194	heart tube poorly differentiated, abnormal
ZP:0001195	optic cup morphology, abnormal
ZP:0001196	motor neuron quality, abnormal
ZP:0001197	neuron apoptotic, abnormal
ZP:0001198	response to external stimulus quality, abnormal
ZP:0001199	ventricular system development disrupted, abnormal
ZP:0001200	hypothalamus cell differentiation process quality, abnormal
ZP:0001201	dopamine metabolic process quality, abnormal
ZP:0001202	swim bladder inflation disrupted, abnormal
ZP:0001203	musculoskeletal movement disrupted, abnormal
ZP:0001204	sensory perception of touch disrupted, abnormal
ZP:0001205	cell-cell adhesion involved in gastrulation disrupted, abnormal
ZP:0001206	dopaminergic neuron differentiation process quality, abnormal
ZP:0001207	cardiac ventricle increased size, abnormal
ZP:0001208	cardiac ventricle decreased thickness, abnormal
ZP:0001209	neurosecretory neuron hypothalamus decreased amount, abnormal
ZP:0001210	dopaminergic neuron hypothalamus decreased amount, abnormal
ZP:0001211	swim bladder uninflated, abnormal
ZP:0001212	neurosecretory neuron preoptic area decreased amount, abnormal
ZP:0001213	neurosecretory neuron caudal tuberculum decreased amount, abnormal
ZP:0001214	dopaminergic neuron caudal tuberculum decreased amount, abnormal
ZP:0001215	neuron projection ventricular zone decreased amount, abnormal
ZP:0001216	head cuboid, abnormal
ZP:0001217	blastoderm cell blastoderm circular, abnormal
ZP:0001218	ventricular system increased volume, abnormal
ZP:0001219	hepatic sinusoid morphology, abnormal
ZP:0001220	hepatic sinusoid increased size, abnormal
ZP:0001221	blood hepatic sinusoid increased volume, abnormal
ZP:0001222	neuron projection anterior neural keel decreased amount, abnormal
ZP:0001223	dopaminergic neuron decreased amount, abnormal
ZP:0001224	embryonic heart tube formation disrupted, abnormal
ZP:0001226	midbrain-hindbrain boundary morphogenesis disrupted, abnormal
ZP:0001227	extracellular matrix organization disrupted, abnormal
ZP:0001228	embryonic heart tube elongation delayed, abnormal
ZP:0001229	embryonic heart tube elongation disrupted, abnormal
ZP:0001230	cell migration involved in heart formation disrupted, abnormal
ZP:0001231	brain flat, abnormal
ZP:0001232	brain degenerate, abnormal
ZP:0001233	brain unstructured, abnormal
ZP:0001234	brain decreased diameter, abnormal
ZP:0001235	brain surface feature shape, abnormal
ZP:0001236	midbrain hindbrain boundary morphology, abnormal
ZP:0001237	otic vesicle increased size, abnormal
ZP:0001238	otic vesicle decreased width, abnormal
ZP:0001239	otic vesicle elongated, abnormal
ZP:0001240	epithelium otic vesicle morphology, abnormal
ZP:0001241	pericardium increased size, abnormal
ZP:0001242	yolk swollen, abnormal
ZP:0001243	heart rudiment lacks parts or has fewer parts of type extracellular matrix heart rudiment, abnormal
ZP:0001244	heart rudiment has fewer parts of type extracellular matrix heart rudiment, abnormal
ZP:0001245	extracellular matrix heart rudiment composition, abnormal
ZP:0001246	inner ear morphology, abnormal
ZP:0001247	inner ear lacks all parts of type otolith, abnormal
ZP:0001248	heart tube decreased length, abnormal
ZP:0001249	semicircular canal aplastic, abnormal
ZP:0001250	central canal decreased thickness, abnormal
ZP:0001251	whole organism degenerate, abnormal
ZP:0001252	embryonic structure inverted, abnormal
ZP:0001253	head surface feature shape, abnormal
ZP:0001254	trunk curved dorsal, abnormal
ZP:0001255	post-vent region curved dorsal, abnormal
ZP:0001256	forebrain ventricle decreased size, abnormal
ZP:0001257	ventricular system structure, cavities, abnormal
ZP:0001258	otolith decreased size, abnormal
ZP:0001259	otolith decreased distance otolith, abnormal
ZP:0001260	melanocyte morphology, abnormal
ZP:0001261	apical part of cell neuroepithelial cell decreased width, abnormal
ZP:0001262	thigmotaxis disrupted, abnormal
ZP:0001263	mechanosensory behavior process quality, abnormal
ZP:0001264	fluid transport disrupted, abnormal
ZP:0001265	membrane depolarization process quality, abnormal
ZP:0001266	regulation of resting membrane potential disrupted, abnormal
ZP:0001267	cilium Kupffer's vesicle movement quality, abnormal
ZP:0001268	gut mislocalised, abnormal
ZP:0001269	thigmotaxis process quality, abnormal
ZP:0001270	ventricular system dilated, abnormal
ZP:0001272	retinal photoreceptor layer quality, abnormal
ZP:0001273	retinal photoreceptor layer decreased thickness, abnormal
ZP:0001274	retinal photoreceptor layer lacks parts or has fewer parts of type photoreceptor cell, abnormal
ZP:0001275	retina increased occurrence cell death, abnormal
ZP:0001276	cell retina disorganized, abnormal
ZP:0001277	photoreceptor cell circular, abnormal
ZP:0001278	photoreceptor cell apoptotic, abnormal
ZP:0001279	photoreceptor outer segment photoreceptor cell deformed, abnormal
ZP:0001280	Muller cell decreased amount, abnormal
ZP:0001281	retinal bipolar neuron decreased amount, abnormal
ZP:0001282	microtubule cytoskeleton organization decreased process quality, abnormal
ZP:0001283	endodermal cell fate specification process quality, abnormal
ZP:0001284	invagination involved in gastrulation with mouth forming second delayed, abnormal
ZP:0001285	forerunner cell group split, abnormal
ZP:0001286	yolk elongated, abnormal
ZP:0001287	yolk flattened, abnormal
ZP:0001288	microtubule yolk spatial pattern, abnormal
ZP:0001289	nucleus yolk syncytial layer morphology, abnormal
ZP:0001290	extension distended, abnormal
ZP:0001291	dorsal fin absent, abnormal
ZP:0001292	deep blastomere blastodisc shape, abnormal
ZP:0001293	deep blastomere blastodisc crowded, abnormal
ZP:0001294	mesodermal cell migration decreased rate, abnormal
ZP:0001295	endothelial cell dorsal aorta decreased amount, abnormal
ZP:0001296	prechordal plate decreased length, abnormal
ZP:0001297	mesodermal cell hypoblast decreased speed, abnormal
ZP:0001298	neural keel decreased length, abnormal
ZP:0001299	filopodium retina increased amount, abnormal
ZP:0001300	endothelial cell posterior cardinal vein decreased amount, abnormal
ZP:0001301	intersegmental vessel morphology, abnormal
ZP:0001302	endothelial cell intersegmental vessel decreased amount, abnormal
ZP:0001303	caudal vein plexus decreased length, abnormal
ZP:0001304	caudal vein plexus decreased width, abnormal
ZP:0001305	caudal vein plexus decreased area, abnormal
ZP:0001306	dorsal longitudinal anastomotic vessel disorganized, abnormal
ZP:0001307	endothelial cell dorsal longitudinal anastomotic vessel decreased amount, abnormal
ZP:0001308	subintestinal vein deformed, abnormal
ZP:0001309	nucleate erythrocyte increased accumulation blood island, abnormal
ZP:0001310	basophilic erythroblast increased size, abnormal
ZP:0001311	erythroblast increased amount, abnormal
ZP:0001312	nucleate erythrocyte desaturated blue, abnormal
ZP:0001313	nucleate erythrocyte lacks all parts of type hemoglobin complex nucleate erythrocyte, abnormal
ZP:0001314	convergent extension involved in axis elongation disrupted, abnormal
ZP:0001315	palatoquadrate cartilage decreased length, abnormal
ZP:0001316	pharyngeal arch cartilage bent, abnormal
ZP:0001317	pharyngeal arch cartilage condensed, abnormal
ZP:0001318	ceratobranchial cartilage decreased amount, abnormal
ZP:0001319	dorsal/ventral pattern formation process quality, abnormal
ZP:0001321	neural plate development disrupted, abnormal
ZP:0001322	gastrulation decreased occurrence, abnormal
ZP:0001323	brain development disrupted, abnormal
ZP:0001324	anterior neural plate formation disrupted, abnormal
ZP:0001325	epiboly delayed, abnormal
ZP:0001326	epiboly decreased occurrence, abnormal
ZP:0001330	tail bud aplastic, abnormal
ZP:0001331	axis shortened, abnormal
ZP:0001332	neural plate increased width, abnormal
ZP:0001333	notochord broad, abnormal
ZP:0001334	somite malformed, abnormal
ZP:0001335	caudal fin deformed, abnormal
ZP:0001337	whole organism increased occurrence apoptotic process, abnormal
ZP:0001338	whole organism arrested embryo development, abnormal
ZP:0001339	whole organism occurrence gene expression, abnormal
ZP:0001340	whole organism decreased occurrence cell cycle phase transition, abnormal
ZP:0001341	whole organism increased occurrence activation of cysteine-type endopeptidase activity involved in apoptotic signaling pathway, abnormal
ZP:0001342	head aplastic, abnormal
ZP:0001343	post-vent region absent, abnormal
ZP:0001346	midbrain hindbrain boundary neural keel physical object quality, abnormal
ZP:0001348	anterior-most region hindbrain apoptotic, abnormal
ZP:0001349	eye apoptotic, abnormal
ZP:0001350	forebrain apoptotic, abnormal
ZP:0001353	hatching gland aplastic, abnormal
ZP:0001354	polster aplastic, abnormal
ZP:0001355	EVL physical object quality, abnormal
ZP:0001356	EVL poorly differentiated, abnormal
ZP:0001357	nucleus nucleate erythrocyte immature, abnormal
ZP:0001358	hemoglobin complex nucleate erythrocyte absent, abnormal
ZP:0001359	retinoic acid receptor signaling pathway disrupted, abnormal
ZP:0001360	response to auditory stimulus decreased process quality, abnormal
ZP:0001361	axonogenesis involved in innervation decreased process quality, abnormal
ZP:0001362	clustering of voltage-gated calcium channels decreased process quality, abnormal
ZP:0001363	presynaptic membrane assembly decreased process quality, abnormal
ZP:0001365	eye movement quality, abnormal
ZP:0001366	retina apoptotic, abnormal
ZP:0001368	dendrite posterior lateral line nerve unbranched, abnormal
ZP:0001370	melanocyte head increased amount, abnormal
ZP:0001371	melanocyte increased amount, abnormal
ZP:0001372	cytoskeleton of presynaptic active zone eye photoreceptor cell decreased length, abnormal
ZP:0001373	cytoskeleton of presynaptic active zone retinal bipolar neuron morphology, abnormal
ZP:0001374	rod bipolar cell decreased amount, abnormal
ZP:0001375	voltage-gated calcium channel complex neuromast hair cell decreased distribution, abnormal
ZP:0001376	cytoskeleton of presynaptic active zone neuromast hair cell decreased amount, abnormal
ZP:0001377	cyclin-dependent protein serine/threonine kinase activity decreased occurrence, abnormal
ZP:0001378	retina morphogenesis in camera-type eye disrupted, abnormal
ZP:0001379	motor neuron brain increased amount, abnormal
ZP:0001380	retinal ganglion cell layer morphology, abnormal
ZP:0001381	motor neuron spinal cord increased amount, abnormal
ZP:0001382	retinal inner nuclear layer morphology, abnormal
ZP:0001383	retinal outer plexiform layer morphology, abnormal
ZP:0001384	retinal outer nuclear layer morphology, abnormal
ZP:0001385	Rohon-Beard neuron displaced to axis spinal cord, abnormal
ZP:0001387	proneural cluster decreased size, abnormal
ZP:0001388	sensory neuron decreased amount, abnormal
ZP:0001389	Rohon-Beard neuron decreased amount, abnormal
ZP:0001390	integument increased pigmentation, abnormal
ZP:0001391	whole organism wholly ventralized, abnormal
ZP:0001392	somite border U-shaped, abnormal
ZP:0001393	posterior lateral line neuromast increased amount, abnormal
ZP:0001394	afferent neuron truncated, abnormal
ZP:0001395	vasculogenesis disrupted, abnormal
ZP:0001396	lens development in camera-type eye delayed, abnormal
ZP:0001397	retina layer formation delayed, abnormal
ZP:0001398	closure of optic fissure arrested, abnormal
ZP:0001399	central nervous system hemorrhagic, abnormal
ZP:0001400	dorsal aorta morphology, abnormal
ZP:0001402	eye hemorrhagic, abnormal
ZP:0001405	somite decreased height, abnormal
ZP:0001406	somite decreased size, abnormal
ZP:0001408	ventricular system distended, abnormal
ZP:0001409	intersegmental vessel decreased amount, abnormal
ZP:0001410	intersegmental vessel increased branchiness, abnormal
ZP:0001411	endocardium morphology, abnormal
ZP:0001412	endocardium decreased size, abnormal
ZP:0001414	interrenal primordium increased size, abnormal
ZP:0001415	pronephric tubule morphology, abnormal
ZP:0001416	pronephric tubule absent, abnormal
ZP:0001417	pronephric podocyte decreased amount, abnormal
ZP:0001420	hyaloid vessel morphology, abnormal
ZP:0001422	hyaloid vessel decreased amount, abnormal
ZP:0001423	hyaloid vessel branchiness, abnormal
ZP:0001425	vasculature broken, abnormal
ZP:0001428	epiboly involved in gastrulation with mouth forming second disrupted, abnormal
ZP:0001429	microtubule yolk decreased thickness, abnormal
ZP:0001430	endocardial progenitor cell migration to the midline involved in heart field formation decreased process quality, abnormal
ZP:0001431	endocardium formation decreased process quality, abnormal
ZP:0001432	whole organism morphology, abnormal
ZP:0001433	establishment of spindle orientation process quality, abnormal
ZP:0001434	post-vent region deformed, abnormal
ZP:0001435	neural tube formation disrupted, abnormal
ZP:0001436	cloaca development disrupted, abnormal
ZP:0001437	epithelial cell migration involved in distal tubule morphogenesis disrupted, abnormal
ZP:0001438	proctodeum unfused from anatomical region cloacal chamber, abnormal
ZP:0001439	gut malformed, abnormal
ZP:0001440	lateral plate mesoderm malformed, abnormal
ZP:0001441	retinal pigmented epithelium morphology, abnormal
ZP:0001442	pronephric duct decreased length, abnormal
ZP:0001443	pronephric duct dilated, abnormal
ZP:0001444	cilium pronephric duct disoriented, abnormal
ZP:0001445	pronephros cystic, abnormal
ZP:0001446	cloacal chamber distended, abnormal
ZP:0001447	central canal malformed, abnormal
ZP:0001448	whole organism curved, abnormal
ZP:0001449	whole organism curved dorsal, abnormal
ZP:0001450	myocardium malformed, abnormal
ZP:0001451	head edematous, abnormal
ZP:0001452	trunk edematous, abnormal
ZP:0001453	extension decreased size, abnormal
ZP:0001454	extension aplastic, abnormal
ZP:0001455	trunk decreased width, abnormal
ZP:0001456	visual behavior disrupted, abnormal
ZP:0001457	melanosome transport delayed, abnormal
ZP:0001458	detection of light stimulus involved in sensory perception decreased occurrence, abnormal
ZP:0001459	intermediate cell mass of mesoderm aplastic, abnormal
ZP:0001460	notochord deformed, abnormal
ZP:0001461	somite U-shaped, abnormal
ZP:0001462	heart looping arrested, abnormal
ZP:0001463	epiboly involved in gastrulation with mouth forming second arrested, abnormal
ZP:0001464	heart position, abnormal
ZP:0001465	atrium structure, abnormal
ZP:0001466	ventral region whole organism edematous, abnormal
ZP:0001469	central nervous system neuron differentiation disrupted, abnormal
ZP:0001470	synaptic transmission, glycinergic arrested, abnormal
ZP:0001471	cellular response to mechanical stimulus disrupted, abnormal
ZP:0001472	motor neuron spinal cord decreased functionality, abnormal
ZP:0001473	motor neuron decreased functionality, abnormal
ZP:0001474	polarity specification of dorsal/ventral axis disrupted, abnormal
ZP:0001475	pronephros development disrupted, abnormal
ZP:0001476	intermediate cell mass of mesoderm increased width, abnormal
ZP:0001477	whole organism spindle-shaped, abnormal
ZP:0001478	pronephric glomerulus morphology, abnormal
ZP:0001479	platelet aggregation disrupted, abnormal
ZP:0001480	thrombocyte activation disrupted, abnormal
ZP:0001481	caudal artery decreased accumulation thrombocyte, abnormal
ZP:0001482	thrombocyte distributed, abnormal
ZP:0001483	thigmotaxis decreased rate, abnormal
ZP:0001484	muscle contraction process quality, abnormal
ZP:0001485	larval locomotory behavior decreased rate, abnormal
ZP:0001486	skeletal muscle satellite cell proliferation increased occurrence, abnormal
ZP:0001487	skeletal muscle fiber development process quality, abnormal
ZP:0001488	somite disorganized, abnormal
ZP:0001489	somite saccular, abnormal
ZP:0001490	myofibril somite structure, abnormal
ZP:0001491	myofibril somite necrotic, abnormal
ZP:0001492	myofibril somite disorganized, abnormal
ZP:0001493	myofibril somite mononucleate, abnormal
ZP:0001494	somite detached from myofibril somite, abnormal
ZP:0001495	trunk musculature quality, abnormal
ZP:0001496	trunk musculature dystrophic, abnormal
ZP:0001497	vertical myoseptum physical object quality, abnormal
ZP:0001498	myotome degenerate, abnormal
ZP:0001499	myotome refractivity, abnormal
ZP:0001500	sarcolemma myotome disorganized, abnormal
ZP:0001501	skeletal muscle myotome degenerate, abnormal
ZP:0001502	muscle cell myotome degenerate, abnormal
ZP:0001503	muscle cell myotome broken, abnormal
ZP:0001504	skeletal muscle cell myotome decreased amount, abnormal
ZP:0001505	skeletal muscle cell myotome degeneration, abnormal
ZP:0001506	whole organism refractivity, abnormal
ZP:0001507	muscle structure, abnormal
ZP:0001508	muscle damaged, abnormal
ZP:0001509	muscle refractivity, abnormal
ZP:0001510	muscle decreased functionality, abnormal
ZP:0001511	muscle decreased strength, abnormal
ZP:0001512	muscle dystrophic, abnormal
ZP:0001513	muscle organization quality, abnormal
ZP:0001514	skeletal muscle atrophied, abnormal
ZP:0001515	skeletal muscle increased accumulation fibrillar collagen trimer skeletal muscle cell, abnormal
ZP:0001516	neutrophil skeletal muscle present, abnormal
ZP:0001517	neutrophil skeletal muscle aggregated, abnormal
ZP:0001518	skeletal muscle cell degenerate, abnormal
ZP:0001519	skeletal muscle cell broken, abnormal
ZP:0001520	skeletal muscle cell increased variability of size, abnormal
ZP:0001521	skeletal muscle cell detached from myoseptum, abnormal
ZP:0001522	nucleus skeletal muscle cell mislocalised, abnormal
ZP:0001523	mitochondrion skeletal muscle cell irregular spatial pattern, abnormal
ZP:0001524	mitochondrion skeletal muscle cell broken, abnormal
ZP:0001525	myofibril skeletal muscle cell increased contractility, abnormal
ZP:0001526	slow muscle cell detached from myoseptum, abnormal
ZP:0001527	fast muscle cell detached from myoseptum, abnormal
ZP:0001528	histone H3-K9 methylation decreased occurrence, abnormal
ZP:0001529	endocrine pancreas development process quality, abnormal
ZP:0001530	endocrine pancreas malformed, abnormal
ZP:0001531	blood circulation decreased rate, abnormal
ZP:0001532	blood circulation increased rate, abnormal
ZP:0001533	cardiac muscle cell proliferation increased occurrence, abnormal
ZP:0001534	heart contraction increased rate, abnormal
ZP:0001535	oncosis increased occurrence, abnormal
ZP:0001536	cardiac muscle cell cardiac ventricle increased amount, abnormal
ZP:0001537	cardiac muscle cell cardiac ventricle decreased amount, abnormal
ZP:0001538	bulbus arteriosus increased size, abnormal
ZP:0001539	nucleate erythrocyte basophilic, abnormal
ZP:0001540	hemoglobin complex nucleate erythrocyte decreased amount, abnormal
ZP:0001541	cardiac muscle cell hypertrophic, abnormal
ZP:0001542	cardiac muscle cell increased size, abnormal
ZP:0001543	cardiac muscle cell decreased size, abnormal
ZP:0001544	cardiac muscle cell hyperplastic, abnormal
ZP:0001545	myofibril cardiac muscle cell disorganized, abnormal
ZP:0001546	yolk grey, abnormal
ZP:0001547	cell-cell adhesion involved in mesendodermal cell migration disrupted, abnormal
ZP:0001548	homotypic cell-cell adhesion arrested, abnormal
ZP:0001549	embryonic cleavage arrested, abnormal
ZP:0001550	cell migration involved in gastrulation decreased rate, abnormal
ZP:0001551	chordate embryonic development arrested, abnormal
ZP:0001552	hatching gland increased size, abnormal
ZP:0001553	polster morphology, abnormal
ZP:0001554	polster decreased length, abnormal
ZP:0001555	tail bud decreased size, abnormal
ZP:0001556	notochord kinked, abnormal
ZP:0001557	mesodermal cell lateral mesoderm decreased speed, abnormal
ZP:0001558	mesodermal cell lateral mesoderm misrouted, abnormal
ZP:0001560	whole organism broken, abnormal
ZP:0001561	cell neural tube mislocalised, abnormal
ZP:0001562	neuron migration disrupted, abnormal
ZP:0001563	axon guidance process quality, abnormal
ZP:0001564	germ cell migration process quality, abnormal
ZP:0001565	axon extension involved in axon guidance disrupted, abnormal
ZP:0001566	posterior lateral line neuromast primordium migration process quality, abnormal
ZP:0001567	posterior lateral line neuromast primordium migration disrupted, abnormal
ZP:0001568	somite cellular quality, abnormal
ZP:0001569	axon trigeminal ganglion position, abnormal
ZP:0001570	posterior lateral line primordium physical object quality, abnormal
ZP:0001571	olfactory receptor cell mislocalised, abnormal
ZP:0001572	olfactory receptor cell mislocalised ventrally, abnormal
ZP:0001573	olfactory receptor cell mislocalised medially, abnormal
ZP:0001574	axon olfactory receptor cell misrouted, abnormal
ZP:0001575	primordial germ cell quality, abnormal
ZP:0001576	primordial germ cell mislocalised, abnormal
ZP:0001579	sensory perception of light stimulus process quality, abnormal
ZP:0001580	regulation of synaptic transmission, glutamatergic process quality, abnormal
ZP:0001581	gap junction hemi-channel activity process quality, abnormal
ZP:0001582	optomotor response decreased occurrence, abnormal
ZP:0001583	gap junction horizontal cell increased amount, abnormal
ZP:0001584	gap junction horizontal cell decreased size, abnormal
ZP:0001585	connexin complex horizontal cell functionality, abnormal
ZP:0001586	gastrulation delayed, abnormal
ZP:0001587	gastrulation process quality, abnormal
ZP:0001589	embryo development disrupted, abnormal
ZP:0001590	dorsal convergence process quality, abnormal
ZP:0001591	epiboly process quality, abnormal
ZP:0001596	cell migration disrupted, abnormal
ZP:0001597	definitive erythrocyte differentiation disrupted, abnormal
ZP:0001598	hypothalamus increased size, abnormal
ZP:0001599	optic vesicle increased size, abnormal
ZP:0001600	optic vesicle has extra parts of type neurectodermal cell, abnormal
ZP:0001601	otic vesicle morphology, abnormal
ZP:0001602	telencephalon increased length, abnormal
ZP:0001603	diencephalon increased length, abnormal
ZP:0001604	diencephalon increased size, abnormal
ZP:0001605	eye increased size, abnormal
ZP:0001606	neural plate increased size, abnormal
ZP:0001607	optic stalk increased size, abnormal
ZP:0001608	retina increased size, abnormal
ZP:0001609	head morphology, abnormal
ZP:0001610	pectoral fin morphology, abnormal
ZP:0001611	thalamus development disrupted, abnormal
ZP:0001614	zona limitans intrathalamica morphology, abnormal
ZP:0001615	embryonic camera-type eye morphogenesis disrupted, abnormal
ZP:0001616	eye malformed, abnormal
ZP:0001617	retinal pigmented epithelium split, abnormal
ZP:0001618	rhombomere 5 aplastic, abnormal
ZP:0001619	ocular blood vessel malformed, abnormal
ZP:0001620	inner ear morphogenesis disrupted, abnormal
ZP:0001621	otic vesicle shape, abnormal
ZP:0001622	neuromast hair cell posterior lateral line neuromast decreased amount, abnormal
ZP:0001623	otolith protruding, abnormal
ZP:0001624	otolith decreased amount, abnormal
ZP:0001625	pillar of the anterior semicircular canal malformed, abnormal
ZP:0001626	pillar of the lateral semicircular canal malformed, abnormal
ZP:0001627	pillar of the posterior semicircular canal malformed, abnormal
ZP:0001628	semicircular canal development disrupted, abnormal
ZP:0001629	notochord development quality, abnormal
ZP:0001630	developmental pigmentation disrupted, abnormal
ZP:0001631	notochord decreased length, abnormal
ZP:0001632	notochord apoptotic, abnormal
ZP:0001633	notochord undifferentiated, abnormal
ZP:0001634	notochord poorly differentiated, abnormal
ZP:0001635	basement membrane notochord decreased thickness, abnormal
ZP:0001636	basement membrane notochord disorganized, abnormal
ZP:0001638	endoplasmic reticulum notochord swollen, abnormal
ZP:0001639	Golgi apparatus notochord structure, abnormal
ZP:0001640	cell notochord structure, abnormal
ZP:0001641	somite size, abnormal
ZP:0001642	somite condensed, abnormal
ZP:0001643	melanosome trunk absent, abnormal
ZP:0001644	melanosome melanocyte absent, abnormal
ZP:0001645	endoplasmic reticulum muscle cell swollen, abnormal
ZP:0001646	Golgi apparatus muscle cell structure, abnormal
ZP:0001647	central nervous system hypoplastic, abnormal
ZP:0001648	thyroid follicle hypoplastic, abnormal
ZP:0001649	whole organism lacks all parts of type extension, abnormal
ZP:0001650	blood vessel remodeling disrupted, abnormal
ZP:0001651	rhombomere formation decreased process quality, abnormal
ZP:0001652	neural plate decreased length, abnormal
ZP:0001653	common cardinal vein morphology, abnormal
ZP:0001654	rhombomere 5 physical object quality, abnormal
ZP:0001655	rhombomere 5 increased area, abnormal
ZP:0001656	rhombomere 3 increased area, abnormal
ZP:0001657	rhombomere 3 fused with rhombomere 5, abnormal
ZP:0001658	rhombomere 4 decreased area, abnormal
ZP:0001659	heart morphogenesis process quality, abnormal
ZP:0001660	axon extension process quality, abnormal
ZP:0001661	axon extension disrupted, abnormal
ZP:0001662	axon caudal commissure decreased length, abnormal
ZP:0001663	axon motor neuron increased branchiness, abnormal
ZP:0001664	skeletal muscle contraction disrupted, abnormal
ZP:0001665	acetylcholinesterase activity arrested, abnormal
ZP:0001666	acetylcholinesterase activity disrupted, abnormal
ZP:0001667	synaptic transmission, cholinergic increased duration, abnormal
ZP:0001668	neuromuscular junction development process quality, abnormal
ZP:0001669	behavior quality, abnormal
ZP:0001670	locomotory behavior arrested, abnormal
ZP:0001671	locomotory behavior disrupted, abnormal
ZP:0001672	associative learning increased rate, abnormal
ZP:0001673	locomotion behavioral quality of a process, abnormal
ZP:0001674	Rohon-Beard neuron spinal cord apoptotic, abnormal
ZP:0001675	notochord damaged, abnormal
ZP:0001676	trunk musculature contractility, abnormal
ZP:0001677	nuclear envelope trunk musculature shape, abnormal
ZP:0001678	nuclear envelope trunk musculature vacuolated, abnormal
ZP:0001679	acetylcholine-gated channel complex trunk musculature position, abnormal
ZP:0001680	sarcoplasm trunk musculature vacuolated, abnormal
ZP:0001681	myofibril trunk musculature decreased length, abnormal
ZP:0001682	myofibril trunk musculature disorganized, abnormal
ZP:0001683	whole organism paralysed, abnormal
ZP:0001684	Rohon-Beard neuron neural tube apoptotic, abnormal
ZP:0001685	axon motor neuron decreased size, abnormal
ZP:0001686	axon motor neuron decreased thickness, abnormal
ZP:0001687	acetylcholine-gated channel complex muscle cell decreased size, abnormal
ZP:0001688	acetylcholine-gated channel complex muscle cell decreased amount, abnormal
ZP:0001689	myosin filament slow muscle cell decreased amount, abnormal
ZP:0001690	dendrite Rohon-Beard neuron decreased length, abnormal
ZP:0001691	dendrite Rohon-Beard neuron decreased amount, abnormal
ZP:0001692	pectoral fin development disrupted, abnormal
ZP:0001693	pronephric duct development delayed, abnormal
ZP:0001694	retinoic acid receptor signaling pathway process quality, abnormal
ZP:0001695	otic vesicle decreased distance somite 1, abnormal
ZP:0001696	swim bladder quality, abnormal
ZP:0001697	yolk deformed, abnormal
ZP:0001698	pharyngeal arch 3-7 skeleton absent, abnormal
ZP:0001699	proximal region pronephric duct decreased length, abnormal
ZP:0001700	distal region pronephric duct increased length, abnormal
ZP:0001702	mandibular muscle morphology, abnormal
ZP:0001703	myofibril medial rectus disorganized, abnormal
ZP:0001704	cornea increased thickness, abnormal
ZP:0001705	head misaligned with trunk, abnormal
ZP:0001706	anterior-posterior axis head decreased length, abnormal
ZP:0001707	pectoral fin absent, abnormal
ZP:0001708	mandibular arch skeleton malformed, abnormal
ZP:0001709	retinal outer plexiform layer disorganized, abnormal
ZP:0001710	photoreceptor outer segment layer absent, abnormal
ZP:0001711	anterior region vertebral column decreased length, abnormal
ZP:0001712	pharyngeal arch 3-7 physical object quality, abnormal
ZP:0001713	pronephric proximal convoluted tubule decreased length, abnormal
ZP:0001714	pronephric distal late tubule increased length, abnormal
ZP:0001715	corneal epithelium scalloped, abnormal
ZP:0001716	corneal endothelium absent, abnormal
ZP:0001717	heart valve formation disrupted, abnormal
ZP:0001718	hyaluronan biosynthetic process disrupted, abnormal
ZP:0001719	head decreased length, abnormal
ZP:0001720	pectoral fin kinked, abnormal
ZP:0001721	pharyngeal arch cartilage decreased size, abnormal
ZP:0001722	atrioventricular valve morphology, abnormal
ZP:0001723	atrioventricular valve aplastic, abnormal
ZP:0001724	endocardial cushion morphology, abnormal
ZP:0001725	lymph vessel development process quality, abnormal
ZP:0001727	dendrite development disrupted, abnormal
ZP:0001728	branching involved in lymph vessel morphogenesis process quality, abnormal
ZP:0001729	olfactory bulb axon guidance disrupted, abnormal
ZP:0001730	horizontal myoseptum lacks parts or has fewer parts of type axon RoP motor neuron, abnormal
ZP:0001731	horizontal myoseptum lacks parts or has fewer parts of type axon motor neuron, abnormal
ZP:0001732	parachordal vessel immature, abnormal
ZP:0001733	parachordal vessel arrested venous endothelial cell migration involved in lymph vessel development, abnormal
ZP:0001734	thoracic duct aplastic, abnormal
ZP:0001735	VaP motor neuron protruding into axon muscle pioneer, abnormal
ZP:0001737	neuron projection dorso-rostral cluster mislocalised dorsally, abnormal
ZP:0001738	neuron projection dorso-rostral cluster multiple, abnormal
ZP:0001739	axon olfactory receptor cell position, abnormal
ZP:0001741	olfactory receptor cell attached to axon anterior commissure, abnormal
ZP:0001746	olfactory receptor cell attached to axon lateral protoglomerulus 1, abnormal
ZP:0001747	olfactory receptor cell attached to axon lateral protoglomerulus 2, abnormal
ZP:0001748	dendrite efferent neuron mislocalised, abnormal
ZP:0001749	dendrite efferent neuron decreased amount, abnormal
ZP:0001750	hyaloid vessel irregular spatial pattern, abnormal
ZP:0001751	hyaloid vessel increased thickness, abnormal
ZP:0001753	nuclear migration disrupted, abnormal
ZP:0001754	retina layer formation arrested, abnormal
ZP:0001755	neuroblast development disrupted, abnormal
ZP:0001757	dorsal motor nucleus of vagus nerve development disrupted, abnormal
ZP:0001758	melanocyte differentiation delayed, abnormal
ZP:0001759	tube formation disrupted, abnormal
ZP:0001760	maintenance of epithelial cell apical/basal polarity disrupted, abnormal
ZP:0001761	eye pigmentation disrupted, abnormal
ZP:0001762	brain shape, abnormal
ZP:0001763	retinal ganglion cell layer disorganized, abnormal
ZP:0001764	heart decreased size, abnormal
ZP:0001765	heart disorganized, abnormal
ZP:0001766	heart dense, abnormal
ZP:0001767	liver morphology, abnormal
ZP:0001768	retinal pigmented epithelium structure, abnormal
ZP:0001769	retinal pigmented epithelium patchy, abnormal
ZP:0001770	retinal pigmented epithelium poorly differentiated, abnormal
ZP:0001771	pronephros quality, abnormal
ZP:0001772	retina quality, abnormal
ZP:0001773	retina degenerate, abnormal
ZP:0001774	retina cellular quality, abnormal
ZP:0001775	retina unstratified, abnormal
ZP:0001776	neuroepithelial cell retina positional polarity, abnormal
ZP:0001777	atrium aplastic, abnormal
ZP:0001778	cornea structure, abnormal
ZP:0001779	anatomical surface cornea structure, abnormal
ZP:0001780	ceratobranchial 5 bone has fewer parts of type ceratobranchial 5 tooth, abnormal
ZP:0001781	corneal epithelium saccular, abnormal
ZP:0001782	desmosome corneal epithelium decreased amount, abnormal
ZP:0001783	corneal stroma disorganized, abnormal
ZP:0001784	dorsolateral motor nucleus of vagal nerve malformed, abnormal
ZP:0001785	nucleus neuroblast position, abnormal
ZP:0001786	pigmented epithelial cell shape, abnormal
ZP:0001787	pigment granule pigmented epithelial cell mislocalised, abnormal
ZP:0001788	amacrine cell spatial pattern, abnormal
ZP:0001789	corneal epithelial cell cellular adhesivity corneal epithelial cell, abnormal
ZP:0001790	cell-cell junction neuroepithelial cell broken, abnormal
ZP:0001791	endoderm decreased size, abnormal
ZP:0001792	liver disorganized, abnormal
ZP:0001793	pancreas decreased size, abnormal
ZP:0001794	intestine decreased size, abnormal
ZP:0001795	hepatoblast decreased size, abnormal
ZP:0001796	atrioventricular valve formation disrupted, abnormal
ZP:0001797	mesodermal cell fate specification increased process quality, abnormal
ZP:0001798	atrioventricular canal development disrupted, abnormal
ZP:0001799	presumptive mesoderm margin differentiated, abnormal
ZP:0001800	atrioventricular canal morphology, abnormal
ZP:0001801	cell endocardial cushion decreased amount, abnormal
ZP:0001802	aortic arch 5 absent, abnormal
ZP:0001803	heart contraction arrhythmic, abnormal
ZP:0001804	cardiac ventricle increased diameter, abnormal
ZP:0001805	heart tube increased size, abnormal
ZP:0001806	cell morphogenesis disrupted, abnormal
ZP:0001807	mesodermal cell migration delayed, abnormal
ZP:0001808	notochord formation disrupted, abnormal
ZP:0001809	muscle cell migration disrupted, abnormal
ZP:0001810	glycosaminoglycan metabolic process disrupted, abnormal
ZP:0001811	cell migration involved in gastrulation delayed, abnormal
ZP:0001812	notochord morphogenesis disrupted, abnormal
ZP:0001813	dorsal convergence delayed, abnormal
ZP:0001814	Kupffer's vesicle oriented towards ciliated cell anterior region Kupffer's vesicle, abnormal
ZP:0001815	adaxial cell shape, abnormal
ZP:0001816	floor plate oriented towards ciliated cell anterior region floor plate, abnormal
ZP:0001817	prechordal plate elongated, abnormal
ZP:0001818	axis increased width, abnormal
ZP:0001819	forebrain increased width, abnormal
ZP:0001820	cell notochord disorganized, abnormal
ZP:0001821	pronephric duct oriented towards ciliated cell anterior region pronephric duct, abnormal
ZP:0001822	somite decreased length, abnormal
ZP:0001823	myotome decreased length, abnormal
ZP:0001824	rhombomere increased width, abnormal
ZP:0001825	ventral fin fold dislocated cell proctodeum, abnormal
ZP:0001826	anterior-posterior axis whole organism dwarf-like, abnormal
ZP:0001827	medial-lateral axis whole organism increased length, abnormal
ZP:0001828	post-vent region malformed, abnormal
ZP:0001829	notochord post-vent region folded, abnormal
ZP:0001830	Meckel's cartilage structure, abnormal
ZP:0001831	chondrocyte Meckel's cartilage disorganized, abnormal
ZP:0001832	chondrocyte ceratohyal cartilage disorganized, abnormal
ZP:0001833	cranial cartilage deformed, abnormal
ZP:0001834	extracellular matrix cranial cartilage composition, abnormal
ZP:0001835	notochord posterior region folded, abnormal
ZP:0001836	notochord posterior region separated from cell cell notochord posterior region, abnormal
ZP:0001837	anterior neural plate increased width, abnormal
ZP:0001838	slow muscle cell decreased length, abnormal
ZP:0001839	slow muscle cell disorganized, abnormal
ZP:0001841	visual behavior quality, abnormal
ZP:0001842	thyroid gland development decreased process quality, abnormal
ZP:0001843	endocrine system has fewer parts of type thyroid follicle, abnormal
ZP:0001845	motor neuron spinal cord mislocalised, abnormal
ZP:0001846	GABAergic neuron spinal cord increased amount, abnormal
ZP:0001847	GABAergic neuron spinal cord mislocalised, abnormal
ZP:0001848	cilium pronephros increased amount, abnormal
ZP:0001849	multi-ciliated epithelial cell pronephros increased amount, abnormal
ZP:0001850	contractile fiber pectoral fin musculature malformed, abnormal
ZP:0001851	actin filament pectoral fin mislocalised, abnormal
ZP:0001852	pectoral fin endoskeletal disc disorganized, abnormal
ZP:0001853	inner ear development paedomorphic growth, abnormal
ZP:0001854	anterior-posterior axis otic vesicle decreased length, abnormal
ZP:0001855	inner ear decreased length, abnormal
ZP:0001856	lateral semicircular canal decreased size, abnormal
ZP:0001857	hair cell posterior crista absent, abnormal
ZP:0001858	hair cell anterior crista absent, abnormal
ZP:0001859	thyroid primordium malformed, abnormal
ZP:0001860	hyosymplectic cartilage malformed, abnormal
ZP:0001861	otic vesicle protrusion shape, abnormal
ZP:0001862	otic vesicle protrusion malformed, abnormal
ZP:0001863	pillar of the anterior semicircular canal increased thickness, abnormal
ZP:0001864	pillar of the lateral semicircular canal increased thickness, abnormal
ZP:0001866	retina dystrophic, abnormal
ZP:0001867	photoreceptor outer segment layer shortened, abnormal
ZP:0001868	optokinetic behavior arrested, abnormal
ZP:0001869	optomotor response arrested, abnormal
ZP:0001870	glial cell migration disrupted, abnormal
ZP:0001871	Schwann cell differentiation arrested, abnormal
ZP:0001872	Schwann cell development arrested, abnormal
ZP:0001873	Schwann cell development disrupted, abnormal
ZP:0001874	myelin assembly disrupted, abnormal
ZP:0001875	oligodendrocyte differentiation arrested, abnormal
ZP:0001876	semicircular canal morphogenesis disrupted, abnormal
ZP:0001877	semicircular canal fusion arrested, abnormal
ZP:0001878	melanocyte migration disrupted, abnormal
ZP:0001879	otic vesicle distended, abnormal
ZP:0001880	epithelial cell otic vesicle apoptotic, abnormal
ZP:0001881	hair cell otic vesicle increased amount, abnormal
ZP:0001882	anterior macula mislocalised, abnormal
ZP:0001883	posterior lateral line nerve mislocalised, abnormal
ZP:0001884	posterior lateral line nerve defasciculated, abnormal
ZP:0001885	axon posterior lateral line nerve decreased amount, abnormal
ZP:0001886	sodium channel complex posterior lateral line nerve asymmetrical, abnormal
ZP:0001887	sodium channel complex posterior lateral line nerve elongated, abnormal
ZP:0001888	sodium channel complex posterior lateral line nerve undistributed, abnormal
ZP:0001889	sodium channel complex posterior lateral line nerve decreased amount, abnormal
ZP:0001890	myelin sheath posterior lateral line nerve absent, abnormal
ZP:0001891	myelinating Schwann cell posterior lateral line nerve absent, abnormal
ZP:0001892	dorsal root ganglion absent, abnormal
ZP:0001893	dorsal root ganglion increased amount, abnormal
ZP:0001894	dorsal root ganglion mislocalised, abnormal
ZP:0001895	inner ear malformed, abnormal
ZP:0001896	lateral crista primordium aplastic, abnormal
ZP:0001897	neuromast quality, abnormal
ZP:0001898	posterior semicircular canal aplastic, abnormal
ZP:0001899	anterior semicircular canal aplastic, abnormal
ZP:0001900	integument lacks all parts of type pigment cell, abnormal
ZP:0001901	hair cell macula mislocalised, abnormal
ZP:0001902	semicircular canal morphology, abnormal
ZP:0001903	semicircular canal decreased thickness, abnormal
ZP:0001904	semicircular canal disorganized, abnormal
ZP:0001905	posterior macula mislocalised, abnormal
ZP:0001906	otolith organ decreased size, abnormal
ZP:0001907	hair cell posterior crista increased amount, abnormal
ZP:0001908	neuron statoacoustic (VIII) ganglion apoptotic, abnormal
ZP:0001909	hair cell anterior crista increased amount, abnormal
ZP:0001910	posterior lateral line neuromast quality, abnormal
ZP:0001911	glial cell posterior lateral line absent, abnormal
ZP:0001912	whole organism lacks all parts of type melanoblast, abnormal
ZP:0001913	pigment cell head absent, abnormal
ZP:0001914	pigment cell trunk absent, abnormal
ZP:0001915	melanoblast post-vent region decreased amount, abnormal
ZP:0001916	glial cell enteric nervous system decreased amount, abnormal
ZP:0001917	neuron enteric nervous system absent, abnormal
ZP:0001918	presumptive enteric nervous system aplastic, abnormal
ZP:0001919	lateral line quality, abnormal
ZP:0001920	otolith quality, abnormal
ZP:0001921	vagal ganglion malformed, abnormal
ZP:0001922	axon motor neuron structure, abnormal
ZP:0001923	axon motor neuron defasciculated, abnormal
ZP:0001924	glial cell mislocalised, abnormal
ZP:0001925	filopodium glial cell increased speed, abnormal
ZP:0001926	filopodium glial cell increased length, abnormal
ZP:0001927	pigment cell spatial pattern, abnormal
ZP:0001928	melanocyte absent, abnormal
ZP:0001929	myelinating Schwann cell morphology, abnormal
ZP:0001930	myelinating Schwann cell absent, abnormal
ZP:0001931	xanthophore morphology, abnormal
ZP:0001932	melanoblast absent, abnormal
ZP:0001933	melanoblast decreased amount, abnormal
ZP:0001934	hatching arrested, abnormal
ZP:0001935	hatching gland development arrested, abnormal
ZP:0001936	secretory granule hatching gland cell decreased size, abnormal
ZP:0001937	secretory granule hatching gland cell decreased amount, abnormal
ZP:0001938	peripheral nervous system development disrupted, abnormal
ZP:0001939	melanocyte differentiation disrupted, abnormal
ZP:0001941	autonomic nervous system development disrupted, abnormal
ZP:0001944	otic vesicle hypoplastic, abnormal
ZP:0001945	postoptic commissure decreased size, abnormal
ZP:0001946	pharyngeal arch 3-7 skeleton morphology, abnormal
ZP:0001947	pharyngeal arch 3-7 skeleton has fewer parts of type ceratobranchial cartilage, abnormal
ZP:0001951	neuron peripheral nervous system distributed, abnormal
ZP:0001952	retinal pigmented epithelium protruding, abnormal
ZP:0001954	neuron dorsal root ganglion decreased amount, abnormal
ZP:0001955	gill decreased size, abnormal
ZP:0001956	adrenergic neuron locus coeruleus absent, abnormal
ZP:0001957	adrenergic neuron medulla oblongata absent, abnormal
ZP:0001958	quadrate decreased length, abnormal
ZP:0001959	quadrate decreased size, abnormal
ZP:0001960	whole organism lacks all parts of type neuron sympathetic nervous system, abnormal
ZP:0001963	Meckel's cartilage sloped downward, abnormal
ZP:0001964	Meckel's cartilage fused with Meckel's cartilage, abnormal
ZP:0001965	mandibular arch skeleton decreased size, abnormal
ZP:0001966	mandibular arch skeleton disorganized, abnormal
ZP:0001967	mandibular arch skeleton protruding, abnormal
ZP:0001968	mandibular arch skeleton mislocalised ventrally, abnormal
ZP:0001969	pharyngeal arch 3 skeleton decreased size, abnormal
ZP:0001970	pharyngeal arch 7 skeleton decreased size, abnormal
ZP:0001971	pharyngeal arch 6 skeleton absent, abnormal
ZP:0001972	pharyngeal arch 4 skeleton absent, abnormal
ZP:0001973	pharyngeal arch 5 skeleton absent, abnormal
ZP:0001974	pharyngeal arch 2 skeleton morphology, abnormal
ZP:0001975	palatoquadrate cartilage mislocalised, abnormal
ZP:0001976	palatoquadrate cartilage disorganized, abnormal
ZP:0001977	ceratohyal cartilage hypoplastic, abnormal
ZP:0001978	ceratohyal cartilage medially rotated, abnormal
ZP:0001979	ethmoid cartilage split, abnormal
ZP:0001981	trabecula cranii decreased length, abnormal
ZP:0001982	trabecula cranii decreased thickness, abnormal
ZP:0001983	trabecula communis absent, abnormal
ZP:0001984	basihyal cartilage decreased length, abnormal
ZP:0001985	basihyal cartilage decreased size, abnormal
ZP:0001986	basihyal cartilage mislocalised laterally, abnormal
ZP:0001988	neurocranium decreased size, abnormal
ZP:0001989	pharyngeal arch 2 disorganized, abnormal
ZP:0001992	anterior catecholaminergic tract decreased size, abnormal
ZP:0001995	response to light stimulus disrupted, abnormal
ZP:0001996	circadian regulation of gene expression disrupted, abnormal
ZP:0001997	intersegmental vessel increased length, abnormal
ZP:0001998	female germ-line stem cell population maintenance disrupted, abnormal
ZP:0001999	oocyte absent, abnormal
ZP:0002000	primordial germ cell decreased amount, abnormal
ZP:0002001	vasculogenesis process quality, abnormal
ZP:0002002	cell migration involved in sprouting angiogenesis disrupted, abnormal
ZP:0002003	cell migration involved in gastrulation process quality, abnormal
ZP:0002004	blood vessel endothelial cell migration process quality, abnormal
ZP:0002005	muscle cell development disrupted, abnormal
ZP:0002006	dorsal convergence disrupted, abnormal
ZP:0002007	endoderm mislocalised anteriorly, abnormal
ZP:0002008	gut morphology, abnormal
ZP:0002009	gut bifurcated, abnormal
ZP:0002010	pancreas morphology, abnormal
ZP:0002011	pancreatic B cell pancreas dispersed, abnormal
ZP:0002012	angiogenic sprout primordial hindbrain channel mislocalised, abnormal
ZP:0002013	angiogenic sprout primordial hindbrain channel decreased amount, abnormal
ZP:0002014	lateral dorsal aorta malformed, abnormal
ZP:0002015	intestine duplicated, abnormal
ZP:0002016	basilar artery absent, abnormal
ZP:0002017	basilar artery unlumenized, abnormal
ZP:0002018	basilar artery agenesis, abnormal
ZP:0002019	blood vessel endothelial cell mislocalised, abnormal
ZP:0002020	endodermal cell circular, abnormal
ZP:0002021	endodermal cell mislocalised anteriorly, abnormal
ZP:0002022	endodermal cell displaced to margin, abnormal
ZP:0002023	filopodium endodermal cell decreased amount, abnormal
ZP:0002024	endodermal cell orientation filopodium dorsal-ventral axis whole organism, abnormal
ZP:0002025	regionalization disrupted, abnormal
ZP:0002026	cardiac conduction system development disrupted, abnormal
ZP:0002027	type B pancreatic cell development disrupted, abnormal
ZP:0002028	hindbrain morphogenesis disrupted, abnormal
ZP:0002029	pancreas development disrupted, abnormal
ZP:0002030	digestive tract morphogenesis disrupted, abnormal
ZP:0002031	cardiac ventricle non-contractile, abnormal
ZP:0002032	hindbrain irregular spatial pattern, abnormal
ZP:0002033	otic vesicle circular, abnormal
ZP:0002034	otic vesicle wholly anterioralized, abnormal
ZP:0002035	rhombomere 6 morphology, abnormal
ZP:0002036	swim bladder agenesis, abnormal
ZP:0002037	liver aplastic, abnormal
ZP:0002038	liver agenesis, abnormal
ZP:0002039	pancreas hypoplastic, abnormal
ZP:0002040	pancreas aplastic, abnormal
ZP:0002041	pancreas variability of size, abnormal
ZP:0002042	pancreas agenesis, abnormal
ZP:0002043	semicircular canal shape, abnormal
ZP:0002044	kidney cystic, abnormal
ZP:0002045	rhombomere 5 morphology, abnormal
ZP:0002046	intestinal bulb structure, abnormal
ZP:0002047	endocrine pancreas quality, abnormal
ZP:0002048	pancreatic bud aplastic, abnormal
ZP:0002049	otolith shape, abnormal
ZP:0002050	atrioventricular node closed, abnormal
ZP:0002051	atrioventricular node decreased functionality, abnormal
ZP:0002052	intrahepatic bile duct decreased length, abnormal
ZP:0002053	intrahepatic bile duct hypoplastic, abnormal
ZP:0002054	intrahepatic bile duct dilated, abnormal
ZP:0002055	islet disorganized, abnormal
ZP:0002056	pancreatic B cell disorganized, abnormal
ZP:0002057	dorsal convergence decreased rate, abnormal
ZP:0002058	mediolateral intercalation disrupted, abnormal
ZP:0002059	retinal neural layer hypoplastic, abnormal
ZP:0002060	yolk edematous, abnormal
ZP:0002061	obsolete cell retina decreased amount, abnormal
ZP:0002062	cranial nerve II defasciculated, abnormal
ZP:0002063	sensory neuron axon guidance disrupted, abnormal
ZP:0002064	axon Rohon-Beard neuron mislocalized adaxially, abnormal
ZP:0002065	axon Rohon-Beard neuron subdermal, abnormal
ZP:0002066	slow muscle cell decreased amount, abnormal
ZP:0002068	lens separated from cell lens epithelium, abnormal
ZP:0002070	cell population proliferation disrupted, abnormal
ZP:0002071	lens fiber cell differentiation disrupted, abnormal
ZP:0002072	retina decreased thickness, abnormal
ZP:0002074	optic tectum morphology, abnormal
ZP:0002075	amacrine cell decreased amount, abnormal
ZP:0002076	anterior-posterior axis hindbrain decreased length, abnormal
ZP:0002077	anterior region hindbrain decreased size, abnormal
ZP:0002078	spinal cord decreased length, abnormal
ZP:0002079	neural keel wholly anterioralized, abnormal
ZP:0002080	neural plate wholly anterioralized, abnormal
ZP:0002081	spinal cord neural keel decreased length, abnormal
ZP:0002082	midbrain hindbrain boundary neural plate mislocalised posteriorly, abnormal
ZP:0002083	midbrain hindbrain boundary neural keel morphology, abnormal
ZP:0002084	angiogenesis disrupted, abnormal
ZP:0002085	hemopoiesis decreased process quality, abnormal
ZP:0002086	erythrocyte differentiation disrupted, abnormal
ZP:0002087	selective angioblast sprouting disrupted, abnormal
ZP:0002088	regulation of fibroblast growth factor receptor signaling pathway disrupted, abnormal
ZP:0002089	artery morphogenesis disrupted, abnormal
ZP:0002090	embryonic retina morphogenesis in camera-type eye disrupted, abnormal
ZP:0002091	dorsal aorta fused with posterior cardinal vein, abnormal
ZP:0002092	macrophage blood island decreased amount, abnormal
ZP:0002093	heart inverted, abnormal
ZP:0002094	grey matter optic tectum decreased mass, abnormal
ZP:0002095	optic cup wholly ventralized, abnormal
ZP:0002096	Meckel's cartilage fused with hyosymplectic cartilage, abnormal
ZP:0002097	palatoquadrate cartilage rotated, abnormal
ZP:0002098	palatoquadrate cartilage flattened, abnormal
ZP:0002099	ceratohyal cartilage fused with ceratobranchial cartilage, abnormal
ZP:0002100	cranial cartilage morphology, abnormal
ZP:0002101	cranial cartilage mislocalised, abnormal
ZP:0002102	ceratobranchial cartilage fused with ceratobranchial cartilage, abnormal
ZP:0002103	thrombocyte absent, abnormal
ZP:0002104	cranial cartilage fused with cranial cartilage, abnormal
ZP:0002105	brain segmentation disrupted, abnormal
ZP:0002106	facial nerve motor nucleus mislocalised, abnormal
ZP:0002107	neuron rhombomere organization quality, abnormal
ZP:0002108	whole organism lacks all parts of type mandibular arch skeleton, abnormal
ZP:0002109	pectoral fin atrophied, abnormal
ZP:0002110	ethmoid cartilage deformed, abnormal
ZP:0002111	trabecula cranii decreased size, abnormal
ZP:0002112	trabecula cranii deformed, abnormal
ZP:0002113	CNS interneuron decreased amount, abnormal
ZP:0002114	endoderm development process quality, abnormal
ZP:0002115	neural crest cell differentiation process quality, abnormal
ZP:0002116	embryonic viscerocranium morphogenesis process quality, abnormal
ZP:0002117	pharyngeal system development process quality, abnormal
ZP:0002118	pectoral fin bud physical object quality, abnormal
ZP:0002119	pharyngeal pouch 3 aplastic, abnormal
ZP:0002120	pharyngeal pouch 6 aplastic, abnormal
ZP:0002121	pharyngeal pouch 5 aplastic, abnormal
ZP:0002122	pharyngeal pouch 4 aplastic, abnormal
ZP:0002123	pharyngeal arch 7 skeleton aplastic, abnormal
ZP:0002124	pharyngeal arch 6 skeleton aplastic, abnormal
ZP:0002125	pharyngeal arch 4 skeleton aplastic, abnormal
ZP:0002126	pharyngeal arch 5 skeleton aplastic, abnormal
ZP:0002127	mesodermal cell migration persistence, abnormal
ZP:0002128	mesodermal cell migration increased rate, abnormal
ZP:0002130	anterior lateral line neuromast hair cell development disrupted, abnormal
ZP:0002131	posterior lateral line neuromast hair cell development disrupted, abnormal
ZP:0002132	involution involved in gastrulation with mouth forming second disrupted, abnormal
ZP:0002133	otic vesicle morphogenesis disrupted, abnormal
ZP:0002134	prechordal plate flat, abnormal
ZP:0002135	prechordal plate increased length, abnormal
ZP:0002136	prechordal plate increased width, abnormal
ZP:0002137	heart rudiment malformed, abnormal
ZP:0002138	mesodermal cell hypoblast spatial pattern, abnormal
ZP:0002140	mesodermal cell hypoblast cellular motility, abnormal
ZP:0002141	liver bilateral, abnormal
ZP:0002142	neural keel increased length, abnormal
ZP:0002143	notochord increased thickness, abnormal
ZP:0002144	saccule decreased size, abnormal
ZP:0002145	semicircular canal broken into two pieces, abnormal
ZP:0002146	utricle increased size, abnormal
ZP:0002147	posterior lateral line neuromast decreased size, abnormal
ZP:0002148	posterior lateral line has fewer parts of type posterior lateral line neuromast, abnormal
ZP:0002149	caudal fin blistered, abnormal
ZP:0002150	endoderm caudal fin blistered, abnormal
ZP:0002151	pharyngeal endoderm disorganized, abnormal
ZP:0002152	pharyngeal endoderm mislocalised posteriorly, abnormal
ZP:0002153	Meckel's cartilage hypoplastic, abnormal
ZP:0002154	Meckel's cartilage disorganized, abnormal
ZP:0002155	mandibular arch skeleton shape, abnormal
ZP:0002156	mandibular arch skeleton size, abnormal
ZP:0002157	mandibular arch skeleton mislocalised, abnormal
ZP:0002158	neurocranial trabecula hypoplastic, abnormal
ZP:0002159	pharyngeal ectoderm disorganized, abnormal
ZP:0002160	pharyngeal ectoderm increased area, abnormal
ZP:0002161	ethmoid cartilage hypoplastic, abnormal
ZP:0002162	neuromast hair cell anterior lateral line decreased amount, abnormal
ZP:0002163	otolith increased size, abnormal
ZP:0002164	otolith malformed, abnormal
ZP:0002165	oral ectoderm hypoplastic, abnormal
ZP:0002166	oral ectoderm disorganized, abnormal
ZP:0002167	oral ectoderm mislocalised anteriorly, abnormal
ZP:0002169	neuromast hair cell apoptotic, abnormal
ZP:0002170	heart contraction process quality, abnormal
ZP:0002172	cardiac muscle contraction irregular rhythm, abnormal
ZP:0002173	cardiac conduction rhythm quality, abnormal
ZP:0002174	cardiac ventricle non-functional, abnormal
ZP:0002175	cardiac muscle cell cardiac ventricle non-contractile, abnormal
ZP:0002176	heart contractility, abnormal
ZP:0002177	chondrocyte Meckel's cartilage decreased size, abnormal
ZP:0002178	atrial myocardium contractility, abnormal
ZP:0002179	pronephric podocyte unfused from pronephric podocyte, abnormal
ZP:0002180	ventricular myocardium decreased thickness, abnormal
ZP:0002181	ventricular myocardium non-functional, abnormal
ZP:0002182	sprouting angiogenesis decreased process quality, abnormal
ZP:0002183	axonogenesis disrupted, abnormal
ZP:0002184	midbrain development disrupted, abnormal
ZP:0002185	neuron projection development disrupted, abnormal
ZP:0002186	yolk decreased size, abnormal
ZP:0002187	brain vasculature has fewer parts of type central artery, abnormal
ZP:0002188	somite deformed, abnormal
ZP:0002189	axon facial nerve motor nucleus decreased length, abnormal
ZP:0002190	trunk deformed, abnormal
ZP:0002191	axon trigeminal motor nucleus decreased length, abnormal
ZP:0002192	cytoskeleton motor neuron disorganized, abnormal
ZP:0002193	axon motor neuron decreased branchiness, abnormal
ZP:0002194	microtubule Mauthner neuron decreased amount, abnormal
ZP:0002195	microtubule cytoskeleton Mauthner neuron decreased mass density, abnormal
ZP:0002196	cell aging increased magnitude, abnormal
ZP:0002197	yolk necrotic, abnormal
ZP:0002198	yolk opaque, abnormal
ZP:0002199	yolk dark grey, abnormal
ZP:0002200	extension absent, abnormal
ZP:0002201	liver composition, abnormal
ZP:0002202	whole organism edematous, abnormal
ZP:0002203	trunk decreased thickness, abnormal
ZP:0002204	muscle composition, abnormal
ZP:0002205	cardiac atrium development disrupted, abnormal
ZP:0002207	retinoic acid receptor signaling pathway decreased process quality, abnormal
ZP:0002210	posterior lateral line neuromast primordium migration arrested, abnormal
ZP:0002211	protoneuromast posterior lateral line primordium morphology, abnormal
ZP:0002212	thigmotaxis decreased process quality, abnormal
ZP:0002213	central nervous system projection neuron axonogenesis disrupted, abnormal
ZP:0002214	sclerotome development disrupted, abnormal
ZP:0002215	centrum length, abnormal
ZP:0002216	adaxial cell somite decreased amount, abnormal
ZP:0002217	hemal arch irregular spatial pattern, abnormal
ZP:0002218	horizontal myoseptum absent, abnormal
ZP:0002219	myotome shape, abnormal
ZP:0002220	neural arch irregular spatial pattern, abnormal
ZP:0002221	sclerotome spatial pattern, abnormal
ZP:0002222	post-vent region shape, abnormal
ZP:0002223	vertebra structure, abnormal
ZP:0002224	somite border absent, abnormal
ZP:0002225	somite border inconspicuous, abnormal
ZP:0002226	axon MiP motor neuron irregular spatial pattern, abnormal
ZP:0002227	axon MiP motor neuron decreased length, abnormal
ZP:0002228	axon CaP motoneuron irregular spatial pattern, abnormal
ZP:0002229	axon CaP motoneuron increased amount, abnormal
ZP:0002230	axon CaP motoneuron decreased length, abnormal
ZP:0002231	head pointed, abnormal
ZP:0002232	habenula development disrupted, abnormal
ZP:0002233	neurogenesis increased occurrence, abnormal
ZP:0002234	cell division increased occurrence, abnormal
ZP:0002235	cerebellum has extra parts of type neuron, abnormal
ZP:0002236	epithelium third ventricle morphology, abnormal
ZP:0002237	columnar/cuboidal epithelial cell third ventricle circular, abnormal
ZP:0002238	third ventricle cellular adhesivity columnar/cuboidal epithelial cell columnar/cuboidal epithelial cell third ventricle, abnormal
ZP:0002239	dorsal habenular nucleus morphology, abnormal
ZP:0002240	dorsal habenular nucleus has extra parts of type right side neuron, abnormal
ZP:0002241	dorsal habenular nucleus has extra parts of type lateral region neuron, abnormal
ZP:0002242	dorsal habenular nucleus has fewer parts of type medial region neuron, abnormal
ZP:0002243	neuron dorsal habenular nucleus spatial pattern, abnormal
ZP:0002244	habenula has extra parts of type left side neuron, abnormal
ZP:0002245	habenula has extra parts of type right side neuron, abnormal
ZP:0002246	hyomandibula decreased size, abnormal
ZP:0002247	anterior-posterior axis whole organism curved dorsal, abnormal
ZP:0002248	head decreased volume, abnormal
ZP:0002249	extracellular matrix mandibular arch skeleton sparse, abnormal
ZP:0002250	chondrocyte mandibular arch skeleton cellular quality, abnormal
ZP:0002251	cartilage element morphology, abnormal
ZP:0002252	cell-cell junction columnar/cuboidal epithelial cell decreased amount, abnormal
ZP:0002253	endoplasmic reticulum chondrocyte decreased volume, abnormal
ZP:0002254	filamentous actin neuroepithelial cell decreased amount, abnormal
ZP:0002255	midbrain hindbrain boundary condensed, abnormal
ZP:0002256	fourth ventricle distended, abnormal
ZP:0002257	cranium hypoplastic, abnormal
ZP:0002258	cranium malformed, abnormal
ZP:0002259	notochord morphogenesis decreased process quality, abnormal
ZP:0002260	notochord cell vacuolation decreased process quality, abnormal
ZP:0002261	retina morphogenesis in camera-type eye process quality, abnormal
ZP:0002262	vacuole notochord broken, abnormal
ZP:0002263	retinal pigmented epithelium physical object quality, abnormal
ZP:0002264	retinal pigmented epithelium translucent, abnormal
ZP:0002265	post-vent region decreased pigmentation, abnormal
ZP:0002266	pharyngeal arch 3-7 shape, abnormal
ZP:0002267	melanocyte larval melanophore stripe translucent, abnormal
ZP:0002268	pigment cell patchy, abnormal
ZP:0002269	melanocyte malformed, abnormal
ZP:0002270	melanocyte translucent, abnormal
ZP:0002271	photoreceptor outer segment eye photoreceptor cell decreased size, abnormal
ZP:0002272	brain necrotic, abnormal
ZP:0002273	yolk non-functional, abnormal
ZP:0002274	chromosome peripheral nervous system amount, abnormal
ZP:0002275	trunk necrotic, abnormal
ZP:0002276	mandibular arch skeleton increased thickness, abnormal
ZP:0002277	cell aging decreased magnitude, abnormal
ZP:0002278	heart necrotic, abnormal
ZP:0002279	pectoral fin shape, abnormal
ZP:0002280	pectoral fin stubby, abnormal
ZP:0002281	cartilage element decreased length, abnormal
ZP:0002282	cartilage element rough, abnormal
ZP:0002283	cartilage element wrinkled, abnormal
ZP:0002284	ball opaque, abnormal
ZP:0002285	hindbrain undulate, abnormal
ZP:0002286	midbrain hindbrain boundary decreased thickness, abnormal
ZP:0002287	forebrain protruding, abnormal
ZP:0002288	nerve peripheral nervous system neoplastic, abnormal
ZP:0002289	optic tectum opaque, abnormal
ZP:0002290	otolith organ deformed, abnormal
ZP:0002291	pigmentation decreased occurrence, abnormal
ZP:0002292	eye color, abnormal
ZP:0002293	fin malformed, abnormal
ZP:0002294	gut decreased size, abnormal
ZP:0002295	retinal pigmented epithelium malformed, abnormal
ZP:0002296	whole organism low saturation, abnormal
ZP:0002297	whole organism unpigmented, abnormal
ZP:0002298	pectoral fin ruffled, abnormal
ZP:0002299	melanocyte punctate, abnormal
ZP:0002300	thymus decreased occurrence cell population proliferation, abnormal
ZP:0002301	epithelial cell thymus decreased amount, abnormal
ZP:0002302	trunk undulate, abnormal
ZP:0002303	pharyngeal arch 3-7 aplastic, abnormal
ZP:0002304	telencephalon deformed, abnormal
ZP:0002305	extension deformed, abnormal
ZP:0002306	otic placode shape, abnormal
ZP:0002307	alternative mRNA splicing, via spliceosome process quality, abnormal
ZP:0002308	regulation of alternative mRNA splicing, via spliceosome disrupted, abnormal
ZP:0002309	eye necrotic, abnormal
ZP:0002310	whole organism circling, abnormal
ZP:0002311	head necrotic, abnormal
ZP:0002312	S phase increased duration, abnormal
ZP:0002313	hindbrain surface feature shape, abnormal
ZP:0002314	head shape, abnormal
ZP:0002316	heparan sulfate proteoglycan biosynthetic process decreased occurrence, abnormal
ZP:0002317	chondroitin sulfate biosynthetic process process quality, abnormal
ZP:0002318	chondroitin sulfate proteoglycan biosynthetic process decreased occurrence, abnormal
ZP:0002319	sulfation decreased occurrence, abnormal
ZP:0002320	endochondral bone morphogenesis delayed, abnormal
ZP:0002321	opercle malformed, abnormal
ZP:0002322	mandibular arch skeleton decreased length, abnormal
ZP:0002323	mandibular arch skeleton condensed, abnormal
ZP:0002324	collagen trimer cranial cartilage morphology, abnormal
ZP:0002325	collagen type I trimer cranial cartilage decreased amount, abnormal
ZP:0002326	collagen type II trimer cranial cartilage decreased amount, abnormal
ZP:0002327	collagen type VI trimer cranial cartilage absent, abnormal
ZP:0002328	pharyngeal arch cartilage decreased length, abnormal
ZP:0002329	pharyngeal arch cartilage increased thickness, abnormal
ZP:0002330	pharyngeal arch cartilage oriented, abnormal
ZP:0002331	chondrocyte pharyngeal arch cartilage circular, abnormal
ZP:0002332	chondrocyte pharyngeal arch cartilage disorganized, abnormal
ZP:0002333	liver development paedomorphic growth, abnormal
ZP:0002334	exocrine pancreas development paedomorphic growth, abnormal
ZP:0002335	regulation of cell cycle disrupted, abnormal
ZP:0002336	yolk shape, abnormal
ZP:0002337	melanophore stripe yolk absent, abnormal
ZP:0002338	gut increased width, abnormal
ZP:0002339	cell gut increased amount, abnormal
ZP:0002340	anterior region notochord increased width, abnormal
ZP:0002341	retina perforate, abnormal
ZP:0002342	retina increased occurrence intrinsic apoptotic signaling pathway by p53 class mediator, abnormal
ZP:0002343	cell retina apoptotic, abnormal
ZP:0002344	facial nerve motor nucleus morphology, abnormal
ZP:0002345	neuron statoacoustic (VIII) ganglion decreased amount, abnormal
ZP:0002346	common lymphoid progenitor thymus primordium absent, abnormal
ZP:0002347	trunk curved, abnormal
ZP:0002348	trunk degenerate, abnormal
ZP:0002349	neural crest cell post-vent region present, abnormal
ZP:0002350	exocrine pancreas aplastic, abnormal
ZP:0002351	optic fissure open, abnormal
ZP:0002352	melanophore stripe decreased amount, abnormal
ZP:0002353	melanocyte melanophore stripe decreased amount, abnormal
ZP:0002354	hematopoietic stem cell ventral wall of dorsal aorta absent, abnormal
ZP:0002355	motor neuron mislocalised, abnormal
ZP:0002356	CNS neuron (sensu Vertebrata) decreased amount, abnormal
ZP:0002357	melanocyte position, abnormal
ZP:0002358	melanocyte mislocalised, abnormal
ZP:0002359	melanocyte cellular motility, abnormal
ZP:0002360	endocrine cell mislocalised, abnormal
ZP:0002361	endodermal cell decreased amount, abnormal
ZP:0002362	vacuole notochord disorganized, abnormal
ZP:0002363	trunk has fewer parts of type melanocyte, abnormal
ZP:0002364	trunk has fewer parts of type iridophore, abnormal
ZP:0002365	iridophore quality, abnormal
ZP:0002366	spindle pole proliferative region increased amount, abnormal
ZP:0002367	chondrocyte intercalation involved in growth plate cartilage morphogenesis disrupted, abnormal
ZP:0002368	cell junction organization disrupted, abnormal
ZP:0002369	ceratohyal bone absent, abnormal
ZP:0002370	hyomandibula absent, abnormal
ZP:0002371	Meckel's cartilage decreased distance anterior side posterior side ceratohyal cartilage, abnormal
ZP:0002372	fibrillar collagen trimer cranial cartilage absent, abnormal
ZP:0002373	collagen type II trimer cranial cartilage absent, abnormal
ZP:0002374	extracellular matrix cranial cartilage decreased size, abnormal
ZP:0002376	pharyngeal arch cartilage aplastic, abnormal
ZP:0002377	chondrocyte pharyngeal arch cartilage crowded, abnormal
ZP:0002378	chondrocranium cartilage aplastic, abnormal
ZP:0002379	perichondral bone aplastic, abnormal
ZP:0002380	perichondrium aplastic, abnormal
ZP:0002381	chondrocyte morphology, abnormal
ZP:0002382	chondrocyte fused with chondrocyte, abnormal
ZP:0002383	chondrocyte attached to chondrocyte, abnormal
ZP:0002384	fibrillar collagen trimer chondrocyte decreased amount, abnormal
ZP:0002385	plasma membrane chondrocyte smooth, abnormal
ZP:0002386	extracellular matrix chondrocyte condensed, abnormal
ZP:0002387	extracellular matrix chondrocyte decreased area, abnormal
ZP:0002388	cell projection membrane chondrocyte absent, abnormal
ZP:0002389	mitotic M phase temporally extended, abnormal
ZP:0002390	spindle organization disrupted, abnormal
ZP:0002391	mitotic chromosome movement towards spindle pole disrupted, abnormal
ZP:0002392	mitotic metaphase plate congression disrupted, abnormal
ZP:0002393	spindle assembly disrupted, abnormal
ZP:0002394	lens protruding out of eye, abnormal
ZP:0002395	retinal neural layer disorganized, abnormal
ZP:0002397	retina has fewer parts of type cell retina, abnormal
ZP:0002398	retina lacks parts or has fewer parts of type centrosome cell, abnormal
ZP:0002399	retina increased duration mitotic M phase, abnormal
ZP:0002400	retina arrested mitotic prometaphase, abnormal
ZP:0002401	retina increased duration mitotic prometaphase, abnormal
ZP:0002402	retina increased duration M phase, abnormal
ZP:0002403	retina increased occurrence apoptotic process, abnormal
ZP:0002407	retina increased duration cell division, abnormal
ZP:0002408	caudal fin curved, abnormal
ZP:0002409	neuron head apoptotic, abnormal
ZP:0002410	trunk sigmoid, abnormal
ZP:0002411	gamma-tubulin complex cell mislocalised, abnormal
ZP:0002412	spindle cell disorganized, abnormal
ZP:0002413	spindle pole centrosome cell absent, abnormal
ZP:0002414	optic tectum necrotic, abnormal
ZP:0002415	cytokinesis disrupted, abnormal
ZP:0002416	chromosome segregation disrupted, abnormal
ZP:0002417	swim bladder collapsed, abnormal
ZP:0002418	germ plasm blastomere mislocalised, abnormal
ZP:0002419	mouth protruding, abnormal
ZP:0002420	blastoderm morphology, abnormal
ZP:0002421	cleavage furrow blastoderm absent, abnormal
ZP:0002422	cleavage furrow blastoderm decreased length, abnormal
ZP:0002423	cleavage furrow blastoderm malformed, abnormal
ZP:0002424	nucleus cell condensed, abnormal
ZP:0002425	midbody cell decreased mass density, abnormal
ZP:0002426	melanosome transport disrupted, abnormal
ZP:0002427	Kupffer's vesicle decreased size, abnormal
ZP:0002428	embryo development process quality, abnormal
ZP:0002429	hindbrain opaque, abnormal
ZP:0002430	lens increased size, abnormal
ZP:0002431	yolk extension absent, abnormal
ZP:0002432	fin deformed, abnormal
ZP:0002433	retinal pigment epithelium development process quality, abnormal
ZP:0002434	eye pigment granule organization process quality, abnormal
ZP:0002436	melanosome organization process quality, abnormal
ZP:0002437	retinal cell programmed cell death increased rate, abnormal
ZP:0002438	developmental pigmentation process quality, abnormal
ZP:0002439	eye pigmentation process quality, abnormal
ZP:0002440	swim bladder formation process quality, abnormal
ZP:0002441	neuron apoptotic process increased rate, abnormal
ZP:0002442	retinal pigmented epithelium increased thickness, abnormal
ZP:0002443	retinal pigmented epithelium vacuolated, abnormal
ZP:0002444	retinal pigmented epithelium mottled, abnormal
ZP:0002445	melanosome retinal pigmented epithelium decreased size, abnormal
ZP:0002446	melanosome retinal pigmented epithelium malformed, abnormal
ZP:0002447	melanosome retinal pigmented epithelium broken, abnormal
ZP:0002448	retinal outer nuclear layer disorganized, abnormal
ZP:0002449	intrahepatic bile duct distended, abnormal
ZP:0002450	intrahepatic bile duct decreased amount, abnormal
ZP:0002451	melanocyte degree of pigmentation, abnormal
ZP:0002452	eye photoreceptor cell malformed, abnormal
ZP:0002453	photoreceptor outer segment eye photoreceptor cell malformed, abnormal
ZP:0002454	photoreceptor outer segment eye photoreceptor cell elongated, abnormal
ZP:0002455	swim bladder formation delayed, abnormal
ZP:0002456	whole organism decreased weight, abnormal
ZP:0002457	muscle contraction decreased occurrence, abnormal
ZP:0002458	locomotion decreased occurrence, abnormal
ZP:0002459	swim bladder formation arrested, abnormal
ZP:0002460	striated muscle myosin thick filament assembly disrupted, abnormal
ZP:0002461	muscle thin filament assembly disrupted, abnormal
ZP:0002462	myofibril slow muscle cell disorganized, abnormal
ZP:0002463	sarcomere fast muscle cell decreased amount, abnormal
ZP:0002464	mitotic S phase duration, abnormal
ZP:0002465	mitotic M phase duration, abnormal
ZP:0002466	regulation of heart rate disrupted, abnormal
ZP:0002467	fat cell differentiation decreased occurrence, abnormal
ZP:0002468	cellular senescence increased occurrence, abnormal
ZP:0002469	sinus venosus increased accumulation blood, abnormal
ZP:0002470	integument rough, abnormal
ZP:0002471	slow muscle cell myotome undulate, abnormal
ZP:0002472	slow muscle cell myotome decreased amount, abnormal
ZP:0002473	trunk apoptotic, abnormal
ZP:0002474	Meckel's cartilage alignment palatoquadrate cartilage, abnormal
ZP:0002475	ceratohyal cartilage mislocalised posteriorly, abnormal
ZP:0002476	pharyngeal arch cartilage physical object quality, abnormal
ZP:0002477	fat cell decreased amount, abnormal
ZP:0002478	axis increased curvature, abnormal
ZP:0002479	dorsal longitudinal anastomotic vessel morphology, abnormal
ZP:0002480	dorsal longitudinal anastomotic vessel absent, abnormal
ZP:0002481	vasculature branchiness, abnormal
ZP:0002482	heart morphogenesis delayed, abnormal
ZP:0002484	ear development disrupted, abnormal
ZP:0002485	cardiac ventricle hypoplastic, abnormal
ZP:0002486	spinal cord apoptotic, abnormal
ZP:0002487	hair cell inner ear absent, abnormal
ZP:0002488	posterior crista primordium aplastic, abnormal
ZP:0002489	anterior crista primordium aplastic, abnormal
ZP:0002490	fast muscle cell decreased amount, abnormal
ZP:0002491	CaP motoneuron decreased amount, abnormal
ZP:0002492	axon CaP motoneuron decreased functionality, abnormal
ZP:0002493	retinal ganglion cell absent, abnormal
ZP:0002494	muscle contraction arrested, abnormal
ZP:0002495	germ cell migration disrupted, abnormal
ZP:0002496	primordial germ cell misrouted, abnormal
ZP:0002497	retina layer formation process quality, abnormal
ZP:0002498	growth disrupted, abnormal
ZP:0002499	hindbrain decreased size, abnormal
ZP:0002500	midbrain hindbrain boundary deformed, abnormal
ZP:0002501	pericardium dilated, abnormal
ZP:0002502	heart dilated, abnormal
ZP:0002503	midbrain decreased size, abnormal
ZP:0002506	heart looping process quality, abnormal
ZP:0002507	opsin transport disrupted, abnormal
ZP:0002508	left/right pattern formation disrupted, abnormal
ZP:0002509	cloacal chamber deformed, abnormal
ZP:0002512	kidney edematous, abnormal
ZP:0002513	anterior-posterior axis whole organism curved, abnormal
ZP:0002516	pronephric glomerulus cystic, abnormal
ZP:0002517	pronephric tubule pronephric glomerulus increased diameter, abnormal
ZP:0002518	pronephric proximal convoluted tubule increased diameter, abnormal
ZP:0002520	establishment of mitotic spindle orientation disrupted, abnormal
ZP:0002521	cilium movement decreased frequency, abnormal
ZP:0002522	neural fold folding delayed, abnormal
ZP:0002523	facial nerve development disrupted, abnormal
ZP:0002524	establishment of cell polarity disrupted, abnormal
ZP:0002525	convergent extension involved in gastrulation process quality, abnormal
ZP:0002526	Kupffer's vesicle increased size, abnormal
ZP:0002527	ventral region brain condensed, abnormal
ZP:0002528	central nervous system degenerate, abnormal
ZP:0002529	floor plate increased width, abnormal
ZP:0002530	floor plate distended, abnormal
ZP:0002532	ciliated cell floor plate increased amount, abnormal
ZP:0002533	hindbrain process quality motor neuron migration, abnormal
ZP:0002534	rhombomere 6 lacks all parts of type branchiomotor neuron, abnormal
ZP:0002535	spinal cord duplicated, abnormal
ZP:0002536	axial chorda mesoderm decreased length, abnormal
ZP:0002537	axial chorda mesoderm increased width, abnormal
ZP:0002538	extension increased width, abnormal
ZP:0002539	eye decreased width, abnormal
ZP:0002540	fourth ventricle duplicated, abnormal
ZP:0002541	neural keel increased thickness, abnormal
ZP:0002542	neural keel increased width, abnormal
ZP:0002543	neural rod morphology, abnormal
ZP:0002544	neural rod increased thickness, abnormal
ZP:0002545	neural rod increased width, abnormal
ZP:0002546	cilium pronephric duct disorganized, abnormal
ZP:0002547	cilium pronephric duct decreased functionality, abnormal
ZP:0002548	multi-ciliated epithelial cell pronephric duct disorganized, abnormal
ZP:0002549	ciliated cell pronephros decreased amount, abnormal
ZP:0002550	somite flat, abnormal
ZP:0002551	motor neuron facial nerve motor nucleus mislocalised, abnormal
ZP:0002552	gall bladder mislocalised laterally, abnormal
ZP:0002553	gall bladder left side of whole organism, abnormal
ZP:0002554	paraxial mesoderm decreased length, abnormal
ZP:0002555	paraxial mesoderm increased width, abnormal
ZP:0002556	cloacal chamber malformed, abnormal
ZP:0002557	ciliated cell cloacal chamber decreased amount, abnormal
ZP:0002558	rhombomere 5 lacks all parts of type branchiomotor neuron, abnormal
ZP:0002559	rhombomere 7 lacks all parts of type branchiomotor neuron, abnormal
ZP:0002560	branchiomotor neuron rhombomere 4 mislocalised, abnormal
ZP:0002561	presumptive pronephric mesoderm mislocalised laterally, abnormal
ZP:0002562	whole organism increased curvature, abnormal
ZP:0002563	head hydrocephalic, abnormal
ZP:0002564	trunk increased curvature, abnormal
ZP:0002565	somite trunk morphology, abnormal
ZP:0002566	post-vent region vacuolated, abnormal
ZP:0002567	post-vent region clavate, abnormal
ZP:0002568	somite post-vent region morphology, abnormal
ZP:0002569	neural tube increased thickness, abnormal
ZP:0002570	neural tube increased width, abnormal
ZP:0002571	cell projection branchiomotor neuron lateral orientation, abnormal
ZP:0002573	ciliated cell increased angle to mitotic spindle apical-basal axis relative to substrate pronephros, abnormal
ZP:0002574	neuroepithelial cell mislocalised, abnormal
ZP:0002575	heart centered, abnormal
ZP:0002576	pronephric duct detached from cell pronephric glomerular basement membrane pronephros, abnormal
ZP:0002577	cell proliferation in forebrain decreased occurrence, abnormal
ZP:0002578	anterior region hindbrain truncated, abnormal
ZP:0002579	neuronal cell body cranial nerve V position, abnormal
ZP:0002580	motor neuron cranial nerve V disorganized, abnormal
ZP:0002581	rhombomere 2 apoptotic, abnormal
ZP:0002582	rhombomere 5 apoptotic, abnormal
ZP:0002583	rhombomere 3 decreased width, abnormal
ZP:0002584	rhombomere 3 apoptotic, abnormal
ZP:0002585	rhombomere 4 apoptotic, abnormal
ZP:0002586	caudal tuberculum has fewer parts of type dopaminergic neuron, abnormal
ZP:0002587	trunk decreased size, abnormal
ZP:0002588	larval locomotory behavior process quality, abnormal
ZP:0002589	whole organism unbalanced, abnormal
ZP:0002590	whole organism decreased behavioural activity, abnormal
ZP:0002591	exit from mitosis disrupted, abnormal
ZP:0002592	establishment or maintenance of apical/basal cell polarity disrupted, abnormal
ZP:0002593	motor neuron precursor migration involved in dorsal motor nucleus of vagus nerve formation disrupted, abnormal
ZP:0002594	apical junction assembly disrupted, abnormal
ZP:0002595	lens perforate, abnormal
ZP:0002596	retinal neural layer positional polarity, abnormal
ZP:0002597	apical junction complex retinal neural layer mislocalised, abnormal
ZP:0002598	proliferative region eye increased size, abnormal
ZP:0002599	proliferative region eye mislocalised, abnormal
ZP:0002600	fourth ventricle decreased volume, abnormal
ZP:0002601	heart immature, abnormal
ZP:0002602	retinal pigmented epithelium perforate, abnormal
ZP:0002603	retina immature, abnormal
ZP:0002604	cardiac muscle cell heart tube size, abnormal
ZP:0002605	cardiac muscle cell heart tube structure, abnormal
ZP:0002606	post-vent region curled, abnormal
ZP:0002607	neuron optic cup decreased amount, abnormal
ZP:0002608	retinal inner plexiform layer patchy, abnormal
ZP:0002609	retinal outer plexiform layer patchy, abnormal
ZP:0002610	pericardial cavity increased size, abnormal
ZP:0002611	vagal ganglion fused with vagal ganglion, abnormal
ZP:0002612	neuroepithelial cell positional polarity, abnormal
ZP:0002613	apical junction complex cardiac muscle cell structure, abnormal
ZP:0002614	axonal defasciculation process quality, abnormal
ZP:0002615	learning or memory process quality, abnormal
ZP:0002616	locomotory behavior increased rate, abnormal
ZP:0002617	long-term synaptic potentiation decreased magnitude, abnormal
ZP:0002618	innervation decreased occurrence, abnormal
ZP:0002619	brain disorganized, abnormal
ZP:0002620	ventral region diencephalon morphology, abnormal
ZP:0002621	fourth ventricle morphology, abnormal
ZP:0002622	trigeminal ganglion has fewer parts of type sensory neuron, abnormal
ZP:0002623	axon terminus trigeminal ganglion increased amount, abnormal
ZP:0002624	ventral telencephalon morphology, abnormal
ZP:0002625	lateral longitudinal fasciculus decreased length, abnormal
ZP:0002626	axon lateral longitudinal fasciculus defasciculated, abnormal
ZP:0002627	cranial nerve position, abnormal
ZP:0002628	whole organism increased behavioural activity, abnormal
ZP:0002629	anterior-most region head truncated, abnormal
ZP:0002630	anterior-most region head flattened, abnormal
ZP:0002631	Meckel's cartilage increased width, abnormal
ZP:0002632	Meckel's cartilage increased angle to anterior-posterior axis whole organism, abnormal
ZP:0002633	forebrain ventricle morphology, abnormal
ZP:0002634	ceratohyal cartilage increased angle to basihyal cartilage, abnormal
ZP:0002635	axon Rohon-Beard neuron increased branchiness, abnormal
ZP:0002636	axon terminus Rohon-Beard neuron increased amount, abnormal
ZP:0002637	bone mineralization delayed, abnormal
ZP:0002638	posterior lateral line neuromast primordium migration decreased rate, abnormal
ZP:0002639	posterior lateral line primordium decreased speed, abnormal
ZP:0002640	posterior lateral line primordium mislocalised, abnormal
ZP:0002641	cardioblast migration decreased process quality, abnormal
ZP:0002642	cell myocardium malformed, abnormal
ZP:0002643	midbrain hindbrain boundary structure, abnormal
ZP:0002644	forebrain structure, abnormal
ZP:0002645	intersegmental vein malformed, abnormal
ZP:0002646	posterior caudal vein malformed, abnormal
ZP:0002647	dorsal longitudinal anastomotic vessel malformed, abnormal
ZP:0002648	alkaline phosphatase activity decreased occurrence, abnormal
ZP:0002649	post-vent region curvature, abnormal
ZP:0002650	pronephric tubule increased distance plasma membrane plasma membrane pronephric tubule, abnormal
ZP:0002651	microvillus pronephric tubule decreased amount, abnormal
ZP:0002652	epithelium pronephric tubule structure, abnormal
ZP:0002653	brush border epithelial cell pronephric tubule disorganized, abnormal
ZP:0002654	gut epithelium structure, abnormal
ZP:0002655	gut epithelium increased distance plasma membrane plasma membrane gut epithelium, abnormal
ZP:0002656	podocyte morphology, abnormal
ZP:0002657	heart jogging decreased process quality, abnormal
ZP:0002658	atrioventricular valve formation decreased process quality, abnormal
ZP:0002659	cell migration in hindbrain disrupted, abnormal
ZP:0002660	endocardial cell differentiation decreased process quality, abnormal
ZP:0002661	heart rudiment mislocalised, abnormal
ZP:0002662	heart rudiment bilateral symmetry, abnormal
ZP:0002663	heart rudiment rotated, abnormal
ZP:0002664	caudal fin decreased size, abnormal
ZP:0002665	lateral mesoderm mislocalised, abnormal
ZP:0002666	epithelium neural tube duplicated, abnormal
ZP:0002667	endocardium atrioventricular canal decreased length, abnormal
ZP:0002669	cardiac jelly decreased volume, abnormal
ZP:0002670	endothelial cell atrioventricular canal endocardium scaly, abnormal
ZP:0002671	neurosecretory neuron diencephalon mislocalised, abnormal
ZP:0002672	preoptic area morphology, abnormal
ZP:0002673	neuroendocrine cell decreased amount, abnormal
ZP:0002674	notochord degenerate, abnormal
ZP:0002675	notochord condensed, abnormal
ZP:0002676	yolk morphology, abnormal
ZP:0002677	melanosome post-vent region absent, abnormal
ZP:0002678	regulation of cell population proliferation disrupted, abnormal
ZP:0002679	maintenance of DNA repeat elements disrupted, abnormal
ZP:0002680	whole organism neoplastic, abnormal
ZP:0002682	pharyngeal arch cartilage malformed, abnormal
ZP:0002683	chondrocranium cartilage malformed, abnormal
ZP:0002684	ceratobranchial cartilage curved, abnormal
ZP:0002685	ceratobranchial cartilage shortened, abnormal
ZP:0002686	S phase delayed, abnormal
ZP:0002687	retinal bipolar neuron differentiation disrupted, abnormal
ZP:0002688	embryonic retina morphogenesis in camera-type eye delayed, abnormal
ZP:0002689	camera-type eye photoreceptor cell differentiation disrupted, abnormal
ZP:0002690	regulation of neural retina development disrupted, abnormal
ZP:0002691	retinal inner nuclear layer unstructured, abnormal
ZP:0002692	cell retinal inner nuclear layer undifferentiated, abnormal
ZP:0002693	retinal outer nuclear layer unstructured, abnormal
ZP:0002694	cell retinal outer nuclear layer undifferentiated, abnormal
ZP:0002695	amacrine cell absent, abnormal
ZP:0002696	retinal cone cell absent, abnormal
ZP:0002697	retinal rod cell decreased amount, abnormal
ZP:0002698	retinal bipolar neuron absent, abnormal
ZP:0002699	digestive system development disrupted, abnormal
ZP:0002700	liver absent, abnormal
ZP:0002701	exocrine pancreas decreased size, abnormal
ZP:0002702	endoplasmic reticulum chondrocyte morphology, abnormal
ZP:0002703	larval locomotory behavior arrested, abnormal
ZP:0002704	larval locomotory behavior disrupted, abnormal
ZP:0002705	muscle attachment decreased occurrence, abnormal
ZP:0002706	skeletal muscle organ development process quality, abnormal
ZP:0002707	heart structure, abnormal
ZP:0002708	basibranchial structure, abnormal
ZP:0002709	basibranchial mislocalised ventrally, abnormal
ZP:0002710	basihyal bone decreased length, abnormal
ZP:0002711	basihyal bone mislocalised ventrally, abnormal
ZP:0002712	trunk musculature structure, abnormal
ZP:0002713	trunk musculature disorganized, abnormal
ZP:0002714	ceratobranchial bone structure, abnormal
ZP:0002715	ceratobranchial bone mislocalised ventrally, abnormal
ZP:0002716	vertical myoseptum malformed, abnormal
ZP:0002717	myotome malformed, abnormal
ZP:0002718	Meckel's cartilage displaced, abnormal
ZP:0002719	intercalated disc myocardium disorganized, abnormal
ZP:0002720	ceratohyal cartilage mislocalised ventrally, abnormal
ZP:0002721	myofibril skeletal muscle cell disorganized, abnormal
ZP:0002722	sarcomere skeletal muscle cell structure, abnormal
ZP:0002723	actin filament slow muscle cell disorganized, abnormal
ZP:0002724	myosin filament slow muscle cell disorganized, abnormal
ZP:0002725	myofibril cardiac muscle cell absent, abnormal
ZP:0002726	caudal commissure defasciculated, abnormal
ZP:0002727	diencephalic white matter split, abnormal
ZP:0002728	diencephalic white matter decreased amount, abnormal
ZP:0002729	blood vessel remodeling decreased occurrence, abnormal
ZP:0002730	ball edematous, abnormal
ZP:0002731	caudal division of the internal carotid artery increased size, abnormal
ZP:0002732	primordial hindbrain channel increased size, abnormal
ZP:0002733	blood vasculature quality, abnormal
ZP:0002734	cranial vasculature malformed, abnormal
ZP:0002735	basal communicating artery increased size, abnormal
ZP:0002736	basal communicating artery attached to primordial midbrain channel, abnormal
ZP:0002737	blood vessel endothelial cell basal communicating artery increased amount, abnormal
ZP:0002739	endothelial cell basal communicating artery decreased amount, abnormal
ZP:0002740	posterior communicating artery increased size, abnormal
ZP:0002741	blood vessel endothelial cell posterior communicating artery increased amount, abnormal
ZP:0002743	basilar artery increased size, abnormal
ZP:0002744	basilar artery attached to primordial hindbrain channel, abnormal
ZP:0002745	central artery atretic, abnormal
ZP:0002746	cranial blood vessel dilated, abnormal
ZP:0002747	endothelial cell increased amount, abnormal
ZP:0002748	thymus development disrupted, abnormal
ZP:0002749	brain vasculature fragile, abnormal
ZP:0002750	cranial vasculature fragile, abnormal
ZP:0002751	cranial vasculature hemorrhagic, abnormal
ZP:0002752	basihyal bone aplastic, abnormal
ZP:0002753	mandibular arch skeleton duplicated, abnormal
ZP:0002754	pharyngeal arch 2 skeleton aplastic, abnormal
ZP:0002755	ceratobranchial 1 cartilage malformed, abnormal
ZP:0002756	pharyngeal arch 2 physical object quality, abnormal
ZP:0002757	myeloid cell decreased amount, abnormal
ZP:0002758	multicellular organism development disrupted, abnormal
ZP:0002759	nervous system development disrupted, abnormal
ZP:0002760	neural tube development disrupted, abnormal
ZP:0002761	brain structure, abnormal
ZP:0002762	anterior-posterior axis brain decreased size, abnormal
ZP:0002763	neuron hindbrain decreased amount, abnormal
ZP:0002764	cerebellum morphology, abnormal
ZP:0002765	diencephalon morphology, abnormal
ZP:0002766	diencephalon lacks all parts of type third ventricle, abnormal
ZP:0002767	somite decreased thickness, abnormal
ZP:0002768	somite elongated, abnormal
ZP:0002769	somite flattened, abnormal
ZP:0002770	tegmentum morphology, abnormal
ZP:0002771	neuron trigeminal ganglion decreased amount, abnormal
ZP:0002772	axon brainstem and spinal white matter decreased amount, abnormal
ZP:0002773	medial longitudinal fasciculus decreased thickness, abnormal
ZP:0002774	head flattened, abnormal
ZP:0002775	neural tube unlumenized, abnormal
ZP:0002776	hindbrain interneuron decreased amount, abnormal
ZP:0002777	dorsal longitudinal fasciculus decreased thickness, abnormal
ZP:0002778	neuron dorso-rostral cluster decreased amount, abnormal
ZP:0002779	axon CaP motoneuron decreased amount, abnormal
ZP:0002780	primary motor neuron decreased amount, abnormal
ZP:0002781	neuroepithelial cell decreased amount, abnormal
ZP:0002782	ribosomal small subunit assembly disrupted, abnormal
ZP:0002783	ribosome biogenesis disrupted, abnormal
ZP:0002784	intestinal bulb decreased size, abnormal
ZP:0002785	epithelial cell intestine cuboid, abnormal
ZP:0002786	intestinal epithelium shape, abnormal
ZP:0002787	intestinal epithelium decreased size, abnormal
ZP:0002788	intestinal epithelium decreased thickness, abnormal
ZP:0002789	autolysosome intestinal epithelium increased amount, abnormal
ZP:0002790	intestinal villus sparse, abnormal
ZP:0002791	apical-basal axis relative to substrate intestinal bulb epithelium decreased length, abnormal
ZP:0002792	neural crest cell migration process quality, abnormal
ZP:0002793	motor neuron axon guidance process quality, abnormal
ZP:0002794	spinal cord motor neuron differentiation process quality, abnormal
ZP:0002795	axon MiP motor neuron absent, abnormal
ZP:0002796	neural crest cell lacks parts or has fewer parts of type filopodium neural crest cell, abnormal
ZP:0002797	bone mineralization disrupted, abnormal
ZP:0002798	ceratobranchial 5 tooth absent, abnormal
ZP:0002799	ceratobranchial 5 tooth decreased size, abnormal
ZP:0002800	ceratohyal cartilage flattened, abnormal
ZP:0002801	cranial cartilage absent, abnormal
ZP:0002802	mitotic cell cycle disrupted, abnormal
ZP:0002803	intramembranous ossification postdisplaced growth, abnormal
ZP:0002804	endochondral ossification predisplaced growth, abnormal
ZP:0002805	thigmotaxis arrested, abnormal
ZP:0002806	renal system process decreased process quality, abnormal
ZP:0002807	adult locomotory behavior behavioral quality of a process, abnormal
ZP:0002808	magnesium ion homeostasis decreased process quality, abnormal
ZP:0002809	swimming behavior duration, abnormal
ZP:0002810	swimming behavior decreased process quality, abnormal
ZP:0002811	growth decreased magnitude, abnormal
ZP:0002812	melanin biosynthetic process delayed, abnormal
ZP:0002813	melanin biosynthetic process disrupted, abnormal
ZP:0002814	epithelial cell proliferation decreased occurrence, abnormal
ZP:0002815	calcium ion homeostasis decreased process quality, abnormal
ZP:0002816	centrum composition, abnormal
ZP:0002817	pronephric duct obstructed, abnormal
ZP:0002818	urostyle composition, abnormal
ZP:0002819	metapterygoid ossified, abnormal
ZP:0002820	maxilla composition, abnormal
ZP:0002821	basihyal bone ossified, abnormal
ZP:0002822	caudal vertebra condensed, abnormal
ZP:0002823	hypural composition, abnormal
ZP:0002824	integument decreased pigmentation, abnormal
ZP:0002826	skeletal system quality, abnormal
ZP:0002827	frontal bone composition, abnormal
ZP:0002828	hemal arch composition, abnormal
ZP:0002829	kidney calcified, abnormal
ZP:0002830	kidney decreased functionality, abnormal
ZP:0002831	parasphenoid composition, abnormal
ZP:0002832	premaxilla composition, abnormal
ZP:0002833	ceratohyal bone ossified, abnormal
ZP:0002834	quadrate ossified, abnormal
ZP:0002835	epihyal ossified, abnormal
ZP:0002836	ectopterygoid composition, abnormal
ZP:0002837	entopterygoid composition, abnormal
ZP:0002838	epural composition, abnormal
ZP:0002839	hyomandibula ossified, abnormal
ZP:0002840	symplectic ossified, abnormal
ZP:0002841	neural arch composition, abnormal
ZP:0002842	trunk lacks all parts of type melanocyte, abnormal
ZP:0002843	Weberian apparatus malformed, abnormal
ZP:0002844	Weberian apparatus condensed, abnormal
ZP:0002845	Weberian vertebra condensed, abnormal
ZP:0002846	corpuscles of Stannius physical object quality, abnormal
ZP:0002847	ceratobranchial 1 bone ossified, abnormal
ZP:0002848	ceratobranchial 4 bone ossified, abnormal
ZP:0002849	ceratobranchial 3 bone ossified, abnormal
ZP:0002850	ceratobranchial 2 bone ossified, abnormal
ZP:0002851	exocrine pancreas hypoplastic, abnormal
ZP:0002852	renal tubule calcified, abnormal
ZP:0002853	parapophysis/rib malformed, abnormal
ZP:0002854	caudal fin lepidotrichium composition, abnormal
ZP:0002855	vertebral column kinked, abnormal
ZP:0002856	epithelial cell of pancreas decreased area, abnormal
ZP:0002857	melanocyte intensity, abnormal
ZP:0002858	melanocyte low saturation, abnormal
ZP:0002859	melanocyte colorless, abnormal
ZP:0002860	melanocyte decreased size, abnormal
ZP:0002861	melanocyte necrotic, abnormal
ZP:0002862	melanocyte decreased pigmentation, abnormal
ZP:0002863	melanocyte disrupted regulation of membrane potential, abnormal
ZP:0002864	melanosome melanocyte malformed, abnormal
ZP:0002865	melanosome melanocyte aggregated, abnormal
ZP:0002866	melanoblast decreased pigmentation, abnormal
ZP:0002867	acinar cell decreased size, abnormal
ZP:0002868	mitotic prometaphase arrested, abnormal
ZP:0002869	mitotic centrosome separation disrupted, abnormal
ZP:0002870	chromosome condensation increased occurrence, abnormal
ZP:0002871	mitotic cell cycle, embryonic disrupted, abnormal
ZP:0002872	mitotic sister chromatid separation disrupted, abnormal
ZP:0002873	mitotic spindle assembly disrupted, abnormal
ZP:0002874	median fin fold apoptotic, abnormal
ZP:0002875	tail bud apoptotic, abnormal
ZP:0002876	integument fragile, abnormal
ZP:0002877	head deformed, abnormal
ZP:0002878	centrosome cell position, abnormal
ZP:0002879	centrosome cell variability of size, abnormal
ZP:0002880	mitotic spindle cell disorganized, abnormal
ZP:0002881	neuron decreased amount, abnormal
ZP:0002882	intestinal villus absent, abnormal
ZP:0002883	heart congested, abnormal
ZP:0002884	detection of light stimulus involved in visual perception decreased process quality, abnormal
ZP:0002885	retina decreased functionality, abnormal
ZP:0002886	swim bladder development disrupted, abnormal
ZP:0002887	liver shape, abnormal
ZP:0002888	liver primordium decreased size, abnormal
ZP:0002889	blastema quality, abnormal
ZP:0002890	determination of left/right asymmetry in lateral mesoderm process quality, abnormal
ZP:0002891	regulation of fibroblast growth factor receptor signaling pathway process quality, abnormal
ZP:0002893	apical protein localization disrupted, abnormal
ZP:0002894	epithelial cilium movement involved in determination of left/right asymmetry process quality, abnormal
ZP:0002895	cell migration involved in heart development disrupted, abnormal
ZP:0002896	Kupffer's vesicle development process quality, abnormal
ZP:0002897	basement membrane organization disrupted, abnormal
ZP:0002898	Kupffer's vesicle malformed, abnormal
ZP:0002899	Kupffer's vesicle physical object quality, abnormal
ZP:0002901	forerunner cell group decreased size, abnormal
ZP:0002902	forerunner cell group physical object quality, abnormal
ZP:0002903	extension morphology, abnormal
ZP:0002904	heart symmetry, abnormal
ZP:0002905	lateral plate mesoderm symmetry, abnormal
ZP:0002906	post-vent region distended, abnormal
ZP:0002907	regulation of mitotic cell cycle, embryonic disrupted, abnormal
ZP:0002908	hypoblast apoptotic, abnormal
ZP:0002909	whole organism dwarf-like, abnormal
ZP:0002910	anatomical surface whole organism decreased area, abnormal
ZP:0002911	adherens junction organization process quality, abnormal
ZP:0002912	blood vessel lumenization process quality, abnormal
ZP:0002913	intersegmental vessel unlumenized, abnormal
ZP:0002914	adherens junction blood vessel endothelial cell physical object quality, abnormal
ZP:0002915	whole organism atrophied, abnormal
ZP:0002916	ceratohyal cartilage bent, abnormal
ZP:0002917	musculature system quality, abnormal
ZP:0002918	muscle degenerate, abnormal
ZP:0002919	exocrine pancreas development disrupted, abnormal
ZP:0002920	intestine hypoplastic, abnormal
ZP:0002921	gut epithelium morphology, abnormal
ZP:0002922	epithelial cilium movement involved in extracellular fluid movement decreased rate, abnormal
ZP:0002923	determination of left/right symmetry process quality, abnormal
ZP:0002925	heart bilateral symmetry, abnormal
ZP:0002926	lateral plate mesoderm bilateral symmetry, abnormal
ZP:0002927	pronephric duct increased diameter, abnormal
ZP:0002928	cilium pronephric duct decreased length, abnormal
ZP:0002929	cilium pronephric duct decreased amount, abnormal
ZP:0002930	trunk increased width, abnormal
ZP:0002931	pronephric tubule cystic, abnormal
ZP:0002932	pharyngeal arch 3-7 decreased length, abnormal
ZP:0002933	extension constricted, abnormal
ZP:0002934	neurocranium shape, abnormal
ZP:0002935	muscle attachment disrupted, abnormal
ZP:0002936	muscle attachment decreased process quality, abnormal
ZP:0002937	locomotion involved in locomotory behavior decreased rate, abnormal
ZP:0002938	locomotion involved in locomotory behavior disrupted, abnormal
ZP:0002939	T-tubule organization process quality, abnormal
ZP:0002940	receptor clustering disrupted, abnormal
ZP:0002941	camera-type eye morphogenesis process quality, abnormal
ZP:0002942	dorsal aorta separated from intersegmental vessel dorsal longitudinal anastomotic vessel, abnormal
ZP:0002943	lens malformed, abnormal
ZP:0002944	swim bladder absent, abnormal
ZP:0002945	myoseptum somite deformed, abnormal
ZP:0002946	intersegmental vessel somite absent, abnormal
ZP:0002947	intersegmental vessel somite disorganized, abnormal
ZP:0002948	granular layer corpus cerebelli disorganized, abnormal
ZP:0002949	skeletal muscle cell trunk musculature retracted, abnormal
ZP:0002950	vertical myoseptum increased width, abnormal
ZP:0002951	vertical myoseptum deformed, abnormal
ZP:0002952	vertical myoseptum U-shaped, abnormal
ZP:0002953	basement membrane vertical myoseptum irregular spatial pattern, abnormal
ZP:0002954	cornea absent, abnormal
ZP:0002955	basement membrane myotome malformed, abnormal
ZP:0002956	muscle tendon junction myotome malformed, abnormal
ZP:0002957	muscle tendon junction myotome disorganized, abnormal
ZP:0002958	muscle tendon junction myotome U-shaped, abnormal
ZP:0002959	myotome detached from muscle cell muscle tendon junction myotome, abnormal
ZP:0002960	caudal fin kinked, abnormal
ZP:0002961	myoseptum broken, abnormal
ZP:0002962	whole organism decreased speed, abnormal
ZP:0002963	whole organism dystrophic, abnormal
ZP:0002964	muscle cell post-vent region morphology, abnormal
ZP:0002965	skeletal muscle cell post-vent region retracted, abnormal
ZP:0002966	muscle necrotic, abnormal
ZP:0002967	sarcoplasmic reticulum muscle unstructured, abnormal
ZP:0002968	sarcomere muscle morphology, abnormal
ZP:0002969	sarcomere muscle decreased amount, abnormal
ZP:0002970	skeletal muscle dystrophic, abnormal
ZP:0002971	muscle cell detached from vertical myoseptum, abnormal
ZP:0002972	muscle cell detached from muscle cell, abnormal
ZP:0002973	skeletal muscle cell detached from vertical myoseptum, abnormal
ZP:0002974	terminal cisterna skeletal muscle cell malformed, abnormal
ZP:0002975	T-tubule skeletal muscle cell malformed, abnormal
ZP:0002976	skeletal muscle cell separated from sarcolemma sarcolemma skeletal muscle cell, abnormal
ZP:0002977	feeding behavior increased process quality, abnormal
ZP:0002978	whole organism increased length, abnormal
ZP:0002979	determination of left/right asymmetry in lateral mesoderm decreased process quality, abnormal
ZP:0002980	optokinetic behavior decreased rate, abnormal
ZP:0002981	protein localization disrupted, abnormal
ZP:0002982	determination of pancreatic left/right asymmetry decreased process quality, abnormal
ZP:0002984	lateral mesoderm morphogenesis decreased process quality, abnormal
ZP:0002985	detection of light stimulus involved in visual perception arrested, abnormal
ZP:0002986	notochord cell development decreased process quality, abnormal
ZP:0002987	epithelial cilium movement involved in determination of left/right asymmetry decreased process quality, abnormal
ZP:0002988	muscle tissue development disrupted, abnormal
ZP:0002989	Kupffer's vesicle development decreased process quality, abnormal
ZP:0002990	basement membrane assembly decreased process quality, abnormal
ZP:0002991	determination of digestive tract left/right asymmetry decreased process quality, abnormal
ZP:0002992	determination of liver left/right asymmetry decreased process quality, abnormal
ZP:0002994	retinal ganglion cell layer dispersed, abnormal
ZP:0002995	hypochord morphology, abnormal
ZP:0002996	lens mislocalised, abnormal
ZP:0002997	lens degenerate, abnormal
ZP:0002998	lens hypoplastic, abnormal
ZP:0002999	lens disorganized, abnormal
ZP:0003000	lens displaced, abnormal
ZP:0003001	midbrain hindbrain boundary shape, abnormal
ZP:0003002	eye shape, abnormal
ZP:0003003	eye mislocalised ventrally, abnormal
ZP:0003004	lateral plate mesoderm mislocalised, abnormal
ZP:0003005	lateral plate mesoderm disorganized, abnormal
ZP:0003006	laminin complex lateral plate mesoderm decreased amount, abnormal
ZP:0003007	liver bilateral symmetry, abnormal
ZP:0003008	liver primordium bilateral symmetry, abnormal
ZP:0003009	notochord hypotrophic, abnormal
ZP:0003010	notochord decreased thickness, abnormal
ZP:0003011	notochord cellular quality, abnormal
ZP:0003012	notochord moderately well differentiated, abnormal
ZP:0003013	vacuole notochord decreased size, abnormal
ZP:0003014	vacuole notochord decreased amount, abnormal
ZP:0003015	pancreas bilateral symmetry, abnormal
ZP:0003016	endocrine cell pancreas mislocalised, abnormal
ZP:0003017	laminin complex somite decreased amount, abnormal
ZP:0003018	pancreas primordium bilateral symmetry, abnormal
ZP:0003019	cranial nerve II morphology, abnormal
ZP:0003020	myotome decreased thickness, abnormal
ZP:0003021	myotome U-shaped, abnormal
ZP:0003022	post-vent region shortened, abnormal
ZP:0003023	laminin complex neural tube decreased amount, abnormal
ZP:0003024	forebrain midbrain boundary increased width, abnormal
ZP:0003025	intestinal bulb primordium bilateral symmetry, abnormal
ZP:0003026	myosin filament fast muscle cell disorganized, abnormal
ZP:0003027	retinal ganglion cell ipsilateral to axon eye, abnormal
ZP:0003028	fast muscle myoblast decreased length, abnormal
ZP:0003029	actin filament organization disrupted, abnormal
ZP:0003030	spermatogenesis disrupted, abnormal
ZP:0003031	muscle organ morphogenesis delayed, abnormal
ZP:0003032	extension quality, abnormal
ZP:0003033	notochord structure, cavities, abnormal
ZP:0003034	notochord lacks parts or has fewer parts of type rough endoplasmic reticulum cell, abnormal
ZP:0003035	collagen type IV trimer notochord absent, abnormal
ZP:0003036	muscle pioneer somite absent, abnormal
ZP:0003037	testis structure, abnormal
ZP:0003038	head swollen, abnormal
ZP:0003039	axon Mauthner neuron mislocalised medially, abnormal
ZP:0003040	basal part of cell neuroepithelial cell increased width, abnormal
ZP:0003041	pharyngeal arch shape, abnormal
ZP:0003042	epithelial cilium movement involved in extracellular fluid movement arrested, abnormal
ZP:0003043	outer dynein arm assembly decreased occurrence, abnormal
ZP:0003044	inner dynein arm assembly decreased occurrence, abnormal
ZP:0003045	intestinal epithelial cell differentiation disrupted, abnormal
ZP:0003046	brain increased occurrence cellular response to DNA damage stimulus, abnormal
ZP:0003047	cardiac ventricle hypertrophic, abnormal
ZP:0003048	cardiac ventricle hyperplastic, abnormal
ZP:0003049	pronephric duct has fewer parts of type motile cilium inner dynein arm pronephric duct, abnormal
ZP:0003050	pronephric duct has fewer parts of type motile cilium outer dynein arm pronephric duct, abnormal
ZP:0003051	motile cilium posterior pronephric duct immobile, abnormal
ZP:0003052	sarcomere cardiac muscle cell increased amount, abnormal
ZP:0003053	muscle contraction disrupted, abnormal
ZP:0003054	visceral muscle development disrupted, abnormal
ZP:0003055	regulation of blood pressure disrupted, abnormal
ZP:0003056	larval locomotory behavior absent, abnormal
ZP:0003057	skeletal myofibril assembly disrupted, abnormal
ZP:0003058	growth decreased occurrence, abnormal
ZP:0003059	peripheral nervous system neuron axonogenesis increased rate, abnormal
ZP:0003060	cardiac myofibril assembly disrupted, abnormal
ZP:0003061	ventricular cardiac myofibril assembly disrupted, abnormal
ZP:0003062	heart contraction amplitude, abnormal
ZP:0003063	cardiac ventricle contractility, abnormal
ZP:0003064	heart decreased strength, abnormal
ZP:0003065	somite grey, abnormal
ZP:0003066	atrium contractility, abnormal
ZP:0003067	skeletal muscle quality, abnormal
ZP:0003068	sensory neuron morphology, abnormal
ZP:0003069	sensory neuron mislocalised, abnormal
ZP:0003070	Z disc skeletal muscle cell disorganized, abnormal
ZP:0003071	A band skeletal muscle cell disorganized, abnormal
ZP:0003072	Rohon-Beard neuron morphology, abnormal
ZP:0003073	cardiac muscle cell decreased thickness, abnormal
ZP:0003074	cardiac muscle cell decreased contractility, abnormal
ZP:0003075	myofibril cardiac muscle cell decreased size, abnormal
ZP:0003076	myofibril cardiac muscle cell decreased amount, abnormal
ZP:0003077	Z disc cardiac muscle cell disorganized, abnormal
ZP:0003078	A band cardiac muscle cell disorganized, abnormal
ZP:0003079	brain development process quality, abnormal
ZP:0003080	hatching disrupted, abnormal
ZP:0003081	developmental growth delayed, abnormal
ZP:0003082	yolk increased volume, abnormal
ZP:0003083	extension edematous, abnormal
ZP:0003084	neuromast absent, abnormal
ZP:0003085	neuromast decreased amount, abnormal
ZP:0003086	caudal fin hypoplastic, abnormal
ZP:0003087	whole organism apoptotic, abnormal
ZP:0003088	Meckel's cartilage stubby, abnormal
ZP:0003089	splanchnocranium morphology, abnormal
ZP:0003090	palatoquadrate cartilage bent, abnormal
ZP:0003091	ceratohyal cartilage orientation basibranchial, abnormal
ZP:0003092	ventral region epithelium hypertrophic, abnormal
ZP:0003093	ceratobranchial cartilage decreased length, abnormal
ZP:0003094	subintestinal vein hypoplastic, abnormal
ZP:0003095	subintestinal vein aplastic, abnormal
ZP:0003096	muscle esophagus decreased size, abnormal
ZP:0003097	gill morphology, abnormal
ZP:0003098	sagitta mislocalised, abnormal
ZP:0003099	pharyngeal arch morphology, abnormal
ZP:0003100	epithelium pneumatic duct morphology, abnormal
ZP:0003101	epithelial cell pneumatic duct disoriented, abnormal
ZP:0003102	epithelial cell pneumatic duct increased variability of size, abnormal
ZP:0003103	epithelial cell pneumatic duct decreased amount, abnormal
ZP:0003104	mucus secreting cell esophageal epithelium decreased amount, abnormal
ZP:0003105	otic vesicle protrusion absent, abnormal
ZP:0003106	joint Meckel's cartilage absent, abnormal
ZP:0003107	palatoquadrate cartilage malformed, abnormal
ZP:0003109	joint pharyngeal arch 1 absent, abnormal
ZP:0003110	mesoderm hypoplastic, abnormal
ZP:0003111	notochord hypoplastic, abnormal
ZP:0003112	muscle hypoplastic, abnormal
ZP:0003113	gastrulation disrupted, abnormal
ZP:0003114	Kupffer's vesicle morphology, abnormal
ZP:0003115	intermediate cell mass of mesoderm increased size, abnormal
ZP:0003116	response to osmotic stress increased magnitude, abnormal
ZP:0003117	cytolysis increased occurrence, abnormal
ZP:0003118	erythrocyte differentiation arrested, abnormal
ZP:0003119	erythrocyte maturation arrested, abnormal
ZP:0003120	gall bladder increased size, abnormal
ZP:0003121	spleen increased size, abnormal
ZP:0003122	nucleate erythrocyte kidney apoptotic, abnormal
ZP:0003123	nucleate erythrocyte morphology, abnormal
ZP:0003124	nucleate erythrocyte broken, abnormal
ZP:0003125	nucleate erythrocyte increased fragility, abnormal
ZP:0003126	nucleus nucleate erythrocyte condensed, abnormal
ZP:0003127	microtubule nucleate erythrocyte disorganized, abnormal
ZP:0003128	plasma membrane nucleate erythrocyte morphology, abnormal
ZP:0003129	plasma membrane nucleate erythrocyte pointleted, abnormal
ZP:0003130	cell projection membrane nucleate erythrocyte present, abnormal
ZP:0003131	telencephalon development disrupted, abnormal
ZP:0003132	whole organism hypoplastic, abnormal
ZP:0003133	post-vent region structure, abnormal
ZP:0003134	axonal defasciculation increased occurrence, abnormal
ZP:0003135	motor neuron axon guidance disrupted, abnormal
ZP:0003136	branchiomotor neuron axon guidance disrupted, abnormal
ZP:0003137	neuron differentiation disrupted, abnormal
ZP:0003138	midbrain-hindbrain boundary development disrupted, abnormal
ZP:0003139	retinal ganglion cell layer decreased size, abnormal
ZP:0003140	retinal ganglion cell layer apoptotic, abnormal
ZP:0003141	neuron projection retinal ganglion cell layer mislocalised, abnormal
ZP:0003142	neuron spinal cord decreased amount, abnormal
ZP:0003143	axon cranial nerve VI decreased length, abnormal
ZP:0003144	cranial nerve II decreased size, abnormal
ZP:0003145	axon cranial nerve II decreased amount, abnormal
ZP:0003146	axon cranial nerve X decreased length, abnormal
ZP:0003147	axon cranial nerve IX decreased length, abnormal
ZP:0003148	axon cranial nerve V decreased length, abnormal
ZP:0003149	axon cranial nerve V defasciculated, abnormal
ZP:0003150	pharyngeal pouch morphology, abnormal
ZP:0003151	facial ganglion decreased size, abnormal
ZP:0003152	trigeminal motor nucleus decreased size, abnormal
ZP:0003153	somite border morphology, abnormal
ZP:0003154	axon lateral line nerve decreased length, abnormal
ZP:0003155	axon Rohon-Beard neuron decreased length, abnormal
ZP:0003156	axon Rohon-Beard neuron decreased amount, abnormal
ZP:0003158	intestine decreased length, abnormal
ZP:0003159	intestine decreased thickness, abnormal
ZP:0003160	actin binding arrested, abnormal
ZP:0003161	intestine smooth muscle contraction arrested, abnormal
ZP:0003162	peristalsis disrupted, abnormal
ZP:0003163	smooth muscle intestine non-contractile, abnormal
ZP:0003164	atrium decreased size, abnormal
ZP:0003165	intersegmental vessel decreased length, abnormal
ZP:0003168	GTPase activity decreased process quality, abnormal
ZP:0003170	brain development delayed, abnormal
ZP:0003171	camera-type eye development disrupted, abnormal
ZP:0003172	lens composition, abnormal
ZP:0003173	diencephalon decreased size, abnormal
ZP:0003174	somite unstructured, abnormal
ZP:0003175	cell proliferation in midbrain decreased rate, abnormal
ZP:0003176	midbrain hindbrain boundary physical object quality, abnormal
ZP:0003177	neuron midbrain decreased amount, abnormal
ZP:0003178	pigment granule maturation disrupted, abnormal
ZP:0003179	Kupffer's vesicle has fewer parts of type cilium epithelial cell, abnormal
ZP:0003180	melanocyte structure, abnormal
ZP:0003182	sprouting angiogenesis disrupted, abnormal
ZP:0003183	intersegmental vessel disorganized, abnormal
ZP:0003184	dorsal longitudinal anastomotic vessel aplastic, abnormal
ZP:0003185	renal system process disrupted, abnormal
ZP:0003186	pronephros decreased functionality, abnormal
ZP:0003187	neuron spinal cord disorganized, abnormal
ZP:0003188	spindle cell structure, abnormal
ZP:0003189	response to endoplasmic reticulum stress increased process quality, abnormal
ZP:0003190	fin decreased size, abnormal
ZP:0003191	liver increased size, abnormal
ZP:0003192	liver fatty, abnormal
ZP:0003193	postero-ventral region pharyngeal arch 1 decreased size, abnormal
ZP:0003194	endoplasmic reticulum hepatocyte dilated, abnormal
ZP:0003195	lipid droplet hepatocyte increased amount, abnormal
ZP:0003196	glycogen granule hepatocyte decreased amount, abnormal
ZP:0003197	locomotion disrupted, abnormal
ZP:0003198	regulation of transmission of nerve impulse decreased process quality, abnormal
ZP:0003199	cell brain decreased amount, abnormal
ZP:0003200	fourth ventricle hydrocephalic, abnormal
ZP:0003202	nucleus brain apoptotic, abnormal
ZP:0003203	olfactory system apoptotic, abnormal
ZP:0003204	forebrain cell migration delayed, abnormal
ZP:0003205	neuron differentiation decreased rate, abnormal
ZP:0003206	axonogenesis involved in innervation disrupted, abnormal
ZP:0003207	forebrain neural keel physical object quality, abnormal
ZP:0003208	motor neuron spinal cord truncated, abnormal
ZP:0003209	motor neuron spinal cord branchiness, abnormal
ZP:0003210	whole organism decreased mobility, abnormal
ZP:0003211	hatching delayed, abnormal
ZP:0003212	hatching gland development disrupted, abnormal
ZP:0003213	hatching gland structure, abnormal
ZP:0003214	hatching gland cell mislocalised, abnormal
ZP:0003215	secretory granule hatching gland cell morphology, abnormal
ZP:0003216	secretory granule hatching gland cell movement quality, abnormal
ZP:0003217	cell lacks parts or has fewer parts of type filopodium cell, abnormal
ZP:0003218	filamentous actin cell disorganized, abnormal
ZP:0003219	cilium or flagellum-dependent cell motility arrested, abnormal
ZP:0003220	muscle pioneer decreased amount, abnormal
ZP:0003221	otolith morphology, abnormal
ZP:0003222	regulation of neurogenesis disrupted, abnormal
ZP:0003223	primary neuron increased amount, abnormal
ZP:0003224	axon hindbrain decreased length, abnormal
ZP:0003225	axon hindbrain disorganized, abnormal
ZP:0003226	forebrain decreased width, abnormal
ZP:0003227	axon forebrain decreased size, abnormal
ZP:0003228	axon forebrain disorganized, abnormal
ZP:0003229	midbrain shape, abnormal
ZP:0003230	whole organism pigmented, abnormal
ZP:0003231	cardiac ventricle deformed, abnormal
ZP:0003232	pericardial cavity edematous, abnormal
ZP:0003233	midbrain hindbrain boundary quality, abnormal
ZP:0003234	glomerular filtration disrupted, abnormal
ZP:0003235	mesonephric podocyte structure, abnormal
ZP:0003236	rhombomere 4 development disrupted, abnormal
ZP:0003237	hindbrain tangential cell migration disrupted, abnormal
ZP:0003238	protein localization to nucleus process quality, abnormal
ZP:0003239	facial nerve motor nucleus mislocalised anteriorly, abnormal
ZP:0003240	nucleus facial nerve motor nucleus physical object quality, abnormal
ZP:0003242	protein phosphorylation increased occurrence, abnormal
ZP:0003243	non-canonical Wnt signaling pathway disrupted, abnormal
ZP:0003244	protein initiator methionine removal decreased occurrence, abnormal
ZP:0003245	mesoderm development disrupted, abnormal
ZP:0003246	embryonic heart tube morphogenesis process quality, abnormal
ZP:0003247	heart valve morphogenesis arrested, abnormal
ZP:0003248	cardiac ventricle morphogenesis decreased process quality, abnormal
ZP:0003249	cardiac muscle progenitor cell migration to the midline involved in heart field formation decreased process quality, abnormal
ZP:0003250	endocardial cushion formation disrupted, abnormal
ZP:0003251	cardiocyte differentiation process quality, abnormal
ZP:0003252	heart contraction decreased process quality, abnormal
ZP:0003253	cardiac ventricle malformed, abnormal
ZP:0003254	cardiac ventricle bifurcated, abnormal
ZP:0003255	otic vesicle lacks all parts of type otolith, abnormal
ZP:0003256	somite obtuse, abnormal
ZP:0003257	heart tube mislocalised radially, abnormal
ZP:0003258	atrium bifurcated, abnormal
ZP:0003259	post-vent region increased accumulation blood, abnormal
ZP:0003260	ventricular system decreased volume, abnormal
ZP:0003261	atrioventricular canal distended, abnormal
ZP:0003262	myocardium split medially, abnormal
ZP:0003263	endocardium split medially, abnormal
ZP:0003264	cardiac muscle cell atrial myocardium shape, abnormal
ZP:0003265	ventricular endocardium physical object quality, abnormal
ZP:0003266	ventricular endocardium increased distance ventricular myocardium, abnormal
ZP:0003267	muscle attachment process quality, abnormal
ZP:0003268	embryonic neurocranium morphogenesis disrupted, abnormal
ZP:0003269	cartilage morphogenesis decreased process quality, abnormal
ZP:0003270	median fin fold decreased length, abnormal
ZP:0003271	median fin fold increased thickness, abnormal
ZP:0003272	median fin fold rough, abnormal
ZP:0003273	median fin fold deformed, abnormal
ZP:0003274	axis increased length, abnormal
ZP:0003275	fin degenerate, abnormal
ZP:0003276	fin edge shape, abnormal
ZP:0003277	pectoral fin bud hypoplastic, abnormal
ZP:0003278	dorsal root ganglion hypoplastic, abnormal
ZP:0003279	dorsal root ganglion lacks parts or has fewer parts of type neuron, abnormal
ZP:0003280	cephalic musculature morphology, abnormal
ZP:0003281	ceratohyal bone inverted, abnormal
ZP:0003282	ventral transverse aplastic, abnormal
ZP:0003283	horizontal myoseptum aplastic, abnormal
ZP:0003284	pectoral fin skeleton decreased size, abnormal
ZP:0003285	pectoral fin skeleton aplastic, abnormal
ZP:0003286	mesenchyme caudal fin hypoplastic, abnormal
ZP:0003287	ventral fin fold increased size, abnormal
ZP:0003288	ventral fin fold duplicated, abnormal
ZP:0003289	myoseptum quality, abnormal
ZP:0003290	whole organism lacks all parts of type ceratobranchial 5 tooth, abnormal
ZP:0003291	whole organism has fewer parts of type pharyngeal pouch, abnormal
ZP:0003292	whole organism lacks all parts of type ceratobranchial 2 cartilage, abnormal
ZP:0003293	whole organism lacks all parts of type ceratobranchial 3 cartilage, abnormal
ZP:0003294	whole organism lacks all parts of type ceratobranchial 4 cartilage, abnormal
ZP:0003295	whole organism lacks all parts of type ceratobranchial 5 cartilage, abnormal
ZP:0003296	whole organism lacks parts or has fewer parts of type dermal bone, abnormal
ZP:0003297	pharyngeal pouch disorganized, abnormal
ZP:0003298	pectoral fin rough, abnormal
ZP:0003299	pectoral fin truncated, abnormal
ZP:0003300	Meckel's cartilage shortened, abnormal
ZP:0003301	lateral line curved, abnormal
ZP:0003302	ceratobranchial cartilage malformed, abnormal
ZP:0003303	ceratobranchial 2 cartilage absent, abnormal
ZP:0003304	ceratobranchial 3 cartilage absent, abnormal
ZP:0003305	ceratobranchial 4 cartilage absent, abnormal
ZP:0003306	ceratobranchial 5 cartilage absent, abnormal
ZP:0003307	neurocranium decreased thickness, abnormal
ZP:0003308	neurocranium decreased width, abnormal
ZP:0003309	ventral larval melanophore stripe has fewer parts of type melanocyte, abnormal
ZP:0003310	lateral larval melanophore stripe lacks all parts of type melanocyte, abnormal
ZP:0003311	dorsal longitudinal fasciculus hypoplastic, abnormal
ZP:0003312	melanocyte degenerate, abnormal
ZP:0003313	slow muscle cell multinucleate, abnormal
ZP:0003314	Rohon-Beard neuron absent, abnormal
ZP:0003315	Rohon-Beard neuron aplastic, abnormal
ZP:0003316	xanthophore desaturated yellow, abnormal
ZP:0003317	xanthophore decreased amount, abnormal
ZP:0003318	xanthophore decreased pigmentation, abnormal
ZP:0003319	iridophore low saturation, abnormal
ZP:0003320	iridophore decreased pigmentation, abnormal
ZP:0003321	secondary motor neuron morphology, abnormal
ZP:0003322	secondary motor neuron defasciculated, abnormal
ZP:0003323	swimming behavior process quality, abnormal
ZP:0003324	motor neuron spinal cord decreased length, abnormal
ZP:0003325	motor neuron spinal cord decreased branchiness, abnormal
ZP:0003326	neuromuscular junction motor neuron disorganized, abnormal
ZP:0003327	cerebellum development disrupted, abnormal
ZP:0003328	cerebellum decreased volume, abnormal
ZP:0003329	forebrain decreased volume, abnormal
ZP:0003330	axon target recognition disrupted, abnormal
ZP:0003331	optic tract disorganized, abnormal
ZP:0003332	basement membrane optic tectum deformed, abnormal
ZP:0003333	extracellular matrix optic tectum deformed, abnormal
ZP:0003334	radial glial cell optic tectum deformed, abnormal
ZP:0003335	photoreceptor cell outer segment organization decreased process quality, abnormal
ZP:0003336	pronephric duct cystic, abnormal
ZP:0003337	retina has fewer parts of type eye photoreceptor cell, abnormal
ZP:0003338	photoreceptor outer segment eye photoreceptor cell decreased length, abnormal
ZP:0003339	photoreceptor outer segment eye photoreceptor cell disorganized, abnormal
ZP:0003340	axoneme eye photoreceptor cell decreased length, abnormal
ZP:0003342	photoreceptor outer segment membrane eye photoreceptor cell disorganized, abnormal
ZP:0003343	photoreceptor outer segment retinal cone cell decreased length, abnormal
ZP:0003344	photoreceptor outer segment retinal cone cell malformed, abnormal
ZP:0003345	photoreceptor outer segment retinal rod cell decreased length, abnormal
ZP:0003346	photoreceptor outer segment retinal rod cell malformed, abnormal
ZP:0003347	caudal vein dilated, abnormal
ZP:0003348	caudal vein plexus morphology, abnormal
ZP:0003349	blood vasculature broken, abnormal
ZP:0003350	axon motor neuron morphology, abnormal
ZP:0003351	notochord cell development disrupted, abnormal
ZP:0003352	notochord cell vacuolation disrupted, abnormal
ZP:0003353	tail bud protruding, abnormal
ZP:0003354	actin cytoskeleton epidermis disorganized, abnormal
ZP:0003355	cell epidermis size, abnormal
ZP:0003356	notochord malformed, abnormal
ZP:0003357	basement membrane notochord increased thickness, abnormal
ZP:0003358	vacuole notochord circular, abnormal
ZP:0003359	caveola notochord decreased mass density, abnormal
ZP:0003360	caveola notochord decreased amount, abnormal
ZP:0003361	cell notochord circular, abnormal
ZP:0003362	cell notochord vacuolated, abnormal
ZP:0003363	notochord increased distance cell cell notochord, abnormal
ZP:0003364	retinal pigmented epithelium disorganized, abnormal
ZP:0003365	pigment granule retinal pigmented epithelium movement quality, abnormal
ZP:0003366	caveola somite absent, abnormal
ZP:0003367	myofibril somite absent, abnormal
ZP:0003368	nervous system decreased size, abnormal
ZP:0003369	nervous system vacuolated, abnormal
ZP:0003370	caveola nervous system absent, abnormal
ZP:0003371	ventricular system structure, abnormal
ZP:0003372	cranial vasculature spatial pattern, abnormal
ZP:0003373	post-vent vasculature spatial pattern, abnormal
ZP:0003374	caveola peridermal cell absent, abnormal
ZP:0003375	pigment granule melanocyte movement quality, abnormal
ZP:0003376	sarcoplasmic reticulum muscle cell disorganized, abnormal
ZP:0003377	myofibril muscle cell disorganized, abnormal
ZP:0003378	posterior lateral line neuromast deposition process quality, abnormal
ZP:0003379	posterior lateral line neuromast spatial pattern, abnormal
ZP:0003380	posterior lateral line primordium shape, abnormal
ZP:0003381	posterior lateral line primordium organization quality, abnormal
ZP:0003382	animal organ regeneration disrupted, abnormal
ZP:0003383	lens necrotic, abnormal
ZP:0003384	forebrain atrophied, abnormal
ZP:0003385	regenerating tissue liver hypoplastic, abnormal
ZP:0003386	midbrain atrophied, abnormal
ZP:0003387	retina necrotic, abnormal
ZP:0003388	whole organism ploidy, abnormal
ZP:0003389	whole organism polyploid, abnormal
ZP:0003390	whole organism aneuploid, abnormal
ZP:0003391	condensed chromosome whole organism spatial pattern, abnormal
ZP:0003392	condensed chromosome whole organism tangled, abnormal
ZP:0003393	whole organism attached to nucleus nucleus whole organism, abnormal
ZP:0003394	trunk atrophied, abnormal
ZP:0003395	spindle post-vent region positional polarity, abnormal
ZP:0003396	neural tube apoptotic, abnormal
ZP:0003397	ciliary marginal zone poorly differentiated, abnormal
ZP:0003398	cell death increased frequency, abnormal
ZP:0003399	rRNA catabolic process disrupted, abnormal
ZP:0003400	amyloid precursor protein metabolic process disrupted, abnormal
ZP:0003401	white matter brain damaged, abnormal
ZP:0003402	ventricular zone damaged, abnormal
ZP:0003403	astrocyte ventricular zone increased amount, abnormal
ZP:0003404	cerebral spinal fluid increased volume, abnormal
ZP:0003405	lysosome CNS neuron (sensu Vertebrata) increased size, abnormal
ZP:0003406	intersegmental vessel immature, abnormal
ZP:0003407	intersegmental vessel lacks all parts of type angiogenic sprout, abnormal
ZP:0003408	histone H3-K36 methylation disrupted, abnormal
ZP:0003409	bone development disrupted, abnormal
ZP:0003410	brain increased size, abnormal
ZP:0003411	motor neuron spinal cord sparse, abnormal
ZP:0003412	Meckel's cartilage deformed, abnormal
ZP:0003413	ceratohyal cartilage deformed, abnormal
ZP:0003414	cartilage element malformed, abnormal
ZP:0003415	ceratobranchial cartilage deformed, abnormal
ZP:0003416	motor neuron branched, abnormal
ZP:0003417	motor neuron truncated, abnormal
ZP:0003418	leukocyte migration involved in inflammatory response increased occurrence, abnormal
ZP:0003419	inflammatory response increased occurrence, abnormal
ZP:0003420	cell death increased rate, abnormal
ZP:0003421	apoptotic chromosome condensation increased occurrence, abnormal
ZP:0003422	neutrophil chemotaxis disrupted, abnormal
ZP:0003423	epithelial cell proliferation increased rate, abnormal
ZP:0003424	yolk present, abnormal
ZP:0003425	neutrophil dorsal fin fold mislocalised, abnormal
ZP:0003426	epidermis malformed, abnormal
ZP:0003427	hemidesmosome epidermis decreased amount, abnormal
ZP:0003428	neutrophil epidermis mislocalised, abnormal
ZP:0003429	integument texture, abnormal
ZP:0003430	integument rugose, abnormal
ZP:0003431	epidermis caudal fin hyperplastic, abnormal
ZP:0003432	ventral fin fold malformed, abnormal
ZP:0003433	leukocyte ventral fin fold mislocalised, abnormal
ZP:0003434	neutrophil ventral fin fold mislocalised, abnormal
ZP:0003435	autophagy increased occurrence, abnormal
ZP:0003436	musculoskeletal movement, spinal reflex action disrupted, abnormal
ZP:0003437	trunk morphology, abnormal
ZP:0003438	trunk hypoplastic, abnormal
ZP:0003439	skeletal muscle cell morphology, abnormal
ZP:0003441	mitochondrion skeletal muscle cell morphology, abnormal
ZP:0003445	potassium:chloride symporter activity increased process quality, abnormal
ZP:0003446	posterior lateral line development decreased process quality, abnormal
ZP:0003447	posterior lateral line neuromast development decreased process quality, abnormal
ZP:0003448	posterior lateral line neuromast has fewer parts of type neuromast hair cell, abnormal
ZP:0003449	posterior lateral line primordium decreased area, abnormal
ZP:0003450	epithelial cell morphogenesis heterochronic, abnormal
ZP:0003451	negative regulation of TOR signaling disrupted, abnormal
ZP:0003454	anterior region diencephalon disorganized, abnormal
ZP:0003457	dorsal region ventral telencephalon increased width, abnormal
ZP:0003458	dorsal region ventral telencephalon disorganized, abnormal
ZP:0003459	dorsal telencephalon increased size, abnormal
ZP:0003460	dorsal telencephalon disorganized, abnormal
ZP:0003462	telencephalic white matter composition, abnormal
ZP:0003463	telencephalic ventricle morphology, abnormal
ZP:0003465	blood vessel increased diameter, abnormal
ZP:0003466	CNS neuron (sensu Vertebrata) mislocalised, abnormal
ZP:0003467	larval locomotory behavior decreased process quality, abnormal
ZP:0003468	collateral sprouting process quality, abnormal
ZP:0003469	regulation of actin cytoskeleton reorganization decreased process quality, abnormal
ZP:0003470	cardiac ventricle decreased contractility, abnormal
ZP:0003471	cardiac muscle cell cardiac ventricle circular, abnormal
ZP:0003472	cardiac muscle cell cardiac ventricle decreased size, abnormal
ZP:0003473	filamentous actin ventricular myocardium mislocalised, abnormal
ZP:0003474	heart rudiment development disrupted, abnormal
ZP:0003475	cellular pigmentation decreased occurrence, abnormal
ZP:0003476	heart primordium decreased size, abnormal
ZP:0003477	heart primordium decreased width, abnormal
ZP:0003478	heart primordium lacks parts or has fewer parts of type cardiac muscle cell, abnormal
ZP:0003479	bulbus arteriosus malformed, abnormal
ZP:0003480	bulbus arteriosus cylindrical, abnormal
ZP:0003481	whole organism lacks parts or has fewer parts of type pharyngeal arch, abnormal
ZP:0003482	cranial neural crest disrupted neural crest cell development, abnormal
ZP:0003483	cranial neural crest cell apoptotic, abnormal
ZP:0003484	regulation of transcription elongation from RNA polymerase II promoter process quality, abnormal
ZP:0003485	blood morphology, abnormal
ZP:0003486	intermediate cell mass of mesoderm physical object quality, abnormal
ZP:0003487	median fin fold edge shape, abnormal
ZP:0003488	fin erose, abnormal
ZP:0003489	trunk musculature morphology, abnormal
ZP:0003490	caudal fin has extra parts of type iridophore, abnormal
ZP:0003491	post-vent region has extra parts of type ventral larval melanophore stripe iridophore, abnormal
ZP:0003492	dorsal larval melanophore stripe has extra parts of type iridophore, abnormal
ZP:0003493	yolk larval melanophore stripe has extra parts of type iridophore, abnormal
ZP:0003494	median fin shape, abnormal
ZP:0003495	median fin decreased area, abnormal
ZP:0003496	iridophore irregular spatial pattern, abnormal
ZP:0003497	iridophore increased amount, abnormal
ZP:0003498	iridophore degree of pigmentation, abnormal
ZP:0003499	iridophore displaced to median fin, abnormal
ZP:0003500	tRNA transcription disrupted, abnormal
ZP:0003501	enteric nervous system complexity, abnormal
ZP:0003502	exocrine pancreas quality, abnormal
ZP:0003503	pharyngeal arch decreased size, abnormal
ZP:0003504	intestine surface feature shape, abnormal
ZP:0003505	smooth muscle contractile fiber intestine organization quality, abnormal
ZP:0003506	intestinal epithelium flat, abnormal
ZP:0003507	intestinal epithelium degenerate, abnormal
ZP:0003508	intestinal epithelium positional polarity, abnormal
ZP:0003509	intestinal epithelium undifferentiated, abnormal
ZP:0003510	intestinal epithelium has fewer parts of type anterior region microvillus epithelial cell, abnormal
ZP:0003511	microvillus intestinal epithelium decreased size, abnormal
ZP:0003512	epithelial cell intestinal epithelium cuboid, abnormal
ZP:0003513	exocrine cell undifferentiated, abnormal
ZP:0003515	germ cell migration decreased process quality, abnormal
ZP:0003519	primordial germ cell mislocalised medially, abnormal
ZP:0003520	regulation of ossification disrupted, abnormal
ZP:0003521	pancreas development process quality, abnormal
ZP:0003522	retinoic acid catabolic process disrupted, abnormal
ZP:0003524	centrum ossified, abnormal
ZP:0003525	pancreas increased length, abnormal
ZP:0003526	pancreas mislocalised anteriorly, abnormal
ZP:0003527	basibranchial malformed, abnormal
ZP:0003529	hypural malformed, abnormal
ZP:0003530	frontal bone decreased length, abnormal
ZP:0003531	frontal bone fused with parietal bone, abnormal
ZP:0003532	mouth decreased size, abnormal
ZP:0003533	supraorbital bone morphology, abnormal
ZP:0003534	rhombomere 5 decreased width, abnormal
ZP:0003535	rhombomere 4 increased size, abnormal
ZP:0003536	rhombomere 4 decreased size, abnormal
ZP:0003538	pectoral fin malformed, abnormal
ZP:0003539	cartilage element pectoral fin mislocalised, abnormal
ZP:0003540	vertebra malformed, abnormal
ZP:0003541	vertebra fused with vertebra, abnormal
ZP:0003542	optic cup decreased size, abnormal
ZP:0003543	mandibular arch skeleton decreased width, abnormal
ZP:0003544	palatoquadrate arch protruding, abnormal
ZP:0003545	ventral mandibular arch protruding, abnormal
ZP:0003546	ceratohyal cartilage fused with ceratohyal cartilage, abnormal
ZP:0003547	ethmoid cartilage malformed, abnormal
ZP:0003548	ethmoid cartilage arrow-shaped, abnormal
ZP:0003549	hyosymplectic cartilage composition, abnormal
ZP:0003550	parachordal cartilage decreased size, abnormal
ZP:0003551	parachordal cartilage malformed, abnormal
ZP:0003552	pectoral fin endoskeletal disc hyperplastic, abnormal
ZP:0003553	trabecula cranii aplastic, abnormal
ZP:0003554	basihyal cartilage malformed, abnormal
ZP:0003555	bone element malformed, abnormal
ZP:0003556	epibranchial ganglion disorganized, abnormal
ZP:0003557	neuron epibranchial ganglion decreased amount, abnormal
ZP:0003558	vertebral column ossified, abnormal
ZP:0003559	neurocranium malformed, abnormal
ZP:0003560	pharyngeal arch 3-7 malformed, abnormal
ZP:0003561	extracellular matrix inter-frontal joint decreased amount, abnormal
ZP:0003562	inter-parietal joint open, abnormal
ZP:0003563	extracellular matrix inter-parietal joint decreased amount, abnormal
ZP:0003564	frontal-parietal joint closed, abnormal
ZP:0003565	extracellular matrix frontal-parietal joint decreased amount, abnormal
ZP:0003566	osteoblast star shaped, abnormal
ZP:0003567	rough endoplasmic reticulum osteoblast decreased amount, abnormal
ZP:0003568	sprouting angiogenesis decreased occurrence, abnormal
ZP:0003569	dorsal/ventral axis specification disrupted, abnormal
ZP:0003570	notochord development delayed, abnormal
ZP:0003571	convergent extension involved in axis elongation delayed, abnormal
ZP:0003572	heart contraction decreased occurrence, abnormal
ZP:0003573	blood decreased fluid flow, abnormal
ZP:0003574	intermediate cell mass of mesoderm distended, abnormal
ZP:0003575	forebrain morphology, abnormal
ZP:0003576	neural keel apoptotic, abnormal
ZP:0003577	pronephric duct fused with medial side medial side pronephric duct, abnormal
ZP:0003578	bulbus arteriosus morphology, abnormal
ZP:0003579	trunk has fewer parts of type somite, abnormal
ZP:0003580	trunk vasculature increased accumulation blood, abnormal
ZP:0003581	parachordal vessel morphology, abnormal
ZP:0003582	parachordal vessel hypoplastic, abnormal
ZP:0003583	post-vent vasculature increased accumulation blood, abnormal
ZP:0003585	vasculature increased accumulation blood, abnormal
ZP:0003587	spinal cord neural keel apoptotic, abnormal
ZP:0003588	ocular blood vessel decreased size, abnormal
ZP:0003589	gut endothelial cell morphology, abnormal
ZP:0003591	phagolysosome assembly arrested, abnormal
ZP:0003594	axial chorda mesoderm decreased size, abnormal
ZP:0003598	cell notochord decreased size, abnormal
ZP:0003600	head hypotrophic, abnormal
ZP:0003601	retinal ganglion cell layer hyperplastic, abnormal
ZP:0003602	medial region forebrain aplastic, abnormal
ZP:0003603	optic stalk morphology, abnormal
ZP:0003604	retinal pigmented epithelium hyperplastic, abnormal
ZP:0003605	retina fused with retina, abnormal
ZP:0003606	pectoral fin cartilage disorganized, abnormal
ZP:0003607	optic primordium fused with optic primordium, abnormal
ZP:0003608	whole organism lacks parts or has fewer parts of type pectoral fin, abnormal
ZP:0003609	head bulbous, abnormal
ZP:0003610	Meckel's cartilage increased thickness, abnormal
ZP:0003611	optic fissure present, abnormal
ZP:0003612	atrioventricular canal aplastic, abnormal
ZP:0003613	ceratohyal cartilage increased thickness, abnormal
ZP:0003614	pectoral fin endoskeletal disc hypoplastic, abnormal
ZP:0003615	trabecula cranii malformed, abnormal
ZP:0003616	pectoral fin fold decreased size, abnormal
ZP:0003617	pectoral fin fold variability of size, abnormal
ZP:0003618	pars superior ear morphology, abnormal
ZP:0003619	optic furrow open, abnormal
ZP:0003620	glucose import decreased rate, abnormal
ZP:0003621	head opaque, abnormal
ZP:0003622	regulation of cholesterol storage disrupted, abnormal
ZP:0003623	programmed cell death increased occurrence, abnormal
ZP:0003624	actin cytoskeleton organization disrupted, abnormal
ZP:0003625	thrombocyte blood island absent, abnormal
ZP:0003626	thrombocyte blood island decreased amount, abnormal
ZP:0003627	segmental plate increased width, abnormal
ZP:0003628	lateral mesoderm increased width, abnormal
ZP:0003629	actinotrichium absent, abnormal
ZP:0003630	kidney development disrupted, abnormal
ZP:0003631	pronephros malformed, abnormal
ZP:0003632	mitotic sister chromatid cohesion process quality, abnormal
ZP:0003634	cerebellum necrotic, abnormal
ZP:0003635	somite structure, abnormal
ZP:0003636	caudal fin aplastic, abnormal
ZP:0003637	whole organism deformed, abnormal
ZP:0003638	spindle cell morphology, abnormal
ZP:0003639	heart development quality, abnormal
ZP:0003640	dorsal aorta lacks parts or has fewer parts of type blood vessel endothelial cell, abnormal
ZP:0003641	heart non-functional, abnormal
ZP:0003642	heart tube position, abnormal
ZP:0003643	posterior cardinal vein lacks parts or has fewer parts of type blood vessel endothelial cell, abnormal
ZP:0003644	cranial vasculature degenerate, abnormal
ZP:0003645	intersegmental vessel lacks parts or has fewer parts of type blood vessel endothelial cell, abnormal
ZP:0003646	endocardium collapsed, abnormal
ZP:0003647	vascular endothelium broken, abnormal
ZP:0003648	trunk vasculature hemorrhagic, abnormal
ZP:0003649	dorsal longitudinal anastomotic vessel broken, abnormal
ZP:0003650	blood vessel endothelial cell decreased amount, abnormal
ZP:0003651	erythrocyte differentiation decreased occurrence, abnormal
ZP:0003652	polysome whole organism decreased amount, abnormal
ZP:0003654	epidermal basal stratum malformed, abnormal
ZP:0003655	median fin absent, abnormal
ZP:0003656	median fin broken, abnormal
ZP:0003657	median fin ruffled, abnormal
ZP:0003658	neuromuscular junction development disrupted, abnormal
ZP:0003659	skeletal muscle acetylcholine-gated channel clustering disrupted, abnormal
ZP:0003660	axon motor neuron truncated, abnormal
ZP:0003661	axon motor neuron branchiness, abnormal
ZP:0003662	canonical Wnt signaling pathway increased process quality, abnormal
ZP:0003663	brain decreased width, abnormal
ZP:0003664	neuromere forebrain disheveled, abnormal
ZP:0003665	compartment boundary third ventricle inconspicuous, abnormal
ZP:0003666	larval development arrested, abnormal
ZP:0003667	pre-miRNA processing disrupted, abnormal
ZP:0003668	forerunner cell group decreased amount, abnormal
ZP:0003669	sarcomerogenesis disrupted, abnormal
ZP:0003670	sarcomere cardiac ventricle immature, abnormal
ZP:0003671	sarcomere cardiac ventricle decreased amount, abnormal
ZP:0003675	intersegmental artery malformed, abnormal
ZP:0003677	intersegmental artery decreased process quality branching involved in blood vessel morphogenesis, abnormal
ZP:0003678	head hemorrhagic, abnormal
ZP:0003680	dorsal longitudinal anastomotic vessel hypoplastic, abnormal
ZP:0003682	convergent extension involved in neural plate elongation disrupted, abnormal
ZP:0003683	cell cycle process disrupted, abnormal
ZP:0003684	polster increased distance notochord, abnormal
ZP:0003685	neuronal stem cell spinal cord increased amount, abnormal
ZP:0003686	oligodendrocyte spinal cord decreased amount, abnormal
ZP:0003687	whole organism increased angle to anterior-most region posterior-most region whole organism, abnormal
ZP:0003688	oligodendrocyte decreased amount, abnormal
ZP:0003689	cranial nerve X position, abnormal
ZP:0003690	axis specification disrupted, abnormal
ZP:0003691	oocyte differentiation process quality, abnormal
ZP:0003692	oocyte morphogenesis process quality, abnormal
ZP:0003693	oocyte animal/vegetal axis specification process quality, abnormal
ZP:0003694	blastodisc absent, abnormal
ZP:0003695	nucleus oocyte stage II mislocalised, abnormal
ZP:0003696	mitochondrion oocyte stage II mislocalised, abnormal
ZP:0003697	endoplasmic reticulum oocyte stage II mislocalised, abnormal
ZP:0003699	cortical granule oocyte stage II mislocalised, abnormal
ZP:0003700	cortical granule oocyte stage III mislocalised, abnormal
ZP:0003701	oocyte stage I physical object quality, abnormal
ZP:0003702	nucleus oocyte stage I mislocalised, abnormal
ZP:0003703	mitochondrion oocyte stage I mislocalised, abnormal
ZP:0003704	endoplasmic reticulum oocyte stage I mislocalised, abnormal
ZP:0003705	microtubule oocyte stage I mislocalised, abnormal
ZP:0003706	mitochondrial cloud oocyte stage I increased size, abnormal
ZP:0003707	mitochondrial cloud oocyte stage I mislocalised, abnormal
ZP:0003708	unfertilized egg decreased size, abnormal
ZP:0003709	unfertilized egg malformed, abnormal
ZP:0003710	cytoplasm unfertilized egg mislocalised, abnormal
ZP:0003711	chorion unfertilized egg malformed, abnormal
ZP:0003712	otolith morphogenesis disrupted, abnormal
ZP:0003713	caudal fin upper lobe fused with caudal fin lower lobe, abnormal
ZP:0003715	atrial myocardium decreased contractility, abnormal
ZP:0003716	ventricular myocardium decreased contractility, abnormal
ZP:0003717	actin cytoskeleton EVL disorganized, abnormal
ZP:0003718	actin cytoskeleton yolk syncytial layer disorganized, abnormal
ZP:0003719	axon trigeminal ganglion decreased amount, abnormal
ZP:0003720	axon motor neuron branched, abnormal
ZP:0003721	EVL structure, abnormal
ZP:0003722	cell EVL shape, abnormal
ZP:0003723	lipid phosphatase activity disrupted, abnormal
ZP:0003724	phosphatidylinositol dephosphorylation decreased occurrence, abnormal
ZP:0003725	semicircular canal formation disrupted, abnormal
ZP:0003726	epithelial cell inner ear disorganized, abnormal
ZP:0003727	epithelial cell inner ear aggregated, abnormal
ZP:0003728	head domed, abnormal
ZP:0003729	head mislocalised ventrally, abnormal
ZP:0003730	intersegmental vessel shape, abnormal
ZP:0003731	locomotory behavior having decreased processual parts skeletal muscle contraction, abnormal
ZP:0003732	axon motor neuron decreased length, abnormal
ZP:0003733	peripheral neuron branchiness, abnormal
ZP:0003734	embryonic heart tube morphogenesis disrupted, abnormal
ZP:0003735	cardiac muscle progenitor cell migration to the midline involved in heart field formation delayed, abnormal
ZP:0003736	pigmentation arrested, abnormal
ZP:0003737	cardiac muscle cell differentiation decreased occurrence, abnormal
ZP:0003738	cardiac cell fate specification process quality, abnormal
ZP:0003739	heart tube hypoplastic, abnormal
ZP:0003740	heart tube aplastic, abnormal
ZP:0003741	somite border trunk disorganized, abnormal
ZP:0003742	somite border post-vent region disorganized, abnormal
ZP:0003743	myocardial precursor decreased amount, abnormal
ZP:0003744	pigment cell absent, abnormal
ZP:0003745	neural crest cell absent, abnormal
ZP:0003746	angiogenesis delayed, abnormal
ZP:0003747	sprouting angiogenesis delayed, abnormal
ZP:0003748	negative regulation of angiogenesis increased occurrence, abnormal
ZP:0003749	intersegmental vessel hypoplastic, abnormal
ZP:0003750	caudal vein plexus decreased thickness, abnormal
ZP:0003751	caudal vein plexus complexity, abnormal
ZP:0003752	endothelial tip cell caudal vein plexus absent, abnormal
ZP:0003753	endothelial tip cell caudal vein plexus decreased amount, abnormal
ZP:0003754	neutrophil chemotaxis process quality, abnormal
ZP:0003756	rhombomere 5 increased width, abnormal
ZP:0003757	rhombomere 3 increased width, abnormal
ZP:0003758	neutrophil whole organism decreased amount, abnormal
ZP:0003760	animal organ development disrupted, abnormal
ZP:0003761	mandibular arch skeleton immature, abnormal
ZP:0003762	oligodendrocyte development disrupted, abnormal
ZP:0003763	ventral spinal cord interneuron differentiation disrupted, abnormal
ZP:0003764	cell differentiation in hindbrain disrupted, abnormal
ZP:0003765	abducens nucleus development disrupted, abnormal
ZP:0003766	oligodendrocyte differentiation disrupted, abnormal
ZP:0003767	glioblast (sensu Vertebrata) hindbrain decreased amount, abnormal
ZP:0003768	GABAergic neuron spinal cord amount, abnormal
ZP:0003769	motor neuron cranial nerve VI decreased amount, abnormal
ZP:0003770	spinal cord interneuron cellular quality, abnormal
ZP:0003771	Kolmer-Agduhr neuron lateral floor plate cellular quality, abnormal
ZP:0003772	motor neuron lacks parts or has fewer parts of type axon motor neuron, abnormal
ZP:0003773	posterior-most region pharyngeal arch hypoplastic, abnormal
ZP:0003774	DNA replication disrupted, abnormal
ZP:0003776	cell cycle disrupted, abnormal
ZP:0003777	multicellular organism development arrested, abnormal
ZP:0003778	cell death increased process quality, abnormal
ZP:0003779	caudal fin curved ventral, abnormal
ZP:0003780	cell whole organism polyploid, abnormal
ZP:0003781	cell whole organism tetraploid, abnormal
ZP:0003782	cell whole organism endopolyploid, abnormal
ZP:0003783	head increased process quality cell death, abnormal
ZP:0003784	anterior neural tube decreased width, abnormal
ZP:0003785	cell increased size, abnormal
ZP:0003786	chromosome cell polyploid, abnormal
ZP:0003787	chromosome cell undivided, abnormal
ZP:0003788	granulocyte decreased amount, abnormal
ZP:0003789	macrophage decreased amount, abnormal
ZP:0003790	erythroid lineage cell increased variability of size, abnormal
ZP:0003791	myeloid lineage restricted progenitor cell increased size, abnormal
ZP:0003792	myeloid lineage restricted progenitor cell decreased amount, abnormal
ZP:0003793	regulation of cyclin-dependent protein serine/threonine kinase activity decreased process quality, abnormal
ZP:0003794	re-entry into mitotic cell cycle increased occurrence, abnormal
ZP:0003795	cell proliferation in hindbrain ventricular zone increased occurrence, abnormal
ZP:0003796	neuron differentiation increased occurrence, abnormal
ZP:0003797	regulation of neural precursor cell proliferation decreased process quality, abnormal
ZP:0003798	spinal cord has extra parts of type primary motor neuron, abnormal
ZP:0003799	spinal cord has extra parts of type primary interneuron, abnormal
ZP:0003800	spinal cord has extra parts of type neuron, abnormal
ZP:0003801	proliferative region mislocalised, abnormal
ZP:0003802	whole organism opaque, abnormal
ZP:0003803	primary neuron proliferative, abnormal
ZP:0003804	voltage-gated calcium channel activity disrupted, abnormal
ZP:0003805	brain morphogenesis disrupted, abnormal
ZP:0003806	optic vesicle malformed, abnormal
ZP:0003807	forebrain condensed, abnormal
ZP:0003808	neural rod disorganized, abnormal
ZP:0003809	neural rod Y-shaped, abnormal
ZP:0003810	neural rod collapsed, abnormal
ZP:0003811	epithelium ventricular system morphology, abnormal
ZP:0003812	neurocranial trabecula fused with neurocranial trabecula, abnormal
ZP:0003813	otic vesicle has extra parts of type otolith, abnormal
ZP:0003814	cilium pronephros decreased length, abnormal
ZP:0003815	anterior-posterior axis whole organism curved lateral, abnormal
ZP:0003816	post-vent region necrotic, abnormal
ZP:0003817	myoblast fusion disrupted, abnormal
ZP:0003818	melanophore stripe disorganized, abnormal
ZP:0003819	fast muscle cell increased amount, abnormal
ZP:0003820	fast muscle cell mononucleate, abnormal
ZP:0003821	CaP motoneuron has fewer parts of type filopodium CaP motoneuron, abnormal
ZP:0003822	CaP motoneuron has fewer parts of type neuron projection primary motor neuron, abnormal
ZP:0003823	neuron projection CaP motoneuron decreased length, abnormal
ZP:0003824	neuron projection CaP motoneuron decreased branchiness, abnormal
ZP:0003825	CaP motoneuron decreased process quality collateral sprouting, abnormal
ZP:0003826	eye discolored, abnormal
ZP:0003827	integument colorless, abnormal
ZP:0003828	blood vessel endothelial cell migration disrupted, abnormal
ZP:0003829	branching morphogenesis of an epithelial tube disrupted, abnormal
ZP:0003830	caudal fin decreased thickness, abnormal
ZP:0003831	posterior region trunk decreased size, abnormal
ZP:0003832	intersegmental vessel dilated, abnormal
ZP:0003833	intersegmental vessel decreased functionality, abnormal
ZP:0003834	lipid metabolic process disrupted, abnormal
ZP:0003835	central nervous system myelination disrupted, abnormal
ZP:0003836	regulation of fatty acid beta-oxidation disrupted, abnormal
ZP:0003837	mitochondrion brain swollen, abnormal
ZP:0003838	lipid droplet brain increased amount, abnormal
ZP:0003839	neuroblast (sensu Vertebrata) brain increased amount, abnormal
ZP:0003840	neuroblast (sensu Vertebrata) brain hyperplastic, abnormal
ZP:0003841	mitochondrion spinal cord swollen, abnormal
ZP:0003842	liver color, abnormal
ZP:0003843	mitochondrion liver swollen, abnormal
ZP:0003844	lipid droplet liver increased amount, abnormal
ZP:0003845	mitochondrial crista liver decreased mass density, abnormal
ZP:0003846	kinocilium neuromast absent, abnormal
ZP:0003847	kinocilium neuromast decreased length, abnormal
ZP:0003848	kidney morphology, abnormal
ZP:0003849	mitochondrion kidney swollen, abnormal
ZP:0003850	glial cell (sensu Vertebrata) ventricular zone increased size, abnormal
ZP:0003851	mitochondrion whole organism decreased functionality, abnormal
ZP:0003852	lipid droplet intestine increased amount, abnormal
ZP:0003853	grey matter morphology, abnormal
ZP:0003854	axon sensory neuron disorganized, abnormal
ZP:0003855	hepatocyte increased size, abnormal
ZP:0003856	mitochondrion Mauthner neuron swollen, abnormal
ZP:0003857	chondrocyte differentiation arrested, abnormal
ZP:0003858	extracellular matrix constituent secretion decreased occurrence, abnormal
ZP:0003859	pectoral fin cartilage malformed, abnormal
ZP:0003860	pharyngeal arch cartilage immature, abnormal
ZP:0003861	extracellular matrix pharyngeal arch cartilage decreased volume, abnormal
ZP:0003862	auditory capsule malformed, abnormal
ZP:0003863	caudal vein plexus malformed, abnormal
ZP:0003864	subintestinal vein malformed, abnormal
ZP:0003865	nucleate erythrocyte position, abnormal
ZP:0003866	nucleate erythrocyte mislocalised, abnormal
ZP:0003867	immature eye morphology, abnormal
ZP:0003868	rRNA processing disrupted, abnormal
ZP:0003869	regulation of mitotic cell cycle disrupted, abnormal
ZP:0003870	exit from mitosis delayed, abnormal
ZP:0003871	lens opacity, abnormal
ZP:0003872	liver necrotic, abnormal
ZP:0003873	nucleolus liver morphology, abnormal
ZP:0003874	nucleolus liver increased size, abnormal
ZP:0003875	ciliary marginal zone decreased size, abnormal
ZP:0003876	nucleolus ciliary marginal zone morphology, abnormal
ZP:0003877	nucleolus ciliary marginal zone increased size, abnormal
ZP:0003878	lens epithelium increased thickness, abnormal
ZP:0003879	nucleolus retinal ganglion cell morphology, abnormal
ZP:0003880	nucleolus retinal ganglion cell increased size, abnormal
ZP:0003881	cysteine-type peptidase activity decreased process quality, abnormal
ZP:0003882	peptidyl-serine phosphorylation increased occurrence, abnormal
ZP:0003883	otolith mineralization disrupted, abnormal
ZP:0003884	branchiostegal ray disorganized, abnormal
ZP:0003885	chondrocyte branchiostegal ray spheroid, abnormal
ZP:0003886	collagen type II trimer Meckel's cartilage increased amount, abnormal
ZP:0003887	ventral mandibular arch retracted, abnormal
ZP:0003888	collagen type II trimer neurocranial trabecula increased amount, abnormal
ZP:0003889	collagen type II trimer cranial cartilage increased amount, abnormal
ZP:0003890	chondrocyte cranial cartilage increased size, abnormal
ZP:0003891	chondrocyte cranial cartilage hyperplastic, abnormal
ZP:0003892	neurocranium blunt, abnormal
ZP:0003893	apical region Muller cell molecular quality, abnormal
ZP:0003894	endocytosis arrested, abnormal
ZP:0003895	protein localization arrested, abnormal
ZP:0003896	cell population proliferation quality, abnormal
ZP:0003897	inner ear morphogenesis paedomorphic growth, abnormal
ZP:0003898	median fin fold increased size, abnormal
ZP:0003899	median fin fold undulate, abnormal
ZP:0003900	epithelium median fin fold undulate, abnormal
ZP:0003901	otic vesicle quality, abnormal
ZP:0003902	inner ear structure, abnormal
ZP:0003903	optic tectum quality, abnormal
ZP:0003904	caudal fin has extra parts of type lepidotrichium, abnormal
ZP:0003905	epithelium ventral fin fold undulate, abnormal
ZP:0003906	muscle pioneer increased amount, abnormal
ZP:0003907	whole organism sterile, abnormal
ZP:0003908	head increased volume, abnormal
ZP:0003909	pectoral fin increased size, abnormal
ZP:0003910	pectoral fin undulate, abnormal
ZP:0003911	pectoral fin has extra parts of type lepidotrichium, abnormal
ZP:0003912	anal fin absent, abnormal
ZP:0003913	anal fin aplastic, abnormal
ZP:0003914	dorsal fin has extra parts of type lepidotrichium, abnormal
ZP:0003915	pelvic fin has extra parts of type lepidotrichium, abnormal
ZP:0003916	pupil quality, abnormal
ZP:0003917	pupil size, abnormal
ZP:0003918	pupil decreased length, abnormal
ZP:0003919	pupil decreased size, abnormal
ZP:0003920	pupil decreased width, abnormal
ZP:0003921	lepidotrichium increased amount, abnormal
ZP:0003922	dorsolateral septum aplastic, abnormal
ZP:0003923	slow muscle cell increased amount, abnormal
ZP:0003924	urea transport decreased rate, abnormal
ZP:0003925	oligodendrocyte progenitor proliferation increased occurrence, abnormal
ZP:0003926	atrioventricular valve decreased functionality, abnormal
ZP:0003927	oligodendrocyte increased amount, abnormal
ZP:0003931	lipid localization disrupted, abnormal
ZP:0003932	chondrocyte morphogenesis disrupted, abnormal
ZP:0003933	liver circular, abnormal
ZP:0003934	collagen type II trimer cartilage element aggregated, abnormal
ZP:0003935	pharyngeal arch 3-7 increased size, abnormal
ZP:0003936	chondrocyte pharyngeal arch 3-7 disorganized, abnormal
ZP:0003937	midbrain hindbrain boundary decreased size, abnormal
ZP:0003938	forebrain malformed, abnormal
ZP:0003939	ethmoid cartilage morphology, abnormal
ZP:0003940	cartilage element neurocranium decreased size, abnormal
ZP:0003941	pharyngeal arch 3-7 disorganized, abnormal
ZP:0003942	chondrocyte trabecular layer decreased amount, abnormal
ZP:0003943	leukocyte differentiation disrupted, abnormal
ZP:0003944	pronephric capsular space distended, abnormal
ZP:0003945	photoreceptor outer segment photoreceptor cell decreased amount, abnormal
ZP:0003946	brain deformed, abnormal
ZP:0003947	cerebellum aplastic, abnormal
ZP:0003948	cytochrome-c oxidase activity decreased occurrence, abnormal
ZP:0003949	spinal cord motor neuron differentiation disrupted, abnormal
ZP:0003950	digestive tract development arrested, abnormal
ZP:0003951	secondary motor neuron spatial pattern, abnormal
ZP:0003952	secondary motor neuron decreased amount, abnormal
ZP:0003953	axon secondary motor neuron decreased size, abnormal
ZP:0003954	forebrain ventricle dilated, abnormal
ZP:0003955	ventral mandibular arch hypoplastic, abnormal
ZP:0003957	mitotic spindle organization process quality, abnormal
ZP:0003958	mitotic cell cycle, embryonic increased duration, abnormal
ZP:0003959	post-vent region apoptotic, abnormal
ZP:0003960	endochondral ossification decreased process quality, abnormal
ZP:0003961	chondrocyte differentiation decreased process quality, abnormal
ZP:0003962	branchiomeric skeletal muscle development decreased process quality, abnormal
ZP:0003963	histone H2A monoubiquitination disrupted, abnormal
ZP:0003964	direct ossification decreased process quality, abnormal
ZP:0003965	cleithrum poorly ossified, abnormal
ZP:0003966	opercle poorly ossified, abnormal
ZP:0003967	parasphenoid poorly ossified, abnormal
ZP:0003968	pharyngeal pouch cellular quality, abnormal
ZP:0003969	head lacks all parts of type Meckel's cartilage, abnormal
ZP:0003970	head lacks all parts of type neurocranial trabecula, abnormal
ZP:0003971	head lacks all parts of type palatoquadrate cartilage, abnormal
ZP:0003972	head lacks all parts of type ceratohyal cartilage, abnormal
ZP:0003973	head lacks all parts of type ethmoid cartilage, abnormal
ZP:0003974	head lacks all parts of type hyosymplectic cartilage, abnormal
ZP:0003975	head lacks all parts of type parachordal cartilage, abnormal
ZP:0003976	head lacks all parts of type sternohyoid, abnormal
ZP:0003977	head lacks all parts of type ventral intermandibularis anterior, abnormal
ZP:0003978	head lacks all parts of type ventral intermandibularis posterior, abnormal
ZP:0003979	head lacks all parts of type adductor mandibulae, abnormal
ZP:0003980	head lacks all parts of type interhyoideus, abnormal
ZP:0003981	head lacks all parts of type hyohyoideus, abnormal
ZP:0003982	pectoral fin lacks all parts of type scapulocoracoid, abnormal
ZP:0003983	pectoral fin lacks all parts of type mesocoracoid cartilage, abnormal
ZP:0003984	pharyngeal arch apoptotic, abnormal
ZP:0003985	chondrocyte pharyngeal arch undifferentiated, abnormal
ZP:0003986	chondrocyte neurocranial trabecula undifferentiated, abnormal
ZP:0003987	pharyngeal arch cartilage poorly ossified, abnormal
ZP:0003988	sternohyoid decreased size, abnormal
ZP:0003989	melanocyte increased branchiness, abnormal
ZP:0003990	xanthophore decreased size, abnormal
ZP:0003991	xanthophore decreased branchiness, abnormal
ZP:0003992	proximal region pronephric duct increased length, abnormal
ZP:0003993	pronephric distal early tubule absent, abnormal
ZP:0003994	whole organism structure, abnormal
ZP:0003995	seminoma testis present, abnormal
ZP:0003996	lymphoid neoplasms whole organism neoplastic, malignant, abnormal
ZP:0003997	cerebellum decreased size, abnormal
ZP:0003998	cerebellum disorganized, abnormal
ZP:0003999	brain degeneration, abnormal
ZP:0004000	retinal ganglion cell layer decayed, abnormal
ZP:0004001	neuron retinal ganglion cell layer degenerate, abnormal
ZP:0004002	diencephalon apoptotic, abnormal
ZP:0004003	nucleus diencephalon aggregated, abnormal
ZP:0004004	cell diencephalon decreased amount, abnormal
ZP:0004005	eye size, abnormal
ZP:0004006	eye degeneration, abnormal
ZP:0004007	nucleus eye aggregated, abnormal
ZP:0004008	cranial nerve II decreased width, abnormal
ZP:0004009	head size, abnormal
ZP:0004010	retinal inner plexiform layer decayed, abnormal
ZP:0004011	neuron retinal inner plexiform layer degenerate, abnormal
ZP:0004012	fast muscle myoblast binucleate, abnormal
ZP:0004013	fast muscle myoblast unfused from fast muscle myoblast, abnormal
ZP:0004014	cell proliferation in hindbrain disrupted, abnormal
ZP:0004015	hindbrain morphogenesis delayed, abnormal
ZP:0004016	hindbrain decreased width, abnormal
ZP:0004020	optic fissure unfused from optic fissure, abnormal
ZP:0004021	otolith increased amount, abnormal
ZP:0004022	somite development disrupted, abnormal
ZP:0004023	cardiac ventricle tubular, abnormal
ZP:0004024	atrium elongated, abnormal
ZP:0004025	atrium tubular, abnormal
ZP:0004026	atrium separated from sinus venosus, abnormal
ZP:0004027	myofibril myotome irregular spatial pattern, abnormal
ZP:0004028	muscle cell disorganized, abnormal
ZP:0004029	nucleus skeletal muscle myoblast circular, abnormal
ZP:0004030	trunk immature, abnormal
ZP:0004031	erythroblast binucleate, abnormal
ZP:0004032	margin constricted, abnormal
ZP:0004033	yolk broken, abnormal
ZP:0004034	yolk syncytial layer morphology, abnormal
ZP:0004035	nucleus yolk syncytial layer decreased amount, abnormal
ZP:0004036	filamentous actin yolk syncytial layer absent, abnormal
ZP:0004037	blastomere displaced to dorsal region blastoderm, abnormal
ZP:0004038	whole organism lacks parts or has fewer parts of type presumptive endoderm, abnormal
ZP:0004039	endocardial cushion quality, abnormal
ZP:0004040	hindbrain distended, abnormal
ZP:0004041	whole organism malformed, abnormal
ZP:0004042	positive regulation of cytosolic calcium ion concentration occurrence, abnormal
ZP:0004043	yolk constricted, abnormal
ZP:0004044	nucleus internal yolk syncytial layer aggregated, abnormal
ZP:0004045	head immature, abnormal
ZP:0004046	angiogenesis process quality, abnormal
ZP:0004047	vacuole organization process quality, abnormal
ZP:0004049	endothelial tube morphogenesis process quality, abnormal
ZP:0004050	blood vessel endothelial cell yolk increased distribution, abnormal
ZP:0004051	sinus venosus dilated, abnormal
ZP:0004052	caudal vein morphology, abnormal
ZP:0004053	endothelial cell caudal vein morphology, abnormal
ZP:0004054	posterior cardinal vein decreased thickness, abnormal
ZP:0004055	posterior cardinal vein dilated, abnormal
ZP:0004056	posterior cardinal vein increased diameter, abnormal
ZP:0004057	endothelial cell posterior cardinal vein increased distribution, abnormal
ZP:0004058	intersegmental vein unlumenized, abnormal
ZP:0004059	intersegmental artery unlumenized, abnormal
ZP:0004060	cranial vasculature morphology, abnormal
ZP:0004061	vacuole intersegmental vessel absent, abnormal
ZP:0004062	caudal vein plexus dilated, abnormal
ZP:0004063	myocardium distended, abnormal
ZP:0004064	myocardium decreased distance endocardium, abnormal
ZP:0004065	vascular endothelium apoptotic, abnormal
ZP:0004066	primordial midbrain channel dilated, abnormal
ZP:0004067	trunk vasculature dilated, abnormal
ZP:0004068	dorsal longitudinal anastomotic vessel unlumenized, abnormal
ZP:0004069	subintestinal vein dilated, abnormal
ZP:0004070	subintestinal vein increased diameter, abnormal
ZP:0004071	inner optic circle unlumenized, abnormal
ZP:0004072	endothelial cell increased distribution, abnormal
ZP:0004073	neural crest formation disrupted, abnormal
ZP:0004074	neural crest cell differentiation disrupted, abnormal
ZP:0004075	BMP signaling pathway disrupted, abnormal
ZP:0004076	hindbrain bulbous, abnormal
ZP:0004077	mitotic cell cycle process quality, abnormal
ZP:0004078	cell migration arrested, abnormal
ZP:0004079	intraciliary transport disrupted, abnormal
ZP:0004082	hindbrain has fewer parts of type branchiomotor neuron, abnormal
ZP:0004083	cilium otic vesicle decreased length, abnormal
ZP:0004084	cilium otic vesicle decreased amount, abnormal
ZP:0004085	eye photoreceptor cell retinal photoreceptor layer apoptotic, abnormal
ZP:0004086	mitotic spindle pronephric duct direction, abnormal
ZP:0004087	photoreceptor outer segment retina absent, abnormal
ZP:0004088	anterior side whole organism disorganized, abnormal
ZP:0004089	axoneme neural tube absent, abnormal
ZP:0004090	retinal outer nuclear layer perforate, abnormal
ZP:0004091	eye photoreceptor cell retinal outer nuclear layer apoptotic, abnormal
ZP:0004092	cilium posterior neural tube decreased amount, abnormal
ZP:0004093	photoreceptor outer segment eye photoreceptor cell absent, abnormal
ZP:0004094	nucleus eye photoreceptor cell decreased length, abnormal
ZP:0004095	cilium eye photoreceptor cell absent, abnormal
ZP:0004096	photoreceptor connecting cilium eye photoreceptor cell absent, abnormal
ZP:0004097	photoreceptor inner segment membrane eye photoreceptor cell disorganized, abnormal
ZP:0004098	photoreceptor inner segment membrane eye photoreceptor cell displaced, abnormal
ZP:0004099	blue sensitive photoreceptor cell morphology, abnormal
ZP:0004100	retinal cone cell morphology, abnormal
ZP:0004101	retinal cone cell decreased length, abnormal
ZP:0004102	retinal rod cell morphology, abnormal
ZP:0004103	retinal rod cell pigmented, abnormal
ZP:0004104	spliceosomal tri-snRNP complex assembly disrupted, abnormal
ZP:0004105	mRNA splicing, via spliceosome disrupted, abnormal
ZP:0004106	myeloid leukocyte differentiation disrupted, abnormal
ZP:0004107	regulation of apoptotic process disrupted, abnormal
ZP:0004108	central nervous system apoptotic, abnormal
ZP:0004109	spinal cord degenerate, abnormal
ZP:0004110	myeloid leukocyte decreased amount, abnormal
ZP:0004111	pigment cell development disrupted, abnormal
ZP:0004112	ovary morphology, abnormal
ZP:0004113	whole organism female sterile, abnormal
ZP:0004114	melanophore stripe trunk absent, abnormal
ZP:0004115	pigment cell (sensu Vertebrata) trunk decreased amount, abnormal
ZP:0004116	iridophore trunk decreased amount, abnormal
ZP:0004117	xanthophore hypodermis decreased amount, abnormal
ZP:0004118	iridophore hypodermis decreased amount, abnormal
ZP:0004119	pigment cell (sensu Vertebrata) decreased amount, abnormal
ZP:0004120	cell population proliferation absent, abnormal
ZP:0004121	chordate embryonic development delayed, abnormal
ZP:0004122	liver and biliary system decreased functionality, abnormal
ZP:0004123	exocrine pancreas decreased thickness, abnormal
ZP:0004124	exocrine pancreas degenerate, abnormal
ZP:0004125	intrahepatic bile duct unbranched, abnormal
ZP:0004126	intrahepatic bile duct absent, abnormal
ZP:0004127	intrahepatic bile duct apoptotic, abnormal
ZP:0004128	intrahepatic bile duct degenerate, abnormal
ZP:0004129	epithelial cell intrahepatic bile duct decreased amount, abnormal
ZP:0004130	endoderm shape, abnormal
ZP:0004131	endoderm structure, abnormal
ZP:0004133	glomerular filtration decreased process quality, abnormal
ZP:0004134	glomerulus morphogenesis disrupted, abnormal
ZP:0004135	glomerular capillary formation disrupted, abnormal
ZP:0004136	dorsal aorta distended, abnormal
ZP:0004137	renal glomerulus pronephros malformed, abnormal
ZP:0004138	capillary loop nephron pronephros closure incomplete, abnormal
ZP:0004139	capillary loop nephron pronephros decreased amount, abnormal
ZP:0004140	mesangial cell pronephros decreased amount, abnormal
ZP:0004141	dorsal-ventral axis whole organism decreased length, abnormal
ZP:0004142	pronephric podocyte attached to dorsal aorta, abnormal
ZP:0004143	cell projection pronephric podocyte folded, abnormal
ZP:0004144	pronephric podocyte inserted into cell projection pronephric capsular space, abnormal
ZP:0004145	lamina densa surrounding cell projection pronephric podocyte, abnormal
ZP:0004146	pronephric glomerular basement membrane increased thickness, abnormal
ZP:0004147	pronephric glomerular basement membrane decreased permeability, abnormal
ZP:0004148	intersegmental vessel branched, abnormal
ZP:0004149	neural crest cell migration delayed, abnormal
ZP:0004150	eye increased distance eye, abnormal
ZP:0004151	neuron dorsal root ganglion displaced, abnormal
ZP:0004152	trigeminal ganglion decreased amount, abnormal
ZP:0004153	neuron posterior lateral line decreased amount, abnormal
ZP:0004154	neuron sympathetic nervous system decreased amount, abnormal
ZP:0004155	pharyngeal arch 2 structure, abnormal
ZP:0004156	pharyngeal arch 2 displaced, abnormal
ZP:0004157	pharyngeal arch 1 structure, abnormal
ZP:0004158	pharyngeal arch 1 displaced, abnormal
ZP:0004159	otolith position, abnormal
ZP:0004160	pharyngeal arch 3-7 skeleton aplastic, abnormal
ZP:0004161	nervous system apoptotic, abnormal
ZP:0004162	erythrocyte maturation decreased process quality, abnormal
ZP:0004163	blood chromatic property, abnormal
ZP:0004164	angiogenesis decreased process quality, abnormal
ZP:0004165	establishment of blood-brain barrier decreased process quality, abnormal
ZP:0004166	brain vasculature increased permeability, abnormal
ZP:0004167	central artery malformed, abnormal
ZP:0004168	phospholipase activity disrupted, abnormal
ZP:0004169	peptidase activity disrupted, abnormal
ZP:0004170	bile acid secretion disrupted, abnormal
ZP:0004171	glucose homeostasis disrupted, abnormal
ZP:0004172	liver and biliary system malformed, abnormal
ZP:0004173	trunk female organism increased size, abnormal
ZP:0004174	hepatic duct physical object quality, abnormal
ZP:0004175	intestine fatty, abnormal
ZP:0004176	hepatocyte decreased functionality, abnormal
ZP:0004178	gut absent, abnormal
ZP:0004179	gut decreased thickness, abnormal
ZP:0004182	hyosymplectic cartilage decreased amount, abnormal
ZP:0004185	ovarian follicle development premature, abnormal
ZP:0004186	oocyte maturation increased occurrence, abnormal
ZP:0004187	oocyte maturity, abnormal
ZP:0004188	ovarian follicle maturity, abnormal
ZP:0004189	neuron differentiation delayed, abnormal
ZP:0004190	retina development in camera-type eye delayed, abnormal
ZP:0004191	retinal ganglion cell layer immature, abnormal
ZP:0004192	retinal neural layer poorly differentiated, abnormal
ZP:0004193	central region retinal neural layer proliferative, abnormal
ZP:0004194	retinal inner nuclear layer immature, abnormal
ZP:0004195	optic tectum apoptotic, abnormal
ZP:0004196	retinal outer nuclear layer immature, abnormal
ZP:0004197	translation decreased process quality, abnormal
ZP:0004199	chondrocyte differentiation disrupted, abnormal
ZP:0004200	optic cup morphogenesis involved in camera-type eye development disrupted, abnormal
ZP:0004201	somite obtuse angle to somite, abnormal
ZP:0004202	muscle pioneer myotome increased amount, abnormal
ZP:0004203	fast muscle cell myotome increased amount, abnormal
ZP:0004204	muscle pioneer absent, abnormal
ZP:0004205	muscle pioneer mislocalised, abnormal
ZP:0004206	pectoral fin folded, abnormal
ZP:0004207	ceratohyal cartilage physical object quality, abnormal
ZP:0004208	ceratohyal cartilage ossified, abnormal
ZP:0004209	hyosymplectic cartilage physical object quality, abnormal
ZP:0004210	hyosymplectic cartilage ossified, abnormal
ZP:0004211	chondrocyte pharyngeal arch 3-7 irregular spatial pattern, abnormal
ZP:0004212	sprouting angiogenesis increased occurrence, abnormal
ZP:0004214	intersegmental vessel has extra parts of type vascular sprouts, abnormal
ZP:0004216	vascular sprouts disorganized, abnormal
ZP:0004218	basement membrane renal glomerulus increased thickness, abnormal
ZP:0004221	podocyte malformed, abnormal
ZP:0004222	podocyte variant shape, abnormal
ZP:0004223	podocyte increased variability of size, abnormal
ZP:0004224	brain hypoplastic, abnormal
ZP:0004225	midbrain hindbrain boundary apoptotic, abnormal
ZP:0004226	olfactory region hypoplastic, abnormal
ZP:0004227	optic primordium malformed, abnormal
ZP:0004228	head truncated, abnormal
ZP:0004229	Meckel's cartilage shape, abnormal
ZP:0004230	ceratohyal cartilage obtuse angle to ceratohyal cartilage, abnormal
ZP:0004231	cranial cartilage hypoplastic, abnormal
ZP:0004232	chondrocyte cranial cartilage circular, abnormal
ZP:0004233	chondrocyte cranial cartilage disorganized, abnormal
ZP:0004234	neuron brain necrotic, abnormal
ZP:0004235	lateral line truncated, abnormal
ZP:0004236	erythroblast decreased amount, abnormal
ZP:0004237	photoreceptor outer segment layer aplastic, abnormal
ZP:0004238	myofibril slow muscle cell decreased diameter, abnormal
ZP:0004239	myofibril slow muscle cell decreased amount, abnormal
ZP:0004240	Z disc slow muscle cell malformed, abnormal
ZP:0004242	erythroid lineage cell intermediate cell mass of mesoderm decreased amount, abnormal
ZP:0004243	erythroid lineage cell blood island decreased amount, abnormal
ZP:0004244	erythroid progenitor cell lateral plate mesoderm decreased amount, abnormal
ZP:0004245	trunk curvature, abnormal
ZP:0004246	response to ionizing radiation disrupted, abnormal
ZP:0004247	melanocyte integument morphology, abnormal
ZP:0004248	melanocyte trunk aggregated, abnormal
ZP:0004249	face development disrupted, abnormal
ZP:0004250	capillary pharyngeal arch hypoplastic, abnormal
ZP:0004251	palatoquadrate cartilage deformed, abnormal
ZP:0004252	aortic arch hypoplastic, abnormal
ZP:0004253	neuromuscular junction development decreased occurrence, abnormal
ZP:0004254	synaptic growth at neuromuscular junction disrupted, abnormal
ZP:0004255	skeletal muscle acetylcholine-gated channel clustering arrested, abnormal
ZP:0004256	skeletal muscle acetylcholine-gated channel clustering decreased occurrence, abnormal
ZP:0004257	neuromuscular junction myotome decreased amount, abnormal
ZP:0004258	peripheral neuron quality, abnormal
ZP:0004259	growth cone CaP motoneuron malformed, abnormal
ZP:0004260	axon primary motor neuron morphology, abnormal
ZP:0004261	adaxial cell disorganized, abnormal
ZP:0004263	primitive hemopoiesis disrupted, abnormal
ZP:0004264	necrotic cell death increased occurrence, abnormal
ZP:0004265	whole organism undulate, abnormal
ZP:0004266	axis elongation decreased process quality, abnormal
ZP:0004267	notochord shortened, abnormal
ZP:0004272	regulation of smoothened signaling pathway process quality, abnormal
ZP:0004273	spinal cord dorsal/ventral patterning process quality, abnormal
ZP:0004274	forebrain regionalization process quality, abnormal
ZP:0004275	adenohypophysis development process quality, abnormal
ZP:0004276	forebrain development process quality, abnormal
ZP:0004277	dorsal/ventral axon guidance disrupted, abnormal
ZP:0004278	axon extension involved in axon guidance process quality, abnormal
ZP:0004279	postoptic commissure absent, abnormal
ZP:0004280	glial cell diencephalon mislocalised, abnormal
ZP:0004281	ventral region midbrain physical object quality, abnormal
ZP:0004282	axon caudal commissure mislocalised, abnormal
ZP:0004283	cranial nerve II decreased length, abnormal
ZP:0004284	cranial nerve II misrouted, abnormal
ZP:0004285	lateral floor plate physical object quality, abnormal
ZP:0004286	ventral mandibular arch increased width, abnormal
ZP:0004287	adenohypophysis physical object quality, abnormal
ZP:0004288	dorsoventral diencephalic tract morphology, abnormal
ZP:0004289	axon tract of the postoptic commissure mislocalised laterally, abnormal
ZP:0004290	phagocytosis, engulfment decreased occurrence, abnormal
ZP:0004291	locomotion increased occurrence, abnormal
ZP:0004292	neural precursor cell proliferation disrupted, abnormal
ZP:0004293	lysosome hindbrain increased size, abnormal
ZP:0004294	cerebellum absent, abnormal
ZP:0004295	lysosome forebrain increased size, abnormal
ZP:0004296	retina absent, abnormal
ZP:0004297	lysosome retina increased size, abnormal
ZP:0004298	axon caudal commissure deformed, abnormal
ZP:0004299	axon cranial nerve II deformed, abnormal
ZP:0004300	optic tectum absent, abnormal
ZP:0004301	axon cranial nerve IV deformed, abnormal
ZP:0004302	mandibular arch skeleton absent, abnormal
ZP:0004303	skeletal muscle contraction arrested, abnormal
ZP:0004304	potassium channel activity decreased occurrence, abnormal
ZP:0004305	neuromuscular synaptic transmission arrested, abnormal
ZP:0004306	skeletal myofibril assembly decreased occurrence, abnormal
ZP:0004307	hatching gland quality, abnormal
ZP:0004308	slow muscle cell somite morphology, abnormal
ZP:0004309	fast muscle cell somite degenerate, abnormal
ZP:0004310	skeletal muscle cell myotome atrophied, abnormal
ZP:0004311	acetylcholine-gated channel complex skeletal muscle absent, abnormal
ZP:0004312	potassium channel complex skeletal muscle decreased amount, abnormal
ZP:0004313	slow muscle cell membrane potential, abnormal
ZP:0004314	myosin complex slow muscle cell decreased object quality, abnormal
ZP:0004315	myosin complex fast muscle cell decreased object quality, abnormal
ZP:0004316	mRNA splicing, via spliceosome process quality, abnormal
ZP:0004317	posterior intestine apoptotic, abnormal
ZP:0004318	intestinal epithelium smooth, abnormal
ZP:0004319	hyaloid vessel hypoplastic, abnormal
ZP:0004320	blood vessel endothelial cell hyaloid vessel aggregated, abnormal
ZP:0004321	embryonic heart tube morphogenesis arrested, abnormal
ZP:0004322	cardiac muscle progenitor cell migration to the midline involved in heart field formation arrested, abnormal
ZP:0004323	embryonic heart tube development arrested, abnormal
ZP:0004324	melanosome melanocyte decreased pigmentation, abnormal
ZP:0004325	cardiac muscle cell absent, abnormal
ZP:0004326	histone H4-R3 methylation decreased occurrence, abnormal
ZP:0004328	prechordal plate formation decreased process quality, abnormal
ZP:0004329	cell migration involved in mesendoderm migration decreased process quality, abnormal
ZP:0004330	bleb anterior axial hypoblast increased amount, abnormal
ZP:0004331	pronephric glomerulus permeability, abnormal
ZP:0004332	rRNA processing decreased process quality, abnormal
ZP:0004333	rRNA transcription decreased process quality, abnormal
ZP:0004334	blood accumulation heart, abnormal
ZP:0004335	heart decreased rate, abnormal
ZP:0004336	pigmentation delayed, abnormal
ZP:0004337	fin rough, abnormal
ZP:0004339	intersegmental vessel has extra parts of type endothelial cell, abnormal
ZP:0004342	photoreceptor cell morphogenesis process quality, abnormal
ZP:0004343	retinal photoreceptor layer physical object quality, abnormal
ZP:0004344	melanocyte distended, abnormal
ZP:0004345	photoreceptor inner segment eye photoreceptor cell absent, abnormal
ZP:0004346	photoreceptor inner segment eye photoreceptor cell malformed, abnormal
ZP:0004347	nucleus eye photoreceptor cell circular, abnormal
ZP:0004348	mitochondrion eye photoreceptor cell mislocalised, abnormal
ZP:0004349	Golgi apparatus eye photoreceptor cell mislocalised, abnormal
ZP:0004350	organelle eye photoreceptor cell mislocalised, abnormal
ZP:0004351	organelle eye photoreceptor cell positional polarity, abnormal
ZP:0004352	synapse eye photoreceptor cell malformed, abnormal
ZP:0004353	retinal cone cell malformed, abnormal
ZP:0004354	organelle retinal cone cell mislocalised, abnormal
ZP:0004355	retinal rod cell malformed, abnormal
ZP:0004356	photoreceptor outer segment retinal rod cell physical object quality, abnormal
ZP:0004357	peptidyl-lysine trimethylation decreased occurrence, abnormal
ZP:0004358	peptidyl-lysine monomethylation increased occurrence, abnormal
ZP:0004359	determination of left/right asymmetry in diencephalon disrupted, abnormal
ZP:0004360	histone methyltransferase activity (H3-K9 specific) magnitude, abnormal
ZP:0004361	cilium Kupffer's vesicle decreased amount, abnormal
ZP:0004362	shield distended, abnormal
ZP:0004363	diencephalon structure, abnormal
ZP:0004364	gut mislocalised radially, abnormal
ZP:0004365	gut centered, abnormal
ZP:0004366	lateral plate mesoderm structure, abnormal
ZP:0004367	liver mislocalised radially, abnormal
ZP:0004368	liver centered, abnormal
ZP:0004369	pancreas mislocalised radially, abnormal
ZP:0004370	pancreas centered, abnormal
ZP:0004371	primitive heart tube mislocalised radially, abnormal
ZP:0004372	primitive heart tube centered, abnormal
ZP:0004373	caudal vein plexus decreased branchiness, abnormal
ZP:0004374	sensory perception of touch process quality, abnormal
ZP:0004375	pharyngeal arch cartilage morphology, abnormal
ZP:0004376	neurocranium morphology, abnormal
ZP:0004377	muscle fiber development disrupted, abnormal
ZP:0004378	myofibril myotome decreased thickness, abnormal
ZP:0004379	myofibril myotome undulate, abnormal
ZP:0004380	myotome detached from myofibril myofibril myotome, abnormal
ZP:0004381	myofibril fast muscle cell decreased amount, abnormal
ZP:0004382	neuromast has fewer parts of type hair cell, abnormal
ZP:0004383	locomotory behavior decreased occurrence, abnormal
ZP:0004384	median fin fold structure, abnormal
ZP:0004385	median fin fold immature, abnormal
ZP:0004386	inner ear aplastic, abnormal
ZP:0004387	pancreas development delayed, abnormal
ZP:0004388	pancreas morphogenesis disrupted, abnormal
ZP:0004389	pancreas decreased volume, abnormal
ZP:0004390	cell migration involved in sprouting angiogenesis arrested, abnormal
ZP:0004392	primordial hindbrain channel dilated, abnormal
ZP:0004393	intersegmental vessel truncated, abnormal
ZP:0004394	intersegmental vessel cellular adhesivity blood vessel endothelial cell blood vessel endothelial cell intersegmental vessel, abnormal
ZP:0004395	endothelial tip cell intersegmental vessel positional polarity, abnormal
ZP:0004396	endothelial tip cell circular, abnormal
ZP:0004397	filopodium endothelial tip cell absent, abnormal
ZP:0004398	filopodium endothelial tip cell decreased amount, abnormal
ZP:0004399	EVL detached from external yolk syncytial layer, abnormal
ZP:0004400	somite absent, abnormal
ZP:0004401	neural crest cell migration decreased rate, abnormal
ZP:0004402	anterior region neurocranium decreased size, abnormal
ZP:0004403	anterior region neurocranium deformed, abnormal
ZP:0004404	pharyngeal arch 2 decreased length, abnormal
ZP:0004405	cranial neural crest cell position, abnormal
ZP:0004406	neural crest cell position, abnormal
ZP:0004407	response to auditory stimulus arrested, abnormal
ZP:0004408	skeletal muscle contraction amplitude, abnormal
ZP:0004409	skeletal muscle contraction increased frequency, abnormal
ZP:0004410	musculoskeletal movement process quality, abnormal
ZP:0004411	whole organism partially paralysed, abnormal
ZP:0004412	CaP motoneuron functionality, abnormal
ZP:0004413	central nervous system neuron development disrupted, abnormal
ZP:0004414	axial mesoderm structural organization disrupted, abnormal
ZP:0004415	dorsal-ventral axis brain decreased length, abnormal
ZP:0004416	neuron brain disorganized, abnormal
ZP:0004417	neuron brain decreased amount, abnormal
ZP:0004418	germ ring increased thickness, abnormal
ZP:0004419	midbrain decreased width, abnormal
ZP:0004420	muscle cell migration arrested, abnormal
ZP:0004421	adaxial cell position, abnormal
ZP:0004422	myofibril slow muscle cell bent, abnormal
ZP:0004423	myofibril slow muscle cell elongated, abnormal
ZP:0004424	locomotory behavior increased process quality, abnormal
ZP:0004425	locomotion increased speed, abnormal
ZP:0004426	neuron caudal tuberculum disorganized, abnormal
ZP:0004427	dopaminergic neuron caudal tuberculum mislocalised, abnormal
ZP:0004428	telencephalon increased size, abnormal
ZP:0004429	whole organism wholly anterioralized, abnormal
ZP:0004430	axial vasculature has fewer parts of type intersegmental vessel, abnormal
ZP:0004431	post-vent region wholly dorsalized, abnormal
ZP:0004432	vasculature morphology, abnormal
ZP:0004433	somitogenesis arrested, abnormal
ZP:0004434	pigmentation process quality, abnormal
ZP:0004435	somite 26 aplastic, abnormal
ZP:0004436	ventral region retina aplastic, abnormal
ZP:0004437	somite 20 aplastic, abnormal
ZP:0004438	somite 30 aplastic, abnormal
ZP:0004439	inner ear has fewer parts of type otolith, abnormal
ZP:0004440	atrium position, abnormal
ZP:0004441	atrium attached to bulbus arteriosus, abnormal
ZP:0004442	somite 11 aplastic, abnormal
ZP:0004443	somite 14 aplastic, abnormal
ZP:0004444	somite 17 aplastic, abnormal
ZP:0004445	somite 23 aplastic, abnormal
ZP:0004446	somite 27 aplastic, abnormal
ZP:0004447	somite 7 malformed, abnormal
ZP:0004448	somite 12 aplastic, abnormal
ZP:0004449	somite 15 aplastic, abnormal
ZP:0004450	somite 18 aplastic, abnormal
ZP:0004451	somite 21 aplastic, abnormal
ZP:0004452	somite 24 aplastic, abnormal
ZP:0004453	somite 28 aplastic, abnormal
ZP:0004454	somite 8 aplastic, abnormal
ZP:0004455	somite 10 aplastic, abnormal
ZP:0004456	somite 13 aplastic, abnormal
ZP:0004457	somite 16 aplastic, abnormal
ZP:0004458	somite 19 aplastic, abnormal
ZP:0004459	somite 22 aplastic, abnormal
ZP:0004460	somite 25 aplastic, abnormal
ZP:0004461	somite 29 aplastic, abnormal
ZP:0004462	somite 6 malformed, abnormal
ZP:0004463	somite 9 aplastic, abnormal
ZP:0004464	somite border degenerate, abnormal
ZP:0004465	multicellular organismal locomotion decreased rate, abnormal
ZP:0004466	peripheral neuron decreased thickness, abnormal
ZP:0004467	axon primary motor neuron branched, abnormal
ZP:0004468	axon secondary motor neuron mislocalised, abnormal
ZP:0004469	dorsal aorta malformed, abnormal
ZP:0004470	caudal vein malformed, abnormal
ZP:0004471	intersegmental vessel post-vent region decreased mass density, abnormal
ZP:0004472	caudal vein plexus increased accumulation blood, abnormal
ZP:0004473	blood vessel decreased width, abnormal
ZP:0004474	podocyte structure, abnormal
ZP:0004475	thrombocyte shape, abnormal
ZP:0004476	cartilage condensation decreased occurrence, abnormal
ZP:0004477	chondrocyte differentiation decreased occurrence, abnormal
ZP:0004478	chondrocyte proliferation decreased occurrence, abnormal
ZP:0004482	chondrocyte ceratobranchial cartilage decreased size, abnormal
ZP:0004483	chondrocyte ceratobranchial cartilage immature, abnormal
ZP:0004484	ammonium transport decreased rate, abnormal
ZP:0004485	blood circulation decreased process quality, abnormal
ZP:0004486	hemopoiesis process quality, abnormal
ZP:0004487	dorsal aorta shortened, abnormal
ZP:0004488	blood island increased occurrence apoptotic process, abnormal
ZP:0004490	intersegmental vessel absent, abnormal
ZP:0004491	blood cell absent, abnormal
ZP:0004492	cell fate specification disrupted, abnormal
ZP:0004493	dorsal aorta increased accumulation blood, abnormal
ZP:0004494	posterior cardinal vein increased size, abnormal
ZP:0004495	posterior cardinal vein increased accumulation blood, abnormal
ZP:0004496	axial vasculature morphology, abnormal
ZP:0004497	axial vasculature decreased functionality, abnormal
ZP:0004498	contractile fiber somite disorganized, abnormal
ZP:0004499	contractile fiber somite undulate, abnormal
ZP:0004500	nervous system development process quality, abnormal
ZP:0004501	hepatocyte differentiation disrupted, abnormal
ZP:0004502	hepatocyte proliferation decreased occurrence, abnormal
ZP:0004503	liver morphogenesis disrupted, abnormal
ZP:0004504	hepatocyte apoptotic, abnormal
ZP:0004505	hepatocyte decreased amount, abnormal
ZP:0004506	hepatocyte decreased area, abnormal
ZP:0004507	ball deformed, abnormal
ZP:0004508	telencephalon hypoplastic, abnormal
ZP:0004509	fin decreased thickness, abnormal
ZP:0004510	midbrain aplastic, abnormal
ZP:0004511	cell migration involved in gastrulation decreased occurrence, abnormal
ZP:0004512	forebrain pointed, abnormal
ZP:0004513	anterior-posterior axis whole organism bent, abnormal
ZP:0004514	blastoderm increased thickness, abnormal
ZP:0004515	telencephalon morphology, abnormal
ZP:0004516	tegmentum opaque, abnormal
ZP:0004517	lens absent, abnormal
ZP:0004518	eye immature, abnormal
ZP:0004519	forebrain increased size, abnormal
ZP:0004520	spinal cord bent, abnormal
ZP:0004521	caudal fin bent, abnormal
ZP:0004522	caudal fin increased occurrence apoptotic process, abnormal
ZP:0004523	head increased occurrence apoptotic process, abnormal
ZP:0004524	nucleate erythrocyte blood absent, abnormal
ZP:0004525	myocardium bent, abnormal
ZP:0004526	cardiac muscle cell shape, abnormal
ZP:0004527	trabecula communis aplastic, abnormal
ZP:0004528	optokinetic behavior decreased occurrence, abnormal
ZP:0004529	axon extension delayed, abnormal
ZP:0004530	CaP motoneuron myotome hypoplastic, abnormal
ZP:0004531	otic vesicle formation disrupted, abnormal
ZP:0004532	anterior macula position, abnormal
ZP:0004533	lateral semicircular canal aplastic, abnormal
ZP:0004534	pectoral fin cartilage morphology, abnormal
ZP:0004535	posterior macula position, abnormal
ZP:0004536	otolith organ lacks parts or has fewer parts of type otolith, abnormal
ZP:0004537	otolith organ has extra parts of type otolith, abnormal
ZP:0004538	immature posterior macula aplastic, abnormal
ZP:0004539	vestibuloauditory system functionality, abnormal
ZP:0004540	chondrocranium cartilage decreased size, abnormal
ZP:0004541	otolith composition, abnormal
ZP:0004542	otolith mislocalised, abnormal
ZP:0004543	median fin fold decreased size, abnormal
ZP:0004544	fin undulate, abnormal
ZP:0004545	vertebra decreased mass density, abnormal
ZP:0004546	lepidotrichium increased thickness, abnormal
ZP:0004547	lepidotrichium decreased mass density, abnormal
ZP:0004548	actinotrichium malformed, abnormal
ZP:0004550	cilium otic vesicle increased length, abnormal
ZP:0004551	cilium pronephric duct increased length, abnormal
ZP:0004552	heart tube bilateral symmetry, abnormal
ZP:0004553	hindbrain elongated, abnormal
ZP:0004554	lymph vessel development disrupted, abnormal
ZP:0004555	optic tectum structure, abnormal
ZP:0004556	forerunner cell group disorganized, abnormal
ZP:0004557	atrioventricular valve development disrupted, abnormal
ZP:0004558	cell proliferation involved in heart valve development disrupted, abnormal
ZP:0004559	atrioventricular canal endocardium morphology, abnormal
ZP:0004560	cell atrioventricular canal endocardium decreased amount, abnormal
ZP:0004561	chemical synaptic transmission disrupted, abnormal
ZP:0004562	optokinetic behavior absent, abnormal
ZP:0004563	vestibular reflex decreased magnitude, abnormal
ZP:0004564	axon terminus retinal cone cell morphology, abnormal
ZP:0004565	plasma membrane neuromast hair cell protruding, abnormal
ZP:0004566	synaptic vesicle neuromast hair cell amount, abnormal
ZP:0004567	blood lacks parts or has fewer parts of type nucleate erythrocyte, abnormal
ZP:0004568	intermediate cell mass of mesoderm increased accumulation blood, abnormal
ZP:0004569	epidermis aggregated, abnormal
ZP:0004570	extension structure, abnormal
ZP:0004571	post-vent region edematous, abnormal
ZP:0004572	whole organism lacks parts or has fewer parts of type hemoglobin complex nucleate erythrocyte, abnormal
ZP:0004573	lateral line development process quality, abnormal
ZP:0004574	neuromast primordium migration process quality, abnormal
ZP:0004575	neuromast deposition decreased process quality, abnormal
ZP:0004576	somite decreased width, abnormal
ZP:0004577	somite tight, abnormal
ZP:0004578	somite has fewer parts of type muscle pioneer, abnormal
ZP:0004579	somite has fewer parts of type fast muscle cell, abnormal
ZP:0004580	neuromast decreased size, abnormal
ZP:0004581	neuromast dispersed, abnormal
ZP:0004582	caudal fin increased width, abnormal
ZP:0004584	lateral larval melanophore stripe absent, abnormal
ZP:0004585	lateral larval melanophore stripe has fewer parts of type melanocyte, abnormal
ZP:0004586	muscle cell sparse, abnormal
ZP:0004588	midbrain hindbrain boundary absent, abnormal
ZP:0004593	notochord increased size, abnormal
ZP:0004594	endocrine pancreas increased size, abnormal
ZP:0004595	pancreatic B cell increased amount, abnormal
ZP:0004596	determination of left/right asymmetry in diencephalon process quality, abnormal
ZP:0004597	metapterygoid morphology, abnormal
ZP:0004598	Meckel's cartilage aplastic/hypoplastic, abnormal
ZP:0004599	cartilaginous joint mandibular arch skeleton morphology, abnormal
ZP:0004600	palatoquadrate cartilage aplastic/hypoplastic, abnormal
ZP:0004601	ammonium homeostasis disrupted, abnormal
ZP:0004602	vH ionocyte flux, abnormal
ZP:0004603	keratinocyte flux, abnormal
ZP:0004604	eye hypoplastic, abnormal
ZP:0004605	heart elongated, abnormal
ZP:0004606	myofibril myocardium disorganized, abnormal
ZP:0004607	sarcoplasmic reticulum skeletal muscle cell disorganized, abnormal
ZP:0004608	sarcomere skeletal muscle cell decreased length, abnormal
ZP:0004609	Z disc skeletal muscle cell irregular spatial pattern, abnormal
ZP:0004610	H zone skeletal muscle cell absent, abnormal
ZP:0004611	I band skeletal muscle cell absent, abnormal
ZP:0004612	Z disc cardiac muscle cell irregular spatial pattern, abnormal
ZP:0004613	H zone cardiac muscle cell absent, abnormal
ZP:0004614	I band cardiac muscle cell absent, abnormal
ZP:0004615	calmodulin-dependent protein kinase activity decreased rate, abnormal
ZP:0004616	hindbrain swollen, abnormal
ZP:0004617	notochord posterior region kinked, abnormal
ZP:0004618	head absent, abnormal
ZP:0004619	regulation of RNA splicing disrupted, abnormal
ZP:0004620	adenohypophysis increased size, abnormal
ZP:0004621	adenohypophysis disorganized, abnormal
ZP:0004622	proximal pars anterior morphology, abnormal
ZP:0004623	convergent extension delayed, abnormal
ZP:0004624	cardiac conduction disrupted, abnormal
ZP:0004625	prechordal plate structure, abnormal
ZP:0004626	eye position, abnormal
ZP:0004627	eye decreased amount, abnormal
ZP:0004633	cell-cell junction endothelial cell absent, abnormal
ZP:0004634	mitotic G1 phase arrested, abnormal
ZP:0004635	DNA damage response, signal transduction by p53 class mediator resulting in cell cycle arrest increased occurrence, abnormal
ZP:0004636	brain edematous, abnormal
ZP:0004637	hematopoietic stem cell dorsal aorta decreased amount, abnormal
ZP:0004638	hematopoietic stem cell blood island decreased amount, abnormal
ZP:0004639	extension shortened, abnormal
ZP:0004640	leukocyte decreased amount, abnormal
ZP:0004641	embryonic camera-type eye development disrupted, abnormal
ZP:0004642	optic vesicle apoptotic, abnormal
ZP:0004643	ceratobranchial cartilage morphology, abnormal
ZP:0004644	cranial neural crest cell mislocalised, abnormal
ZP:0004645	optic stalk decreased length, abnormal
ZP:0004646	optic stalk increased thickness, abnormal
ZP:0004647	whole organism lacks all parts of type optic chiasm, abnormal
ZP:0004648	bleb assembly increased occurrence, abnormal
ZP:0004649	heart primordium morphology, abnormal
ZP:0004650	liver primordium morphology, abnormal
ZP:0004651	pancreas primordium morphology, abnormal
ZP:0004652	bleb mesodermal cell increased amount, abnormal
ZP:0004653	eye pigmented, abnormal
ZP:0004654	xanthophore absent, abnormal
ZP:0004655	protein phosphorylation decreased occurrence, abnormal
ZP:0004656	cortical actin cytoskeleton organization disrupted, abnormal
ZP:0004657	filopodium assembly disrupted, abnormal
ZP:0004658	convergent extension decreased rate, abnormal
ZP:0004659	polster mislocalised, abnormal
ZP:0004660	whole organism lacks all parts of type parachordal vessel, abnormal
ZP:0004661	cortical actin cytoskeleton whole organism disorganized, abnormal
ZP:0004662	cortical actin cytoskeleton whole organism decreased mass density, abnormal
ZP:0004663	forerunner cell group whole organism cellular motility, abnormal
ZP:0004664	EVL whole organism cellular motility, abnormal
ZP:0004665	yolk syncytial layer whole organism cellular motility, abnormal
ZP:0004666	DEL whole organism cellular motility, abnormal
ZP:0004667	blood vessel endothelial cell intersegmental vessel decreased amount, abnormal
ZP:0004668	blood vessel unlumenized, abnormal
ZP:0004669	medial fin morphogenesis process quality, abnormal
ZP:0004670	median fin fold blistered, abnormal
ZP:0004671	blood island blistered, abnormal
ZP:0004672	epidermis morphogenesis disrupted, abnormal
ZP:0004673	epidermis morphology, abnormal
ZP:0004674	cell surface keratinocyte disorganized, abnormal
ZP:0004675	dorsal aorta hypoplastic, abnormal
ZP:0004676	retinal pigmented epithelium unpigmented, abnormal
ZP:0004677	larval melanophore stripe low saturation, abnormal
ZP:0004678	neoplasm orbit protruding, abnormal
ZP:0004679	melanocyte broken, abnormal
ZP:0004680	melanocyte aggregated, abnormal
ZP:0004681	melanosome melanocyte degenerate, abnormal
ZP:0004682	cell adhesion disrupted, abnormal
ZP:0004683	medial fin development disrupted, abnormal
ZP:0004684	protein localization to adherens junction arrested, abnormal
ZP:0004685	median fin fold malformed, abnormal
ZP:0004686	median fin fold edematous, abnormal
ZP:0004687	basement membrane median fin fold punctate, abnormal
ZP:0004689	epidermis median fin fold disorganized, abnormal
ZP:0004690	epidermal cell median fin fold positional polarity, abnormal
ZP:0004691	extension hypoplastic, abnormal
ZP:0004692	fin necrotic, abnormal
ZP:0004693	caudal fin has fewer parts of type lepidotrichium, abnormal
ZP:0004694	pectoral fin structure, abnormal
ZP:0004695	pectoral fin degenerate, abnormal
ZP:0004696	pectoral fin edematous, abnormal
ZP:0004697	pectoral fin has fewer parts of type lepidotrichium, abnormal
ZP:0004698	anal fin has fewer parts of type lepidotrichium, abnormal
ZP:0004699	dorsal fin has fewer parts of type lepidotrichium, abnormal
ZP:0004700	epidermal cell shape, abnormal
ZP:0004701	neuron optic tectum decreased amount, abnormal
ZP:0004702	locomotory behavior decreased frequency, abnormal
ZP:0004703	cell migration process quality, abnormal
ZP:0004704	endocrine pancreas development disrupted, abnormal
ZP:0004705	axon cranial nerve V immature, abnormal
ZP:0004706	axon Mauthner neuron morphology, abnormal
ZP:0004707	axon Rohon-Beard neuron truncated, abnormal
ZP:0004708	atrioventricular valve constricted, abnormal
ZP:0004709	skeletal muscle decreased size, abnormal
ZP:0004710	skeletal muscle refractivity, abnormal
ZP:0004711	myofibril skeletal muscle disorganized, abnormal
ZP:0004713	Z disc skeletal muscle increased thickness, abnormal
ZP:0004714	epithelial to mesenchymal transition occurrence, abnormal
ZP:0004715	negative regulation of epithelial to mesenchymal transition disrupted, abnormal
ZP:0004716	posterior lateral line neuromast development disrupted, abnormal
ZP:0004717	negative regulation of epithelial cell proliferation disrupted, abnormal
ZP:0004718	epidermis quality, abnormal
ZP:0004719	integument quality, abnormal
ZP:0004720	cell integument circular, abnormal
ZP:0004721	epithelial cell increased amount, abnormal
ZP:0004722	lamellipodium epithelial cell increased amount, abnormal
ZP:0004723	epidermal cell morphology, abnormal
ZP:0004724	mandibular muscle aplastic, abnormal
ZP:0004725	whole organism mobility, abnormal
ZP:0004726	myofibril skeletal muscle cell structure, abnormal
ZP:0004727	myofibril skeletal muscle cell decreased width, abnormal
ZP:0004728	macrophage mislocalised, abnormal
ZP:0004729	neutrophil mislocalised, abnormal
ZP:0004730	basement membrane assembly disrupted, abnormal
ZP:0004735	integument detached from whole organism, abnormal
ZP:0004736	dermis broken, abnormal
ZP:0004737	retinal ganglion cell layer decreased thickness, abnormal
ZP:0004738	retinal inner nuclear layer decreased thickness, abnormal
ZP:0004739	retinal outer nuclear layer decreased thickness, abnormal
ZP:0004740	regulation of transcription by RNA polymerase II disrupted, abnormal
ZP:0004741	neuron development process quality, abnormal
ZP:0004742	trigeminal ganglion decreased size, abnormal
ZP:0004743	chromosome whole organism disorganized, abnormal
ZP:0004744	chromosome whole organism condensed, abnormal
ZP:0004745	eye mislocalised anteriorly, abnormal
ZP:0004746	digestive tract development delayed, abnormal
ZP:0004747	digestive tract development process quality, abnormal
ZP:0004748	gut poorly differentiated, abnormal
ZP:0004749	mid intestine epithelium morphology, abnormal
ZP:0004750	visual perception disrupted, abnormal
ZP:0004751	otic vesicle formation process quality, abnormal
ZP:0004752	otic placode formation process quality, abnormal
ZP:0004753	intermediate cell mass of mesoderm morphology, abnormal
ZP:0004754	otic vesicle malformed, abnormal
ZP:0004756	caudal vein aplastic, abnormal
ZP:0004757	caudal vein plexus absent, abnormal
ZP:0004758	post-vent vasculature morphology, abnormal
ZP:0004759	cell differentiation disrupted, abnormal
ZP:0004760	exocrine pancreas morphology, abnormal
ZP:0004761	angiogenesis arrested, abnormal
ZP:0004762	embryonic pectoral fin morphogenesis disrupted, abnormal
ZP:0004763	scapulocoracoid morphology, abnormal
ZP:0004764	scapulocoracoid increased size, abnormal
ZP:0004765	ventral mandibular arch shortened, abnormal
ZP:0004766	pharyngeal arch 2 shortened, abnormal
ZP:0004767	negative regulation of heart rate disrupted, abnormal
ZP:0004768	regulation of cell migration quality, abnormal
ZP:0004771	pectoral fin musculature aplastic, abnormal
ZP:0004772	neuromast posterior lateral line decreased amount, abnormal
ZP:0004773	myotome cellular quality, abnormal
ZP:0004774	thymus lacks parts or has fewer parts of type lymphocyte, abnormal
ZP:0004775	hypaxial myotome region aplastic, abnormal
ZP:0004776	protein prenylation disrupted, abnormal
ZP:0004777	melanosome organization disrupted, abnormal
ZP:0004778	pigmentation increased occurrence, abnormal
ZP:0004779	lens opaque, abnormal
ZP:0004780	retinal neural layer lacks parts or has fewer parts of type retinal outer plexiform layer, abnormal
ZP:0004781	spinal cord increased curvature, abnormal
ZP:0004782	iridophore eye decreased amount, abnormal
ZP:0004783	retinal pigmented epithelium irregular spatial pattern, abnormal
ZP:0004784	retinal pigmented epithelium hypertrophic, abnormal
ZP:0004785	retinal pigmented epithelium irregular thickness, abnormal
ZP:0004786	melanosome retinal pigmented epithelium decreased amount, abnormal
ZP:0004787	retinal outer nuclear layer apoptotic, abnormal
ZP:0004788	retinal outer nuclear layer has fewer parts of type photoreceptor cell, abnormal
ZP:0004789	photoreceptor outer segment layer disheveled, abnormal
ZP:0004790	photoreceptor cell morphology, abnormal
ZP:0004791	photoreceptor cell disorganized, abnormal
ZP:0004792	pigmented epithelial cell vacuolated, abnormal
ZP:0004793	retinal ganglion cell apoptotic, abnormal
ZP:0004794	cation transport arrested, abnormal
ZP:0004795	cation transport decreased occurrence, abnormal
ZP:0004796	adenohypophysis morphogenesis process quality, abnormal
ZP:0004797	somatotropin secreting cell differentiation process quality, abnormal
ZP:0004798	prolactin secreting cell differentiation process quality, abnormal
ZP:0004799	corticotropin hormone secreting cell differentiation process quality, abnormal
ZP:0004800	central nervous system has fewer parts of type white matter, abnormal
ZP:0004801	facial nerve motor nucleus absent, abnormal
ZP:0004802	motor nucleus of vagal nerve absent, abnormal
ZP:0004803	optic chiasm malformed, abnormal
ZP:0004804	cranial nerve IX absent, abnormal
ZP:0004805	abducens motor nucleus absent, abnormal
ZP:0004806	central canal quality, abnormal
ZP:0004807	central canal morphology, abnormal
ZP:0004808	adenohypophyseal placode decreased size, abnormal
ZP:0004809	lateral floor plate composition, abnormal
ZP:0004810	trigeminal motor nucleus absent, abnormal
ZP:0004811	ethmoid cartilage decreased width, abnormal
ZP:0004812	somatotropin secreting cell decreased amount, abnormal
ZP:0004813	prolactin secreting cell decreased amount, abnormal
ZP:0004814	adrenocorticotropic hormone secreting cell decreased amount, abnormal
ZP:0004815	axon primary motor neuron misrouted, abnormal
ZP:0004816	retinal ganglion cell displaced to axon diencephalon, abnormal
ZP:0004817	cell proliferation in midbrain decreased occurrence, abnormal
ZP:0004818	optic tectum physical object quality, abnormal
ZP:0004819	ventral mandibular arch quality, abnormal
ZP:0004820	developmental pigmentation delayed, abnormal
ZP:0004821	embryonic morphogenesis paedomorphic growth, abnormal
ZP:0004822	inner ear hypoplastic, abnormal
ZP:0004823	head orientation trunk, abnormal
ZP:0004824	taxis arrested, abnormal
ZP:0004825	swim bladder formation growth quality of occurrent, abnormal
ZP:0004826	myotome disorganized, abnormal
ZP:0004827	myotome vacuolated, abnormal
ZP:0004828	myoseptum perforate, abnormal
ZP:0004829	sarcomere muscle cell disorganized, abnormal
ZP:0004830	sarcomere muscle cell collapsed, abnormal
ZP:0004831	melanocyte lateral larval melanophore stripe decreased amount, abnormal
ZP:0004832	skeletal muscle degenerate, abnormal
ZP:0004833	endothelial cell development disrupted, abnormal
ZP:0004834	spinal cord development disrupted, abnormal
ZP:0004835	ventral spinal cord interneuron specification disrupted, abnormal
ZP:0004836	auditory receptor cell fate specification process quality, abnormal
ZP:0004837	generation of neurons increased rate, abnormal
ZP:0004838	taste bud formation decreased process quality, abnormal
ZP:0004839	endothelial cell artery morphology, abnormal
ZP:0004840	cell brain circular, abnormal
ZP:0004841	cell brain dispersed, abnormal
ZP:0004842	neuron central nervous system disorganized, abnormal
ZP:0004843	epiphysis has extra parts of type neuron, abnormal
ZP:0004844	hindbrain has fewer parts of type radial glial cell, abnormal
ZP:0004845	hindbrain has fewer parts of type dorsal region neuron, abnormal
ZP:0004846	radial glial cell hindbrain increased amount, abnormal
ZP:0004847	radial glial cell hindbrain disorganized, abnormal
ZP:0004848	midbrain hindbrain boundary increased size, abnormal
ZP:0004849	retinal neural layer morphology, abnormal
ZP:0004850	retinal neural layer undifferentiated, abnormal
ZP:0004851	pericardium distended, abnormal
ZP:0004852	polster increased size, abnormal
ZP:0004853	somite 5 increased length, abnormal
ZP:0004854	glial cell spinal cord decreased amount, abnormal
ZP:0004856	primary motor neuron spinal cord increased amount, abnormal
ZP:0004857	GABAergic neuron spinal cord decreased amount, abnormal
ZP:0004858	cell notochord spherical, abnormal
ZP:0004859	pronephric duct increased size, abnormal
ZP:0004860	somite increased length, abnormal
ZP:0004861	habenula cellular quality, abnormal
ZP:0004862	neuron habenula morphology, abnormal
ZP:0004863	hair cell posterior macula increased amount, abnormal
ZP:0004864	trigeminal ganglion has extra parts of type sensory neuron, abnormal
ZP:0004865	sensory neuron trigeminal ganglion apoptotic, abnormal
ZP:0004866	integument has fewer parts of type pigment cell, abnormal
ZP:0004867	semicircular canal spatial pattern, abnormal
ZP:0004868	tela chorioidea morphology, abnormal
ZP:0004869	tela chorioidea mislocalised, abnormal
ZP:0004870	medial longitudinal fasciculus increased width, abnormal
ZP:0004871	caudal tuberculum morphology, abnormal
ZP:0004872	hair cell anterior macula increased amount, abnormal
ZP:0004873	somite 2 increased length, abnormal
ZP:0004874	somite 3 increased length, abnormal
ZP:0004875	somite 4 increased length, abnormal
ZP:0004877	rhombomere morphology, abnormal
ZP:0004878	rhombomere increased size, abnormal
ZP:0004879	primary neuron rhombomere increased amount, abnormal
ZP:0004880	taste bud physical quality, abnormal
ZP:0004881	thyroid primordium increased size, abnormal
ZP:0004882	thyroid primordium increased volume, abnormal
ZP:0004883	thyroid primordium mislocalised, abnormal
ZP:0004884	thyroid primordium disorganized, abnormal
ZP:0004885	thyroid primordium physical object quality, abnormal
ZP:0004886	thyroid primordium mislocalised ventrally, abnormal
ZP:0004887	whole organism has extra parts of type anterior-posterior axis Rohon-Beard neuron, abnormal
ZP:0004888	whole organism has extra parts of type anterior-posterior axis primary motor neuron, abnormal
ZP:0004889	whole organism has extra parts of type medial-lateral axis Rohon-Beard neuron, abnormal
ZP:0004890	trunk has fewer parts of type anterior region melanocyte, abnormal
ZP:0004891	melanocyte trunk absent, abnormal
ZP:0004892	post-vent region lacks all parts of type pigment cell, abnormal
ZP:0004893	posterior lateral line placode has extra parts of type sensory neuron, abnormal
ZP:0004894	cell posterior lateral line primordium decreased amount, abnormal
ZP:0004895	myofibril pectoral fin disheveled, abnormal
ZP:0004896	myoblast pectoral fin decreased amount, abnormal
ZP:0004897	roof plate spinal cord region malformed, abnormal
ZP:0004898	roof plate spinal cord region separated from roof plate spinal cord region, abnormal
ZP:0004899	cell projection roof plate spinal cord region absent, abnormal
ZP:0004900	optic cup has fewer parts of type radial glial cell, abnormal
ZP:0004901	intersegmental vessel increased mass density, abnormal
ZP:0004902	intersegmental vessel has extra parts of type blood vessel, abnormal
ZP:0004903	anterior lateral line placode has extra parts of type sensory neuron, abnormal
ZP:0004904	rhombic lip cellular motility, abnormal
ZP:0004905	epithelium pharyngeal arch 3 physical object quality, abnormal
ZP:0004906	pharyngeal vasculature separated from thyroid primordium, abnormal
ZP:0004907	CoSA increased amount, abnormal
ZP:0004908	VeLD decreased amount, abnormal
ZP:0004909	hindbrain interneuron increased amount, abnormal
ZP:0004910	CiD increased amount, abnormal
ZP:0004911	pectoral fin fold morphology, abnormal
ZP:0004912	hindbrain neural keel concave, abnormal
ZP:0004913	Mauthner neuron increased amount, abnormal
ZP:0004914	axon Mauthner neuron fasciculation, abnormal
ZP:0004915	axon primary neuron fasciculation, abnormal
ZP:0004917	neuroepithelial cell circular, abnormal
ZP:0004918	retinal ganglion cell dead, abnormal
ZP:0004919	angiogenesis decreased occurrence, abnormal
ZP:0004920	ion homeostasis disrupted, abnormal
ZP:0004921	somatic stem cell epidermis decreased amount, abnormal
ZP:0004922	vasculature neurohypophysis malformed, abnormal
ZP:0004923	NaK ionocyte decreased amount, abnormal
ZP:0004924	vH ionocyte decreased amount, abnormal
ZP:0004925	sprouting angiogenesis arrested, abnormal
ZP:0004926	granulocyte differentiation disrupted, abnormal
ZP:0004927	artery aplastic, abnormal
ZP:0004928	cardiac ventricle decreased strength, abnormal
ZP:0004929	posterior cardinal vein morphology, abnormal
ZP:0004930	posterior cardinal vein aplastic, abnormal
ZP:0004931	intersegmental artery decreased length, abnormal
ZP:0004932	granulocyte immature, abnormal
ZP:0004933	proctodeum apoptotic, abnormal
ZP:0004934	ventricular zone forebrain apoptotic, abnormal
ZP:0004935	presumptive telencephalon necrotic, abnormal
ZP:0004936	slow muscle cell somite decreased amount, abnormal
ZP:0004937	muscle cell increased occurrence apoptotic process, abnormal
ZP:0004938	muscle cell increased occurrence cell death, abnormal
ZP:0004939	apoptotic process decreased occurrence, abnormal
ZP:0004940	delamination involved in gastrulation with mouth forming second disrupted, abnormal
ZP:0004941	Kupffer's vesicle development disrupted, abnormal
ZP:0004942	heart mislocalised radially, abnormal
ZP:0004943	hypoblast decreased thickness, abnormal
ZP:0004944	whole organism lacks all parts of type Kupffer's vesicle, abnormal
ZP:0004945	epithelial cell differentiation process quality, abnormal
ZP:0004947	otic placode split, abnormal
ZP:0004949	inner ear duplicated, abnormal
ZP:0004950	inner ear split, abnormal
ZP:0004951	integument physical object quality, abnormal
ZP:0004952	pharyngeal arch 2 skeleton quality, abnormal
ZP:0004953	cranial cartilage mislocalised posteriorly, abnormal
ZP:0004954	pharyngeal arch cartilage mislocalised posteriorly, abnormal
ZP:0004955	auditory capsule decreased size, abnormal
ZP:0004956	ceratobranchial cartilage bent, abnormal
ZP:0004957	pharyngeal arch 1 aplastic, abnormal
ZP:0004958	otic vesicle protrusion morphology, abnormal
ZP:0004959	pillar of the semicircular canal aplastic, abnormal
ZP:0004960	epiphysis decreased size, abnormal
ZP:0004961	apoptotic DNA fragmentation increased rate, abnormal
ZP:0004962	apoptotic process increased rate, abnormal
ZP:0004963	immature eye apoptotic, abnormal
ZP:0004964	blood vessel endothelial cell proliferation involved in sprouting angiogenesis disrupted, abnormal
ZP:0004965	canonical Wnt signaling pathway involved in neural crest cell differentiation disrupted, abnormal
ZP:0004966	cell-cell junction organization disrupted, abnormal
ZP:0004967	negative regulation of Notch signaling pathway disrupted, abnormal
ZP:0004968	pigment cell differentiation disrupted, abnormal
ZP:0004969	caudal fin morphology, abnormal
ZP:0004970	trunk neural crest cell positional polarity, abnormal
ZP:0004971	trunk neural crest cell decreased amount, abnormal
ZP:0004972	axon habenula misrouted, abnormal
ZP:0004973	interpeduncular nucleus tegmentum structure, abnormal
ZP:0004974	blood vessel endothelial cell apoptotic, abnormal
ZP:0004975	axon CaP motoneuron branched, abnormal
ZP:0004976	cardiac ventricle development disrupted, abnormal
ZP:0004977	blood circulation decreased occurrence, abnormal
ZP:0004978	cardiac ventricle shape, abnormal
ZP:0004979	sarcomere ventricular myocardium sparse, abnormal
ZP:0004980	ball size, abnormal
ZP:0004981	nucleate erythrocyte blood decreased amount, abnormal
ZP:0004982	hindbrain apoptotic, abnormal
ZP:0004983	hindbrain edematous, abnormal
ZP:0004984	hindbrain aplastic, abnormal
ZP:0004985	midbrain hindbrain boundary amorphous, abnormal
ZP:0004986	extension degenerate, abnormal
ZP:0004987	heart tube decreased thickness, abnormal
ZP:0004988	heart tube collapsed, abnormal
ZP:0004989	forebrain midbrain boundary amorphous, abnormal
ZP:0004990	fin development disrupted, abnormal
ZP:0004991	cell migration involved in heart development decreased rate, abnormal
ZP:0004992	fin morphology, abnormal
ZP:0004993	heart constricted, abnormal
ZP:0004994	post-vent region curved lateral, abnormal
ZP:0004995	atrioventricular canal increased length, abnormal
ZP:0004996	melanocyte scale decreased amount, abnormal
ZP:0004997	iridophore spatial pattern, abnormal
ZP:0004998	swim bladder development process quality, abnormal
ZP:0004999	habenular commissure aplastic, abnormal
ZP:0005000	xanthophore low saturation, abnormal
ZP:0005001	xanthophore increased distribution, abnormal
ZP:0005002	axon retinal ganglion cell irregular spatial pattern, abnormal
ZP:0005003	axon retinal ganglion cell aggregated, abnormal
ZP:0005004	axon retinal ganglion cell displaced, abnormal
ZP:0005005	retinal ganglion cell displaced to axon ipsilateral side eye, abnormal
ZP:0005006	neuron-neuron synaptic transmission process quality, abnormal
ZP:0005007	posterior lateral line neuromast hair cell development process quality, abnormal
ZP:0005008	neuromast hair cell physical object quality, abnormal
ZP:0005009	nucleate erythrocyte increased amount, abnormal
ZP:0005010	hair cell quality, abnormal
ZP:0005011	hair cell morphology, abnormal
ZP:0005012	axis curved, abnormal
ZP:0005013	cilium ciliated olfactory receptor neuron paralysed, abnormal
ZP:0005014	ciliated olfactory receptor neuron increased rate cilium-dependent cell motility, abnormal
ZP:0005015	ciliated olfactory receptor neuron decreased process quality cilium-dependent cell motility, abnormal
ZP:0005016	startle response occurrence, abnormal
ZP:0005017	hypothalamus development disrupted, abnormal
ZP:0005018	afferent axon development in posterior lateral line nerve decreased occurrence, abnormal
ZP:0005019	melanocyte dispersed, abnormal
ZP:0005020	muscle pioneer somite decreased amount, abnormal
ZP:0005021	heart tube elongated, abnormal
ZP:0005022	post-vent region coiled, abnormal
ZP:0005023	nucleus slow muscle cell decreased amount, abnormal
ZP:0005024	skeletal muscle cell somite disorganized, abnormal
ZP:0005025	nucleus skeletal muscle cell shape, abnormal
ZP:0005026	establishment or maintenance of epithelial cell apical/basal polarity process quality, abnormal
ZP:0005027	retinal inner nuclear layer distributed, abnormal
ZP:0005028	third ventricle absent, abnormal
ZP:0005029	third ventricle decreased volume, abnormal
ZP:0005030	neuroblast (sensu Vertebrata) neural tube mislocalised, abnormal
ZP:0005031	outer limiting membrane aplastic, abnormal
ZP:0005032	retinal outer nuclear layer distributed, abnormal
ZP:0005033	retinal cone cell mislocalised, abnormal
ZP:0005034	retinal rod cell mislocalised, abnormal
ZP:0005035	retinal rod cell disorganized, abnormal
ZP:0005036	retinal rod cell deformed, abnormal
ZP:0005037	retinal rod cell increased distribution, abnormal
ZP:0005038	photoreceptor outer segment retinal rod cell decreased volume, abnormal
ZP:0005039	Muller cell mislocalised, abnormal
ZP:0005040	centrosome neuroepithelial cell mislocalised, abnormal
ZP:0005041	retinal ganglion cell disorganized, abnormal
ZP:0005042	retinal ganglion cell increased distribution, abnormal
ZP:0005043	actin filament polymerization increased occurrence, abnormal
ZP:0005044	eye neoplastic, abnormal
ZP:0005047	caudal fin falciform, abnormal
ZP:0005048	myeloid lineage restricted progenitor cell mislocalised, abnormal
ZP:0005049	cardiovascular system morphology, abnormal
ZP:0005050	cardiovascular system non-functional, abnormal
ZP:0005051	gut edematous, abnormal
ZP:0005053	intersegmental artery attached to intersegmental vessel, abnormal
ZP:0005054	intersegmental vessel irregular spatial pattern, abnormal
ZP:0005055	dorsal longitudinal anastomotic vessel irregular spatial pattern, abnormal
ZP:0005056	subintestinal vein irregular spatial pattern, abnormal
ZP:0005057	supraintestinal artery irregular spatial pattern, abnormal
ZP:0005058	thoracic duct decreased size, abnormal
ZP:0005059	chemical synaptic transmission amplitude, abnormal
ZP:0005060	chemical synaptic transmission decreased intensity, abnormal
ZP:0005061	visual perception decreased occurrence, abnormal
ZP:0005062	retinal ganglion cell structure, abnormal
ZP:0005063	axon retinal ganglion cell defasciculated, abnormal
ZP:0005064	cell proliferation in hindbrain increased occurrence, abnormal
ZP:0005065	cell proliferation in forebrain increased occurrence, abnormal
ZP:0005066	forebrain neuron development decreased process quality, abnormal
ZP:0005067	cell proliferation in midbrain increased occurrence, abnormal
ZP:0005068	Rohon-Beard neuron spinal cord decreased amount, abnormal
ZP:0005069	neuron cerebellum decreased amount, abnormal
ZP:0005070	forebrain has fewer parts of type neuron, abnormal
ZP:0005071	Meckel's cartilage decreased distance ceratohyal cartilage, abnormal
ZP:0005072	neuron projection motor neuron decreased size, abnormal
ZP:0005073	motor neuron perpendicular to neuron projection spinal cord, abnormal
ZP:0005074	establishment of mitotic spindle orientation decreased process quality, abnormal
ZP:0005075	secondary neural tube formation decreased process quality, abnormal
ZP:0005076	neuroepithelial cell neural keel disorganized, abnormal
ZP:0005077	neuroepithelial cell neural rod disorganized, abnormal
ZP:0005078	central canal branched, abnormal
ZP:0005079	central canal disorganized, abnormal
ZP:0005080	neuroepithelial cell neural tube disorganized, abnormal
ZP:0005082	mitotic spindle neuroepithelial cell direction, abnormal
ZP:0005083	exocrine pancreas development delayed, abnormal
ZP:0005084	anterior pancreatic bud decreased size, abnormal
ZP:0005085	pancreatic duct aplastic, abnormal
ZP:0005086	exocrine cell absent, abnormal
ZP:0005087	calcium ion transport disrupted, abnormal
ZP:0005088	embryonic digestive tract morphogenesis disrupted, abnormal
ZP:0005089	cardiac ventricle orientation atrium, abnormal
ZP:0005090	heart rudiment morphology, abnormal
ZP:0005091	pancreatic bud mislocalised, abnormal
ZP:0005092	anterior lateral plate mesoderm morphology, abnormal
ZP:0005093	regulation of cell cycle arrest disrupted, abnormal
ZP:0005094	mitotic cell cycle arrest increased occurrence, abnormal
ZP:0005095	somite lacks parts or has fewer parts of type fast muscle cell, abnormal
ZP:0005096	pharyngeal arch 3-7 skeleton decreased length, abnormal
ZP:0005097	mouth open, abnormal
ZP:0005098	cranium has extra parts of type cranial cartilage, abnormal
ZP:0005099	branchiostegal ray 3 shape, abnormal
ZP:0005100	branchiostegal ray 3 aplastic, abnormal
ZP:0005101	palatoquadrate cartilage curved lateral, abnormal
ZP:0005102	palatoquadrate cartilage curved medial, abnormal
ZP:0005103	cartilage element mislocalised, abnormal
ZP:0005104	osteoblast decreased amount, abnormal
ZP:0005105	nucleate erythrocyte increased accumulation ventral wall of dorsal aorta, abnormal
ZP:0005107	muscle misaligned with myofibril myofibril muscle, abnormal
ZP:0005108	T-tubule muscle broken, abnormal
ZP:0005109	muscle misaligned with T-tubule T-tubule muscle, abnormal
ZP:0005110	sarcolemma muscle broken, abnormal
ZP:0005111	myofibril muscle cell damaged, abnormal
ZP:0005113	axis elongation disrupted, abnormal
ZP:0005114	anterior/posterior axis specification disrupted, abnormal
ZP:0005115	gut lateralized, abnormal
ZP:0005116	heart mislocalised laterally, abnormal
ZP:0005117	liver mislocalised laterally, abnormal
ZP:0005118	pancreas mislocalised laterally, abnormal
ZP:0005119	head increased distance post-vent region, abnormal
ZP:0005120	anterior-posterior axis trunk shortened, abnormal
ZP:0005121	branching morphogenesis of a nerve disrupted, abnormal
ZP:0005122	peripheral nervous system neuron axonogenesis disrupted, abnormal
ZP:0005123	cranial nerve morphology, abnormal
ZP:0005124	pancreas development decreased process quality, abnormal
ZP:0005125	swim bladder decreased size, abnormal
ZP:0005126	epithelium swim bladder decreased size, abnormal
ZP:0005127	parasphenoid shape, abnormal
ZP:0005128	parasphenoid decreased length, abnormal
ZP:0005129	hepatic duct morphology, abnormal
ZP:0005130	hepatic duct decreased size, abnormal
ZP:0005131	hepatic duct aplastic, abnormal
ZP:0005132	intestine decreased width, abnormal
ZP:0005133	palatoquadrate cartilage shape, abnormal
ZP:0005134	ethmoid cartilage decreased length, abnormal
ZP:0005135	esophageal epithelium decreased size, abnormal
ZP:0005136	trabecula cranii shape, abnormal
ZP:0005137	extrapancreatic duct physical object quality, abnormal
ZP:0005138	palate shape, abnormal
ZP:0005139	palate square, abnormal
ZP:0005140	hepatocyte mislocalised, abnormal
ZP:0005141	pectoral fin morphogenesis arrested, abnormal
ZP:0005142	pectoral fin field morphology, abnormal
ZP:0005145	mesodermal cell migration decreased occurrence, abnormal
ZP:0005146	paraxial mesodermal cell differentiation process quality, abnormal
ZP:0005147	paraxial mesodermal cell differentiation decreased process quality, abnormal
ZP:0005148	tail bud increased size, abnormal
ZP:0005149	tail bud cellular quality, abnormal
ZP:0005150	tail bud decreased cellular motility, abnormal
ZP:0005151	segmental plate poorly differentiated, abnormal
ZP:0005152	segmental plate decreased cellular motility, abnormal
ZP:0005153	somite trunk absent, abnormal
ZP:0005155	post-vent region has extra parts of type somite, abnormal
ZP:0005156	protein N-linked glycosylation decreased occurrence, abnormal
ZP:0005157	lipooligosaccharide catabolic process increased occurrence, abnormal
ZP:0005158	secondary motor neuron spinal cord increased amount, abnormal
ZP:0005159	ethmoid cartilage shape, abnormal
ZP:0005160	cartilage development process quality, abnormal
ZP:0005161	pharyngeal arch 3-7 skeleton hypoplastic, abnormal
ZP:0005162	cleithrum ossified, abnormal
ZP:0005163	opercle ossified, abnormal
ZP:0005164	osteoblast opercle poorly differentiated, abnormal
ZP:0005165	maxilla ossified, abnormal
ZP:0005166	branchiostegal ray ossified, abnormal
ZP:0005167	osteoblast branchiostegal ray poorly differentiated, abnormal
ZP:0005168	mouth ventrally rotated head, abnormal
ZP:0005169	parasphenoid ossified, abnormal
ZP:0005170	entopterygoid ossified, abnormal
ZP:0005171	vertebra ossified, abnormal
ZP:0005172	ceratobranchial 5 bone ossified, abnormal
ZP:0005173	palatoquadrate cartilage hypoplastic, abnormal
ZP:0005174	hyosymplectic cartilage hypoplastic, abnormal
ZP:0005175	notochordal ossification ossified, abnormal
ZP:0005176	cell population proliferation decreased process quality, abnormal
ZP:0005177	neuron projection morphogenesis disrupted, abnormal
ZP:0005178	Kupffer's vesicle deformed, abnormal
ZP:0005179	forerunner cell group shape, abnormal
ZP:0005180	forerunner cell group increased width, abnormal
ZP:0005181	forerunner cell group malformed, abnormal
ZP:0005182	bile ductule liver and biliary system increased amount, abnormal
ZP:0005183	intrahepatic bile duct liver and biliary system decreased amount, abnormal
ZP:0005184	prechordal plate mislocalised posteriorly, abnormal
ZP:0005185	liver decreased functionality, abnormal
ZP:0005186	anatomical axis whole organism curved, abnormal
ZP:0005187	mesoderm head increased width, abnormal
ZP:0005188	exocrine pancreas mislocalised, abnormal
ZP:0005189	retinal inner plexiform layer disorganized, abnormal
ZP:0005190	synapse retinal inner plexiform layer disorganized, abnormal
ZP:0005191	intestine mislocalised, abnormal
ZP:0005192	photoreceptor inner segment layer disorganized, abnormal
ZP:0005193	cell intrahepatic bile duct decreased amount, abnormal
ZP:0005194	multicellular organism growth decreased rate, abnormal
ZP:0005195	adipose tissue development disrupted, abnormal
ZP:0005196	adipose tissue increased mass, abnormal
ZP:0005197	fat cell hypertrophic, abnormal
ZP:0005198	lipid droplet fat cell increased size, abnormal
ZP:0005199	DNA methylation on cytosine decreased occurrence, abnormal
ZP:0005200	intermediate cell mass of mesoderm apoptotic, abnormal
ZP:0005201	blood vasculature decreased amount, abnormal
ZP:0005202	lens apoptotic, abnormal
ZP:0005203	retina distended, abnormal
ZP:0005204	pioneer neuron olfactory placode absent, abnormal
ZP:0005205	pioneer neuron olfactory placode decreased amount, abnormal
ZP:0005206	optic tract branchiness, abnormal
ZP:0005207	cell population proliferation decreased rate, abnormal
ZP:0005208	pharyngeal muscle development disrupted, abnormal
ZP:0005209	semicircular canal morphogenesis arrested, abnormal
ZP:0005210	pharynx development hypotrophic growth, abnormal
ZP:0005211	cardiac ventricle increased width, abnormal
ZP:0005212	cardiac ventricle shortened, abnormal
ZP:0005213	neural crest cell hindbrain decreased amount, abnormal
ZP:0005214	pharynx malformed, abnormal
ZP:0005215	heart straight, abnormal
ZP:0005216	neural crest cell midbrain decreased amount, abnormal
ZP:0005217	notochord mislocalised anteriorly, abnormal
ZP:0005218	bulbus arteriosus decreased length, abnormal
ZP:0005219	bulbus arteriosus immature, abnormal
ZP:0005220	smooth muscle bulbus arteriosus morphology, abnormal
ZP:0005221	levator arcus palatini aplastic, abnormal
ZP:0005222	macula hypoplastic, abnormal
ZP:0005223	macula decreased amount, abnormal
ZP:0005224	mesenchyme decreased size, abnormal
ZP:0005225	semicircular canal hypoplastic, abnormal
ZP:0005226	atrium increased width, abnormal
ZP:0005227	atrium decreased angle to cardiac ventricle, abnormal
ZP:0005228	dilatator operculi aplastic, abnormal
ZP:0005229	mouth closure incomplete, abnormal
ZP:0005230	mouth mislocalised posteriorly, abnormal
ZP:0005231	thymus hypoplastic, abnormal
ZP:0005232	thymus aplastic, abnormal
ZP:0005233	pharyngeal pouch malformed, abnormal
ZP:0005234	pharyngeal pouch aplastic, abnormal
ZP:0005235	pharyngeal pouch decreased amount, abnormal
ZP:0005236	Meckel's cartilage inverted, abnormal
ZP:0005237	Meckel's cartilage mislocalised ventrally, abnormal
ZP:0005238	glossopharyngeal ganglion absent, abnormal
ZP:0005239	muscle pharyngeal arch aplastic, abnormal
ZP:0005240	parachordal cartilage mislocalised posteriorly, abnormal
ZP:0005241	pharyngeal arch cartilage fused with pharyngeal arch cartilage, abnormal
ZP:0005242	epibranchial ganglion increased size, abnormal
ZP:0005243	epibranchial ganglion fused with epibranchial ganglion, abnormal
ZP:0005244	neural crest cell pharyngeal arch 2 absent, abnormal
ZP:0005245	neural crest cell pharyngeal arch 2 decreased amount, abnormal
ZP:0005246	neural crest cell pharyngeal arch 1 present, abnormal
ZP:0005247	neural crest cell pharyngeal arch 1 decreased amount, abnormal
ZP:0005248	neural crest cell pharyngeal arch 3-7 absent, abnormal
ZP:0005249	pharyngeal arch 3-7 fused with neural crest cell neural crest cell pharyngeal arch 3-7, abnormal
ZP:0005250	aortic arch decreased amount, abnormal
ZP:0005251	constrictor dorsalis morphology, abnormal
ZP:0005252	cardiac muscle cell circular, abnormal
ZP:0005253	gonad morphology, abnormal
ZP:0005254	gonad apoptotic, abnormal
ZP:0005255	whole organism lacks all parts of type sperm, abnormal
ZP:0005256	sperm decreased amount, abnormal
ZP:0005257	germ line cell absent, abnormal
ZP:0005258	germ line cell apoptotic, abnormal
ZP:0005259	germ line cell decreased amount, abnormal
ZP:0005260	olfactory placode morphology, abnormal
ZP:0005261	basibranchial decreased size, abnormal
ZP:0005262	basibranchial undulate, abnormal
ZP:0005263	palatoquadrate cartilage mislocalised posteriorly, abnormal
ZP:0005264	ceratohyal cartilage displaced, abnormal
ZP:0005265	hyosymplectic cartilage mislocalised posteriorly, abnormal
ZP:0005266	cranial cartilage shape, abnormal
ZP:0005267	cranial cartilage malformed, abnormal
ZP:0005268	basihyal cartilage undulate, abnormal
ZP:0005269	compact myelin hindbrain decreased amount, abnormal
ZP:0005270	oligodendrocyte hindbrain morphology, abnormal
ZP:0005271	axon spinal cord decreased length, abnormal
ZP:0005272	oligodendrocyte spinal cord morphology, abnormal
ZP:0005273	cortical actin cytoskeleton organization absent, abnormal
ZP:0005274	epiboly disrupted, abnormal
ZP:0005275	blood mislocalised, abnormal
ZP:0005276	blood vessel endothelial cell dorsal aorta apoptotic, abnormal
ZP:0005277	blood vessel endothelial cell posterior cardinal vein apoptotic, abnormal
ZP:0005278	blood vasculature degenerate, abnormal
ZP:0005279	head color, abnormal
ZP:0005280	intersegmental vessel decreased diameter, abnormal
ZP:0005281	intersegmental vessel absent blood circulation, abnormal
ZP:0005282	endothelial cell apoptotic, abnormal
ZP:0005283	blood vessel development delayed, abnormal
ZP:0005284	hemopoiesis decreased occurrence, abnormal
ZP:0005285	neuron apoptotic process increased occurrence, abnormal
ZP:0005286	G1 to G0 transition disrupted, abnormal
ZP:0005287	angioblastic mesenchymal cell lateral plate mesoderm cellular motility, abnormal
ZP:0005288	axial vasculature apoptotic, abnormal
ZP:0005289	axial vasculature decreased diameter, abnormal
ZP:0005290	motor neuron head disorganized, abnormal
ZP:0005291	proliferative region neural tube decreased functionality, abnormal
ZP:0005292	caudal vein plexus apoptotic, abnormal
ZP:0005293	proliferative region caudal vein plexus decreased functionality, abnormal
ZP:0005294	neural crest cell pharyngeal arch 3-7 decreased amount, abnormal
ZP:0005295	optic vein morphology, abnormal
ZP:0005296	inner optic circle morphology, abnormal
ZP:0005297	atrioventricular valve amorphous, abnormal
ZP:0005298	endocardial ring amorphous, abnormal
ZP:0005299	posterior neural tube apoptotic, abnormal
ZP:0005300	egg activation disrupted, abnormal
ZP:0005301	meiotic sister chromatid cohesion involved in meiosis II disrupted, abnormal
ZP:0005302	oocyte microtubule cytoskeleton organization disrupted, abnormal
ZP:0005303	ribonucleoprotein complex assembly disrupted, abnormal
ZP:0005304	embryonic camera-type eye development delayed, abnormal
ZP:0005305	actin cytoskeleton reorganization disrupted, abnormal
ZP:0005306	sperm aster formation disrupted, abnormal
ZP:0005307	meiotic metaphase II plate congression disrupted, abnormal
ZP:0005309	sister chromosome movement towards spindle pole involved in meiotic sister chromatid segregation disrupted, abnormal
ZP:0005311	astral microtubule blastomere disorganized, abnormal
ZP:0005312	aster blastomere mislocalised, abnormal
ZP:0005313	actin filament blastomere branched, abnormal
ZP:0005314	cortical actin cytoskeleton blastomere morphology, abnormal
ZP:0005315	blastomere disrupted astral microtubule organization, abnormal
ZP:0005316	cortical microtubule cytoskeleton blastomere disorganized, abnormal
ZP:0005317	cleavage furrow blastomere absent, abnormal
ZP:0005318	P granule blastomere decreased size, abnormal
ZP:0005319	mitotic spindle blastomere disorganized, abnormal
ZP:0005320	sinus venosus decreased functionality, abnormal
ZP:0005321	meiotic spindle unfertilized egg bent, abnormal
ZP:0005322	microtubule bundle unfertilized egg absent, abnormal
ZP:0005323	atrioventricular valve decreased diameter, abnormal
ZP:0005324	endocardial ring decreased size, abnormal
ZP:0005325	erythroid lineage cell decreased amount, abnormal
ZP:0005326	interkinetic nuclear migration disrupted, abnormal
ZP:0005327	presumptive neural retina decreased thickness, abnormal
ZP:0005328	microtubule cytoskeleton presumptive neural retina disorganized, abnormal
ZP:0005329	whole organism semi-lethal (sensu genetics), abnormal
ZP:0005330	intersegmental vessel arrested, abnormal
ZP:0005331	intersegmental vessel variability of size, abnormal
ZP:0005332	endothelial tip cell intersegmental vessel shape, abnormal
ZP:0005334	anterior region head truncated, abnormal
ZP:0005335	EVL lacks parts or has fewer parts of type bicellular tight junction EVL, abnormal
ZP:0005336	bicellular tight junction EVL decreased amount, abnormal
ZP:0005337	blood island increased size, abnormal
ZP:0005338	male gonad development delayed, abnormal
ZP:0005339	male gonad development postdisplaced growth, abnormal
ZP:0005340	female gonad development arrested, abnormal
ZP:0005341	female gonad development aplastic growth, abnormal
ZP:0005342	female organism absent, abnormal
ZP:0005343	ovary aplastic, abnormal
ZP:0005344	ovarian follicle stage I aplastic, abnormal
ZP:0005345	primordial germ cell shape, abnormal
ZP:0005346	primordial germ cell decreased cellular motility, abnormal
ZP:0005347	primordial germ cell lacks all parts of type bleb primordial germ cell, abnormal
ZP:0005348	primordial germ cell decreased occurrence cell motility, abnormal
ZP:0005349	somitogenesis increased duration, abnormal
ZP:0005350	proctodeum mislocalised anteriorly, abnormal
ZP:0005351	anterior-posterior axis somite increased length, abnormal
ZP:0005352	trunk has fewer parts of type myotome, abnormal
ZP:0005353	anal fin mislocalised anteriorly, abnormal
ZP:0005354	dorsal fin mislocalised anteriorly, abnormal
ZP:0005355	vertebral column has fewer parts of type vertebra, abnormal
ZP:0005357	cell proliferation involved in compound eye morphogenesis increased occurrence, abnormal
ZP:0005358	retina lacks all parts of type amacrine cell, abnormal
ZP:0005359	retina has fewer parts of type amacrine cell, abnormal
ZP:0005360	proliferative region retina increased size, abnormal
ZP:0005361	cranial nerve II decreased thickness, abnormal
ZP:0005362	cranial nerve II hypoplastic, abnormal
ZP:0005364	ciliary marginal zone increased size, abnormal
ZP:0005367	auditory capsule morphology, abnormal
ZP:0005369	left-right axis whole organism increased width, abnormal
ZP:0005370	retinal pigmented epithelium forebrain mislocalized adaxially, abnormal
ZP:0005371	macula utricle increased occurrence cell death, abnormal
ZP:0005372	caudal fin upturned, abnormal
ZP:0005373	macula saccule increased occurrence cell death, abnormal
ZP:0005374	Kupffer's vesicle decreased volume, abnormal
ZP:0005375	Kupffer's vesicle unlumenized, abnormal
ZP:0005376	epithelial cell Kupffer's vesicle apical-basal polarity, abnormal
ZP:0005377	forerunner cell group spatial pattern, abnormal
ZP:0005378	forerunner cell group circular, abnormal
ZP:0005379	forerunner cell group mislocalised, abnormal
ZP:0005380	forerunner cell group orientation forerunner cell group, abnormal
ZP:0005381	forerunner cell group detached from forerunner cell group, abnormal
ZP:0005382	pseudopodium forerunner cell group direction, abnormal
ZP:0005383	heart tube positional polarity, abnormal
ZP:0005384	post-vent region undulate, abnormal
ZP:0005385	ventricular system increased accumulation cerebral spinal fluid, abnormal
ZP:0005386	caudal vein plexus perforate, abnormal
ZP:0005387	JNK cascade disrupted, abnormal
ZP:0005388	Wnt signaling pathway disrupted, abnormal
ZP:0005389	heart split, abnormal
ZP:0005390	chondrocyte differentiation process quality, abnormal
ZP:0005391	retinal ganglion cell axon guidance arrested, abnormal
ZP:0005392	embryonic cranial skeleton morphogenesis process quality, abnormal
ZP:0005393	embryonic skeletal joint morphogenesis process quality, abnormal
ZP:0005394	face morphogenesis process quality, abnormal
ZP:0005395	floor plate hypoplastic, abnormal
ZP:0005396	inner ear wholly anterioralized, abnormal
ZP:0005397	inner ear has extra parts of type anterior macula, abnormal
ZP:0005398	optic chiasm aplastic, abnormal
ZP:0005399	posterior macula aplastic, abnormal
ZP:0005400	horizontal myoseptum hypoplastic, abnormal
ZP:0005401	head retracted, abnormal
ZP:0005402	neural tube decreased thickness, abnormal
ZP:0005403	joint mandibular arch skeleton malformed, abnormal
ZP:0005404	pharyngeal arch 2 skeleton hypoplastic, abnormal
ZP:0005405	joint pharyngeal arch 2 skeleton malformed, abnormal
ZP:0005406	chondrocyte pharyngeal arch 3-7 absent, abnormal
ZP:0005407	pars superior ear has extra parts of type anterior crista, abnormal
ZP:0005408	axon primary motor neuron disorganized, abnormal
ZP:0005409	axon primary motor neuron decreased amount, abnormal
ZP:0005410	axon secondary motor neuron absent, abnormal
ZP:0005411	cell body secondary motor neuron decreased amount, abnormal
ZP:0005412	axon retinal ganglion cell disorganized, abnormal
ZP:0005413	retinal ganglion cell displaced to axon eye, abnormal
ZP:0005414	regulation of BMP signaling pathway disrupted, abnormal
ZP:0005415	cardiac ventricle morphology, abnormal
ZP:0005416	atrium deformed, abnormal
ZP:0005417	cilium or flagellum-dependent cell motility disrupted, abnormal
ZP:0005418	smoothened signaling pathway disrupted, abnormal
ZP:0005419	axoneme assembly disrupted, abnormal
ZP:0005421	Kupffer's vesicle altered number of axonemal microtubule ciliated cell, abnormal
ZP:0005422	axoneme Kupffer's vesicle disorganized, abnormal
ZP:0005423	gut position, abnormal
ZP:0005424	liver position, abnormal
ZP:0005425	liver inverted, abnormal
ZP:0005426	pancreas position, abnormal
ZP:0005427	pancreas inverted, abnormal
ZP:0005428	heart tube inverted, abnormal
ZP:0005429	heart tube symmetry, abnormal
ZP:0005430	heart tube straight, abnormal
ZP:0005431	nervous system necrotic, abnormal
ZP:0005432	atrium inverted, abnormal
ZP:0005433	lateral floor plate aplastic, abnormal
ZP:0005434	medial floor plate morphology, abnormal
ZP:0005435	roof of mouth development disrupted, abnormal
ZP:0005436	trabecula communis cleft, abnormal
ZP:0005437	sensory perception of sound decreased occurrence, abnormal
ZP:0005438	hair cell macula utricle decreased amount, abnormal
ZP:0005439	hair cell lateral crista decreased amount, abnormal
ZP:0005440	hair cell posterior macula absent, abnormal
ZP:0005441	hair cell posterior macula decreased amount, abnormal
ZP:0005442	semicircular canal immature, abnormal
ZP:0005443	hair cell posterior crista decreased amount, abnormal
ZP:0005444	hair cell anterior crista decreased amount, abnormal
ZP:0005445	sagitta decreased size, abnormal
ZP:0005446	sagitta immature, abnormal
ZP:0005447	integument ionocyte morphology, abnormal
ZP:0005448	hair cell macula saccule decreased amount, abnormal
ZP:0005449	neuromast hair cell has fewer parts of type stereocilium neuromast hair cell, abnormal
ZP:0005450	neuromast hair cell has fewer parts of type kinocilium neuromast hair cell, abnormal
ZP:0005451	kinocilium neuromast hair cell truncated, abnormal
ZP:0005452	establishment or maintenance of epithelial cell apical/basal polarity disrupted, abnormal
ZP:0005453	ventral region diencephalon structure, abnormal
ZP:0005454	centrosome neural rod mislocalised, abnormal
ZP:0005455	axoneme neural rod irregular spatial pattern, abnormal
ZP:0005456	centrosome neural tube mislocalised, abnormal
ZP:0005457	protein localization to adherens junction disrupted, abnormal
ZP:0005459	DEL position, abnormal
ZP:0005460	cerebellar central artery disorganized, abnormal
ZP:0005461	inner optic circle decreased amount, abnormal
ZP:0005462	primary motor neuron branched, abnormal
ZP:0005463	intersegmental artery disrupted sprouting angiogenesis, abnormal
ZP:0005464	subintestinal vein disrupted sprouting angiogenesis, abnormal
ZP:0005466	respiratory burst decreased process quality, abnormal
ZP:0005467	neuron-neuron synaptic transmission decreased process quality, abnormal
ZP:0005468	sensory perception of sound decreased process quality, abnormal
ZP:0005469	regulation of proton-transporting ATPase activity, rotational mechanism decreased process quality, abnormal
ZP:0005470	synaptic vesicle maturation decreased process quality, abnormal
ZP:0005471	regulation of cellular pH reduction decreased process quality, abnormal
ZP:0005472	synaptic vesicle lumen acidification decreased process quality, abnormal
ZP:0005473	vacuolar proton-transporting V-type ATPase, V1 domain neuromast hair cell mislocalised, abnormal
ZP:0005474	synaptic vesicle lumen neuromast hair cell decreased acidity, abnormal
ZP:0005475	dorsal telencephalon morphology, abnormal
ZP:0005477	xanthoblast axis mislocalised medially, abnormal
ZP:0005479	melanoblast axis mislocalised medially, abnormal
ZP:0005480	glomerular capillary pronephros dilated, abnormal
ZP:0005481	anatomical axis whole organism curved dorsal, abnormal
ZP:0005482	cell projection pronephric podocyte absent, abnormal
ZP:0005483	pericardium broken, abnormal
ZP:0005484	neuron differentiation decreased occurrence, abnormal
ZP:0005485	neuron brain undifferentiated, abnormal
ZP:0005486	hindbrain has fewer parts of type neuron, abnormal
ZP:0005488	tail bud umbonate, abnormal
ZP:0005489	cardiac ventricle elliptic, abnormal
ZP:0005490	cardiac ventricle immature, abnormal
ZP:0005491	cardiac ventricle curvature, abnormal
ZP:0005492	cardiac muscle cell cardiac ventricle shape, abnormal
ZP:0005493	bulbus arteriosus increased length, abnormal
ZP:0005494	atrium malformed, abnormal
ZP:0005495	atrium decreased contractility, abnormal
ZP:0005496	atrium non-contractile, abnormal
ZP:0005497	atrium decreased strength, abnormal
ZP:0005498	myofibril atrium disorganized, abnormal
ZP:0005499	cardiac jelly distended, abnormal
ZP:0005500	digestive tract mesoderm development disrupted, abnormal
ZP:0005501	anterior/posterior axis specification process quality, abnormal
ZP:0005502	cerebellum morphogenesis disrupted, abnormal
ZP:0005503	cerebellum structural organization disrupted, abnormal
ZP:0005504	midbrain-hindbrain boundary maturation disrupted, abnormal
ZP:0005505	forebrain anterior/posterior pattern specification disrupted, abnormal
ZP:0005506	forebrain dorsal/ventral pattern formation disrupted, abnormal
ZP:0005507	cerebellar granule cell precursor proliferation increased occurrence, abnormal
ZP:0005508	chemokine production disrupted, abnormal
ZP:0005509	DNA hypomethylation chronic, abnormal
ZP:0005510	canonical Wnt signaling pathway disrupted, abnormal
ZP:0005511	canonical Wnt signaling pathway decreased process quality, abnormal
ZP:0005512	endodermal digestive tract morphogenesis disrupted, abnormal
ZP:0005513	DNA demethylation increased occurrence, abnormal
ZP:0005514	negative regulation of canonical Wnt signaling pathway disrupted, abnormal
ZP:0005515	cardiac ventricle mislocalised radially, abnormal
ZP:0005516	dorsal aorta decreased process quality blood circulation, abnormal
ZP:0005517	blood dorsal aorta decreased fluid flow, abnormal
ZP:0005518	pharynx immature, abnormal
ZP:0005519	postoptic commissure morphology, abnormal
ZP:0005520	dorsal region cerebellum curved, abnormal
ZP:0005521	dorsal region cerebellum increased size, abnormal
ZP:0005522	ventral region cerebellum decreased thickness, abnormal
ZP:0005523	diencephalon flattened, abnormal
ZP:0005524	forebrain wholly dorsalized, abnormal
ZP:0005525	liver has extra parts of type hepatocyte, abnormal
ZP:0005526	liver primordium increased size, abnormal
ZP:0005527	liver primordium aplastic, abnormal
ZP:0005528	neuromast has extra parts of type neuromast hair cell, abnormal
ZP:0005530	caudal commissure morphology, abnormal
ZP:0005531	abnormal(ly) disrupted neutrophil aggregation
ZP:0005532	optic tectum flattened, abnormal
ZP:0005533	ventral fin fold morphology, abnormal
ZP:0005534	anterior commissure morphology, abnormal
ZP:0005535	anterior region neuroectoderm decreased size, abnormal
ZP:0005536	posterior lateral line primordium morphology, abnormal
ZP:0005537	atrioventricular canal obstructed, abnormal
ZP:0005538	endocardium hyperplastic, abnormal
ZP:0005539	intestine immature, abnormal
ZP:0005540	intestine poorly differentiated, abnormal
ZP:0005541	fin bud immature, abnormal
ZP:0005542	pancreatic bud decreased size, abnormal
ZP:0005543	atrioventricular canal endocardium fused with atrioventricular canal endocardium, abnormal
ZP:0005544	optic nerve head decreased thickness, abnormal
ZP:0005545	presumptive atrium heart tube mislocalised radially, abnormal
ZP:0005546	atrioventricular valve malformed, abnormal
ZP:0005547	hepatocyte increased amount, abnormal
ZP:0005548	heart morphogenesis occurrence, abnormal
ZP:0005549	excretion disrupted, abnormal
ZP:0005550	post-anal tail morphogenesis process quality, abnormal
ZP:0005551	cell proliferation involved in kidney development increased occurrence, abnormal
ZP:0005552	cilium Kupffer's vesicle spatial pattern, abnormal
ZP:0005553	cilium Kupffer's vesicle immobile, abnormal
ZP:0005554	brush border pronephric duct irregular spatial pattern, abnormal
ZP:0005555	brush border pronephric duct decreased size, abnormal
ZP:0005556	cilium pronephros immobile, abnormal
ZP:0005557	axoneme pronephros structure, abnormal
ZP:0005558	testis hyperplastic, abnormal
ZP:0005559	germ cell tumor testis increased amount, abnormal
ZP:0005560	germ cell tumor testis proliferative, abnormal
ZP:0005561	spermatogonium testis increased amount, abnormal
ZP:0005562	kinocilium lateral line decreased length, abnormal
ZP:0005563	kinocilium lateral line decreased amount, abnormal
ZP:0005564	pronephric glomerulus increased size, abnormal
ZP:0005565	pronephric tubule dilated, abnormal
ZP:0005566	cornea development in camera-type eye disrupted, abnormal
ZP:0005567	extracellular matrix assembly disrupted, abnormal
ZP:0005568	symplectic quality, abnormal
ZP:0005569	posterior lateral line primordium split, abnormal
ZP:0005570	cell posterior lateral line primordium increased length, abnormal
ZP:0005571	primordial germ cell cellular motility, abnormal
ZP:0005572	primordial germ cell positional polarity, abnormal
ZP:0005576	somite spatial pattern, abnormal
ZP:0005578	intersegmental artery structure, abnormal
ZP:0005579	blood vessel endothelial cell intersegmental artery increased amount, abnormal
ZP:0005582	intersegmental vessel mislocalised, abnormal
ZP:0005584	angiogenic sprout increased amount, abnormal
ZP:0005585	blood vessel endothelial cell increased amount, abnormal
ZP:0005586	motor neuron increased amount, abnormal
ZP:0005587	Rohon-Beard neuron increased amount, abnormal
ZP:0005588	definitive hemopoiesis decreased process quality, abnormal
ZP:0005589	signal transduction by p53 class mediator increased process quality, abnormal
ZP:0005590	fin regeneration arrested, abnormal
ZP:0005591	cardiac muscle cell proliferation arrested, abnormal
ZP:0005592	heart trabecula formation arrested, abnormal
ZP:0005593	cardiac conduction process quality, abnormal
ZP:0005594	neuron dorsal root ganglion absent, abnormal
ZP:0005595	myocardium lacks all parts of type trabecular layer, abnormal
ZP:0005596	neuron sympathetic nervous system absent, abnormal
ZP:0005597	alpha-(1->6)-fucosyltransferase activity disrupted, abnormal
ZP:0005598	spinal cord lacks all parts of type neuron projection motor neuron, abnormal
ZP:0005599	eye physical object quality, abnormal
ZP:0005600	fourth ventricle swollen, abnormal
ZP:0005601	retina lacks parts or has fewer parts of type Muller cell, abnormal
ZP:0005602	retina lacks parts or has fewer parts of type retinal ganglion cell, abnormal
ZP:0005603	somite has fewer parts of type slow muscle cell, abnormal
ZP:0005604	muscle cell somite decreased length, abnormal
ZP:0005605	whole organism lacks all parts of type neuron projection dorsal root ganglion, abnormal
ZP:0005606	splanchnocranium lacks all parts of type mandibular arch skeleton, abnormal
ZP:0005607	hindbrain commissure decreased amount, abnormal
ZP:0005608	motor neuron position, abnormal
ZP:0005609	motor neuron disorganized, abnormal
ZP:0005610	photoreceptor cell decreased amount, abnormal
ZP:0005611	primitive erythrocyte differentiation arrested, abnormal
ZP:0005612	hemoglobin complex blood absent, abnormal
ZP:0005613	erythroblast immature, abnormal
ZP:0005614	nucleus nucleate erythrocyte broken, abnormal
ZP:0005615	palatoquadrate arch malformed, abnormal
ZP:0005616	ventral mandibular arch decreased length, abnormal
ZP:0005617	cilium posterior neural tube disorganized, abnormal
ZP:0005618	cilium posterior neural tube distended, abnormal
ZP:0005619	transcription, DNA-templated decreased occurrence, abnormal
ZP:0005620	negative regulation of apoptotic process disrupted, abnormal
ZP:0005621	positive regulation of cell cycle disrupted, abnormal
ZP:0005622	eye disrupted cell division, abnormal
ZP:0005623	liver apoptotic, abnormal
ZP:0005624	liver development process quality, abnormal
ZP:0005625	alkaline phosphatase activity process quality, abnormal
ZP:0005626	endoderm development discontinuous, abnormal
ZP:0005627	morphogenesis of embryonic epithelium process quality, abnormal
ZP:0005628	basal protein localization disrupted, abnormal
ZP:0005629	pancreas quality, abnormal
ZP:0005630	digestive system hypoplastic, abnormal
ZP:0005631	whole organism decreased acidity, abnormal
ZP:0005632	whole organism organismal quality, abnormal
ZP:0005633	brush border whole organism structure, abnormal
ZP:0005634	mandibular arch skeleton structure, abnormal
ZP:0005635	sodium ion transport disrupted, abnormal
ZP:0005636	cellular calcium ion homeostasis disrupted, abnormal
ZP:0005637	epidermal cell differentiation disrupted, abnormal
ZP:0005638	water homeostasis disrupted, abnormal
ZP:0005639	pore complex epidermis absent, abnormal
ZP:0005640	integument ionocyte integument absent, abnormal
ZP:0005641	pore complex epidermis decreased amount, abnormal
ZP:0005642	head development process quality, abnormal
ZP:0005644	notochord curled, abnormal
ZP:0005645	epithelium hyperplastic, abnormal
ZP:0005646	caudal fin actinotrichium malformed, abnormal
ZP:0005647	cellular pigmentation process quality, abnormal
ZP:0005648	melanin biosynthetic process arrested, abnormal
ZP:0005649	retinal pigmented epithelium color, abnormal
ZP:0005650	pigment granule retinal pigmented epithelium decreased amount, abnormal
ZP:0005651	melanocyte integument decreased amount, abnormal
ZP:0005652	melanocyte unpigmented, abnormal
ZP:0005653	cardiac conduction system development process quality, abnormal
ZP:0005654	cardiac muscle tissue morphogenesis process quality, abnormal
ZP:0005655	heart contraction asynchronous, abnormal
ZP:0005656	ventricular myocardium contractility, abnormal
ZP:0005657	cardiac muscle cell malformed, abnormal
ZP:0005658	carbonate dehydratase activity decreased occurrence, abnormal
ZP:0005659	respiratory gaseous exchange by respiratory system process quality, abnormal
ZP:0005660	intrahepatic bile duct development arrested, abnormal
ZP:0005661	nucleus liver increased size, abnormal
ZP:0005662	lipid droplet liver present, abnormal
ZP:0005663	gall bladder decreased functionality, abnormal
ZP:0005664	bile ductule degenerate, abnormal
ZP:0005665	bile ductule unlumenized, abnormal
ZP:0005666	intrahepatic bile duct decreased branchiness, abnormal
ZP:0005667	mitochondrion hepatocyte structure, abnormal
ZP:0005668	mitochondrial crista hepatocyte condensed, abnormal
ZP:0005673	lateral dorsal aorta morphology, abnormal
ZP:0005676	trunk vasculature disorganized, abnormal
ZP:0005678	solid lens vesicle decreased size, abnormal
ZP:0005679	circulatory system process disrupted, abnormal
ZP:0005680	pigment cell morphology, abnormal
ZP:0005681	heart contraction delayed, abnormal
ZP:0005682	cell brain necrotic, abnormal
ZP:0005683	heart swollen, abnormal
ZP:0005684	posterior intestine morphology, abnormal
ZP:0005685	myoblast fusion involved in skeletal muscle regeneration disrupted, abnormal
ZP:0005686	fast muscle cell disorganized, abnormal
ZP:0005687	fast muscle cell disheveled, abnormal
ZP:0005688	fast muscle cell decreased diameter, abnormal
ZP:0005689	fast muscle cell has fewer parts of type nucleus fast muscle cell, abnormal
ZP:0005690	margin disorganized, abnormal
ZP:0005691	dorsal aorta decreased diameter, abnormal
ZP:0005692	adaxial cell absent, abnormal
ZP:0005693	adaxial cell decreased amount, abnormal
ZP:0005694	head muscle hypoplastic, abnormal
ZP:0005695	fast muscle cell absent, abnormal
ZP:0005696	post-vent region sigmoid, abnormal
ZP:0005697	pharyngeal arch 2 skeleton shape, abnormal
ZP:0005698	chondrocranium cartilage hypoplastic, abnormal
ZP:0005699	activation of innate immune response decreased process quality, abnormal
ZP:0005700	pattern recognition receptor signaling pathway decreased process quality, abnormal
ZP:0005701	caudal vein plexus aplastic, abnormal
ZP:0005702	angiogenic sprout caudal vein plexus decreased amount, abnormal
ZP:0005703	caudal fin decreased pigmentation, abnormal
ZP:0005704	axis whole organism decreased pigmentation, abnormal
ZP:0005705	endothelial cell proliferation decreased rate, abnormal
ZP:0005706	primordial hindbrain channel absent, abnormal
ZP:0005707	primordial hindbrain channel aplastic, abnormal
ZP:0005708	intersegmental vein decreased amount, abnormal
ZP:0005709	intersegmental artery increased amount, abnormal
ZP:0005710	lymph vasculature trunk aplastic, abnormal
ZP:0005711	trunk vasculature branchiness, abnormal
ZP:0005712	lymphangioblast cord absent, abnormal
ZP:0005713	vascular lymphangioblast absent, abnormal
ZP:0005714	vascular lymphangioblast cellular motility, abnormal
ZP:0005715	vascular lymphangioblast decreased amount, abnormal
ZP:0005716	somite misaligned with myofibril myofibril somite, abnormal
ZP:0005717	somite border amorphous, abnormal
ZP:0005718	feeding behavior decreased process quality, abnormal
ZP:0005719	anterior commissure morphogenesis disrupted, abnormal
ZP:0005720	posterior commissure morphogenesis disrupted, abnormal
ZP:0005721	medial longitudinal fasciculus structure, abnormal
ZP:0005722	muscle organ development disrupted, abnormal
ZP:0005723	axon motor neuron misrouted, abnormal
ZP:0005725	actin cap epiblast position, abnormal
ZP:0005726	mitotic spindle epiblast position, abnormal
ZP:0005727	tail bud mislocalised, abnormal
ZP:0005728	tail bud opaque, abnormal
ZP:0005729	inner ear increased size, abnormal
ZP:0005730	otolith organ has fewer parts of type otolith, abnormal
ZP:0005731	head position, abnormal
ZP:0005732	head mislocalised posteriorly, abnormal
ZP:0005733	somite border hypoplastic, abnormal
ZP:0005734	muscle morphology, abnormal
ZP:0005735	ventral region retina mislocalized adaxially, abnormal
ZP:0005737	type B pancreatic cell differentiation decreased occurrence, abnormal
ZP:0005738	pancreatic A cell differentiation increased occurrence, abnormal
ZP:0005739	endocrine pancreas development decreased process quality, abnormal
ZP:0005740	type B pancreatic cell proliferation disrupted, abnormal
ZP:0005741	endocrine pancreas decreased size, abnormal
ZP:0005742	endocrine pancreas has fewer parts of type pancreatic B cell, abnormal
ZP:0005743	endocrine pancreas has extra parts of type pancreatic A cell, abnormal
ZP:0005744	endocrine pancreas has fewer parts of type endodermal cell, abnormal
ZP:0005745	posterior pancreatic bud decreased size, abnormal
ZP:0005748	posterior pancreatic bud has fewer parts of type pancreatic B cell, abnormal
ZP:0005749	posterior pancreatic bud has extra parts of type pancreatic A cell, abnormal
ZP:0005752	axon MiP motor neuron mislocalised, abnormal
ZP:0005754	endocrine cell extrapancreatic duct decreased amount, abnormal
ZP:0005755	post-vent region increased size, abnormal
ZP:0005756	pharyngeal arch non-functional, abnormal
ZP:0005758	subintestinal vein morphology, abnormal
ZP:0005760	neuromuscular synaptic transmission decreased process quality, abnormal
ZP:0005763	slow muscle cell morphology, abnormal
ZP:0005764	pancreas absent, abnormal
ZP:0005765	lens morphogenesis in camera-type eye process quality, abnormal
ZP:0005766	anaphase-promoting complex-dependent catabolic process decreased rate, abnormal
ZP:0005767	proteasome-mediated ubiquitin-dependent protein catabolic process decreased rate, abnormal
ZP:0005768	lens fiber cell differentiation process quality, abnormal
ZP:0005769	nucleus lens circular, abnormal
ZP:0005770	nucleus lens mislocalised anteriorly, abnormal
ZP:0005771	nucleus lens decreased amount, abnormal
ZP:0005772	midbrain hindbrain boundary hemorrhagic, abnormal
ZP:0005773	cell division rate, abnormal
ZP:0005774	EVL increased permeability, abnormal
ZP:0005775	EVL moderately well differentiated, abnormal
ZP:0005776	actin filament EVL disorganized, abnormal
ZP:0005777	bicellular tight junction EVL irregular spatial pattern, abnormal
ZP:0005778	cell junction EVL immature, abnormal
ZP:0005779	extracellular space DEL decreased area, abnormal
ZP:0005780	camera-type eye development arrested, abnormal
ZP:0005781	retinal bipolar neuron differentiation delayed, abnormal
ZP:0005782	axon retina malformed, abnormal
ZP:0005783	pneumatic duct morphology, abnormal
ZP:0005784	neutrophil aggregation disrupted, abnormal
ZP:0005785	neutrophil intermediate cell mass of mesoderm absent, abnormal
ZP:0005786	opercle decreased thickness, abnormal
ZP:0005787	cytosolic small ribosomal subunit whole organism decreased amount, abnormal
ZP:0005788	neutrophil anterior lateral mesoderm absent, abnormal
ZP:0005789	granulocyte position, abnormal
ZP:0005790	integument disorganized, abnormal
ZP:0005791	caudal fin disorganized, abnormal
ZP:0005794	cellular sodium ion homeostasis disrupted, abnormal
ZP:0005796	visual perception arrested, abnormal
ZP:0005797	response to light stimulus arrested, abnormal
ZP:0005798	developmental growth decreased rate, abnormal
ZP:0005799	cilium peripheral olfactory organ decreased length, abnormal
ZP:0005800	eye elliptic, abnormal
ZP:0005801	cilium olfactory pit decreased amount, abnormal
ZP:0005802	retinal photoreceptor layer structure, abnormal
ZP:0005803	retinal photoreceptor layer apoptotic, abnormal
ZP:0005804	cilium pronephric duct morphology, abnormal
ZP:0005805	retina electrical conductivity, abnormal
ZP:0005806	central region retina apoptotic, abnormal
ZP:0005807	retina lacks all parts of type central region eye photoreceptor cell, abnormal
ZP:0005808	retina has fewer parts of type central region eye photoreceptor cell, abnormal
ZP:0005809	retina lacks all parts of type central region retinal cone cell, abnormal
ZP:0005810	photoreceptor outer segment retina decreased size, abnormal
ZP:0005811	photoreceptor outer segment retina disorganized, abnormal
ZP:0005812	anterior-posterior axis whole organism curled, abnormal
ZP:0005813	cilium whole organism morphology, abnormal
ZP:0005814	retinal outer nuclear layer wholeness, abnormal
ZP:0005815	photoreceptor cell degenerate, abnormal
ZP:0005816	eye photoreceptor cell apoptotic, abnormal
ZP:0005817	eye photoreceptor cell decreased amount, abnormal
ZP:0005818	nucleus eye photoreceptor cell condensed, abnormal
ZP:0005819	cilium Kupffer's vesicle decreased volume, abnormal
ZP:0005820	cell Kupffer's vesicle mislocalised, abnormal
ZP:0005821	blood accumulation yolk, abnormal
ZP:0005822	forerunner cell group distributed, abnormal
ZP:0005823	hindbrain molecular quality, abnormal
ZP:0005824	oligodendrocyte hindbrain decreased amount, abnormal
ZP:0005825	gut orientation left-right axis whole organism, abnormal
ZP:0005826	intersegmental artery attached to intersegmental artery, abnormal
ZP:0005827	eye edematous, abnormal
ZP:0005828	orbital region increased accumulation blood, abnormal
ZP:0005829	mitochondrial chromosome whole organism decreased amount, abnormal
ZP:0005830	dorsal-ventral axis head decreased length, abnormal
ZP:0005831	cerebellar central artery hemorrhagic, abnormal
ZP:0005832	cerebellum degenerate, abnormal
ZP:0005833	basihyal bone decreased size, abnormal
ZP:0005834	optic tectum degenerate, abnormal
ZP:0005835	left/right pattern formation occurrence, abnormal
ZP:0005836	motile cilium Kupffer's vesicle decreased length, abnormal
ZP:0005837	motile cilium Kupffer's vesicle decreased amount, abnormal
ZP:0005838	cell Kupffer's vesicle decreased amount, abnormal
ZP:0005839	motile cilium pronephric duct decreased length, abnormal
ZP:0005841	cilium olfactory placode paralysed, abnormal
ZP:0005842	cilium pronephros partially paralysed, abnormal
ZP:0005843	pronephric tubule distended, abnormal
ZP:0005844	motile cilium pronephric duct decreased amount, abnormal
ZP:0005845	axoneme olfactory epithelium swollen, abnormal
ZP:0005847	photoreceptor outer segment photoreceptor cell decreased length, abnormal
ZP:0005848	intraciliary transport particle photoreceptor cell mislocalised, abnormal
ZP:0005849	photoreceptor connecting cilium photoreceptor cell swollen, abnormal
ZP:0005850	photoreceptor outer segment membrane photoreceptor cell disorganized, abnormal
ZP:0005851	photoreceptor outer segment membrane photoreceptor cell vacuolated, abnormal
ZP:0005852	mitotic spindle assembly process quality, abnormal
ZP:0005853	caudal fin increased thickness, abnormal
ZP:0005854	whole organism lacks parts or has fewer parts of type circulating cell blood cell, abnormal
ZP:0005855	hematopoietic system accumulation cell anterior region ball, abnormal
ZP:0005856	erythroblast increased size, abnormal
ZP:0005857	nucleus erythroblast increased size, abnormal
ZP:0005858	blood vessel has fewer parts of type blood cell, abnormal
ZP:0005859	blood vessel lacks parts or has fewer parts of type blood nucleate erythrocyte, abnormal
ZP:0005860	hematopoietic stem cell absent, abnormal
ZP:0005861	nucleate erythrocyte accumulation intermediate cell mass of mesoderm, abnormal
ZP:0005862	nucleate erythrocyte accumulation common cardinal vein, abnormal
ZP:0005863	motor neuron spinal cord disorganized, abnormal
ZP:0005864	brain amorphous, abnormal
ZP:0005865	midbrain hindbrain boundary dorso-ventrally flattened, abnormal
ZP:0005866	paraxial mesoderm formation disrupted, abnormal
ZP:0005867	cell migration involved in mesendoderm migration disrupted, abnormal
ZP:0005868	polster mislocalised posteriorly, abnormal
ZP:0005869	tail bud truncated, abnormal
ZP:0005870	anterior region forebrain aplastic, abnormal
ZP:0005871	paraxial mesoderm increased distance adaxial cell adaxial cell paraxial mesoderm, abnormal
ZP:0005872	segmental plate curved, abnormal
ZP:0005873	anterior region head flattened, abnormal
ZP:0005874	hindbrain neural keel increased width, abnormal
ZP:0005875	midbrain hindbrain boundary neural keel increased width, abnormal
ZP:0005876	glucagon secreting cell decreased amount, abnormal
ZP:0005877	retinal photoreceptor layer aplastic, abnormal
ZP:0005878	photoreceptor outer segment photoreceptor outer segment layer deformed, abnormal
ZP:0005879	photoreceptor outer segment photoreceptor outer segment layer decreased amount, abnormal
ZP:0005880	Muller cell apical-basal polarity, abnormal
ZP:0005881	perikaryon Muller cell mislocalised, abnormal
ZP:0005882	pigmentation abnormal, abnormal
ZP:0005883	embryonic pectoral fin morphogenesis process quality, abnormal
ZP:0005884	otic vesicle morphogenesis process quality, abnormal
ZP:0005885	apical ectodermal ridge pectoral fin bud physical object quality, abnormal
ZP:0005886	intersegmental vessel non-functional, abnormal
ZP:0005887	epibranchial placode decreased size, abnormal
ZP:0005888	axis elongation arrested, abnormal
ZP:0005890	brain vasculature morphology, abnormal
ZP:0005891	brain vasculature dilated, abnormal
ZP:0005892	heart shape, abnormal
ZP:0005896	anterior cerebral vein dilated, abnormal
ZP:0005897	cranial vasculature dilated, abnormal
ZP:0005898	cranial vasculature attachment quality cranial vasculature, abnormal
ZP:0005900	intersegmental vessel increased width, abnormal
ZP:0005901	myocardium decreased thickness, abnormal
ZP:0005905	primordial midbrain channel increased size, abnormal
ZP:0005909	subintestinal vein disorganized, abnormal
ZP:0005911	prosencephalic artery dilated, abnormal
ZP:0005912	mesencephalic vein spatial pattern, abnormal
ZP:0005918	brain vasculature broken, abnormal
ZP:0005919	epithelium brain vasculature decreased thickness, abnormal
ZP:0005920	integument blistered, abnormal
ZP:0005921	endothelial cell morphology, abnormal
ZP:0005922	actin cytoskeleton skeletal muscle cell retracted, abnormal
ZP:0005924	retinal ganglion cell layer hypoplastic, abnormal
ZP:0005925	retinal inner nuclear layer hypoplastic, abnormal
ZP:0005926	retina lacks parts or has fewer parts of type retinal inner plexiform layer, abnormal
ZP:0005927	retina lacks parts or has fewer parts of type retinal outer plexiform layer, abnormal
ZP:0005928	whole organism lacks all parts of type cranial nerve II, abnormal
ZP:0005929	regulation of heart contraction disrupted, abnormal
ZP:0005930	blood accumulation pericardium, abnormal
ZP:0005931	sinus venosus hypoplastic, abnormal
ZP:0005932	myocardium sinus venosus poorly differentiated, abnormal
ZP:0005933	lipid metabolic process process quality, abnormal
ZP:0005934	liver and biliary system morphology, abnormal
ZP:0005935	bile ductule obstructed, abnormal
ZP:0005936	bile ductule aplastic, abnormal
ZP:0005937	bile ductule dilated, abnormal
ZP:0005938	bile ductule lumenized, abnormal
ZP:0005939	bile ductule decreased amount, abnormal
ZP:0005940	intrahepatic bile duct length, abnormal
ZP:0005941	intrahepatic bile duct decreased thickness, abnormal
ZP:0005942	intrahepatic bile duct distributed, abnormal
ZP:0005943	granular layer corpus cerebelli decreased size, abnormal
ZP:0005944	molecular layer corpus cerebelli decreased size, abnormal
ZP:0005945	granular layer valvula cerebelli decreased size, abnormal
ZP:0005946	molecular layer valvula cerebelli decreased size, abnormal
ZP:0005947	motile cilium Kupffer's vesicle movement quality, abnormal
ZP:0005948	cilium olfactory pit decreased length, abnormal
ZP:0005949	cilium macula decreased length, abnormal
ZP:0005951	chondrocyte pharyngeal arch cartilage decreased amount, abnormal
ZP:0005952	cilium anterior lateral line neuromast decreased length, abnormal
ZP:0005953	photoreceptor outer segment eye photoreceptor cell decreased amount, abnormal
ZP:0005954	collateral sprouting decreased process quality, abnormal
ZP:0005955	neuron spinal cord degenerate, abnormal
ZP:0005956	axon collateral primary motor neuron decreased branchiness, abnormal
ZP:0005957	calcium ion import increased rate, abnormal
ZP:0005958	peroxisome yolk decreased amount, abnormal
ZP:0005959	peroxisome pronephric duct decreased amount, abnormal
ZP:0005960	peroxisome hepatocyte decreased amount, abnormal
ZP:0005962	homologous chromosome pairing at meiosis disrupted, abnormal
ZP:0005963	male meiosis I disrupted, abnormal
ZP:0005964	meiotic metaphase I plate congression disrupted, abnormal
ZP:0005965	chiasma assembly disrupted, abnormal
ZP:0005966	male organism male sterile, abnormal
ZP:0005967	male organism triploid, abnormal
ZP:0005968	male organism decreased male fertility, abnormal
ZP:0005969	female organism lethal (sensu genetics), abnormal
ZP:0005970	female organism aneuploid, abnormal
ZP:0005971	testis increased weight, abnormal
ZP:0005972	testis apoptotic, abnormal
ZP:0005973	whole organism increased size, abnormal
ZP:0005974	whole organism brood viability, abnormal
ZP:0005975	spermatocyte increased amount, abnormal
ZP:0005976	spermatocyte decreased amount, abnormal
ZP:0005977	recombination nodule spermatocyte absent, abnormal
ZP:0005978	sperm absent, abnormal
ZP:0005979	spermatogonium increased amount, abnormal
ZP:0005980	eye morphogenesis process quality, abnormal
ZP:0005982	germ cell migration cellular spatiotemporal quality, abnormal
ZP:0005983	rod bipolar cell disorganized, abnormal
ZP:0005984	cone retinal bipolar cell disorganized, abnormal
ZP:0005985	response to light intensity decreased occurrence, abnormal
ZP:0005986	pigmentation decreased intensity, abnormal
ZP:0005987	keratinocyte epidermis morphology, abnormal
ZP:0005988	neuromast action potential, abnormal
ZP:0005989	neuromast non-functional, abnormal
ZP:0005990	neuromast hair cell mislocalised, abnormal
ZP:0005991	positive phototaxis decreased occurrence, abnormal
ZP:0005992	obsolete cell retinal inner nuclear layer decreased amount, abnormal
ZP:0005993	retinal photoreceptor layer morphology, abnormal
ZP:0005994	retina has fewer parts of type retinal cone cell, abnormal
ZP:0005995	photoreceptor cell retina degenerate, abnormal
ZP:0005996	retinal outer plexiform layer irregular thickness, abnormal
ZP:0005997	retinal outer plexiform layer has fewer parts of type synapse neuron, abnormal
ZP:0005998	photoreceptor outer segment eye photoreceptor cell morphology, abnormal
ZP:0005999	UV sensitive photoreceptor cell decreased amount, abnormal
ZP:0006000	blue sensitive photoreceptor cell decreased amount, abnormal
ZP:0006001	green sensitive photoreceptor cell decreased amount, abnormal
ZP:0006002	red sensitive photoreceptor cell decreased amount, abnormal
ZP:0006003	retinal cone cell degenerate, abnormal
ZP:0006004	retinal rod cell degenerate, abnormal
ZP:0006005	photoreceptor outer segment retinal rod cell morphology, abnormal
ZP:0006006	Muller cell morphology, abnormal
ZP:0006007	nucleus retinal bipolar neuron displaced, abnormal
ZP:0006008	axon retinal bipolar neuron displaced, abnormal
ZP:0006009	ON-bipolar cell morphology, abnormal
ZP:0006010	axon ON-bipolar cell increased amount, abnormal
ZP:0006011	axon ON-bipolar cell increased length, abnormal
ZP:0006012	ON-bipolar cell located in axon retinal ganglion cell layer, abnormal
ZP:0006013	dendrite ON-bipolar cell increased amount, abnormal
ZP:0006014	dendrite ON-bipolar cell increased length, abnormal
ZP:0006015	ON-bipolar cell located in dendrite retinal outer nuclear layer, abnormal
ZP:0006016	epidermis atrophied, abnormal
ZP:0006017	locomotor rhythm decreased process quality, abnormal
ZP:0006018	epiphysis decreased magnitude circadian regulation of gene expression, abnormal
ZP:0006019	cell lens apoptotic, abnormal
ZP:0006020	trunk curved lateral, abnormal
ZP:0006021	erythrocyte development disrupted, abnormal
ZP:0006022	heart primordium position, abnormal
ZP:0006023	erythroblast intermediate cell mass of mesoderm increased amount, abnormal
ZP:0006024	forebrain aplastic, abnormal
ZP:0006025	digestive system position, abnormal
ZP:0006026	optic tectum aplastic, abnormal
ZP:0006027	optic primordium decreased size, abnormal
ZP:0006028	ribosome whole organism decreased amount, abnormal
ZP:0006029	pharyngeal arch 3-7 immature, abnormal
ZP:0006030	nucleate erythrocyte apoptotic, abnormal
ZP:0006031	anterior region whole organism necrotic, abnormal
ZP:0006032	hemoglobin complex blood cell decreased amount, abnormal
ZP:0006034	blood vessel endothelial cell posterior cardinal vein decreased amount, abnormal
ZP:0006035	blood vasculature head decreased amount, abnormal
ZP:0006036	angioblastic mesenchymal cell mislocalised, abnormal
ZP:0006037	angioblastic mesenchymal cell apoptotic, abnormal
ZP:0006038	angioblastic mesenchymal cell decreased amount, abnormal
ZP:0006039	erythrocyte differentiation delayed, abnormal
ZP:0006040	endocrine pancreas disorganized, abnormal
ZP:0006041	heart looping decreased process quality, abnormal
ZP:0006042	cardioblast cell fate specification decreased process quality, abnormal
ZP:0006043	atrial cardiac muscle cell differentiation decreased occurrence, abnormal
ZP:0006044	ventricular cardiac muscle cell differentiation decreased occurrence, abnormal
ZP:0006045	heart contraction decreased frequency, abnormal
ZP:0006046	cardiac ventricle decreased length, abnormal
ZP:0006047	cardiac ventricle has fewer parts of type cardiac muscle cell, abnormal
ZP:0006048	heart has fewer parts of type cardiac muscle cell, abnormal
ZP:0006049	atrium decreased length, abnormal
ZP:0006050	atrium has fewer parts of type cardiac muscle cell, abnormal
ZP:0006051	whole organism lacks all parts of type blood, abnormal
ZP:0006052	cranial cartilage decreased object quality, abnormal
ZP:0006053	posterior lateral plate mesoderm physical object quality, abnormal
ZP:0006055	cell cycle process temporally extended, abnormal
ZP:0006056	neuron maturation delayed, abnormal
ZP:0006057	retinal cone cell differentiation disrupted, abnormal
ZP:0006058	retinal rod cell differentiation disrupted, abnormal
ZP:0006059	retinal outer plexiform layer structure, abnormal
ZP:0006060	horizontal cell immature, abnormal
ZP:0006061	retinal bipolar neuron immature, abnormal
ZP:0006062	presumptive atrium heart tube increased size, abnormal
ZP:0006063	presumptive cardiac ventricle heart tube decreased size, abnormal
ZP:0006064	branching involved in blood vessel morphogenesis disrupted, abnormal
ZP:0006065	sprouting angiogenesis premature, abnormal
ZP:0006066	intersegmental artery increased branchiness, abnormal
ZP:0006067	axial vasculature has extra parts of type intersegmental vessel, abnormal
ZP:0006068	intersegmental vessel spatial pattern, abnormal
ZP:0006069	ocular blood vessel structure, abnormal
ZP:0006070	ocular blood vessel increased amount, abnormal
ZP:0006071	ocular blood vessel kinked, abnormal
ZP:0006072	myelination in peripheral nervous system decreased occurrence, abnormal
ZP:0006073	myelination of anterior lateral line nerve axons decreased occurrence, abnormal
ZP:0006074	neuromast increased amount, abnormal
ZP:0006075	neuromast trunk increased amount, abnormal
ZP:0006076	inner dynein arm olfactory placode absent, abnormal
ZP:0006077	outer dynein arm olfactory placode absent, abnormal
ZP:0006078	cilium spinal cord decreased length, abnormal
ZP:0006079	pronephros distended, abnormal
ZP:0006080	pronephros lacks parts or has fewer parts of type microvillus epithelial cell, abnormal
ZP:0006081	brush border pronephros absent, abnormal
ZP:0006082	inner dynein arm pronephros absent, abnormal
ZP:0006083	outer dynein arm pronephros absent, abnormal
ZP:0006084	parapineal organ right side of whole organism, abnormal
ZP:0006085	pronephric glomerulus decreased thickness, abnormal
ZP:0006086	basibranchial absent, abnormal
ZP:0006087	opercular flap absent, abnormal
ZP:0006088	dorsal region neural tube necrotic, abnormal
ZP:0006089	ventral mandibular arch absent, abnormal
ZP:0006090	mesenchyme condensation cell pharyngeal arch decreased amount, abnormal
ZP:0006091	palatoquadrate cartilage absent, abnormal
ZP:0006092	hyosymplectic cartilage absent, abnormal
ZP:0006093	basihyal cartilage absent, abnormal
ZP:0006094	xanthoblast decreased amount, abnormal
ZP:0006095	oculomotor nerve formation decreased process quality, abnormal
ZP:0006096	axon cranial nerve III mislocalised, abnormal
ZP:0006097	cranial nerve III process quality axon extension, abnormal
ZP:0006098	smoothened signaling pathway process quality, abnormal
ZP:0006099	adaxial cell physical object quality, abnormal
ZP:0006100	cilium pronephric duct absent, abnormal
ZP:0006101	cilium pronephric duct deformed, abnormal
ZP:0006102	photoreceptor outer segment layer retina absent, abnormal
ZP:0006103	cilium neuromast absent, abnormal
ZP:0006104	heart tube mislocalised, abnormal
ZP:0006105	renal glomerulus kidney cystic, abnormal
ZP:0006106	nucleus retinal outer nuclear layer decreased amount, abnormal
ZP:0006107	cilium multi-ciliated epithelial cell absent, abnormal
ZP:0006108	renal duct increased size, abnormal
ZP:0006109	Muller cell absent, abnormal
ZP:0006110	yolk physical object quality, abnormal
ZP:0006111	zymogen granule pancreas decreased amount, abnormal
ZP:0006112	intrahepatic bile duct increased width, abnormal
ZP:0006113	intrahepatic bile duct sparse, abnormal
ZP:0006114	intrahepatic bile duct separated from intrahepatic bile duct, abnormal
ZP:0006115	intrahepatic bile duct increased accumulation vesicle intrahepatic bile duct, abnormal
ZP:0006116	cytoplasm intrahepatic bile duct composition, abnormal
ZP:0006117	smooth endoplasmic reticulum intrahepatic bile duct dilated, abnormal
ZP:0006118	Golgi apparatus enterocyte dilated, abnormal
ZP:0006119	mesendoderm development disrupted, abnormal
ZP:0006121	DNA methylation decreased occurrence, abnormal
ZP:0006122	DNA methylation on cytosine within a CG sequence decreased occurrence, abnormal
ZP:0006123	lens capsule absent, abnormal
ZP:0006124	yolk accumulation blood, abnormal
ZP:0006125	parachordal vessel aplastic, abnormal
ZP:0006126	atrial ventricular junction remodeling disrupted, abnormal
ZP:0006127	developmental growth involved in morphogenesis disrupted, abnormal
ZP:0006128	heart tube condensed, abnormal
ZP:0006129	P granule primordial germ cell size, abnormal
ZP:0006130	myofibril muscle decreased diameter, abnormal
ZP:0006131	alpha-tubulin acetylation disrupted, abnormal
ZP:0006132	granuloma formation decreased occurrence, abnormal
ZP:0006133	cell retinal ganglion cell layer decreased amount, abnormal
ZP:0006136	cell retinal outer nuclear layer decreased amount, abnormal
ZP:0006140	midbrain hindbrain boundary poorly differentiated, abnormal
ZP:0006141	epidermis development disrupted, abnormal
ZP:0006142	neutrophil chemotaxis increased rate, abnormal
ZP:0006144	median fin fold morphology, abnormal
ZP:0006145	median fin fold decreased thickness, abnormal
ZP:0006146	median fin fold degenerate, abnormal
ZP:0006147	epidermis increased thickness, abnormal
ZP:0006148	epidermis disorganized, abnormal
ZP:0006149	chorion accumulation keratinocyte, abnormal
ZP:0006150	olfactory epithelium morphology, abnormal
ZP:0006151	keratinocyte epidermal basal stratum aggregated, abnormal
ZP:0006152	keratinocyte mislocalised, abnormal
ZP:0006153	keratinocyte disorganized, abnormal
ZP:0006154	leukocyte aggregated, abnormal
ZP:0006155	neutrophil increased amount, abnormal
ZP:0006156	visual behavior decreased rate, abnormal
ZP:0006157	melanocyte differentiation process quality, abnormal
ZP:0006158	phototaxis arrested, abnormal
ZP:0006159	detection of light stimulus involved in visual perception process quality, abnormal
ZP:0006160	cholinergic neuron retinal neural layer decreased amount, abnormal
ZP:0006161	retinal inner nuclear layer perforate, abnormal
ZP:0006162	melanocyte increased area, abnormal
ZP:0006163	heart contraction occurrence, abnormal
ZP:0006164	cardiac muscle contraction arrested, abnormal
ZP:0006165	posterior lateral line neuromast deposition disrupted, abnormal
ZP:0006166	integument tail bud aggregated, abnormal
ZP:0006167	yolk protruding out of whole organism, abnormal
ZP:0006168	ruffle EVL absent, abnormal
ZP:0006169	keratinocyte aggregated, abnormal
ZP:0006170	detection of visible light disrupted, abnormal
ZP:0006171	photoreceptor outer segment photoreceptor outer segment layer absent, abnormal
ZP:0006172	photoreceptor outer segment retinal cone cell absent, abnormal
ZP:0006173	double-strand break repair via homologous recombination decreased frequency, abnormal
ZP:0006174	somitomeric trunk muscle development disrupted, abnormal
ZP:0006175	skeletal muscle cell proliferation increased rate, abnormal
ZP:0006176	striated muscle cell differentiation disrupted, abnormal
ZP:0006177	somite decreased occurrence cell population proliferation, abnormal
ZP:0006178	fast muscle cell somite disorganized, abnormal
ZP:0006179	medial rectus aplastic, abnormal
ZP:0006180	cephalic musculature decreased process quality skeletal muscle tissue development, abnormal
ZP:0006181	ventral rectus aplastic, abnormal
ZP:0006182	trunk musculature refractivity, abnormal
ZP:0006183	sternohyoid aplastic, abnormal
ZP:0006184	fast muscle cell shape, abnormal
ZP:0006185	myofibril fast muscle cell position, abnormal
ZP:0006186	melanocyte stimulating hormone secreting cell absent, abnormal
ZP:0006187	melanocyte stimulating hormone secreting cell decreased amount, abnormal
ZP:0006188	adrenocorticotropic hormone secreting cell absent, abnormal
ZP:0006189	neuron differentiation premature, abnormal
ZP:0006190	hindbrain physical object quality, abnormal
ZP:0006191	dorsal region diencephalon physical object quality, abnormal
ZP:0006192	midbrain physical object quality, abnormal
ZP:0006193	T cell thymus absent, abnormal
ZP:0006194	trunk altered number of intersegmental vessel, abnormal
ZP:0006195	cytoplasmic microtubule organization process quality, abnormal
ZP:0006196	filopodium assembly process quality, abnormal
ZP:0006197	axon extension decreased occurrence, abnormal
ZP:0006198	microtubule severing decreased occurrence, abnormal
ZP:0006199	Meckel's cartilage fused with ventral region dorsal region palatoquadrate cartilage, abnormal
ZP:0006200	hyosymplectic cartilage fused with dorsal region ventral region ceratohyal cartilage, abnormal
ZP:0006201	interhyal cartilage aplastic, abnormal
ZP:0006202	whole organism lacks parts or has fewer parts of type cartilage element, abnormal
ZP:0006203	whole organism lacks parts or has fewer parts of type pharyngeal arch 3-7, abnormal
ZP:0006204	myofibril trunk musculature decreased size, abnormal
ZP:0006205	anterior-posterior axis whole organism decreased thickness, abnormal
ZP:0006206	eye colorless, abnormal
ZP:0006207	pharyngeal arch cartilage deformed, abnormal
ZP:0006208	myofibril muscle cell decreased amount, abnormal
ZP:0006209	axon primary motor neuron decreased length, abnormal
ZP:0006210	neuron projection primary motor neuron decreased amount, abnormal
ZP:0006211	branching involved in blood vessel morphogenesis process quality, abnormal
ZP:0006212	central nervous system myelination occurrence, abnormal
ZP:0006213	oligodendrocyte progenitor proliferation disrupted, abnormal
ZP:0006214	cardiac ventricle collapsed, abnormal
ZP:0006215	sinus venosus collapsed, abnormal
ZP:0006216	bulbus arteriosus collapsed, abnormal
ZP:0006217	melanocyte head decreased amount, abnormal
ZP:0006218	xanthophore head decreased amount, abnormal
ZP:0006219	melanoblast head decreased amount, abnormal
ZP:0006220	xanthophore trunk decreased amount, abnormal
ZP:0006221	melanoblast trunk decreased amount, abnormal
ZP:0006222	oligodendrocyte morphology, abnormal
ZP:0006223	glial cell (sensu Vertebrata) absent, abnormal
ZP:0006224	establishment of endothelial barrier disrupted, abnormal
ZP:0006225	tectal ventricle decreased volume, abnormal
ZP:0006226	ventricular system lumenized, abnormal
ZP:0006227	hyaloid vessel broken, abnormal
ZP:0006228	bicellular tight junction neuroepithelial cell increased permeability, abnormal
ZP:0006229	centrosome pronephric duct decreased amount, abnormal
ZP:0006230	locomotion involved in locomotory behavior arrested, abnormal
ZP:0006231	axon hindbrain decreased amount, abnormal
ZP:0006232	axon eye decreased amount, abnormal
ZP:0006233	axon forebrain decreased amount, abnormal
ZP:0006234	axon midbrain decreased amount, abnormal
ZP:0006235	third ventricle decreased size, abnormal
ZP:0006236	telencephalic ventricle decreased size, abnormal
ZP:0006242	myofibril muscle disorganized, abnormal
ZP:0006245	long-chain fatty acid metabolic process disrupted, abnormal
ZP:0006246	hepaticobiliary system process disrupted, abnormal
ZP:0006247	gall bladder disrupted lipid storage, abnormal
ZP:0006248	bile canaliculus spheroid, abnormal
ZP:0006249	bile canaliculus decreased branchiness, abnormal
ZP:0006250	bile ductule sparse, abnormal
ZP:0006251	rough endoplasmic reticulum hepatocyte increased amount, abnormal
ZP:0006252	response to bacterium disrupted, abnormal
ZP:0006253	response to bacterium increased process quality, abnormal
ZP:0006254	photoreceptor cell development disrupted, abnormal
ZP:0006255	lens position, abnormal
ZP:0006256	cell lens disorganized, abnormal
ZP:0006257	cell lens poorly differentiated, abnormal
ZP:0006258	liver spheroid, abnormal
ZP:0006259	liver increased pigmentation, abnormal
ZP:0006260	blood vessel liver morphology, abnormal
ZP:0006261	retinal photoreceptor layer lacks parts or has fewer parts of type retinal cone cell, abnormal
ZP:0006262	retinal photoreceptor layer lacks all parts of type retinal cone cell, abnormal
ZP:0006263	retinal photoreceptor layer lacks all parts of type retinal rod cell, abnormal
ZP:0006264	retinal photoreceptor layer has fewer parts of type retinal rod cell, abnormal
ZP:0006265	eye photoreceptor cell retinal photoreceptor layer disorganized, abnormal
ZP:0006266	eye photoreceptor cell retinal photoreceptor layer immature, abnormal
ZP:0006267	retinal cone cell retinal photoreceptor layer disorganized, abnormal
ZP:0006268	retinal rod cell retinal photoreceptor layer disorganized, abnormal
ZP:0006269	retina lacks all parts of type photoreceptor outer segment layer, abnormal
ZP:0006270	cranium increased width, abnormal
ZP:0006271	cranium shortened, abnormal
ZP:0006272	whole organism buoyancy, abnormal
ZP:0006273	trunk swollen, abnormal
ZP:0006274	ciliary marginal zone hyperplastic, abnormal
ZP:0006275	goblet cell mid intestine decreased amount, abnormal
ZP:0006276	lens epithelium disorganized, abnormal
ZP:0006277	columnar/cuboidal epithelial cell lens epithelium morphology, abnormal
ZP:0006278	columnar/cuboidal epithelial cell lens epithelium shape, abnormal
ZP:0006279	columnar/cuboidal epithelial cell lens epithelium disorganized, abnormal
ZP:0006280	intestine decreased volume, abnormal
ZP:0006281	mucus layer intestine decreased thickness, abnormal
ZP:0006282	leukocyte intestine increased amount, abnormal
ZP:0006283	hepatic sinusoid decreased size, abnormal
ZP:0006284	intestinal villus damage, abnormal
ZP:0006285	endoplasmic reticulum lumen pancreatic acinar cell distended, abnormal
ZP:0006286	goblet cell increased amount, abnormal
ZP:0006287	goblet cell mislocalised, abnormal
ZP:0006288	goblet cell disorganized, abnormal
ZP:0006289	goblet cell detached from intestinal epithelium, abnormal
ZP:0006290	condensed nuclear chromosome goblet cell increased amount, abnormal
ZP:0006291	cytoskeleton goblet cell disorganized, abnormal
ZP:0006292	exocytic vesicle goblet cell morphology, abnormal
ZP:0006293	autophagosome enteroendocrine cell increased amount, abnormal
ZP:0006294	hepatocyte necrotic, abnormal
ZP:0006295	hepatocyte vacuolated, abnormal
ZP:0006296	hepatocyte fatty, abnormal
ZP:0006297	nucleus hepatocyte mislocalised, abnormal
ZP:0006298	mitochondrion hepatocyte morphology, abnormal
ZP:0006299	endoplasmic reticulum lumen hepatocyte vacuolated, abnormal
ZP:0006300	endoplasmic reticulum lumen hepatocyte swollen, abnormal
ZP:0006302	intestinal epithelial cell shape, abnormal
ZP:0006303	intestinal epithelial cell apoptotic, abnormal
ZP:0006304	intestinal epithelial cell disorganized, abnormal
ZP:0006305	intestinal epithelial cell detached from intestinal epithelium, abnormal
ZP:0006306	intestinal epithelial cell increased process quality autophagy of mitochondrion, abnormal
ZP:0006307	cytoplasm intestinal epithelial cell immature, abnormal
ZP:0006308	mitochondrion intestinal epithelial cell morphology, abnormal
ZP:0006309	mitochondrion intestinal epithelial cell decreased amount, abnormal
ZP:0006310	autophagosome intestinal epithelial cell increased amount, abnormal
ZP:0006311	endoplasmic reticulum intestinal epithelial cell distended, abnormal
ZP:0006312	endoplasmic reticulum lumen intestinal epithelial cell vacuolated, abnormal
ZP:0006313	endoplasmic reticulum lumen intestinal epithelial cell distended, abnormal
ZP:0006314	Golgi apparatus intestinal epithelial cell distended, abnormal
ZP:0006315	brush border intestinal epithelial cell morphology, abnormal
ZP:0006316	brush border intestinal epithelial cell decreased thickness, abnormal
ZP:0006317	brush border intestinal epithelial cell atrophied, abnormal
ZP:0006318	intestinal epithelial cell increased occurrence autophagy, abnormal
ZP:0006319	intestinal epithelial cell decreased process quality cell population proliferation, abnormal
ZP:0006320	cortical actin cytoskeleton intestinal epithelial cell decreased thickness, abnormal
ZP:0006321	vesicle intestinal epithelial cell increased amount, abnormal
ZP:0006322	vesicle intestinal epithelial cell increased size, abnormal
ZP:0006323	intestinal epithelial cell increased process quality positive regulation of autophagy in response to ER overload, abnormal
ZP:0006324	caudal vein plexus edematous, abnormal
ZP:0006325	axis specification arrested, abnormal
ZP:0006326	spinal cord decreased width, abnormal
ZP:0006327	caudal fin multiple, abnormal
ZP:0006328	neural tube distended, abnormal
ZP:0006329	sodium ion transport decreased process quality, abnormal
ZP:0006330	ammonium transport decreased process quality, abnormal
ZP:0006331	cell cycle process arrested, abnormal
ZP:0006332	endoplasmic reticulum unfolded protein response increased occurrence, abnormal
ZP:0006333	photoreceptor cell differentiation disrupted, abnormal
ZP:0006334	extracellular matrix constituent secretion disrupted, abnormal
ZP:0006335	cell eye apoptotic, abnormal
ZP:0006336	fin kinked, abnormal
ZP:0006338	retinal photoreceptor layer absent, abnormal
ZP:0006340	neuroepithelial cell retinal pigmented epithelium disorganized, abnormal
ZP:0006341	pronephric duct decreased thickness, abnormal
ZP:0006342	nucleus retina condensed, abnormal
ZP:0006343	endoplasmic reticulum intestinal epithelium dilated, abnormal
ZP:0006344	endoplasmic reticulum intestinal epithelium distended, abnormal
ZP:0006345	cell junction intestinal epithelium loose, abnormal
ZP:0006346	intestinal villus decreased length, abnormal
ZP:0006347	intestinal villus disorganized, abnormal
ZP:0006348	intestinal villus decreased amount, abnormal
ZP:0006349	Bruch's membrane aplastic, abnormal
ZP:0006350	chondrocyte deformed, abnormal
ZP:0006351	chondrocyte increased accumulation vacuole cytoplasm chondrocyte, abnormal
ZP:0006352	extracellular matrix chondrocyte decreased mass density, abnormal
ZP:0006353	endoplasmic reticulum hepatocyte morphology, abnormal
ZP:0006354	endoplasmic reticulum hepatocyte vacuolated, abnormal
ZP:0006355	endoplasmic reticulum eye photoreceptor cell dilated, abnormal
ZP:0006356	retinal rod cell aplastic, abnormal
ZP:0006357	Muller cell disoriented, abnormal
ZP:0006358	swimming decreased speed, abnormal
ZP:0006359	brain decreased volume, abnormal
ZP:0006360	brain has fewer parts of type cell, abnormal
ZP:0006361	dopaminergic neuron diencephalon spatial pattern, abnormal
ZP:0006362	positive regulation of gene expression disrupted, abnormal
ZP:0006363	heart deformed, abnormal
ZP:0006364	axon extension involved in axon guidance decreased process quality, abnormal
ZP:0006365	axon CaP motoneuron increased branchiness, abnormal
ZP:0006366	nuclear division disrupted, abnormal
ZP:0006367	mitotic spindle organization disrupted, abnormal
ZP:0006368	centriole replication disrupted, abnormal
ZP:0006369	embryonic cleavage disrupted, abnormal
ZP:0006370	centrosome duplication disrupted, abnormal
ZP:0006371	yolk syncytial layer increased size, abnormal
ZP:0006372	blastomere size, abnormal
ZP:0006373	blastomere decreased amount, abnormal
ZP:0006374	nucleus blastomere increased size, abnormal
ZP:0006375	centrosome blastomere decreased amount, abnormal
ZP:0006376	whole organism tetraploid, abnormal
ZP:0006377	chromosome whole organism increased amount, abnormal
ZP:0006378	centriole sperm composition, abnormal
ZP:0006379	photoreceptor cell morphogenesis disrupted, abnormal
ZP:0006380	photoreceptor cell outer segment organization disrupted, abnormal
ZP:0006381	retinal cone cell development disrupted, abnormal
ZP:0006382	determination of heart left/right asymmetry process quality, abnormal
ZP:0006383	retinal ganglion cell layer absent, abnormal
ZP:0006384	midbrain hindbrain boundary blurry, abnormal
ZP:0006385	extension decreased width, abnormal
ZP:0006386	eye opaque, abnormal
ZP:0006387	retinal inner nuclear layer absent, abnormal
ZP:0006388	lateral mesoderm bilateral symmetry, abnormal
ZP:0006389	retinal outer nuclear layer absent, abnormal
ZP:0006390	photoreceptor outer segment retinal rod cell absent, abnormal
ZP:0006391	cranium quality, abnormal
ZP:0006392	prechordal plate malformed, abnormal
ZP:0006393	neural plate malformed, abnormal
ZP:0006394	eye development process quality, abnormal
ZP:0006395	somitogenesis process quality, abnormal
ZP:0006396	extension disorganized, abnormal
ZP:0006397	forebrain bulbous, abnormal
ZP:0006398	palate malformed, abnormal
ZP:0006399	somite cuboid, abnormal
ZP:0006400	intersegmental vessel branchiness, abnormal
ZP:0006401	cranial neural crest pharyngeal arch mislocalised, abnormal
ZP:0006402	neurocranial trabecula decreased length, abnormal
ZP:0006403	parachordal cartilage morphology, abnormal
ZP:0006404	cranial cartilage decreased size, abnormal
ZP:0006405	cranial ganglion decreased size, abnormal
ZP:0006406	cranial neural crest cell rhombomere 6 decreased amount, abnormal
ZP:0006407	fourth ventricle edematous, abnormal
ZP:0006408	olfactory pit decreased size, abnormal
ZP:0006409	mouth malformed, abnormal
ZP:0006410	oral cavity mislocalised posteriorly, abnormal
ZP:0006411	trigeminal motor nucleus fused with trigeminal motor nucleus, abnormal
ZP:0006412	neural tube closure disrupted, abnormal
ZP:0006413	protein localization to centrosome disrupted, abnormal
ZP:0006414	cranial ganglion irregular spatial pattern, abnormal
ZP:0006415	myoblast fusion decreased occurrence, abnormal
ZP:0006416	fast muscle cell circular, abnormal
ZP:0006417	pancreatic bud morphology, abnormal
ZP:0006419	hypobranchial bone aplastic, abnormal
ZP:0006420	ceratobranchial bone increased width, abnormal
ZP:0006421	ceratohyal bone morphology, abnormal
ZP:0006422	ceratohyal bone shape, abnormal
ZP:0006423	symplectic decreased length, abnormal
ZP:0006424	pharyngeal arch 2 skeleton decreased length, abnormal
ZP:0006425	pharyngeal arch 2 skeleton increased width, abnormal
ZP:0006426	pharyngeal arch 2 skeleton bifurcated, abnormal
ZP:0006427	hyosymplectic cartilage shape, abnormal
ZP:0006428	interhyal cartilage shape, abnormal
ZP:0006429	hypobranchial cartilage decreased size, abnormal
ZP:0006430	hypobranchial 1 cartilage aplastic, abnormal
ZP:0006431	hypobranchial 2 cartilage aplastic, abnormal
ZP:0006441	sensory neuron spinal cord decreased amount, abnormal
ZP:0006442	glial cell proliferation decreased process quality, abnormal
ZP:0006443	retinal rod cell development decreased process quality, abnormal
ZP:0006444	retinal neural layer has fewer parts of type retinal rod cell, abnormal
ZP:0006445	eye lacks all parts of type lens, abnormal
ZP:0006448	establishment of anatomical structure orientation disrupted, abnormal
ZP:0006449	embryonic morphogenesis disrupted, abnormal
ZP:0006450	liver cystic, abnormal
ZP:0006451	endoplasmic reticulum liver disoriented, abnormal
ZP:0006452	endoplasmic reticulum liver swollen, abnormal
ZP:0006453	whole organism curved lateral, abnormal
ZP:0006454	trunk malformed, abnormal
ZP:0006455	endoderm aplastic, abnormal
ZP:0006456	cilium Kupffer's vesicle increased amount, abnormal
ZP:0006457	cilium macula saccule decreased length, abnormal
ZP:0006458	cilium macula saccule decreased amount, abnormal
ZP:0006459	cell macula saccule decreased amount, abnormal
ZP:0006460	spinal cord interneuron morphology, abnormal
ZP:0006461	skeletal muscle decreased functionality, abnormal
ZP:0006462	motor neuron absent, abnormal
ZP:0006463	central nervous system degeneration, abnormal
ZP:0006464	retinal pigmented epithelium distance retinal outer nuclear layer, abnormal
ZP:0006465	photoreceptor outer segment retinal cone cell decreased amount, abnormal
ZP:0006466	protein phosphorylation disrupted, abnormal
ZP:0006467	chordate embryonic development disrupted, abnormal
ZP:0006468	heart decreased thickness, abnormal
ZP:0006469	notochord formation process quality, abnormal
ZP:0006470	notochord cell differentiation process quality, abnormal
ZP:0006471	notochord coiled, abnormal
ZP:0006472	vacuole notochord increased amount, abnormal
ZP:0006473	hindbrain decreased length, abnormal
ZP:0006474	whole organism wholly posterioralized, abnormal
ZP:0006475	anterior/posterior pattern specification process quality, abnormal
ZP:0006476	pelvic fin mislocalised posteriorly, abnormal
ZP:0006477	exocrine pancreas increased size, abnormal
ZP:0006478	optic nerve development delayed, abnormal
ZP:0006479	positive phototaxis decreased frequency, abnormal
ZP:0006480	retinal ganglion cell retina decreased amount, abnormal
ZP:0006481	axon retinal ganglion cell morphology, abnormal
ZP:0006482	dorsal aorta obstructed, abnormal
ZP:0006483	dorsal aorta mislocalised dorsally, abnormal
ZP:0006484	blood vessel endothelial cell dorsal aorta positional polarity, abnormal
ZP:0006485	posterior cardinal vein duplicated, abnormal
ZP:0006486	posterior cardinal vein deformed, abnormal
ZP:0006487	posterior cardinal vein mislocalised dorsally, abnormal
ZP:0006488	blood vessel endothelial cell posterior cardinal vein structure, abnormal
ZP:0006489	axial vasculature decreased area, abnormal
ZP:0006490	ventral wall of dorsal aorta deformed, abnormal
ZP:0006491	bicellular tight junction blood vessel endothelial cell increased amount, abnormal
ZP:0006492	bicellular tight junction blood vessel endothelial cell mislocalised, abnormal
ZP:0006493	detection of mechanical stimulus involved in sensory perception of sound process quality, abnormal
ZP:0006494	vestibular reflex absent, abnormal
ZP:0006495	stereocilium bundle auditory receptor cell splayed, abnormal
ZP:0006496	afferent neuron has extra parts of type neuron projection afferent neuron, abnormal
ZP:0006497	afferent neuron process quality neuron projection development, abnormal
ZP:0006498	neuron projection afferent neuron complexity, abnormal
ZP:0006499	neuron projection afferent neuron transient, abnormal
ZP:0006500	blood vessel development process quality, abnormal
ZP:0006501	blood vessel morphogenesis process quality, abnormal
ZP:0006502	cilium assembly disrupted, abnormal
ZP:0006503	cell brain morphology, abnormal
ZP:0006504	floor plate patchy, abnormal
ZP:0006506	motile cilium floor plate decreased amount, abnormal
ZP:0006507	lens increased amount, abnormal
ZP:0006508	motile cilium otic vesicle absent, abnormal
ZP:0006509	somite hemorrhagic, abnormal
ZP:0006510	ventral mesenchyme physical object quality, abnormal
ZP:0006511	central canal decreased size, abnormal
ZP:0006512	lateral dorsal aorta decreased diameter, abnormal
ZP:0006513	posterior region myoseptum morphology, abnormal
ZP:0006514	axoneme whole organism absent, abnormal
ZP:0006518	adenohypophysis aplastic, abnormal
ZP:0006519	trabecula cranii morphology, abnormal
ZP:0006520	otolith deformed, abnormal
ZP:0006521	pharyngeal vasculature hemorrhagic, abnormal
ZP:0006522	kinocilium auditory receptor cell absent, abnormal
ZP:0006523	thoracic duct decreased length, abnormal
ZP:0006524	TOR signaling disrupted, abnormal
ZP:0006525	photoreceptor outer segment retina decreased length, abnormal
ZP:0006526	photoreceptor outer segment eye photoreceptor cell disheveled, abnormal
ZP:0006527	vesicle membrane eye photoreceptor cell present, abnormal
ZP:0006529	gall bladder quality, abnormal
ZP:0006530	heart primordium increased size, abnormal
ZP:0006531	tail bud deformed, abnormal
ZP:0006532	yolk protruding, abnormal
ZP:0006533	epidermis separated from muscle, abnormal
ZP:0006534	immature eye decreased size, abnormal
ZP:0006535	muscle malformed, abnormal
ZP:0006536	epidermal cell permeable, abnormal
ZP:0006537	epidermal cell separated from epidermal cell, abnormal
ZP:0006538	bicellular tight junction epidermal cell decreased length, abnormal
ZP:0006539	ossification decreased process quality, abnormal
ZP:0006540	bone mineralization decreased process quality, abnormal
ZP:0006541	integument ball physical object quality, abnormal
ZP:0006542	integument extension physical object quality, abnormal
ZP:0006543	postcranial axial skeleton cartilaginous, abnormal
ZP:0006544	integument gill physical object quality, abnormal
ZP:0006545	corpuscles of Stannius cellular quality, abnormal
ZP:0006546	convergent extension involved in organogenesis disrupted, abnormal
ZP:0006550	whole organism decreased width, abnormal
ZP:0006551	regulation of transcription, DNA-templated disrupted, abnormal
ZP:0006552	regulation of glucose metabolic process disrupted, abnormal
ZP:0006553	midbrain-hindbrain boundary structural organization disrupted, abnormal
ZP:0006554	nucleate erythrocyte maturation disrupted, abnormal
ZP:0006555	eye pigmentation delayed, abnormal
ZP:0006556	hematopoietic multipotent progenitor cell intermediate cell mass of mesoderm decreased amount, abnormal
ZP:0006557	liver immature, abnormal
ZP:0006558	erythroid lineage cell increased size, abnormal
ZP:0006564	statoacoustic (VIII) ganglion decreased size, abnormal
ZP:0006566	mechanosensory behavior arrested, abnormal
ZP:0006567	protein localization to cell surface arrested, abnormal
ZP:0006568	detection of mechanical stimulus involved in sensory perception of touch arrested, abnormal
ZP:0006569	voltage-gated sodium channel complex Rohon-Beard neuron mislocalised, abnormal
ZP:0006570	protein sumoylation disrupted, abnormal
ZP:0006571	collagen fibril organization process quality, abnormal
ZP:0006572	embryonic camera-type eye morphogenesis process quality, abnormal
ZP:0006573	eye distended, abnormal
ZP:0006575	anterior region sclera decreased thickness, abnormal
ZP:0006576	posterior region sclera decreased thickness, abnormal
ZP:0006577	fibroblast sclera decreased amount, abnormal
ZP:0006578	neutrophil homeostasis disrupted, abnormal
ZP:0006579	neutrophil spatial pattern, abnormal
ZP:0006580	swim bladder increased length, abnormal
ZP:0006581	swim bladder increased volume, abnormal
ZP:0006582	anterior macula morphology, abnormal
ZP:0006583	inner ear collapsed, abnormal
ZP:0006584	macula crowded, abnormal
ZP:0006585	intermediate mesoderm morphology, abnormal
ZP:0006586	G2/M transition of mitotic cell cycle delayed, abnormal
ZP:0006587	mitotic cell cycle delayed, abnormal
ZP:0006589	gastrulation decreased rate, abnormal
ZP:0006590	embryonic cleavage delayed, abnormal
ZP:0006591	epiboly involved in gastrulation with mouth forming second decreased rate, abnormal
ZP:0006592	intrinsic apoptotic signaling pathway increased process quality, abnormal
ZP:0006593	blastoderm cell increased size, abnormal
ZP:0006594	blastoderm cell decreased amount, abnormal
ZP:0006595	blastoderm cell cellular adhesivity blastoderm cell, abnormal
ZP:0006596	nucleus blastoderm cell increased size, abnormal
ZP:0006597	nucleus blastoderm cell decreased amount, abnormal
ZP:0006598	cardiac ventricle hypotrophic, abnormal
ZP:0006599	dorsal aorta absent, abnormal
ZP:0006600	yolk concave, abnormal
ZP:0006601	caudal vein absent, abnormal
ZP:0006602	common cardinal vein decreased width, abnormal
ZP:0006604	posterior cardinal vein increased thickness, abnormal
ZP:0006605	trunk vasculature hypoplastic, abnormal
ZP:0006606	striated muscle myosin thick filament cardiac muscle cell disorganized, abnormal
ZP:0006607	striated muscle thin filament cardiac muscle cell disorganized, abnormal
ZP:0006608	myofibril cardiac muscle cell sparse, abnormal
ZP:0006609	sarcomere cardiac muscle cell increased length, abnormal
ZP:0006610	defense response to bacterium disrupted, abnormal
ZP:0006611	hypophysis quality, abnormal
ZP:0006613	cell cycle decreased rate, abnormal
ZP:0006614	swimming decreased rate, abnormal
ZP:0006615	regulation of ventricular cardiac muscle cell membrane repolarization process quality, abnormal
ZP:0006616	cardiac conduction arrested, abnormal
ZP:0006617	cardiac conduction increased duration, abnormal
ZP:0006618	cardiac conduction decreased rate, abnormal
ZP:0006619	nucleate erythrocyte blood increased amount, abnormal
ZP:0006620	cardiac ventricle action potential, abnormal
ZP:0006621	cardiac ventricle functionality, abnormal
ZP:0006622	whole organism semi-viable, abnormal
ZP:0006623	vertebral artery present, abnormal
ZP:0006624	parachordal vessel present, abnormal
ZP:0006625	pharyngeal arch disorganized, abnormal
ZP:0006626	epithelial cilium movement involved in extracellular fluid movement disrupted, abnormal
ZP:0006627	tubulin-glutamic acid ligase activity disrupted, abnormal
ZP:0006628	cilium Kupffer's vesicle non-functional, abnormal
ZP:0006629	axonemal microtubule pronephric duct increased amount, abnormal
ZP:0006630	axonemal microtubule pronephric duct decreased size, abnormal
ZP:0006631	axoneme pronephric duct morphology, abnormal
ZP:0006632	inner ear altered number of otolith, abnormal
ZP:0006633	ventral mandibular arch increased thickness, abnormal
ZP:0006634	somite increased size, abnormal
ZP:0006635	whole organism elongated, abnormal
ZP:0006636	caudal fin lower lobe absent, abnormal
ZP:0006637	blood accumulation cranial vasculature, abnormal
ZP:0006638	blood accumulation trunk vasculature, abnormal
ZP:0006639	intersegmental vein absent, abnormal
ZP:0006640	intersegmental vein decreased length, abnormal
ZP:0006641	liver development decreased rate, abnormal
ZP:0006642	eye photoreceptor cell differentiation disrupted, abnormal
ZP:0006643	antero-ventral region hindbrain apoptotic, abnormal
ZP:0006644	serotonergic neuron hindbrain decreased amount, abnormal
ZP:0006645	retinal inner nuclear layer malformed, abnormal
ZP:0006646	neuron retinal inner nuclear layer decreased amount, abnormal
ZP:0006647	neuron retina decreased amount, abnormal
ZP:0006648	whole organism increased pigmentation, abnormal
ZP:0006649	retinal outer nuclear layer malformed, abnormal
ZP:0006650	melanosome melanocyte increased distribution, abnormal
ZP:0006651	mesoderm cellular motility, abnormal
ZP:0006652	hypophyseal fenestra increased width, abnormal
ZP:0006653	anterior neural plate decreased length, abnormal
ZP:0006654	mRNA polyadenylation disrupted, abnormal
ZP:0006655	iridophore post-vent region decreased amount, abnormal
ZP:0006656	ventral mandibular arch shape, abnormal
ZP:0006657	hematopoietic stem cell apoptotic, abnormal
ZP:0006658	heart contraction decreased magnitude, abnormal
ZP:0006659	heart increased accumulation blood, abnormal
ZP:0006660	common cardinal vein decreased size, abnormal
ZP:0006661	blood vasculature obstructed, abnormal
ZP:0006662	aortic arch constricted, abnormal
ZP:0006663	cell-cell junction blood vessel endothelial cell decreased length, abnormal
ZP:0006664	multicellular organism growth disrupted, abnormal
ZP:0006665	caudal fin truncated, abnormal
ZP:0006666	neuromast hair cell posterior lateral line decreased amount, abnormal
ZP:0006667	growth cone motor neuron increased size, abnormal
ZP:0006668	swimming disrupted, abnormal
ZP:0006669	axon neuron decreased length, abnormal
ZP:0006670	axon neuron decreased branchiness, abnormal
ZP:0006671	glutamatergic neuron decreased amount, abnormal
ZP:0006672	forebrain neuron development disrupted, abnormal
ZP:0006673	locomotion involved in locomotory behavior increased occurrence, abnormal
ZP:0006674	neuron brain apoptotic, abnormal
ZP:0006676	retina lacks parts or has fewer parts of type dopaminergic neuron, abnormal
ZP:0006677	adrenergic neuron olfactory bulb decreased amount, abnormal
ZP:0006678	periventricular nucleus of caudal tuberculum has fewer parts of type dopaminergic neuron, abnormal
ZP:0006679	pretectum lacks parts or has fewer parts of type dopaminergic neuron, abnormal
ZP:0006680	adrenergic neuron pretectum decreased amount, abnormal
ZP:0006681	ventral thalamus has fewer parts of type dopaminergic neuron, abnormal
ZP:0006682	preoptic area lacks parts or has fewer parts of type dopaminergic neuron, abnormal
ZP:0006683	adrenergic neuron preoptic area decreased amount, abnormal
ZP:0006684	adrenergic neuron caudal tuberculum decreased amount, abnormal
ZP:0006686	neuron fate commitment disrupted, abnormal
ZP:0006687	pancreas primordium has fewer parts of type endocrine cell, abnormal
ZP:0006688	pancreatic bud has fewer parts of type endocrine cell, abnormal
ZP:0006689	pancreatic bud has fewer parts of type pancreatic B cell, abnormal
ZP:0006691	pancreatic bud has fewer parts of type pancreatic A cell, abnormal
ZP:0006692	VeLD increased amount, abnormal
ZP:0006694	eye development delayed, abnormal
ZP:0006695	optic vesicle morphology, abnormal
ZP:0006696	nucleus retinal inner nuclear layer apoptotic, abnormal
ZP:0006697	cell retinal inner nuclear layer degenerate, abnormal
ZP:0006698	retinal pigmented epithelium discolored, abnormal
ZP:0006699	axon cranial nerve II decreased length, abnormal
ZP:0006700	axon cranial nerve II defasciculated, abnormal
ZP:0006701	whole organism colorless, abnormal
ZP:0006702	ciliary marginal zone damaged, abnormal
ZP:0006703	retinal inner plexiform layer decreased thickness, abnormal
ZP:0006704	nucleus retinal ganglion cell apoptotic, abnormal
ZP:0006711	left/right axis specification disrupted, abnormal
ZP:0006712	floor plate morphology, abnormal
ZP:0006713	cilium pronephric duct immobile, abnormal
ZP:0006714	inner dynein arm pronephric duct absent, abnormal
ZP:0006715	outer dynein arm pronephric duct absent, abnormal
ZP:0006716	cilium olfactory bulb immobile, abnormal
ZP:0006717	anatomical axis trunk curved, abnormal
ZP:0006718	trunk unpigmented, abnormal
ZP:0006719	cell cycle arrest disrupted, abnormal
ZP:0006720	regulation of cell cycle process disrupted, abnormal
ZP:0006722	mandibular arch skeleton physical object quality, abnormal
ZP:0006723	cranium morphology, abnormal
ZP:0006724	myelination in peripheral nervous system disrupted, abnormal
ZP:0006725	endoplasmic reticulum unfolded protein response increased process quality, abnormal
ZP:0006726	myelination of posterior lateral line nerve axons decreased process quality, abnormal
ZP:0006727	axon spinal cord morphology, abnormal
ZP:0006728	node of Ranvier spinal cord morphology, abnormal
ZP:0006729	node of Ranvier spinal cord decreased amount, abnormal
ZP:0006730	mitochondrion liver decreased size, abnormal
ZP:0006731	endoplasmic reticulum liver broken, abnormal
ZP:0006732	endoplasmic reticulum lumen liver morphology, abnormal
ZP:0006733	mitochondrial crista liver increased width, abnormal
ZP:0006734	bile canaliculus liver disorganized, abnormal
ZP:0006735	node of Ranvier posterior lateral line nerve morphology, abnormal
ZP:0006736	node of Ranvier posterior lateral line nerve decreased amount, abnormal
ZP:0006737	endoplasmic reticulum oligodendrocyte swollen, abnormal
ZP:0006738	endoplasmic reticulum myelinating Schwann cell swollen, abnormal
ZP:0006739	neuron death increased occurrence, abnormal
ZP:0006740	hindbrain degenerate, abnormal
ZP:0006741	telencephalon degenerate, abnormal
ZP:0006742	diencephalon degenerate, abnormal
ZP:0006743	dorsal region neural tube degenerate, abnormal
ZP:0006744	macrophage absent, abnormal
ZP:0006747	maintenance of blood-brain barrier disrupted, abnormal
ZP:0006748	glucose import decreased process quality, abnormal
ZP:0006749	brain vasculature decreased functionality, abnormal
ZP:0006750	adherens junction blood vessel endothelium decreased object quality, abnormal
ZP:0006751	bicellular tight junction blood vessel endothelium decreased object quality, abnormal
ZP:0006752	blood vessel permeable, abnormal
ZP:0006753	lymph vasculature trunk absent, abnormal
ZP:0006754	endothelial cell trunk decreased amount, abnormal
ZP:0006755	cerebellar central artery absent, abnormal
ZP:0006756	anterior mesencephalic central artery absent, abnormal
ZP:0006757	middle mesencephalic central artery absent, abnormal
ZP:0006758	posterior mesencephalic central artery absent, abnormal
ZP:0006759	filopodium vascular sprouts absent, abnormal
ZP:0006760	cloacal chamber cystic, abnormal
ZP:0006761	protein localization to cilium disrupted, abnormal
ZP:0006762	caudal fin upper lobe rough, abnormal
ZP:0006763	caudal fin lower lobe rough, abnormal
ZP:0006764	spliceosomal complex assembly disrupted, abnormal
ZP:0006765	epithelial cell thymus decreased thickness, abnormal
ZP:0006766	U6 snRNP whole organism decreased amount, abnormal
ZP:0006767	head decreased circumference, abnormal
ZP:0006768	splanchnocranium malformed, abnormal
ZP:0006769	osteoblast differentiation predisplaced growth, abnormal
ZP:0006770	chondrocyte development premature, abnormal
ZP:0006771	proteoglycan biosynthetic process disrupted, abnormal
ZP:0006772	eye protruding, abnormal
ZP:0006773	extracellular matrix cranium decreased volume, abnormal
ZP:0006774	perichondral bone cranium hyperplastic, abnormal
ZP:0006775	splanchnocranium structure, abnormal
ZP:0006776	chondrocranium structure, abnormal
ZP:0006777	anterior region neurocranium hypoplastic, abnormal
ZP:0006778	perichondral bone hyperplastic, abnormal
ZP:0006779	perichondral bone has extra parts of type osteoblast, abnormal
ZP:0006780	atrium decreased functionality, abnormal
ZP:0006781	bone mineralization increased process quality, abnormal
ZP:0006782	cleithrum nodular, abnormal
ZP:0006783	axial fin skeleton mineralized, abnormal
ZP:0006784	vertebra fused with centrum centrum, abnormal
ZP:0006785	myotome morphology, abnormal
ZP:0006786	skeletal muscle cell apoptotic, abnormal
ZP:0006787	slow muscle cell mislocalised, abnormal
ZP:0006788	cardiovascular system hypertrophic, abnormal
ZP:0006789	DNA replication checkpoint disrupted, abnormal
ZP:0006790	mitotic prophase temporally extended, abnormal
ZP:0006791	S phase increased occurrence, abnormal
ZP:0006792	startle response sporadic, abnormal
ZP:0006794	tonic skeletal muscle contraction sporadic, abnormal
ZP:0006796	axis whole organism shortened, abnormal
ZP:0006797	dorsal region retinal pigmented epithelium aplastic, abnormal
ZP:0006798	exocrine pancreas undifferentiated, abnormal
ZP:0006799	thrombocyte differentiation disrupted, abnormal
ZP:0006800	blood decreased volume, abnormal
ZP:0006801	yolk vacuolated, abnormal
ZP:0006802	common cardinal vein congested, abnormal
ZP:0006803	intestine edematous, abnormal
ZP:0006806	Wnt signaling pathway, calcium modulating pathway disrupted, abnormal
ZP:0006807	convergent extension involved in somitogenesis disrupted, abnormal
ZP:0006808	mitotic sister chromatid segregation arrested, abnormal
ZP:0006809	mitotic prometaphase increased duration, abnormal
ZP:0006811	mitotic metaphase plate congression process quality, abnormal
ZP:0006814	spindle assembly checkpoint increased occurrence, abnormal
ZP:0006815	intrinsic apoptotic signaling pathway by p53 class mediator increased occurrence, abnormal
ZP:0006816	brain immature, abnormal
ZP:0006817	proliferative region increased occurrence intrinsic apoptotic signaling pathway by p53 class mediator, abnormal
ZP:0006818	optic primordium immature, abnormal
ZP:0006819	caudal fin shortened, abnormal
ZP:0006820	caudal fin increased occurrence intrinsic apoptotic signaling pathway by p53 class mediator, abnormal
ZP:0006821	whole organism increased occurrence intrinsic apoptotic signaling pathway by p53 class mediator, abnormal
ZP:0006822	head increased occurrence intrinsic apoptotic signaling pathway by p53 class mediator, abnormal
ZP:0006823	trunk increased occurrence intrinsic apoptotic signaling pathway by p53 class mediator, abnormal
ZP:0006824	blood vessel decreased amount, abnormal
ZP:0006825	lens non-functional, abnormal
ZP:0006826	eye deformed, abnormal
ZP:0006827	iridophore absent, abnormal
ZP:0006828	blood island distended, abnormal
ZP:0006829	hematopoietic stem cell increased amount, abnormal
ZP:0006830	monocyte increased amount, abnormal
ZP:0006831	leukocyte proportionality to nucleate erythrocyte, abnormal
ZP:0006832	pancreatic epsilon cell decreased amount, abnormal
ZP:0006833	protein glycosylation decreased process quality, abnormal
ZP:0006834	myoseptum increased width, abnormal
ZP:0006835	myoseptum damaged, abnormal
ZP:0006836	sarcolemma muscle damaged, abnormal
ZP:0006837	skeletal muscle cell disorganized, abnormal
ZP:0006838	skeletal muscle cell sparse, abnormal
ZP:0006839	prechordal plate mislocalised, abnormal
ZP:0006840	lens rough, abnormal
ZP:0006841	calcium ion homeostasis disrupted, abnormal
ZP:0006842	muscle post-vent region shortened, abnormal
ZP:0006843	leucine metabolic process disrupted, abnormal
ZP:0006844	spinal cord curved, abnormal
ZP:0006845	synaptic transmission, cholinergic amplitude, abnormal
ZP:0006846	nucleate erythrocyte cardiovascular system absent, abnormal
ZP:0006847	intersegmental vessel brochidodromous, abnormal
ZP:0006848	ceratohyal cartilage straight, abnormal
ZP:0006849	blood vessel endothelial cell delamination involved in blood vessel lumen ensheathment disrupted, abnormal
ZP:0006850	endothelial tube lumen extension involved in blood vessel lumen ensheathment disrupted, abnormal
ZP:0006851	cardiac ventricle elongated, abnormal
ZP:0006852	common cardinal vein decreased length, abnormal
ZP:0006853	common cardinal vein disrupted blood vessel endothelial cell migration, abnormal
ZP:0006854	intersegmental vessel absent blood vessel lumenization, abnormal
ZP:0006855	cardiac jelly physical quality, abnormal
ZP:0006856	atrial endocardium structure, abnormal
ZP:0006857	cell-cell junction atrial endocardium decreased size, abnormal
ZP:0006858	cell-cell junction atrial endocardium decreased amount, abnormal
ZP:0006859	developmental growth process quality, abnormal
ZP:0006860	angioblast cell migration from lateral mesoderm to midline disrupted, abnormal
ZP:0006861	artery development disrupted, abnormal
ZP:0006862	blood vessel endothelial cell intersegmental vessel slender, abnormal
ZP:0006863	axial blood vessel malformed, abnormal
ZP:0006864	mitotic cell cycle arrested, abnormal
ZP:0006865	chromosome segregation process quality, abnormal
ZP:0006866	mitotic cell cycle arrest increased duration, abnormal
ZP:0006867	exocrine pancreas decreased length, abnormal
ZP:0006868	exocrine pancreas retracted, abnormal
ZP:0006869	spindle ciliary marginal zone structure, abnormal
ZP:0006870	spindle ciliary marginal zone increased amount, abnormal
ZP:0006871	spindle ciliary marginal zone apical-basal polarity, abnormal
ZP:0006872	ciliary marginal zone orientation spindle retinal pigmented epithelium, abnormal
ZP:0006873	dorsal aorta decreased size, abnormal
ZP:0006874	lateral dorsal aorta decreased thickness, abnormal
ZP:0006875	lateral dorsal aorta unlumenized, abnormal
ZP:0006876	myeloid cell development disrupted, abnormal
ZP:0006877	blood island has fewer parts of type myeloid cell, abnormal
ZP:0006878	olfactory placode decreased size, abnormal
ZP:0006879	cilium olfactory placode aggregated, abnormal
ZP:0006880	ventricular system edematous, abnormal
ZP:0006881	whole organism color, abnormal
ZP:0006882	whole organism curled, abnormal
ZP:0006883	head structure, abnormal
ZP:0006884	cilium olfactory pit truncated, abnormal
ZP:0006885	cilium olfactory pit shortened, abnormal
ZP:0006887	photoreceptor outer segment layer decreased size, abnormal
ZP:0006888	centriole eye photoreceptor cell displaced, abnormal
ZP:0006889	cilium or flagellum-dependent cell motility decreased rate, abnormal
ZP:0006890	epithelial cilium movement involved in extracellular fluid movement decreased frequency, abnormal
ZP:0006891	establishment of epithelial cell apical/basal polarity disrupted, abnormal
ZP:0006892	cilium movement involved in cell motility disrupted, abnormal
ZP:0006893	cilium Kupffer's vesicle functionality, abnormal
ZP:0006894	cilium floor plate functionality, abnormal
ZP:0006895	optic vesicle decreased size, abnormal
ZP:0006896	tail bud increased length, abnormal
ZP:0006897	pronephric duct morphology, abnormal
ZP:0006898	mesodermal cell paraxial mesoderm disoriented, abnormal
ZP:0006899	cilium cloacal chamber functionality, abnormal
ZP:0006900	motile cilium olfactory epithelium decreased speed, abnormal
ZP:0006901	cilium neural tube functionality, abnormal
ZP:0006902	pronephric glomerulus dilated, abnormal
ZP:0006903	cilium pronephric tubule functionality, abnormal
ZP:0006904	cilium pronephric tubule decreased amount, abnormal
ZP:0006905	pronephric proximal straight tubule dilated, abnormal
ZP:0006906	motile cilium posterior pronephric duct decreased speed, abnormal
ZP:0006907	neural crest apoptotic, abnormal
ZP:0006908	trigeminal ganglion disorganized, abnormal
ZP:0006909	calmodulin-dependent protein kinase activity decreased occurrence, abnormal
ZP:0006910	regulation of cardiac muscle contraction by calcium ion signaling decreased process quality, abnormal
ZP:0006911	regulation of collagen biosynthetic process process quality, abnormal
ZP:0006912	cell migration involved in kidney development disrupted, abnormal
ZP:0006913	cell proliferation involved in pronephros development increased occurrence, abnormal
ZP:0006914	protein autophosphorylation decreased occurrence, abnormal
ZP:0006915	ventricular cardiac muscle cell action potential decreased process quality, abnormal
ZP:0006916	notochord physical object quality, abnormal
ZP:0006917	distal region pronephric duct obstructed, abnormal
ZP:0006918	anterior region pronephros structure, abnormal
ZP:0006919	anterior region pronephros truncated, abnormal
ZP:0006920	inner ear increased distance posterior-most region anterior-most region pronephric duct, abnormal
ZP:0006921	cilium cloacal chamber decreased length, abnormal
ZP:0006922	cilium cloacal chamber decreased amount, abnormal
ZP:0006923	digestive system morphology, abnormal
ZP:0006924	pronephric duct opening decreased size, abnormal
ZP:0006925	renal glomerulus cystic, abnormal
ZP:0006926	angiogenesis increased occurrence, abnormal
ZP:0006927	blood vasculature hindbrain branched, abnormal
ZP:0006928	brain vasculature branched, abnormal
ZP:0006929	cranial vasculature increased diameter, abnormal
ZP:0006930	cranial vasculature branchiness, abnormal
ZP:0006931	cell intersegmental vessel increased amount, abnormal
ZP:0006932	aortic arch dilated, abnormal
ZP:0006933	aortic arch increased diameter, abnormal
ZP:0006934	locomotory behavior decreased process quality, abnormal
ZP:0006935	axon extension decreased process quality, abnormal
ZP:0006936	sensory perception of touch decreased process quality, abnormal
ZP:0006937	neuronal stem cell population maintenance decreased process quality, abnormal
ZP:0006938	spinal cord decreased size, abnormal
ZP:0006939	spinal cord has fewer parts of type motor neuron, abnormal
ZP:0006940	spinal cord lacks parts or has fewer parts of type secondary motor neuron, abnormal
ZP:0006941	neuronal stem cell spinal cord apoptotic, abnormal
ZP:0006942	integument edematous, abnormal
ZP:0006943	ciliary marginal zone apoptotic, abnormal
ZP:0006944	intestinal epithelium morphology, abnormal
ZP:0006945	axon motor neuron disorganized, abnormal
ZP:0006946	symplectic increased length, abnormal
ZP:0006947	symplectic in contact with Meckel's cartilage, abnormal
ZP:0006948	caudal fin ruffled, abnormal
ZP:0006949	pharyngeal arch 4 skeleton decreased size, abnormal
ZP:0006950	joint pharyngeal arch absent, abnormal
ZP:0006951	ceratohyal cartilage fused with hyosymplectic cartilage, abnormal
ZP:0006952	basihyal cartilage shape, abnormal
ZP:0006953	basihyal cartilage hyperplastic, abnormal
ZP:0006954	cardiac muscle cell differentiation arrested, abnormal
ZP:0006955	cardiac muscle cell differentiation process quality, abnormal
ZP:0006957	heart aplastic, abnormal
ZP:0006958	bulbus arteriosus decreased size, abnormal
ZP:0006959	bulbus arteriosus aplastic, abnormal
ZP:0006960	heart tube shortened, abnormal
ZP:0006961	atrium physical object quality, abnormal
ZP:0006962	presumptive atrium heart tube decreased volume, abnormal
ZP:0006963	presumptive cardiac ventricle heart tube decreased volume, abnormal
ZP:0006964	cardiac muscle cell undifferentiated, abnormal
ZP:0006965	Kupffer's vesicle decreased functionality, abnormal
ZP:0006966	bicellular tight junction Kupffer's vesicle disorganized, abnormal
ZP:0006967	motor neuron migration abnormal, abnormal
ZP:0006968	glycolytic process increased rate, abnormal
ZP:0006969	neuroblast proliferation increased rate, abnormal
ZP:0006970	aerobic respiration decreased rate, abnormal
ZP:0006971	respiratory electron transport chain process quality, abnormal
ZP:0006972	cilium pronephric duct malformed, abnormal
ZP:0006973	mitochondrion motor neuron mislocalised, abnormal
ZP:0006974	axon motor neuron unbranched, abnormal
ZP:0006975	axon terminus motor neuron decreased amount, abnormal
ZP:0006976	glial cell spatial pattern, abnormal
ZP:0006977	glial cell malformed, abnormal
ZP:0006978	neutrophil blood island increased amount, abnormal
ZP:0006979	vasculogenesis decreased process quality, abnormal
ZP:0006980	erythrocyte maturation disrupted, abnormal
ZP:0006981	primitive erythrocyte differentiation disrupted, abnormal
ZP:0006982	blood heart absent, abnormal
ZP:0006983	blood blood vessel absent, abnormal
ZP:0006984	pharyngeal arch deformed, abnormal
ZP:0006985	head protruding, abnormal
ZP:0006987	trunk kinked, abnormal
ZP:0006988	outer dynein arm ciliated olfactory receptor neuron absent, abnormal
ZP:0006989	somite rostral/caudal axis specification disrupted, abnormal
ZP:0006990	tail bud increased width, abnormal
ZP:0006991	somite anterior-posterior polarity, abnormal
ZP:0006992	anterior-posterior axis somite condensed, abnormal
ZP:0006993	medial-lateral axis somite increased width, abnormal
ZP:0006994	medial-lateral axis whole organism increased width, abnormal
ZP:0006996	sinus venosus edematous, abnormal
ZP:0006997	skeletal muscle morphology, abnormal
ZP:0006998	epidermis trunk morphology, abnormal
ZP:0006999	epidermis post-vent region morphology, abnormal
ZP:0007000	post-vent vasculature increased accumulation postero-ventral region nucleate erythrocyte, abnormal
ZP:0007001	vasculature degenerate, abnormal
ZP:0007002	chondrocyte ventral mandibular arch decreased amount, abnormal
ZP:0007003	pharyngeal arch cartilage fragile, abnormal
ZP:0007004	mitotic cell cycle, embryonic arrested, abnormal
ZP:0007005	neuron projection optic tectum mislocalised, abnormal
ZP:0007006	neuron projection optic tectum disorganized, abnormal
ZP:0007007	retinal inner plexiform layer deformed, abnormal
ZP:0007008	stratum fibrosum et griseum superficiale increased width, abnormal
ZP:0007009	axon stratum fibrosum et griseum superficiale mislocalised, abnormal
ZP:0007010	neuron projection amacrine cell morphology, abnormal
ZP:0007011	dendrite retinal ganglion cell morphology, abnormal
ZP:0007012	axon retinal bipolar neuron morphology, abnormal
ZP:0007013	head damaged, abnormal
ZP:0007014	muscle cell cellular homeostasis disrupted, abnormal
ZP:0007015	myosin complex somite border aggregated, abnormal
ZP:0007016	slow muscle cell quality, abnormal
ZP:0007017	slow muscle cell broken, abnormal
ZP:0007018	slow muscle cell non-functional, abnormal
ZP:0007019	actin filament slow muscle cell irregular spatial pattern, abnormal
ZP:0007020	myosin filament slow muscle cell irregular spatial pattern, abnormal
ZP:0007021	type III intermediate filament slow muscle cell irregular spatial pattern, abnormal
ZP:0007023	Z disc cardiac muscle increased width, abnormal
ZP:0007024	Z disc cardiac muscle disorganized, abnormal
ZP:0007025	sarcomere cardiac muscle cell decreased thickness, abnormal
ZP:0007026	sarcomere cardiac muscle cell decreased amount, abnormal
ZP:0007027	heart jogging process quality, abnormal
ZP:0007028	embryonic heart tube left/right pattern formation process quality, abnormal
ZP:0007029	left/right pattern formation process quality, abnormal
ZP:0007030	determination of digestive tract left/right asymmetry process quality, abnormal
ZP:0007031	Kupffer's vesicle decreased width, abnormal
ZP:0007032	Kupffer's vesicle functionality, abnormal
ZP:0007033	Kupffer's vesicle lacks parts or has fewer parts of type motile cilium Kupffer's vesicle, abnormal
ZP:0007034	Kupffer's vesicle process quality cilium movement, abnormal
ZP:0007035	motile cilium Kupffer's vesicle immobile, abnormal
ZP:0007036	motile cilium Kupffer's vesicle malformed, abnormal
ZP:0007037	Kupffer's vesicle lacks parts or has fewer parts of type motile cilium axonemal central pair Kupffer's vesicle, abnormal
ZP:0007038	ciliated cell Kupffer's vesicle decreased length, abnormal
ZP:0007039	ciliated cell Kupffer's vesicle decreased amount, abnormal
ZP:0007040	heart rudiment split bilaterally, abnormal
ZP:0007041	heart rudiment displaced to right side whole organism, abnormal
ZP:0007042	heart rudiment displaced to axis whole organism, abnormal
ZP:0007043	musculature system caudal fin decreased thickness, abnormal
ZP:0007045	cardiac muscle cell ventricular myocardium decreased amount, abnormal
ZP:0007046	cell-cell junction maintenance disrupted, abnormal
ZP:0007047	aconitate hydratase activity decreased process quality, abnormal
ZP:0007048	cytochrome-c oxidase activity decreased process quality, abnormal
ZP:0007049	nucleate erythrocyte heart decreased amount, abnormal
ZP:0007050	myelination of lateral line nerve axons disrupted, abnormal
ZP:0007051	melanocyte dilated, abnormal
ZP:0007052	myelinating Schwann cell decreased amount, abnormal
ZP:0007053	neural rod decreased length, abnormal
ZP:0007054	otic placode increased distance otic placode, abnormal
ZP:0007055	neuroepithelial cell apical-basal polarity, abnormal
ZP:0007056	apical surface neuroepithelial cell morphology, abnormal
ZP:0007058	lamellipodium anterior axial hypoblast decreased amount, abnormal
ZP:0007059	filopodium anterior axial hypoblast decreased amount, abnormal
ZP:0007060	endodermal cell gut disorganized, abnormal
ZP:0007061	lateral plate mesoderm morphology, abnormal
ZP:0007062	lateral plate mesoderm apoptotic, abnormal
ZP:0007063	actin filament bundle lateral plate mesoderm increased size, abnormal
ZP:0007064	mesodermal cell lateral plate mesoderm disorganized, abnormal
ZP:0007065	liver mislocalised ventrally, abnormal
ZP:0007066	hepatocyte liver apoptotic, abnormal
ZP:0007067	liver primordium mislocalised posteriorly, abnormal
ZP:0007068	actin filament bundle endodermal cell increased size, abnormal
ZP:0007069	cell proliferation in hindbrain decreased rate, abnormal
ZP:0007070	cerebellar granule cell differentiation disrupted, abnormal
ZP:0007071	neurotransmitter biosynthetic process process quality, abnormal
ZP:0007072	musculoskeletal movement, spinal reflex action decreased rate, abnormal
ZP:0007073	secondary motor neuron floor plate decreased amount, abnormal
ZP:0007074	cerebellar granule cell cerebellum decreased amount, abnormal
ZP:0007075	pancreas spheroid, abnormal
ZP:0007076	pectoral fin musculature decreased tonicity, abnormal
ZP:0007077	pancreatic duct disrupted cell migration, abnormal
ZP:0007079	pancreatic ductal cell located in hepatic duct, abnormal
ZP:0007080	muscle organ morphogenesis disrupted, abnormal
ZP:0007081	skeletal muscle cell myotome disorganized, abnormal
ZP:0007082	sarcomere skeletal muscle cell disorganized, abnormal
ZP:0007083	trunk disorganized, abnormal
ZP:0007084	post-vent region disorganized, abnormal
ZP:0007085	endocrine cell endocrine pancreas undifferentiated, abnormal
ZP:0007086	epidermis ventral fin fold morphology, abnormal
ZP:0007087	endoplasmic reticulum unfolded protein response process quality, abnormal
ZP:0007088	locomotory behavior decreased speed, abnormal
ZP:0007089	posterior lateral line nerve decreased thickness, abnormal
ZP:0007090	myelin sheath posterior lateral line nerve morphology, abnormal
ZP:0007091	myelin sheath posterior lateral line nerve decreased thickness, abnormal
ZP:0007092	compact myelin posterior lateral line nerve absent, abnormal
ZP:0007093	inner ear swollen, abnormal
ZP:0007095	vertebra mineralized, abnormal
ZP:0007096	otic vesicle protrusion disorganized, abnormal
ZP:0007097	regulation of blood vessel endothelial cell migration disrupted, abnormal
ZP:0007098	branching involved in lymph vessel morphogenesis disrupted, abnormal
ZP:0007099	venous endothelial cell migration involved in lymph vessel development disrupted, abnormal
ZP:0007100	cellular response to growth factor stimulus increased occurrence, abnormal
ZP:0007101	dorsal aorta has extra parts of type endothelial tip cell, abnormal
ZP:0007102	blood vasculature gut increased amount, abnormal
ZP:0007103	posterior cardinal vein lacks parts or has fewer parts of type endothelial tip cell, abnormal
ZP:0007104	intersegmental artery absent, abnormal
ZP:0007106	blood vasculature pectoral fin increased amount, abnormal
ZP:0007109	thoracic duct hypotrophic, abnormal
ZP:0007110	lymphangiogenic sprout decreased amount, abnormal
ZP:0007111	median fin fold hypoplastic, abnormal
ZP:0007112	ventral region caudal fin hypoplastic, abnormal
ZP:0007113	ventral fin fold hypoplastic, abnormal
ZP:0007114	post-vent region has extra parts of type muscle, abnormal
ZP:0007115	protein kinase activity decreased occurrence, abnormal
ZP:0007116	epithelial structure maintenance disrupted, abnormal
ZP:0007117	formation of anatomical boundary delayed, abnormal
ZP:0007118	actin cytoskeleton somite disorganized, abnormal
ZP:0007119	epithelial cell somite morphology, abnormal
ZP:0007120	lamellipodium cell decreased amount, abnormal
ZP:0007121	spinal cord physical object quality, abnormal
ZP:0007122	thigmotaxis absent, abnormal
ZP:0007123	post-vent region decreased thickness, abnormal
ZP:0007124	skeletal muscle contractility, abnormal
ZP:0007125	skeletal muscle decreased force, abnormal
ZP:0007126	striated muscle thin filament skeletal muscle decreased length, abnormal
ZP:0007127	sarcomere skeletal muscle decreased length, abnormal
ZP:0007128	filamentous actin skeletal muscle cell aggregated, abnormal
ZP:0007129	epidermis post-vent region irregular spatial pattern, abnormal
ZP:0007130	cloacal septation disrupted, abnormal
ZP:0007131	brain decreased mass, abnormal
ZP:0007132	brain infiltrative, abnormal
ZP:0007133	cerebellum organization quality, abnormal
ZP:0007134	fourth ventricle composition, abnormal
ZP:0007135	retinal photoreceptor layer lacks all parts of type photoreceptor outer segment photoreceptor cell, abnormal
ZP:0007136	renal system cystic, abnormal
ZP:0007137	anterior-posterior axis whole organism increased curvature, abnormal
ZP:0007138	photoreceptor outer segment layer disorganized, abnormal
ZP:0007139	erythrocyte homeostasis disrupted, abnormal
ZP:0007140	homeostasis of number of cells within a tissue disrupted, abnormal
ZP:0007141	nucleate erythrocyte dorsal aorta decreased amount, abnormal
ZP:0007142	nucleate erythrocyte common cardinal vein decreased amount, abnormal
ZP:0007143	integument increased accumulation epidermal cell, abnormal
ZP:0007144	ventral fin fold increased accumulation epidermal cell, abnormal
ZP:0007145	whole organism monstrous, abnormal
ZP:0007146	nucleate erythrocyte increased volume, abnormal
ZP:0007147	nucleate erythrocyte deformed, abnormal
ZP:0007148	nucleus nucleate erythrocyte swollen, abnormal
ZP:0007149	plasma membrane nucleate erythrocyte broken, abnormal
ZP:0007150	plasma membrane nucleate erythrocyte deformed, abnormal
ZP:0007151	mitotic sister chromatid segregation disrupted, abnormal
ZP:0007152	nucleus retina morphology, abnormal
ZP:0007153	nucleus retina variability of size, abnormal
ZP:0007154	chromosome gastrula cell morphology, abnormal
ZP:0007155	M phase increased duration, abnormal
ZP:0007156	retina morphogenesis in camera-type eye delayed, abnormal
ZP:0007157	hematopoietic stem cell proliferation decreased rate, abnormal
ZP:0007158	blood island has fewer parts of type hematopoietic stem cell, abnormal
ZP:0007159	T cell absent, abnormal
ZP:0007160	embryonic neurocranium morphogenesis process quality, abnormal
ZP:0007161	neural crest cell mislocalised, abnormal
ZP:0007162	intestinal epithelial structure maintenance decreased process quality, abnormal
ZP:0007163	intestine well differentiated, abnormal
ZP:0007165	intestinal epithelium has fewer parts of type epithelial cell, abnormal
ZP:0007166	slow-twitch skeletal muscle fiber contraction decreased process quality, abnormal
ZP:0007167	taxis decreased process quality, abnormal
ZP:0007168	axis curved ventral, abnormal
ZP:0007169	slow muscle cell has fewer parts of type myofibril slow muscle cell, abnormal
ZP:0007170	striated muscle thin filament slow muscle cell disorganized, abnormal
ZP:0007171	myofibril slow muscle cell decreased size, abnormal
ZP:0007172	sarcomere slow muscle cell malformed, abnormal
ZP:0007173	sarcomere slow muscle cell decreased amount, abnormal
ZP:0007174	animal organ morphogenesis disrupted, abnormal
ZP:0007176	melanosome transport decreased rate, abnormal
ZP:0007177	startle response decreased process quality, abnormal
ZP:0007178	cellular respiration decreased process quality, abnormal
ZP:0007179	midbrain hindbrain boundary inconspicuous, abnormal
ZP:0007180	contractile fiber muscle disorganized, abnormal
ZP:0007181	mitochondrion muscle cell broken, abnormal
ZP:0007182	nucleate erythrocyte accumulation heart, abnormal
ZP:0007183	sarcomere heart malformed, abnormal
ZP:0007184	Z disc heart malformed, abnormal
ZP:0007185	telencephalon cellular quality, abnormal
ZP:0007186	postero-dorsal region telencephalon cellular quality, abnormal
ZP:0007187	heparan sulfate proteoglycan biosynthetic process process quality, abnormal
ZP:0007188	chondroitin sulfate biosynthetic process increased occurrence, abnormal
ZP:0007189	tooth mineralization delayed, abnormal
ZP:0007190	chondroitin sulfate proteoglycan biosynthetic process increased occurrence, abnormal
ZP:0007191	sulfation increased occurrence, abnormal
ZP:0007192	pharyngeal arch 3-7 skeleton increased thickness, abnormal
ZP:0007193	pharyngeal arch 3-7 skeleton increased width, abnormal
ZP:0007194	dorsal region diencephalon flattened, abnormal
ZP:0007195	dorsal region midbrain flattened, abnormal
ZP:0007196	optic tract structure, abnormal
ZP:0007197	dorsomedial optic tract composition, abnormal
ZP:0007198	distal region pectoral fin degenerate, abnormal
ZP:0007199	cell pectoral fin circular, abnormal
ZP:0007200	mandibular arch skeleton increased width, abnormal
ZP:0007201	mandibular arch skeleton increased mass, abnormal
ZP:0007202	mandibular arch skeleton sloped downward, abnormal
ZP:0007203	ventral mandibular arch morphology, abnormal
ZP:0007204	pharyngeal arch 2 skeleton increased thickness, abnormal
ZP:0007205	chondrocyte pharyngeal arch cartilage organization quality, abnormal
ZP:0007206	pectoral fin fold aplastic, abnormal
ZP:0007207	distal region pectoral fin fold aplastic, abnormal
ZP:0007208	chondrocyte shape, abnormal
ZP:0007209	axon retinal ganglion cell branched, abnormal
ZP:0007210	axon retinal ganglion cell organization quality, abnormal
ZP:0007211	skeletal system development disrupted, abnormal
ZP:0007212	ossification decreased occurrence, abnormal
ZP:0007213	chondrocyte intercalation involved in growth plate cartilage morphogenesis arrested, abnormal
ZP:0007214	pectoral fin development arrested, abnormal
ZP:0007215	olfactory placode hypoplastic, abnormal
ZP:0007216	apical ectodermal ridge pectoral fin bud aplastic, abnormal
ZP:0007217	pectoral girdle decreased size, abnormal
ZP:0007218	ceratobranchial 5 tooth decreased length, abnormal
ZP:0007219	ceratobranchial 5 tooth increased thickness, abnormal
ZP:0007220	ceratobranchial 5 tooth increased width, abnormal
ZP:0007221	ceratobranchial 5 tooth ossified, abnormal
ZP:0007222	ceratobranchial 5 tooth mislocalised posteriorly, abnormal
ZP:0007223	ceratobranchial 5 tooth increased distance ceratobranchial 5 tooth, abnormal
ZP:0007224	ceratobranchial 5 tooth decreased concentration enameloid, abnormal
ZP:0007225	distal surface ceratobranchial 5 tooth split, abnormal
ZP:0007226	ventral tooth row has extra parts of type ceratobranchial 5 tooth, abnormal
ZP:0007227	dorsal tooth row has fewer parts of type ceratobranchial 5 tooth, abnormal
ZP:0007228	pharyngeal epithelium decreased thickness, abnormal
ZP:0007229	Meckel's cartilage increased size, abnormal
ZP:0007230	mandibular arch skeleton mislocalised posteriorly, abnormal
ZP:0007231	ceratobranchial 5 bone apoptotic, abnormal
ZP:0007232	pectoral fin endoskeletal disc absent, abnormal
ZP:0007233	cartilage element increased thickness, abnormal
ZP:0007234	ceratobranchial 4 cartilage decreased size, abnormal
ZP:0007235	neurocranium decreased length, abnormal
ZP:0007236	neurocranium increased thickness, abnormal
ZP:0007237	dermal bone hypoplastic, abnormal
ZP:0007238	pharyngeal arch 3-7 increased width, abnormal
ZP:0007239	fin fold pectoral fin bud absent, abnormal
ZP:0007240	chondrocyte circular, abnormal
ZP:0007241	axon retinal ganglion cell fasciculation, abnormal
ZP:0007242	hair cell absent, abnormal
ZP:0007243	hair cell decreased amount, abnormal
ZP:0007244	pronuclear fusion disrupted, abnormal
ZP:0007245	pronuclear migration disrupted, abnormal
ZP:0007246	female pronucleus blastomere movement quality, abnormal
ZP:0007247	blastomere misaligned with female pronucleus aster blastomere, abnormal
ZP:0007248	blastomere detached from centrosome male pronucleus blastomere, abnormal
ZP:0007249	blood increased accumulation yolk, abnormal
ZP:0007250	cell-cell junction heart structure, abnormal
ZP:0007251	desmosome heart decreased amount, abnormal
ZP:0007252	excretion decreased magnitude, abnormal
ZP:0007253	pancreatic epsilon cell increased amount, abnormal
ZP:0007254	ghrelin secreting cell increased amount, abnormal
ZP:0007255	glucagon secreting cell increased amount, abnormal
ZP:0007256	pharynx decreased width, abnormal
ZP:0007257	pigment granule whole organism decreased amount, abnormal
ZP:0007258	ceratobranchial 3 cartilage aplastic, abnormal
ZP:0007259	ceratobranchial 4 cartilage aplastic, abnormal
ZP:0007260	ceratobranchial 5 cartilage aplastic, abnormal
ZP:0007261	cell brain degenerate, abnormal
ZP:0007262	hindbrain increased size, abnormal
ZP:0007263	cell eye degenerate, abnormal
ZP:0007264	startle response process quality, abnormal
ZP:0007265	otolith development disrupted, abnormal
ZP:0007266	whole organism lacks all parts of type lateral crista, abnormal
ZP:0007268	cilium movement increased rate, abnormal
ZP:0007269	regulation of cilium beat frequency disrupted, abnormal
ZP:0007270	cilium pronephros disoriented, abnormal
ZP:0007271	cilium pronephros disorganized, abnormal
ZP:0007272	cilium pronephros shortened, abnormal
ZP:0007273	blood vessel development arrested, abnormal
ZP:0007274	endothelial cell proliferation decreased occurrence, abnormal
ZP:0007275	head mesenchyme position, abnormal
ZP:0007276	ventral aorta has fewer parts of type vascular associated smooth muscle cell, abnormal
ZP:0007277	primordial hindbrain channel fragile, abnormal
ZP:0007278	head increased accumulation blood, abnormal
ZP:0007279	ventricular system hemorrhagic, abnormal
ZP:0007280	ventricular system increased accumulation blood, abnormal
ZP:0007281	cranial vasculature immature, abnormal
ZP:0007282	blood vessel endothelial cell cranial vasculature morphology, abnormal
ZP:0007283	cranial vasculature separated from blood vessel endothelial cell mesenchymal cell head mesenchyme, abnormal
ZP:0007284	pharyngeal vasculature has fewer parts of type vascular associated smooth muscle cell, abnormal
ZP:0007285	mid cerebral vein fragile, abnormal
ZP:0007286	primordial midbrain channel fragile, abnormal
ZP:0007287	central artery morphology, abnormal
ZP:0007288	central artery irregular spatial pattern, abnormal
ZP:0007289	central artery unlumenized, abnormal
ZP:0007290	cytoplasm blood vessel endothelial cell decreased thickness, abnormal
ZP:0007291	eye disorganized, abnormal
ZP:0007292	retinal cone cell retinal photoreceptor layer disheveled, abnormal
ZP:0007293	kinocilium inner ear decreased length, abnormal
ZP:0007294	nucleus photoreceptor inner segment layer condensed, abnormal
ZP:0007295	photoreceptor outer segment layer malformed, abnormal
ZP:0007296	nucleus photoreceptor outer segment layer condensed, abnormal
ZP:0007297	photoreceptor outer segment membrane photoreceptor outer segment layer disorganized, abnormal
ZP:0007298	cell photoreceptor outer segment layer decreased amount, abnormal
ZP:0007299	photoreceptor cell degeneration, abnormal
ZP:0007300	catalase activity decreased process quality, abnormal
ZP:0007301	central nervous system neuron axonogenesis disrupted, abnormal
ZP:0007302	post-anal tail morphogenesis arrested, abnormal
ZP:0007303	vascular endothelial growth factor signaling pathway cellular spatiotemporal quality, abnormal
ZP:0007304	sensory perception of touch arrested, abnormal
ZP:0007305	head development arrested, abnormal
ZP:0007306	regulation of superoxide dismutase activity disrupted, abnormal
ZP:0007307	regulation of hypoxia-inducible factor-1alpha signaling pathway disrupted, abnormal
ZP:0007308	regulation of reactive oxygen species metabolic process disrupted, abnormal
ZP:0007309	proliferative region brain increased size, abnormal
ZP:0007310	spinal cord curved ventral, abnormal
ZP:0007311	primary motor neuron spinal cord decreased amount, abnormal
ZP:0007312	dopaminergic neuron diencephalon distributed, abnormal
ZP:0007313	dopaminergic neuron diencephalon mislocalised ventrally, abnormal
ZP:0007314	brainstem and spinal white matter disorganized, abnormal
ZP:0007315	dopaminergic neuron pretectum decreased amount, abnormal
ZP:0007316	ansulate commissure aplastic, abnormal
ZP:0007317	dopaminergic neuron caudal tuberculum dead, abnormal
ZP:0007318	dopaminergic neuron caudal tuberculum disheveled, abnormal
ZP:0007319	caudal fin shape, abnormal
ZP:0007320	head low brightness, abnormal
ZP:0007321	white matter shape, abnormal
ZP:0007322	peripheral neuron decreased amount, abnormal
ZP:0007323	axon dopaminergic neuron absent, abnormal
ZP:0007324	axon dopaminergic neuron decreased length, abnormal
ZP:0007325	axon dopaminergic neuron broken, abnormal
ZP:0007326	cranial ganglion absent, abnormal
ZP:0007329	median fin fold aplastic, abnormal
ZP:0007331	whole organism lacks all parts of type melanocyte, abnormal
ZP:0007333	neuromast hair cell absent, abnormal
ZP:0007334	hematopoietic stem cell caudal vein plexus decreased amount, abnormal
ZP:0007335	parachordal vessel disorganized, abnormal
ZP:0007336	parachordal vessel agenesis, abnormal
ZP:0007337	motile cilium otic vesicle decreased amount, abnormal
ZP:0007338	heart right side of anterior-posterior axis whole organism, abnormal
ZP:0007339	heart rudiment bilateral, abnormal
ZP:0007340	heart rudiment right side of anterior-posterior axis whole organism, abnormal
ZP:0007341	liver right side of anterior-posterior axis whole organism, abnormal
ZP:0007342	somite loose, abnormal
ZP:0007343	kinocilium auditory receptor cell decreased amount, abnormal
ZP:0007344	cilium renal tubule curled, abnormal
ZP:0007349	pharyngeal endoderm increased amount, abnormal
ZP:0007350	pharyngeal arch increased amount, abnormal
ZP:0007351	Kupffer's vesicle aplastic, abnormal
ZP:0007353	nucleate erythrocyte decreased size, abnormal
ZP:0007354	nucleate erythrocyte undifferentiated, abnormal
ZP:0007356	diencephalon lacks all parts of type dopaminergic neuron, abnormal
ZP:0007357	diencephalon has fewer parts of type dopaminergic neuron, abnormal
ZP:0007358	dopaminergic neuron diencephalon disorganized, abnormal
ZP:0007359	retinal inner nuclear layer lacks all parts of type amacrine cell, abnormal
ZP:0007360	retinal inner nuclear layer has fewer parts of type amacrine cell, abnormal
ZP:0007361	pretectum lacks all parts of type dopaminergic neuron, abnormal
ZP:0007362	pretectum has fewer parts of type dopaminergic neuron, abnormal
ZP:0007363	locus coeruleus has fewer parts of type dopaminergic neuron, abnormal
ZP:0007364	pathway-restricted SMAD protein phosphorylation disrupted, abnormal
ZP:0007365	margin increased thickness, abnormal
ZP:0007366	hypoblast has extra parts of type somatic stem cell, abnormal
ZP:0007367	epithelial cell fin disorganized, abnormal
ZP:0007368	epithelial cell notochord circular, abnormal
ZP:0007369	epithelial cell notochord disorganized, abnormal
ZP:0007370	integument apoptotic, abnormal
ZP:0007371	epithelial cell integument circular, abnormal
ZP:0007372	epithelial cell integument disorganized, abnormal
ZP:0007373	caudal fin collapsed, abnormal
ZP:0007374	cell ventral fin fold circular, abnormal
ZP:0007375	integument trunk rough, abnormal
ZP:0007376	pectoral fin apoptotic, abnormal
ZP:0007377	startle response arrested, abnormal
ZP:0007378	inhibitory postsynaptic potential process quality, abnormal
ZP:0007379	regulation of synaptic transmission, glycinergic process quality, abnormal
ZP:0007380	sensory perception of sound arrested, abnormal
ZP:0007381	chemosensory behavior decreased occurrence, abnormal
ZP:0007382	glial cell migration arrested, abnormal
ZP:0007383	fin regeneration decreased occurrence, abnormal
ZP:0007384	developmental pigmentation arrested, abnormal
ZP:0007385	posterior lateral line nerve has extra parts of type posterior lateral line neuromast, abnormal
ZP:0007386	posterior lateral line nerve has fewer parts of type glial cell, abnormal
ZP:0007387	trunk has extra parts of type posterior lateral line neuromast, abnormal
ZP:0007388	trunk has fewer parts of type melanophore stripe melanocyte, abnormal
ZP:0007389	melanophore stripe post-vent region decreased pigmentation, abnormal
ZP:0007390	post-vent region has fewer parts of type melanophore stripe melanocyte, abnormal
ZP:0007391	melanocyte post-vent region poorly differentiated, abnormal
ZP:0007392	blastema decreased size, abnormal
ZP:0007393	sympathetic chain ganglion absent, abnormal
ZP:0007394	glial cell decreased amount, abnormal
ZP:0007395	lymphangiogenesis decreased occurrence, abnormal
ZP:0007396	lymph vessel endothelium aplastic, abnormal
ZP:0007397	BMP signaling pathway process quality, abnormal
ZP:0007398	scale aplastic, abnormal
ZP:0007399	scale decreased amount, abnormal
ZP:0007400	gill raker decreased size, abnormal
ZP:0007401	gill raker aplastic, abnormal
ZP:0007402	ceratobranchial 5 tooth aplastic, abnormal
ZP:0007403	ceratobranchial 5 tooth decreased amount, abnormal
ZP:0007404	whole organism lacks all parts of type fin, abnormal
ZP:0007405	endochondral bone pectoral fin size, abnormal
ZP:0007406	anal fin lepidotrichium aplastic, abnormal
ZP:0007407	caudal fin lepidotrichium aplastic, abnormal
ZP:0007408	lepidotrichium morphology, abnormal
ZP:0007409	lepidotrichium malformed, abnormal
ZP:0007410	eye morphogenesis disrupted, abnormal
ZP:0007415	retinal pigmented epithelium decreased thickness, abnormal
ZP:0007418	posterior crista increased size, abnormal
ZP:0007419	posterior crista disorganized, abnormal
ZP:0007420	anterior crista increased size, abnormal
ZP:0007421	anterior crista disorganized, abnormal
ZP:0007425	pillar of the lateral semicircular canal shape, abnormal
ZP:0007426	brain V-shaped, abnormal
ZP:0007427	protein kinase activity increased occurrence, abnormal
ZP:0007428	receptor-mediated endocytosis arrested, abnormal
ZP:0007429	stem cell population maintenance disrupted, abnormal
ZP:0007430	renal absorption arrested, abnormal
ZP:0007431	retinal ganglion cell layer hypotrophic, abnormal
ZP:0007432	neuron retinal ganglion cell layer increased amount, abnormal
ZP:0007433	neuron retinal ganglion cell layer sparse, abnormal
ZP:0007434	retinal neural layer decreased thickness, abnormal
ZP:0007435	cell retinal neural layer decreased mass density, abnormal
ZP:0007436	eye refractivity, abnormal
ZP:0007437	eye increased diameter, abnormal
ZP:0007438	eye variability of size, abnormal
ZP:0007439	retinal inner nuclear layer hypotrophic, abnormal
ZP:0007440	endosome pronephric duct absent, abnormal
ZP:0007441	recycling endosome membrane pronephric duct absent, abnormal
ZP:0007442	retina increased area, abnormal
ZP:0007443	visual system decreased functionality, abnormal
ZP:0007444	ciliary zone hypertrophic, abnormal
ZP:0007445	neuronal stem cell ciliary marginal zone decreased amount, abnormal
ZP:0007446	retinal outer nuclear layer hypotrophic, abnormal
ZP:0007447	optic nerve head increased size, abnormal
ZP:0007448	optic nerve head increased diameter, abnormal
ZP:0007449	vitreous increased size, abnormal
ZP:0007450	aqueous humor anterior segment eye increased pressure, abnormal
ZP:0007451	posterior segment eye increased depth, abnormal
ZP:0007452	photoreceptor cell outer segment organization delayed, abnormal
ZP:0007453	axoneme retinal photoreceptor layer absent, abnormal
ZP:0007454	cilium lateral crista decreased variability of size, abnormal
ZP:0007455	cilium anterior macula absent, abnormal
ZP:0007456	cilium olfactory epithelium decreased length, abnormal
ZP:0007457	cilium olfactory epithelium decreased amount, abnormal
ZP:0007458	cilium posterior lateral line neuromast absent, abnormal
ZP:0007459	cilium posterior lateral line neuromast decreased length, abnormal
ZP:0007460	cilium posterior lateral line neuromast decreased amount, abnormal
ZP:0007461	photoreceptor connecting cilium photoreceptor outer segment layer decreased length, abnormal
ZP:0007462	myotome development disrupted, abnormal
ZP:0007463	postcranial axial skeleton behavioral quality of a process skeletal system development, abnormal
ZP:0007464	axis whole organism decreased length, abnormal
ZP:0007465	cranial vault dorso-ventrally flattened, abnormal
ZP:0007467	ventral mandibular arch exserted, abnormal
ZP:0007468	integument ionocyte decreased amount, abnormal
ZP:0007469	NCC ionocyte increased amount, abnormal
ZP:0007470	ceratohyal cartilage increased angle to ceratohyal cartilage, abnormal
ZP:0007471	axon trigeminal ganglion decreased length, abnormal
ZP:0007472	roof plate formation disrupted, abnormal
ZP:0007473	roof plate midbrain region increased width, abnormal
ZP:0007476	neuron hyperplastic, abnormal
ZP:0007477	pigment granule dispersal disrupted, abnormal
ZP:0007478	hepatic duct decreased length, abnormal
ZP:0007479	hepatic duct disorganized, abnormal
ZP:0007480	hepatic duct decreased amount, abnormal
ZP:0007481	intersegmental vessel disrupted membrane raft distribution, abnormal
ZP:0007482	endothelial tip cell disrupted membrane raft distribution, abnormal
ZP:0007484	response to light stimulus decreased strength, abnormal
ZP:0007485	retina decreased pigmentation, abnormal
ZP:0007486	anterior-most region telencephalon truncated, abnormal
ZP:0007487	pharyngeal arch 3-7 skeleton increased size, abnormal
ZP:0007488	cranial cartilage apoptotic, abnormal
ZP:0007489	perichondrium increased thickness, abnormal
ZP:0007490	perichondrium rough, abnormal
ZP:0007491	cell perichondrium increased size, abnormal
ZP:0007492	chondrocyte color, abnormal
ZP:0007493	nucleus chondrocyte shape, abnormal
ZP:0007494	plasma membrane chondrocyte undulate, abnormal
ZP:0007496	cell population proliferation occurrence, abnormal
ZP:0007497	brain wholly posterioralized, abnormal
ZP:0007498	posterior lateral line truncated, abnormal
ZP:0007499	pectoral fin hypoplastic, abnormal
ZP:0007500	skeletal muscle contraction decreased process quality, abnormal
ZP:0007501	SCF-dependent proteasomal ubiquitin-dependent protein catabolic process decreased occurrence, abnormal
ZP:0007502	cardiac muscle contraction decreased process quality, abnormal
ZP:0007503	determination of left/right symmetry decreased process quality, abnormal
ZP:0007504	motile cilium assembly decreased process quality, abnormal
ZP:0007505	determination of heart left/right asymmetry decreased process quality, abnormal
ZP:0007506	determination of intestine left/right asymmetry decreased process quality, abnormal
ZP:0007507	gut symmetry, abnormal
ZP:0007508	liver symmetry, abnormal
ZP:0007509	post-vent vasculature increased branchiness, abnormal
ZP:0007510	blood vessel inner optic circle increased branchiness, abnormal
ZP:0007511	cranial blood vessel increased branchiness, abnormal
ZP:0007512	Schwann cell proliferation decreased process quality, abnormal
ZP:0007513	eurydendroid cell differentiation disrupted, abnormal
ZP:0007514	oligodendrocyte cell fate specification disrupted, abnormal
ZP:0007515	peripheral nervous system myelin formation decreased occurrence, abnormal
ZP:0007516	Schwann cell migration decreased process quality, abnormal
ZP:0007517	lateral line nerve glial cell migration decreased process quality, abnormal
ZP:0007518	lateral line system has extra parts of type posterior lateral line neuromast, abnormal
ZP:0007519	eurydendroid cell cerebellum decreased amount, abnormal
ZP:0007520	posterior lateral line nerve located in epidermis, abnormal
ZP:0007521	posterior lateral line nerve lateral to basement membrane epidermis, abnormal
ZP:0007522	posterior lateral line nerve lacks parts or has fewer parts of type myelinating Schwann cell, abnormal
ZP:0007523	neuron dorsal root ganglion mislocalised, abnormal
ZP:0007526	contractile fiber somite decreased amount, abnormal
ZP:0007527	blood circulation delayed, abnormal
ZP:0007528	muscle pioneer trunk decreased amount, abnormal
ZP:0007530	fast muscle cell trunk decreased amount, abnormal
ZP:0007532	contractile fiber post-vent region patchy, abnormal
ZP:0007533	slow muscle cell post-vent region decreased amount, abnormal
ZP:0007534	axon regeneration decreased process quality, abnormal
ZP:0007535	sensory epithelium regeneration decreased process quality, abnormal
ZP:0007536	skeletal muscle cell increased length, abnormal
ZP:0007537	Muller cell cellular potency, abnormal
ZP:0007538	positive regulation of deoxyribonuclease activity decreased process quality, abnormal
ZP:0007539	lens fiber cell differentiation decreased process quality, abnormal
ZP:0007540	lens nucleate quality, abnormal
ZP:0007541	chromatin lens damaged, abnormal
ZP:0007542	obsolete cell head apoptotic, abnormal
ZP:0007543	pharyngeal arch hypoplastic, abnormal
ZP:0007544	digestive system malformed, abnormal
ZP:0007545	endocardial ring malformed, abnormal
ZP:0007546	cartilage development decreased process quality, abnormal
ZP:0007547	spinal cord increased process quality apoptotic DNA fragmentation, abnormal
ZP:0007548	eye increased process quality apoptotic DNA fragmentation, abnormal
ZP:0007549	cartilage element pharyngeal arch immature, abnormal
ZP:0007550	cartilage element chondrocranium cartilage immature, abnormal
ZP:0007551	endoplasmic reticulum chondrocyte increased size, abnormal
ZP:0007552	endoplasmic reticulum chondrocyte disorganized, abnormal
ZP:0007553	endoplasmic reticulum lumen chondrocyte distended, abnormal
ZP:0007554	respiratory electron transport chain disrupted, abnormal
ZP:0007555	nucleus nucleate erythrocyte increased size, abnormal
ZP:0007556	myotome decreased width, abnormal
ZP:0007557	muscle cell myotome increased length, abnormal
ZP:0007558	I band skeletal muscle cell disorganized, abnormal
ZP:0007559	branched-chain amino acid metabolic process disrupted, abnormal
ZP:0007560	central nervous system functionality, abnormal
ZP:0007561	spinal cord hypoplastic, abnormal
ZP:0007562	epithelial cell pronephros morphology, abnormal
ZP:0007563	pronephric glomerulus structure, abnormal
ZP:0007564	cilium Kupffer's vesicle decreased functionality, abnormal
ZP:0007565	cilium central canal decreased length, abnormal
ZP:0007566	cilium central canal decreased functionality, abnormal
ZP:0007567	vesicle-mediated transport process quality, abnormal
ZP:0007568	cytoplasm liver and biliary system composition, abnormal
ZP:0007569	epithelial cell liver and biliary system structure, abnormal
ZP:0007570	cytoplasm enterocyte composition, abnormal
ZP:0007571	Golgi stack enterocyte dilated, abnormal
ZP:0007572	stereocilium hair cell anterior macula malformed, abnormal
ZP:0007573	stereocilium hair cell anterior macula decreased amount, abnormal
ZP:0007574	hatching decreased occurrence, abnormal
ZP:0007576	Z disc skeletal muscle absent, abnormal
ZP:0007577	T-tubule skeletal muscle absent, abnormal
ZP:0007578	T-tubule skeletal muscle disorganized, abnormal
ZP:0007579	muscle cell displaced to nucleus central region muscle cell, abnormal
ZP:0007580	spinal cord has fewer parts of type CNS neuron (sensu Vertebrata), abnormal
ZP:0007582	endothelial tip cell intersegmental vessel increased width, abnormal
ZP:0007583	vascular sprouts has extra parts of type endothelial tip cell, abnormal
ZP:0007585	convergent extension involved in gastrulation delayed, abnormal
ZP:0007586	sympathetic ganglion development disrupted, abnormal
ZP:0007587	angioblast cell migration from lateral mesoderm to midline delayed, abnormal
ZP:0007588	angioblastic mesenchymal cell vascular cord mislocalised laterally, abnormal
ZP:0007589	angioblastic mesenchymal cell vascular cord decreased amount, abnormal
ZP:0007590	cell median fin fold circular, abnormal
ZP:0007591	ventral fin fold rough, abnormal
ZP:0007592	mitochondrial electron transport, NADH to ubiquinone decreased rate, abnormal
ZP:0007593	T-tubule fast muscle cell unlumenized, abnormal
ZP:0007594	blood vessel morphogenesis delayed, abnormal
ZP:0007595	ventral aorta morphology, abnormal
ZP:0007596	ceratobranchial cartilage decreased distance ceratobranchial cartilage, abnormal
ZP:0007597	ceratobranchial cartilage dislocated ceratobranchial cartilage, abnormal
ZP:0007598	pharyngeal vasculature morphology, abnormal
ZP:0007599	aortic arch 5 unlumenized, abnormal
ZP:0007600	aortic arch 6 unlumenized, abnormal
ZP:0007601	primary head sinus morphology, abnormal
ZP:0007603	epithalamus development process quality, abnormal
ZP:0007604	forebrain neuron differentiation decreased process quality, abnormal
ZP:0007605	cell pretectum mislocalised, abnormal
ZP:0007607	dorsal thalamus fused with pretectum, abnormal
ZP:0007608	cell dorsal thalamus mislocalised, abnormal
ZP:0007610	GABAergic neuron dorsal thalamus mislocalised posteriorly, abnormal
ZP:0007611	goblet cell cellular quality, abnormal
ZP:0007612	goblet cell immature, abnormal
ZP:0007613	secretory granule goblet cell decreased amount, abnormal
ZP:0007614	intermediate cell mass of mesoderm decreased size, abnormal
ZP:0007615	pharynx hemorrhagic, abnormal
ZP:0007616	vasculature hemorrhagic, abnormal
ZP:0007617	whole organism fragile, abnormal
ZP:0007618	cell post-vent region apoptotic, abnormal
ZP:0007619	cardiac muscle cell heart disorganized, abnormal
ZP:0007620	muscle deformed, abnormal
ZP:0007621	sarcomere skeletal muscle cell morphology, abnormal
ZP:0007622	M band skeletal muscle cell morphology, abnormal
ZP:0007623	midbrain hindbrain boundary decreased distance otic vesicle, abnormal
ZP:0007624	otic vesicle increased distance otic vesicle, abnormal
ZP:0007625	cilium pronephros paralysed, abnormal
ZP:0007626	pronephros decreased process quality cilium-dependent cell motility, abnormal
ZP:0007627	leukocyte chemotaxis process quality, abnormal
ZP:0007628	leukocyte morphology, abnormal
ZP:0007629	leukocyte cellular motility, abnormal
ZP:0007630	pseudopodium leukocyte increased amount, abnormal
ZP:0007631	anterior region forebrain non-functional, abnormal
ZP:0007632	notochord absent, abnormal
ZP:0007633	glandular epithelial cell development heterochronic, abnormal
ZP:0007634	feeding behavior quality, abnormal
ZP:0007635	metabolic process increased rate, abnormal
ZP:0007636	regulation of phosphatidylinositol 3-kinase signaling disrupted, abnormal
ZP:0007637	TOR signaling occurrence, abnormal
ZP:0007638	epithelial cell proliferation decreased rate, abnormal
ZP:0007639	whole organism increased acidity, abnormal
ZP:0007640	intestine increased diameter, abnormal
ZP:0007641	goblet cell intestine present, abnormal
ZP:0007642	intestinal epithelium flattened, abnormal
ZP:0007643	brush border intestinal epithelium increased height, abnormal
ZP:0007644	epithelial cell intestinal epithelium increased amount, abnormal
ZP:0007645	oocyte development delayed, abnormal
ZP:0007646	RNA 3' uridylation increased occurrence, abnormal
ZP:0007647	embryonic pectoral fin morphogenesis arrested, abnormal
ZP:0007648	cell division decreased occurrence, abnormal
ZP:0007649	hepatocyte proliferation disrupted, abnormal
ZP:0007651	brain decreased occurrence branching morphogenesis of a nerve, abnormal
ZP:0007652	telencephalon disorganized, abnormal
ZP:0007653	neuron telencephalon decreased amount, abnormal
ZP:0007654	dorsal region neural plate apoptotic, abnormal
ZP:0007655	neuron neural tube decreased amount, abnormal
ZP:0007656	neuronal stem cell apoptotic, abnormal
ZP:0007657	axon motor neuron decreased amount, abnormal
ZP:0007658	lymph vessel morphogenesis disrupted, abnormal
ZP:0007659	whole organism lacks all parts of type lymphangioblast cord, abnormal
ZP:0007660	intersegmental vessel increased amount, abnormal
ZP:0007661	neural crest cell development decreased process quality, abnormal
ZP:0007662	embryonic camera-type eye morphogenesis decreased process quality, abnormal
ZP:0007663	cornea disorganized, abnormal
ZP:0007664	cranial neural crest physical object quality, abnormal
ZP:0007665	neurocranial trabecula absent, abnormal
ZP:0007666	yolk increased accumulation blood, abnormal
ZP:0007667	atrium increased accumulation blood, abnormal
ZP:0007668	ventricular myocardium hypoplastic, abnormal
ZP:0007669	cilium movement disrupted, abnormal
ZP:0007670	axonemal dynein complex Kupffer's vesicle decreased amount, abnormal
ZP:0007671	cilium Kupffer's vesicle decreased coordination, abnormal
ZP:0007672	axoneme Kupffer's vesicle structure, abnormal
ZP:0007673	neuronal action potential ictal, abnormal
ZP:0007674	swimming process quality, abnormal
ZP:0007675	anterior region pronephros dilated, abnormal
ZP:0007676	motile cilium pronephros immobile, abnormal
ZP:0007677	ciliary rootlet ciliated cell absent, abnormal
ZP:0007678	fucose biosynthetic process disrupted, abnormal
ZP:0007679	glycosylation decreased occurrence, abnormal
ZP:0007680	dorsolateral motor nucleus of vagal nerve mislocalised medially, abnormal
ZP:0007681	dorsolateral motor nucleus of vagal nerve fused with dorsolateral motor nucleus of vagal nerve, abnormal
ZP:0007682	secondary motor neuron irregular spatial pattern, abnormal
ZP:0007683	axon secondary motor neuron morphology, abnormal
ZP:0007684	cardiac muscle cell atrioventricular canal morphology, abnormal
ZP:0007685	otolith inner ear malformed, abnormal
ZP:0007686	sagitta malformed, abnormal
ZP:0007687	glomerulus development disrupted, abnormal
ZP:0007688	pronephric duct malformed, abnormal
ZP:0007689	pronephric glomerulus aplastic, abnormal
ZP:0007690	pronephric tubule aplastic, abnormal
ZP:0007691	intersegmental vessel decreased thickness, abnormal
ZP:0007692	trunk vasculature malformed, abnormal
ZP:0007693	skeletal muscle cell vacuolated, abnormal
ZP:0007694	intercalated disc cardiac muscle cell decreased thickness, abnormal
ZP:0007695	intercalated disc cardiac muscle cell decreased amount, abnormal
ZP:0007696	sarcomere cardiac muscle cell mislocalised, abnormal
ZP:0007697	nucleus retina increased size, abnormal
ZP:0007698	nucleus retina variability of shape, abnormal
ZP:0007699	sarcomere skeletal muscle decreased thickness, abnormal
ZP:0007700	Z disc skeletal muscle increased width, abnormal
ZP:0007701	lipid storage disrupted, abnormal
ZP:0007702	cell migration delayed, abnormal
ZP:0007703	hindbrain-spinal cord boundary formation disrupted, abnormal
ZP:0007704	hindbrain increased length, abnormal
ZP:0007709	trunk mesenchyme distended, abnormal
ZP:0007711	pancreas primordium mislocalised posteriorly, abnormal
ZP:0007719	pancreatic bud mislocalised posteriorly, abnormal
ZP:0007725	podocyte mislocalised posteriorly, abnormal
ZP:0007726	respiratory burst involved in inflammatory response disrupted, abnormal
ZP:0007727	iris perforate, abnormal
ZP:0007728	pupil morphology, abnormal
ZP:0007729	detection of muscle stretch process quality, abnormal
ZP:0007730	sarcomere organization decreased process quality, abnormal
ZP:0007731	myotome detached from myofibril vertical myoseptum, abnormal
ZP:0007732	Z disc skeletal muscle cell decreased amount, abnormal
ZP:0007733	Z disc cardiac muscle cell malformed, abnormal
ZP:0007734	skeletal muscle cell differentiation disrupted, abnormal
ZP:0007735	respiratory system development disrupted, abnormal
ZP:0007736	retinal neural layer absent, abnormal
ZP:0007737	gill filament malformed, abnormal
ZP:0007738	epithelium gill filament disorganized, abnormal
ZP:0007739	chondrocyte gill filament absent, abnormal
ZP:0007740	skeletal muscle cell curved, abnormal
ZP:0007741	nucleus skeletal muscle cell increased amount, abnormal
ZP:0007742	nucleus skeletal muscle cell increased diameter, abnormal
ZP:0007743	planar cell polarity pathway involved in axis elongation disrupted, abnormal
ZP:0007744	medial-lateral axis neural plate distended, abnormal
ZP:0007745	whole organism increased width, abnormal
ZP:0007746	anterior-posterior axis whole organism condensed, abnormal
ZP:0007747	whole organism oblong, abnormal
ZP:0007748	anterior-posterior axis whole organism elongated, abnormal
ZP:0007749	post-vent region increased thickness, abnormal
ZP:0007750	odontogenesis paedomorphic growth, abnormal
ZP:0007751	cartilage development delayed, abnormal
ZP:0007752	embryonic skeletal joint morphogenesis disrupted, abnormal
ZP:0007753	intermandibularis disorganized, abnormal
ZP:0007754	ceratobranchial 5 tooth immature, abnormal
ZP:0007755	ceratobranchial 5 tooth detached from ceratobranchial 5 bone, abnormal
ZP:0007756	cartilage tissue Meckel's cartilage decreased amount, abnormal
ZP:0007757	bony projection palatoquadrate arch decreased length, abnormal
ZP:0007758	ventral mandibular arch notched, abnormal
ZP:0007759	mesenchyme pharyngeal arch morphology, abnormal
ZP:0007760	joint pharyngeal arch increased amount, abnormal
ZP:0007761	hyosymplectic cartilage notched, abnormal
ZP:0007762	chondroblast pharyngeal arch cartilage disorganized, abnormal
ZP:0007763	joint mislocalised, abnormal
ZP:0007764	sternohyoid decreased length, abnormal
ZP:0007765	sternohyoid detached from bone tissue, abnormal
ZP:0007766	head muscle detached from bone element, abnormal
ZP:0007767	hyohyoideus inverted, abnormal
ZP:0007768	extracellular matrix chondroblast absent, abnormal
ZP:0007769	epidermis blistered, abnormal
ZP:0007770	anterior-posterior axis whole organism increased length, abnormal
ZP:0007771	lens cellularity, abnormal
ZP:0007772	retina process quality cell population proliferation, abnormal
ZP:0007773	mandibular arch skeleton shortened, abnormal
ZP:0007774	midbrain elongated, abnormal
ZP:0007775	retina degeneration, abnormal
ZP:0007776	myoseptum partially broken, abnormal
ZP:0007777	otolith formation disrupted, abnormal
ZP:0007779	defecation disrupted, abnormal
ZP:0007780	cortical granule exocytosis disrupted, abnormal
ZP:0007781	positive regulation of cortical granule exocytosis by positive regulation of cytosolic calcium ion concentration disrupted, abnormal
ZP:0007782	intestinal epithelial structure maintenance disrupted, abnormal
ZP:0007783	microtubule blastomere disorganized, abnormal
ZP:0007784	chorion soft, abnormal
ZP:0007785	microtubule marginal blastomere disorganized, abnormal
ZP:0007786	microtubule marginal blastomere sparse, abnormal
ZP:0007787	intestinal bulb lacks parts or has fewer parts of type intestinal villus, abnormal
ZP:0007788	muscle intestinal bulb degenerate, abnormal
ZP:0007789	blastodisc decreased size, abnormal
ZP:0007790	intestinal villus mid intestine increased circumference, abnormal
ZP:0007791	muscle mid intestine degenerate, abnormal
ZP:0007792	intestinal villus intestinal bulb epithelium increased circumference, abnormal
ZP:0007793	goblet cell intestinal bulb epithelium decreased amount, abnormal
ZP:0007794	goblet cell mid intestine epithelium decreased amount, abnormal
ZP:0007795	startle response increased process quality, abnormal
ZP:0007796	visual behavior decreased process quality, abnormal
ZP:0007797	swimming decreased occurrence, abnormal
ZP:0007798	light adaption decreased process quality, abnormal
ZP:0007799	regulation of dopamine receptor signaling pathway decreased process quality, abnormal
ZP:0007800	calcium ion import process quality, abnormal
ZP:0007801	liver decreased mass, abnormal
ZP:0007802	melanocyte myoseptum disorganized, abnormal
ZP:0007803	Meckel's cartilage disoriented, abnormal
ZP:0007804	ceratohyal cartilage fused with hypobranchial cartilage, abnormal
ZP:0007805	ethmoid cartilage curled, abnormal
ZP:0007806	ethmoid cartilage retracted, abnormal
ZP:0007807	subintestinal vein absent, abnormal
ZP:0007808	subintestinal vein decreased amount, abnormal
ZP:0007809	hematopoietic progenitor cell differentiation decreased functionality, abnormal
ZP:0007810	erythroid progenitor cell decreased amount, abnormal
ZP:0007811	thrombocyte increased amount, abnormal
ZP:0007812	hemoglobin complex erythroid lineage cell decreased amount, abnormal
ZP:0007814	myeloid lineage restricted progenitor cell increased amount, abnormal
ZP:0007815	angiogenic sprout decreased length, abnormal
ZP:0007816	angiogenic sprout decreased amount, abnormal
ZP:0007817	astrocyte hindbrain decreased amount, abnormal
ZP:0007818	facial nerve motor nucleus mislocalised laterally, abnormal
ZP:0007820	vagal lobe aplastic, abnormal
ZP:0007821	abducens motor nucleus aplastic, abnormal
ZP:0007822	pars anterior physical object quality, abnormal
ZP:0007823	floor plate rhombomere region increased width, abnormal
ZP:0007824	adenohypophysis wholly anterioralized, abnormal
ZP:0007825	trigeminal motor nucleus aplastic, abnormal
ZP:0007826	trigeminal motor nucleus mislocalised laterally, abnormal
ZP:0007827	prolactin secreting cell increased amount, abnormal
ZP:0007828	thyroid stimulating hormone secreting cell increased amount, abnormal
ZP:0007829	posterior intestine undulate, abnormal
ZP:0007830	posterior intestine distended, abnormal
ZP:0007831	posterior intestine cystic, abnormal
ZP:0007832	mesenchyme posterior intestine distended, abnormal
ZP:0007833	mesenchymal cell posterior intestine morphology, abnormal
ZP:0007834	mesenchymal cell posterior intestine increased amount, abnormal
ZP:0007835	mesenchymal cell posterior intestine degenerate, abnormal
ZP:0007836	smooth muscle cell posterior intestine irregular spatial pattern, abnormal
ZP:0007837	posterior intestine epithelium morphology, abnormal
ZP:0007838	posterior intestine epithelium disorganized, abnormal
ZP:0007839	posterior intestine epithelium stratification, abnormal
ZP:0007840	basement membrane posterior intestine epithelium morphology, abnormal
ZP:0007841	myosin complex smooth muscle morphology, abnormal
ZP:0007842	regulation of myeloid leukocyte differentiation disrupted, abnormal
ZP:0007843	blood vasculature morphology, abnormal
ZP:0007844	posterior lateral mesoderm morphology, abnormal
ZP:0007845	spinal cord decreased thickness, abnormal
ZP:0007846	pancreatic B cell mislocalised, abnormal
ZP:0007847	peripheral nervous system neuron axonogenesis decreased occurrence, abnormal
ZP:0007848	double-strand break repair via single-strand annealing decreased frequency, abnormal
ZP:0007849	cysteine-type peptidase activity increased process quality, abnormal
ZP:0007850	regulation of autophagy disrupted, abnormal
ZP:0007851	melanocyte apoptotic process increased occurrence, abnormal
ZP:0007852	retinal neural layer detached from retinal pigmented epithelium, abnormal
ZP:0007853	chromatin retinal neural layer condensed, abnormal
ZP:0007854	liver hyperplastic, abnormal
ZP:0007855	chromatin retinal pigmented epithelium condensed, abnormal
ZP:0007856	melanocyte retinal pigmented epithelium immature, abnormal
ZP:0007857	melanocyte head decreased pigmentation, abnormal
ZP:0007858	iridophore head decreased amount, abnormal
ZP:0007859	melanosome melanophore stripe morphology, abnormal
ZP:0007860	photoreceptor outer segment layer collapsed, abnormal
ZP:0007861	photoreceptor outer segment layer displaced to photoreceptor outer segment membrane vacuolar lumen photoreceptor outer segment layer, abnormal
ZP:0007862	retinal rod cell photoreceptor outer segment layer vacuolated, abnormal
ZP:0007863	retinal rod cell photoreceptor outer segment layer collapsed, abnormal
ZP:0007864	larval melanophore stripe decreased pigmentation, abnormal
ZP:0007865	melanocyte larval melanophore stripe decreased pigmentation, abnormal
ZP:0007866	vacuole dorsal larval melanophore stripe increased amount, abnormal
ZP:0007867	melanosome dorsal larval melanophore stripe decreased amount, abnormal
ZP:0007868	nucleus retinal rod cell mislocalised, abnormal
ZP:0007869	Muller cell hypertrophic, abnormal
ZP:0007870	regulation of cell projection assembly process quality, abnormal
ZP:0007871	anterior axial hypoblast decreased cellular motility, abnormal
ZP:0007872	bleb anterior axial hypoblast increased size, abnormal
ZP:0007873	cardiac ventricle quality, abnormal
ZP:0007874	myofibril cardiac ventricle decreased thickness, abnormal
ZP:0007875	sarcomere cardiac ventricle irregular spatial pattern, abnormal
ZP:0007876	Z disc cardiac ventricle morphology, abnormal
ZP:0007877	atrium collapsed, abnormal
ZP:0007878	myocardium uncoordinated, abnormal
ZP:0007879	melanosome transport increased duration, abnormal
ZP:0007880	anatomical axis whole organism asymmetrical, abnormal
ZP:0007881	cell division disrupted, abnormal
ZP:0007882	mRNA splicing, via endonucleolytic cleavage and ligation process quality, abnormal
ZP:0007883	forerunner cell group position, abnormal
ZP:0007884	shield morphology, abnormal
ZP:0007885	dolichol-linked oligosaccharide biosynthetic process disrupted, abnormal
ZP:0007886	oligosaccharide-lipid intermediate biosynthetic process disrupted, abnormal
ZP:0007887	head development abnormal, abnormal
ZP:0007888	midbrain hindbrain boundary neural tube cleft, abnormal
ZP:0007889	trunk shortened, abnormal
ZP:0007890	ventricular system morphology, abnormal
ZP:0007891	digestive system inverted, abnormal
ZP:0007892	digestive system centered, abnormal
ZP:0007893	epithalamus bilateral, abnormal
ZP:0007894	epithalamus inverted, abnormal
ZP:0007895	epithalamus aplastic, abnormal
ZP:0007896	negative regulation of TOR signaling increased occurrence, abnormal
ZP:0007897	pectoral fin deformed, abnormal
ZP:0007898	cell pectoral fin decreased size, abnormal
ZP:0007899	cell pectoral fin condensed, abnormal
ZP:0007900	basihyal cartilage deformed, abnormal
ZP:0007901	hypobranchial cartilage decreased thickness, abnormal
ZP:0007902	chromosome cell disorganized, abnormal
ZP:0007903	mitotic spindle cell deformed, abnormal
ZP:0007904	central nervous system development process quality, abnormal
ZP:0007905	embryonic camera-type eye formation disrupted, abnormal
ZP:0007908	posterior lateral line neuromast has fewer parts of type kinocilium neuromast, abnormal
ZP:0007909	stereocilium posterior lateral line neuromast decreased length, abnormal
ZP:0007910	kinocilium posterior lateral line neuromast decreased length, abnormal
ZP:0007911	pharyngeal pouch decreased length, abnormal
ZP:0007912	pharyngeal pouch increased width, abnormal
ZP:0007913	pharyngeal epithelium disorganized, abnormal
ZP:0007914	pharyngeal arch 3-7 lacks all parts of type ceratobranchial 2 cartilage, abnormal
ZP:0007915	pharyngeal arch 3-7 lacks all parts of type ceratobranchial 3 cartilage, abnormal
ZP:0007916	pharyngeal arch 3-7 lacks all parts of type ceratobranchial 4 cartilage, abnormal
ZP:0007917	pharyngeal arch 3-7 lacks all parts of type ceratobranchial 1 cartilage, abnormal
ZP:0007918	pharyngeal arch 3-7 lacks all parts of type ceratobranchial 5 cartilage, abnormal
ZP:0007919	cranial neural crest cell decreased amount, abnormal
ZP:0007920	Kupffer's vesicle hypoplastic, abnormal
ZP:0007921	cilium Kupffer's vesicle increased length, abnormal
ZP:0007923	somite apoptotic, abnormal
ZP:0007924	thigmotaxis decreased functionality, abnormal
ZP:0007926	heart apoptotic, abnormal
ZP:0007927	Z disc heart blurry, abnormal
ZP:0007928	sarcolemma heart edematous, abnormal
ZP:0007929	somite shortened, abnormal
ZP:0007930	myocardium degenerate, abnormal
ZP:0007931	presumptive mesoderm decreased length, abnormal
ZP:0007933	mitochondrion cardiac muscle cell vacuolated, abnormal
ZP:0007934	midbrain hemorrhagic, abnormal
ZP:0007935	heart dysplastic, abnormal
ZP:0007936	myofibril skeletal muscle undulate, abnormal
ZP:0007937	myofibril skeletal muscle loose, abnormal
ZP:0007940	osteoblast differentiation process quality, abnormal
ZP:0007941	intramembranous ossification decreased rate, abnormal
ZP:0007942	endochondral ossification decreased occurrence, abnormal
ZP:0007943	osteoclast differentiation delayed, abnormal
ZP:0007944	osteoblast proliferation disrupted, abnormal
ZP:0007945	swim bladder morphogenesis disrupted, abnormal
ZP:0007946	swim bladder formation disrupted, abnormal
ZP:0007947	swim bladder hypoplastic, abnormal
ZP:0007948	mesenchyme swim bladder decreased size, abnormal
ZP:0007949	mesenchyme swim bladder disorganized, abnormal
ZP:0007950	smooth muscle swim bladder aplastic, abnormal
ZP:0007951	mesothelial cell swim bladder decreased amount, abnormal
ZP:0007952	mesenchyme gut decreased size, abnormal
ZP:0007953	neuron gut absent, abnormal
ZP:0007954	opercle fused with subopercle, abnormal
ZP:0007955	opercle fused with interopercle, abnormal
ZP:0007956	dorsal-ventral axis opercle decreased length, abnormal
ZP:0007957	opercle has fewer parts of type antero-ventral margin bone tissue, abnormal
ZP:0007958	opercle has fewer parts of type antero-ventral margin osteoblast, abnormal
ZP:0007959	postero-ventral margin opercle decreased length, abnormal
ZP:0007960	opercle has fewer parts of type postero-ventral margin osteoblast, abnormal
ZP:0007961	interopercle fused with subopercle, abnormal
ZP:0007962	osteoblast Meckel's cartilage decreased amount, abnormal
ZP:0007963	osteoclast pharyngeal arch 7 skeleton undifferentiated, abnormal
ZP:0007964	osteoclast pharyngeal arch 7 skeleton poorly differentiated, abnormal
ZP:0007965	anterior chamber swim bladder absent, abnormal
ZP:0007966	ceratohyal cartilage cartilaginous, abnormal
ZP:0007967	osteoblast ceratohyal cartilage absent, abnormal
ZP:0007968	pneumatic duct decreased size, abnormal
ZP:0007969	intramembranous bone has extra parts of type branchiostegal ray, abnormal
ZP:0007970	gut epithelium decreased size, abnormal
ZP:0007971	swim bladder bud hypoplastic, abnormal
ZP:0007972	regulation of transcription from RNA polymerase II promoter in response to stress disrupted, abnormal
ZP:0007973	cardiac ventricle increased distance atrium, abnormal
ZP:0007974	somite immature, abnormal
ZP:0007975	blood coagulation disrupted, abnormal
ZP:0007976	intersegmental vein physical quality, abnormal
ZP:0007977	whole organism kinked, abnormal
ZP:0007978	caudal vein plexus branchiness, abnormal
ZP:0007980	thrombocyte decreased functionality, abnormal
ZP:0007981	posterior kidney cystic, abnormal
ZP:0007982	skeletal muscle tissue development process quality, abnormal
ZP:0007983	muscle cell myotome decreased length, abnormal
ZP:0007984	nucleate erythrocyte pericardium decreased amount, abnormal
ZP:0007985	heart mislocalised medially, abnormal
ZP:0007986	myocardium position, abnormal
ZP:0007987	phosphatidylinositol dephosphorylation disrupted, abnormal
ZP:0007988	trunk musculature decreased size, abnormal
ZP:0007989	skeletal muscle cell hypotrophic, abnormal
ZP:0007990	skeletal muscle cell decreased functionality, abnormal
ZP:0007991	skeletal muscle cell separated from skeletal muscle cell, abnormal
ZP:0007992	nucleus skeletal muscle cell increased size, abnormal
ZP:0007993	sarcoplasmic reticulum skeletal muscle cell morphology, abnormal
ZP:0007994	T-tubule skeletal muscle cell morphology, abnormal
ZP:0007995	T-tubule skeletal muscle cell disorganized, abnormal
ZP:0007996	perinuclear region of cytoplasm skeletal muscle cell disorganized, abnormal
ZP:0007997	ceratobranchial 3 cartilage decreased length, abnormal
ZP:0007998	ceratobranchial 4 cartilage decreased length, abnormal
ZP:0007999	ceratobranchial 5 cartilage decreased length, abnormal
ZP:0008000	T cell differentiation arrested, abnormal
ZP:0008001	alpha-beta T cell differentiation arrested, abnormal
ZP:0008002	thymus increased occurrence apoptotic process, abnormal
ZP:0008003	T cell aplastic/hypoplastic, abnormal
ZP:0008004	alpha-beta T cell aplastic/hypoplastic, abnormal
ZP:0008007	voltage-gated sodium channel complex spinal cord decreased amount, abnormal
ZP:0008008	voltage-gated sodium channel complex posterior lateral line nerve decreased amount, abnormal
ZP:0008009	node of Ranvier posterior lateral line nerve increased length, abnormal
ZP:0008010	head muscle absent, abnormal
ZP:0008011	olfactory pit obstructed, abnormal
ZP:0008012	cilium olfactory pit non-functional, abnormal
ZP:0008013	cilium olfactory pit decreased functionality, abnormal
ZP:0008014	gall bladder lacks parts or has fewer parts of type cell, abnormal
ZP:0008015	intrahepatic bile duct decreased functionality, abnormal
ZP:0008016	extrahepatic duct decreased amount, abnormal
ZP:0008017	endocardial ring absent, abnormal
ZP:0008018	cardiac muscle cell apoptotic, abnormal
ZP:0008019	cardiac muscle cell elongated, abnormal
ZP:0008020	hemoglobin binding disrupted, abnormal
ZP:0008021	yolk autofluorescence, abnormal
ZP:0008022	whole organism autofluorescence, abnormal
ZP:0008023	post-vent vasculature autofluorescence, abnormal
ZP:0008024	nucleate erythrocyte autofluorescence, abnormal
ZP:0008025	cell lens nucleate quality, abnormal
ZP:0008026	eye lacks all parts of type retinal photoreceptor layer, abnormal
ZP:0008027	atrium lacks parts or has fewer parts of type sarcomere cardiac muscle cell, abnormal
ZP:0008028	atrium lacks parts or has fewer parts of type Z disc cardiac muscle cell, abnormal
ZP:0008029	ventricular myocardium decreased size, abnormal
ZP:0008030	ventricular myocardium decreased volume, abnormal
ZP:0008031	ventricular myocardium decreased occurrence cardiac chamber ballooning, abnormal
ZP:0008032	skeletal muscle lacks parts or has fewer parts of type myofibril slow muscle cell, abnormal
ZP:0008033	myofibril skeletal muscle morphology, abnormal
ZP:0008034	contractile fiber skeletal muscle decreased size, abnormal
ZP:0008035	myofibril cardiac muscle disorganized, abnormal
ZP:0008036	slow muscle cell decreased diameter, abnormal
ZP:0008037	nucleus slow muscle cell circular, abnormal
ZP:0008038	Z disc cardiac muscle cell decreased size, abnormal
ZP:0008039	Z disc cardiac muscle cell increased width, abnormal
ZP:0008040	Z disc cardiac muscle cell broken, abnormal
ZP:0008041	whole organism circular, abnormal
ZP:0008042	optokinetic behavior process quality, abnormal
ZP:0008043	optomotor response disrupted, abnormal
ZP:0008044	lens increased distance retinal pigmented epithelium, abnormal
ZP:0008045	lens increased distance iridophore, abnormal
ZP:0008046	eye degree of pigmentation, abnormal
ZP:0008047	neoplasm eye protruding, abnormal
ZP:0008048	retinal pigmented epithelium spatial pattern, abnormal
ZP:0008049	retinal pigmented epithelium organization quality, abnormal
ZP:0008050	retinal pigmented epithelium dislocated lens, abnormal
ZP:0008051	optic chiasm absent, abnormal
ZP:0008052	retinal ganglion cell ipsilateral to axon ipsilateral region brain, abnormal
ZP:0008053	habenula development process quality, abnormal
ZP:0008054	regulation of dendrite morphogenesis process quality, abnormal
ZP:0008055	dendrite ventral habenular nucleus increased volume, abnormal
ZP:0008056	axonogenesis neotenous growth, abnormal
ZP:0008057	anterior region notochord undifferentiated, abnormal
ZP:0008058	medial longitudinal fasciculus morphology, abnormal
ZP:0008059	axon medial longitudinal fasciculus branched, abnormal
ZP:0008060	vertical myoseptum morphology, abnormal
ZP:0008061	retinal ganglion cell poorly differentiated, abnormal
ZP:0008062	cell body retinal ganglion cell mislocalised, abnormal
ZP:0008063	apoptotic process delayed, abnormal
ZP:0008064	skeletal muscle tissue development decreased process quality, abnormal
ZP:0008065	myotome structure, abnormal
ZP:0008066	myotome decreased size, abnormal
ZP:0008067	myotome dystrophic, abnormal
ZP:0008068	extracellular matrix myotome structure, abnormal
ZP:0008069	skeletal muscle cell retracted, abnormal
ZP:0008070	skeletal muscle cell dystrophic, abnormal
ZP:0008071	skeletal muscle cell detached from myofibril muscle tendon junction myotome, abnormal
ZP:0008072	skeletal muscle cell detached from myofibril myofibril skeletal muscle cell, abnormal
ZP:0008073	M band skeletal muscle cell disorganized, abnormal
ZP:0008074	myeloid leukocyte differentiation process quality, abnormal
ZP:0008075	thrombocyte differentiation process quality, abnormal
ZP:0008076	T cell differentiation delayed, abnormal
ZP:0008077	neutrophil differentiation process quality, abnormal
ZP:0008078	hematopoietic stem cell migration process quality, abnormal
ZP:0008079	cranial ganglion has fewer parts of type sensory neuron, abnormal
ZP:0008080	hindbrain lacks all parts of type fourth ventricle, abnormal
ZP:0008081	hindbrain has fewer parts of type serotonergic neuron, abnormal
ZP:0008082	blood island aplastic, abnormal
ZP:0008083	forebrain has fewer parts of type dopaminergic neuron, abnormal
ZP:0008084	midbrain deformed, abnormal
ZP:0008085	locus coeruleus has fewer parts of type norepinephrine secreting cell, abnormal
ZP:0008086	exocrine pancreas increased amount, abnormal
ZP:0008087	parapineal organ aplastic, abnormal
ZP:0008088	anterior pancreatic bud increased amount, abnormal
ZP:0008089	sympathetic nervous system has fewer parts of type norepinephrine secreting cell, abnormal
ZP:0008090	neuron hindbrain commissure decreased amount, abnormal
ZP:0008091	hepatocyte morphology, abnormal
ZP:0008092	cilium Kupffer's vesicle symmetry, abnormal
ZP:0008093	portion of organism substance Kupffer's vesicle decreased fluid flow, abnormal
ZP:0008094	portion of organism substance Kupffer's vesicle circling direction, abnormal
ZP:0008095	cell Kupffer's vesicle shape, abnormal
ZP:0008096	cell Kupffer's vesicle structure, abnormal
ZP:0008097	cell Kupffer's vesicle cellular quality, abnormal
ZP:0008098	pancreas symmetry, abnormal
ZP:0008099	apical side cell increased width, abnormal
ZP:0008100	apical surface cell increased size, abnormal
ZP:0008102	convergent extension process quality, abnormal
ZP:0008103	somite broad, abnormal
ZP:0008104	cilium pronephric tubule increased length, abnormal
ZP:0008105	rhodopsin metabolic process disrupted, abnormal
ZP:0008106	photoreceptor inner segment layer structure, abnormal
ZP:0008107	cilium olfactory pit disorganized, abnormal
ZP:0008108	filamentous actin somite disorganized, abnormal
ZP:0008110	brain morphogenesis decreased process quality, abnormal
ZP:0008111	tectal ventricle hydrocephalic, abnormal
ZP:0008112	ventral wall of dorsal aorta morphology, abnormal
ZP:0008113	eye agenesis, abnormal
ZP:0008114	forebrain agenesis, abnormal
ZP:0008115	midbrain agenesis, abnormal
ZP:0008116	vertical myoseptum obtuse angle to vertical myoseptum, abnormal
ZP:0008117	myofibril myotome disorganized, abnormal
ZP:0008118	motor neuron spatial pattern, abnormal
ZP:0008119	motor neuron defasciculated, abnormal
ZP:0008120	swimming behavior behavioral quality of a process, abnormal
ZP:0008121	skeletal muscle cell has extra parts of type membrane skeletal muscle cell, abnormal
ZP:0008122	sarcoplasmic reticulum skeletal muscle cell dilated, abnormal
ZP:0008123	sarcoplasmic reticulum skeletal muscle cell swollen, abnormal
ZP:0008124	T-tubule skeletal muscle cell dilated, abnormal
ZP:0008125	cell lens morphology, abnormal
ZP:0008126	cell lens decreased length, abnormal
ZP:0008127	cell lens vacuolated, abnormal
ZP:0008128	synapse assembly disrupted, abnormal
ZP:0008129	detection of light stimulus involved in visual perception disrupted, abnormal
ZP:0008130	postsynaptic density assembly disrupted, abnormal
ZP:0008131	synapse retinal outer plexiform layer disorganized, abnormal
ZP:0008132	kinocilium auditory receptor cell bent, abnormal
ZP:0008133	retinal cone cell detached from cytoskeleton of presynaptic active zone postsynaptic density retinal outer plexiform layer, abnormal
ZP:0008134	posterior cardinal vein absent, abnormal
ZP:0008135	fibroblast growth factor receptor signaling pathway decreased process quality, abnormal
ZP:0008136	cell-cell adhesion mediated by cadherin decreased process quality, abnormal
ZP:0008137	endodermal cell mislocalised, abnormal
ZP:0008138	glycosphingolipid biosynthetic process process quality, abnormal
ZP:0008139	hindbrain increased occurrence cell death, abnormal
ZP:0008140	midbrain increased occurrence cell death, abnormal
ZP:0008141	caudal fin curved dorsal, abnormal
ZP:0008142	intersegmental vessel decreased process quality sprouting angiogenesis, abnormal
ZP:0008143	ethmoid cartilage immature, abnormal
ZP:0008144	pharyngeal arch 3 deformed, abnormal
ZP:0008145	pharyngeal arch 4 deformed, abnormal
ZP:0008146	pharyngeal arch 5 deformed, abnormal
ZP:0008147	pharyngeal arch 2 inverted, abnormal
ZP:0008148	nucleus yolk syncytial layer increased size, abnormal
ZP:0008149	nucleus yolk syncytial layer decreased size, abnormal
ZP:0008150	nucleus yolk syncytial layer mislocalised, abnormal
ZP:0008151	nucleus yolk syncytial layer dispersed, abnormal
ZP:0008152	marginal blastomere necrotic, abnormal
ZP:0008153	somitogenesis decreased process quality, abnormal
ZP:0008154	neural tube formation decreased process quality, abnormal
ZP:0008155	convergent extension involved in gastrulation decreased process quality, abnormal
ZP:0008156	neural tube has extra parts of type central canal, abnormal
ZP:0008157	cell neural tube disorganized, abnormal
ZP:0008158	Meckel's cartilage decreased width, abnormal
ZP:0008159	Meckel's cartilage sharp, abnormal
ZP:0008160	ceratohyal cartilage mislocalised dorsally, abnormal
ZP:0008162	dorsal longitudinal anastomotic vessel immature, abnormal
ZP:0008163	neural crest cell migration decreased occurrence, abnormal
ZP:0008164	pigment cell post-vent region decreased amount, abnormal
ZP:0008165	trunk neural crest cell morphology, abnormal
ZP:0008166	neural crest cell increased amount, abnormal
ZP:0008167	retinal neural layer stratification, abnormal
ZP:0008168	eye spherical, abnormal
ZP:0008169	oral cavity decreased size, abnormal
ZP:0008170	nerve midbrain hindbrain boundary sparse, abnormal
ZP:0008172	glial cell (sensu Vertebrata) decreased amount, abnormal
ZP:0008173	regulation of synapse structure or activity disrupted, abnormal
ZP:0008174	synaptic vesicle hair cell decreased amount, abnormal
ZP:0008175	neuromast hair cell decreased functionality, abnormal
ZP:0008176	endoderm decreased amount, abnormal
ZP:0008177	positive regulation of apoptotic process disrupted, abnormal
ZP:0008178	brain hydrophilic, abnormal
ZP:0008179	proctodeum atretic, abnormal
ZP:0008180	pronephric duct increased thickness, abnormal
ZP:0008181	cilium pronephric duct curved, abnormal
ZP:0008182	pronephros obstructed, abnormal
ZP:0008183	cloacal chamber dilated, abnormal
ZP:0008184	cilium cloacal chamber absent, abnormal
ZP:0008185	cilium cloacal chamber decreased mobility, abnormal
ZP:0008186	heart tube left side of axis, abnormal
ZP:0008187	renal glomerulus dilated, abnormal
ZP:0008188	posterior pronephric duct bent, abnormal
ZP:0008189	otolith absent, abnormal
ZP:0008190	cilium or flagellum-dependent cell motility increased rate, abnormal
ZP:0008191	axonemal microtubule pronephros increased amount, abnormal
ZP:0008192	axonemal microtubule pronephros displaced, abnormal
ZP:0008193	cilium pronephric tubule decreased length, abnormal
ZP:0008194	glomerular visceral epithelial cell development disrupted, abnormal
ZP:0008195	glomerular basement membrane disorganized, abnormal
ZP:0008196	orbit edematous, abnormal
ZP:0008197	cell projection podocyte disorganized, abnormal
ZP:0008200	female sex determination arrested, abnormal
ZP:0008201	ovary absent, abnormal
ZP:0008202	testis neoplastic, abnormal
ZP:0008203	testis degeneration, abnormal
ZP:0008204	testis has fewer parts of type spermatocyte, abnormal
ZP:0008205	spermatocyte apoptotic, abnormal
ZP:0008206	cartilage condensation disrupted, abnormal
ZP:0008207	cranial cartilage pharyngeal arch decreased size, abnormal
ZP:0008209	brain bulbous, abnormal
ZP:0008210	cardiac muscle cell differentiation disrupted, abnormal
ZP:0008211	extracellular matrix atrium increased size, abnormal
ZP:0008212	cardiac muscle cell atrium decreased amount, abnormal
ZP:0008213	cardiac muscle cell atrioventricular canal mislocalised, abnormal
ZP:0008214	heart electrical conductivity, abnormal
ZP:0008215	fin musculature disorganized, abnormal
ZP:0008216	cephalic musculature hypoplastic, abnormal
ZP:0008217	cephalic musculature malformed, abnormal
ZP:0008218	atrium orientation cardiac ventricle, abnormal
ZP:0008219	myotome irregular spatial pattern, abnormal
ZP:0008220	muscle tendon junction myotome structure, abnormal
ZP:0008221	muscle tendon junction myotome irregular spatial pattern, abnormal
ZP:0008222	muscle tendon junction myotome decreased thickness, abnormal
ZP:0008223	myofibril myotome distributed, abnormal
ZP:0008224	myofibril myotome decreased amount, abnormal
ZP:0008225	whole organism uncoordinated, abnormal
ZP:0008226	skeletal muscle cell decreased mass, abnormal
ZP:0008227	slow muscle cell undulate, abnormal
ZP:0008228	slow muscle cell misaligned with slow muscle cell, abnormal
ZP:0008229	fast muscle cell variant shape, abnormal
ZP:0008230	pharynx lacks parts or has fewer parts of type pharyngeal arch 3-7, abnormal
ZP:0008231	melanophore stripe decreased thickness, abnormal
ZP:0008232	trunk vasculature increased branchiness, abnormal
ZP:0008233	cardiac muscle myosin thick filament assembly disrupted, abnormal
ZP:0008234	slow muscle cell disrupted myofibril assembly, abnormal
ZP:0008235	sarcomere fast muscle cell disorganized, abnormal
ZP:0008236	Z disc fast muscle cell disorganized, abnormal
ZP:0008237	M band fast muscle cell disorganized, abnormal
ZP:0008238	fast muscle cell disrupted sarcomere organization, abnormal
ZP:0008239	fast muscle cell disrupted striated muscle myosin thick filament assembly, abnormal
ZP:0008240	fast muscle cell disrupted muscle thin filament assembly, abnormal
ZP:0008241	sarcomere cardiac muscle cell absent, abnormal
ZP:0008242	shield increased size, abnormal
ZP:0008244	trunk truncated, abnormal
ZP:0008245	post-vent region branched, abnormal
ZP:0008246	outflow tract morphogenesis decreased process quality, abnormal
ZP:0008247	transforming growth factor beta receptor signaling pathway decreased process quality, abnormal
ZP:0008248	cardiac ventricle physical object quality, abnormal
ZP:0008249	cardiac ventricle has fewer parts of type ventricular endocardium, abnormal
ZP:0008250	bulbus arteriosus lacks all parts of type smooth muscle myoblast, abnormal
ZP:0008251	whole organism lacks all parts of type ventral aorta, abnormal
ZP:0008252	presumptive bulbus arteriosus hypoplastic, abnormal
ZP:0008253	presumptive cardiac ventricle heart tube decreased length, abnormal
ZP:0008254	pharyngeal vasculature hypoplastic, abnormal
ZP:0008255	pharyngeal vasculature malformed, abnormal
ZP:0008256	obsolete cell EVL morphology, abnormal
ZP:0008257	hematopoietic stem cell differentiation increased occurrence, abnormal
ZP:0008258	endothelial to hematopoietic transition increased occurrence, abnormal
ZP:0008259	blood increased accumulation blood island, abnormal
ZP:0008260	blood increased accumulation post-vent region, abnormal
ZP:0008261	blood increased accumulation vasculature, abnormal
ZP:0008262	caudal vein disorganized, abnormal
ZP:0008263	caudal vein functionality, abnormal
ZP:0008264	posterior cardinal vein functionality, abnormal
ZP:0008265	mouth structure, abnormal
ZP:0008266	central artery hemorrhagic, abnormal
ZP:0008267	hematopoietic stem cell ventral wall of dorsal aorta increased amount, abnormal
ZP:0008268	optic choroid vascular plexus hemorrhagic, abnormal
ZP:0008269	ventral fin fold aplastic, abnormal
ZP:0008270	renal filtration decreased process quality, abnormal
ZP:0008272	cilium pronephric duct kinked, abnormal
ZP:0008273	cilium pronephric duct shortened, abnormal
ZP:0008274	pronephric duct lacks parts or has fewer parts of type epithelial cell microvillus epithelial cell, abnormal
ZP:0008275	caudal fin curvature, abnormal
ZP:0008277	ventral fin fold edematous, abnormal
ZP:0008278	dorsal compartment pharyngeal pouch 1 morphology, abnormal
ZP:0008279	segmentation decreased rate, abnormal
ZP:0008280	anatomical axis whole organism decreased length, abnormal
ZP:0008281	neuromast development disrupted, abnormal
ZP:0008282	lateral line morphology, abnormal
ZP:0008283	regulation of neuron apoptotic process disrupted, abnormal
ZP:0008284	neuron brain absent, abnormal
ZP:0008285	axon central nervous system decreased amount, abnormal
ZP:0008286	neuronal stem cell decreased amount, abnormal
ZP:0008287	pronephric glomerulus physical object quality, abnormal
ZP:0008288	pronephric podocyte morphology, abnormal
ZP:0008289	cell projection pronephric podocyte disorganized, abnormal
ZP:0008290	apical junction complex neural tube structure, abnormal
ZP:0008291	photoreceptor cell decreased adhesivity, abnormal
ZP:0008292	cilium movement amplitude, abnormal
ZP:0008294	tubulin-glycine ligase activity arrested, abnormal
ZP:0008295	epiphysis bilateral symmetry, abnormal
ZP:0008296	cilium olfactory placode decreased length, abnormal
ZP:0008297	cilium olfactory placode malformed, abnormal
ZP:0008298	cilium olfactory placode decreased amount, abnormal
ZP:0008300	cilium pronephros direction, abnormal
ZP:0008301	cilium pronephros inverted, abnormal
ZP:0008303	inner ear lacks parts or has fewer parts of type otolith, abnormal
ZP:0008304	retinoid metabolic process disrupted, abnormal
ZP:0008305	presumptive neural retina decreased size, abnormal
ZP:0008306	forerunner cell group stratification, abnormal
ZP:0008307	fourth ventricle increased accumulation cerebral spinal fluid, abnormal
ZP:0008310	skeletal system morphogenesis disrupted, abnormal
ZP:0008311	telencephalon wholly dorsalized, abnormal
ZP:0008312	retina fused with cranial nerve II, abnormal
ZP:0008313	gill absent, abnormal
ZP:0008314	semicircular canal quality, abnormal
ZP:0008315	pharyngeal arch 3 skeleton absent, abnormal
ZP:0008316	palatoquadrate arch morphology, abnormal
ZP:0008317	ventral mandibular arch fused with palatoquadrate arch, abnormal
ZP:0008318	pharyngeal arch 2 skeleton inverted, abnormal
ZP:0008319	palatoquadrate cartilage quality, abnormal
ZP:0008320	ceratohyal cartilage quality, abnormal
ZP:0008321	ceratohyal cartilage kinked, abnormal
ZP:0008322	brain morphogenesis process quality, abnormal
ZP:0008323	MAP kinase activity disrupted, abnormal
ZP:0008324	MAP kinase activity increased occurrence, abnormal
ZP:0008325	angiogenic sprout dorsal aorta immature, abnormal
ZP:0008326	vascular sprouts posterior cardinal vein absent, abnormal
ZP:0008327	vascular sprouts posterior cardinal vein decreased amount, abnormal
ZP:0008328	inner ear morphogenesis decreased process quality, abnormal
ZP:0008329	camera-type eye morphogenesis decreased process quality, abnormal
ZP:0008330	kidney morphogenesis decreased process quality, abnormal
ZP:0008331	Kupffer's vesicle lacks all parts of type cilium ciliated epithelial cell, abnormal
ZP:0008332	pronephric duct lacks parts or has fewer parts of type cilium ciliated epithelial cell, abnormal
ZP:0008333	pronephros dilated, abnormal
ZP:0008334	gamma-delta T cell differentiation arrested, abnormal
ZP:0008335	ventral wall of dorsal aorta decreased process quality hematopoietic stem cell differentiation, abnormal
ZP:0008336	gamma-delta T cell aplastic/hypoplastic, abnormal
ZP:0008337	pronephric duct morphogenesis disrupted, abnormal
ZP:0008338	epithelial tube formation disrupted, abnormal
ZP:0008339	pronephric duct structure, abnormal
ZP:0008342	phosphatidylcholine-retinol O-acyltransferase activity disrupted, abnormal
ZP:0008344	collagen fibril organization decreased process quality, abnormal
ZP:0008345	collagen metabolic process disrupted, abnormal
ZP:0008346	fin shape, abnormal
ZP:0008347	fin decreased length, abnormal
ZP:0008348	fin has fewer parts of type lepidotrichium, abnormal
ZP:0008349	fibrillar collagen trimer fin disorganized, abnormal
ZP:0008350	fibrillar collagen trimer centrum disorganized, abnormal
ZP:0008351	postcranial axial skeleton increased curvature, abnormal
ZP:0008352	lepidotrichium caudal fin decreased size, abnormal
ZP:0008353	ventral fin fold decreased length, abnormal
ZP:0008354	ventral fin fold undulate, abnormal
ZP:0008355	lepidotrichium anal fin decreased size, abnormal
ZP:0008356	lepidotrichium dorsal fin decreased size, abnormal
ZP:0008357	pelvic fin decreased size, abnormal
ZP:0008358	vertebra shape, abnormal
ZP:0008359	vertebra increased mass density, abnormal
ZP:0008360	lepidotrichium undulate, abnormal
ZP:0008361	lepidotrichium broken, abnormal
ZP:0008362	lepidotrichium fused with lepidotrichium, abnormal
ZP:0008363	osteoblast cuboid, abnormal
ZP:0008364	post-anal tail morphogenesis delayed, abnormal
ZP:0008365	liver development arrested, abnormal
ZP:0008366	liver development having decreased processual parts cell population proliferation, abnormal
ZP:0008367	swim bladder development having decreased processual parts cell population proliferation, abnormal
ZP:0008368	liver increased variability of size, abnormal
ZP:0008369	gall bladder morphology, abnormal
ZP:0008370	gall bladder absent, abnormal
ZP:0008371	extrahepatic duct morphology, abnormal
ZP:0008372	extrahepatic duct decreased size, abnormal
ZP:0008373	neuron brain increased amount, abnormal
ZP:0008374	diencephalon hypoplastic, abnormal
ZP:0008375	forebrain asymmetrical, abnormal
ZP:0008376	midbrain hypoplastic, abnormal
ZP:0008377	white matter spatial pattern, abnormal
ZP:0008378	cardiac ventricle mislocalised, abnormal
ZP:0008379	yolk lacks parts or has fewer parts of type granulocyte, abnormal
ZP:0008380	yolk lacks parts or has fewer parts of type macrophage, abnormal
ZP:0008381	blood island lacks parts or has fewer parts of type granulocyte, abnormal
ZP:0008382	blood island lacks parts or has fewer parts of type macrophage, abnormal
ZP:0008383	histone methyltransferase activity (H4-K20 specific) disrupted, abnormal
ZP:0008384	shield increased width, abnormal
ZP:0008385	ossification increased magnitude, abnormal
ZP:0008386	skeletal system morphology, abnormal
ZP:0008387	exit from mitosis decreased occurrence, abnormal
ZP:0008388	retinal neural layer structure, abnormal
ZP:0008389	apical region retinal neural layer increased area, abnormal
ZP:0008390	cell retinal neural layer aggregated, abnormal
ZP:0008391	heart decreased object quality, abnormal
ZP:0008392	adherens junction retina increased size, abnormal
ZP:0008393	adherens junction retina distributed, abnormal
ZP:0008394	stomodeum shape, abnormal
ZP:0008395	proximal region neurocranial trabecula decreased length, abnormal
ZP:0008396	proximal region neurocranial trabecula truncated, abnormal
ZP:0008397	chondrocyte neurocranial trabecula circular, abnormal
ZP:0008398	chondrocyte neurocranial trabecula disorganized, abnormal
ZP:0008399	ethmoid cartilage has fewer parts of type chondrocyte, abnormal
ZP:0008400	ethmoid cartilage decreased occurrence chondrocyte proliferation, abnormal
ZP:0008401	chondrocyte ethmoid cartilage shape, abnormal
ZP:0008402	chondrocyte ethmoid cartilage disorganized, abnormal
ZP:0008403	postero-lateral region parachordal cartilage aplastic, abnormal
ZP:0008404	cranial neural crest cell lateralized, abnormal
ZP:0008405	dorsal region cranial neural crest cell mislocalised laterally, abnormal
ZP:0008406	hindbrain structure, abnormal
ZP:0008407	determination of left/right symmetry arrested, abnormal
ZP:0008408	response to wounding decreased process quality, abnormal
ZP:0008409	cilium Kupffer's vesicle absent, abnormal
ZP:0008410	cilium floor plate decreased amount, abnormal
ZP:0008411	motile cilium central canal immobile, abnormal
ZP:0008412	ventral fin fold absent, abnormal
ZP:0008413	pharyngeal arch decreased process quality chondrocyte differentiation, abnormal
ZP:0008414	pharyngeal arch decreased process quality transforming growth factor beta receptor signaling pathway, abnormal
ZP:0008415	pharyngeal arch decreased occurrence cell population proliferation, abnormal
ZP:0008416	chondrocyte pharyngeal arch differentiated, abnormal
ZP:0008417	floor plate deformed, abnormal
ZP:0008418	post-vent region hemorrhagic, abnormal
ZP:0008419	dopamine metabolic process disrupted, abnormal
ZP:0008420	pronephros deformed, abnormal
ZP:0008421	mid cerebral vein immature, abnormal
ZP:0008422	cell lymphangioblast cord decreased amount, abnormal
ZP:0008423	somite border curvature, abnormal
ZP:0008424	Kupffer's vesicle non-functional, abnormal
ZP:0008425	Kupffer's vesicle has fewer parts of type cilium inner dynein arm Kupffer's vesicle, abnormal
ZP:0008426	ciliary basal body floor plate mislocalised, abnormal
ZP:0008427	anterior-most region head decreased size, abnormal
ZP:0008428	anterior-most region head antero-posteriorly flattened, abnormal
ZP:0008429	anterior-most region head shortened, abnormal
ZP:0008430	cranial neural crest morphology, abnormal
ZP:0008431	cranial neural crest lacks all parts of type antero-ventral region cranial neural crest cell, abnormal
ZP:0008432	cranial neural crest has fewer parts of type medial region cranial neural crest cell, abnormal
ZP:0008433	ethmoid cartilage notched, abnormal
ZP:0008434	ethmoid cartilage perforate, abnormal
ZP:0008435	ethmoid cartilage shortened, abnormal
ZP:0008436	trabecula communis hypoplastic, abnormal
ZP:0008437	trabecula communis deformed, abnormal
ZP:0008438	palate cleft, abnormal
ZP:0008439	epithelial cell notochord irregular spatial pattern, abnormal
ZP:0008440	epithelial cell notochord variant shape, abnormal
ZP:0008441	epithelial cell notochord variability of size, abnormal
ZP:0008442	cellular sodium ion homeostasis decreased process quality, abnormal
ZP:0008443	detection of mechanical stimulus involved in sensory perception of sound decreased process quality, abnormal
ZP:0008444	angular vestibuloocular reflex decreased process quality, abnormal
ZP:0008445	hair cell lateral crista morphology, abnormal
ZP:0008446	hair cell anterior macula has extra parts of type multivesicular body hair cell anterior macula, abnormal
ZP:0008447	vesicle hair cell anterior macula increased diameter, abnormal
ZP:0008448	sodium:potassium-exchanging ATPase complex hair cell mislocalised, abnormal
ZP:0008449	stereocilium bundle hair cell decreased width, abnormal
ZP:0008450	neuromast hair cell cellular quality, abnormal
ZP:0008451	neuromast hair cell functionality, abnormal
ZP:0008452	skeletal muscle contraction decreased force, abnormal
ZP:0008454	swimming behavior decreased occurrence, abnormal
ZP:0008456	myoseptum decreased thickness, abnormal
ZP:0008458	convergent extension involved in gastrulation decreased magnitude, abnormal
ZP:0008459	tissue development disrupted, abnormal
ZP:0008460	embryonic organ development disrupted, abnormal
ZP:0008461	musculature system disorganized, abnormal
ZP:0008462	keratinocyte detached from whole organism, abnormal
ZP:0008463	midbrain increased size, abnormal
ZP:0008464	heart primordium bifurcated, abnormal
ZP:0008465	prechordal plate position, abnormal
ZP:0008466	organizer inducing center increased width, abnormal
ZP:0008467	brain morphogenesis arrested, abnormal
ZP:0008468	muscle tendon junction muscle disorganized, abnormal
ZP:0008469	myofibril muscle degenerate, abnormal
ZP:0008470	sarcolemma muscle collapsed, abnormal
ZP:0008471	phosphatidylinositol-4,5-bisphosphate 5-phosphatase activity decreased occurrence, abnormal
ZP:0008472	cellular response to heat increased duration, abnormal
ZP:0008473	neural precursor cell proliferation decreased occurrence, abnormal
ZP:0008474	cellular response to epinephrine stimulus delayed, abnormal
ZP:0008475	renal filtration disrupted, abnormal
ZP:0008476	Kupffer's vesicle has fewer parts of type cilium ciliated epithelial cell, abnormal
ZP:0008477	neuron forebrain electrical conductivity, abnormal
ZP:0008478	anterior region pronephros cystic, abnormal
ZP:0008479	retina deformed, abnormal
ZP:0008480	neuromast immature, abnormal
ZP:0008481	heart tube displaced to right side whole organism, abnormal
ZP:0008482	heart tube displaced to central region whole organism, abnormal
ZP:0008483	anterior-posterior axis whole organism asymmetrical, abnormal
ZP:0008484	ethmoid cartilage absent, abnormal
ZP:0008485	pronephric tubule increased width, abnormal
ZP:0008486	cilium pronephric tubule disorganized, abnormal
ZP:0008487	pharyngeal arch 3-7 lacks parts or has fewer parts of type cartilage tissue, abnormal
ZP:0008488	white matter cystic, abnormal
ZP:0008489	white matter increased accumulation astrocyte, abnormal
ZP:0008490	anterior region cranial vault flattened, abnormal
ZP:0008491	growth plate cartilage chondrocyte proliferation disrupted, abnormal
ZP:0008492	ventral mandibular arch deformed, abnormal
ZP:0008493	hyosymplectic cartilage decreased length, abnormal
ZP:0008494	locomotion irregular rhythm, abnormal
ZP:0008495	semicircular canal morphogenesis process quality, abnormal
ZP:0008496	lateral line development delayed, abnormal
ZP:0008497	posterior lateral line neuromast primordium migration delayed, abnormal
ZP:0008498	equilibrioception delayed, abnormal
ZP:0008499	hair cell anterior macula decreased amount, abnormal
ZP:0008500	neuromast physical object quality, abnormal
ZP:0008501	pronephric podocyte structure, abnormal
ZP:0008502	pronephric podocyte disorganized, abnormal
ZP:0008503	pronephric glomerular basement membrane disorganized, abnormal
ZP:0008504	lens fiber cell fate commitment disrupted, abnormal
ZP:0008505	lens epithelial cell proliferation increased occurrence, abnormal
ZP:0008506	lens physical object quality, abnormal
ZP:0008507	lens pigmented, abnormal
ZP:0008508	actin filament lens spatial pattern, abnormal
ZP:0008509	actin filament lens decreased amount, abnormal
ZP:0008510	cell lens shape, abnormal
ZP:0008511	cornea composition, abnormal
ZP:0008512	cornea nucleate quality, abnormal
ZP:0008513	pupil absent, abnormal
ZP:0008514	lens epithelium composition, abnormal
ZP:0008515	lens epithelium structure, abnormal
ZP:0008516	lens epithelium has extra parts of type epithelial cell, abnormal
ZP:0008517	lens epithelium has extra parts of type nucleus epithelial cell, abnormal
ZP:0008518	nucleus lens epithelium increased size, abnormal
ZP:0008519	nucleus lens epithelium disorganized, abnormal
ZP:0008520	epithelial cell lens epithelium nucleate quality, abnormal
ZP:0008521	epithelial cell lens epithelium immature, abnormal
ZP:0008522	epithelial cell lens epithelium swollen, abnormal
ZP:0008523	locomotory behavior process quality, abnormal
ZP:0008524	swimming occurrence, abnormal
ZP:0008525	motor neuron axon guidance decreased process quality, abnormal
ZP:0008526	axon motor neuron mislocalised, abnormal
ZP:0008527	vasculature yolk decreased amount, abnormal
ZP:0008528	pharyngeal arch 3-7 deformed, abnormal
ZP:0008529	posterior-most region somite decreased amount, abnormal
ZP:0008530	vertical myoseptum structure, abnormal
ZP:0008531	vertical myoseptum decreased length, abnormal
ZP:0008532	post-vent region decreased flexibility, abnormal
ZP:0008533	hindbrain development delayed, abnormal
ZP:0008534	EVL constricted, abnormal
ZP:0008535	rhombomere 5 decreased thickness, abnormal
ZP:0008536	rhombomere 3 decreased thickness, abnormal
ZP:0008537	cell detached from post-vent region, abnormal
ZP:0008538	hemostasis delayed, abnormal
ZP:0008539	yolk hemorrhagic, abnormal
ZP:0008540	regulation of vascular endothelial growth factor receptor signaling pathway process quality, abnormal
ZP:0008541	retina edematous, abnormal
ZP:0008542	ocular blood vessel retinal inner plexiform layer mislocalised, abnormal
ZP:0008543	pronephric podocyte physical object quality, abnormal
ZP:0008544	blood vessel trunk vasculature increased amount, abnormal
ZP:0008545	optic artery increased permeability, abnormal
ZP:0008546	hyaloid vessel branched, abnormal
ZP:0008547	hyaloid vessel malformed, abnormal
ZP:0008548	optic choroid vascular plexus branched, abnormal
ZP:0008549	optic choroid vascular plexus malformed, abnormal
ZP:0008550	cranial blood vessel increased amount, abnormal
ZP:0008551	ocular blood vessel branched, abnormal
ZP:0008552	nucleate erythrocyte optical quality, abnormal
ZP:0008553	endoplasmic reticulum to Golgi vesicle-mediated transport decreased process quality, abnormal
ZP:0008554	melanosome organization decreased process quality, abnormal
ZP:0008555	collagen biosynthetic process decreased process quality, abnormal
ZP:0008556	extracellular matrix constituent secretion decreased process quality, abnormal
ZP:0008557	collagen trimer notochord mislocalised, abnormal
ZP:0008558	extracellular matrix notochord decreased thickness, abnormal
ZP:0008559	chondrocyte Meckel's cartilage malformed, abnormal
ZP:0008560	fibrillar collagen trimer cranial cartilage decreased mass, abnormal
ZP:0008561	extracellular matrix cranial cartilage decreased mass, abnormal
ZP:0008562	chondroblast spatial pattern, abnormal
ZP:0008563	endoplasmic reticulum chondrocyte distended, abnormal
ZP:0008564	melanosome melanocyte circular, abnormal
ZP:0008565	melanosome melanocyte immature, abnormal
ZP:0008566	caudal artery increased accumulation thrombocyte, abnormal
ZP:0008567	thrombocyte aggregated, abnormal
ZP:0008571	retinal outer plexiform layer aplastic, abnormal
ZP:0008572	retinal outer nuclear layer aplastic, abnormal
ZP:0008573	photoreceptor outer segment photoreceptor cell aplastic/hypoplastic, abnormal
ZP:0008574	nucleus photoreceptor cell shape, abnormal
ZP:0008576	Golgi cisterna photoreceptor cell hypoplastic, abnormal
ZP:0008577	horizontal cell absent, abnormal
ZP:0008579	EVL cellular motility, abnormal
ZP:0008580	deep blastomere circular, abnormal
ZP:0008581	deep blastomere cellular adhesivity, abnormal
ZP:0008582	portion of tissue cardiac ventricle increased thickness, abnormal
ZP:0008583	portion of tissue atrium decreased thickness, abnormal
ZP:0008584	pericardium hypertrophic, abnormal
ZP:0008585	cellular response to DNA damage stimulus disrupted, abnormal
ZP:0008586	cardiac muscle contraction decreased rate, abnormal
ZP:0008587	cardiac muscle contraction decreased strength, abnormal
ZP:0008588	brain atrophied, abnormal
ZP:0008589	brain decreased occurrence cell population proliferation, abnormal
ZP:0008590	brain disrupted axon extension, abnormal
ZP:0008591	brain disrupted innervation, abnormal
ZP:0008592	ventricular system brain decreased volume, abnormal
ZP:0008593	neuron brain mislocalised, abnormal
ZP:0008594	heart primordium decreased occurrence cell population proliferation, abnormal
ZP:0008595	midbrain decreased occurrence cell population proliferation, abnormal
ZP:0008596	tectal ventricle decreased width, abnormal
ZP:0008597	atrium shortened, abnormal
ZP:0008598	plasma membrane neuron structure, abnormal
ZP:0008599	spinal cord interneuron increased amount, abnormal
ZP:0008600	microtubule cytoskeleton organization disrupted, abnormal
ZP:0008601	efferent axon development in posterior lateral line nerve disrupted, abnormal
ZP:0008602	spinal cord structure, abnormal
ZP:0008603	mitochondrion spinal cord vacuolated, abnormal
ZP:0008604	axon spinal cord discolored, abnormal
ZP:0008605	axon spinal cord decreased amount, abnormal
ZP:0008606	compact myelin spinal cord decreased amount, abnormal
ZP:0008607	synaptic vesicle enteric nervous system mislocalised, abnormal
ZP:0008608	microtubule cytoskeleton enteric nervous system disorganized, abnormal
ZP:0008609	microtubule cytoskeleton neuron disorganized, abnormal
ZP:0008610	fin absent, abnormal
ZP:0008611	caudal fin absent, abnormal
ZP:0008612	mesoderm caudal fin immature, abnormal
ZP:0008613	mesoderm anal fin immature, abnormal
ZP:0008614	pelvic fin absent, abnormal
ZP:0008615	pectoral fin distal radial fused with pectoral fin distal radial, abnormal
ZP:0008617	retinal ganglion cell retinal ganglion cell layer increased amount, abnormal
ZP:0008618	retinal photoreceptor layer poorly differentiated, abnormal
ZP:0008619	nucleus retina mislocalised, abnormal
ZP:0008620	eye photoreceptor cell shape, abnormal
ZP:0008621	retinal ganglion cell increased amount, abnormal
ZP:0008622	retinal ganglion cell mislocalised, abnormal
ZP:0008623	notochord broken, abnormal
ZP:0008624	post-vent region increased amount, abnormal
ZP:0008625	pectoral fin physical object quality, abnormal
ZP:0008626	primitive erythrocyte differentiation decreased occurrence, abnormal
ZP:0008627	whole organism has fewer parts of type hemoglobin complex nucleate erythrocyte, abnormal
ZP:0008628	neuroectoderm apoptotic, abnormal
ZP:0008629	nucleate erythrocyte hypoplastic, abnormal
ZP:0008630	collagen biosynthetic process increased rate, abnormal
ZP:0008632	chondrocyte Meckel's cartilage length, abnormal
ZP:0008633	chondrocyte Meckel's cartilage obtuse, abnormal
ZP:0008634	chondrocyte ceratohyal cartilage obtuse, abnormal
ZP:0008635	chondrocyte pharyngeal arch cartilage malformed, abnormal
ZP:0008636	chondrocyte malformed, abnormal
ZP:0008637	chondrocyte undifferentiated, abnormal
ZP:0008638	endoplasmic reticulum lumen chondrocyte swollen, abnormal
ZP:0008639	Golgi apparatus chondrocyte decreased size, abnormal
ZP:0008640	Golgi apparatus chondrocyte disorganized, abnormal
ZP:0008641	actin filament chondrocyte disorganized, abnormal
ZP:0008643	neural crest cell migration increased rate, abnormal
ZP:0008644	parachordal vessel absent, abnormal
ZP:0008645	cellular response to light stimulus increased intensity, abnormal
ZP:0008646	ON-bipolar cell functionality, abnormal
ZP:0008647	axon terminus ON-bipolar cell morphology, abnormal
ZP:0008648	pigmentation occurrence, abnormal
ZP:0008649	membrane depolarization increased occurrence, abnormal
ZP:0008650	melanocyte membrane potential, abnormal
ZP:0008651	xanthophore spatial pattern, abnormal
ZP:0008652	midbrain hindbrain boundary decreased width, abnormal
ZP:0008653	tegmentum increased size, abnormal
ZP:0008654	tegmentum deformed, abnormal
ZP:0008655	mouth prominent, abnormal
ZP:0008656	rhombomere deformed, abnormal
ZP:0008657	optic cup prominent, abnormal
ZP:0008658	caudal vein plexus decreased occurrence blood circulation, abnormal
ZP:0008659	release of sequestered calcium ion into cytosol decreased occurrence, abnormal
ZP:0008660	rhombomere hindbrain condensed, abnormal
ZP:0008661	somite trunk increased width, abnormal
ZP:0008662	developmental growth neotenous growth, abnormal
ZP:0008663	atrioventricular canal increased width, abnormal
ZP:0008664	fin bud decreased size, abnormal
ZP:0008665	sprouting angiogenesis sporadic, abnormal
ZP:0008666	central region dorsal aorta decreased width, abnormal
ZP:0008667	common cardinal vein increased accumulation blood cell, abnormal
ZP:0008668	central region posterior cardinal vein decreased width, abnormal
ZP:0008669	caudal vein plexus increased accumulation blood cell, abnormal
ZP:0008670	dorsal longitudinal anastomotic vessel non-functional, abnormal
ZP:0008671	central region subintestinal vein decreased width, abnormal
ZP:0008672	fin vasculature decreased functionality, abnormal
ZP:0008673	central region pectoral fin blood vessel decreased width, abnormal
ZP:0008674	melatonin biosynthetic process disrupted, abnormal
ZP:0008675	circadian sleep/wake cycle, sleep decreased duration, abnormal
ZP:0008676	circadian sleep/wake cycle, sleep disrupted, abnormal
ZP:0008677	spleen decreased size, abnormal
ZP:0008678	spleen agenesis, abnormal
ZP:0008679	pharyngeal arch 5 immature, abnormal
ZP:0008680	presumptive cardiac ventricle heart tube mislocalised, abnormal
ZP:0008681	cell body intrahepatic bile duct increased size, abnormal
ZP:0008682	lateral mesodermal cell differentiation disrupted, abnormal
ZP:0008683	intermediate mesodermal cell differentiation disrupted, abnormal
ZP:0008684	hemangioblast cell differentiation disrupted, abnormal
ZP:0008685	pronephros morphology, abnormal
ZP:0008686	common cardinal vein increased diameter, abnormal
ZP:0008687	presumptive endoderm increased width, abnormal
ZP:0008688	pharyngeal endoderm increased width, abnormal
ZP:0008689	pronephric tubule decreased diameter, abnormal
ZP:0008690	pronephric proximal convoluted tubule morphology, abnormal
ZP:0008691	anterior lateral mesoderm morphology, abnormal
ZP:0008692	epiphysis apoptotic, abnormal
ZP:0008693	telencephalon apoptotic, abnormal
ZP:0008694	caudal artery poorly differentiated, abnormal
ZP:0008695	caudal vein poorly differentiated, abnormal
ZP:0008696	whole organism hemorrhagic, abnormal
ZP:0008697	nucleate erythrocyte increased accumulation caudal artery, abnormal
ZP:0008698	nucleate erythrocyte increased accumulation dorsal aorta, abnormal
ZP:0008699	whole organism swollen, abnormal
ZP:0008700	trunk shape, abnormal
ZP:0008701	hemoglobin complex blood decreased amount, abnormal
ZP:0008702	melanocyte yolk decreased amount, abnormal
ZP:0008703	melanosome retinal pigmented epithelium immature, abnormal
ZP:0008704	melanosome retinal pigmented epithelium decreased circumference, abnormal
ZP:0008705	retinal pigmented epithelium displaced to melanosome retinal pigmented epithelium, abnormal
ZP:0008706	retinal pigmented epithelium displaced to melanosome central region retinal pigmented epithelium, abnormal
ZP:0008707	retinal pigmented epithelium displaced to melanosome dorsal region retinal pigmented epithelium, abnormal
ZP:0008708	retinal pigmented epithelium displaced to melanosome retina, abnormal
ZP:0008709	retinal pigmented epithelium displaced to melanosome optic choroid, abnormal
ZP:0008710	retinal pigmented epithelium lacks all parts of type cell projection melanosome retinal pigmented epithelium, abnormal
ZP:0008711	lipid biosynthetic process process quality, abnormal
ZP:0008712	nucleus notochord morphology, abnormal
ZP:0008713	endoplasmic reticulum notochord increased size, abnormal
ZP:0008714	Golgi apparatus notochord morphology, abnormal
ZP:0008715	myofibril somite unstructured, abnormal
ZP:0008716	blood vessel inner optic circle decreased size, abnormal
ZP:0008717	blood vessel inner optic circle elliptic, abnormal
ZP:0008718	ocular blood vessel deformed, abnormal
ZP:0008719	protein glycosylation disrupted, abnormal
ZP:0008720	voluntary musculoskeletal movement disrupted, abnormal
ZP:0008721	head morphogenesis disrupted, abnormal
ZP:0008722	notochord disorganized, abnormal
ZP:0008723	vertical myoseptum curved, abnormal
ZP:0008724	myotome decreased mass, abnormal
ZP:0008725	basement membrane myotome morphology, abnormal
ZP:0008726	myofibril myotome spatial pattern, abnormal
ZP:0008727	myofibril myotome decreased length, abnormal
ZP:0008728	myofibril myotome refractivity, abnormal
ZP:0008729	myoseptum disorganized, abnormal
ZP:0008730	myoseptum increased distance myoseptum, abnormal
ZP:0008732	contractile fiber trunk disorganized, abnormal
ZP:0008733	neural tube disorganized, abnormal
ZP:0008734	muscle cell irregular spatial pattern, abnormal
ZP:0008735	chondrocyte development disrupted, abnormal
ZP:0008736	neuromuscular junction development delayed, abnormal
ZP:0008737	somite curved, abnormal
ZP:0008738	clathrin-sculpted acetylcholine transport vesicle somite mislocalised medially, abnormal
ZP:0008739	hyosymplectic cartilage disorganized, abnormal
ZP:0008740	melanocyte apoptotic, abnormal
ZP:0008741	neuron fate determination disrupted, abnormal
ZP:0008742	anatomical compartment boundary somite shape, abnormal
ZP:0008743	myofibril muscle misrouted, abnormal
ZP:0008744	voluntary musculoskeletal movement arrested, abnormal
ZP:0008745	T-tubule myotome mislocalised, abnormal
ZP:0008746	T-tubule myotome decreased amount, abnormal
ZP:0008747	myofibril skeletal muscle cell disoriented, abnormal
ZP:0008748	myofibril skeletal muscle cell undulate, abnormal
ZP:0008749	myofibril skeletal muscle cell increased variability of size, abnormal
ZP:0008750	muscle cell apoptotic, abnormal
ZP:0008751	collagen trimer skeletal muscle cell spatial pattern, abnormal
ZP:0008752	mitochondrion skeletal muscle cell increased amount, abnormal
ZP:0008753	mitochondrion skeletal muscle cell swollen, abnormal
ZP:0008754	endoplasmic reticulum skeletal muscle cell dilated, abnormal
ZP:0008755	mitochondrial crista skeletal muscle cell structure, abnormal
ZP:0008756	sarcolemma skeletal muscle cell structure, abnormal
ZP:0008757	intersegmental vessel has extra parts of type filopodium endothelial tip cell, abnormal
ZP:0008758	intersegmental vessel process quality sprouting angiogenesis, abnormal
ZP:0008759	intersegmental vessel detached from endothelial tip cell dorsal aorta, abnormal
ZP:0008760	chromatin binding disrupted, abnormal
ZP:0008761	pharynx has fewer parts of type goblet cell, abnormal
ZP:0008762	goblet cell pharynx decreased amount, abnormal
ZP:0008763	retinal photoreceptor layer decreased size, abnormal
ZP:0008764	retinal pigmented epithelium increased size, abnormal
ZP:0008765	nuclear pore retina mislocalised, abnormal
ZP:0008766	nuclear pore retina disorganized, abnormal
ZP:0008767	nuclear pore retina decreased amount, abnormal
ZP:0008768	cranial nerve II decreased diameter, abnormal
ZP:0008769	nuclear pore posterior intestine decreased amount, abnormal
ZP:0008770	enterocyte intestinal bulb decreased amount, abnormal
ZP:0008771	retinal outer plexiform layer decreased size, abnormal
ZP:0008772	intestine apoptotic, abnormal
ZP:0008773	intestine has fewer parts of type goblet cell, abnormal
ZP:0008774	nuclear pore intestine mislocalised, abnormal
ZP:0008775	nuclear pore intestine disorganized, abnormal
ZP:0008776	intestinal epithelium surface feature shape, abnormal
ZP:0008777	intestinal epithelium detached from obsolete cell intestinal epithelium, abnormal
ZP:0008778	nuclear pore intestinal epithelium decreased amount, abnormal
ZP:0008779	cell intestinal epithelium disorganized, abnormal
ZP:0008780	enteroendocrine cell intestinal epithelium decreased amount, abnormal
ZP:0008781	intestinal bulb epithelium decreased thickness, abnormal
ZP:0008782	intestinal bulb epithelium surface feature shape, abnormal
ZP:0008783	nuclear pore intestinal bulb epithelium absent, abnormal
ZP:0008784	goblet cell posterior intestine epithelium absent, abnormal
ZP:0008785	nucleus enterocyte shape, abnormal
ZP:0008786	nucleus enterocyte mislocalised, abnormal
ZP:0008787	caudal artery malformed, abnormal
ZP:0008788	heart hemorrhagic, abnormal
ZP:0008789	intersegmental vessel fused with intersegmental vessel, abnormal
ZP:0008790	filopodium intersegmental vessel decreased length, abnormal
ZP:0008791	dorsal longitudinal anastomotic vessel shape, abnormal
ZP:0008792	filopodium endothelial tip cell decreased length, abnormal
ZP:0008793	motor neuron spinal cord morphology, abnormal
ZP:0008794	axon neuron truncated, abnormal
ZP:0008795	anterior region whole organism truncated, abnormal
ZP:0008796	pronephric duct distended, abnormal
ZP:0008797	sodium:potassium-exchanging ATPase complex pronephric duct mislocalised, abnormal
ZP:0008798	cilium pronephric duct increased behavioural activity, abnormal
ZP:0008799	actin cytoskeleton pronephric duct disorganized, abnormal
ZP:0008800	otolith organ increased amount, abnormal
ZP:0008801	collateral sprouting in absence of injury premature, abnormal
ZP:0008802	regulation of collateral sprouting in absence of injury process quality, abnormal
ZP:0008803	branching morphogenesis of a nerve sporadic, abnormal
ZP:0008804	branching morphogenesis of a nerve increased occurrence, abnormal
ZP:0008805	motor neuron spinal cord malformed, abnormal
ZP:0008806	primary motor neuron spinal cord malformed, abnormal
ZP:0008807	cranial nerve VII malformed, abnormal
ZP:0008808	cranial nerve V malformed, abnormal
ZP:0008809	axon MiP motor neuron increased branchiness, abnormal
ZP:0008810	axon RoP motor neuron mislocalised, abnormal
ZP:0008811	axon RoP motor neuron increased branchiness, abnormal
ZP:0008812	axon motor neuron increased amount, abnormal
ZP:0008813	axon collateral CaP motoneuron increased amount, abnormal
ZP:0008814	axon collateral CaP motoneuron mislocalised proximally, abnormal
ZP:0008815	epithelial cell differentiation disrupted, abnormal
ZP:0008816	basal plate midbrain region decreased size, abnormal
ZP:0008817	intestinal bulb morphology, abnormal
ZP:0008818	zona limitans intrathalamica decreased size, abnormal
ZP:0008819	goblet cell intestinal epithelium absent, abnormal
ZP:0008820	enterocyte intestinal epithelium absent, abnormal
ZP:0008821	epithelial cell mid intestine epithelium cuboid, abnormal
ZP:0008822	epithelial cell posterior intestine epithelium cuboid, abnormal
ZP:0008823	enteroendocrine cell absent, abnormal
ZP:0008824	mesodermal cell decreased amount, abnormal
ZP:0008825	lymph vasculature inverted, abnormal
ZP:0008826	regulation of growth hormone secretion disrupted, abnormal
ZP:0008827	branchiomeric skeletal muscle development process quality, abnormal
ZP:0008828	abductor hyohyoid has fewer parts of type skeletal muscle cell, abnormal
ZP:0008829	adductor operculi has fewer parts of type skeletal muscle cell, abnormal
ZP:0008830	dilatator operculi has fewer parts of type skeletal muscle cell, abnormal
ZP:0008831	levator operculi has fewer parts of type skeletal muscle cell, abnormal
ZP:0008832	adductor hyohyoid has fewer parts of type skeletal muscle cell, abnormal
ZP:0008833	pronephric duct opening morphology, abnormal
ZP:0008834	neuromast increased size, abnormal
ZP:0008835	neuromast increased area, abnormal
ZP:0008837	parapineal organ inverted, abnormal
ZP:0008841	ryanodine-sensitive calcium-release channel activity decreased occurrence, abnormal
ZP:0008842	voltage-gated calcium channel activity decreased occurrence, abnormal
ZP:0008843	muscle contraction decreased intensity, abnormal
ZP:0008844	protein oxidation increased occurrence, abnormal
ZP:0008845	fast-twitch skeletal muscle fiber contraction process quality, abnormal
ZP:0008846	fast-twitch skeletal muscle fiber contraction decreased occurrence, abnormal
ZP:0008848	locomotion involved in locomotory behavior occurrence, abnormal
ZP:0008850	fast muscle cell trunk musculature decreased contractility, abnormal
ZP:0008853	fast muscle cell myotome decreased functionality, abnormal
ZP:0008855	fast muscle cell post-vent region decreased contractility, abnormal
ZP:0008857	longitudinal sarcoplasmic reticulum skeletal muscle swollen, abnormal
ZP:0008858	sarcoplasmic reticulum membrane skeletal muscle dilated, abnormal
ZP:0008859	sarcoplasmic reticulum fast muscle cell absent, abnormal
ZP:0008860	sarcoplasmic reticulum fast muscle cell disorganized, abnormal
ZP:0008864	neural tube formation occurrence, abnormal
ZP:0008865	midbrain-hindbrain boundary morphogenesis occurrence, abnormal
ZP:0008866	ventricular system development occurrence, abnormal
ZP:0008867	midbrain-hindbrain boundary development occurrence, abnormal
ZP:0008868	cranium deformed, abnormal
ZP:0008869	neuroectoderm deformed, abnormal
ZP:0008870	T cell differentiation disrupted, abnormal
ZP:0008871	thymus cellularity, abnormal
ZP:0008872	thymus lacks parts or has fewer parts of type pro-T cell, abnormal
ZP:0008873	pro-T cell decreased amount, abnormal
ZP:0008874	blood vasculature hemorrhagic, abnormal
ZP:0008875	trunk vasculature spatial pattern, abnormal
ZP:0008877	P granule primordial germ cell physical object quality, abnormal
ZP:0008878	P granule primordial germ cell decreased amount, abnormal
ZP:0008879	primordial germ cell increased distance P granule mitochondrion primordial germ cell, abnormal
ZP:0008880	exocrine pancreas disorganized, abnormal
ZP:0008881	double-strand break repair via homologous recombination increased frequency, abnormal
ZP:0008882	double-strand break repair via nonhomologous end joining decreased frequency, abnormal
ZP:0008884	vasculogenesis paedomorphic growth, abnormal
ZP:0008885	filopodium assembly paedomorphic growth, abnormal
ZP:0008886	intersegmental vein decreased size, abnormal
ZP:0008887	filopodium intersegmental vein decreased length, abnormal
ZP:0008888	response to cytokine decreased process quality, abnormal
ZP:0008889	anatomical structure aplastic, abnormal
ZP:0008890	tail bud increased amount, abnormal
ZP:0008891	notochord increased amount, abnormal
ZP:0008892	whole organism radial symmetry, abnormal
ZP:0008893	glomerular basement membrane increased permeability, abnormal
ZP:0008894	neural crest formation process quality, abnormal
ZP:0008895	bone mineralization process quality, abnormal
ZP:0008896	heart tubular, abnormal
ZP:0008897	facial nerve motor nucleus has fewer parts of type motor neuron, abnormal
ZP:0008898	motor neuron cranial nerve position, abnormal
ZP:0008899	motor neuron cranial nerve disorganized, abnormal
ZP:0008900	anterior-posterior axis whole organism kinked, abnormal
ZP:0008901	anterior-posterior axis trunk curved, abnormal
ZP:0008902	vertebra increased distance vertebra, abnormal
ZP:0008903	vertebra has fewer parts of type neural spine, abnormal
ZP:0008904	vertebra has fewer parts of type hemal spine, abnormal
ZP:0008905	cranial neural crest disorganized, abnormal
ZP:0008906	cranial neural crest has fewer parts of type cranial neural crest cell, abnormal
ZP:0008907	facial ganglion hypoplastic, abnormal
ZP:0008908	axon facial ganglion decreased length, abnormal
ZP:0008909	axon facial ganglion decreased amount, abnormal
ZP:0008910	pharyngeal arch decreased amount, abnormal
ZP:0008911	neural spine decreased size, abnormal
ZP:0008912	hemal spine decreased size, abnormal
ZP:0008913	somite border malformed, abnormal
ZP:0008914	pharyngeal arch 3-7 absent, abnormal
ZP:0008916	otolith increased variability of size, abnormal
ZP:0008918	external yolk syncytial layer immature, abnormal
ZP:0008919	actin filament whole organism disorganized, abnormal
ZP:0008920	protein secretion disrupted, abnormal
ZP:0008921	hypochord development disrupted, abnormal
ZP:0008922	rough endoplasmic reticulum hypochord increased size, abnormal
ZP:0008923	rough endoplasmic reticulum notochord increased size, abnormal
ZP:0008924	otolith organ altered number of otolith, abnormal
ZP:0008925	otolith aplastic, abnormal
ZP:0008926	transmission of nerve impulse process quality, abnormal
ZP:0008927	blood cell intermediate cell mass of mesoderm decreased amount, abnormal
ZP:0008928	midbrain degenerate, abnormal
ZP:0008929	notochord immature, abnormal
ZP:0008930	fourth ventricle dilated, abnormal
ZP:0008931	tectal ventricle dilated, abnormal
ZP:0008933	neural tube closure arrested, abnormal
ZP:0008934	glial cell differentiation decreased occurrence, abnormal
ZP:0008935	caudal vein absent blood circulation, abnormal
ZP:0008936	ceratobranchial cartilage hypoplastic, abnormal
ZP:0008937	dorsal longitudinal anastomotic vessel absent blood circulation, abnormal
ZP:0008939	epithelial cell pronephros shortened, abnormal
ZP:0008941	cilium olfactory epithelium shortened, abnormal
ZP:0008942	pronephric tubule increased size, abnormal
ZP:0008943	pronephric proximal convoluted tubule closed, abnormal
ZP:0008944	multi-ciliated epithelial cell accumulation pronephric duct, abnormal
ZP:0008948	cilium multi-ciliated epithelial cell disorganized, abnormal
ZP:0008950	definitive hemopoiesis arrested, abnormal
ZP:0008951	midbrain disorganized, abnormal
ZP:0008952	axon nervous system spatial pattern, abnormal
ZP:0008953	cranial nerve III decreased size, abnormal
ZP:0008954	cranial nerve X morphology, abnormal
ZP:0008955	cranial nerve IV decreased size, abnormal
ZP:0008956	cranial nerve VII decreased size, abnormal
ZP:0008957	cranial nerve VII disorganized, abnormal
ZP:0008958	cranial nerve V decreased size, abnormal
ZP:0008959	cranial nerve V disorganized, abnormal
ZP:0008960	cardiac ventricle decreased volume, abnormal
ZP:0008961	heart insufficient, abnormal
ZP:0008962	nucleate erythrocyte decreased fluid flow, abnormal
ZP:0008963	cranial ganglion morphology, abnormal
ZP:0008964	glial cell lateral line decreased amount, abnormal
ZP:0008965	T cell differentiation in thymus disrupted, abnormal
ZP:0008966	T cell decreased amount, abnormal
ZP:0008967	muscle contraction decreased rate, abnormal
ZP:0008968	sarcomere organization process quality, abnormal
ZP:0008969	fast muscle cell myotome physical object quality, abnormal
ZP:0008970	dopaminergic neuron diencephalon irregular spatial pattern, abnormal
ZP:0008971	axon optic tectum decreased amount, abnormal
ZP:0008972	neuromuscular synaptic transmission amplitude, abnormal
ZP:0008973	neuromuscular synaptic transmission process quality, abnormal
ZP:0008974	receptor clustering process quality, abnormal
ZP:0008975	post-vent region mislocalised, abnormal
ZP:0008976	ventricular zone increased size, abnormal
ZP:0008977	cell ventricular zone increased mass density, abnormal
ZP:0008978	pharyngeal arch decreased length, abnormal
ZP:0008979	cell pharyngeal arch increased mass density, abnormal
ZP:0008980	atrioventricular valve non-functional, abnormal
ZP:0008981	blood cell aggregated, abnormal
ZP:0008982	regulation of neurotransmitter levels disrupted, abnormal
ZP:0008983	response to light stimulus decreased duration, abnormal
ZP:0008984	oxygen metabolic process decreased rate, abnormal
ZP:0008985	ball increased circumference, abnormal
ZP:0008986	dorsal region brain physical object quality, abnormal
ZP:0008987	axon secondary motor neuron branchiness, abnormal
ZP:0008988	regulation of hydrogen peroxide metabolic process disrupted, abnormal
ZP:0008989	neutrophil differentiation disrupted, abnormal
ZP:0008990	macrophage differentiation disrupted, abnormal
ZP:0008991	mononuclear phagocyte rostral blood island aggregated, abnormal
ZP:0008992	mononuclear phagocyte rostral blood island decreased amount, abnormal
ZP:0008993	neutrophil rostral blood island decreased amount, abnormal
ZP:0008994	myeloid cell aggregated, abnormal
ZP:0008995	cranial nerve X mislocalised, abnormal
ZP:0008996	thymus has fewer parts of type pro-T cell, abnormal
ZP:0008997	lymphangioblast cord malformed, abnormal
ZP:0008998	pronephric glomerulus disorganized, abnormal
ZP:0008999	retina layer formation decreased process quality, abnormal
ZP:0009000	retinal cone cell differentiation delayed, abnormal
ZP:0009001	retina morphogenesis in camera-type eye decreased process quality, abnormal
ZP:0009002	brain increased occurrence apoptotic process, abnormal
ZP:0009003	lens increased occurrence apoptotic process, abnormal
ZP:0009004	retinal inner nuclear layer increased occurrence cell population proliferation, abnormal
ZP:0009005	retina increased occurrence cell population proliferation, abnormal
ZP:0009006	optic cup increased occurrence apoptotic process, abnormal
ZP:0009007	retinal outer nuclear layer increased occurrence cell population proliferation, abnormal
ZP:0009008	solid lens vesicle decreased occurrence apoptotic process, abnormal
ZP:0009009	vasculature development arrested, abnormal
ZP:0009010	notochord curved, abnormal
ZP:0009011	caudal vein plexus irregular spatial pattern, abnormal
ZP:0009012	vasculature irregular spatial pattern, abnormal
ZP:0009013	neurogenesis process quality, abnormal
ZP:0009014	primary neuron decreased amount, abnormal
ZP:0009015	median fin fold collapsed, abnormal
ZP:0009016	epidermis damaged, abnormal
ZP:0009017	telomerase activity process quality, abnormal
ZP:0009018	telomerase activity decreased occurrence, abnormal
ZP:0009020	telomere maintenance via telomerase decreased occurrence, abnormal
ZP:0009021	cell cycle arrest increased occurrence, abnormal
ZP:0009022	spermatogonial cell division decreased occurrence, abnormal
ZP:0009024	determination of adult lifespan decreased duration, abnormal
ZP:0009025	fertilization having decreased processual parts fertilization, abnormal
ZP:0009026	animal organ senescence premature, abnormal
ZP:0009027	chromosome breakage increased occurrence, abnormal
ZP:0009028	hematopoietic stem cell homeostasis disrupted, abnormal
ZP:0009029	regulation of signal transduction by p53 class mediator increased process quality, abnormal
ZP:0009030	spinal cord curvature, abnormal
ZP:0009031	retinal photoreceptor layer atrophied, abnormal
ZP:0009032	male organism decreased fertility, abnormal
ZP:0009033	male organism has fewer parts of type renal tubule head kidney, abnormal
ZP:0009034	male organism has fewer parts of type hematopoietic multipotent progenitor cell head kidney, abnormal
ZP:0009035	gut male organism increased thickness, abnormal
ZP:0009036	gut male organism apoptotic, abnormal
ZP:0009037	gut male organism degenerate, abnormal
ZP:0009038	gut male organism senescent, abnormal
ZP:0009039	gut male organism inflamed, abnormal
ZP:0009040	liver male organism degenerate, abnormal
ZP:0009041	trunk musculature male organism degenerate, abnormal
ZP:0009042	head kidney male organism apoptotic, abnormal
ZP:0009043	head kidney male organism degenerate, abnormal
ZP:0009044	head kidney male organism senescent, abnormal
ZP:0009045	renal tubule male organism apoptotic, abnormal
ZP:0009046	intestinal epithelium male organism dysplastic, abnormal
ZP:0009047	intestinal villus male organism decreased length, abnormal
ZP:0009048	blood cell male organism decreased amount, abnormal
ZP:0009049	hematopoietic multipotent progenitor cell male organism apoptotic, abnormal
ZP:0009050	female organism decreased fertility, abnormal
ZP:0009051	chromosome, telomeric region integument decreased length, abnormal
ZP:0009052	testis degenerate, abnormal
ZP:0009053	testis senescent, abnormal
ZP:0009054	testis atrophied, abnormal
ZP:0009055	testis decreased occurrence telomere maintenance, abnormal
ZP:0009056	sperm testis decreased amount, abnormal
ZP:0009057	germ line cell testis apoptotic, abnormal
ZP:0009058	chromosome, telomeric region caudal fin decreased length, abnormal
ZP:0009059	whole organism decreased female fertility, abnormal
ZP:0009060	whole organism decreased male fertility, abnormal
ZP:0009062	neural tube closure incomplete, abnormal
ZP:0009063	ventral wall of dorsal aorta apoptotic, abnormal
ZP:0009064	chromosome, telomeric region gut epithelium decreased length, abnormal
ZP:0009065	chromosome, telomeric region gut epithelium decreased variability of size, abnormal
ZP:0009066	blood cell apoptotic, abnormal
ZP:0009067	developmental process arrested, abnormal
ZP:0009068	spinal cord oligodendrocyte cell differentiation disrupted, abnormal
ZP:0009069	dorsal/ventral neural tube patterning disrupted, abnormal
ZP:0009070	smoothened signaling pathway involved in dorsal/ventral neural tube patterning disrupted, abnormal
ZP:0009071	neuronal cell body cranial nerve VII mislocalised anteriorly, abnormal
ZP:0009072	neuronal cell body rhombomere 5 mislocalised, abnormal
ZP:0009073	neuronal cell body rhombomere 7 mislocalised, abnormal
ZP:0009074	neuronal cell body rhombomere 4 mislocalised, abnormal
ZP:0009075	whole organism decreased fertility, abnormal
ZP:0009076	posterior region whole organism morphology, abnormal
ZP:0009077	neural tube wholly ventralized, abnormal
ZP:0009078	striated muscle tissue development disrupted, abnormal
ZP:0009079	myoseptum curved, abnormal
ZP:0009080	myofibril muscle loose, abnormal
ZP:0009083	endocardium aplastic, abnormal
ZP:0009084	locomotion involved in locomotory behavior process quality, abnormal
ZP:0009085	neural crest physical object quality, abnormal
ZP:0009086	extraocular musculature decreased amount, abnormal
ZP:0009087	ventricular system malformed, abnormal
ZP:0009088	pharyngeal musculature decreased amount, abnormal
ZP:0009090	otic vesicle has fewer parts of type otolith, abnormal
ZP:0009091	ventral side eye decreased pigmentation, abnormal
ZP:0009093	epithelium sensory system decreased thickness, abnormal
ZP:0009094	whole organism rough, abnormal
ZP:0009097	otolith broken, abnormal
ZP:0009099	neuroepithelial cell dislocated dorsal side ventricular system, abnormal
ZP:0009100	phagolysosome assembly disrupted, abnormal
ZP:0009101	vesicle-mediated transport disrupted, abnormal
ZP:0009102	retinal neural layer apoptotic, abnormal
ZP:0009103	liver discolored, abnormal
ZP:0009104	retinal pigmented epithelium swollen, abnormal
ZP:0009105	microvillus retinal pigmented epithelium decreased amount, abnormal
ZP:0009106	vesicle retinal pigmented epithelium present, abnormal
ZP:0009107	melanosome retinal pigmented epithelium shape, abnormal
ZP:0009108	melanocyte retinal pigmented epithelium colored, abnormal
ZP:0009109	melanocyte retinal pigmented epithelium colorless, abnormal
ZP:0009110	integument colored, abnormal
ZP:0009111	melanosome integument shape, abnormal
ZP:0009112	melanosome integument decreased amount, abnormal
ZP:0009113	melanocyte integument colored, abnormal
ZP:0009114	melanocyte integument colorless, abnormal
ZP:0009115	intestine discolored, abnormal
ZP:0009116	vesicle intestine increased amount, abnormal
ZP:0009117	vesicle intestine decreased size, abnormal
ZP:0009118	photoreceptor outer segment layer decreased length, abnormal
ZP:0009119	hepatocyte disorganized, abnormal
ZP:0009120	vesicle hepatocyte present, abnormal
ZP:0009121	vesicle macrophage increased size, abnormal
ZP:0009122	vesicle macrophage variant shape, abnormal
ZP:0009123	iridophore reflectivity, abnormal
ZP:0009124	smoothened signaling pathway increased process quality, abnormal
ZP:0009130	cell proliferation involved in heart morphogenesis decreased rate, abnormal
ZP:0009131	retinal ganglion cell decreased functionality, abnormal
ZP:0009132	retina shape, abnormal
ZP:0009133	optic tectum swollen, abnormal
ZP:0009134	lens epithelium vacuolated, abnormal
ZP:0009136	photoreceptor connecting cilium photoreceptor outer segment layer decreased variability of size, abnormal
ZP:0009137	head lacks parts or has fewer parts of type otic placode, abnormal
ZP:0009138	bile ductule intrahepatic bile duct decreased amount, abnormal
ZP:0009139	1-phosphatidylinositol-4-phosphate 5-kinase activity decreased occurrence, abnormal
ZP:0009140	muscle cell proliferation increased occurrence, abnormal
ZP:0009141	muscle has fewer parts of type sarcoplasmic reticulum muscle cell, abnormal
ZP:0009142	muscle precursor cell decreased amount, abnormal
ZP:0009143	brainstem and spinal white matter decreased amount, abnormal
ZP:0009144	photoreceptor outer segment photoreceptor cell decreased size, abnormal
ZP:0009145	retinal cone cell cellular quality, abnormal
ZP:0009146	retinal rod cell cellular quality, abnormal
ZP:0009147	optic tract composition, abnormal
ZP:0009148	cranial nerve II composition, abnormal
ZP:0009149	optic tectum composition, abnormal
ZP:0009150	amacrine cell mislocalised, abnormal
ZP:0009151	primary motor neuron has fewer parts of type neuron projection primary motor neuron, abnormal
ZP:0009152	neuron projection primary motor neuron decreased branchiness, abnormal
ZP:0009153	primary motor neuron decreased process quality collateral sprouting, abnormal
ZP:0009154	acetylcholine receptor activity disrupted, abnormal
ZP:0009155	mitochondrial matrix trunk musculature absent, abnormal
ZP:0009156	striated muscle thin filament trunk musculature decreased amount, abnormal
ZP:0009157	trunk musculature misaligned with myofibril myofibril trunk musculature, abnormal
ZP:0009158	sarcomere trunk musculature morphology, abnormal
ZP:0009159	actin filament bundle trunk musculature disorganized, abnormal
ZP:0009160	myoseptum U-shaped, abnormal
ZP:0009162	cell proliferation involved in heart morphogenesis decreased occurrence, abnormal
ZP:0009163	cell adhesion involved in heart morphogenesis decreased process quality, abnormal
ZP:0009164	cardiac muscle cell cardiac ventricle decreased area, abnormal
ZP:0009165	heart tube increased fragility, abnormal
ZP:0009167	mastication decreased process quality, abnormal
ZP:0009168	esophagus lacks parts or has fewer parts of type skeletal muscle cell, abnormal
ZP:0009169	skeletal muscle cell esophagus poorly differentiated, abnormal
ZP:0009172	pectoral fin musculature decreased size, abnormal
ZP:0009173	pectoral fin musculature disorganized, abnormal
ZP:0009174	musculoskeletal movement arrested, abnormal
ZP:0009175	basement membrane notochord distributed, abnormal
ZP:0009176	whole organism behavioural inactive, abnormal
ZP:0009177	perichordal connective tissue decreased thickness, abnormal
ZP:0009178	perichordal connective tissue disorganized, abnormal
ZP:0009179	slow muscle cell misaligned with myofibril myofibril slow muscle cell, abnormal
ZP:0009180	fast muscle cell misaligned with myofibril myofibril fast muscle cell, abnormal
ZP:0009181	axon primary motor neuron shape, abnormal
ZP:0009182	neuron projection motor neuron morphology, abnormal
ZP:0009183	neuron projection motor neuron decreased amount, abnormal
ZP:0009184	heart contraction decreased volume, abnormal
ZP:0009185	heart contraction decreased fluid flow, abnormal
ZP:0009186	otic vesicle development arrested, abnormal
ZP:0009187	dorsal region cerebellum morphology, abnormal
ZP:0009188	postero-dorsal region optic tectum morphology, abnormal
ZP:0009189	whole organism disorganized, abnormal
ZP:0009190	G1/S transition of mitotic cell cycle decreased rate, abnormal
ZP:0009191	ethmoid cartilage increased length, abnormal
ZP:0009192	trabecula communis increased length, abnormal
ZP:0009193	pronephros apoptotic, abnormal
ZP:0009194	olfactory bulb apoptotic, abnormal
ZP:0009195	olfactory placode apoptotic, abnormal
ZP:0009196	vertebra 1 malformed, abnormal
ZP:0009197	vertebra 2 malformed, abnormal
ZP:0009198	ventral fin fold apoptotic, abnormal
ZP:0009199	nucleate erythrocyte development decreased occurrence, abnormal
ZP:0009200	action potential disrupted, abnormal
ZP:0009201	basement membrane vertical myoseptum malformed, abnormal
ZP:0009202	myoseptum myotome mislocalised, abnormal
ZP:0009203	muscle cell myotome retracted, abnormal
ZP:0009204	sarcolemma skeletal muscle cell broken, abnormal
ZP:0009205	slow muscle cell retracted, abnormal
ZP:0009206	tectal ventricle morphology, abnormal
ZP:0009207	neuromast deposition disrupted, abnormal
ZP:0009208	parachordal vessel decreased size, abnormal
ZP:0009209	cysteine-type endopeptidase activity increased rate, abnormal
ZP:0009210	chromatin central nervous system condensed, abnormal
ZP:0009211	spinal cord opaque, abnormal
ZP:0009212	protein kinase regulator activity disrupted, abnormal
ZP:0009213	urea cycle disrupted, abnormal
ZP:0009214	epidermis morphogenesis decreased process quality, abnormal
ZP:0009215	epidermis separated from epidermal cell epidermal cell epidermis, abnormal
ZP:0009216	epidermal cell increased variability of size, abnormal
ZP:0009217	neuromuscular junction development decreased process quality, abnormal
ZP:0009218	axonal transport of mitochondrion decreased occurrence, abnormal
ZP:0009219	yolk distended, abnormal
ZP:0009220	somite irregular spatial pattern, abnormal
ZP:0009221	RoP motor neuron decreased length, abnormal
ZP:0009222	RoP motor neuron immature, abnormal
ZP:0009223	axon motor neuron absent, abnormal
ZP:0009224	presynaptic active zone motor neuron decreased area, abnormal
ZP:0009225	neuromuscular junction muscle cell decreased area, abnormal
ZP:0009226	myofibril skeletal muscle cell decreased thickness, abnormal
ZP:0009227	CaP motoneuron disorganized, abnormal
ZP:0009228	CaP motoneuron branchiness, abnormal
ZP:0009229	mitochondrion neuron circular, abnormal
ZP:0009230	mitochondrion neuron mislocalised, abnormal
ZP:0009231	neuron decreased process quality mitochondrion localization, abnormal
ZP:0009232	protein lipidation disrupted, abnormal
ZP:0009233	Wnt protein secretion disrupted, abnormal
ZP:0009234	neural tube shortened, abnormal
ZP:0009235	TOR signaling increased occurrence, abnormal
ZP:0009237	diencephalon bilateral symmetry, abnormal
ZP:0009238	motile cilium pronephric duct increased length, abnormal
ZP:0009239	pancreas primordium mislocalised, abnormal
ZP:0009240	dorsal root ganglion position, abnormal
ZP:0009241	caudal fin skeleton deformed, abnormal
ZP:0009242	trunk neural crest cell mislocalised, abnormal
ZP:0009243	hypophysis disorganized, abnormal
ZP:0009244	adenohypophysis morphology, abnormal
ZP:0009245	somatotropin secreting cell spatial pattern, abnormal
ZP:0009246	prolactin secreting cell spatial pattern, abnormal
ZP:0009247	cilium movement arrested, abnormal
ZP:0009248	induction of programmed cell death increased occurrence, abnormal
ZP:0009249	brain decreased object quality, abnormal
ZP:0009250	neuroepithelial cell hindbrain decreased amount, abnormal
ZP:0009251	heart displaced to right side whole organism, abnormal
ZP:0009252	heart displaced to medial side whole organism, abnormal
ZP:0009253	cell ventricular zone apoptotic, abnormal
ZP:0009254	somite border disorganized, abnormal
ZP:0009255	Mauthner neuron decreased amount, abnormal
ZP:0009256	dopaminergic neuron central nervous system apoptotic, abnormal
ZP:0009257	epidermis median fin fold morphology, abnormal
ZP:0009258	anal fin increased length, abnormal
ZP:0009259	endothelial cell decreased amount, abnormal
ZP:0009260	neuron remodeling disrupted, abnormal
ZP:0009261	peripheral olfactory organ morphology, abnormal
ZP:0009262	synaptic vesicle olfactory receptor cell decreased amount, abnormal
ZP:0009263	axon terminus olfactory receptor cell morphology, abnormal
ZP:0009264	axon terminus olfactory receptor cell increased size, abnormal
ZP:0009267	posterior cardinal vein decreased width, abnormal
ZP:0009268	cranium hemorrhagic, abnormal
ZP:0009269	intersegmental vessel deformed, abnormal
ZP:0009270	myocardium decreased size, abnormal
ZP:0009271	atrial myocardium decreased size, abnormal
ZP:0009274	endocardium development decreased process quality, abnormal
ZP:0009275	median fin fold attenuate, abnormal
ZP:0009276	notochord delaminated, abnormal
ZP:0009277	caudal vein structure, cavities, abnormal
ZP:0009278	blood vessel endothelial cell caudal vein disorganized, abnormal
ZP:0009279	atrium has fewer parts of type atrial endocardium, abnormal
ZP:0009280	posterior cardinal vein decreased diameter, abnormal
ZP:0009281	integument trunk distended, abnormal
ZP:0009282	caudal vein plexus disorganized, abnormal
ZP:0009283	myocardium attached to endocardium, abnormal
ZP:0009284	bleb assembly disrupted, abnormal
ZP:0009285	filamentous actin margin decreased amount, abnormal
ZP:0009286	bleb margin absent, abnormal
ZP:0009287	cell projection prechordal plate decreased amount, abnormal
ZP:0009288	cell projection hypoblast decreased amount, abnormal
ZP:0009289	hindbrain cellular quality, abnormal
ZP:0009290	neuron hindbrain disorganized, abnormal
ZP:0009291	swim bladder malformed, abnormal
ZP:0009292	forebrain truncated, abnormal
ZP:0009293	basibranchial aplastic, abnormal
ZP:0009294	glial cell trigeminal ganglion increased amount, abnormal
ZP:0009295	diencephalic white matter lacks parts or has fewer parts of type postoptic commissure, abnormal
ZP:0009296	telencephalic white matter lacks parts or has fewer parts of type anterior commissure, abnormal
ZP:0009297	whole organism lacks parts or has fewer parts of type facial nerve motor nucleus, abnormal
ZP:0009298	whole organism lacks parts or has fewer parts of type motor nucleus of vagal nerve, abnormal
ZP:0009299	whole organism lacks parts or has fewer parts of type cranial nerve X, abnormal
ZP:0009300	whole organism lacks parts or has fewer parts of type cranial nerve VII, abnormal
ZP:0009301	whole organism lacks parts or has fewer parts of type cranial nerve V, abnormal
ZP:0009302	whole organism lacks parts or has fewer parts of type trigeminal motor nucleus, abnormal
ZP:0009303	cranial neural crest increased size, abnormal
ZP:0009304	axial mesoderm increased width, abnormal
ZP:0009305	axial mesoderm sigmoid, abnormal
ZP:0009306	glial cell posterior lateral line ganglion increased amount, abnormal
ZP:0009307	white matter lacks parts or has fewer parts of type supraoptic tract, abnormal
ZP:0009308	MiP motor neuron decreased amount, abnormal
ZP:0009309	primary motor neuron increased branchiness, abnormal
ZP:0009310	synapse maturation disrupted, abnormal
ZP:0009311	dendrite dorsal habenular nucleus decreased volume, abnormal
ZP:0009312	dendrite habenula absent, abnormal
ZP:0009313	dendrite habenula decreased volume, abnormal
ZP:0009314	dendrite ventral habenular nucleus decreased volume, abnormal
ZP:0009315	ectoderm delaminated, abnormal
ZP:0009316	yolk protruding out of ball, abnormal
ZP:0009317	retrograde axonal transport decreased occurrence, abnormal
ZP:0009318	lysosome localization decreased process quality, abnormal
ZP:0009319	regulation of JNK cascade decreased process quality, abnormal
ZP:0009320	dynein light intermediate chain binding decreased process quality, abnormal
ZP:0009321	central nervous system physical object quality, abnormal
ZP:0009322	peripheral nervous system physical object quality, abnormal
ZP:0009323	axon medial longitudinal fasciculus decreased length, abnormal
ZP:0009324	lysosome posterior lateral line mislocalised, abnormal
ZP:0009325	axon posterior lateral line decreased length, abnormal
ZP:0009326	axon terminus posterior lateral line swollen, abnormal
ZP:0009327	posterior lateral line has extra parts of type axon terminus lysosome posterior lateral line, abnormal
ZP:0009328	neuromuscular junction myotome decreased size, abnormal
ZP:0009329	myotome misaligned with slow muscle cell slow muscle cell myotome, abnormal
ZP:0009330	slow muscle cell curved, abnormal
ZP:0009331	axon extension involved in axon guidance arrested, abnormal
ZP:0009332	heart trabecula formation disrupted, abnormal
ZP:0009333	endocardium atrioventricular canal increased length, abnormal
ZP:0009334	cardiac muscle cell atrioventricular canal increased amount, abnormal
ZP:0009335	cardiac jelly mislocalised, abnormal
ZP:0009336	endocardium far from myocardium, abnormal
ZP:0009337	trabecular layer morphology, abnormal
ZP:0009338	atrioventricular valve increased length, abnormal
ZP:0009339	pectoral fin morphogenesis process quality, abnormal
ZP:0009340	calcium- and calmodulin-dependent protein kinase complex Kupffer's vesicle mislocalised posteriorly, abnormal
ZP:0009341	epidermis structure, abnormal
ZP:0009342	epidermis vacuolated, abnormal
ZP:0009343	basement membrane integument structure, abnormal
ZP:0009344	eye photoreceptor cell development process quality, abnormal
ZP:0009345	inner ear receptor cell development process quality, abnormal
ZP:0009346	stereocilium bundle anterior crista malformed, abnormal
ZP:0009347	photoreceptor connecting cilium eye photoreceptor cell physical object quality, abnormal
ZP:0009348	ceratohyal cartilage orientation axis, abnormal
ZP:0009349	morphogenesis of an epithelial sheet disrupted, abnormal
ZP:0009350	cardiac muscle cell proliferation disrupted, abnormal
ZP:0009351	trunk vasculature broken, abnormal
ZP:0009352	subintestinal vein structure, abnormal
ZP:0009353	subintestinal vein decreased functionality, abnormal
ZP:0009354	nucleate erythrocyte aggregated, abnormal
ZP:0009355	nucleate erythrocyte fluid flow rate, abnormal
ZP:0009356	blood vessel lumenization decreased process quality, abnormal
ZP:0009357	endocardium dilated, abnormal
ZP:0009358	subintestinal vein disheveled, abnormal
ZP:0009359	dorsal convergence decreased duration, abnormal
ZP:0009360	shield increased thickness, abnormal
ZP:0009361	anterior-posterior axis axis elongated, abnormal
ZP:0009362	anterior-posterior axis axis shortened, abnormal
ZP:0009363	anatomical axis trunk increased curvature, abnormal
ZP:0009364	post-vent region increased width, abnormal
ZP:0009366	spinal cord has extra parts of type dorsal region glioblast (sensu Vertebrata), abnormal
ZP:0009367	whole organism lacks all parts of type dorsal longitudinal anastomotic vessel, abnormal
ZP:0009368	oligodendrocyte mislocalised medially, abnormal
ZP:0009369	neuroblast (sensu Vertebrata) increased amount, abnormal
ZP:0009370	glioblast (sensu Vertebrata) increased amount, abnormal
ZP:0009371	axonogenesis increased occurrence, abnormal
ZP:0009372	cranial nerve I fasciculation, abnormal
ZP:0009373	frontonasal suture morphogenesis arrested, abnormal
ZP:0009374	intersegmental lymph vessel aplastic, abnormal
ZP:0009375	dorsal longitudinal lymphatic vessel aplastic, abnormal
ZP:0009376	neuromuscular synaptic transmission decreased occurrence, abnormal
ZP:0009377	high voltage-gated calcium channel activity decreased process quality, abnormal
ZP:0009378	response to external stimulus arrested, abnormal
ZP:0009379	swimming decreased process quality, abnormal
ZP:0009380	swimming behavior absent, abnormal
ZP:0009381	sensory perception of touch decreased intensity, abnormal
ZP:0009382	slow muscle cell non-contractile, abnormal
ZP:0009383	axon terminus motor neuron physical object quality, abnormal
ZP:0009384	retinal inner plexiform layer decreased size, abnormal
ZP:0009385	oocyte maturation decreased occurrence, abnormal
ZP:0009386	germ cell development disrupted, abnormal
ZP:0009387	female organism female sterile, abnormal
ZP:0009388	testis increased size, abnormal
ZP:0009389	testis increased accumulation primordial germ cell, abnormal
ZP:0009390	germ cell tumor testis present, abnormal
ZP:0009391	oocyte stage IV absent, abnormal
ZP:0009392	spermatocyte absent, abnormal
ZP:0009393	synchronous neurotransmitter secretion decreased occurrence, abnormal
ZP:0009394	calcium ion import disrupted, abnormal
ZP:0009395	vH ionocyte decreased functionality, abnormal
ZP:0009396	lens morphogenesis in camera-type eye delayed, abnormal
ZP:0009397	striated muscle contraction disrupted, abnormal
ZP:0009398	heart increased width, abnormal
ZP:0009399	heart tube increased width, abnormal
ZP:0009400	actin filament myotome absent, abnormal
ZP:0009401	sarcomere myotome disorganized, abnormal
ZP:0009402	Z disc myotome structure, abnormal
ZP:0009403	myosin filament myotome absent, abnormal
ZP:0009404	chloride transport disrupted, abnormal
ZP:0009405	erythrocyte maturation delayed, abnormal
ZP:0009406	hemoglobin complex erythroid progenitor cell decreased amount, abnormal
ZP:0009407	anterior side head collapsed, abnormal
ZP:0009408	cilium assembly process quality, abnormal
ZP:0009409	ciliated epithelial cell Kupffer's vesicle physical object quality, abnormal
ZP:0009410	motile cilium pronephric duct direction, abnormal
ZP:0009411	pronephric tubule increased diameter, abnormal
ZP:0009412	filamentous actin ciliated epithelial cell decreased mass, abnormal
ZP:0009413	apical cortex ciliated epithelial cell composition, abnormal
ZP:0009414	mandibular arch skeleton dysplastic, abnormal
ZP:0009415	atrium mislocalised, abnormal
ZP:0009416	cilium olfactory placode structure, abnormal
ZP:0009417	cilium olfactory placode immobile, abnormal
ZP:0009418	cilium spinal cord decreased mobility, abnormal
ZP:0009419	inner dynein arm ciliated cell decreased amount, abnormal
ZP:0009420	outer dynein arm ciliated cell decreased amount, abnormal
ZP:0009421	caudal vein plexus immature, abnormal
ZP:0009422	notochord collapsed, abnormal
ZP:0009423	hemal spine caudal vertebra decreased amount, abnormal
ZP:0009424	vertebra deformed, abnormal
ZP:0009425	neural spine decreased amount, abnormal
ZP:0009426	vertebral column curved lateral, abnormal
ZP:0009427	mesenchymal cell proliferation decreased rate, abnormal
ZP:0009428	vascular sprouts increased amount, abnormal
ZP:0009429	pronephric duct collapsed, abnormal
ZP:0009430	intraciliary transport particle photoreceptor cell spatial pattern, abnormal
ZP:0009431	metallopeptidase activity disrupted, abnormal
ZP:0009432	heart contraction rate, abnormal
ZP:0009433	yolk width, abnormal
ZP:0009434	melanosome integument decreased size, abnormal
ZP:0009435	melanosome integument variant shape, abnormal
ZP:0009436	melanosome integument decreased pigmentation, abnormal
ZP:0009437	phosphate ion homeostasis disrupted, abnormal
ZP:0009438	fast muscle myoblast morphology, abnormal
ZP:0009439	fast muscle myoblast irregular spatial pattern, abnormal
ZP:0009440	voltage-gated sodium channel activity decreased rate, abnormal
ZP:0009441	neuronal action potential process quality, abnormal
ZP:0009442	neuron apoptotic process decreased occurrence, abnormal
ZP:0009443	Rohon-Beard neuron alive, abnormal
ZP:0009444	Rohon-Beard neuron increased age, abnormal
ZP:0009446	chondrocyte Meckel's cartilage circular, abnormal
ZP:0009448	mitotic spindle neural plate decreased functionality, abnormal
ZP:0009449	neuron medial longitudinal fasciculus decreased amount, abnormal
ZP:0009450	neuron rhombomere decreased amount, abnormal
ZP:0009451	axon anterior commissure organization quality, abnormal
ZP:0009452	neural tube decreased size, abnormal
ZP:0009453	cell neural tube decreased amount, abnormal
ZP:0009454	Rohon-Beard neuron decreased branchiness, abnormal
ZP:0009455	platelet formation disrupted, abnormal
ZP:0009456	cranial nerve development disrupted, abnormal
ZP:0009457	glial cell hindbrain decreased amount, abnormal
ZP:0009458	adherens junction assembly disrupted, abnormal
ZP:0009459	caudal vein increased permeability, abnormal
ZP:0009460	caudal vein plexus broken, abnormal
ZP:0009461	dorsal longitudinal anastomotic vessel increased permeability, abnormal
ZP:0009462	blood vessel endothelial cell has fewer parts of type cell-cell junction blood vessel endothelial cell, abnormal
ZP:0009463	adherens junction blood vessel endothelial cell immature, abnormal
ZP:0009465	margin poorly differentiated, abnormal
ZP:0009466	optic primordium shape, abnormal
ZP:0009467	optic primordium hypoplastic, abnormal
ZP:0009468	blastoderm thickness, abnormal
ZP:0009469	nucleus lens epithelium mislocalised, abnormal
ZP:0009470	pronephric podocyte shape, abnormal
ZP:0009471	pronephric glomerular capsule dilated, abnormal
ZP:0009472	pronephric glomerular basement membrane broken, abnormal
ZP:0009473	basement membrane lens capsule decreased thickness, abnormal
ZP:0009474	basement membrane lens capsule broken, abnormal
ZP:0009475	neutral lipid metabolic process process quality, abnormal
ZP:0009476	monocarboxylic acid transmembrane transporter activity decreased process quality, abnormal
ZP:0009477	response to starvation process quality, abnormal
ZP:0009478	response to starvation decreased process quality, abnormal
ZP:0009479	hepaticobiliary system process decreased process quality, abnormal
ZP:0009480	anatomical compartment boundary paraxial mesoderm disorganized, abnormal
ZP:0009481	anatomical compartment boundary paraxial mesoderm distributed, abnormal
ZP:0009482	anatomical axis whole organism shortened, abnormal
ZP:0009483	whole organism dissociated from cell yolk, abnormal
ZP:0009484	regulation of pH process quality, abnormal
ZP:0009485	sodium ion homeostasis process quality, abnormal
ZP:0009486	thymus development delayed, abnormal
ZP:0009487	thymocyte migration disrupted, abnormal
ZP:0009488	ventral region retina morphology, abnormal
ZP:0009489	ceratobranchial bone deformed, abnormal
ZP:0009490	ceratohyal bone deformed, abnormal
ZP:0009492	retinal inner plexiform layer morphology, abnormal
ZP:0009493	locomotion process quality, abnormal
ZP:0009494	abductor hyohyoid lacks parts or has fewer parts of type skeletal muscle cell, abnormal
ZP:0009495	adductor operculi physical object quality, abnormal
ZP:0009496	myoblast adductor operculi decreased amount, abnormal
ZP:0009497	myoblast dilatator operculi decreased amount, abnormal
ZP:0009498	levator operculi physical object quality, abnormal
ZP:0009499	myoblast levator operculi decreased amount, abnormal
ZP:0009500	adductor hyohyoid lacks parts or has fewer parts of type skeletal muscle cell, abnormal
ZP:0009501	muscle organ development arrested, abnormal
ZP:0009502	somite dispersed, abnormal
ZP:0009503	thyroid follicle decreased size, abnormal
ZP:0009504	thyroid follicle poorly differentiated, abnormal
ZP:0009505	hemoglobin complex intermediate cell mass of mesoderm absent, abnormal
ZP:0009506	nucleate erythrocyte proportionality to nucleus cytoplasm nucleate erythrocyte, abnormal
ZP:0009507	cerebellar Purkinje cell differentiation disrupted, abnormal
ZP:0009508	cerebellar granule cell decreased amount, abnormal
ZP:0009509	Purkinje cell decreased amount, abnormal
ZP:0009510	hypophysis has fewer parts of type vasculature blood vessel endothelial cell, abnormal
ZP:0009511	vasculature neurohypophysis hypoplastic, abnormal
ZP:0009512	hyaloid vessel structure, abnormal
ZP:0009513	hyaloid vessel decreased diameter, abnormal
ZP:0009514	enteroendocrine cell differentiation disrupted, abnormal
ZP:0009515	goblet cell posterior intestine decreased amount, abnormal
ZP:0009516	goblet cell intestinal bulb decreased amount, abnormal
ZP:0009517	intestine distended, abnormal
ZP:0009518	goblet cell decreased amount, abnormal
ZP:0009519	goblet cell poorly differentiated, abnormal
ZP:0009520	chondrocyte hypertrophy premature, abnormal
ZP:0009521	hypertrophic chondrocyte increased amount, abnormal
ZP:0009525	spinal cord deformed, abnormal
ZP:0009526	determination of bilateral symmetry decreased process quality, abnormal
ZP:0009527	pectoral fin development process quality, abnormal
ZP:0009528	skeletal muscle cell differentiation process quality, abnormal
ZP:0009529	motile cilium Kupffer's vesicle absent, abnormal
ZP:0009531	motile cilium pronephric duct absent, abnormal
ZP:0009533	pectoral fin bilateral symmetry, abnormal
ZP:0009534	exocrine pancreas absent, abnormal
ZP:0009535	exocrine pancreas bilateral symmetry, abnormal
ZP:0009536	cerebellar central artery branchiness, abnormal
ZP:0009537	retinal bipolar neuron decreased functionality, abnormal
ZP:0009538	intestine lacks all parts of type goblet cell, abnormal
ZP:0009539	blood accumulation sinus venosus, abnormal
ZP:0009540	apical-basal axis relative to substrate whole organism increased curvature, abnormal
ZP:0009541	protoneuromast disorganized, abnormal
ZP:0009542	signal transduction in response to DNA damage decreased process quality, abnormal
ZP:0009543	myofibril muscle morphology, abnormal
ZP:0009544	sarcolemma muscle perforate, abnormal
ZP:0009545	neutrophil activation involved in immune response disrupted, abnormal
ZP:0009546	collateral sprouting decreased occurrence, abnormal
ZP:0009547	upper region head flattened, abnormal
ZP:0009548	main axon Rohon-Beard neuron decreased length, abnormal
ZP:0009549	ceratobranchial cartilage increased width, abnormal
ZP:0009550	hypophyseal fenestra absent, abnormal
ZP:0009551	hypophyseal fenestra decreased size, abnormal
ZP:0009552	neural precursor cell proliferation increased rate, abnormal
ZP:0009553	retina vasculature development in camera-type eye disrupted, abnormal
ZP:0009554	vascular sprouts morphology, abnormal
ZP:0009555	ocular blood vessel morphology, abnormal
ZP:0009556	thigmotropism decreased occurrence, abnormal
ZP:0009557	whole organism increased contractility, abnormal
ZP:0009558	mandibular arch skeleton movement quality, abnormal
ZP:0009559	neuroblast decreased amount, abnormal
ZP:0009560	steroid biosynthetic process disrupted, abnormal
ZP:0009561	cortisol biosynthetic process disrupted, abnormal
ZP:0009562	motor neuron migration disrupted, abnormal
ZP:0009565	neuroectoderm increased width, abnormal
ZP:0009569	endocardial cushion development arrested, abnormal
ZP:0009570	endocardial cushion development disrupted, abnormal
ZP:0009571	heart lacks all parts of type endocardial cushion, abnormal
ZP:0009572	locomotion arrested, abnormal
ZP:0009573	atrial cardiac muscle cell differentiation disrupted, abnormal
ZP:0009574	endocrine pancreas lacks parts or has fewer parts of type insulin secreting cell, abnormal
ZP:0009575	endocrine pancreas lacks parts or has fewer parts of type glucagon secreting cell, abnormal
ZP:0009576	endocrine pancreas lacks parts or has fewer parts of type somatostatin secreting cell, abnormal
ZP:0009577	posterior pancreatic bud lacks parts or has fewer parts of type insulin secreting cell, abnormal
ZP:0009578	posterior pancreatic bud lacks parts or has fewer parts of type somatostatin secreting cell, abnormal
ZP:0009579	Kolmer-Agduhr neuron increased amount, abnormal
ZP:0009580	axon pectoral fin motor nerve decreased amount, abnormal
ZP:0009581	axon motor neuron mislocalised posteriorly, abnormal
ZP:0009582	axon CaP motoneuron absent, abnormal
ZP:0009583	secondary motor neuron absent, abnormal
ZP:0009584	axon secondary motor neuron disorganized, abnormal
ZP:0009585	neuron posterior lateral line ganglion decreased amount, abnormal
ZP:0009586	somite border somite 1 amorphous, abnormal
ZP:0009587	somite border somite 2 amorphous, abnormal
ZP:0009588	somite border somite 3 amorphous, abnormal
ZP:0009590	positive regulation of transcription, DNA-templated disrupted, abnormal
ZP:0009591	neuron locus coeruleus decreased amount, abnormal
ZP:0009592	neuromuscular synaptic transmission increased duration, abnormal
ZP:0009593	acetylcholine receptor activity increased duration, abnormal
ZP:0009594	acetylcholine receptor activity physiological state, abnormal
ZP:0009595	fast-twitch skeletal muscle fiber contraction decreased rate, abnormal
ZP:0009596	behavioral response to nicotine decreased occurrence, abnormal
ZP:0009597	membrane repolarization decreased rate, abnormal
ZP:0009598	mouth morphology, abnormal
ZP:0009599	muscle cell increased permeability, abnormal
ZP:0009600	pharyngeal arch 3-7 skeleton malformed, abnormal
ZP:0009601	neuron peripheral nervous system decreased amount, abnormal
ZP:0009602	whole organism lacks all parts of type neuron dorsal root ganglion, abnormal
ZP:0009603	pharyngeal arch 2 skeleton malformed, abnormal
ZP:0009604	phagocytosis decreased occurrence, abnormal
ZP:0009605	blood vessel endothelial cell common cardinal vein increased amount, abnormal
ZP:0009606	erythroid progenitor cell increased amount, abnormal
ZP:0009607	microglial cell absent, abnormal
ZP:0009608	leukocyte absent, abnormal
ZP:0009609	myeloid cell absent, abnormal
ZP:0009610	erythroid lineage cell increased amount, abnormal
ZP:0009611	neutrophil absent, abnormal
ZP:0009613	odontogenesis delayed, abnormal
ZP:0009614	muscle cell differentiation decreased occurrence, abnormal
ZP:0009615	striated muscle cell differentiation delayed, abnormal
ZP:0009616	striated muscle cell differentiation process quality, abnormal
ZP:0009617	adaxial cell immature, abnormal
ZP:0009618	somite has extra parts of type muscle precursor cell, abnormal
ZP:0009619	segmental plate has fewer parts of type anterior region adaxial cell, abnormal
ZP:0009620	pectoral girdle morphology, abnormal
ZP:0009621	myoseptum aplastic, abnormal
ZP:0009623	pectoral fin variability of size, abnormal
ZP:0009624	fin fold pectoral fin bud disorganized, abnormal
ZP:0009625	retinal cone cell irregular spatial pattern, abnormal
ZP:0009626	brain lacks all parts of type midbrain hindbrain boundary, abnormal
ZP:0009628	hindbrain cellular adhesivity cell cell hindbrain, abnormal
ZP:0009629	macula morphology, abnormal
ZP:0009630	lateral longitudinal fasciculus decreased size, abnormal
ZP:0009631	medial longitudinal fasciculus decreased size, abnormal
ZP:0009632	rhombomere 5 shape, abnormal
ZP:0009633	rhombomere 3 shape, abnormal
ZP:0009634	post-vent region cystic, abnormal
ZP:0009635	post-vent region cellular adhesivity cell cell post-vent region, abnormal
ZP:0009636	locus ceruleus development disrupted, abnormal
ZP:0009637	parasympathetic nervous system development disrupted, abnormal
ZP:0009639	pars intermedia physical object quality, abnormal
ZP:0009640	epibranchial placode morphology, abnormal
ZP:0009642	osteoblast proliferation increased occurrence, abnormal
ZP:0009643	pigmentation decreased process quality, abnormal
ZP:0009645	cell retinal ganglion cell layer increased amount, abnormal
ZP:0009646	cell retinal inner nuclear layer increased amount, abnormal
ZP:0009647	dorsal region retina disorganized, abnormal
ZP:0009648	cell retina increased amount, abnormal
ZP:0009649	muscle pioneer somite increased amount, abnormal
ZP:0009651	postero-ventral margin opercle increased length, abnormal
ZP:0009652	inner limiting membrane disorganized, abnormal
ZP:0009653	inner limiting membrane broken, abnormal
ZP:0009654	osteoblast Meckel's cartilage increased amount, abnormal
ZP:0009655	iris increased size, abnormal
ZP:0009656	neuronal stem cell ciliary marginal zone increased amount, abnormal
ZP:0009657	cell retinal outer nuclear layer increased amount, abnormal
ZP:0009658	retinal outer nuclear layer displaced to photoreceptor cell ciliary marginal zone, abnormal
ZP:0009659	slow muscle cell absent, abnormal
ZP:0009660	fast muscle cell mislocalised, abnormal
ZP:0009661	photoreceptor cell mislocalised, abnormal
ZP:0009662	axon terminus Muller cell physical object quality, abnormal
ZP:0009663	negative regulation of neurogenesis decreased occurrence, abnormal
ZP:0009664	neuron rhombomere 2 mislocalised, abnormal
ZP:0009665	neuron rhombomere 4 mislocalised, abnormal
ZP:0009666	hypothalamus morphology, abnormal
ZP:0009667	cranial neural crest apoptotic, abnormal
ZP:0009668	palatoquadrate cartilage morphology, abnormal
ZP:0009669	hyosymplectic cartilage morphology, abnormal
ZP:0009670	chondrocyte ceratobranchial cartilage decreased amount, abnormal
ZP:0009671	vertebral artery aplastic, abnormal
ZP:0009672	vasculature lacks parts or has fewer parts of type intersegmental vessel, abnormal
ZP:0009673	eye swollen, abnormal
ZP:0009674	eye mislocalised laterally, abnormal
ZP:0009675	maxilla shape, abnormal
ZP:0009676	maxilla fused with maxilla, abnormal
ZP:0009677	pharyngeal arch 2 skeleton disorganized, abnormal
ZP:0009678	branchiostegal ray 1 aplastic, abnormal
ZP:0009679	branchiostegal ray 3 decreased size, abnormal
ZP:0009680	palatoquadrate cartilage structure, abnormal
ZP:0009681	hyosymplectic cartilage structure, abnormal
ZP:0009682	ceratobranchial 2 cartilage aplastic, abnormal
ZP:0009683	ceratobranchial 1 cartilage truncated, abnormal
ZP:0009684	ceratobranchial 5 cartilage truncated, abnormal
ZP:0009685	endochondral bone aplastic, abnormal
ZP:0009688	axon VaP motor neuron mislocalised, abnormal
ZP:0009689	axon CaP motoneuron mislocalised, abnormal
ZP:0009693	opercle increased variability, abnormal
ZP:0009694	opercle distended, abnormal
ZP:0009695	opercle fused with branchiostegal ray 3, abnormal
ZP:0009696	branchiostegal ray fan-shaped, abnormal
ZP:0009697	bone tissue cranium mislocalised, abnormal
ZP:0009698	myotome decreased volume, abnormal
ZP:0009699	branchiostegal ray 3 increased variability, abnormal
ZP:0009700	ceratohyal cartilage split, abnormal
ZP:0009701	myofibril skeletal muscle cell decreased diameter, abnormal
ZP:0009705	skin morphogenesis process quality, abnormal
ZP:0009706	scale increased size, abnormal
ZP:0009707	scale patchy, abnormal
ZP:0009708	dorsal aorta morphogenesis disrupted, abnormal
ZP:0009709	blood decreased viscosity, abnormal
ZP:0009710	circulating cell blood absent, abnormal
ZP:0009711	circulating cell blood decreased amount, abnormal
ZP:0009712	lateral dorsal aorta dilated, abnormal
ZP:0009713	Kolmer-Agduhr neuron lateral floor plate undifferentiated, abnormal
ZP:0009714	atrioventricular valve absent, abnormal
ZP:0009716	cephalic musculature aplastic, abnormal
ZP:0009718	heme biosynthetic process arrested, abnormal
ZP:0009719	monocyte differentiation increased occurrence, abnormal
ZP:0009720	macrophage differentiation increased occurrence, abnormal
ZP:0009721	nucleate erythrocyte present, abnormal
ZP:0009722	myeloid cell increased amount, abnormal
ZP:0009724	eye perforate, abnormal
ZP:0009726	ventral region retinal pigmented epithelium absent, abnormal
ZP:0009728	post-vent region wholly ventralized, abnormal
ZP:0009731	hindbrain structural organization disrupted, abnormal
ZP:0009732	hindbrain deformed, abnormal
ZP:0009733	choroid plexus fourth ventricle increased size, abnormal
ZP:0009734	otic vesicle development disrupted, abnormal
ZP:0009735	thymus lacks all parts of type lymphocyte, abnormal
ZP:0009736	thymus has fewer parts of type lymphocyte, abnormal
ZP:0009737	epithelium thymus morphology, abnormal
ZP:0009738	digestive system process disrupted, abnormal
ZP:0009739	mouth closed, abnormal
ZP:0009740	neuron posterior intestine absent, abnormal
ZP:0009741	neuron projection posterior lateral line primordium absent, abnormal
ZP:0009747	heart tube shape, abnormal
ZP:0009748	atrium shape, abnormal
ZP:0009753	atrial myocardium increased size, abnormal
ZP:0009754	atrial myocardium increased width, abnormal
ZP:0009755	atrial myocardium dilated, abnormal
ZP:0009756	atrial myocardium distended, abnormal
ZP:0009757	atrial myocardium bulbous, abnormal
ZP:0009758	ventricular myocardium decreased width, abnormal
ZP:0009759	ventricular myocardium shortened, abnormal
ZP:0009760	blood vessel endothelial cell intersegmental artery decreased amount, abnormal
ZP:0009761	foregut morphogenesis disrupted, abnormal
ZP:0009762	ball constricted, abnormal
ZP:0009763	liver mislocalised posteriorly, abnormal
ZP:0009764	pancreas mislocalised posteriorly, abnormal
ZP:0009765	whole organism spherical, abnormal
ZP:0009766	corpuscles of Stannius decreased size, abnormal
ZP:0009767	corpuscles of Stannius mislocalised posteriorly, abnormal
ZP:0009768	exocrine pancreas mislocalised posteriorly, abnormal
ZP:0009769	endocrine pancreas mislocalised posteriorly, abnormal
ZP:0009770	pronephric proximal convoluted tubule increased length, abnormal
ZP:0009771	pronephric proximal straight tubule decreased length, abnormal
ZP:0009772	pronephric distal early tubule decreased length, abnormal
ZP:0009773	posterior pronephric duct decreased length, abnormal
ZP:0009774	pronephric distal late tubule decreased length, abnormal
ZP:0009775	neural crest cell mislocalised posteriorly, abnormal
ZP:0009776	mesoderm formation disrupted, abnormal
ZP:0009777	brain poorly differentiated, abnormal
ZP:0009778	presumptive neural plate wholly anterioralized, abnormal
ZP:0009779	axis mislocalised posteriorly, abnormal
ZP:0009780	forebrain prominent, abnormal
ZP:0009781	forebrain distended, abnormal
ZP:0009782	somite aplastic, abnormal
ZP:0009784	mesoderm trunk decreased size, abnormal
ZP:0009785	mesoderm post-vent region decreased size, abnormal
ZP:0009786	presumptive mesoderm wholly dorsalized, abnormal
ZP:0009787	neural crest cell morphology, abnormal
ZP:0009788	nucleus brain decreased amount, abnormal
ZP:0009789	nucleus spinal cord decreased amount, abnormal
ZP:0009790	central canal unlumenized, abnormal
ZP:0009791	neurogenic placode morphology, abnormal
ZP:0009793	heart tube fused with heart tube, abnormal
ZP:0009794	iron ion transport disrupted, abnormal
ZP:0009795	habenular commissure absent, abnormal
ZP:0009796	habenular commissure decreased thickness, abnormal
ZP:0009797	habenular commissure discontinuous, abnormal
ZP:0009798	habenular commissure decreased process quality axon extension involved in axon guidance, abnormal
ZP:0009799	fin morphogenesis process quality, abnormal
ZP:0009800	caudal fin lepidotrichium undivided, abnormal
ZP:0009801	joint caudal fin lepidotrichium absent, abnormal
ZP:0009802	pectoral fin lepidotrichium undivided, abnormal
ZP:0009803	joint pectoral fin lepidotrichium absent, abnormal
ZP:0009804	lepidotrichium undivided, abnormal
ZP:0009805	joint lepidotrichium absent, abnormal
ZP:0009806	posterior side notochord disorganized, abnormal
ZP:0009807	melanocyte disorganized, abnormal
ZP:0009809	lens vacuolated, abnormal
ZP:0009810	GABAergic neuron retina mislocalised, abnormal
ZP:0009811	ventral region optic tectum morphology, abnormal
ZP:0009812	ventrolateral optic tract quality, abnormal
ZP:0009813	ventrolateral optic tract agenesis, abnormal
ZP:0009814	axial vasculature hemorrhagic, abnormal
ZP:0009815	optic fissure morphology, abnormal
ZP:0009816	optic fissure mislocalised, abnormal
ZP:0009817	ceratohyal cartilage mislocalised medially, abnormal
ZP:0009818	ceratohyal cartilage overlap with ceratohyal cartilage, abnormal
ZP:0009819	ceratobranchial 2 cartilage mislocalised anteriorly, abnormal
ZP:0009820	ceratobranchial 2 cartilage orientation ceratobranchial 2 cartilage, abnormal
ZP:0009821	ceratobranchial 1 cartilage mislocalised anteriorly, abnormal
ZP:0009822	ceratobranchial 1 cartilage orientation ceratobranchial 1 cartilage, abnormal
ZP:0009823	hypobranchial cartilage decreased width, abnormal
ZP:0009824	hypobranchial cartilage notched, abnormal
ZP:0009825	Muller cell disorganized, abnormal
ZP:0009826	liver development decreased process quality, abnormal
ZP:0009827	epiphysis has fewer parts of type photoreceptor cell, abnormal
ZP:0009828	anterior pancreatic bud hypoplastic, abnormal
ZP:0009829	anterior pancreatic bud aplastic, abnormal
ZP:0009830	musculoskeletal movement decreased occurrence, abnormal
ZP:0009834	primary motor neuron decreased process quality axon extension, abnormal
ZP:0009836	secondary motor neuron decreased process quality axon extension, abnormal
ZP:0009837	lymphatic endothelial cell differentiation disrupted, abnormal
ZP:0009838	neuron hypothalamus decreased amount, abnormal
ZP:0009839	somatic stem cell neuromast immature, abnormal
ZP:0009840	kinocilium neuromast hair cell absent, abnormal
ZP:0009841	hyomandibula bifurcated, abnormal
ZP:0009842	hyomandibula cylindrical, abnormal
ZP:0009843	trabecula cranii unfused from posterior region neurocranium, abnormal
ZP:0009844	chondrocyte trabecula cranii disorganized, abnormal
ZP:0009845	spinal cord oligodendrocyte cell differentiation delayed, abnormal
ZP:0009846	spinal cord oligodendrocyte cell fate specification process quality, abnormal
ZP:0009847	oligodendrocyte differentiation decreased frequency, abnormal
ZP:0009848	spinal cord has fewer parts of type oligodendrocyte, abnormal
ZP:0009849	spinal cord has extra parts of type oligodendrocyte, abnormal
ZP:0009850	endocrine pancreas physical object quality, abnormal
ZP:0009851	bicellular tight junction glial cell absent, abnormal
ZP:0009852	myelinating Schwann cell mislocalised, abnormal
ZP:0009854	floor plate disorganized, abnormal
ZP:0009855	floor plate undifferentiated, abnormal
ZP:0009857	hypochord decreased length, abnormal
ZP:0009858	hypochord disorganized, abnormal
ZP:0009859	hypochord aplastic, abnormal
ZP:0009860	axial chorda mesoderm decreased width, abnormal
ZP:0009863	paraxial mesoderm increased area, abnormal
ZP:0009864	paraxial mesoderm fused with left side right side paraxial mesoderm, abnormal
ZP:0009866	extrahepatic duct absent, abnormal
ZP:0009867	embryonic retina morphogenesis in camera-type eye decreased process quality, abnormal
ZP:0009868	retinal blood vessel morphogenesis decreased process quality, abnormal
ZP:0009869	whole organism lacks all parts of type nucleate erythrocyte, abnormal
ZP:0009870	optic fissure increased width, abnormal
ZP:0009871	hyaloid artery constricted, abnormal
ZP:0009872	hyaloid vein dilated, abnormal
ZP:0009873	ocular blood vessel dilated, abnormal
ZP:0009874	ocular blood vessel increased permeability, abnormal
ZP:0009875	ocular blood vessel increased diameter, abnormal
ZP:0009876	anterior axial hypoblast morphology, abnormal
ZP:0009877	prechordal plate poorly differentiated, abnormal
ZP:0009878	ventral mesenchyme distended, abnormal
ZP:0009879	protein autophosphorylation arrested, abnormal
ZP:0009881	posterior region gut increased thickness, abnormal
ZP:0009882	primitive heart tube bilateral symmetry, abnormal
ZP:0009883	mesoderm post-vent region decreased amount, abnormal
ZP:0009884	notochord posterior region absent, abnormal
ZP:0009885	osteoclast differentiation premature, abnormal
ZP:0009886	eye structure, abnormal
ZP:0009887	eye curved lateral, abnormal
ZP:0009888	eye protruding into diencephalon, abnormal
ZP:0009889	optic stalk mislocalised, abnormal
ZP:0009890	optic stalk distended, abnormal
ZP:0009891	optic stalk kinked, abnormal
ZP:0009892	retinal pigmented epithelium displaced, abnormal
ZP:0009893	retina protruding, abnormal
ZP:0009894	retina displaced, abnormal
ZP:0009895	somite orientation somite, abnormal
ZP:0009896	optic tectum proliferative, abnormal
ZP:0009897	osteoclast opercular flap differentiated, abnormal
ZP:0009898	osteoclast caudal fin skeleton differentiated, abnormal
ZP:0009899	osteoclast neural arch differentiated, abnormal
ZP:0009901	osteoclast Meckel's cartilage differentiated, abnormal
ZP:0009902	osteoclast pharyngeal arch 7 skeleton differentiated, abnormal
ZP:0009903	ventral mandibular arch proliferative, abnormal
ZP:0009904	photoreceptor outer segment layer protruding, abnormal
ZP:0009905	skeletal muscle cell has fewer parts of type myosin filament skeletal muscle cell, abnormal
ZP:0009906	cardiac muscle cell has fewer parts of type myosin filament cardiac muscle cell, abnormal
ZP:0009907	intercalated disc cardiac muscle cell malformed, abnormal
ZP:0009908	melanocyte migration arrested, abnormal
ZP:0009909	gut decreased contractility, abnormal
ZP:0009910	gut distended, abnormal
ZP:0009911	melanocyte head absent, abnormal
ZP:0009912	melanocyte head mislocalised, abnormal
ZP:0009913	melanocyte ventral larval melanophore stripe decreased amount, abnormal
ZP:0009914	melanocyte shape, abnormal
ZP:0009915	melanocyte circular, abnormal
ZP:0009917	melanocyte increased occurrence apoptotic process, abnormal
ZP:0009918	melanosome melanocyte low saturation, abnormal
ZP:0009919	melanoblast increased amount, abnormal
ZP:0009920	ependymal cell spinal cord proliferative, abnormal
ZP:0009921	convergent extension involved in axis elongation process quality, abnormal
ZP:0009922	myofibril cardiac ventricle disorganized, abnormal
ZP:0009923	optic vesicle mislocalised, abnormal
ZP:0009924	axis thickness, abnormal
ZP:0009925	pronephric duct aplastic, abnormal
ZP:0009926	rhombomere 3 fused with left side right side rhombomere 3, abnormal
ZP:0009927	neuron spinal cord neural rod absent, abnormal
ZP:0009928	heart looping decreased occurrence, abnormal
ZP:0009929	posterior lateral line lacks parts or has fewer parts of type neuromast, abnormal
ZP:0009930	neuron projection posterior lateral line mislocalised, abnormal
ZP:0009931	neuron posterior lateral line decreased branchiness, abnormal
ZP:0009932	caudal fin decreased process quality blood circulation, abnormal
ZP:0009933	trunk lacks parts or has fewer parts of type neuromast, abnormal
ZP:0009934	nucleate erythrocyte differentiation disrupted, abnormal
ZP:0009935	solid lens vesicle morphology, abnormal
ZP:0009936	endothelial cell migration disrupted, abnormal
ZP:0009938	presumptive endocardium heart primordium aplastic, abnormal
ZP:0009939	epithelium ventricular endocardium aplastic, abnormal
ZP:0009940	trunk vasculature decreased size, abnormal
ZP:0009941	post-vent vasculature decreased size, abnormal
ZP:0009942	medial longitudinal fasciculus defasciculated, abnormal
ZP:0009943	interhyal cartilage fused with ceratohyal cartilage, abnormal
ZP:0009944	interhyal cartilage fused with hyosymplectic cartilage, abnormal
ZP:0009946	polster increased length, abnormal
ZP:0009947	prechordal plate shape, abnormal
ZP:0009948	prechordal plate increased size, abnormal
ZP:0009949	rhombomere 5 development disrupted, abnormal
ZP:0009950	rhombomere 6 development disrupted, abnormal
ZP:0009951	semicircular canal formation process quality, abnormal
ZP:0009952	rhombomere 6 aplastic, abnormal
ZP:0009953	anterior/posterior compartment boundary rhombomere 6 absent, abnormal
ZP:0009954	rhombomere 6 arrested rhombomere boundary formation, abnormal
ZP:0009955	anterior/posterior compartment boundary rhombomere 5 absent, abnormal
ZP:0009956	rhombomere 5 arrested rhombomere boundary formation, abnormal
ZP:0009957	anterior/posterior compartment boundary rhombomere 7 absent, abnormal
ZP:0009958	cartilage element pharyngeal arch malformed, abnormal
ZP:0009959	cartilage element pharyngeal arch 3 increased thickness, abnormal
ZP:0009960	cartilage element pharyngeal arch 3 truncated, abnormal
ZP:0009961	axon hindbrain commissure decussate, abnormal
ZP:0009962	neural crest hindbrain process quality neural crest cell migration, abnormal
ZP:0009963	xanthophore differentiation disrupted, abnormal
ZP:0009964	sensory neuron dorsal root ganglion mislocalised dorsally, abnormal
ZP:0009965	pterinosome head decreased amount, abnormal
ZP:0009966	pterinosome trunk absent, abnormal
ZP:0009967	melanocyte trunk increased amount, abnormal
ZP:0009968	melanocyte trunk decreased size, abnormal
ZP:0009969	melanocyte trunk mislocalised, abnormal
ZP:0009970	xanthophore trunk colorless, abnormal
ZP:0009971	xanthophore trunk absent, abnormal
ZP:0009973	neuron neural crest derived presumptive enteric nervous system decreased amount, abnormal
ZP:0009974	melanocyte melanophore stripe increased amount, abnormal
ZP:0009975	neural crest cell delaminated, abnormal
ZP:0009976	cranial nerve VI hypoplastic, abnormal
ZP:0009977	cranial nerve X hypoplastic, abnormal
ZP:0009978	cranial nerve VII hypoplastic, abnormal
ZP:0009979	cranial nerve IX hypoplastic, abnormal
ZP:0009980	ceratobranchial 5 tooth malformed, abnormal
ZP:0009981	pharyngeal arch mislocalised laterally, abnormal
ZP:0009982	adrenal gland development disrupted, abnormal
ZP:0009983	pronephros morphogenesis disrupted, abnormal
ZP:0009984	pronephros decreased size, abnormal
ZP:0009985	interrenal primordium decreased size, abnormal
ZP:0009986	coelom edematous, abnormal
ZP:0009987	head muscle poorly differentiated, abnormal
ZP:0009988	CaP motoneuron physical quality of a process axon guidance, abnormal
ZP:0009989	axon CaP motoneuron truncated, abnormal
ZP:0009990	axon CaP motoneuron branchiness, abnormal
ZP:0009991	CaP motoneuron decreased process quality axon extension, abnormal
ZP:0009992	Muller cell retinal neural layer decreased amount, abnormal
ZP:0009993	retinal cone cell retinal photoreceptor layer decreased amount, abnormal
ZP:0009994	anterior macula has fewer parts of type hair cell anterior macula, abnormal
ZP:0009995	Muller cell proliferative, abnormal
ZP:0009997	tail bud duplicated, abnormal
ZP:0009999	caudal fin duplicated, abnormal
ZP:0010000	scapulocoracoid pectoral fin fold absent, abnormal
ZP:0010001	endochondral bone pectoral fin fold absent, abnormal
ZP:0010002	unidimensional cell growth disrupted, abnormal
ZP:0010003	cell projection hypoblast deviation, abnormal
ZP:0010004	cell hypoblast circular, abnormal
ZP:0010005	central canal bent, abnormal
ZP:0010006	central canal kinked, abnormal
ZP:0010007	anterior cerebral vein morphology, abnormal
ZP:0010008	anterior cerebral vein decreased size, abnormal
ZP:0010009	anterior region whole organism morphology, abnormal
ZP:0010010	head increased width, abnormal
ZP:0010011	head condensed, abnormal
ZP:0010013	anterior-posterior axis trunk bifurcated, abnormal
ZP:0010014	ceratohyal cartilage increased size, abnormal
ZP:0010015	cranial cartilage decreased length, abnormal
ZP:0010016	chondrocyte pharyngeal arch cartilage increased amount, abnormal
ZP:0010017	chondrocyte pharyngeal arch cartilage decreased size, abnormal
ZP:0010018	notochord posterior region bent, abnormal
ZP:0010019	mid cerebral vein decreased size, abnormal
ZP:0010020	ectodermal cell circular, abnormal
ZP:0010021	cell projection ectodermal cell deviation, abnormal
ZP:0010022	muscle cell differentiation process quality, abnormal
ZP:0010023	mesodermal cell heart primordium decreased amount, abnormal
ZP:0010024	cardiac muscle myoblast heart primordium decreased amount, abnormal
ZP:0010025	proctodeum malformed, abnormal
ZP:0010026	swim bladder disorganized, abnormal
ZP:0010027	cerebellum physical object quality, abnormal
ZP:0010028	anterior macula increased size, abnormal
ZP:0010029	common cardinal vein increased width, abnormal
ZP:0010030	pancreas primordium hypoplastic, abnormal
ZP:0010031	segmental plate lacks all parts of type anterior region adaxial cell, abnormal
ZP:0010032	macula fused with macula, abnormal
ZP:0010033	tela chorioidea decreased size, abnormal
ZP:0010034	tela chorioidea hypoplastic, abnormal
ZP:0010035	cell tela chorioidea fragility, abnormal
ZP:0010036	cell tela chorioidea decreased amount, abnormal
ZP:0010037	lapillus decreased size, abnormal
ZP:0010038	melanocyte caudal fin mislocalised, abnormal
ZP:0010039	cell projection roof plate spinal cord region decreased length, abnormal
ZP:0010040	ventricular system apoptotic, abnormal
ZP:0010041	smooth muscle aplastic, abnormal
ZP:0010042	pillar of the anterior semicircular canal shape, abnormal
ZP:0010043	mesothelial cell distributed, abnormal
ZP:0010044	mesothelial cell decreased amount, abnormal
ZP:0010045	endocrine cell decreased amount, abnormal
ZP:0010046	slow muscle cell decreased size, abnormal
ZP:0010047	slow muscle cell aplastic, abnormal
ZP:0010048	Muller cell decreased occurrence cell population proliferation, abnormal
ZP:0010049	notochord development peramorphic growth, abnormal
ZP:0010050	gut decreased curvature, abnormal
ZP:0010051	liver orientation left-right axis whole organism, abnormal
ZP:0010052	notochord decreased diameter, abnormal
ZP:0010053	cell notochord decreased amount, abnormal
ZP:0010054	pancreas orientation left-right axis whole organism, abnormal
ZP:0010055	cloacal chamber morphology, abnormal
ZP:0010056	pronephric duct opening closed, abnormal
ZP:0010057	chordo neural hinge decreased size, abnormal
ZP:0010058	epicardium hypoplastic, abnormal
ZP:0010059	notochord decreased width, abnormal
ZP:0010060	interneuron hindbrain increased amount, abnormal
ZP:0010061	facial nerve motor nucleus increased amount, abnormal
ZP:0010062	vagal lobe increased amount, abnormal
ZP:0010063	trigeminal motor nucleus increased amount, abnormal
ZP:0010064	rostrocaudal neural tube patterning disrupted, abnormal
ZP:0010065	negative regulation of Wnt signaling pathway disrupted, abnormal
ZP:0010066	eye morphogenesis arrested, abnormal
ZP:0010068	forebrain morphogenesis disrupted, abnormal
ZP:0010070	trigeminal neural crest distended, abnormal
ZP:0010072	neuron trigeminal placode irregular spatial pattern, abnormal
ZP:0010073	neuron hindbrain mislocalised, abnormal
ZP:0010074	posterior lateral line neuromast primordium migration increased duration, abnormal
ZP:0010075	posterior lateral line primordium has fewer parts of type posterior-most region cell, abnormal
ZP:0010076	posterior lateral line primordium decreased process quality cell population proliferation, abnormal
ZP:0010077	glucose metabolic process disrupted, abnormal
ZP:0010078	determination of pancreatic left/right asymmetry process quality, abnormal
ZP:0010079	determination of liver left/right asymmetry process quality, abnormal
ZP:0010080	digestive system positional polarity, abnormal
ZP:0010081	endocrine pancreas hypoplastic, abnormal
ZP:0010082	endocrine pancreas decreased functionality, abnormal
ZP:0010083	acinar cell decreased amount, abnormal
ZP:0010084	whole organism lacks all parts of type telencephalon, abnormal
ZP:0010085	whole organism lacks all parts of type eye, abnormal
ZP:0010086	regulation of brain-derived neurotrophic factor receptor signaling pathway disrupted, abnormal
ZP:0010087	pigment accumulation delayed, abnormal
ZP:0010088	blood low saturation, abnormal
ZP:0010089	olfactory placode composition, abnormal
ZP:0010090	olfactory receptor cell olfactory placode absent, abnormal
ZP:0010091	pharyngeal arch 3-7 skeleton has fewer parts of type pharyngeal arch cartilage, abnormal
ZP:0010092	neuroblast head dispersed, abnormal
ZP:0010093	trunk misaligned with larval melanophore stripe anterior-posterior axis whole organism, abnormal
ZP:0010094	melanocyte trunk disorganized, abnormal
ZP:0010095	neural tube shape, abnormal
ZP:0010096	ceratohyal cartilage curved caudal, abnormal
ZP:0010097	neuromast lateral line decreased amount, abnormal
ZP:0010098	pharyngeal arch 2 disoriented, abnormal
ZP:0010099	pharyngeal arch 2 mislocalised ventrally, abnormal
ZP:0010100	pharyngeal arch 1 disoriented, abnormal
ZP:0010101	pharyngeal arch 1 mislocalised ventrally, abnormal
ZP:0010102	dopaminergic neuron ventral thalamus decreased amount, abnormal
ZP:0010103	dopaminergic neuron preoptic area decreased amount, abnormal
ZP:0010104	somite post-vent region apoptotic, abnormal
ZP:0010105	posterior region somite border surface feature shape, abnormal
ZP:0010111	whole organism lacks parts or has fewer parts of type intersegmental vessel, abnormal
ZP:0010112	whole organism lacks parts or has fewer parts of type parachordal vessel, abnormal
ZP:0010113	trunk vasculature lacks all parts of type parachordal vessel, abnormal
ZP:0010114	axon VaP motor neuron increased branchiness, abnormal
ZP:0010115	neuromast hair cell posterior lateral line neuromast absent, abnormal
ZP:0010116	brain disoriented, abnormal
ZP:0010117	epiphysis split, abnormal
ZP:0010118	retinal ganglion cell layer mislocalised, abnormal
ZP:0010119	hindbrain decreased thickness, abnormal
ZP:0010120	cell hindbrain aggregated, abnormal
ZP:0010121	cell hindbrain loose, abnormal
ZP:0010122	lens disoriented, abnormal
ZP:0010123	tail bud vacuolated, abnormal
ZP:0010124	paraxial mesoderm tail bud disorganized, abnormal
ZP:0010125	eye fused with brain, abnormal
ZP:0010126	cell fourth ventricle mislocalised, abnormal
ZP:0010127	fourth ventricle midbrain mislocalised anteriorly, abnormal
ZP:0010128	cell midbrain loose, abnormal
ZP:0010129	neural rod shape, abnormal
ZP:0010130	cartilage element pectoral fin bud absent, abnormal
ZP:0010131	cartilage element pectoral fin bud disorganized, abnormal
ZP:0010132	retinal pigmented epithelium position, abnormal
ZP:0010133	mesodermal cell paraxial mesoderm spherical, abnormal
ZP:0010134	stereocilium bundle hair cell posterior macula decreased length, abnormal
ZP:0010135	kinocilium hair cell posterior macula decreased length, abnormal
ZP:0010136	kinocilium hair cell anterior macula decreased length, abnormal
ZP:0010137	spinal cord interneuron disorganized, abnormal
ZP:0010138	presumptive neural retina detached from adherens junction presumptive retinal pigmented epithelium, abnormal
ZP:0010139	photoreceptor outer segment whole organism decreased length, abnormal
ZP:0010140	neuroectoderm malformed, abnormal
ZP:0010141	mesodermal cell axial mesoderm mislocalised, abnormal
ZP:0010142	ventricular system composition, abnormal
ZP:0010143	retinal inner plexiform layer structure, abnormal
ZP:0010144	pillar of the semicircular canal structure, abnormal
ZP:0010145	hindbrain interneuron disorganized, abnormal
ZP:0010146	anterior neural keel increased width, abnormal
ZP:0010147	hindbrain neural keel umbonate, abnormal
ZP:0010148	posterior neural tube T-shaped, abnormal
ZP:0010149	filopodium cell present, abnormal
ZP:0010150	mesodermal cell mislocalised, abnormal
ZP:0010151	Mauthner neuron mislocalised, abnormal
ZP:0010152	Mauthner neuron displaced to posterior region rhombomere, abnormal
ZP:0010153	posterior lateral line development disrupted, abnormal
ZP:0010154	neuromast shape, abnormal
ZP:0010156	neuron migration arrested, abnormal
ZP:0010157	axon extension heterochronic, abnormal
ZP:0010158	olfactory placode development delayed, abnormal
ZP:0010159	mitotic cell cycle arrest delayed, abnormal
ZP:0010160	dopaminergic neuron forebrain absent, abnormal
ZP:0010161	posterior lateral line nerve aplastic, abnormal
ZP:0010162	dorsal root ganglion morphology, abnormal
ZP:0010163	neuromast mislocalised, abnormal
ZP:0010164	primary olfactory fiber layer morphology, abnormal
ZP:0010165	glomerular layer morphology, abnormal
ZP:0010166	nerve opercular lateral line absent, abnormal
ZP:0010167	posterior lateral line ganglion absent, abnormal
ZP:0010168	ventral anterior lateral line nerve decreased size, abnormal
ZP:0010169	atrial myocardium disorganized, abnormal
ZP:0010170	atrial myocardium swollen, abnormal
ZP:0010171	cardiac muscle cell atrial myocardium loose, abnormal
ZP:0010172	ventricular myocardium increased width, abnormal
ZP:0010173	cardiac muscle cell ventricular myocardium condensed, abnormal
ZP:0010174	camera-type eye morphogenesis disrupted, abnormal
ZP:0010175	medial region brain decreased size, abnormal
ZP:0010176	prechordal plate hypoplastic, abnormal
ZP:0010177	shield aplastic, abnormal
ZP:0010178	shield decreased amount, abnormal
ZP:0010179	eye decreased distance anterior region anterior region eye, abnormal
ZP:0010180	ventral region forebrain constricted, abnormal
ZP:0010181	immature eye malformed, abnormal
ZP:0010182	immature eye decreased amount, abnormal
ZP:0010183	neuronal stem cell population maintenance decreased occurrence, abnormal
ZP:0010184	dorsal telencephalon has extra parts of type ventricular zone neuron, abnormal
ZP:0010185	radial glial cell dorsal telencephalon cellular potency, abnormal
ZP:0010186	endoderm formation disrupted, abnormal
ZP:0010187	anterior axial hypoblast increased thickness, abnormal
ZP:0010188	mesoderm morphology, abnormal
ZP:0010189	mesoderm aplastic, abnormal
ZP:0010190	polster absent, abnormal
ZP:0010191	prechordal plate decreased size, abnormal
ZP:0010192	prechordal plate aplastic, abnormal
ZP:0010193	gut physical object quality, abnormal
ZP:0010194	retina aplastic, abnormal
ZP:0010195	retina stratification, abnormal
ZP:0010196	presumptive dorsal mesoderm morphology, abnormal
ZP:0010197	rhombomere 4 morphology, abnormal
ZP:0010198	mesoderm head aplastic, abnormal
ZP:0010199	mesoderm trunk aplastic, abnormal
ZP:0010200	medial floor plate aplastic, abnormal
ZP:0010201	facial placode morphology, abnormal
ZP:0010202	glossopharyngeal placode morphology, abnormal
ZP:0010203	mandibular neural crest fused with hyoid neural crest, abnormal
ZP:0010204	hatching gland cell absent, abnormal
ZP:0010205	xanthophore head colored, abnormal
ZP:0010206	xanthophore trunk colored, abnormal
ZP:0010207	pterinosome xanthophore morphology, abnormal
ZP:0010208	mitotic S phase arrested, abnormal
ZP:0010209	central nervous system has fewer parts of type myelin sheath oligodendrocyte, abnormal
ZP:0010210	spinal cord has fewer parts of type cell projection radial glial cell, abnormal
ZP:0010211	spinal cord has fewer parts of type dorsal region oligodendrocyte, abnormal
ZP:0010212	spinal cord has extra parts of type ventral region oligodendrocyte, abnormal
ZP:0010213	spinal cord has extra parts of type grey matter oligodendrocyte, abnormal
ZP:0010214	spinal cord has fewer parts of type white matter oligodendrocyte, abnormal
ZP:0010215	head opacity, abnormal
ZP:0010216	oligodendrocyte distributed, abnormal
ZP:0010217	plasma membrane oligodendrocyte disorganized, abnormal
ZP:0010218	axon oligodendrocyte misrouted, abnormal
ZP:0010219	axon oligodendrocyte split, abnormal
ZP:0010220	axonal growth cone oligodendrocyte collapsed, abnormal
ZP:0010221	neurectodermal cell increased amount, abnormal
ZP:0010222	cell projection radial glial cell disorganized, abnormal
ZP:0010223	cranial vasculature perforate, abnormal
ZP:0010224	ethmoid cartilage unfused from ethmoid cartilage, abnormal
ZP:0010225	palate hypoplastic, abnormal
ZP:0010226	lip decreased size, abnormal
ZP:0010227	regulation of canonical Wnt signaling pathway disrupted, abnormal
ZP:0010228	floor plate undulate, abnormal
ZP:0010230	adaxial cell mislocalised, abnormal
ZP:0010231	dermomyotome increased amount, abnormal
ZP:0010232	fast muscle cell immature, abnormal
ZP:0010233	immunoglobulin heavy chain V-D-J recombination disrupted, abnormal
ZP:0010234	T cell head kidney absent, abnormal
ZP:0010235	B cell head kidney absent, abnormal
ZP:0010236	granulocyte increased amount, abnormal
ZP:0010237	retina lacks all parts of type Muller cell, abnormal
ZP:0010238	optic vesicle morphogenesis process quality, abnormal
ZP:0010239	adenohypophysis development disrupted, abnormal
ZP:0010240	retinal neural layer quality, abnormal
ZP:0010241	adenohypophysis decreased amount, abnormal
ZP:0010243	whole organism sigmoid, abnormal
ZP:0010244	trunk vasculature non-functional, abnormal
ZP:0010245	post-vent vasculature structure, abnormal
ZP:0010246	thoracic duct immature, abnormal
ZP:0010247	ossification increased occurrence, abnormal
ZP:0010248	segmental plate increased cellular motility, abnormal
ZP:0010249	postcranial axial skeleton ossified, abnormal
ZP:0010250	embryonic axis specification disrupted, abnormal
ZP:0010251	endodermal cell endoderm increased amount, abnormal
ZP:0010252	epiphysis oblong, abnormal
ZP:0010253	forerunner cell group increased amount, abnormal
ZP:0010254	prechordal plate quality, abnormal
ZP:0010255	ventral region diencephalon decreased size, abnormal
ZP:0010256	chorion present, abnormal
ZP:0010257	head sharpness, abnormal
ZP:0010258	nucleus of the tract of the postoptic commissure absent, abnormal
ZP:0010259	dorsal rectus morphology, abnormal
ZP:0010260	ventral rectus morphology, abnormal
ZP:0010262	dorsal oblique extraocular muscle morphology, abnormal
ZP:0010263	ventral oblique extraocular muscle morphology, abnormal
ZP:0010264	corneal epithelium increased thickness, abnormal
ZP:0010265	cell cycle rate, abnormal
ZP:0010266	forebrain neuron differentiation disrupted, abnormal
ZP:0010267	neuron differentiation arrested, abnormal
ZP:0010268	serotonin metabolic process disrupted, abnormal
ZP:0010269	defense response to fungus process quality, abnormal
ZP:0010270	retinal rod cell differentiation delayed, abnormal
ZP:0010271	retinal rod cell differentiation process quality, abnormal
ZP:0010272	oncogene-induced cell senescence decreased occurrence, abnormal
ZP:0010274	nucleus retinal neural layer apoptotic, abnormal
ZP:0010275	ventricular zone telencephalon increased width, abnormal
ZP:0010276	eye adjacent to eye, abnormal
ZP:0010277	gut neoplastic, abnormal
ZP:0010278	hepatocellular carcinoma liver present, abnormal
ZP:0010279	peripheral nervous system neoplastic, malignant, abnormal
ZP:0010280	neurofibrosarcoma peripheral nervous system increased amount, abnormal
ZP:0010281	cranial nerve I defasciculated, abnormal
ZP:0010282	motor neuron vagal lobe decreased amount, abnormal
ZP:0010283	gill neoplastic, abnormal
ZP:0010284	glomerular layer decreased size, abnormal
ZP:0010285	integument neoplastic, abnormal
ZP:0010286	paraventricular organ absent neurotransmitter metabolic process, abnormal
ZP:0010287	posterior cardinal vein structure, abnormal
ZP:0010288	posterior intestine neoplastic, abnormal
ZP:0010292	sarcoma trunk present, abnormal
ZP:0010293	post-vent region neoplastic, abnormal
ZP:0010294	optic nerve head decreased size, abnormal
ZP:0010295	axon optic nerve head absent, abnormal
ZP:0010296	supraoptic tract decreased thickness, abnormal
ZP:0010297	supraoptic tract fasciculation, abnormal
ZP:0010298	anterior swim bladder bud absent, abnormal
ZP:0010299	anterior swim bladder bud decreased size, abnormal
ZP:0010300	cardiac muscle cell decreased process quality cell population proliferation, abnormal
ZP:0010301	neutrophil decreased process quality phagocytosis, abnormal
ZP:0010302	positive regulation of ERK1 and ERK2 cascade decreased magnitude, abnormal
ZP:0010303	positive regulation of vascular endothelial growth factor signaling pathway decreased occurrence, abnormal
ZP:0010304	intersegmental vessel has fewer parts of type blood vessel endothelial cell, abnormal
ZP:0010305	atrioventricular canal decreased size, abnormal
ZP:0010306	posterior side hypothalamus morphology, abnormal
ZP:0010307	optic tectum hypoplastic, abnormal
ZP:0010308	splanchnocranium decreased length, abnormal
ZP:0010309	interhyal cartilage absent, abnormal
ZP:0010310	Kupffer's vesicle bilateral, abnormal
ZP:0010311	Kupffer's vesicle inverted, abnormal
ZP:0010312	Kupffer's vesicle dislocated yolk, abnormal
ZP:0010313	anterior region brain decreased size, abnormal
ZP:0010314	median fin fold increased amount, abnormal
ZP:0010315	median fin fold duplicated, abnormal
ZP:0010317	somite 1 decreased size, abnormal
ZP:0010318	somite 5 decreased size, abnormal
ZP:0010319	tail bud shape, abnormal
ZP:0010320	tail bud increased thickness, abnormal
ZP:0010321	tail bud wholly anterioralized, abnormal
ZP:0010322	tail bud everted, abnormal
ZP:0010323	blood island increased amount, abnormal
ZP:0010324	blood island increased width, abnormal
ZP:0010325	extension increased size, abnormal
ZP:0010326	lateral plate mesoderm increased width, abnormal
ZP:0010327	neural plate decreased thickness, abnormal
ZP:0010328	primitive heart tube bilateral, abnormal
ZP:0010329	primitive heart tube inverted, abnormal
ZP:0010330	ventral region pronephros increased width, abnormal
ZP:0010331	caudal vein truncated, abnormal
ZP:0010332	somite 11 increased size, abnormal
ZP:0010333	somite 11 fused with dorso-medial margin dorso-medial margin somite 11, abnormal
ZP:0010334	somite 14 increased size, abnormal
ZP:0010335	somite 14 fused with dorso-medial margin dorso-medial margin somite 14, abnormal
ZP:0010336	somite 2 decreased size, abnormal
ZP:0010337	somite 3 decreased size, abnormal
ZP:0010338	somite 12 increased size, abnormal
ZP:0010339	somite 12 fused with dorso-medial margin dorso-medial margin somite 12, abnormal
ZP:0010340	somite 15 increased size, abnormal
ZP:0010341	somite 15 fused with dorso-medial margin dorso-medial margin somite 15, abnormal
ZP:0010342	somite 4 decreased size, abnormal
ZP:0010343	somite 13 increased size, abnormal
ZP:0010344	somite 13 fused with dorso-medial margin dorso-medial margin somite 13, abnormal
ZP:0010345	caudal fin increased amount, abnormal
ZP:0010346	ventral fin fold multiple, abnormal
ZP:0010347	head decreased thickness, abnormal
ZP:0010349	ventral region trunk increased thickness, abnormal
ZP:0010350	somite trunk decreased size, abnormal
ZP:0010351	post-vent region folded, abnormal
ZP:0010352	somite post-vent region increased size, abnormal
ZP:0010353	somite post-vent region decreased size, abnormal
ZP:0010354	notochord posterior region has fewer parts of type cell, abnormal
ZP:0010355	Kupffer's vesicle development arrested, abnormal
ZP:0010356	gall bladder mislocalised radially, abnormal
ZP:0010357	pancreatic bud mislocalised radially, abnormal
ZP:0010358	atrium increased thickness, abnormal
ZP:0010359	forebrain neuron development extra or missing processual parts neuron fate specification, abnormal
ZP:0010360	medial longitudinal catecholaminergic tract increased size, abnormal
ZP:0010361	cellular pigmentation disrupted, abnormal
ZP:0010363	intersegmental vein truncated, abnormal
ZP:0010364	cell-cell junction blood vessel endothelium mislocalised, abnormal
ZP:0010366	pronephros development process quality, abnormal
ZP:0010367	pronephric glomerulus hypoplastic, abnormal
ZP:0010369	fibroblast growth factor receptor signaling pathway process quality, abnormal
ZP:0010370	regulation of bone remodeling occurrence, abnormal
ZP:0010371	pharyngeal arch 3-7 skeleton disorganized, abnormal
ZP:0010372	heart rudiment decreased size, abnormal
ZP:0010373	opercle bilateral symmetry, abnormal
ZP:0010374	semicircular canal truncated, abnormal
ZP:0010375	locus coeruleus aplastic, abnormal
ZP:0010376	oral epithelium has fewer parts of type taste bud, abnormal
ZP:0010377	rhombomere 1 morphology, abnormal
ZP:0010378	ventral mandibular arch bilateral symmetry, abnormal
ZP:0010379	alar plate midbrain region morphology, abnormal
ZP:0010380	chondrocranium bilateral symmetry, abnormal
ZP:0010381	midbrain neural rod morphology, abnormal
ZP:0010382	midbrain neural rod increased thickness, abnormal
ZP:0010383	midbrain neural rod prominent, abnormal
ZP:0010384	midbrain hindbrain boundary neural rod morphology, abnormal
ZP:0010385	embryonic medial fin morphogenesis decreased process quality, abnormal
ZP:0010388	median fin fold decreased height, abnormal
ZP:0010401	endocardium morphogenesis disrupted, abnormal
ZP:0010402	pineal gland development disrupted, abnormal
ZP:0010403	endocrine cell pancreas decreased amount, abnormal
ZP:0010404	somite fused with medial side medial side somite, abnormal
ZP:0010405	caudal fin physical object quality, abnormal
ZP:0010406	post-vent region increased distance somite somite post-vent region, abnormal
ZP:0010407	melanocyte displaced to ventral surface neural tube, abnormal
ZP:0010408	midbrain-hindbrain boundary initiation process quality, abnormal
ZP:0010409	optic nerve development disrupted, abnormal
ZP:0010410	midbrain-hindbrain boundary development arrested, abnormal
ZP:0010411	neuron cranial ganglion decreased amount, abnormal
ZP:0010412	epiphysis decreased width, abnormal
ZP:0010413	retinal neural layer closure incomplete, abnormal
ZP:0010414	otic vesicle physical object quality, abnormal
ZP:0010415	diencephalon distended, abnormal
ZP:0010416	retinal pigmented epithelium closure incomplete, abnormal
ZP:0010417	pronephric duct absent, abnormal
ZP:0010418	pronephric duct physical object quality, abnormal
ZP:0010419	pronephric duct lacks all parts of type brush border epithelial cell, abnormal
ZP:0010420	central region pronephric duct distended, abnormal
ZP:0010421	epithelial cell pronephric duct flattened, abnormal
ZP:0010422	pronephros absent, abnormal
ZP:0010423	pronephros physical object quality, abnormal
ZP:0010424	caudal commissure increased size, abnormal
ZP:0010425	optic tectum malformed, abnormal
ZP:0010426	cell optic tectum degenerate, abnormal
ZP:0010427	cell optic tectum refractile, abnormal
ZP:0010428	trochlear motor nucleus has fewer parts of type neuron, abnormal
ZP:0010429	commissura cerebelli aplastic, abnormal
ZP:0010430	oculomotor nucleus has fewer parts of type neuron, abnormal
ZP:0010431	optic chiasm ipsilateral to cranial nerve II cranial nerve II optic chiasm, abnormal
ZP:0010432	cranial nerve IV aplastic, abnormal
ZP:0010433	ansulate commissure decreased size, abnormal
ZP:0010434	thyroid follicle aplastic, abnormal
ZP:0010435	forebrain midbrain boundary decreased distance hindbrain commissure, abnormal
ZP:0010436	anterior region pronephric tubule malformed, abnormal
ZP:0010437	gut epithelium edematous, abnormal
ZP:0010438	regulation of cellular response to stress increased process quality, abnormal
ZP:0010439	otic vesicle has fewer parts of type hair cell, abnormal
ZP:0010440	Kolmer-Agduhr neuron spinal cord undifferentiated, abnormal
ZP:0010441	internal gill bud decreased length, abnormal
ZP:0010442	internal gill bud decreased amount, abnormal
ZP:0010443	neurocranium lacks all parts of type neurocranial trabecula, abnormal
ZP:0010444	pronephric distal late tubule decreased object quality, abnormal
ZP:0010445	mandibular muscle refractivity, abnormal
ZP:0010446	striated muscle myosin thick filament myotome absent, abnormal
ZP:0010447	striated muscle myosin thick filament myotome decreased amount, abnormal
ZP:0010448	striated muscle thin filament myotome decreased amount, abnormal
ZP:0010449	Z disc myotome disorganized, abnormal
ZP:0010450	M band myotome disorganized, abnormal
ZP:0010451	nucleus skeletal muscle cell circular, abnormal
ZP:0010452	myofibril skeletal muscle cell decreased amount, abnormal
ZP:0010453	striated muscle myosin thick filament slow muscle cell disorganized, abnormal
ZP:0010454	striated muscle myosin thick filament fast muscle cell disorganized, abnormal
ZP:0010455	striated muscle thin filament fast muscle cell disorganized, abnormal
ZP:0010457	intracellularly ATP-gated chloride channel activity increased occurrence, abnormal
ZP:0010458	exocrine pancreas development process quality, abnormal
ZP:0010459	gut swollen, abnormal
ZP:0010460	gut epithelium flattened, abnormal
ZP:0010461	intestinal villus flattened, abnormal
ZP:0010462	enterocyte decreased height, abnormal
ZP:0010463	microvillus enterocyte decreased length, abnormal
ZP:0010464	prechordal plate formation disrupted, abnormal
ZP:0010465	ventral region central nervous system decreased length, abnormal
ZP:0010466	polster decreased size, abnormal
ZP:0010467	polster elongated, abnormal
ZP:0010468	polster anterior-posterior polarity, abnormal
ZP:0010469	polster flattened, abnormal
ZP:0010470	posterior region prechordal plate decreased length, abnormal
ZP:0010471	posterior region prechordal plate increased width, abnormal
ZP:0010472	notochord protruding, abnormal
ZP:0010473	optic stalk fused with optic stalk, abnormal
ZP:0010474	axial mesoderm decreased length, abnormal
ZP:0010475	mandibular arch skeleton deformed, abnormal
ZP:0010476	axial hypoblast decreased length, abnormal
ZP:0010477	axial hypoblast increased width, abnormal
ZP:0010478	regulation of heart contraction increased duration, abnormal
ZP:0010479	whole organism has fewer parts of type nucleate erythrocyte, abnormal
ZP:0010481	ectodermal cell fate commitment disrupted, abnormal
ZP:0010482	hindbrain condensed, abnormal
ZP:0010483	pronephros increased width, abnormal
ZP:0010484	dorsal region retina cellular quality, abnormal
ZP:0010485	cloacal chamber cellular quality, abnormal
ZP:0010486	rhombomere 5 increased length, abnormal
ZP:0010487	caudal fin increased accumulation blood cell, abnormal
ZP:0010488	ventral fin fold flattened, abnormal
ZP:0010489	ventral fin fold edge shape, abnormal
ZP:0010490	postero-ventral region ventral fin fold hypoplastic, abnormal
ZP:0010491	neuroectoderm degenerate, abnormal
ZP:0010492	anal fin hypoplastic, abnormal
ZP:0010493	Meckel's cartilage position, abnormal
ZP:0010494	Meckel's cartilage overlap with Meckel's cartilage, abnormal
ZP:0010495	ceratohyal cartilage fused with ceratobranchial 1 cartilage, abnormal
ZP:0010496	cell division decreased rate, abnormal
ZP:0010497	ceratobranchial bone malformed, abnormal
ZP:0010498	chondrocyte palatoquadrate cartilage decreased amount, abnormal
ZP:0010499	chondrocyte increased size, abnormal
ZP:0010501	retina increased duration cell cycle process, abnormal
ZP:0010502	retina increased duration S phase, abnormal
ZP:0010503	behavioral fear response arrested, abnormal
ZP:0010504	dopamine biosynthetic process from tyrosine decreased occurrence, abnormal
ZP:0010505	multicellular organismal response to stress arrested, abnormal
ZP:0010506	mRNA binding disrupted, abnormal
ZP:0010507	lateral plate mesoderm asymmetrical, abnormal
ZP:0010508	heart primordium fused with left side right side heart primordium, abnormal
ZP:0010509	trigeminal ganglion dispersed, abnormal
ZP:0010510	smoothened signaling pathway decreased occurrence, abnormal
ZP:0010511	optic nerve formation disrupted, abnormal
ZP:0010512	striated muscle cell development arrested, abnormal
ZP:0010514	somite lacks all parts of type muscle pioneer, abnormal
ZP:0010515	third ventricle increased size, abnormal
ZP:0010516	horizontal myoseptum morphology, abnormal
ZP:0010517	anterior commissure decreased size, abnormal
ZP:0010518	pharyngeal arch 3-7 mislocalised ventrally, abnormal
ZP:0010519	axon MiP motor neuron decreased amount, abnormal
ZP:0010521	gastrulation physical quality of a process, abnormal
ZP:0010522	cell migration involved in gastrulation increased rate, abnormal
ZP:0010523	Wnt signaling pathway process quality, abnormal
ZP:0010524	neural tube patterning disrupted, abnormal
ZP:0010527	neuroendocrine cell poorly differentiated, abnormal
ZP:0010528	dopaminergic neuron disorganized, abnormal
ZP:0010529	photopic photoreceptor cell retina absent, abnormal
ZP:0010530	smooth muscle tissue development disrupted, abnormal
ZP:0010531	smooth muscle tunica interna swim bladder absent, abnormal
ZP:0010532	visceral peritoneum disorganized, abnormal
ZP:0010533	adenohypophysis development paedomorphic growth, abnormal
ZP:0010534	otic vesicle apoptotic, abnormal
ZP:0010535	otic vesicle oblong, abnormal
ZP:0010536	lateral crista absent, abnormal
ZP:0010537	mandibular muscle hypoplastic, abnormal
ZP:0010538	cranial nerve VIII increased length, abnormal
ZP:0010539	cranial nerve VIII decreased thickness, abnormal
ZP:0010540	macula shape, abnormal
ZP:0010541	posterior crista absent, abnormal
ZP:0010542	anterior crista absent, abnormal
ZP:0010543	posterior-most region posterior lateral line neuromast absent, abnormal
ZP:0010544	posterior lateral line primordium apoptotic, abnormal
ZP:0010545	mandibular arch skeleton circular, abnormal
ZP:0010546	neurohypophysis quality, abnormal
ZP:0010547	adenohypophysis poorly differentiated, abnormal
ZP:0010548	secretory granule adenohypophysis mislocalised, abnormal
ZP:0010549	peptide hormone secreting cell structure, abnormal
ZP:0010550	somatotropin secreting cell absent, abnormal
ZP:0010551	prolactin secreting cell mislocalised, abnormal
ZP:0010552	thyroid stimulating hormone secreting cell absent, abnormal
ZP:0010553	DNA methylation on cytosine increased occurrence, abnormal
ZP:0010554	lens poorly differentiated, abnormal
ZP:0010555	dorsal region retinal pigmented epithelium absent, abnormal
ZP:0010556	nucleus exocrine pancreas condensed, abnormal
ZP:0010557	gut endothelial cell intestinal epithelium absent, abnormal
ZP:0010558	hepatocyte degenerate, abnormal
ZP:0010559	hepatocyte aggregated, abnormal
ZP:0010560	hepatocyte mislocalised posteriorly, abnormal
ZP:0010562	pigment accumulation process quality, abnormal
ZP:0010563	dendrite retinal ganglion cell mislocalised, abnormal
ZP:0010564	retinal ganglion cell displaced to dendrite retinal inner nuclear layer, abnormal
ZP:0010565	retinal ganglion cell displaced to dendrite retinal inner plexiform layer, abnormal
ZP:0010566	retinal ganglion cell displaced to dendrite retinal outer plexiform layer, abnormal
ZP:0010567	neuron projection retinal ganglion cell mislocalised, abnormal
ZP:0010568	retinal ganglion cell displaced to neuron projection optic tectum, abnormal
ZP:0010569	retinal ganglion cell process quality dendrite guidance, abnormal
ZP:0010570	retinal ganglion cell process quality neuron projection guidance, abnormal
ZP:0010571	Wnt signaling pathway decreased process quality, abnormal
ZP:0010572	hypothalamus cell differentiation disrupted, abnormal
ZP:0010573	fin development decreased process quality, abnormal
ZP:0010574	regulation of cell proliferation involved in tissue homeostasis decreased process quality, abnormal
ZP:0010575	posterior region hypothalamus decreased size, abnormal
ZP:0010576	axon hypothalamus decreased amount, abnormal
ZP:0010577	neuron hypothalamus morphology, abnormal
ZP:0010578	posterior lateral line nerve truncated, abnormal
ZP:0010579	neuromast has fewer parts of type neuromast hair cell, abnormal
ZP:0010580	paraxial mesoderm decreased size, abnormal
ZP:0010581	posterior lateral line neuromast mislocalised anteriorly, abnormal
ZP:0010582	posterior lateral line primordium increased length, abnormal
ZP:0010583	posterior lateral line primordium self-renewal, abnormal
ZP:0010584	anal fin decreased length, abnormal
ZP:0010585	dorsal fin decreased length, abnormal
ZP:0010586	caudal fin lepidotrichium hypoplastic, abnormal
ZP:0010587	pectoral fin lepidotrichium hypoplastic, abnormal
ZP:0010588	anterior-posterior axis eye decreased length, abnormal
ZP:0010589	dorsal-ventral axis eye decreased length, abnormal
ZP:0010590	retinal inner nuclear layer disorganized, abnormal
ZP:0010591	basibranchial hypoplastic, abnormal
ZP:0010593	medial rectus increased thickness, abnormal
ZP:0010594	cornea morphology, abnormal
ZP:0010595	oral cavity malformed, abnormal
ZP:0010596	iris morphology, abnormal
ZP:0010597	ventral mandibular arch mislocalised ventrally, abnormal
ZP:0010598	pharyngeal arch 2 skeleton mislocalised ventrally, abnormal
ZP:0010599	ceratohyal cartilage position, abnormal
ZP:0010600	basihyal cartilage hypoplastic, abnormal
ZP:0010601	corneal epithelium disorganized, abnormal
ZP:0010602	hyaloid vessel disorganized, abnormal
ZP:0010603	anterior segment eye structure, abnormal
ZP:0010604	anterior segment eye increased accumulation cell, abnormal
ZP:0010605	cell anterior segment eye disorganized, abnormal
ZP:0010606	ocular blood vessel has extra parts of type hyaloid vessel, abnormal
ZP:0010607	heart valve aplastic, abnormal
ZP:0010608	spinal cord malformed, abnormal
ZP:0010609	maxilla hyperplastic, abnormal
ZP:0010610	Meckel's cartilage flat, abnormal
ZP:0010611	palatoquadrate cartilage increased variability of size, abnormal
ZP:0010612	ceratohyal cartilage shortened, abnormal
ZP:0010613	axon development disrupted, abnormal
ZP:0010614	neuromuscular junction myotome physical object quality, abnormal
ZP:0010615	axon motor neuron bifurcated, abnormal
ZP:0010616	presynaptic active zone motor neuron physical object quality, abnormal
ZP:0010617	CaP motoneuron morphology, abnormal
ZP:0010618	bulbus arteriosus amorphous, abnormal
ZP:0010619	epithalamus development disrupted, abnormal
ZP:0010621	cell migration in diencephalon disrupted, abnormal
ZP:0010622	retina has extra parts of type retinal rod cell, abnormal
ZP:0010623	pineal complex morphology, abnormal
ZP:0010624	obsolete cell parapineal organ mislocalised, abnormal
ZP:0010625	retinal rod cell increased amount, abnormal
ZP:0010627	whole organism lacks parts or has fewer parts of type melanocyte, abnormal
ZP:0010628	whole organism lacks parts or has fewer parts of type melanoblast, abnormal
ZP:0010629	melanocyte aplastic, abnormal
ZP:0010630	swim bladder inflation decreased process quality, abnormal
ZP:0010631	pharyngeal system development decreased process quality, abnormal
ZP:0010632	axis whole organism curved, abnormal
ZP:0010633	pharyngeal pouch arrested, abnormal
ZP:0010634	pharyngeal arch arrested, abnormal
ZP:0010635	pharyngeal arch fused with mesenchyme condensation cell mesenchyme condensation cell pharyngeal arch, abnormal
ZP:0010637	sarcomere cardiac muscle cell decreased length, abnormal
ZP:0010638	melanin biosynthetic process from tyrosine disrupted, abnormal
ZP:0010639	iridophore morphology, abnormal
ZP:0010640	melanoblast unpigmented, abnormal
ZP:0010641	fin regeneration hypotrophic growth, abnormal
ZP:0010642	intermediate cell mass of mesoderm vacuolated, abnormal
ZP:0010643	regenerating fin decreased length, abnormal
ZP:0010644	rhombomere morphogenesis disrupted, abnormal
ZP:0010645	hindbrain constricted, abnormal
ZP:0010646	midbrain hindbrain boundary closure incomplete, abnormal
ZP:0010647	axon Mauthner neuron decreased length, abnormal
ZP:0010648	hematopoietic stem cell migration disrupted, abnormal
ZP:0010649	ossification involved in bone maturation arrested, abnormal
ZP:0010650	hematopoietic stem cell proliferation decreased occurrence, abnormal
ZP:0010651	head kidney lacks parts or has fewer parts of type hematopoietic multipotent progenitor cell, abnormal
ZP:0010652	head kidney has fewer parts of type hemoglobin complex hematopoietic multipotent progenitor cell, abnormal
ZP:0010653	blood cell head kidney decreased amount, abnormal
ZP:0010654	hemoglobin complex whole organism decreased amount, abnormal
ZP:0010655	hematopoietic stem cell increased accumulation ventral wall of dorsal aorta, abnormal
ZP:0010656	pro-T cell absent, abnormal
ZP:0010657	lymphoid progenitor cell decreased amount, abnormal
ZP:0010658	zinc ion homeostasis disrupted, abnormal
ZP:0010659	swimming decreased distance swimming behavior, abnormal
ZP:0010660	pancreatic bud has extra parts of type pancreatic epsilon cell, abnormal
ZP:0010661	epiphysis cellular quality, abnormal
ZP:0010662	median fin fold cellular quality, abnormal
ZP:0010663	heart cellular quality, abnormal
ZP:0010664	pectoral fin cellular quality, abnormal
ZP:0010665	stomodeum cellular quality, abnormal
ZP:0010666	cardiac muscle cell cardiac ventricle increased size, abnormal
ZP:0010667	cardiac muscle cell cardiac ventricle elongated, abnormal
ZP:0010668	fin agenesis, abnormal
ZP:0010669	pectoral girdle aplastic, abnormal
ZP:0010670	trunk curled, abnormal
ZP:0010671	pectoral fin curved dorsal, abnormal
ZP:0010672	myocardium disorganized, abnormal
ZP:0010673	pectoral fin lepidotrichium decreased amount, abnormal
ZP:0010674	atrioventricular valve structure, abnormal
ZP:0010675	mitochondrion cardiac muscle cell increased amount, abnormal
ZP:0010676	mitochondrion cardiac muscle cell swollen, abnormal
ZP:0010677	cardiac muscle cell dissociated from bicellular tight junction bicellular tight junction cardiac muscle cell, abnormal
ZP:0010678	telencephalon protruding, abnormal
ZP:0010680	amacrine cell differentiation disrupted, abnormal
ZP:0010681	retinal ganglion cell layer sparse, abnormal
ZP:0010682	compartment boundary retinal ganglion cell layer rough, abnormal
ZP:0010683	retina hypoplastic, abnormal
ZP:0010684	retina lacks parts or has fewer parts of type photoreceptor cell, abnormal
ZP:0010685	retina lacks parts or has fewer parts of type amacrine cell, abnormal
ZP:0010686	cranial nerve II truncated, abnormal
ZP:0010687	cranial nerve II sparse, abnormal
ZP:0010688	cranial nerve II fasciculation, abnormal
ZP:0010689	cranial nerve decreased size, abnormal
ZP:0010690	lateral line nerve decreased size, abnormal
ZP:0010691	retinal ganglion cell lacks parts or has fewer parts of type neuron projection retinal ganglion cell, abnormal
ZP:0010692	neuron projection retinal ganglion cell physical object quality, abnormal
ZP:0010693	cell-cell junction heart decreased amount, abnormal
ZP:0010694	adherens junction heart composition, abnormal
ZP:0010695	adherens junction heart decreased amount, abnormal
ZP:0010696	endothelial cell heart morphology, abnormal
ZP:0010697	skeletal muscle cell differentiated, abnormal
ZP:0010698	bone tissue decreased mass density, abnormal
ZP:0010699	brain symmetry, abnormal
ZP:0010700	endocrine pancreas inverted, abnormal
ZP:0010701	pronephric duct lacks all parts of type motile cilium pronephric duct, abnormal
ZP:0010702	motile cilium peripheral olfactory organ decreased length, abnormal
ZP:0010703	motile cilium peripheral olfactory organ decreased mobility, abnormal
ZP:0010704	pronephric duct disorganized, abnormal
ZP:0010705	motile cilium pronephric duct uncoordinated, abnormal
ZP:0010706	motile cilium pronephric duct decreased mobility, abnormal
ZP:0010707	pronephros morphogenesis process quality, abnormal
ZP:0010708	pronephros lacks all parts of type pronephric glomerulus, abnormal
ZP:0010709	pronephric glomerulus split bilaterally, abnormal
ZP:0010710	centrum irregular spatial pattern, abnormal
ZP:0010711	centrum malformed, abnormal
ZP:0010712	centrum disorganized, abnormal
ZP:0010713	vertebral column deviation, abnormal
ZP:0010714	notochord outer sheath cell disorganized, abnormal
ZP:0010715	notochord outer sheath cell deformed, abnormal
ZP:0010716	activation of cysteine-type endopeptidase activity involved in apoptotic process increased process quality, abnormal
ZP:0010718	cardioblast migration to the midline involved in heart rudiment formation disrupted, abnormal
ZP:0010721	ventral mandibular arch disorganized, abnormal
ZP:0010722	pharyngeal arch 1 decreased length, abnormal
ZP:0010723	pharyngeal arch 1 disrupted embryonic morphogenesis, abnormal
ZP:0010724	cardioblast migration to the midline involved in heart rudiment formation decreased process quality, abnormal
ZP:0010725	heart tube increased amount, abnormal
ZP:0010726	heart tube mislocalised laterally, abnormal
ZP:0010727	mitotic cell cycle temporally extended, abnormal
ZP:0010728	pronephric glomerulus morphogenesis process quality, abnormal
ZP:0010729	centrum fused with centrum, abnormal
ZP:0010730	osteoblast vertebral column mislocalised, abnormal
ZP:0010731	whole organism lacks all parts of type ventral region brain, abnormal
ZP:0010732	hypochord undulate, abnormal
ZP:0010733	dorsal fin decreased size, abnormal
ZP:0010734	blood ventricular system mislocalised, abnormal
ZP:0010735	cranial blood vessel decreased branchiness, abnormal
ZP:0010736	intestine increased occurrence peristalsis, abnormal
ZP:0010737	retinal pigmented epithelium broken, abnormal
ZP:0010739	melanosome retinal pigmented epithelium displaced, abnormal
ZP:0010740	retinal pigmented epithelium has fewer parts of type cell melanosome retinal pigmented epithelium, abnormal
ZP:0010741	basement membrane assembly involved in embryonic body morphogenesis process quality, abnormal
ZP:0010742	collagen type IV trimer whole organism physical object quality, abnormal
ZP:0010743	pericyte cranial blood vessel decreased amount, abnormal
ZP:0010744	liver has fewer parts of type hepatocyte, abnormal
ZP:0010745	skeletal muscle broken, abnormal
ZP:0010746	response to light stimulus decreased process quality, abnormal
ZP:0010747	retinal cone cell increased process quality cell death, abnormal
ZP:0010748	thigmotropism absent, abnormal
ZP:0010749	thigmotropism decreased process quality, abnormal
ZP:0010750	sarcoplasmic reticulum skeletal muscle swollen, abnormal
ZP:0010751	muscle cell broken, abnormal
ZP:0010752	slow muscle cell process quality muscle contraction, abnormal
ZP:0010753	fast muscle cell process quality muscle contraction, abnormal
ZP:0010754	lymphoid lineage cell migration into thymus disrupted, abnormal
ZP:0010755	lymphocyte ventral wall of dorsal aorta decreased amount, abnormal
ZP:0010756	centriole peripheral olfactory organ physical object quality, abnormal
ZP:0010757	ciliary basal body peripheral olfactory organ physical object quality, abnormal
ZP:0010758	skeletal muscle cell myotome morphology, abnormal
ZP:0010759	whole organism lacks all parts of type macrophage, abnormal
ZP:0010760	lymphoid lineage cell migration into thymus involved in thymus epithelium morphogenesis disrupted, abnormal
ZP:0010761	cranial suture morphogenesis process quality, abnormal
ZP:0010762	scale malformed, abnormal
ZP:0010763	pectoral girdle alignment pectoral fin, abnormal
ZP:0010764	parietal bone malformed, abnormal
ZP:0010765	parasphenoid malformed, abnormal
ZP:0010766	premaxilla malformed, abnormal
ZP:0010767	dermatocranium decreased occurrence ossification involved in bone remodeling, abnormal
ZP:0010768	dermatocranium increased occurrence bone resorption, abnormal
ZP:0010769	preopercular sensory canal malformed, abnormal
ZP:0010770	inter-frontal joint branched, abnormal
ZP:0010771	cranial vault malformed, abnormal
ZP:0010772	cranial vault increased occurrence bone resorption, abnormal
ZP:0010773	cone photoresponse recovery process quality, abnormal
ZP:0010774	retinal cone cell photosensitive, abnormal
ZP:0010775	retinal cone cell increased process quality detection of light stimulus involved in visual perception, abnormal
ZP:0010776	myotube cell development disrupted, abnormal
ZP:0010777	muscle trunk musculature morphology, abnormal
ZP:0010778	muscle cell trunk musculature disorganized, abnormal
ZP:0010779	myoseptum muscle decreased thickness, abnormal
ZP:0010780	myotome broken, abnormal
ZP:0010781	muscle broken, abnormal
ZP:0010782	posterior lateral line primordium process quality actin filament bundle organization, abnormal
ZP:0010783	brain aplastic, abnormal
ZP:0010784	apoptotic process increased process quality, abnormal
ZP:0010785	posterior lateral line neuromast deposition decreased process quality, abnormal
ZP:0010788	blood accumulation caudal vein plexus, abnormal
ZP:0010789	caudal artery morphology, abnormal
ZP:0010790	caudal artery immature, abnormal
ZP:0010791	dorsal aorta disrupted blood circulation, abnormal
ZP:0010792	axial vasculature disrupted blood circulation, abnormal
ZP:0010793	cranial vasculature lacks parts or has fewer parts of type central artery, abnormal
ZP:0010794	cranial vasculature disrupted blood circulation, abnormal
ZP:0010795	central artery immature, abnormal
ZP:0010796	central artery disrupted blood vessel lumenization, abnormal
ZP:0010797	post-vent vasculature disrupted blood circulation, abnormal
ZP:0010798	joint fin irregular spatial pattern, abnormal
ZP:0010799	caudal fin increased length, abnormal
ZP:0010800	pectoral fin increased length, abnormal
ZP:0010801	dorsal fin increased length, abnormal
ZP:0010802	pelvic fin increased length, abnormal
ZP:0010803	lepidotrichium structure, abnormal
ZP:0010804	lepidotrichium increased length, abnormal
ZP:0010805	mitotic S phase temporally extended, abnormal
ZP:0010806	microglial cell activation increased process quality, abnormal
ZP:0010807	mitochondrial electron transport, ubiquinol to cytochrome c decreased rate, abnormal
ZP:0010808	mitochondrion muscle increased size, abnormal
ZP:0010809	mitochondrion muscle decreased functionality, abnormal
ZP:0010811	CaP motoneuron increased duration motor neuron axon guidance, abnormal
ZP:0010812	Mauthner neuron process quality action potential, abnormal
ZP:0010813	Mauthner neuron increased occurrence action potential, abnormal
ZP:0010814	Mauthner neuron temporal distribution quality action potential, abnormal
ZP:0010815	Mauthner neuron process quality transmission of nerve impulse, abnormal
ZP:0010816	microglia development arrested, abnormal
ZP:0010817	mRNA splicing, via spliceosome decreased process quality, abnormal
ZP:0010818	inner ear receptor cell stereocilium organization disrupted, abnormal
ZP:0010819	stereocilium bundle auditory receptor cell shape, abnormal
ZP:0010820	inflammatory response increased process quality, abnormal
ZP:0010821	yolk syncytial layer edematous, abnormal
ZP:0010822	blood island lacks all parts of type leukocyte, abnormal
ZP:0010823	eye damaged, abnormal
ZP:0010825	integument damaged, abnormal
ZP:0010826	leukocyte accumulation anatomical region heart, abnormal
ZP:0010827	striated muscle thin filament skeletal muscle disorganized, abnormal
ZP:0010828	Z disc slow muscle cell disorganized, abnormal
ZP:0010829	pronephric duct morphogenesis decreased process quality, abnormal
ZP:0010830	Kupffer's vesicle has fewer parts of type motile cilium Kupffer's vesicle, abnormal
ZP:0010831	Kupffer's vesicle decreased process quality motile cilium assembly, abnormal
ZP:0010832	otic vesicle decreased volume, abnormal
ZP:0010833	otic vesicle has fewer parts of type motile cilium otic vesicle, abnormal
ZP:0010834	motile cilium otic vesicle decreased length, abnormal
ZP:0010835	otic vesicle decreased process quality motile cilium assembly, abnormal
ZP:0010836	motile cilium pronephric duct disorganized, abnormal
ZP:0010837	peripheral olfactory organ disorganized, abnormal
ZP:0010838	eye atrophied, abnormal
ZP:0010839	caudal fin atrophied, abnormal
ZP:0010840	axis whole organism truncated, abnormal
ZP:0010841	determination of intestine left/right asymmetry process quality, abnormal
ZP:0010842	dermal bone decreased process quality ossification, abnormal
ZP:0010843	ceratohyal cartilage decreased angle to ceratohyal cartilage, abnormal
ZP:0010845	oxidative DNA demethylation process quality, abnormal
ZP:0010846	erythroid progenitor cell intermediate cell mass of mesoderm decreased amount, abnormal
ZP:0010847	polychromatophilic erythroblast increased amount, abnormal
ZP:0010848	erythroid progenitor cell increased accumulation intermediate cell mass of mesoderm, abnormal
ZP:0010849	trunk lacks all parts of type anterior region thoracic duct, abnormal
ZP:0010850	tooth 4V delayed odontogenesis, abnormal
ZP:0010851	tooth 3V absent, abnormal
ZP:0010853	notochord cell differentiation disrupted, abnormal
ZP:0010854	somite development process quality, abnormal
ZP:0010855	axial chorda mesoderm disrupted cell fate commitment, abnormal
ZP:0010856	floor plate spinal cord region patchy, abnormal
ZP:0010857	muscle displaced to axis, abnormal
ZP:0010858	dorsal side spinal cord apoptotic, abnormal
ZP:0010859	olfactory epithelium lacks parts or has fewer parts of type microvillous olfactory receptor neuron olfactory epithelium, abnormal
ZP:0010860	microvillous olfactory receptor neuron olfactory epithelium disorganized, abnormal
ZP:0010861	neural crest cell apoptotic, abnormal
ZP:0010862	xanthophore dead, abnormal
ZP:0010863	pectoral girdle aplastic/hypoplastic, abnormal
ZP:0010864	palatoquadrate cartilage shortened, abnormal
ZP:0010865	sternohyoid displaced, abnormal
ZP:0010866	brain shortened, abnormal
ZP:0010867	caudal fin necrotic, abnormal
ZP:0010868	whole organism increased process quality apoptotic process, abnormal
ZP:0010869	slow muscle cell shortened, abnormal
ZP:0010870	fast muscle cell disoriented, abnormal
ZP:0010871	fast muscle cell shortened, abnormal
ZP:0010872	primary motor neuron morphology, abnormal
ZP:0010873	Kupffer's vesicle decreased area, abnormal
ZP:0010874	basolateral plasma membrane Kupffer's vesicle physical object quality, abnormal
ZP:0010875	cristae formation absent, abnormal
ZP:0010876	otic placode formation increased process quality, abnormal
ZP:0010877	otolith development arrested, abnormal
ZP:0010878	otic vesicle has extra parts of type hair cell, abnormal
ZP:0010879	primary neuron neural plate increased amount, abnormal
ZP:0010880	lapillus hypotrophic, abnormal
ZP:0010881	statoacoustic (VIII) ganglion increased size, abnormal
ZP:0010882	statoacoustic (VIII) ganglion hyperplastic, abnormal
ZP:0010883	sagitta hypotrophic, abnormal
ZP:0010884	hair cell anterior macula absent, abnormal
ZP:0010885	auditory epithelial support cell absent, abnormal
ZP:0010886	vascular sprouts pleuroperitoneal cavity increased amount, abnormal
ZP:0010887	brain increased process quality apoptotic process, abnormal
ZP:0010888	eye increased process quality apoptotic process, abnormal
ZP:0010890	angioblast cell migration premature, abnormal
ZP:0010891	intersegmental vessel position, abnormal
ZP:0010892	vascular sprouts mislocalised, abnormal
ZP:0010893	pronephric glomerulus development disrupted, abnormal
ZP:0010894	pronephric glomerulus decreased size, abnormal
ZP:0010895	cell projection pronephric podocyte morphology, abnormal
ZP:0010896	cell projection pronephric podocyte irregular spatial pattern, abnormal
ZP:0010897	cell projection pronephric podocyte increased area, abnormal
ZP:0010898	pronephric glomerular capillary hypotrophic, abnormal
ZP:0010899	fin bud hypoplastic, abnormal
ZP:0010900	efflux transmembrane transporter activity decreased process quality, abnormal
ZP:0010901	cell pectoral fin skeleton decreased amount, abnormal
ZP:0010902	cleithrum pectoral fin decreased length, abnormal
ZP:0010903	scapulocoracoid pectoral fin decreased size, abnormal
ZP:0010904	pectoral fin actinotrichium decreased size, abnormal
ZP:0010905	macula utricle has extra parts of type immature hair cell anterior macula, abnormal
ZP:0010906	macula utricle has extra parts of type tether cell, abnormal
ZP:0010907	macula utricle has extra parts of type hair cell, abnormal
ZP:0010908	otic vesicle lacks parts or has fewer parts of type auditory epithelial support cell, abnormal
ZP:0010909	otic vesicle has extra parts of type tether cell, abnormal
ZP:0010910	macula has extra parts of type hair cell, abnormal
ZP:0010911	posterior crista has extra parts of type hair cell, abnormal
ZP:0010912	posterior macula increased size, abnormal
ZP:0010913	axial mesoderm formation process quality, abnormal
ZP:0010914	paraxial mesoderm formation process quality, abnormal
ZP:0010915	dorso-medial region anatomical structure disorganized, abnormal
ZP:0010916	spinal cord bifurcated, abnormal
ZP:0010917	angioblast cell migration delayed, abnormal
ZP:0010918	dorsal aorta broken, abnormal
ZP:0010919	vein broken, abnormal
ZP:0010920	angiogenic sprout absent, abnormal
ZP:0010921	caudal fin wholly dorsalized, abnormal
ZP:0010922	dorsal aorta increased size, abnormal
ZP:0010923	dorsal aorta process quality sprouting angiogenesis, abnormal
ZP:0010924	somite 1 morphology, abnormal
ZP:0010925	somite 2 morphology, abnormal
ZP:0010926	somite 3 morphology, abnormal
ZP:0010927	somite 4 morphology, abnormal
ZP:0010928	interstitial matrix trunk morphology, abnormal
ZP:0010929	interrenal primordium morphology, abnormal
ZP:0010930	interrenal primordium position, abnormal
ZP:0010931	interrenal primordium unfused from left side right side interrenal primordium, abnormal
ZP:0010932	interrenal vessel absent, abnormal
ZP:0010933	interrenal  angiogenic sprout absent, abnormal
ZP:0010934	artery absent, abnormal
ZP:0010935	vein morphology, abnormal
ZP:0010936	interrenal primordium centered, abnormal
ZP:0010937	pronephric glomerular capillary absent, abnormal
ZP:0010938	adrenal gland development lacking processual parts cell migration, abnormal
ZP:0010939	pronephric glomerulus unfused from right side left side pronephric glomerulus, abnormal
ZP:0010940	vascular endothelium increased size, abnormal
ZP:0010941	vascular endothelium mislocalised, abnormal
ZP:0010942	pronephric glomerular capillary increased size, abnormal
ZP:0010943	interrenal  angiogenic sprout mislocalised laterally, abnormal
ZP:0010944	embryonic pectoral fin morphogenesis decreased process quality, abnormal
ZP:0010945	axial mesoderm development decreased process quality, abnormal
ZP:0010946	paraxial mesoderm development process quality, abnormal
ZP:0010947	paraxial mesoderm development decreased process quality, abnormal
ZP:0010948	somite 1 fused with somite 2, abnormal
ZP:0010949	lateral plate mesoderm physical object quality, abnormal
ZP:0010950	anterior region notochord apoptotic, abnormal
ZP:0010951	rhombomere 5 decreased distance somite 1, abnormal
ZP:0010952	whole organism lacks all parts of type pectoral fin cartilage, abnormal
ZP:0010953	whole organism lacks all parts of type pharyngeal pouch 3, abnormal
ZP:0010954	whole organism lacks all parts of type pharyngeal pouch 4, abnormal
ZP:0010955	whole organism lacks all parts of type pectoral fin, abnormal
ZP:0010956	head has fewer parts of type notochord cell notochord, abnormal
ZP:0010957	pectoral fin field physical object quality, abnormal
ZP:0010958	neural crest pharyngeal arch 3-7 apoptotic, abnormal
ZP:0010959	cartilage element cranium shortened, abnormal
ZP:0010960	sarcomere caudal fin musculature disorganized, abnormal
ZP:0010961	muscle cell caudal fin malformed, abnormal
ZP:0010962	muscle cell caudal fin deformed, abnormal
ZP:0010963	muscle cell malformed, abnormal
ZP:0010964	muscle cell deformed, abnormal
ZP:0010965	stereocilium bundle anterior macula bent, abnormal
ZP:0010966	stereocilium bundle anterior macula splayed, abnormal
ZP:0010968	Kupffer's vesicle has fewer parts of type cilium Kupffer's vesicle, abnormal
ZP:0010969	pronephric duct has fewer parts of type cilium pronephric duct, abnormal
ZP:0010971	intestinal epithelium stratified, abnormal
ZP:0010973	invadopodium intestinal epithelium present, abnormal
ZP:0010974	basal lamina intestinal epithelium degenerate, abnormal
ZP:0010975	intestinal epithelial cell mislocalised, abnormal
ZP:0010980	hair cell anterior macula increased occurrence apoptotic process, abnormal
ZP:0010981	posterior lateral line primordium decreased size, abnormal
ZP:0010982	posterior lateral line primordium disorganized, abnormal
ZP:0010983	posterior lateral line primordium lacks parts or has fewer parts of type protoneuromast, abnormal
ZP:0010984	ribbon synapse photoreceptor cell malformed, abnormal
ZP:0010985	pharyngeal arch 2 hypoplastic, abnormal
ZP:0010986	pharyngeal arch 1 hypoplastic, abnormal
ZP:0010987	otic vesicle morphogenesis decreased process quality, abnormal
ZP:0010988	otic vesicle has fewer parts of type immature macula, abnormal
ZP:0010990	otic vesicle decreased process quality neuron differentiation, abnormal
ZP:0010991	neuroblast (sensu Vertebrata) otic vesicle poorly differentiated, abnormal
ZP:0010992	breeding tubercle jaw flap decreased size, abnormal
ZP:0010993	jaw row breeding tubercle decreased size, abnormal
ZP:0010994	jaw row breeding tubercle decreased amount, abnormal
ZP:0010995	motor neuron process quality collateral sprouting, abnormal
ZP:0010996	axon Rohon-Beard neuron decreased branchiness, abnormal
ZP:0010997	ceratobranchial cartilage aplastic/hypoplastic, abnormal
ZP:0010998	optokinetic behavior decreased process quality, abnormal
ZP:0010999	myelination premature, abnormal
ZP:0011000	oligodendrocyte decreased process quality cell migration, abnormal
ZP:0011001	Mauthner neuron decreased diameter, abnormal
ZP:0011002	Mauthner neuron increased process quality myelination, abnormal
ZP:0011003	myelin sheath Mauthner neuron increased thickness, abnormal
ZP:0011004	neuron increased process quality myelination, abnormal
ZP:0011005	myelin sheath neuron increased thickness, abnormal
ZP:0011006	regulation of smooth muscle contraction process quality, abnormal
ZP:0011007	tonic smooth muscle contraction present, abnormal
ZP:0011009	regulation of intestinal epithelial structure maintenance disrupted, abnormal
ZP:0011010	enteric musculature intestine morphology, abnormal
ZP:0011011	intestinal epithelium cystic, abnormal
ZP:0011012	focal adhesion intestinal epithelium degenerate, abnormal
ZP:0011013	basal lamina intestinal epithelium damaged, abnormal
ZP:0011014	interrenal primordium bilateral, abnormal
ZP:0011015	mesoderm migration involved in gastrulation disrupted, abnormal
ZP:0011016	actin polymerization or depolymerization process quality, abnormal
ZP:0011017	regulation of cytosolic calcium ion concentration disrupted, abnormal
ZP:0011018	mitochondrial calcium ion homeostasis disrupted, abnormal
ZP:0011019	filamentous actin mesodermal cell oriented, abnormal
ZP:0011020	renal water transport decreased process quality, abnormal
ZP:0011021	embryonic heart tube left/right pattern formation decreased process quality, abnormal
ZP:0011022	pronephros morphogenesis decreased process quality, abnormal
ZP:0011023	central canal has fewer parts of type cilium ependymal cell, abnormal
ZP:0011024	pronephric tubule has fewer parts of type microvillus pronephric tubule, abnormal
ZP:0011025	actin cytoskeleton pronephric tubule decreased object quality, abnormal
ZP:0011026	motile cilium pronephric tubule decreased length, abnormal
ZP:0011027	motile cilium pronephric tubule disoriented, abnormal
ZP:0011028	ciliary basal body pronephric tubule disorganized, abnormal
ZP:0011029	apical part of cell pronephric tubule physical object quality, abnormal
ZP:0011030	pronephric podocyte lacks parts or has fewer parts of type slit diaphragm pronephric podocyte, abnormal
ZP:0011031	cell projection pronephric podocyte malformed, abnormal
ZP:0011032	apical part of cell pronephric podocyte malformed, abnormal
ZP:0011033	pronephric capsular space dilated, abnormal
ZP:0011034	cilium ependymal cell decreased length, abnormal
ZP:0011035	cilium ependymal cell disoriented, abnormal
ZP:0011036	erythrocyte development process quality, abnormal
ZP:0011037	epiboly abnormal, abnormal
ZP:0011038	endoderm disrupted cell migration involved in gastrulation, abnormal
ZP:0011039	extension malformed, abnormal
ZP:0011040	germ ring constricted, abnormal
ZP:0011041	heart agenesis, abnormal
ZP:0011042	hypoblast movement quality, abnormal
ZP:0011043	presumptive endoderm process quality cell migration involved in gastrulation, abnormal
ZP:0011044	ventral fin fold abnormal, abnormal
ZP:0011045	pharyngeal endoderm malformed, abnormal
ZP:0011046	notochord posterior region malformed, abnormal
ZP:0011047	blood cell increased accumulation trunk, abnormal
ZP:0011048	mesodermal cell accumulation margin, abnormal
ZP:0011049	endodermal cell movement quality, abnormal
ZP:0011050	retinal outer plexiform layer decreased thickness, abnormal
ZP:0011051	retinal cone cell quality, abnormal
ZP:0011054	retinal cone cell lacks parts or has fewer parts of type cone cell pedicle ribbon synapse retinal cone cell, abnormal
ZP:0011055	axon microtubule bundle Rohon-Beard neuron loose, abnormal
ZP:0011058	central canal hindbrain increased amount, abnormal
ZP:0011059	cell hindbrain disoriented, abnormal
ZP:0011061	fourth ventricle separated from fourth ventricle, abnormal
ZP:0011063	rhombomere 3 increased variability establishment of mitotic spindle orientation, abnormal
ZP:0011065	rhombomere 4 increased variability establishment of mitotic spindle orientation, abnormal
ZP:0011066	eye decreased process quality cell population proliferation, abnormal
ZP:0011067	eye increased process quality intrinsic apoptotic signaling pathway, abnormal
ZP:0011068	ciliary marginal zone decreased process quality cell population proliferation, abnormal
ZP:0011069	forebrain dorsal/ventral pattern formation process quality, abnormal
ZP:0011070	floor plate development decreased process quality, abnormal
ZP:0011071	retina development in camera-type eye process quality, abnormal
ZP:0011072	commissural neuron axon guidance process quality, abnormal
ZP:0011073	spinal cord has fewer parts of type anterior region primary motor neuron, abnormal
ZP:0011074	lens eye deformed, abnormal
ZP:0011075	forebrain process quality axon guidance, abnormal
ZP:0011077	somite lacks all parts of type horizontal myoseptum, abnormal
ZP:0011078	cleithrum hypoplastic, abnormal
ZP:0011079	caudal commissure absent, abnormal
ZP:0011081	caudal fin lacks all parts of type primary motor neuron, abnormal
ZP:0011083	anterior commissure absent, abnormal
ZP:0011084	trunk lacks all parts of type posterior region primary motor neuron, abnormal
ZP:0011085	adenohypophyseal placode transformed to lens, abnormal
ZP:0011086	lateral floor plate absent, abnormal
ZP:0011087	medial floor plate broken, abnormal
ZP:0011088	primary motor neuron absent, abnormal
ZP:0011089	retinal ganglion cell process quality axon guidance, abnormal
ZP:0011090	neuroblast (sensu Vertebrata) otic vesicle physical object quality, abnormal
ZP:0011091	notochord mislocalised laterally, abnormal
ZP:0011092	filamentous actin somite deformed, abnormal
ZP:0011093	myelin sheath peripheral neuron neoplastic, abnormal
ZP:0011095	abducens motor nucleus fused with abducens motor nucleus, abnormal
ZP:0011100	cerebellum development decreased process quality, abnormal
ZP:0011101	midbrain-hindbrain boundary development decreased process quality, abnormal
ZP:0011102	somite development decreased process quality, abnormal
ZP:0011103	somite poorly differentiated, abnormal
ZP:0011104	whole organism lacks all parts of type midbrain hindbrain boundary, abnormal
ZP:0011105	whole organism lacks all parts of type cerebellum, abnormal
ZP:0011106	axon VaP motor neuron branchiness, abnormal
ZP:0011107	iridophore dorsal larval melanophore stripe mislocalised anteriorly, abnormal
ZP:0011108	iridophore ventral larval melanophore stripe increased amount, abnormal
ZP:0011109	blood island morphology, abnormal
ZP:0011110	blood island has extra parts of type erythroid lineage cell, abnormal
ZP:0011115	oligodendrocyte differentiation process quality, abnormal
ZP:0011116	embryonic cleavage process quality, abnormal
ZP:0011117	regulation of nodal signaling pathway process quality, abnormal
ZP:0011118	pharyngeal pouch 1 physical object quality, abnormal
ZP:0011119	stomodeum mislocalised ventrally, abnormal
ZP:0011120	palatoquadrate cartilage fused with Meckel's cartilage, abnormal
ZP:0011121	hyosymplectic cartilage fused with ceratohyal cartilage, abnormal
ZP:0011122	ventral region pharyngeal arch 3 physical object quality, abnormal
ZP:0011123	mesenchymal cell pharyngeal arch 3 physical object quality, abnormal
ZP:0011124	ventral region pharyngeal arch 4 physical object quality, abnormal
ZP:0011125	mesenchymal cell pharyngeal arch 4 physical object quality, abnormal
ZP:0011126	ventral region pharyngeal arch 2 physical object quality, abnormal
ZP:0011127	mesenchymal cell pharyngeal arch 2 physical object quality, abnormal
ZP:0011128	ventral region pharyngeal arch 1 physical object quality, abnormal
ZP:0011129	mesenchymal cell pharyngeal arch 1 physical object quality, abnormal
ZP:0011130	ventral intermandibularis anterior physical object quality, abnormal
ZP:0011131	ventral intermandibularis posterior physical object quality, abnormal
ZP:0011132	interhyoideus decreased length, abnormal
ZP:0011133	interhyoideus physical object quality, abnormal
ZP:0011134	hyohyoideus decreased length, abnormal
ZP:0011135	anterior commissure morphogenesis process quality, abnormal
ZP:0011136	supraoptic tract process quality axon extension, abnormal
ZP:0011137	dorso-rostral cluster process quality axon extension, abnormal
ZP:0011138	axon retinal ganglion cell decreased branchiness, abnormal
ZP:0011139	retinal ganglion cell decreased process quality collateral sprouting in absence of injury, abnormal
ZP:0011140	hindbrain morphogenesis process quality, abnormal
ZP:0011141	posterior region hindbrain physical object quality, abnormal
ZP:0011142	rhombomere 6 increased length, abnormal
ZP:0011143	spinal cord has fewer parts of type anterior region spinal cord interneuron, abnormal
ZP:0011144	spinal cord has fewer parts of type anterior region motor neuron, abnormal
ZP:0011145	intermandibularis decreased length, abnormal
ZP:0011146	rhombomere 7 increased length, abnormal
ZP:0011147	rhombomere 7 physical object quality, abnormal
ZP:0011148	neuron projection dorso-rostral cluster physical object quality, abnormal
ZP:0011149	locomotor rhythm process quality, abnormal
ZP:0011150	head decreased pigmentation, abnormal
ZP:0011151	opsin transport decreased process quality, abnormal
ZP:0011152	retinal outer nuclear layer increased process quality apoptotic process, abnormal
ZP:0011153	retinal outer nuclear layer increased process quality cell death, abnormal
ZP:0011154	neuron projection cranial nerve physical object quality, abnormal
ZP:0011155	angiogenic sprout physical object quality, abnormal
ZP:0011156	intersegmental vessel process quality blood vessel lumenization, abnormal
ZP:0011158	Schwann cell migration process quality, abnormal
ZP:0011159	posterior lateral line nerve has fewer parts of type axon myelinating Schwann cell, abnormal
ZP:0011160	posterior lateral line nerve arrested myelination, abnormal
ZP:0011161	posterior lateral line nerve decreased process quality myelination, abnormal
ZP:0011162	immature Schwann cell decreased velocity, abnormal
ZP:0011163	motor neuron has extra parts of type axon myelinating Schwann cell, abnormal
ZP:0011164	motor neuron arrested myelination, abnormal
ZP:0011165	motor neuron decreased process quality myelination, abnormal
ZP:0011166	myelinating Schwann cell loose, abnormal
ZP:0011167	atrioventricular valve formation process quality, abnormal
ZP:0011168	atrioventricular canal development process quality, abnormal
ZP:0011169	atrioventricular canal malformed, abnormal
ZP:0011170	otic vesicle development process quality, abnormal
ZP:0011171	otic vesicle split, abnormal
ZP:0011172	hyomandibula hypoplastic, abnormal
ZP:0011173	pharyngeal pouch 1 increased process quality apoptotic process, abnormal
ZP:0011174	pharyngeal pouch 2 increased process quality apoptotic process, abnormal
ZP:0011175	facial ganglion absent, abnormal
ZP:0011176	neurogenic placode increased process quality apoptotic process, abnormal
ZP:0011177	ventral anterior lateral line ganglion absent, abnormal
ZP:0011178	middle lateral line ganglion absent, abnormal
ZP:0011179	pharyngeal arch 3 hypoplastic, abnormal
ZP:0011180	pharyngeal arch 4 hypoplastic, abnormal
ZP:0011181	neurogenic field increased process quality apoptotic process, abnormal
ZP:0011182	vagal ganglion decreased size, abnormal
ZP:0011183	vagal ganglion lacks parts or has fewer parts of type vagal ganglion, abnormal
ZP:0011184	neuroectoderm wholly dorsalized, abnormal
ZP:0011185	retinal pigmented epithelium process quality melanosome localization, abnormal
ZP:0011186	lapillus decreased width, abnormal
ZP:0011187	lapillus adjacent to sagitta, abnormal
ZP:0011188	sagitta decreased width, abnormal
ZP:0011190	angioblast cell migration process quality, abnormal
ZP:0011192	tonic skeletal muscle contraction process quality, abnormal
ZP:0011193	glomerular filtration process quality, abnormal
ZP:0011194	intersegmental vessel disrupted sprouting angiogenesis, abnormal
ZP:0011195	lens disrupted collagen fibril organization, abnormal
ZP:0011196	Golgi apparatus photoreceptor cell physical object quality, abnormal
ZP:0011197	negative regulation of oxidative stress-induced intrinsic apoptotic signaling pathway disrupted, abnormal
ZP:0011198	epithelial cell pronephros physical object quality, abnormal
ZP:0011199	cilium multi-ciliated epithelial cell physical object quality, abnormal
ZP:0011200	telomere maintenance via telomerase process quality, abnormal
ZP:0011201	chromosome, telomeric region whole organism physical object quality, abnormal
ZP:0011202	retinal cone cell process quality chemical synaptic transmission, abnormal
ZP:0011203	cone cell pedicle retinal cone cell morphology, abnormal
ZP:0011204	brain vasculature malformed, abnormal
ZP:0011205	cerebellum hypoplastic, abnormal
ZP:0011206	diencephalon increased process quality apoptotic process, abnormal
ZP:0011207	fourth ventricle increased process quality apoptotic process, abnormal
ZP:0011208	rhombomere 3 process quality establishment of mitotic spindle orientation, abnormal
ZP:0011209	rhombomere 4 process quality establishment of mitotic spindle orientation, abnormal
ZP:0011210	brain decreased length, abnormal
ZP:0011211	posterior region mesoderm increased length, abnormal
ZP:0011212	cell migration to the midline involved in heart development disrupted, abnormal
ZP:0011213	optic stalk physical object quality, abnormal
ZP:0011214	supraoptic commissure physical object quality, abnormal
ZP:0011215	anterior commissure physical object quality, abnormal
ZP:0011216	anterior commissure process quality axon extension, abnormal
ZP:0011217	cell migration involved in somitogenic axis elongation disrupted, abnormal
ZP:0011218	adherens junction tail bud morphology, abnormal
ZP:0011219	thoracic duct morphology, abnormal
ZP:0011220	rhombomere boundary formation process quality, abnormal
ZP:0011221	rhombomere 5 process quality rhombomere boundary formation, abnormal
ZP:0011222	rhombomere 3 process quality rhombomere boundary formation, abnormal
ZP:0011223	fourth ventricle development process quality, abnormal
ZP:0011224	hindbrain process quality neural keel formation, abnormal
ZP:0011225	rhombomere 3 process quality neural keel formation, abnormal
ZP:0011226	rhombomere 4 process quality neural keel formation, abnormal
ZP:0011227	interrenal gland mislocalised, abnormal
ZP:0011228	interrenal gland decreased occurrence steroid biosynthetic process, abnormal
ZP:0011229	interrenal primordium disrupted cell migration, abnormal
ZP:0011230	splanchnocranium aplastic, abnormal
ZP:0011231	anterior region neurocranium aplastic, abnormal
ZP:0011232	myotome development process quality, abnormal
ZP:0011233	fast muscle cell morphology, abnormal
ZP:0011234	neuromast hair cell process quality synapse organization, abnormal
ZP:0011235	neuromast hair cell process quality cellular response to mechanical stimulus, abnormal
ZP:0011236	ribbon synapse neuromast hair cell morphology, abnormal
ZP:0011237	splanchnocranium hyperplastic, abnormal
ZP:0011238	ceratobranchial cartilage hyperplastic, abnormal
ZP:0011239	diencephalic nucleus displaced to axon lateral region hindbrain, abnormal
ZP:0011240	diencephalic nucleus displaced to axon medial region hindbrain, abnormal
ZP:0011241	hypocretin-secreting neuron displaced to axon medial region hindbrain, abnormal
ZP:0011242	otic vesicle development decreased process quality, abnormal
ZP:0011245	otic placode physical object quality, abnormal
ZP:0011246	lateral crista physical object quality, abnormal
ZP:0011248	pectoral fin bud absent, abnormal
ZP:0011249	pectoral girdle absent, abnormal
ZP:0011250	pharyngeal arch absent, abnormal
ZP:0011251	dopaminergic neuron displaced to axon medial region hindbrain, abnormal
ZP:0011253	anterior-posterior axis whole organism truncated, abnormal
ZP:0011255	cell accumulation dorsal side tail bud, abnormal
ZP:0011256	pectoral fin cartilage absent, abnormal
ZP:0011257	dorsal side whole organism decreased thickness, abnormal
ZP:0011258	blood accumulation head, abnormal
ZP:0011259	blood accumulation post-vent region, abnormal
ZP:0011260	atrioventricular canal shape, abnormal
ZP:0011261	NADH oxidation decreased rate, abnormal
ZP:0011262	trunk decreased occurrence blood circulation, abnormal
ZP:0011263	intestine disrupted epithelial tube morphogenesis, abnormal
ZP:0011264	anatomical space intestine increased amount, abnormal
ZP:0011265	anatomical space intestine trabecular, abnormal
ZP:0011266	epiphysis split bilaterally, abnormal
ZP:0011267	parapineal organ process quality determination of left/right asymmetry in nervous system, abnormal
ZP:0011268	epiphysis morphology, abnormal
ZP:0011269	neural tube open, abnormal
ZP:0011270	hypothalamus has fewer parts of type serotonin secreting cell, abnormal
ZP:0011271	hypothalamus increased duration mitotic S phase, abnormal
ZP:0011272	vH ionocyte process quality regulation of pH, abnormal
ZP:0011274	olfactory epithelium organization quality, abnormal
ZP:0011275	olfactory bulb glomerulus malformed, abnormal
ZP:0011276	olfactory bulb glomerulus aplastic/hypoplastic, abnormal
ZP:0011277	cell detached from neural tube, abnormal
ZP:0011278	olfactory nerve formation process quality, abnormal
ZP:0011279	cranial nerve I morphology, abnormal
ZP:0011280	axon cranial nerve I mislocalised, abnormal
ZP:0011281	olfactory epithelium shape, abnormal
ZP:0011282	olfactory epithelium decreased size, abnormal
ZP:0011283	olfactory bulb glomerulus morphology, abnormal
ZP:0011284	cell-cell adhesion disrupted, abnormal
ZP:0011285	posterior side dorsal fin fold decreased size, abnormal
ZP:0011286	posterior side dorsal fin fold split medially, abnormal
ZP:0011287	hindbrain neural keel shape, abnormal
ZP:0011288	neuroepithelial cell displaced to fourth ventricle, abnormal
ZP:0011289	heart development process quality, abnormal
ZP:0011290	blood circulation decreased functionality, abnormal
ZP:0011291	blood vessel hindbrain absent, abnormal
ZP:0011292	blood vessel midbrain hindbrain boundary absent, abnormal
ZP:0011293	dorsal region brain vasculature absent, abnormal
ZP:0011294	heart decreased length, abnormal
ZP:0011295	anterior cardinal vein absent, abnormal
ZP:0011296	blood vessel optic tectum absent, abnormal
ZP:0011297	blood vessel pharyngeal arch absent, abnormal
ZP:0011299	somite amorphous, abnormal
ZP:0011301	ventral spinal cord interneuron differentiation decreased occurrence, abnormal
ZP:0011302	spinal cord oligodendrocyte cell differentiation decreased occurrence, abnormal
ZP:0011303	spinal cord has fewer parts of type spinal cord interneuron, abnormal
ZP:0011304	spinal cord has fewer parts of type Kolmer-Agduhr neuron, abnormal
ZP:0011305	whole organism lacks all parts of type swim bladder, abnormal
ZP:0011306	mandibular arch skeleton degenerate, abnormal
ZP:0011307	somite antero-posteriorly flattened, abnormal
ZP:0011309	central nervous system disorganized, abnormal
ZP:0011310	neural crest increased size, abnormal
ZP:0011311	whole organism elliptic, abnormal
ZP:0011312	posterior region whole organism wholly dorsalized, abnormal
ZP:0011313	posterior region whole organism truncated, abnormal
ZP:0011314	eye displaced, abnormal
ZP:0011315	locus coeruleus lacks parts or has fewer parts of type neuron, abnormal
ZP:0011316	pharyngeal arch has fewer parts of type neuron, abnormal
ZP:0011317	pharyngeal pouch decreased occurrence protein localization to plasma membrane, abnormal
ZP:0011318	musculoskeletal movement irregular rhythm, abnormal
ZP:0011319	musculoskeletal movement decreased coordination, abnormal
ZP:0011320	musculoskeletal movement episodic, abnormal
ZP:0011321	optic tectum increased frequency neuronal action potential, abnormal
ZP:0011322	optic tectum irregular rhythm neuronal action potential, abnormal
ZP:0011323	optic tectum decreased process quality regulation of neuronal action potential, abnormal
ZP:0011324	whole organism process quality mitotic cell cycle, abnormal
ZP:0011325	whole organism increased process quality cell population proliferation, abnormal
ZP:0011326	cloaca morphology, abnormal
ZP:0011327	embryonic digestive tract morphogenesis process quality, abnormal
ZP:0011328	endoderm decreased process quality cell population proliferation, abnormal
ZP:0011329	endoderm process quality cell migration, abnormal
ZP:0011330	cell endoderm decreased amount, abnormal
ZP:0011331	gut shape, abnormal
ZP:0011332	liver primordium aplastic/hypoplastic, abnormal
ZP:0011333	pancreas primordium aplastic/hypoplastic, abnormal
ZP:0011334	endodermal cell delayed cell migration, abnormal
ZP:0011335	endodermal cell process quality cell migration, abnormal
ZP:0011336	cell migration to the midline involved in heart development delayed, abnormal
ZP:0011337	cell migration to the midline involved in heart development process quality, abnormal
ZP:0011338	endothelial cell ventral wall of dorsal aorta apoptotic, abnormal
ZP:0011339	heart rudiment process quality cardioblast anterior-lateral migration, abnormal
ZP:0011340	presumptive endocardium decreased process quality BMP signaling pathway involved in heart development, abnormal
ZP:0011341	blood vessel morphogenesis decreased process quality, abnormal
ZP:0011342	caudal vein plexus increased occurrence sprouting angiogenesis, abnormal
ZP:0011343	angiogenic sprout caudal vein plexus increased amount, abnormal
ZP:0011344	ventral wall of dorsal aorta has fewer parts of type hematopoietic stem cell, abnormal
ZP:0011345	cell projection cardiac muscle cell transient, abnormal
ZP:0011346	hindbrain increased process quality apoptotic process, abnormal
ZP:0011347	midbrain increased process quality apoptotic process, abnormal
ZP:0011348	horizontal myoseptum increased process quality apoptotic process, abnormal
ZP:0011349	head increased process quality apoptotic process, abnormal
ZP:0011350	trunk increased process quality apoptotic process, abnormal
ZP:0011351	retroarticular absent, abnormal
ZP:0011352	mesenchyme pharyngeal arch 1 decreased area, abnormal
ZP:0011354	retinal ganglion cell decreased process quality neuron remodeling, abnormal
ZP:0011355	axon retinal ganglion cell physical object quality, abnormal
ZP:0011356	axon retinal ganglion cell increased branchiness, abnormal
ZP:0011357	retinal ganglion cell has extra parts of type axon presynaptic active zone retinal ganglion cell, abnormal
ZP:0011358	axon collateral retinal ganglion cell increased length, abnormal
ZP:0011359	axon collateral retinal ganglion cell physical object quality, abnormal
ZP:0011360	retinal ganglion cell occurrence collateral sprouting in absence of injury, abnormal
ZP:0011361	retinal ganglion cell increased occurrence collateral sprouting in absence of injury, abnormal
ZP:0011362	heart lacks all parts of type cell ventricular epicardium, abnormal
ZP:0011363	proepicardial cluster absent, abnormal
ZP:0011364	telencephalon lacks parts or has fewer parts of type dopaminergic neuron, abnormal
ZP:0011365	heart decreased duration cardiac muscle cell action potential, abnormal
ZP:0011366	whole organism spotted, abnormal
ZP:0011367	whole organism desaturated yellow, abnormal
ZP:0011368	whole organism has fewer parts of type melanocyte, abnormal
ZP:0011369	whole organism lacks all parts of type xanthophore, abnormal
ZP:0011370	whole organism has fewer parts of type xanthophore, abnormal
ZP:0011371	head has fewer parts of type xanthophore, abnormal
ZP:0011372	xanthophore head irregular spatial pattern, abnormal
ZP:0011373	trunk lacks all parts of type xanthophore, abnormal
ZP:0011374	trunk has fewer parts of type ventro-lateral region xanthophore, abnormal
ZP:0011375	trunk has fewer parts of type dermis melanocyte, abnormal
ZP:0011376	trunk lacks all parts of type dermis xanthophore, abnormal
ZP:0011377	melanophore stripe trunk malformed, abnormal
ZP:0011378	iridophore trunk mislocalised, abnormal
ZP:0011379	anal fin spotted, abnormal
ZP:0011380	anal fin has fewer parts of type melanophore stripe, abnormal
ZP:0011381	melanophore stripe anal fin patchy, abnormal
ZP:0011382	melanophore stripe low saturation, abnormal
ZP:0011383	melanophore stripe irregular spatial pattern, abnormal
ZP:0011384	melanophore stripe spotted, abnormal
ZP:0011385	melanophore stripe absent, abnormal
ZP:0011386	melanophore stripe patchy, abnormal
ZP:0011387	xanthophore area density, abnormal
ZP:0011388	dopaminergic neuron disrupted neuron development, abnormal
ZP:0011389	hindbrain disrupted anterior/posterior pattern specification, abnormal
ZP:0011390	axon hindbrain morphology, abnormal
ZP:0011391	axon hindbrain mislocalised, abnormal
ZP:0011392	radial glial cell hindbrain morphology, abnormal
ZP:0011393	glial cell (sensu Vertebrata) floor plate spinal cord region amount, abnormal
ZP:0011394	glial cell (sensu Vertebrata) floor plate spinal cord region increased size, abnormal
ZP:0011395	endothelial cell migration delayed, abnormal
ZP:0011396	filopodium assembly increased occurrence, abnormal
ZP:0011397	regulation of blood vessel remodeling process quality, abnormal
ZP:0011398	caudal vein plexus has extra parts of type endothelial cell filopodium endothelial cell, abnormal
ZP:0011399	subintestinal vein has extra parts of type angiogenic sprout, abnormal
ZP:0011400	glial cell projection trunk mislocalised, abnormal
ZP:0011401	enteric neuron decreased amount, abnormal
ZP:0011402	cellular calcium ion homeostasis process quality, abnormal
ZP:0011403	skeletal myofibril assembly decreased process quality, abnormal
ZP:0011404	skeletal muscle myofibril myotome malformed, abnormal
ZP:0011405	skeletal muscle myofibril myotome disorganized, abnormal
ZP:0011406	skeletal muscle myofibril myotome increased fragility, abnormal
ZP:0011407	sarcolemma skeletal muscle cell increased permeability, abnormal
ZP:0011408	trigeminal sensory neuron mislocalised, abnormal
ZP:0011409	trigeminal sensory neuron process quality cell migration, abnormal
ZP:0011410	lipid transport disrupted, abnormal
ZP:0011411	lipid droplet liver decreased amount, abnormal
ZP:0011412	liver decreased occurrence cell population proliferation, abnormal
ZP:0011413	lipid droplet gall bladder decreased amount, abnormal
ZP:0011414	lipid droplet intestine decreased amount, abnormal
ZP:0011415	posterior lateral line nerve development process quality, abnormal
ZP:0011416	spinal cord molecular quality, abnormal
ZP:0011417	anatomical region motor nucleus of vagal nerve decreased size, abnormal
ZP:0011418	somite 4 increased duration somitogenesis, abnormal
ZP:0011419	intestinal bulb hypoplastic, abnormal
ZP:0011420	vertebra 2 absent, abnormal
ZP:0011421	intestine lacks all parts of type intestinal villus, abnormal
ZP:0011422	intestine lacks all parts of type columnar/cuboidal epithelial cell, abnormal
ZP:0011423	intestinal epithelium aplastic, abnormal
ZP:0011424	Kupffer's vesicle increased diameter, abnormal
ZP:0011425	Kupffer's vesicle process quality calcium-mediated signaling, abnormal
ZP:0011426	optic cup flattened, abnormal
ZP:0011427	hyaloid vessel delayed vasculature development, abnormal
ZP:0011428	hyaloid vessel process quality vasculature development, abnormal
ZP:0011429	spinal cord has fewer parts of type radial glial cell, abnormal
ZP:0011430	central canal increased size, abnormal
ZP:0011431	endoderm mislocalised, abnormal
ZP:0011432	pancreatic bud split medially, abnormal
ZP:0011433	extracellular matrix cell increased size, abnormal
ZP:0011434	extracellular matrix cell organization quality, abnormal
ZP:0011435	endothelial cell mislocalised, abnormal
ZP:0011436	macula utricle physical object quality, abnormal
ZP:0011437	anterior region otic vesicle physical object quality, abnormal
ZP:0011438	lateral crista primordium physical object quality, abnormal
ZP:0011439	posterior crista primordium physical object quality, abnormal
ZP:0011440	semicircular canal physical object quality, abnormal
ZP:0011441	posterior crista physical object quality, abnormal
ZP:0011442	anterior crista physical object quality, abnormal
ZP:0011443	primordial germ cell apoptotic, abnormal
ZP:0011444	thoracic duct decreased process quality lymphangiogenesis, abnormal
ZP:0011445	postoptic commissure defasciculated, abnormal
ZP:0011446	postoptic commissure disrupted commissural neuron axon guidance, abnormal
ZP:0011447	forebrain disrupted commissural neuron axon guidance, abnormal
ZP:0011448	cranial nerve II disrupted commissural neuron axon guidance, abnormal
ZP:0011449	anterior commissure defasciculated, abnormal
ZP:0011450	anterior commissure disrupted commissural neuron axon guidance, abnormal
ZP:0011454	anterior region endoderm increased width, abnormal
ZP:0011455	anterior region endoderm perforate, abnormal
ZP:0011456	endoderm process quality convergent extension, abnormal
ZP:0011457	larval locomotory behavior increased rate, abnormal
ZP:0011458	axon primary motor neuron increased branchiness, abnormal
ZP:0011460	cellular senescence increased process quality, abnormal
ZP:0011461	autophagosome maturation process quality, abnormal
ZP:0011462	cell accumulation autophagosome perinuclear region of cytoplasm cell, abnormal
ZP:0011463	cell accumulation autolysosome perinuclear region of cytoplasm cell, abnormal
ZP:0011464	astrocyte postoptic commissure mislocalised, abnormal
ZP:0011465	astrocyte forebrain morphology, abnormal
ZP:0011466	astrocyte anterior commissure mislocalised, abnormal
ZP:0011467	caudal fin lacks parts or has fewer parts of type dorsal root ganglion, abnormal
ZP:0011468	pharyngeal arch 1 has fewer parts of type chondrocyte, abnormal
ZP:0011469	chondrocyte pharyngeal arch 1 shape, abnormal
ZP:0011470	pharyngeal arch 3-7 increased process quality cell death, abnormal
ZP:0011471	glial cell (sensu Vertebrata) hindbrain mislocalised, abnormal
ZP:0011472	spinal cord lacks all parts of type radial glial cell ventricular zone, abnormal
ZP:0011473	cranial nerve II absent, abnormal
ZP:0011474	trunk has fewer parts of type glial cell (sensu Vertebrata) nerve, abnormal
ZP:0011475	trunk has fewer parts of type axon motor neuron, abnormal
ZP:0011476	nerve trunk truncated, abnormal
ZP:0011477	spinal cord has extra parts of type radial glial cell ventricular zone, abnormal
ZP:0011478	neural tube has extra parts of type radial glial cell, abnormal
ZP:0011479	neural tube increased process quality apoptotic process, abnormal
ZP:0011480	forebrain ventricle has extra parts of type astrocyte, abnormal
ZP:0011481	CoSA decreased amount, abnormal
ZP:0011482	VeLD process quality axon guidance, abnormal
ZP:0011483	Kolmer-Agduhr neuron process quality axon guidance, abnormal
ZP:0011484	radial glial cell has fewer parts of type aster radial glial cell, abnormal
ZP:0011485	Kupffer's vesicle increased distance nucleus apical plasma membrane Kupffer's vesicle, abnormal
ZP:0011487	Kupffer's vesicle detached from ciliary basal body apical plasma membrane Kupffer's vesicle, abnormal
ZP:0011488	cell ectoderm shape, abnormal
ZP:0011489	ectoderm orientation cell ectoderm, abnormal
ZP:0011490	floor plate process quality establishment of planar polarity, abnormal
ZP:0011491	cell notochord shape, abnormal
ZP:0011492	notochord orientation cell notochord, abnormal
ZP:0011493	extracellular matrix cell decreased size, abnormal
ZP:0011494	pronephric glomerulus development process quality, abnormal
ZP:0011495	turning behavior process quality, abnormal
ZP:0011496	exploration behavior process quality, abnormal
ZP:0011497	locomotory exploration behavior process quality, abnormal
ZP:0011498	forebrain deformed, abnormal
ZP:0011499	glial cell (sensu Vertebrata) nerve branched, abnormal
ZP:0011500	myofibril assembly delayed, abnormal
ZP:0011501	myofibril somite morphology, abnormal
ZP:0011502	myofibril somite loose, abnormal
ZP:0011503	vasculature development process quality, abnormal
ZP:0011504	basal communicating artery detached from primordial midbrain channel, abnormal
ZP:0011505	posterior margin midbrain increased width, abnormal
ZP:0011506	central region optic tectum proliferative, abnormal
ZP:0011507	optic tectum increased occurrence apoptotic process, abnormal
ZP:0011508	optic tectum increased occurrence cell proliferation in midbrain, abnormal
ZP:0011509	optic tectum process quality regulation of neurogenesis, abnormal
ZP:0011511	postoptic commissure has fewer parts of type astrocyte, abnormal
ZP:0011512	anterior commissure has fewer parts of type astrocyte, abnormal
ZP:0011513	central nervous system morphogenesis decreased process quality, abnormal
ZP:0011514	neural crest poorly differentiated, abnormal
ZP:0011515	neuroectoderm retina necrotic, abnormal
ZP:0011516	head lacks parts or has fewer parts of type pharyngeal arch cartilage, abnormal
ZP:0011517	neural tube necrotic, abnormal
ZP:0011518	pharyngeal arch necrotic, abnormal
ZP:0011519	pharyngeal arch 1 fused with pharyngeal arch 2, abnormal
ZP:0011520	chondrocyte mislocalised, abnormal
ZP:0011521	pancreas molecular quality, abnormal
ZP:0011522	intestine molecular quality, abnormal
ZP:0011524	myelin sheath lateral line nerve absent, abnormal
ZP:0011527	aortic arch malformed, abnormal
ZP:0011528	cell projection organization disrupted, abnormal
ZP:0011529	pseudopodium organization disrupted, abnormal
ZP:0011530	epiboly involved in gastrulation with mouth forming second process quality, abnormal
ZP:0011531	convergent extension involved in axis elongation decreased process quality, abnormal
ZP:0011532	dorsal convergence decreased process quality, abnormal
ZP:0011533	cell-cell adhesion involved in gastrulation decreased occurrence, abnormal
ZP:0011534	DEL circular, abnormal
ZP:0011535	DEL detached from EVL, abnormal
ZP:0011536	axis whole organism increased width, abnormal
ZP:0011537	filamentous actin blastoderm increased amount, abnormal
ZP:0011538	neutrophil migration increased occurrence, abnormal
ZP:0011539	enteric nervous system delayed neuron migration, abnormal
ZP:0011540	enteric nervous system decreased rate neuron migration, abnormal
ZP:0011541	enteric nervous system decreased occurrence cell division, abnormal
ZP:0011542	caudal fin malformed, abnormal
ZP:0011543	ventral wall of dorsal aorta increased process quality apoptotic process, abnormal
ZP:0011544	ventral wall of dorsal aorta decreased process quality Notch signaling pathway, abnormal
ZP:0011545	cell posterior lateral mesoderm shape, abnormal
ZP:0011546	endothelial cell decreased process quality Notch signaling pathway, abnormal
ZP:0011547	neural tube decreased width, abnormal
ZP:0011548	neural tube asymmetrical, abnormal
ZP:0011549	ventricular system closed, abnormal
ZP:0011550	intersegmental vein hypoplastic, abnormal
ZP:0011551	cranial vasculature aplastic, abnormal
ZP:0011552	cranial vasculature process quality angiogenesis, abnormal
ZP:0011553	intersegmental vessel process quality angiogenesis, abnormal
ZP:0011554	pronephric glomerulus morphogenesis decreased process quality, abnormal
ZP:0011555	slit diaphragm pronephric podocyte malformed, abnormal
ZP:0011556	pronephric glomerular capsule cystic, abnormal
ZP:0011557	eye process quality pigmentation, abnormal
ZP:0011558	dorsal aorta decreased distance caudal vein, abnormal
ZP:0011559	posterior cardinal vein increased occurrence endothelial cell apoptotic process, abnormal
ZP:0011560	cytokinesis process quality, abnormal
ZP:0011561	cortical granule exocytosis decreased process quality, abnormal
ZP:0011562	blastomere has extra parts of type nucleus blastomere, abnormal
ZP:0011563	oocyte accumulation secretory granule oocyte, abnormal
ZP:0011564	oocyte stage III has extra parts of type cortical granule oocyte stage III, abnormal
ZP:0011565	lysosome oocyte stage III broken, abnormal
ZP:0011566	cytoplasm unfertilized egg opaque, abnormal
ZP:0011567	egg chorion unfertilized egg elevation, abnormal
ZP:0011568	egg chorion fertilized egg elevation, abnormal
ZP:0011569	spinal cord lacks parts or has fewer parts of type oligodendrocyte, abnormal
ZP:0011570	spinal cord lacks all parts of type primary motor neuron, abnormal
ZP:0011571	JNK cascade decreased process quality, abnormal
ZP:0011572	convergent extension involved in neural plate elongation process quality, abnormal
ZP:0011573	mediolateral intercalation process quality, abnormal
ZP:0011574	hypoblast process quality convergent extension, abnormal
ZP:0011575	caudal fin folded, abnormal
ZP:0011576	hindbrain increased process quality cell death, abnormal
ZP:0011577	intersegmental vein increased amount, abnormal
ZP:0011578	intersegmental artery decreased amount, abnormal
ZP:0011579	post-vent region absent blood circulation, abnormal
ZP:0011580	caudal vein plexus increased size, abnormal
ZP:0011581	post-vent vasculature malformed, abnormal
ZP:0011582	mandibular arch skeleton flattened, abnormal
ZP:0011583	memory decreased process quality, abnormal
ZP:0011584	intersegmental vein arrested, abnormal
ZP:0011585	intersegmental vein shortened, abnormal
ZP:0011586	intersegmental vein lacks parts or has fewer parts of type endothelial cell, abnormal
ZP:0011587	intersegmental vein delayed sprouting angiogenesis, abnormal
ZP:0011588	intersegmental vein disrupted sprouting angiogenesis, abnormal
ZP:0011589	intersegmental vein disrupted blood circulation, abnormal
ZP:0011590	intersegmental vein decreased occurrence cell population proliferation, abnormal
ZP:0011591	motor neuron morphology, abnormal
ZP:0011592	motor neuron broken, abnormal
ZP:0011593	germ cell migration premature, abnormal
ZP:0011594	establishment of mitotic spindle orientation process quality, abnormal
ZP:0011595	cilium mesoderm aplastic, abnormal
ZP:0011596	neural plate process quality establishment of mitotic spindle orientation, abnormal
ZP:0011597	pronephros lacks parts or has fewer parts of type multi-ciliated epithelial cell cilium multi-ciliated epithelial cell, abnormal
ZP:0011598	neural tube lacks all parts of type axoneme neural tube, abnormal
ZP:0011599	xanthophore differentiation delayed, abnormal
ZP:0011600	melanophore stripe malformed, abnormal
ZP:0011601	midbrain hindbrain boundary increased angle to basal side epithelium brain, abnormal
ZP:0011602	cell midbrain hindbrain boundary increased length, abnormal
ZP:0011603	neuroepithelial cell decreased accumulation actin filament apical region midbrain hindbrain boundary, abnormal
ZP:0011604	ceratohyal cartilage shape, abnormal
ZP:0011605	retina disrupted cell population proliferation, abnormal
ZP:0011606	pectoral fin shortened, abnormal
ZP:0011607	optic fissure unfused from anatomical margin anatomical margin optic fissure, abnormal
ZP:0011608	exonucleolytic trimming to generate mature 3'-end of 5.8S rRNA from tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA) disrupted, abnormal
ZP:0011609	fourth ventricle increased volume, abnormal
ZP:0011610	integument discolored, abnormal
ZP:0011611	large ribosomal subunit whole organism decreased amount, abnormal
ZP:0011612	cytosolic ribosome whole organism decreased amount, abnormal
ZP:0011613	forebrain ventricle increased volume, abnormal
ZP:0011614	posterior chamber swim bladder uninflated, abnormal
ZP:0011615	gut has fewer parts of type enteric neuron, abnormal
ZP:0011616	optic tectum increased distance optic tectum, abnormal
ZP:0011617	blood island has fewer parts of type neutrophil, abnormal
ZP:0011618	thigmotaxis decreased strength, abnormal
ZP:0011619	acetylcholine-gated channel complex skeletal muscle cell position, abnormal
ZP:0011620	slow muscle cell decreased magnitude neuromuscular synaptic transmission, abnormal
ZP:0011621	acetylcholine-gated channel complex fast muscle cell non-functional, abnormal
ZP:0011622	fast muscle cell arrested neuromuscular synaptic transmission, abnormal
ZP:0011623	vesicle localization process quality, abnormal
ZP:0011624	eye decreased area, abnormal
ZP:0011626	cell trunk apoptotic, abnormal
ZP:0011627	pigment cell decreased perimeter, abnormal
ZP:0011628	cell projection pigment cell increased amount, abnormal
ZP:0011629	vesicle neuron decreased speed, abnormal
ZP:0011630	renal tubule dilated, abnormal
ZP:0011631	renal glomerulus disorganized, abnormal
ZP:0011632	renal glomerulus distended, abnormal
ZP:0011633	photoreceptor outer segment photoreceptor cell absent, abnormal
ZP:0011635	kidney development process quality, abnormal
ZP:0011636	photoreceptor inner segment retinal cone cell physical object quality, abnormal
ZP:0011637	retinal cone cell has extra parts of type photoreceptor inner segment cytoplasmic vesicle retinal cone cell, abnormal
ZP:0011638	Golgi apparatus retinal cone cell morphology, abnormal
ZP:0011639	Golgi apparatus retinal cone cell disorganized, abnormal
ZP:0011640	Golgi apparatus retinal cone cell broken, abnormal
ZP:0011641	retinal cone cell process quality autophagy, abnormal
ZP:0011642	retinal cone cell process quality lysosome organization, abnormal
ZP:0011643	retinal cone cell process quality endosomal transport, abnormal
ZP:0011644	retinal cone cell decreased process quality maintenance of Golgi location, abnormal
ZP:0011645	ribosomal protein S6 kinase activity increased occurrence, abnormal
ZP:0011646	protein kinase B signaling decreased occurrence, abnormal
ZP:0011647	ventral spinal cord development process quality, abnormal
ZP:0011648	ventral region spinal cord poorly differentiated, abnormal
ZP:0011649	spinal cord decreased process quality smoothened signaling pathway, abnormal
ZP:0011650	neural tube decreased process quality smoothened signaling pathway, abnormal
ZP:0011651	epithelium pronephric duct morphology, abnormal
ZP:0011652	ventral mesoderm increased occurrence cell population proliferation, abnormal
ZP:0011653	eye photoreceptor cell differentiation delayed, abnormal
ZP:0011655	axon optic cup misrouted, abnormal
ZP:0011656	ciliary marginal zone disrupted cell population proliferation, abnormal
ZP:0011657	hemopoiesis delayed, abnormal
ZP:0011658	heart formation delayed, abnormal
ZP:0011659	caudal fin increased process quality apoptotic process, abnormal
ZP:0011660	pharynx increased process quality apoptotic process, abnormal
ZP:0011661	palatoquadrate arch hypoplastic, abnormal
ZP:0011662	ventral mandibular arch decreased process quality cell population proliferation, abnormal
ZP:0011663	axon posterior lateral line nerve mislocalised, abnormal
ZP:0011664	intestine has fewer parts of type enteroendocrine cell, abnormal
ZP:0011665	intestine increased process quality cell population proliferation, abnormal
ZP:0011666	ATP biosynthetic process disrupted, abnormal
ZP:0011667	mitochondrion myocardium disorganized, abnormal
ZP:0011668	mitochondrial crista myocardium decreased amount, abnormal
ZP:0011669	mitochondrion skeletal muscle structure, abnormal
ZP:0011670	mitochondrion skeletal muscle vacuolated, abnormal
ZP:0011671	mitochondrial crista skeletal muscle decreased amount, abnormal
ZP:0011672	medial rectus decreased thickness, abnormal
ZP:0011673	adductor mandibulae decreased thickness, abnormal
ZP:0011674	adductor mandibulae disrupted regulation of myofibril size, abnormal
ZP:0011675	muscle cell adductor mandibulae decreased size, abnormal
ZP:0011676	interhyoideus decreased thickness, abnormal
ZP:0011677	interhyoideus disrupted regulation of myofibril size, abnormal
ZP:0011678	muscle cell interhyoideus decreased size, abnormal
ZP:0011679	dorsal aorta disorganized, abnormal
ZP:0011680	radial glial cell hindbrain mislocalised, abnormal
ZP:0011681	cranial nerve II increased thickness, abnormal
ZP:0011682	posterior cardinal vein disorganized, abnormal
ZP:0011683	trunk decreased process quality pigmentation, abnormal
ZP:0011684	vascular sprouts intersegmental vessel mislocalised, abnormal
ZP:0011685	retinal ganglion cell increased accumulation axon ventral region retina, abnormal
ZP:0011686	whole organism lacks parts or has fewer parts of type hyosymplectic cartilage, abnormal
ZP:0011687	pharyngeal endoderm apoptotic, abnormal
ZP:0011688	pharyngeal arch 6 skeleton decreased size, abnormal
ZP:0011689	pharyngeal arch 5 skeleton decreased size, abnormal
ZP:0011690	pineal complex process quality circadian regulation of gene expression, abnormal
ZP:0011691	iridophore differentiation decreased occurrence, abnormal
ZP:0011692	eye has fewer parts of type iridophore, abnormal
ZP:0011693	caudal fin has fewer parts of type iridophore, abnormal
ZP:0011694	trunk lacks parts or has fewer parts of type melanophore stripe, abnormal
ZP:0011695	trunk has fewer parts of type melanophore stripe, abnormal
ZP:0011696	trunk lacks all parts of type dermis iridophore, abnormal
ZP:0011697	anal fin has fewer parts of type iridophore, abnormal
ZP:0011698	melanocyte increased process quality cell death, abnormal
ZP:0011699	cell midbrain hindbrain boundary increased width, abnormal
ZP:0011700	cell midbrain hindbrain boundary increased area, abnormal
ZP:0011701	inner ear receptor cell stereocilium organization decreased process quality, abnormal
ZP:0011702	stereocilium bundle hair cell direction, abnormal
ZP:0011703	cell projection hypoblast direction, abnormal
ZP:0011704	cell projection hypoblast physical object quality, abnormal
ZP:0011705	liver increased process quality apoptotic process, abnormal
ZP:0011706	forebrain flattened, abnormal
ZP:0011707	retina has fewer parts of type retinal ganglion cell, abnormal
ZP:0011708	neuromast displaced, abnormal
ZP:0011709	cranial nerve II has fewer parts of type axon retinal ganglion cell, abnormal
ZP:0011710	optic tectum has fewer parts of type neuron projection retinal ganglion cell, abnormal
ZP:0011711	head altered number of neuromast, abnormal
ZP:0011712	anterior region floor plate deformed, abnormal
ZP:0011713	hypothalamus deformed, abnormal
ZP:0011714	fourth ventricle deformed, abnormal
ZP:0011715	cranial nerve III absent, abnormal
ZP:0011716	cranial nerve II immature, abnormal
ZP:0011717	optic tectum mislocalised anteriorly, abnormal
ZP:0011718	cranial nerve IV absent, abnormal
ZP:0011719	dorsal thalamus deformed, abnormal
ZP:0011720	pectoral fin aplastic/hypoplastic, abnormal
ZP:0011721	pericardial cavity inflated, abnormal
ZP:0011722	retinal ganglion cell immature, abnormal
ZP:0011723	neuron projection retinal ganglion cell immature, abnormal
ZP:0011725	ectodermal placode development decreased process quality, abnormal
ZP:0011728	head lacks all parts of type glossopharyngeal ganglion, abnormal
ZP:0011729	head lacks all parts of type vagal ganglion 1, abnormal
ZP:0011730	head lacks all parts of type vagal ganglion 2, abnormal
ZP:0011731	head lacks all parts of type vagal ganglion 3, abnormal
ZP:0011733	facial placode poorly differentiated, abnormal
ZP:0011735	glossopharyngeal placode poorly differentiated, abnormal
ZP:0011736	glossopharyngeal placode decreased occurrence neurogenesis, abnormal
ZP:0011737	vagal placode 1 poorly differentiated, abnormal
ZP:0011738	vagal placode 1 decreased occurrence neurogenesis, abnormal
ZP:0011739	vagal placode 2 poorly differentiated, abnormal
ZP:0011740	vagal placode 2 decreased occurrence neurogenesis, abnormal
ZP:0011741	vagal placode 3 poorly differentiated, abnormal
ZP:0011742	vagal placode 3 decreased occurrence neurogenesis, abnormal
ZP:0011743	vagal placode 4 poorly differentiated, abnormal
ZP:0011745	neuroblast (sensu Vertebrata) vagal placode 4 mislocalised ventrally, abnormal
ZP:0011747	heart primordium decreased process quality cell population proliferation, abnormal
ZP:0011748	pharyngeal pouch absent, abnormal
ZP:0011749	pharyngeal pouch process quality pharyngeal system development, abnormal
ZP:0011750	blood island has fewer parts of type macrophage, abnormal
ZP:0011751	caudal fin has fewer parts of type axon caudal fin, abnormal
ZP:0011752	forebrain shape, abnormal
ZP:0011753	blood vessel endothelial cell proliferation involved in sprouting angiogenesis increased occurrence, abnormal
ZP:0011754	angiogenic sprout intersegmental vessel increased amount, abnormal
ZP:0011755	angiogenic sprout mislocalised, abnormal
ZP:0011756	bulbus arteriosus development process quality, abnormal
ZP:0011757	atrium morphology, abnormal
ZP:0011758	whole organism lacks parts or has fewer parts of type portion of tissue, abnormal
ZP:0011759	melanocyte process quality neural crest cell migration, abnormal
ZP:0011760	myelination decreased process quality, abnormal
ZP:0011762	photoreceptor cell pineal complex increased amount, abnormal
ZP:0011763	parapineal organ process quality epithalamus development, abnormal
ZP:0011764	parapineal organ process quality determination of left/right asymmetry in diencephalon, abnormal
ZP:0011766	pronephric duct branched, abnormal
ZP:0011767	pronephric duct undulate, abnormal
ZP:0011768	pronephric duct in contact with pronephric duct, abnormal
ZP:0011769	habenula decreased process quality cytoskeleton organization, abnormal
ZP:0011770	filamentous actin habenula disorganized, abnormal
ZP:0011775	tooth mineralization decreased process quality, abnormal
ZP:0011776	opercle decreased area bone mineralization, abnormal
ZP:0011777	tooth 4V absent tooth mineralization, abnormal
ZP:0011778	tooth 4V disrupted tooth mineralization, abnormal
ZP:0011779	ceratobranchial cartilage absent ossification, abnormal
ZP:0011780	ceratobranchial cartilage disrupted ossification, abnormal
ZP:0011781	dental epithelium lacks parts or has fewer parts of type tooth placode, abnormal
ZP:0011784	trunk neural crest cell migration decreased process quality, abnormal
ZP:0011785	swim bladder dysplastic, abnormal
ZP:0011786	posterior region whole organism curved, abnormal
ZP:0011787	cranial neural crest condensed, abnormal
ZP:0011788	cranial neural crest cell broadly articulated with cranial neural crest cell, abnormal
ZP:0011789	trunk neural crest cell shape, abnormal
ZP:0011790	trunk neural crest cell disorganized, abnormal
ZP:0011791	trunk neural crest cell broadly articulated with trunk neural crest cell, abnormal
ZP:0011792	trunk neural crest cell disrupted contact inhibition, abnormal
ZP:0011793	oligodendrocyte loose, abnormal
ZP:0011794	cardiac muscle cell has fewer parts of type cell projection cardiac muscle cell, abnormal
ZP:0011795	liver neoplastic, spontaneous, abnormal
ZP:0011796	adenoma liver present, abnormal
ZP:0011797	intestine neoplastic, spontaneous, abnormal
ZP:0011798	adenoma intestine present, abnormal
ZP:0011799	adenomatous polyp intestine present, abnormal
ZP:0011800	posterior lateral line lacks all parts of type myelinating Schwann cell, abnormal
ZP:0011801	posterior lateral line arrested myelination in peripheral nervous system, abnormal
ZP:0011802	thoracic duct agenesis, abnormal
ZP:0011803	cell notochord malformed, abnormal
ZP:0011804	DEL increased thickness, abnormal
ZP:0011805	skeletal muscle disorganized, abnormal
ZP:0011806	Notch signaling pathway decreased occurrence, abnormal
ZP:0011807	presumptive neural retina molecular quality, abnormal
ZP:0011808	pigment cell mislocalised, abnormal
ZP:0011809	anal fin has fewer parts of type melanocyte, abnormal
ZP:0011810	melanophore stripe decreased pigmentation, abnormal
ZP:0011811	cholesterol homeostasis process quality, abnormal
ZP:0011812	posterior cardinal vein fatty, abnormal
ZP:0011813	vascular endothelium posterior cardinal vein increased permeability, abnormal
ZP:0011814	posterior region notochord malformed, abnormal
ZP:0011815	atrium decreased thickness, abnormal
ZP:0011816	myotome condensed, abnormal
ZP:0011817	myotome deformed, abnormal
ZP:0011818	presumptive atrium heart tube elongated, abnormal
ZP:0011819	ventricular myocardium disorganized, abnormal
ZP:0011820	skeletal muscle structure, cavities, abnormal
ZP:0011821	endocytosis decreased process quality, abnormal
ZP:0011822	nodal signaling pathway decreased process quality, abnormal
ZP:0011823	shield absent, abnormal
ZP:0011824	secondary lysosome EVL increased amount, abnormal
ZP:0011826	blastoderm separated from yolk, abnormal
ZP:0011827	cardiac ventricle has extra parts of type cell, abnormal
ZP:0011828	atrium has extra parts of type cell, abnormal
ZP:0011829	brain lacks parts or has fewer parts of type ventricular system, abnormal
ZP:0011830	primary motor neuron brain spatial pattern, abnormal
ZP:0011831	primary motor neuron brain decreased amount, abnormal
ZP:0011832	spinal cord has fewer parts of type primary motor neuron, abnormal
ZP:0011833	primary motor neuron spinal cord spatial pattern, abnormal
ZP:0011834	head increased occurrence cell death, abnormal
ZP:0011835	trunk increased occurrence apoptotic process, abnormal
ZP:0011836	primary motor neuron irregular spatial pattern, abnormal
ZP:0011837	posterior cardinal vein lacks parts or has fewer parts of type lymphangiogenic sprout, abnormal
ZP:0011838	lymphatic system cranial vasculature decreased functionality, abnormal
ZP:0011839	intestine decreased process quality lymphangiogenesis, abnormal
ZP:0011840	lymph vasculature absent, abnormal
ZP:0011841	facial lymphatic vessel decreased process quality lymphangiogenesis, abnormal
ZP:0011842	endothelial cell lymph vessel endothelium decreased amount, abnormal
ZP:0011843	lymphangioblast lymphangioblast cord decreased amount, abnormal
ZP:0011844	lipoprotein biosynthetic process disrupted, abnormal
ZP:0011845	MAP kinase kinase activity disrupted, abnormal
ZP:0011846	dorsal aorta development disrupted, abnormal
ZP:0011847	cranial blood vessel morphology, abnormal
ZP:0011848	oligodendrocyte development process quality, abnormal
ZP:0011849	central nervous system myelination decreased process quality, abnormal
ZP:0011850	oligodendrocyte hindbrain poorly differentiated, abnormal
ZP:0011852	spinal cord has fewer parts of type oligodendrocyte spinal cord, abnormal
ZP:0011853	oligodendrocyte spinal cord mislocalised dorsally, abnormal
ZP:0011854	oligodendrocyte spinal cord poorly differentiated, abnormal
ZP:0011855	spinal cord dorsal to oligodendrocyte dorsal longitudinal fasciculus, abnormal
ZP:0011856	spinal cord far from oligodendrocyte dorsal longitudinal fasciculus, abnormal
ZP:0011857	dorsal longitudinal fasciculus decreased process quality axon ensheathment in central nervous system, abnormal
ZP:0011858	oligodendrocyte mislocalised dorsally, abnormal
ZP:0011859	axon trigeminal ganglion decreased branchiness, abnormal
ZP:0011860	trigeminal ganglion decreased occurrence collateral sprouting, abnormal
ZP:0011861	early endosome Rohon-Beard neuron mislocalised, abnormal
ZP:0011862	Rohon-Beard neuron decreased occurrence anterograde axonal transport, abnormal
ZP:0011863	growth cone Rohon-Beard neuron decreased volume, abnormal
ZP:0011864	growth cone Rohon-Beard neuron decreased branchiness, abnormal
ZP:0011865	Rohon-Beard neuron decreased occurrence collateral sprouting, abnormal
ZP:0011866	Rohon-Beard neuron increased rate axon extension, abnormal
ZP:0011867	Rohon-Beard neuron decreased occurrence retrograde transport, endosome to plasma membrane, abnormal
ZP:0011869	lens detached from retina, abnormal
ZP:0011870	retinal neural layer malformed, abnormal
ZP:0011871	ciliated cell pronephric duct irregular density, abnormal
ZP:0011872	cloaca cystic, abnormal
ZP:0011873	trunk neural crest cell migration delayed, abnormal
ZP:0011874	neural crest cell migration involved in autonomic nervous system development disrupted, abnormal
ZP:0011875	retina has fewer parts of type cell, abnormal
ZP:0011876	retina process quality mitotic cell cycle, abnormal
ZP:0011877	retina decreased process quality apoptotic process, abnormal
ZP:0011878	retina decreased process quality exit from mitosis, abnormal
ZP:0011879	vagal neural crest decreased size, abnormal
ZP:0011880	cranial neural crest decreased size, abnormal
ZP:0011881	enteric neuron decreased length, abnormal
ZP:0011882	enteric neuron mislocalised, abnormal
ZP:0011883	slow muscle cell detached from vertical myoseptum, abnormal
ZP:0011884	iridophore eye morphology, abnormal
ZP:0011885	melanophore stripe trunk decreased amount, abnormal
ZP:0011886	melanophore stripe distributed, abnormal
ZP:0011887	optic nerve development decreased process quality, abnormal
ZP:0011888	embryonic camera-type eye development decreased process quality, abnormal
ZP:0011889	cranial nerve II decreased volume, abnormal
ZP:0011890	fin increased length, abnormal
ZP:0011891	caudal fin asymmetrical, abnormal
ZP:0011892	caudal fin drooping, abnormal
ZP:0011893	lepidotrichium increased branchiness, abnormal
ZP:0011894	lepidotrichium segment length, abnormal
ZP:0011895	lepidotrichium segment increased amount, abnormal
ZP:0011896	lepidotrichium segment increased variability of size, abnormal
ZP:0011897	blood increased process quality apoptotic process, abnormal
ZP:0011898	mitochondrion whole organism morphology, abnormal
ZP:0011899	Golgi apparatus whole organism morphology, abnormal
ZP:0011900	whole organism increased occurrence autophagy, abnormal
ZP:0011901	nucleate erythrocyte has extra parts of type autophagosome nucleate erythrocyte, abnormal
ZP:0011902	nucleate erythrocyte has extra parts of type autolysosome nucleate erythrocyte, abnormal
ZP:0011903	nucleate erythrocyte increased occurrence autophagy, abnormal
ZP:0011904	muscle increased distance muscle cell, abnormal
ZP:0011905	muscle cell skeletal muscle loose, abnormal
ZP:0011906	skeletal muscle cell undulate, abnormal
ZP:0011907	fast muscle cell decreased width, abnormal
ZP:0011908	blood circulation decreased speed, abnormal
ZP:0011909	heart disrupted calcium-mediated signaling, abnormal
ZP:0011910	endocardial cushion lacks parts or has fewer parts of type cardiac muscle cell, abnormal
ZP:0011911	cell whole organism decreased amount, abnormal
ZP:0011912	brain agenesis, abnormal
ZP:0011913	liver arrested cell cycle, abnormal
ZP:0011914	inner ear increased process quality cell death, abnormal
ZP:0011915	mandibular arch skeleton increased process quality cell death, abnormal
ZP:0011916	nucleus hepatocyte increased size, abnormal
ZP:0011917	hepatocyte decreased process quality DNA methylation, abnormal
ZP:0011919	pronephric tubule decreased process quality ciliary basal body organization, abnormal
ZP:0011920	ciliary basal body pronephric tubule mislocalised, abnormal
ZP:0011921	pronephric tubule separated from ciliary basal body apical plasma membrane pronephric tubule, abnormal
ZP:0011922	ceratohyal cartilage misaligned with ceratohyal cartilage, abnormal
ZP:0011923	pharyngeal arch cartilage misaligned with pharyngeal arch cartilage, abnormal
ZP:0011924	skeletal muscle cell increased process quality apoptotic process, abnormal
ZP:0011925	cleavage in ITS2 between 5.8S rRNA and LSU-rRNA of tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA) disrupted, abnormal
ZP:0011926	nuclear pore retinal inner nuclear layer malformed, abnormal
ZP:0011927	endoplasmic reticulum retinal inner nuclear layer morphology, abnormal
ZP:0011928	nuclear pore liver malformed, abnormal
ZP:0011929	liver decreased process quality poly(A)+ mRNA export from nucleus, abnormal
ZP:0011930	pancreas decreased process quality poly(A)+ mRNA export from nucleus, abnormal
ZP:0011931	retinal pigmented epithelium distended, abnormal
ZP:0011932	nuclear pore retina malformed, abnormal
ZP:0011933	retina increased process quality apoptotic process, abnormal
ZP:0011934	retina decreased process quality poly(A)+ mRNA export from nucleus, abnormal
ZP:0011935	nuclear pore intestine malformed, abnormal
ZP:0011936	intestine decreased process quality poly(A)+ mRNA export from nucleus, abnormal
ZP:0011937	nuclear pore retinal outer nuclear layer malformed, abnormal
ZP:0011938	endoplasmic reticulum retinal outer nuclear layer morphology, abnormal
ZP:0011939	nuclear pore retinal ganglion cell malformed, abnormal
ZP:0011940	endoplasmic reticulum retinal ganglion cell morphology, abnormal
ZP:0011941	hypothalamus has extra parts of type posterior side dopaminergic neuron, abnormal
ZP:0011942	lens shape, abnormal
ZP:0011943	atrial cardiac muscle cell action potential increased duration, abnormal
ZP:0011944	atrioventricular ring aplastic, abnormal
ZP:0011945	blood accumulation cardiac ventricle, abnormal
ZP:0011946	heart vasculature non-functional, abnormal
ZP:0011947	vasculature malformed, abnormal
ZP:0011948	posterior lateral line molecular quality, abnormal
ZP:0011949	posterior side yolk decreased size, abnormal
ZP:0011950	semicircular canal absent, abnormal
ZP:0011951	hindbrain increased occurrence cell proliferation in hindbrain ventricular zone, abnormal
ZP:0011952	whole organism viable, abnormal
ZP:0011953	mRNA processing process quality, abnormal
ZP:0011954	head muscle malformed, abnormal
ZP:0011955	skeletal muscle cell loose, abnormal
ZP:0011956	endothelial cell increased rate cell population proliferation, abnormal
ZP:0011957	Notch signaling pathway increased occurrence, abnormal
ZP:0011958	neurogenesis decreased occurrence, abnormal
ZP:0011959	negative regulation of neurogenesis increased occurrence, abnormal
ZP:0011960	neural crest cell migration involved in heart formation process quality, abnormal
ZP:0011961	common cardinal vein decreased process quality blood circulation, abnormal
ZP:0011962	slow muscle cell somite disorganized, abnormal
ZP:0011963	fast muscle cell somite decreased amount, abnormal
ZP:0011964	posterior lateral line nerve misrouted, abnormal
ZP:0011965	muscle fin musculature hypoplastic, abnormal
ZP:0011966	muscle trunk musculature hypoplastic, abnormal
ZP:0011967	fast muscle cell myotome decreased amount, abnormal
ZP:0011968	muscle hypaxial myotome region hypoplastic, abnormal
ZP:0011969	muscle hypaxial myotome region malformed, abnormal
ZP:0011970	myoseptum hypoplastic, abnormal
ZP:0011971	whole organism lacks all parts of type horizontal myoseptum, abnormal
ZP:0011972	melanophore stripe trunk branched, abnormal
ZP:0011973	melanophore stripe trunk curved, abnormal
ZP:0011974	posterior lateral line primordium misrouted, abnormal
ZP:0011975	sternohyoid hypoplastic, abnormal
ZP:0011976	somite decreased diameter, abnormal
ZP:0011977	skeletal muscle cell irregular spatial pattern, abnormal
ZP:0011978	skeletal muscle cell decussate, abnormal
ZP:0011979	skeletal muscle cell misaligned with skeletal muscle cell, abnormal
ZP:0011980	macrophage aplastic, abnormal
ZP:0011981	protein localization to synapse disrupted, abnormal
ZP:0011982	synaptic vesicle recycling via endosome disrupted, abnormal
ZP:0011983	terminal bouton hair cell anterior macula increased amount, abnormal
ZP:0011984	terminal bouton neuromast hair cell increased amount, abnormal
ZP:0011985	kinocilium neuromast hair cell decreased length, abnormal
ZP:0011987	integument ball calcified, abnormal
ZP:0011988	eye calcified, abnormal
ZP:0011989	heart calcified, abnormal
ZP:0011990	notochord calcified, abnormal
ZP:0011991	notochord severe intensity bone mineralization, abnormal
ZP:0011992	bulbus arteriosus calcified, abnormal
ZP:0011993	cleithrum calcified, abnormal
ZP:0011994	pectoral fin cartilage calcified, abnormal
ZP:0011995	osteoclast integument mislocalised, abnormal
ZP:0011996	hemal arch fused with hemal arch, abnormal
ZP:0011997	cranium calcified, abnormal
ZP:0011998	osteoclast cranium mislocalised, abnormal
ZP:0011999	neural arch fused with neural arch, abnormal
ZP:0012001	neural tube calcified, abnormal
ZP:0012002	vertebra increased occurrence bone mineralization, abnormal
ZP:0012003	vertebra increased occurrence bone resorption, abnormal
ZP:0012004	osteoclast vertebra mislocalised, abnormal
ZP:0012005	ventricular system calcified, abnormal
ZP:0012006	ceratohyal cartilage increased occurrence bone mineralization, abnormal
ZP:0012007	ceratohyal cartilage premature perichondral ossification, abnormal
ZP:0012008	bone tissue ceratohyal cartilage mislocalised, abnormal
ZP:0012009	ethmoid cartilage calcified, abnormal
ZP:0012010	notochord outer sheath cell mineralized, abnormal
ZP:0012011	notochord outer sheath cell increased occurrence bone mineralization, abnormal
ZP:0012012	skeletal muscle cell accumulation mitochondrion skeletal muscle cell, abnormal
ZP:0012013	Z disc skeletal muscle cell morphology, abnormal
ZP:0012014	skeletal muscle myofibril skeletal muscle cell disorganized, abnormal
ZP:0012015	skeletal muscle myofibril skeletal muscle cell broken, abnormal
ZP:0012016	autophagosome slow muscle cell increased amount, abnormal
ZP:0012017	intersegmental vessel has extra parts of type filopodium intersegmental vessel, abnormal
ZP:0012018	intersegmental vessel lacks parts or has fewer parts of type dorsal region cell junction endothelial cell, abnormal
ZP:0012019	cell junction intersegmental vessel morphology, abnormal
ZP:0012020	intersegmental vessel dissociated from endothelial tip cell vascular sprouts intersegmental vessel, abnormal
ZP:0012021	pronephros process quality cilium movement, abnormal
ZP:0012022	motile cilium pronephros paralysed, abnormal
ZP:0012023	motile cilium pronephros decreased coordination, abnormal
ZP:0012024	whole organism lacks all parts of type ventral fin fold, abnormal
ZP:0012025	anterior-posterior axis whole organism undulate, abnormal
ZP:0012026	cloaca malformed, abnormal
ZP:0012027	whole organism hydrocephalic, abnormal
ZP:0012028	thoracic duct malformed, abnormal
ZP:0012029	facial nerve motor nucleus accumulation rhombomere 4, abnormal
ZP:0012030	facial nerve motor nucleus arrested cell migration, abnormal
ZP:0012031	cell midbrain hindbrain boundary decreased length, abnormal
ZP:0012032	spinal cord has fewer parts of type radial glial cell ventricular zone, abnormal
ZP:0012033	glial cell (sensu Vertebrata) spinal cord mislocalised, abnormal
ZP:0012034	neuron spinal cord mislocalised, abnormal
ZP:0012035	neuroepithelial cell decreased accumulation actin filament basal region midbrain hindbrain boundary, abnormal
ZP:0012036	mitochondrion organization process quality, abnormal
ZP:0012037	myelination of posterior lateral line nerve axons arrested, abnormal
ZP:0012038	myelination of posterior lateral line nerve axons disrupted, abnormal
ZP:0012039	heart lacks all parts of type trabecular layer, abnormal
ZP:0012040	myelin sheath posterior lateral line nerve physical object quality, abnormal
ZP:0012041	inner ear edematous, abnormal
ZP:0012042	mitochondrion myocardium elongated, abnormal
ZP:0012043	mitochondrial crista myocardium increased branchiness, abnormal
ZP:0012044	sprouting angiogenesis growth quality of occurrent, abnormal
ZP:0012045	lymphangioblast decreased amount, abnormal
ZP:0012046	dorsal-ventral axis whole organism absent, abnormal
ZP:0012047	post-vent region bifurcated, abnormal
ZP:0012048	bulbus arteriosus formation process quality, abnormal
ZP:0012049	bulbus arteriosus elongated, abnormal
ZP:0012050	bulbus arteriosus has extra parts of type cardiac muscle cell, abnormal
ZP:0012051	thigmotaxis increased duration, abnormal
ZP:0012052	thigmotaxis increased magnitude, abnormal
ZP:0012053	ventral spinal cord interneuron specification decreased process quality, abnormal
ZP:0012054	hindbrain has fewer parts of type oligodendrocyte, abnormal
ZP:0012055	hindbrain has fewer parts of type glioblast (sensu Vertebrata), abnormal
ZP:0012056	spinal cord lacks all parts of type CiA, abnormal
ZP:0012057	abducens motor nucleus has fewer parts of type motor neuron abducens motor nucleus, abnormal
ZP:0012058	hindbrain interneuron process quality neuron fate specification, abnormal
ZP:0012059	prolactin secreting cell development decreased process quality, abnormal
ZP:0012060	adenohypophysis has extra parts of type follicle stimulating hormone secreting cell, abnormal
ZP:0012061	adenohypophysis has fewer parts of type prolactin secreting cell, abnormal
ZP:0012062	adenohypophysis has fewer parts of type adrenocorticotropic hormone secreting cell, abnormal
ZP:0012063	adenohypophysis increased occurrence apoptotic process, abnormal
ZP:0012064	adenohypophysis decreased occurrence corticotropin hormone secreting cell differentiation, abnormal
ZP:0012065	prolactin secreting cell rostral pars anterior dispersed, abnormal
ZP:0012066	ossification process quality, abnormal
ZP:0012067	adipose tissue development premature, abnormal
ZP:0012069	levator arcus palatini increased width, abnormal
ZP:0012070	levator arcus palatini shortened, abnormal
ZP:0012071	adductor operculi increased width, abnormal
ZP:0012072	adductor operculi shortened, abnormal
ZP:0012073	dilatator operculi increased width, abnormal
ZP:0012074	dilatator operculi shortened, abnormal
ZP:0012075	adductor hyohyoid increased width, abnormal
ZP:0012076	adductor hyohyoid shortened, abnormal
ZP:0012077	sternohyoid increased width, abnormal
ZP:0012078	sternohyoid shortened, abnormal
ZP:0012079	head muscle increased width, abnormal
ZP:0012080	head muscle shortened, abnormal
ZP:0012081	ventral intermandibularis anterior increased width, abnormal
ZP:0012082	ventral intermandibularis anterior shortened, abnormal
ZP:0012083	ventral intermandibularis posterior increased width, abnormal
ZP:0012084	ventral intermandibularis posterior shortened, abnormal
ZP:0012085	adductor mandibulae increased width, abnormal
ZP:0012086	adductor mandibulae shortened, abnormal
ZP:0012087	interhyoideus increased width, abnormal
ZP:0012088	interhyoideus shortened, abnormal
ZP:0012089	hyohyoideus absent, abnormal
ZP:0012091	glial cell absent, abnormal
ZP:0012092	lens increased diameter, abnormal
ZP:0012093	sodium ion homeostasis disrupted, abnormal
ZP:0012095	autophagy decreased process quality, abnormal
ZP:0012096	myosin filament organization disrupted, abnormal
ZP:0012097	myoseptum morphology, abnormal
ZP:0012098	myoseptum unstructured, abnormal
ZP:0012099	mitochondrion muscle morphology, abnormal
ZP:0012100	muscle separated from striated muscle thin filament myosin filament muscle, abnormal
ZP:0012101	sarcoplasmic reticulum muscle dilated, abnormal
ZP:0012102	muscle cell degenerate, abnormal
ZP:0012103	nucleus muscle cell morphology, abnormal
ZP:0012104	nucleus muscle cell increased amount, abnormal
ZP:0012105	fast muscle cell undulate, abnormal
ZP:0012106	magnesium ion homeostasis disrupted, abnormal
ZP:0012107	musculoskeletal movement, spinal reflex action increased occurrence, abnormal
ZP:0012108	interneuromast cell increased process quality Notch signaling pathway, abnormal
ZP:0012109	interneuromast cell increased process quality fibroblast growth factor receptor signaling pathway, abnormal
ZP:0012110	interneuromast cell increased process quality canonical Wnt signaling pathway, abnormal
ZP:0012111	DNA methylation disrupted, abnormal
ZP:0012112	DNA methylation on cytosine within a CG sequence disrupted, abnormal
ZP:0012113	lipid homeostasis disrupted, abnormal
ZP:0012114	Meckel's cartilage circular, abnormal
ZP:0012115	ceratohyal cartilage curved, abnormal
ZP:0012116	telencephalon physical object quality, abnormal
ZP:0012117	cardiac muscle cell action potential increased duration, abnormal
ZP:0012118	blood island has extra parts of type hematopoietic stem cell, abnormal
ZP:0012119	keratinocyte integument decreased amount, abnormal
ZP:0012120	mucus secreting cell integument decreased amount, abnormal
ZP:0012121	melanophore stripe caudal fin spotted, abnormal
ZP:0012122	melanophore stripe caudal fin absent, abnormal
ZP:0012123	melanocyte caudal fin decreased amount, abnormal
ZP:0012124	anal fin has fewer parts of type xanthophore, abnormal
ZP:0012125	melanophore stripe anal fin spotted, abnormal
ZP:0012126	melanophore stripe anal fin absent, abnormal
ZP:0012127	melanophore stripe anal fin undulate, abnormal
ZP:0012128	melanocyte anal fin decreased amount, abnormal
ZP:0012129	melanophore stripe increased width, abnormal
ZP:0012130	melanophore stripe undulate, abnormal
ZP:0012131	melanophore stripe disheveled, abnormal
ZP:0012132	melanocyte distributed, abnormal
ZP:0012133	iridophore dispersed, abnormal
ZP:0012134	otic vesicle decreased length, abnormal
ZP:0012135	kinocilium otic vesicle increased amount, abnormal
ZP:0012136	kinocilium posterior crista deformed, abnormal
ZP:0012137	kinocilium posterior crista decreased amount, abnormal
ZP:0012138	kinocilium hair cell anterior macula deformed, abnormal
ZP:0012139	kinocilium hair cell anterior macula decreased amount, abnormal
ZP:0012140	hindbrain lacks all parts of type radial glial cell, abnormal
ZP:0012141	developmental growth decreased process quality, abnormal
ZP:0012142	opercle decreased process quality bone mineralization, abnormal
ZP:0012143	branchiostegal ray decreased process quality bone mineralization, abnormal
ZP:0012144	ceratohyal bone decreased process quality bone mineralization, abnormal
ZP:0012145	quadrate decreased process quality bone mineralization, abnormal
ZP:0012146	hyomandibula decreased process quality bone mineralization, abnormal
ZP:0012147	vertebra decreased process quality bone mineralization, abnormal
ZP:0012148	cranial vault decreased process quality bone mineralization, abnormal
ZP:0012149	determination of stomach left/right asymmetry disrupted, abnormal
ZP:0012150	transcriptional activation by promoter-enhancer looping decreased process quality, abnormal
ZP:0012151	hypothalamus lacks parts or has fewer parts of type dopaminergic neuron, abnormal
ZP:0012152	diencephalon lacks parts or has fewer parts of type dopaminergic neuron, abnormal
ZP:0012153	pectoral fin bud decreased process quality embryonic pectoral fin morphogenesis, abnormal
ZP:0012154	sympathetic nervous system lacks parts or has fewer parts of type sympathetic neuron, abnormal
ZP:0012155	dopaminergic neuron disrupted axon development, abnormal
ZP:0012156	cell junction diencephalon morphology, abnormal
ZP:0012157	cell diencephalon disorganized, abnormal
ZP:0012158	cell accumulation forebrain ventricle, abnormal
ZP:0012159	smoothened signaling pathway decreased process quality, abnormal
ZP:0012160	GABAergic neuron differentiation disrupted, abnormal
ZP:0012161	hindbrain lacks all parts of type oligodendrocyte, abnormal
ZP:0012162	diencephalon decreased process quality neuron differentiation, abnormal
ZP:0012163	forebrain lacks all parts of type oligodendrocyte, abnormal
ZP:0012164	forebrain has fewer parts of type oligodendrocyte, abnormal
ZP:0012165	forebrain lacks all parts of type GABAergic neuron, abnormal
ZP:0012166	forebrain has fewer parts of type GABAergic neuron, abnormal
ZP:0012167	forebrain increased occurrence apoptotic process, abnormal
ZP:0012168	midbrain increased occurrence apoptotic process, abnormal
ZP:0012169	pectoral fin bud decreased depth, abnormal
ZP:0012170	ventral telencephalon decreased process quality neuron differentiation, abnormal
ZP:0012171	mesenchyme pectoral fin decreased occurrence cell population proliferation, abnormal
ZP:0012172	GABAergic neuron decreased amount, abnormal
ZP:0012173	microglial cell brain decreased amount, abnormal
ZP:0012174	macrophage brain decreased amount, abnormal
ZP:0012175	macrophage central nervous system decreased amount, abnormal
ZP:0012176	macrophage integument decreased amount, abnormal
ZP:0012177	integument lacks parts or has fewer parts of type macrophage cell projection macrophage, abnormal
ZP:0012178	anatomical region hemal arch decreased size, abnormal
ZP:0012179	macrophage head morphology, abnormal
ZP:0012180	neutrophil head increased amount, abnormal
ZP:0012181	vertebra morphology, abnormal
ZP:0012182	vertebra increased volume, abnormal
ZP:0012183	vertebra increased area, abnormal
ZP:0012184	blood vessel mislocalised, abnormal
ZP:0012185	macrophage has fewer parts of type cell projection macrophage, abnormal
ZP:0012186	hair cell saccule decreased amount, abnormal
ZP:0012187	skeletal muscle myofibril muscle disorganized, abnormal
ZP:0012188	myoseptum muscle disorganized, abnormal
ZP:0012189	whole organism lacks parts or has fewer parts of type pectoral fin bud, abnormal
ZP:0012190	NCC ionocyte head increased amount, abnormal
ZP:0012191	hemal arch hypoplastic, abnormal
ZP:0012192	rib hypoplastic, abnormal
ZP:0012193	basipterygium hypoplastic, abnormal
ZP:0012194	neural arch hypoplastic, abnormal
ZP:0012195	dorsal fin lepidotrichium absent, abnormal
ZP:0012196	anal fin lepidotrichium decreased amount, abnormal
ZP:0012197	caudal fin lepidotrichium decreased amount, abnormal
ZP:0012198	pectoral fin lepidotrichium aplastic, abnormal
ZP:0012199	pelvic fin lepidotrichium hypoplastic, abnormal
ZP:0012200	motile cilium Kupffer's vesicle decreased fluid flow, abnormal
ZP:0012201	musculoskeletal movement decreased process quality, abnormal
ZP:0012202	skeletal muscle paralysed, abnormal
ZP:0012203	striated muscle cell misaligned with striated muscle cell, abnormal
ZP:0012204	myofibril striated muscle cell disorganized, abnormal
ZP:0012205	striated muscle cell misaligned with Z disc Z disc striated muscle cell, abnormal
ZP:0012206	myofilament striated muscle cell disorganized, abnormal
ZP:0012207	striated muscle cell detached from myofilament myoseptum, abnormal
ZP:0012208	skeletal muscle cell detached from somite border, abnormal
ZP:0012209	retinal cone cell development decreased process quality, abnormal
ZP:0012210	melanocyte occurrence cellular pigment accumulation, abnormal
ZP:0012211	melanocyte decreased occurrence cellular response to light intensity, abnormal
ZP:0012212	retinal cone cell lacks all parts of type photoreceptor outer segment retinal cone cell, abnormal
ZP:0012213	eye far from eye, abnormal
ZP:0012214	cardiac muscle cell proliferation decreased rate, abnormal
ZP:0012215	pectoral fin development delayed, abnormal
ZP:0012216	pectoral fin immature, abnormal
ZP:0012217	liver decreased process quality cell population proliferation, abnormal
ZP:0012218	caudal fin decreased process quality cell population proliferation, abnormal
ZP:0012219	trunk decreased process quality cell population proliferation, abnormal
ZP:0012220	Meckel's cartilage disrupted cartilage development, abnormal
ZP:0012221	palatoquadrate cartilage disrupted cartilage development, abnormal
ZP:0012222	peripheral olfactory organ has fewer parts of type ciliated olfactory receptor neuron, abnormal
ZP:0012223	thoracic duct has fewer parts of type endothelial cell, abnormal
ZP:0012224	mitochondrial respiratory chain complex I whole organism decreased amount, abnormal
ZP:0012225	caudal vein plexus increased process quality apoptotic process, abnormal
ZP:0012227	precaudal vertebra curved, abnormal
ZP:0012228	caudal vertebra curved, abnormal
ZP:0012229	dorsal-ventral axis whole organism curved, abnormal
ZP:0012230	medial-lateral axis whole organism curved, abnormal
ZP:0012231	vertebra angle vertebra, abnormal
ZP:0012232	vertebral column curved, abnormal
ZP:0012233	dorsal-ventral axis whole organism shortened, abnormal
ZP:0012234	cilium neural tube disorganized, abnormal
ZP:0012235	pharyngeal arch decreased width, abnormal
ZP:0012236	dorsal aorta decreased thickness, abnormal
ZP:0012237	dorsal aorta lacks parts or has fewer parts of type endothelial cell, abnormal
ZP:0012241	ventral wall of dorsal aorta decreased process quality cell population proliferation, abnormal
ZP:0012242	vertical myoseptum decreased size, abnormal
ZP:0012243	vertical myoseptum disorganized, abnormal
ZP:0012244	post-vent region decreased width, abnormal
ZP:0012245	skeletal muscle cell elongated, abnormal
ZP:0012246	striated muscle myosin thick filament skeletal muscle cell disorganized, abnormal
ZP:0012247	skeletal muscle cell orientation myofibril skeletal muscle cell, abnormal
ZP:0012248	Z disc skeletal muscle cell structure, abnormal
ZP:0012249	M band skeletal muscle cell decreased amount, abnormal
ZP:0012250	photoreceptor cell absent, abnormal
ZP:0012251	cardiac muscle cell structure, abnormal
ZP:0012252	intercalated disc cardiac muscle cell absent, abnormal
ZP:0012253	caudal fin has fewer parts of type melanophore stripe, abnormal
ZP:0012254	melanophore stripe anal fin decreased width, abnormal
ZP:0012255	melanocyte confluent with xanthophore, abnormal
ZP:0012256	response to auditory stimulus process quality, abnormal
ZP:0012257	trunk neural crest cell migration process quality, abnormal
ZP:0012258	trunk neural crest cell elongated, abnormal
ZP:0012259	muscle tendon junction muscle morphology, abnormal
ZP:0012260	T-tubule muscle dilated, abnormal
ZP:0012261	mitochondrion muscle cell increased size, abnormal
ZP:0012262	mitochondrion muscle cell aggregated, abnormal
ZP:0012263	mitochondrial intermembrane space muscle cell dilated, abnormal
ZP:0012264	myofibril muscle cell kinked, abnormal
ZP:0012265	muscle cell separated from myofibril muscle tendon junction muscle cell, abnormal
ZP:0012266	muscle cell misaligned with myofibril myofibril muscle cell, abnormal
ZP:0012267	mitochondrial crista muscle cell decreased amount, abnormal
ZP:0012268	parachordal vessel malformed, abnormal
ZP:0012269	basement membrane renal glomerulus morphology, abnormal
ZP:0012270	endothelial cell renal glomerulus swollen, abnormal
ZP:0012271	thoracic duct has fewer parts of type endothelial cell lymphatic system, abnormal
ZP:0012272	neuromast development process quality, abnormal
ZP:0012273	posterior lateral line has fewer parts of type neuromast, abnormal
ZP:0012274	caudal fin lacks all parts of type neuromast, abnormal
ZP:0012275	trunk has fewer parts of type posterior region neuromast, abnormal
ZP:0012276	posterior lateral line primordium increased process quality cell death, abnormal
ZP:0012277	thyroxine 5-deiodinase activity decreased process quality, abnormal
ZP:0012281	hindbrain increased occurrence neurogenesis, abnormal
ZP:0012282	lateral region facial lymphatic vessel decreased length, abnormal
ZP:0012284	phototaxis disrupted, abnormal
ZP:0012285	response to mechanical stimulus decreased process quality, abnormal
ZP:0012286	axonal transport of mitochondrion decreased process quality, abnormal
ZP:0012287	axon posterior lateral line nerve decreased size, abnormal
ZP:0012288	axon posterior lateral line nerve degeneration, abnormal
ZP:0012289	posterior lateral line nerve has fewer parts of type axon mitochondrion posterior lateral line nerve, abnormal
ZP:0012290	caudal fin has fewer parts of type axon mitochondrion neuron, abnormal
ZP:0012291	mitochondrion neuron mobility, abnormal
ZP:0012292	otolith development process quality, abnormal
ZP:0012293	otic vesicle lacks parts or has fewer parts of type otolith, abnormal
ZP:0012294	neuron optic recess mislocalised, abnormal
ZP:0012295	hematopoietic stem cell intermediate cell mass of mesoderm decreased amount, abnormal
ZP:0012296	sternohyoid disorganized, abnormal
ZP:0012297	spinal cord increased process quality apoptotic process, abnormal
ZP:0012298	telencephalon hydrocephalic, abnormal
ZP:0012300	muscle contraction decreased force, abnormal
ZP:0012301	skeletal muscle thin filament assembly disrupted, abnormal
ZP:0012302	trunk musculature decreased functionality, abnormal
ZP:0012303	inclusion body muscle cell increased amount, abnormal
ZP:0012304	M band muscle cell morphology, abnormal
ZP:0012305	muscle cell increased distance skeletal muscle myofibril skeletal muscle myofibril muscle cell, abnormal
ZP:0012306	MAPK cascade disrupted, abnormal
ZP:0012309	intersegmental vessel trunk morphology, abnormal
ZP:0012311	trigeminal nerve morphogenesis decreased process quality, abnormal
ZP:0012312	axon trigeminal ganglion misrouted, abnormal
ZP:0012313	trigeminal sensory neuron decreased occurrence extracellular matrix disassembly, abnormal
ZP:0012314	trigeminal sensory neuron decreased process quality sensory neuron axon guidance, abnormal
ZP:0012315	blood island has extra parts of type neutrophil, abnormal
ZP:0012316	vasculature has fewer parts of type circulating cell neutrophil, abnormal
ZP:0012317	neuromast deposition process quality, abnormal
ZP:0012318	neural crest accumulation axis, abnormal
ZP:0012319	trunk lacks all parts of type posterior region neuromast, abnormal
ZP:0012320	blood cell accumulation bulbus arteriosus, abnormal
ZP:0012322	auditory receptor cell decreased functionality, abnormal
ZP:0012323	xanthophore differentiation premature, abnormal
ZP:0012324	barbel absent, abnormal
ZP:0012325	ventral mandibular arch hypertrophic, abnormal
ZP:0012326	xanthophore increased amount, abnormal
ZP:0012327	sleep process quality, abnormal
ZP:0012329	cerebellum vasculature development disrupted, abnormal
ZP:0012330	neuron cranial nerve V decreased amount, abnormal
ZP:0012331	Rohon-Beard neuron has fewer parts of type dendritic filopodium Rohon-Beard neuron, abnormal
ZP:0012332	neuron projection Rohon-Beard neuron malformed, abnormal
ZP:0012333	neuron projection Rohon-Beard neuron decreased branchiness, abnormal
ZP:0012334	Rohon-Beard neuron decreased process quality collateral sprouting, abnormal
ZP:0012335	startle response delayed, abnormal
ZP:0012336	sensory perception of sound disrupted, abnormal
ZP:0012337	sensory perception of mechanical stimulus disrupted, abnormal
ZP:0012338	posterior lateral line neuromast morphology, abnormal
ZP:0012339	posterior lateral line neuromast decreased functionality, abnormal
ZP:0012340	stereocilium posterior lateral line neuromast decreased amount, abnormal
ZP:0012341	kinocilium posterior lateral line neuromast decreased amount, abnormal
ZP:0012342	neuromuscular junction skeletal muscle decreased size, abnormal
ZP:0012343	neuromuscular junction skeletal muscle broken, abnormal
ZP:0012344	neuromuscular junction skeletal muscle decreased amount, abnormal
ZP:0012345	skeletal muscle cell decreased width, abnormal
ZP:0012346	skeletal muscle cell atrophied, abnormal
ZP:0012347	skeletal muscle myofibril skeletal muscle cell disoriented, abnormal
ZP:0012348	iridophore ridged, abnormal
ZP:0012349	neuron projection dorsal root ganglion morphology, abnormal
ZP:0012350	Rohon-Beard neuron process quality neuronal action potential, abnormal
ZP:0012351	CaP motoneuron process quality neuronal action potential, abnormal
ZP:0012352	neuron projection CaP motoneuron morphology, abnormal
ZP:0012353	neuron projection CaP motoneuron displaced, abnormal
ZP:0012354	CaP motoneuron process quality membrane repolarization, abnormal
ZP:0012355	caudal vein plexus structure, abnormal
ZP:0012356	trunk vasculature disrupted blood circulation, abnormal
ZP:0012357	axial blood vessel disrupted blood circulation, abnormal
ZP:0012358	spinal cord disrupted spinal cord oligodendrocyte cell fate specification, abnormal
ZP:0012359	spinal cord disrupted regulation of oligodendrocyte progenitor proliferation, abnormal
ZP:0012360	neuron spinal cord increased amount, abnormal
ZP:0012361	glioblast (sensu Vertebrata) increased occurrence cell division, abnormal
ZP:0012362	dorsal-ventral axis notochord increased size, abnormal
ZP:0012363	dorsal-ventral axis myotome increased size, abnormal
ZP:0012364	skeletal muscle myofibril skeletal muscle organization quality, abnormal
ZP:0012365	Z disc skeletal muscle cell spatial pattern, abnormal
ZP:0012366	trunk has fewer parts of type dermis iridophore, abnormal
ZP:0012367	melanophore stripe lacks parts or has fewer parts of type melanocyte, abnormal
ZP:0012368	esophagus malformed, abnormal
ZP:0012369	esophageal epithelium disorganized, abnormal
ZP:0012370	esophageal epithelium disrupted epithelial cell differentiation, abnormal
ZP:0012371	primary islet absent, abnormal
ZP:0012372	photoreceptor cell differentiation decreased process quality, abnormal
ZP:0012373	retinal ganglion cell layer has fewer parts of type retinal ganglion cell, abnormal
ZP:0012374	optic stalk shape, abnormal
ZP:0012375	optic stalk decreased size, abnormal
ZP:0012376	cranial nerve II physical object quality, abnormal
ZP:0012377	adenohypophysis formation decreased process quality, abnormal
ZP:0012378	hypothalamus has fewer parts of type posterior side dopaminergic neuron, abnormal
ZP:0012379	blood vasculature lacks all parts of type hypophyseal artery, abnormal
ZP:0012380	blood vasculature lacks all parts of type hypophyseal capillary, abnormal
ZP:0012381	neurohypophysis decreased occurrence vasculogenesis, abnormal
ZP:0012382	neurohypophysis decreased occurrence innervation, abnormal
ZP:0012383	adenohypophysis decreased object quality, abnormal
ZP:0012384	pharyngeal pouch decreased speed cell migration, abnormal
ZP:0012385	rhombomere 6 decreased size, abnormal
ZP:0012386	facial nerve motor nucleus decreased process quality motor neuron migration, abnormal
ZP:0012387	rhombomere 3 increased size, abnormal
ZP:0012388	amacrine cell differentiation decreased process quality, abnormal
ZP:0012389	camera-type eye photoreceptor cell differentiation delayed, abnormal
ZP:0012390	retinal inner nuclear layer physical object quality, abnormal
ZP:0012391	retinal inner nuclear layer poorly differentiated, abnormal
ZP:0012392	retinal inner nuclear layer has fewer parts of type horizontal cell retinal inner nuclear layer, abnormal
ZP:0012393	retinal inner plexiform layer malformed, abnormal
ZP:0012394	retinal inner plexiform layer has fewer parts of type dendrite retinal ganglion cell, abnormal
ZP:0012395	retinal outer nuclear layer poorly differentiated, abnormal
ZP:0012396	amacrine cell poorly differentiated, abnormal
ZP:0012397	retinal cone cell undifferentiated, abnormal
ZP:0012398	retinal rod cell undifferentiated, abnormal
ZP:0012399	Muller cell poorly differentiated, abnormal
ZP:0012400	retinal ganglion cell decreased occurrence dendrite morphogenesis, abnormal
ZP:0012401	retinal bipolar neuron poorly differentiated, abnormal
ZP:0012402	pharyngeal vasculature has fewer parts of type blood vessel endothelial cell, abnormal
ZP:0012403	pharyngeal vasculature decreased process quality vasculogenesis, abnormal
ZP:0012404	pharyngeal vasculature decreased process quality angioblast cell differentiation, abnormal
ZP:0012405	pharyngeal vasculature decreased occurrence blood vessel endothelial cell differentiation, abnormal
ZP:0012406	pharyngeal vasculature decreased process quality pharyngeal arch artery morphogenesis, abnormal
ZP:0012407	lymphangiogenic sprout facial lymphatic vessel aplastic, abnormal
ZP:0012408	pharynx increased amount, abnormal
ZP:0012409	pharynx increased width, abnormal
ZP:0012410	pharyngeal epithelium absent, abnormal
ZP:0012411	pharyngeal pouch increased speed cell migration, abnormal
ZP:0012413	spinal cord lacks parts or has fewer parts of type motor neuron, abnormal
ZP:0012414	retina has fewer parts of type blue sensitive photoreceptor cell, abnormal
ZP:0012415	retina process quality dorsal/ventral pattern formation, abnormal
ZP:0012416	optic tectum decreased process quality innervation, abnormal
ZP:0012417	neuromuscular junction motor neuron increased volume, abnormal
ZP:0012418	neuromuscular junction motor neuron physical object quality, abnormal
ZP:0012419	determination of left/right asymmetry in diencephalon decreased process quality, abnormal
ZP:0012420	lateral plate mesoderm decreased process quality determination of left/right asymmetry in lateral mesoderm, abnormal
ZP:0012421	lateral semicircular canal development disrupted, abnormal
ZP:0012422	anterior macula decreased distance posterior macula, abnormal
ZP:0012423	inner ear lacks all parts of type lateral crista, abnormal
ZP:0012424	inner ear lacks all parts of type lateral semicircular canal, abnormal
ZP:0012425	blood vessel morphology, abnormal
ZP:0012426	nodal signaling pathway involved in determination of left/right asymmetry disrupted, abnormal
ZP:0012427	convergent extension involved in nephron morphogenesis process quality, abnormal
ZP:0012428	habenula disrupted determination of left/right symmetry, abnormal
ZP:0012429	habenula process quality neurogenesis, abnormal
ZP:0012430	epithalamus disrupted determination of left/right symmetry, abnormal
ZP:0012431	trunk wholly dorsalized, abnormal
ZP:0012432	medial floor plate increased width, abnormal
ZP:0012433	melanocyte process quality developmental pigmentation, abnormal
ZP:0012434	neurogenesis decreased process quality, abnormal
ZP:0012435	interneuron increased amount, abnormal
ZP:0012436	atrium lacks all parts of type ventricular endocardium, abnormal
ZP:0012437	endocardium aggregated, abnormal
ZP:0012438	endocardium decreased anterior-posterior diameter, abnormal
ZP:0012439	cell-cell junction endocardium mislocalised, abnormal
ZP:0012440	endocardium decreased process quality cell-cell junction organization, abnormal
ZP:0012441	endocardium process quality cardiac muscle cell differentiation, abnormal
ZP:0012442	endothelial cell endocardium aggregated, abnormal
ZP:0012443	endothelial cell endocardium obtuse, abnormal
ZP:0012444	ventricular endocardium aggregated, abnormal
ZP:0012445	presumptive endocardium decreased process quality morphogenesis of an epithelial sheet, abnormal
ZP:0012446	ventral wall of dorsal aorta lacks all parts of type hematopoietic stem cell, abnormal
ZP:0012447	pronephric glomerulus morphogenesis arrested, abnormal
ZP:0012448	presumptive pronephric mesoderm malformed, abnormal
ZP:0012449	pronephric glomerulus poorly differentiated, abnormal
ZP:0012450	hindbrain decreased occurrence cell proliferation in hindbrain ventricular zone, abnormal
ZP:0012451	hindbrain premature neurogenesis, abnormal
ZP:0012452	spinal cord lacks all parts of type oligodendrocyte, abnormal
ZP:0012453	enteric nervous system development decreased process quality, abnormal
ZP:0012454	intestinal epithelial cell differentiation process quality, abnormal
ZP:0012455	swim bladder decreased volume, abnormal
ZP:0012456	posterior intestine decreased occurrence peristalsis, abnormal
ZP:0012457	enteric nervous system lacks all parts of type enteric neuron, abnormal
ZP:0012458	enteric nervous system has fewer parts of type enteric neuron, abnormal
ZP:0012459	intestinal epithelium lacks parts or has fewer parts of type goblet cell, abnormal
ZP:0012460	intestinal epithelium lacks parts or has fewer parts of type enteroendocrine cell, abnormal
ZP:0012461	intestinal epithelium process quality Notch signaling pathway, abnormal
ZP:0012462	enteroendocrine cell intestinal epithelium undifferentiated, abnormal
ZP:0012463	anterior region intestine lumen increased diameter, abnormal
ZP:0012464	rhombomere 6 has fewer parts of type cranial motor neuron, abnormal
ZP:0012465	rhombomere 7 has fewer parts of type cranial motor neuron, abnormal
ZP:0012466	rhombomere 4 has extra parts of type cranial motor neuron, abnormal
ZP:0012467	ventral aorta separated from bulbus arteriosus, abnormal
ZP:0012468	hypobranchial artery morphology, abnormal
ZP:0012469	hypobranchial artery dysplastic, abnormal
ZP:0012470	thyroid follicle position, abnormal
ZP:0012471	thyroid follicle mislocalised, abnormal
ZP:0012472	cell thyroid follicle decreased amount, abnormal
ZP:0012473	thyroid primordium morphology, abnormal
ZP:0012474	thyroid primordium distended, abnormal
ZP:0012475	aortic arch absent, abnormal
ZP:0012476	parachordal vessel incomplete structure, abnormal
ZP:0012477	neuron cell-cell adhesion disrupted, abnormal
ZP:0012478	glial cell projection trunk truncated, abnormal
ZP:0012479	glial cell projection trunk disorganized, abnormal
ZP:0012480	glial cell projection trunk kinked, abnormal
ZP:0012481	branchiomotor neuron decreased cellular motility, abnormal
ZP:0012482	branchiomotor neuron detached from medial longitudinal fasciculus, abnormal
ZP:0012483	branchiomotor neuron decreased velocity neuron migration, abnormal
ZP:0012484	neural plate morphogenesis process quality, abnormal
ZP:0012485	cardioblast migration to the midline involved in heart field formation process quality, abnormal
ZP:0012486	prechordal plate aplastic/hypoplastic, abnormal
ZP:0012487	neural keel malformed, abnormal
ZP:0012488	neural plate process quality cell motility, abnormal
ZP:0012489	anterior region notochord absent, abnormal
ZP:0012490	neural tube cellular spatiotemporal quality cell division, abnormal
ZP:0012491	pancreatic bud lacks all parts of type pancreatic B cell, abnormal
ZP:0012492	prechordal plate formation process quality, abnormal
ZP:0012493	prechordal plate process quality mesodermal cell migration, abnormal
ZP:0012494	thymus morphology, abnormal
ZP:0012495	thymus has fewer parts of type T cell, abnormal
ZP:0012496	thymus has extra parts of type fat cell, abnormal
ZP:0012497	thymic epithelium has fewer parts of type epithelial cell, abnormal
ZP:0012498	eye field cell fate commitment involved in camera-type eye formation disrupted, abnormal
ZP:0012499	cellular response to light stimulus disrupted, abnormal
ZP:0012500	cranial nerve II shape, abnormal
ZP:0012502	axis malformed, abnormal
ZP:0012503	neuromuscular junction trunk morphology, abnormal
ZP:0012504	cell proliferation in forebrain disrupted, abnormal
ZP:0012505	epithelial cell proliferation disrupted, abnormal
ZP:0012506	olfactory bulb morphology, abnormal
ZP:0012507	ciliated olfactory receptor neuron decreased amount, abnormal
ZP:0012508	microvillous olfactory receptor neuron decreased amount, abnormal
ZP:0012510	postoptic commissure has fewer parts of type axon postoptic commissure, abnormal
ZP:0012511	postoptic commissure has fewer parts of type medial region glial cell (sensu Vertebrata), abnormal
ZP:0012512	postoptic commissure decreased process quality commissural neuron axon guidance, abnormal
ZP:0012513	forebrain lacks all parts of type anterior commissure, abnormal
ZP:0012514	forebrain increased process quality Roundabout signaling pathway involved in axon guidance, abnormal
ZP:0012515	anterior commissure has fewer parts of type axon anterior commissure, abnormal
ZP:0012516	anterior commissure has fewer parts of type medial region glial cell (sensu Vertebrata), abnormal
ZP:0012517	anterior commissure decreased process quality commissural neuron axon guidance, abnormal
ZP:0012518	pharyngeal pouch process quality adherens junction organization, abnormal
ZP:0012519	pharyngeal pouch decreased occurrence apical protein localization, abnormal
ZP:0012520	optic vesicle morphogenesis disrupted, abnormal
ZP:0012521	pharyngeal pouch process quality epithelial cell migration, abnormal
ZP:0012522	pineal complex has extra parts of type photoreceptor cell, abnormal
ZP:0012523	parapineal organ malformed, abnormal
ZP:0012524	parapineal organ has fewer parts of type cell, abnormal
ZP:0012525	axial mesoderm development disrupted, abnormal
ZP:0012526	floor plate split, abnormal
ZP:0012527	spinal cord lacks all parts of type posterior region primary motor neuron, abnormal
ZP:0012528	notochord aplastic/hypoplastic, abnormal
ZP:0012529	sclerotome absent, abnormal
ZP:0012530	whole organism lacks all parts of type notochord, abnormal
ZP:0012531	pineal complex decreased size, abnormal
ZP:0012532	pronephric glomerulus increased amount, abnormal
ZP:0012534	pronephric glomerulus mislocalised laterally, abnormal
ZP:0012535	pronephric glomerular capillary attached to common cardinal vein, abnormal
ZP:0012536	pronephric glomerular capillary detached from membrane pronephric glomerular basement membrane, abnormal
ZP:0012537	glomerular endothelium fenestra pronephric glomerular capillary closed, abnormal
ZP:0012538	anatomical region secondary motor neuron discontinuous, abnormal
ZP:0012539	anatomical region secondary motor neuron split, abnormal
ZP:0012540	podocyte mislocalised laterally, abnormal
ZP:0012541	pharyngeal pouch 2 malformed, abnormal
ZP:0012542	pharyngeal arch 6 absent, abnormal
ZP:0012543	pharyngeal arch 7 absent, abnormal
ZP:0012544	pharyngeal arch 2 fused with pharyngeal arch 3, abnormal
ZP:0012545	trigeminal sensory neuron decreased amount, abnormal
ZP:0012546	DNA methylation decreased process quality, abnormal
ZP:0012547	habenula process quality determination of left/right symmetry, abnormal
ZP:0012548	pineal complex molecular quality, abnormal
ZP:0012549	parapineal organ hyperplastic, abnormal
ZP:0012550	pharyngeal arch increased process quality apoptotic process, abnormal
ZP:0012551	chondrocranium shape, abnormal
ZP:0012552	chondrocranium decreased size, abnormal
ZP:0012553	gut constricted, abnormal
ZP:0012554	dorsal root ganglion has fewer parts of type neuron, abnormal
ZP:0012555	axon dorsal root ganglion morphology, abnormal
ZP:0012556	dendrite motor neuron morphology, abnormal
ZP:0012557	dendrite motor neuron decreased length, abnormal
ZP:0012558	node of Ranvier motor neuron increased width, abnormal
ZP:0012559	myelin sheath motor neuron loose, abnormal
ZP:0012560	motor neuron process quality axon extension, abnormal
ZP:0012561	myelinating Schwann cell structure, abnormal
ZP:0012562	retina has fewer parts of type UV sensitive photoreceptor cell, abnormal
ZP:0012564	cell parapineal organ decreased amount, abnormal
ZP:0012565	UV sensitive photoreceptor cell morphology, abnormal
ZP:0012566	UV sensitive photoreceptor cell deformed, abnormal
ZP:0012567	UV sensitive photoreceptor cell has extra parts of type cone cell pedicle UV sensitive photoreceptor cell, abnormal
ZP:0012568	axon UV sensitive photoreceptor cell bifurcated, abnormal
ZP:0012569	trunk lacks all parts of type dermis melanocyte, abnormal
ZP:0012570	locomotion involved in locomotory behavior decreased speed, abnormal
ZP:0012571	striated muscle thin filament myotome disoriented, abnormal
ZP:0012572	skeletal muscle decreased strength, abnormal
ZP:0012573	hyohyoideus misaligned away from hyohyoideus, abnormal
ZP:0012574	striated muscle thin filament fast muscle cell increased variability of size, abnormal
ZP:0012575	myofibril fast muscle cell malformed, abnormal
ZP:0012576	sarcomere fast muscle cell malformed, abnormal
ZP:0012577	Z disc fast muscle cell increased width, abnormal
ZP:0012578	eye red, abnormal
ZP:0012580	anal fin lacks all parts of type melanocyte, abnormal
ZP:0012582	habenula process quality determination of left/right asymmetry in diencephalon, abnormal
ZP:0012583	neuron projection habenula displaced, abnormal
ZP:0012585	cilium neural tube decreased length, abnormal
ZP:0012586	protein kinase B signaling decreased process quality, abnormal
ZP:0012587	trunk vasculature process quality angiogenesis, abnormal
ZP:0012588	cornea malformed, abnormal
ZP:0012589	corneal endothelium malformed, abnormal
ZP:0012590	anterior segment eye morphology, abnormal
ZP:0012591	anterior segment eye hypoplastic, abnormal
ZP:0012592	mesenchymal cell anterior segment eye morphology, abnormal
ZP:0012593	common lymphoid progenitor decreased amount, abnormal
ZP:0012594	ependymal cell decreased process quality cell population proliferation, abnormal
ZP:0012595	compact layer of ventricle has fewer parts of type apical region cardiac myofibril compact layer of ventricle, abnormal
ZP:0012596	compact layer of ventricle has extra parts of type basal cortex cardiac myofibril compact layer of ventricle, abnormal
ZP:0012597	compact layer of ventricle decreased process quality ventricular cardiac myofibril assembly, abnormal
ZP:0012598	cardiac myofibril compact layer of ventricle increased diameter, abnormal
ZP:0012599	behavior process quality, abnormal
ZP:0012600	learning process quality, abnormal
ZP:0012601	learning decreased process quality, abnormal
ZP:0012602	circadian rhythm rhythm quality, abnormal
ZP:0012603	locomotory exploration behavior increased process quality, abnormal
ZP:0012604	dopaminergic neuron caudal tuberculum disorganized, abnormal
ZP:0012605	cell head necrotic, abnormal
ZP:0012606	motor neuron branchiness, abnormal
ZP:0012607	atrium hypertrophic, abnormal
ZP:0012608	cardiac muscle cell atrium increased size, abnormal
ZP:0012609	cardiac muscle cell disrupted sarcomere organization, abnormal
ZP:0012611	osteoblast differentiation decreased occurrence, abnormal
ZP:0012612	intramembranous ossification decreased occurrence, abnormal
ZP:0012613	thrombocyte differentiation decreased occurrence, abnormal
ZP:0012614	cellular response to oxidative stress increased occurrence, abnormal
ZP:0012615	definitive hemopoiesis occurrence, abnormal
ZP:0012616	centrum decreased occurrence bone mineralization, abnormal
ZP:0012617	opercle decreased volume, abnormal
ZP:0012618	opercle decreased occurrence bone mineralization, abnormal
ZP:0012619	ceratohyal bone decreased occurrence bone mineralization, abnormal
ZP:0012620	cranium decreased occurrence bone mineralization, abnormal
ZP:0012621	hematopoietic system has fewer parts of type nucleate erythrocyte, abnormal
ZP:0012622	hematopoietic system has fewer parts of type thrombocyte, abnormal
ZP:0012623	hematopoietic stem cell mislocalised, abnormal
ZP:0012624	habenula development decreased process quality, abnormal
ZP:0012625	dorsal habenular nucleus poorly differentiated, abnormal
ZP:0012626	midbrain hindbrain boundary hypoplastic, abnormal
ZP:0012627	optic vesicle formation decreased process quality, abnormal
ZP:0012628	optic vesicle decreased process quality regionalization, abnormal
ZP:0012629	optic vesicle increased occurrence apoptotic process, abnormal
ZP:0012630	cell optic vesicle mislocalised, abnormal
ZP:0012631	ovarian follicle development delayed, abnormal
ZP:0012632	spermatogenesis delayed, abnormal
ZP:0012633	vitellogenesis delayed, abnormal
ZP:0012634	sex determination process quality, abnormal
ZP:0012635	female gonad development delayed, abnormal
ZP:0012636	ovary decreased size, abnormal
ZP:0012637	ovary immature, abnormal
ZP:0012638	testis decreased size, abnormal
ZP:0012639	ovulation decreased occurrence, abnormal
ZP:0012640	multi-ciliated epithelial cell pronephros aggregated, abnormal
ZP:0012641	pronephric proximal straight tubule distended, abnormal
ZP:0012642	pronephric distal late tubule decreased size, abnormal
ZP:0012643	vertebral column increased curvature, abnormal
ZP:0012646	dendrite Mauthner neuron increased branchiness, abnormal
ZP:0012647	Mauthner neuron process quality dendrite morphogenesis, abnormal
ZP:0012648	axon spinal cord increased branchiness, abnormal
ZP:0012649	melanophore stripe has fewer parts of type melanocyte, abnormal
ZP:0012650	melanosome melanocyte decreased amount, abnormal
ZP:0012651	optic vesicle unstructured, abnormal
ZP:0012652	optic vesicle looseness, abnormal
ZP:0012653	optic vesicle edge shape, abnormal
ZP:0012654	cell optic vesicle mislocalised medially, abnormal
ZP:0012655	axon cerebellum morphology, abnormal
ZP:0012656	axon cerebellum degenerate, abnormal
ZP:0012657	hematopoietic progenitor cell differentiation process quality, abnormal
ZP:0012658	sclerotome development process quality, abnormal
ZP:0012659	dorsal aorta development process quality, abnormal
ZP:0012660	thymus development process quality, abnormal
ZP:0012661	hematopoietic stem cell differentiation process quality, abnormal
ZP:0012662	Golgi organization disrupted, abnormal
ZP:0012663	lipid digestion disrupted, abnormal
ZP:0012664	Golgi apparatus exocrine pancreas dilated, abnormal
ZP:0012665	Golgi apparatus cholangiocyte dilated, abnormal
ZP:0012666	myelin maintenance decreased process quality, abnormal
ZP:0012667	spinal cord decreased process quality myelination, abnormal
ZP:0012668	cell projection oligodendrocyte decreased amount, abnormal
ZP:0012669	myelin sheath oligodendrocyte decreased length, abnormal
ZP:0012670	myelin sheath oligodendrocyte decreased amount, abnormal
ZP:0012671	respiratory burst involved in defense response decreased process quality, abnormal
ZP:0012672	macrophage heart decreased amount, abnormal
ZP:0012673	macrophage head decreased amount, abnormal
ZP:0012674	blood island increased process quality cell death, abnormal
ZP:0012675	macrophage blood island absent, abnormal
ZP:0012676	macrophage head absent, abnormal
ZP:0012677	macrophage immature, abnormal
ZP:0012678	myeloid cell increased process quality cell death, abnormal
ZP:0012679	swimming behavior increased duration, abnormal
ZP:0012680	female organism increased female fertility, abnormal
ZP:0012681	otolith detached from otolith organ, abnormal
ZP:0012682	posterior crista otic vesicle absent, abnormal
ZP:0012683	posterior crista otic vesicle apoptotic, abnormal
ZP:0012684	anterior crista otic vesicle absent, abnormal
ZP:0012685	gut decreased process quality peristalsis, abnormal
ZP:0012687	glucose import disrupted, abnormal
ZP:0012688	hindbrain increased occurrence apoptotic process, abnormal
ZP:0012689	telencephalon displaced, abnormal
ZP:0012690	lateral longitudinal fasciculus decreased thickness, abnormal
ZP:0012691	lateral longitudinal fasciculus fasciculation, abnormal
ZP:0012692	otic vesicle has fewer parts of type auditory epithelial support cell, abnormal
ZP:0012693	cell periderm decreased amount, abnormal
ZP:0012694	peridermal cell increased size, abnormal
ZP:0012696	epidermal basal stratum increased occurrence cell population proliferation, abnormal
ZP:0012697	periderm increased occurrence cell population proliferation, abnormal
ZP:0012698	cell increased accumulation lysosome periderm, abnormal
ZP:0012699	cell increased accumulation endosome periderm, abnormal
ZP:0012700	cell increased accumulation vesicle periderm, abnormal
ZP:0012701	peridermal cell morphology, abnormal
ZP:0012702	peridermal cell increased amount, abnormal
ZP:0012703	peridermal cell decreased size, abnormal
ZP:0012704	peridermal cell spherical, abnormal
ZP:0012705	basolateral plasma membrane peridermal cell decreased area, abnormal
ZP:0012706	apical plasma membrane peridermal cell decreased area, abnormal
ZP:0012707	cell projection membrane peridermal cell absent, abnormal
ZP:0012708	epidermal cell spherical, abnormal
ZP:0012709	lymphocyte differentiation decreased process quality, abnormal
ZP:0012710	myeloid cell development process quality, abnormal
ZP:0012711	otic vesicle lacks all parts of type tether cell, abnormal
ZP:0012712	pancreas degenerate, abnormal
ZP:0012713	pancreas lacks parts or has fewer parts of type pancreatic acinar cell, abnormal
ZP:0012714	neutrophil pancreas mislocalised, abnormal
ZP:0012715	pancreatic acinar cell decreased amount, abnormal
ZP:0012716	neuromast hair cell decreased efficacy calcium ion import, abnormal
ZP:0012717	posterior macula separated from tether cell sagitta, abnormal
ZP:0012718	sagitta arrested otolith tethering, abnormal
ZP:0012719	acellular anatomical structure utricle physical object quality, abnormal
ZP:0012720	otic vesicle delayed otolith formation, abnormal
ZP:0012721	otic vesicle delayed otolith tethering, abnormal
ZP:0012722	BMP signaling pathway increased process quality, abnormal
ZP:0012723	nodal signaling pathway increased process quality, abnormal
ZP:0012724	pronephric proximal tubule morphogenesis decreased process quality, abnormal
ZP:0012725	glomerular visceral epithelial cell migration decreased process quality, abnormal
ZP:0012726	pronephric proximal convoluted tubule malformed, abnormal
ZP:0012727	pronephric podocyte mislocalised laterally, abnormal
ZP:0012728	pronephros arrested epithelial cilium movement involved in extracellular fluid movement, abnormal
ZP:0012729	cell migration involved in sprouting angiogenesis decreased process quality, abnormal
ZP:0012730	liver right side of gut, abnormal
ZP:0012731	pancreas left side of gut, abnormal
ZP:0012732	macula adjacent to macula, abnormal
ZP:0012733	posterior macula has extra parts of type hair cell, abnormal
ZP:0012734	epiboly decreased duration, abnormal
ZP:0012735	whole organism has fewer parts of type cell, abnormal
ZP:0012736	whole organism has extra parts of type cell, abnormal
ZP:0012737	whole organism altered number of cell, abnormal
ZP:0012738	posterior macula decreased size, abnormal
ZP:0012739	posterior macula has fewer parts of type hair cell, abnormal
ZP:0012740	shield poorly differentiated, abnormal
ZP:0012741	germ ring poorly differentiated, abnormal
ZP:0012742	sympathetic nervous system development process quality, abnormal
ZP:0012743	filopodium cranial neural crest decreased length, abnormal
ZP:0012744	filopodium cranial neural crest decreased amount, abnormal
ZP:0012745	cardiac muscle cell decreased volume, abnormal
ZP:0012746	cranial neural crest misrouted, abnormal
ZP:0012747	cranial neural crest process quality neural crest cell migration, abnormal
ZP:0012748	sympathetic nervous system decreased size, abnormal
ZP:0012749	sympathetic nervous system malformed, abnormal
ZP:0012750	pharyngeal arch 1 absent, abnormal
ZP:0012751	pharyngeal arch 1 process quality neural crest cell migration, abnormal
ZP:0012752	cranial neural crest pharyngeal arch 1 misrouted, abnormal
ZP:0012753	pectoral fin bud increased occurrence cell death, abnormal
ZP:0012754	pectoral fin bud decreased occurrence cell population proliferation, abnormal
ZP:0012755	pectoral fin field decreased size, abnormal
ZP:0012756	pectoral fin field distributed, abnormal
ZP:0012757	scapulocoracoid absent, abnormal
ZP:0012758	scapulocoracoid malformed, abnormal
ZP:0012759	bony projection scapulocoracoid absent, abnormal
ZP:0012760	bony projection scapulocoracoid mislocalised, abnormal
ZP:0012761	pectoral fin endoskeletal disc aplastic, abnormal
ZP:0012762	Notch signaling pathway decreased process quality, abnormal
ZP:0012763	trunk vasculature process quality blood vessel morphogenesis, abnormal
ZP:0012764	retinal cone cell increased amount, abnormal
ZP:0012765	endodermal cell differentiation increased occurrence, abnormal
ZP:0012766	hypoblast has extra parts of type endodermal cell, abnormal
ZP:0012767	swimming behavior increased behavioural activity, abnormal
ZP:0012768	interneuron somite decreased amount, abnormal
ZP:0012769	glutamatergic neuron increased amount, abnormal
ZP:0012770	glycinergic neuron decreased amount, abnormal
ZP:0012782	pronephric duct morphogenesis process quality, abnormal
ZP:0012815	central artery structure, abnormal
ZP:0012852	posterior lateral line morphology, abnormal
ZP:0012870	apoptotic process process quality, abnormal
ZP:0012877	locomotory behavior occurrence, abnormal
ZP:0012890	cardiac atrium development process quality, abnormal
ZP:0012891	cardiac ventricle development process quality, abnormal
ZP:0012926	intersegmental vein morphology, abnormal
ZP:0012943	neural keel morphology, abnormal
ZP:0012953	thigmotaxis occurrence, abnormal
ZP:0012965	central nervous system structure, abnormal
ZP:0012993	endocrine pancreas morphology, abnormal
ZP:0013010	whole organism size, abnormal
ZP:0013026	sarcomere atrium morphology, abnormal
ZP:0013065	rhombomere 3 morphology, abnormal
ZP:0013068	vasculature liver morphology, abnormal
ZP:0013069	hepatocyte structure, abnormal
ZP:0013119	Meckel's cartilage size, abnormal
ZP:0013121	palatoquadrate cartilage size, abnormal
ZP:0013123	ceratohyal cartilage size, abnormal
ZP:0013124	ceratohyal cartilage length, abnormal
ZP:0013125	ceratohyal cartilage distance Meckel's cartilage, abnormal
ZP:0013137	cell division process quality, abnormal
ZP:0013142	pharyngeal endoderm morphology, abnormal
ZP:0013148	habenula symmetry, abnormal
ZP:0013173	visual behavior process quality, abnormal
ZP:0013176	peripheral nervous system development process quality, abnormal
ZP:0013179	testis morphology, abnormal
ZP:0013186	Sertoli cell present, abnormal
ZP:0013224	ventral spinal nerve morphology, abnormal
ZP:0013230	larval development process quality, abnormal
ZP:0013249	lens fiber cell morphogenesis process quality, abnormal
ZP:0013258	circadian rhythm process quality, abnormal
ZP:0013259	pineal gland development process quality, abnormal
ZP:0013279	phototaxis process quality, abnormal
ZP:0013286	myofibril slow muscle cell morphology, abnormal
ZP:0013297	rRNA processing process quality, abnormal
ZP:0013360	angioblast cell differentiation process quality, abnormal
ZP:0013369	whole organism male fertility, abnormal
ZP:0013379	axoneme pronephros morphology, abnormal
ZP:0013388	pronephric tubule shape, abnormal
ZP:0013402	pericardium structure, abnormal
ZP:0013456	photoreceptor outer segment layer morphology, abnormal
ZP:0013470	axoneme pronephric duct structure, abnormal
ZP:0013484	cilium otic vesicle morphology, abnormal
ZP:0013486	fucosylation decreased process quality, abnormal
ZP:0013488	embryonic heart tube development process quality, abnormal
ZP:0013501	cardiac muscle morphology, abnormal
ZP:0013527	perichondral bone absent, abnormal
ZP:0013546	Kupffer's vesicle lumenized, abnormal
ZP:0013554	male gonad development process quality, abnormal
ZP:0013590	notochord shape, abnormal
ZP:0013611	erythrocyte maturation process quality, abnormal
ZP:0013613	whole organism physical object quality, abnormal
ZP:0013619	neural tube spatial pattern, abnormal
ZP:0013651	renal glomerulus morphology, abnormal
ZP:0013664	cardiac ventricle volume, abnormal
ZP:0013670	canonical Wnt signaling pathway process quality, abnormal
ZP:0013681	atrioventricular valve morphogenesis disrupted, abnormal
ZP:0013685	mesencephalic vein morphology, abnormal
ZP:0013689	motor neuron action potential, abnormal
ZP:0013748	posterior lateral line nerve morphology, abnormal
ZP:0013753	lens development in camera-type eye process quality, abnormal
ZP:0013759	trigeminal ganglion morphology, abnormal
ZP:0013760	melanophore stripe morphology, abnormal
ZP:0013779	posterior lateral line neuromast position, abnormal
ZP:0013799	ribosome biogenesis process quality, abnormal
ZP:0013833	cardiac muscle cell morphology, abnormal
ZP:0013848	cranial nerve VII spatial pattern, abnormal
ZP:0013869	sarcomere slow muscle cell morphology, abnormal
ZP:0013876	adrenal gland development process quality, abnormal
ZP:0013877	interrenal gland position, abnormal
ZP:0013878	interrenal gland decreased occurrence epithelial to mesenchymal transition, abnormal
ZP:0013879	interrenal gland process quality animal organ morphogenesis, abnormal
ZP:0013880	pronephric glomerulus separated from pronephric glomerulus, abnormal
ZP:0013881	chromaffin cell mislocalised, abnormal
ZP:0013882	interrenal  angiogenic sprout decreased length, abnormal
ZP:0013883	cardiac muscle progenitor cell migration to the midline involved in heart field formation decreased occurrence, abnormal
ZP:0013884	heart split bilaterally, abnormal
ZP:0013885	heart tube split bilaterally, abnormal
ZP:0013886	myocardial precursor mislocalised laterally, abnormal
ZP:0013887	enterocyte differentiation decreased occurrence, abnormal
ZP:0013888	intestinal epithelium has fewer parts of type enterocyte, abnormal
ZP:0013889	intestinal epithelium decreased occurrence endocytosis, abnormal
ZP:0013890	digestive tract morphogenesis decreased process quality, abnormal
ZP:0013891	intestinal epithelium malformed, abnormal
ZP:0013892	intestinal epithelium has extra parts of type goblet cell, abnormal
ZP:0013893	apical region intestinal epithelium physical object quality, abnormal
ZP:0013894	intestinal epithelium process quality endocytosis, abnormal
ZP:0013895	intestinal epithelium decreased process quality Notch signaling pathway, abnormal
ZP:0013896	apical plasma membrane intestinal epithelium increased area, abnormal
ZP:0013897	epithelial cell intestinal epithelium decreased height, abnormal
ZP:0013898	recycling endosome enterocyte mislocalised radially, abnormal
ZP:0013899	gut disrupted innervation, abnormal
ZP:0013900	bone mineralization increased occurrence, abnormal
ZP:0013901	integument mineralized, abnormal
ZP:0013902	cranium increased occurrence bone mineralization, abnormal
ZP:0013903	vertebral column increased occurrence bone mineralization, abnormal
ZP:0013904	anatomical space vertebral column mineralized, abnormal
ZP:0013905	islet increased amount, abnormal
ZP:0013906	islet decreased size, abnormal
ZP:0013907	antero-medial region endoderm decreased object quality, abnormal
ZP:0013908	anterior region endoderm apoptotic, abnormal
ZP:0013909	endoderm increased occurrence apoptotic process, abnormal
ZP:0013910	pharyngeal endoderm mislocalised laterally, abnormal
ZP:0013911	Notch signaling pathway decreased intensity, abnormal
ZP:0013912	ventral mandibular arch atrophied, abnormal
ZP:0013913	endoderm cellular quality, abnormal
ZP:0013914	cerebellar neuron development disrupted, abnormal
ZP:0013915	prechordal plate decreased speed, abnormal
ZP:0013916	voltage-gated sodium channel activity decreased process quality, abnormal
ZP:0013918	Golgi to plasma membrane protein transport disrupted, abnormal
ZP:0013919	skeletal muscle action potential, abnormal
ZP:0013920	Rohon-Beard neuron action potential, abnormal
ZP:0013921	Rohon-Beard neuron accumulation voltage-gated sodium channel complex endoplasmic reticulum Rohon-Beard neuron, abnormal
ZP:0013922	Rohon-Beard neuron accumulation voltage-gated sodium channel complex Golgi apparatus Rohon-Beard neuron, abnormal
ZP:0013923	response to light stimulus process quality, abnormal
ZP:0013924	spinal cord has fewer parts of type motor neuron synapse motor neuron, abnormal
ZP:0013925	dorsal anterior lateral line nerve has fewer parts of type synapse dorsal anterior lateral line nerve, abnormal
ZP:0013926	dorsal anterior lateral line nerve decreased process quality synapse assembly, abnormal
ZP:0013927	motor neuron decreased process quality synapse assembly, abnormal
ZP:0013931	optic vesicle constricted, abnormal
ZP:0013932	retinal pigmented epithelium disconnected, abnormal
ZP:0013933	retina folded, abnormal
ZP:0013934	cornea pigmented, abnormal
ZP:0013935	ventral region optic cup decreased depth, abnormal
ZP:0013936	lens epithelium decreased occurrence cell population proliferation, abnormal
ZP:0013937	ceratohyal cartilage pharyngeal arch 2 malformed, abnormal
ZP:0013947	caudal fin increased size, abnormal
ZP:0013954	whole organism degree of pigmentation, abnormal
ZP:0013955	microtubule pronephric duct disorganized, abnormal
ZP:0013959	fibroblast vertical myoseptum mislocalised, abnormal
ZP:0013961	endodermal cell differentiation arrested, abnormal
ZP:0013963	nodal signaling pathway decreased occurrence, abnormal
ZP:0013965	hypoblast lacks all parts of type endodermal cell, abnormal
ZP:0013971	caudal fin morphogenesis disrupted, abnormal
ZP:0013972	fin fold actinotrichium decreased size, abnormal
ZP:0013973	ventral fin fold has fewer parts of type fin fold actinotrichium, abnormal
ZP:0013979	photoreceptor outer segment retinal cone cell disorganized, abnormal
ZP:0013992	dorsal longitudinal anastomotic vessel decreased diameter, abnormal
ZP:0013993	subintestinal vein increased occurrence sprouting angiogenesis, abnormal
ZP:0013997	posterior cardinal vein broken, abnormal
ZP:0013998	cranial vasculature physical object quality, abnormal
ZP:0013999	aortic arch physical object quality, abnormal
ZP:0014000	caudal vein decreased size, abnormal
ZP:0014001	angiogenic sprout intersegmental vessel arrested, abnormal
ZP:0014002	subintestinal vein decreased size, abnormal
ZP:0014003	intersegmental vessel increased size, abnormal
ZP:0014004	filopodium intersegmental vessel increased amount, abnormal
ZP:0014007	intersegmental vessel decreased branchiness, abnormal
ZP:0014008	trunk vasculature lacks parts or has fewer parts of type filopodium blood vessel endothelial cell, abnormal
ZP:0014009	filopodium intersegmental vessel decreased size, abnormal
ZP:0014010	blood vessel intestine decreased branchiness, abnormal
ZP:0014012	angioblast cell migration from lateral mesoderm to midline process quality, abnormal
ZP:0014020	chondroblast palatoquadrate cartilage disorganized, abnormal
ZP:0014024	blood vessel increased branchiness, abnormal
ZP:0014032	caudal vein plexus process quality blood vessel development, abnormal
ZP:0014033	cell-cell junction blood vessel endothelial cell decreased amount, abnormal
ZP:0014035	intersegmental vessel extends beyond somite, abnormal
ZP:0014043	eye photoreceptor cell quality, abnormal
ZP:0014044	iridophore intensity, abnormal
ZP:0014050	trunk increased size, abnormal
ZP:0014051	notochord has extra parts of type cell notochord, abnormal
ZP:0014052	notochord posterior region bifurcated, abnormal
ZP:0014053	determination of ventral identity disrupted, abnormal
ZP:0014054	whole organism lacks parts or has fewer parts of type post-vent region, abnormal
ZP:0014055	Meckel's cartilage decreased thickness, abnormal
ZP:0014056	palatoquadrate cartilage decreased thickness, abnormal
ZP:0014058	liver increased amount, abnormal
ZP:0014061	otolith angular, abnormal
ZP:0014062	otolith star shaped, abnormal
ZP:0014066	abducens motor nucleus adjacent to abducens motor nucleus, abnormal
ZP:0014067	trigeminal motor nucleus adjacent to trigeminal motor nucleus, abnormal
ZP:0014087	desmosome heart structure, abnormal
ZP:0014088	renal tubule morphology, abnormal
ZP:0014089	gut endothelial cell decreased size, abnormal
ZP:0014090	pharyngeal arch 3-7 hypoplastic, abnormal
ZP:0014092	fin regeneration decreased rate, abnormal
ZP:0014098	fast muscle myoblast mononucleate, abnormal
ZP:0014099	hindbrain size, abnormal
ZP:0014101	caudal vein edematous, abnormal
ZP:0014102	thyroid follicle morphology, abnormal
ZP:0014103	endocrine pancreas dispersed, abnormal
ZP:0014104	brain vasculature structure, abnormal
ZP:0014106	defense response to bacterium arrested, abnormal
ZP:0014114	margin morphology, abnormal
ZP:0014115	yolk syncytial layer disorganized, abnormal
ZP:0014116	microvillus external yolk syncytial layer decreased length, abnormal
ZP:0014117	microvillus external yolk syncytial layer decreased mass density, abnormal
ZP:0014118	margin irregular spatial pattern, abnormal
ZP:0014120	filamentous actin external yolk syncytial layer disorganized, abnormal
ZP:0014133	cardiac ventricle increased volume, abnormal
ZP:0014143	retinal pigmented epithelium colorless, abnormal
ZP:0014156	cell brain apoptotic, abnormal
ZP:0014182	common cardinal vein aplastic, abnormal
ZP:0014185	liver vacuolated, abnormal
ZP:0014189	epithelium development process quality, abnormal
ZP:0014206	ventricular cardiac myofibril assembly process quality, abnormal
ZP:0014207	striated muscle myosin thick filament cardiac ventricle absent, abnormal
ZP:0014217	sodium ion transport increased occurrence, abnormal
ZP:0014218	chloride transport decreased occurrence, abnormal
ZP:0014219	calcium-independent cell-cell adhesion via plasma membrane cell-adhesion molecules disrupted, abnormal
ZP:0014220	adherens junction maintenance disrupted, abnormal
ZP:0014221	DEL increased accumulation cytoplasmic vesicle DEL, abnormal
ZP:0014222	adherens junction EVL disorganized, abnormal
ZP:0014223	adherens junction DEL disorganized, abnormal
ZP:0014224	cell DEL circular, abnormal
ZP:0014225	cell DEL disorganized, abnormal
ZP:0014226	cell brain dead, abnormal
ZP:0014238	otolith formation process quality, abnormal
ZP:0014239	inner ear morphogenesis process quality, abnormal
ZP:0014240	macula utricle decreased size, abnormal
ZP:0014241	lateral crista aplastic, abnormal
ZP:0014242	posterior crista aplastic, abnormal
ZP:0014243	statoacoustic (VIII) ganglion malformed, abnormal
ZP:0014244	anterior crista aplastic, abnormal
ZP:0014245	macula saccule decreased size, abnormal
ZP:0014246	pillar of the anterior semicircular canal aplastic, abnormal
ZP:0014247	pillar of the lateral semicircular canal aplastic, abnormal
ZP:0014248	pillar of the posterior semicircular canal aplastic, abnormal
ZP:0014256	somite border spatial pattern, abnormal
ZP:0014257	melanocyte black, abnormal
ZP:0014258	midbrain opaque, abnormal
ZP:0014260	intestinal villus gut epithelium absent, abnormal
ZP:0014261	epithelial cell gut circular, abnormal
ZP:0014262	smooth muscle cell gut disorganized, abnormal
ZP:0014269	caudal fin development disrupted, abnormal
ZP:0014275	fin regeneration decreased process quality, abnormal
ZP:0014277	wound healing decreased process quality, abnormal
ZP:0014282	heart primordium has fewer parts of type cardiac muscle cell, abnormal
ZP:0014292	muscle cell undulate, abnormal
ZP:0014293	muscle tendon junction myotome physical object quality, abnormal
ZP:0014294	muscle cell increased length, abnormal
ZP:0014309	endocrine cell posterior pancreatic bud decreased amount, abnormal
ZP:0014312	neural crest absent, abnormal
ZP:0014322	trigeminal ganglion apoptotic, abnormal
ZP:0014323	peripheral neuron head decreased amount, abnormal
ZP:0014324	cardiac chamber formation process quality, abnormal
ZP:0014325	cranial blood vessel hemorrhagic, abnormal
ZP:0014326	response to chemical disrupted, abnormal
ZP:0014332	nucleus yolk syncytial layer shape, abnormal
ZP:0014333	nucleus yolk syncytial layer dense, abnormal
ZP:0014334	nucleus yolk syncytial layer irregular spatial pattern, abnormal
ZP:0014335	margin blastoderm irregular spatial pattern, abnormal
ZP:0014336	yolk syncytial layer fused with chromosome chromosome yolk syncytial layer, abnormal
ZP:0014337	nucleus yolk syncytial layer undivided, abnormal
ZP:0014338	sarcomere slow muscle cell absent, abnormal
ZP:0014339	filamentous actin slow muscle cell dispersed, abnormal
ZP:0014340	myofibril muscle cell absent, abnormal
ZP:0014341	myofibril slow muscle cell undulate, abnormal
ZP:0014347	cytoskeleton of presynaptic active zone neuromast hair cell decreased size, abnormal
ZP:0014350	musculoskeletal movement decreased magnitude, abnormal
ZP:0014353	locomotion involved in locomotory behavior decreased process quality, abnormal
ZP:0014354	mesodermal to mesenchymal transition involved in gastrulation disrupted, abnormal
ZP:0014355	mesodermal cell spatial pattern, abnormal
ZP:0014356	bleb hypoblast increased amount, abnormal
ZP:0014364	retina lacks all parts of type microvillus retinal pigmented epithelium, abnormal
ZP:0014377	response to wounding disrupted, abnormal
ZP:0014379	frontal bone decreased thickness, abnormal
ZP:0014382	pronephric proximal convoluted tubule dilated, abnormal
ZP:0014383	pronephric capsular space increased size, abnormal
ZP:0014384	slow muscle cell trunk musculature decreased contractility, abnormal
ZP:0014385	slow muscle cell post-vent region decreased contractility, abnormal
ZP:0014389	endocardial progenitor cell migration to the midline involved in heart field formation disrupted, abnormal
ZP:0014390	Wnt signaling pathway increased occurrence, abnormal
ZP:0014392	regulation of RNA stability disrupted, abnormal
ZP:0014394	angiogenic sprout intersegmental vessel decreased amount, abnormal
ZP:0014398	pronephric podocyte fused with pronephric podocyte, abnormal
ZP:0014399	anterior region pronephros deformed, abnormal
ZP:0014400	pronephric tubule fused with anterior region anterior region pronephric tubule, abnormal
ZP:0014401	pronephric glomerular capillary hypoplastic, abnormal
ZP:0014402	pronephric glomerular capillary non-functional, abnormal
ZP:0014408	nucleus yolk syncytial layer spatial pattern, abnormal
ZP:0014409	microtubule yolk syncytial layer spatial pattern, abnormal
ZP:0014412	myosin filament assembly arrested, abnormal
ZP:0014413	axon motor neuron disoriented, abnormal
ZP:0014440	embryo development decreased functionality, abnormal
ZP:0014445	fin regeneration process quality, abnormal
ZP:0014454	response to hypoxia decreased process quality, abnormal
ZP:0014462	notochord granular, abnormal
ZP:0014463	vesicle notochord inner cell decreased size, abnormal
ZP:0014464	migratory slow muscle precursor cell decreased amount, abnormal
ZP:0014466	dopaminergic neuron retina decreased amount, abnormal
ZP:0014472	tail bud malformed, abnormal
ZP:0014482	anterior-posterior axis whole organism morphology, abnormal
ZP:0014491	heart tube medial orientation, abnormal
ZP:0014492	anterior region neuroectoderm absent, abnormal
ZP:0014495	whole organism increased permeability, abnormal
ZP:0014497	erythrocyte differentiation decreased process quality, abnormal
ZP:0014499	blood cell heart decreased amount, abnormal
ZP:0014512	musculoskeletal movement increased occurrence, abnormal
ZP:0014524	Kupffer's vesicle increased area, abnormal
ZP:0014525	BMP signaling pathway involved in heart development decreased process quality, abnormal
ZP:0014531	ventral mandibular arch open, abnormal
ZP:0014532	chondrocranium cartilage absent, abnormal
ZP:0014547	cardiac muscle cell proliferation decreased process quality, abnormal
ZP:0014566	heart decreased width, abnormal
ZP:0014571	slow muscle cell adaxial to somite, abnormal
ZP:0014574	cardiac ventricle constricted, abnormal
ZP:0014594	muscle structure development disrupted, abnormal
ZP:0014595	fast muscle cell bent, abnormal
ZP:0014596	rhombomere 5 decreased size, abnormal
ZP:0014597	rhombomere 3 decreased size, abnormal
ZP:0014599	mitochondrial calcium ion transmembrane transport disrupted, abnormal
ZP:0014600	Kupffer's vesicle has fewer parts of type inner dynein arm ciliated cell, abnormal
ZP:0014601	Kupffer's vesicle has fewer parts of type outer dynein arm ciliated cell, abnormal
ZP:0014602	motile cilium Kupffer's vesicle decreased speed, abnormal
ZP:0014603	motile cilium Kupffer's vesicle shortened, abnormal
ZP:0014604	gut process quality left/right pattern formation, abnormal
ZP:0014637	cortisol metabolic process increased process quality, abnormal
ZP:0014638	cortisol metabolic process decreased process quality, abnormal
ZP:0014639	hatching process quality, abnormal
ZP:0014641	hatching premature, abnormal
ZP:0014642	EVL temporally extended epiboly, abnormal
ZP:0014643	yolk syncytial layer temporally extended epiboly, abnormal
ZP:0014644	DEL arrested epiboly, abnormal
ZP:0014645	DEL temporally extended epiboly, abnormal
ZP:0014651	pronephric proximal straight tubule decreased size, abnormal
ZP:0014653	regulation of cardiac muscle contraction by calcium ion signaling process quality, abnormal
ZP:0014655	atrial cardiac muscle cell action potential process quality, abnormal
ZP:0014656	troponin complex heart disorganized, abnormal
ZP:0014657	muscle thin filament tropomyosin heart disorganized, abnormal
ZP:0014658	sarcomere cardiac ventricle disorganized, abnormal
ZP:0014659	sarcomere heart disorganized, abnormal
ZP:0014660	cardiac ventricle decreased process quality heart contraction, abnormal
ZP:0014661	cardiac myofibril heart disorganized, abnormal
ZP:0014674	neutrophil migration decreased process quality, abnormal
ZP:0014681	reactive oxygen species metabolic process process quality, abnormal
ZP:0014682	head kidney decreased size, abnormal
ZP:0014688	cleithrum absent, abnormal
ZP:0014690	parachordal cartilage absent, abnormal
ZP:0014692	mesoderm decreased amount, abnormal
ZP:0014716	whole organism decreased process quality apoptotic process, abnormal
ZP:0014717	whole organism decreased process quality cell population proliferation, abnormal
ZP:0014727	bulbus arteriosus absent, abnormal
ZP:0014734	mesoderm development process quality, abnormal
ZP:0014736	median fin fold decreased width, abnormal
ZP:0014746	muscle detached from tendon, abnormal
ZP:0014747	muscle tendon junction somite border morphology, abnormal
ZP:0014748	cardiac muscle cell action potential process quality, abnormal
ZP:0014759	retina has fewer parts of type retinal rod cell, abnormal
ZP:0014763	BMP signaling pathway decreased process quality, abnormal
ZP:0014774	optic tectum increased process quality cell population proliferation, abnormal
ZP:0014778	photoreceptor cell development process quality, abnormal
ZP:0014779	lens nucleated, abnormal
ZP:0014780	lens process quality enucleation, abnormal
ZP:0014781	adult behavior process quality, abnormal
ZP:0014785	posterior region trunk decreased length, abnormal
ZP:0014803	palatoquadrate arch absent, abnormal
ZP:0014804	palatoquadrate arch decreased size, abnormal
ZP:0014805	interrenal gland decreased size, abnormal
ZP:0014806	neuromuscular process controlling balance process quality, abnormal
ZP:0014814	pronephric glomerular basement membrane increased permeability, abnormal
ZP:0014815	left/right axis specification process quality, abnormal
ZP:0014816	inner ear has extra parts of type otolith, abnormal
ZP:0014817	cilium Kupffer's vesicle disorganized, abnormal
ZP:0014818	Kupffer's vesicle has fewer parts of type cilium axonemal microtubule Kupffer's vesicle, abnormal
ZP:0014819	growth decreased process quality, abnormal
ZP:0014822	posterior lateral line neuromast mislocalised, abnormal
ZP:0014826	oligodendrocyte decreased process quality cell division, abnormal
ZP:0014830	hypothalamus absent, abnormal
ZP:0014848	melanosome trunk increased area, abnormal
ZP:0014851	optic cup deformed, abnormal
ZP:0014852	ventricular system absent, abnormal
ZP:0014858	endodermal cell fate specification decreased process quality, abnormal
ZP:0014859	whole organism lacks all parts of type endoderm, abnormal
ZP:0014860	branchiomotor neuron rhombomere 5 mislocalised anteriorly, abnormal
ZP:0014865	blood desaturated red, abnormal
ZP:0014867	EVL delayed epiboly, abnormal
ZP:0014868	DEL delayed epiboly, abnormal
ZP:0014884	spinal cord has fewer parts of type dorsal side oligodendrocyte, abnormal
ZP:0014885	spinal cord process quality central nervous system myelination, abnormal
ZP:0014890	retinal rod cell degeneration, abnormal
ZP:0014891	chondrocyte decreased amount, abnormal
ZP:0014897	axon fasciculus retroflexus misrouted, abnormal
ZP:0014914	neuromast decreased occurrence cell population proliferation, abnormal
ZP:0014916	posterior lateral line neuromast hair cell differentiation decreased occurrence, abnormal
ZP:0014920	gut inverted, abnormal
ZP:0014921	embryonic heart tube elongation decreased process quality, abnormal
ZP:0014922	primitive heart tube decreased length, abnormal
ZP:0014923	cardiac ventricle process quality heart contraction, abnormal
ZP:0014924	cardiac muscle cell cardiac ventricle decreased volume, abnormal
ZP:0014926	cranial neural crest cell decreased process quality cell population proliferation, abnormal
ZP:0014927	mandibular arch skeleton quality, abnormal
ZP:0014931	endocardial cushion agenesis, abnormal
ZP:0014934	atrioventricular valve development process quality, abnormal
ZP:0014948	cardioblast cell midline fusion disrupted, abnormal
ZP:0014952	midbrain decreased volume, abnormal
ZP:0014956	hemopoiesis quality, abnormal
ZP:0014963	immune response quality, abnormal
ZP:0014965	granulocyte spatial pattern, abnormal
ZP:0014967	brain spatial pattern, abnormal
ZP:0014969	cell migration quality, abnormal
ZP:0014984	fin increased size, abnormal
ZP:0014985	diencephalon spatial pattern, abnormal
ZP:0014987	scale spatial pattern, abnormal
ZP:0014988	pancreas spatial pattern, abnormal
ZP:0014991	testis increased amount, abnormal
ZP:0014992	pectoral fin musculature decreased amount, abnormal
ZP:0014995	caudal fin spatial pattern, abnormal
ZP:0014998	head spatial pattern, abnormal
ZP:0015003	musculature system decreased amount, abnormal
ZP:0015004	epidermal cell circular, abnormal
ZP:0015012	testis absent, abnormal
ZP:0015013	ovary increased amount, abnormal
ZP:0015014	gonad decreased size, abnormal
ZP:0015015	melanophore stripe decreased width, abnormal
ZP:0015016	epidermal cell decreased amount, abnormal
ZP:0015019	gonad absent, abnormal
ZP:0015029	scale size, abnormal
ZP:0015031	branchiostegal ray decreased amount, abnormal
ZP:0015040	granulocyte absent, abnormal
ZP:0015041	mitochondrion posterior lateral line nerve decreased amount, abnormal
ZP:0015042	axon posterior lateral line nerve discolored, abnormal
ZP:0015043	synaptic vesicle posterior lateral line nerve mislocalised, abnormal
ZP:0015049	heart rudiment has fewer parts of type cardiac muscle cell, abnormal
ZP:0015050	cardiac ventricle lacks all parts of type trabecular layer of ventricle, abnormal
ZP:0015051	cardiac muscle cell cardiac ventricle irregular spatial pattern, abnormal
ZP:0015053	fin mislocalised, abnormal
ZP:0015054	ventral larval melanophore stripe duplicated, abnormal
ZP:0015055	extension wholly ventralized, abnormal
ZP:0015056	anal fin duplicated, abnormal
ZP:0015066	cardiac muscle cell increased process quality apoptotic process, abnormal
ZP:0015069	cardiac ventricle has extra parts of type cardiac muscle cell, abnormal
ZP:0015070	heart has extra parts of type cardiac muscle cell, abnormal
ZP:0015071	atrium has extra parts of type cardiac muscle cell, abnormal
ZP:0015078	posterior lateral line primordium decreased process quality cell division, abnormal
ZP:0015079	neuromast increased distance neuromast, abnormal
ZP:0015080	neuromast decreased distance neuromast, abnormal
ZP:0015081	lateral line primordium decreased size, abnormal
ZP:0015084	posterior lateral line primordium decreased process quality adherens junction maintenance, abnormal
ZP:0015093	gonad development quality, abnormal
ZP:0015096	mature neutrophil decreased amount, abnormal
ZP:0015099	mature neutrophil absent, abnormal
ZP:0015106	muscle pioneer spatial pattern, abnormal
ZP:0015114	cranium decreased length, abnormal
ZP:0015115	scale absent, abnormal
ZP:0015119	yolk structure, abnormal
ZP:0015122	melanophore stripe spatial pattern, abnormal
ZP:0015124	intersegmental vessel delayed sprouting angiogenesis, abnormal
ZP:0015147	multi-ciliated epithelial cell pronephros decreased amount, abnormal
ZP:0015151	otic placode absent, abnormal
ZP:0015154	neuroectoderm increased size, abnormal
ZP:0015155	non neural ectoderm decreased size, abnormal
ZP:0015162	testis hypertrophic, abnormal
ZP:0015171	muscle cell somite disorganized, abnormal
ZP:0015172	melanocyte spindle-shaped, abnormal
ZP:0015177	circadian sleep/wake cycle, wakefulness increased occurrence, abnormal
ZP:0015180	response to absence of light increased occurrence, abnormal
ZP:0015184	nucleate erythrocyte accumulation head, abnormal
ZP:0015208	Notch signaling pathway increased process quality, abnormal
ZP:0015240	otic vesicle decreased amount, abnormal
ZP:0015243	otic placode decreased amount, abnormal
ZP:0015250	hatching gland hypoplastic, abnormal
ZP:0015258	primary motor neuron structure, abnormal
ZP:0015259	pronephros edematous, abnormal
ZP:0015260	cilium pronephros decreased amount, abnormal
ZP:0015275	thymus increased size, abnormal
ZP:0015279	cardiac muscle cell mislocalised, abnormal
ZP:0015280	vasculogenesis arrested, abnormal
ZP:0015281	axial vasculature aplastic, abnormal
ZP:0015282	primitive hemopoiesis arrested, abnormal
ZP:0015283	ventral wall of dorsal aorta lacks all parts of type nucleate erythrocyte, abnormal
ZP:0015285	motile cilium pronephric duct immobile, abnormal
ZP:0015286	heart tube decreased functionality, abnormal
ZP:0015287	neural tube bilateral symmetry, abnormal
ZP:0015293	heart tube absent, abnormal
ZP:0015317	macrophage aggregated, abnormal
ZP:0015318	ball decreased size, abnormal
ZP:0015319	inner ear sharpness, abnormal
ZP:0015320	inner ear lacks all parts of type lapillus, abnormal
ZP:0015321	ball morphology, abnormal
ZP:0015324	pillar of the lateral semicircular canal decreased size, abnormal
ZP:0015326	inner ear symmetrical, abnormal
ZP:0015327	posterior macula deformed, abnormal
ZP:0015328	lateral crista hypotrophic, abnormal
ZP:0015329	anterior macula deformed, abnormal
ZP:0015330	inner ear degenerate, abnormal
ZP:0015331	inner ear increased thickness, abnormal
ZP:0015332	stereocilium bundle macula decreased amount, abnormal
ZP:0015333	inner ear lacks all parts of type sagitta, abnormal
ZP:0015334	inner ear flat, abnormal
ZP:0015341	intestine neoplastic, abnormal
ZP:0015349	sleep increased duration, abnormal
ZP:0015352	cilium olfactory placode absent, abnormal
ZP:0015353	retinal rod cell development disrupted, abnormal
ZP:0015354	renal glomerulus increased size, abnormal
ZP:0015355	posterior neural keel increased width, abnormal
ZP:0015356	anterior neural keel flat, abnormal
ZP:0015357	post-vent region spade-shaped, abnormal
ZP:0015358	cell medial floor plate mislocalised, abnormal
ZP:0015359	whole organism has fewer parts of type posterior region muscle, abnormal
ZP:0015360	paraxial mesoderm disorganized, abnormal
ZP:0015361	cell pronephros increased amount, abnormal
ZP:0015362	mesoderm absent, abnormal
ZP:0015363	keratin accumulating cell increased accumulation epidermis, abnormal
ZP:0015366	corpuscles of Stannius increased size, abnormal
ZP:0015368	pronephric distal early tubule increased length, abnormal
ZP:0015373	caudal vein plexus increased diameter, abnormal
ZP:0015374	axial vasculature unlumenized, abnormal
ZP:0015375	axial vasculature perforate, abnormal
ZP:0015376	splanchnocranium decreased size, abnormal
ZP:0015379	posterior cardinal vein collapsed, abnormal
ZP:0015380	cranial vasculature misrouted, abnormal
ZP:0015381	anterior cardinal vein unfused from posterior cardinal vein, abnormal
ZP:0015382	lateral dorsal aorta unfused from lateral dorsal aorta, abnormal
ZP:0015387	sperm decreased cellular motility, abnormal
ZP:0015391	fertilization decreased occurrence, abnormal
ZP:0015392	integument translucent, abnormal
ZP:0015395	iridophore eye absent, abnormal
ZP:0015403	ocular blood vessel irregular spatial pattern, abnormal
ZP:0015404	ocular blood vessel degenerate, abnormal
ZP:0015407	heart process process quality, abnormal
ZP:0015412	thigmotaxis behavioral quality of a process, abnormal
ZP:0015413	response to nicotine decreased process quality, abnormal
ZP:0015414	melanocyte sparse, abnormal
ZP:0015426	blastoderm irregular spatial pattern, abnormal
ZP:0015438	keratinocyte differentiation disrupted, abnormal
ZP:0015439	cell population proliferation increased duration, abnormal
ZP:0015440	epidermal cell increased amount, abnormal
ZP:0015441	cardiac muscle tissue development disrupted, abnormal
ZP:0015442	heart perforate, abnormal
ZP:0015448	blood cell mislocalised, abnormal
ZP:0015458	neuromast hair cell increased amount, abnormal
ZP:0015470	primordial hindbrain channel arrested blood vessel development, abnormal
ZP:0015473	intersegmental vessel arrested blood vessel development, abnormal
ZP:0015475	common cardinal vein malformed, abnormal
ZP:0015476	cranial vasculature structure, abnormal
ZP:0015479	DEL translucent, abnormal
ZP:0015480	actin filament yolk syncytial layer spatial pattern, abnormal
ZP:0015481	cortical cytoskeleton yolk syncytial layer morphology, abnormal
ZP:0015482	germ ring morphology, abnormal
ZP:0015483	lamellipodium EVL increased amount, abnormal
ZP:0015484	blastoderm cell EVL morphology, abnormal
ZP:0015485	microtubule yolk syncytial layer disorganized, abnormal
ZP:0015486	vesicle yolk syncytial layer present, abnormal
ZP:0015489	marginal blastomere constricted, abnormal
ZP:0015490	blastoderm decreased size, abnormal
ZP:0015491	shield decreased size, abnormal
ZP:0015492	shield malformed, abnormal
ZP:0015493	blastoderm cell EVL circular, abnormal
ZP:0015494	posterior lateral line decreased length, abnormal
ZP:0015498	photoreceptor outer segment layer decreased thickness, abnormal
ZP:0015499	photoreceptor outer segment retinal rod cell degenerate, abnormal
ZP:0015503	blastomere shield mislocalised, abnormal
ZP:0015514	mesencephalic vein malformed, abnormal
ZP:0015522	sinoatrial node decreased functionality, abnormal
ZP:0015525	retinal inner nuclear layer structure, abnormal
ZP:0015527	oocyte anterior/posterior axis specification disrupted, abnormal
ZP:0015528	intracellular mRNA localization disrupted, abnormal
ZP:0015529	chorion micropyle formation disrupted, abnormal
ZP:0015530	chorion malformed, abnormal
ZP:0015531	oocyte physical object quality, abnormal
ZP:0015532	oocyte positional polarity, abnormal
ZP:0015533	unfertilized egg positional polarity, abnormal
ZP:0015534	posterior region ovary neoplastic, abnormal
ZP:0015535	mitochondrial cloud oocyte absent, abnormal
ZP:0015553	iridophore decreased size, abnormal
ZP:0015554	melanocyte punctiform, abnormal
ZP:0015556	lymphocyte differentiation disrupted, abnormal
ZP:0015563	anterior region neuroectoderm increased size, abnormal
ZP:0015582	pronephros aplastic, abnormal
ZP:0015584	blood vasculature liver aplastic, abnormal
ZP:0015585	hepatocyte liver morphology, abnormal
ZP:0015589	cellular response to DNA damage stimulus increased occurrence, abnormal
ZP:0015594	endothelial cell trunk absent, abnormal
ZP:0015595	neuromast hair cell differentiation involved in neuromast regeneration decreased occurrence, abnormal
ZP:0015596	gut flattened, abnormal
ZP:0015597	liver structure, abnormal
ZP:0015598	liver low brightness, abnormal
ZP:0015608	oocyte maturation process quality, abnormal
ZP:0015609	pole plasm assembly process quality, abnormal
ZP:0015610	pole plasm mRNA localization arrested, abnormal
ZP:0015611	pole plasm mRNA localization process quality, abnormal
ZP:0015612	oocyte stage II physical object quality, abnormal
ZP:0015613	oocyte stage I symmetry, abnormal
ZP:0015620	molecular layer corpus cerebelli malformed, abnormal
ZP:0015621	axon granule cell decreased length, abnormal
ZP:0015622	granule cell cerebellum decreased amount, abnormal
ZP:0015623	Purkinje cell cerebellum decreased amount, abnormal
ZP:0015632	myelination of posterior lateral line nerve axons decreased occurrence, abnormal
ZP:0015633	posterior lateral line increased diameter, abnormal
ZP:0015634	axon posterior lateral line defasciculated, abnormal
ZP:0015635	Z disc cardiac muscle cell absent, abnormal
ZP:0015636	fin fold actinotrichium disorganized, abnormal
ZP:0015637	fin fold actinotrichium decreased mass density, abnormal
ZP:0015639	caudal fin lepidotrichium malformed, abnormal
ZP:0015640	interray vessel caudal fin disorganized, abnormal
ZP:0015641	osteoblast caudal fin mislocalised, abnormal
ZP:0015642	dorsal fin lepidotrichium undulate, abnormal
ZP:0015643	anal fin lepidotrichium undulate, abnormal
ZP:0015644	fin fold actinotrichium rough, abnormal
ZP:0015645	caudal fin lepidotrichium fused with caudal fin lepidotrichium, abnormal
ZP:0015646	caudal fin lepidotrichium undulate, abnormal
ZP:0015647	fin fold actinotrichium lepidotrichium mislocalised, abnormal
ZP:0015648	response to amphetamine arrested, abnormal
ZP:0015654	skeletal muscle myofibril myotome morphology, abnormal
ZP:0015656	brain folded, abnormal
ZP:0015665	pelvic fin hypoplastic, abnormal
ZP:0015666	pectoral fin lepidotrichium absent, abnormal
ZP:0015667	pelvic fin lepidotrichium absent, abnormal
ZP:0015668	pectoral fin bent, abnormal
ZP:0015669	pectoral fin curved, abnormal
ZP:0015670	otic vesicle protrusion aplastic, abnormal
ZP:0015671	basihyal cartilage mislocalised posteriorly, abnormal
ZP:0015672	melanocyte size, abnormal
ZP:0015673	forebrain ventricle increased size, abnormal
ZP:0015675	skeletal muscle acetylcholine-gated channel clustering process quality, abnormal
ZP:0015681	pigment granule xanthophore composition, abnormal
ZP:0015695	lymphocyte proliferation increased occurrence, abnormal
ZP:0015696	fin neoplastic, abnormal
ZP:0015697	head kidney neoplastic, abnormal
ZP:0015698	common lymphoid progenitor head kidney increased amount, abnormal
ZP:0015699	lymphocyte blood increased amount, abnormal
ZP:0015700	lymphocyte head kidney increased amount, abnormal
ZP:0015701	lymphocyte whole organism increased amount, abnormal
ZP:0015702	lymphocyte whole organism neoplastic, malignant, abnormal
ZP:0015703	erythroid lineage cell head kidney decreased amount, abnormal
ZP:0015704	lymphoid progenitor cell whole organism increased amount, abnormal
ZP:0015705	myeloid lineage restricted progenitor cell head kidney decreased amount, abnormal
ZP:0015708	endoderm absent, abnormal
ZP:0015721	epithelium pectoral fin degenerate, abnormal
ZP:0015722	pectoral fin fold degenerate, abnormal
ZP:0015723	pectoral fin necrotic, abnormal
ZP:0015724	mating decreased efficiency, abnormal
ZP:0015725	pelvic radial decreased amount, abnormal
ZP:0015726	anal fin decreased size, abnormal
ZP:0015727	dorsal fin lepidotrichium decreased length, abnormal
ZP:0015728	dorsal fin lepidotrichium malformed, abnormal
ZP:0015729	dorsal fin lepidotrichium decreased amount, abnormal
ZP:0015730	dorsal fin pterygiophore decreased amount, abnormal
ZP:0015731	anal fin pterygiophore decreased amount, abnormal
ZP:0015732	anal fin lepidotrichium decreased length, abnormal
ZP:0015733	melanophore stripe branched, abnormal
ZP:0015734	pelvic fin lepidotrichium decreased length, abnormal
ZP:0015735	pelvic fin lepidotrichium malformed, abnormal
ZP:0015736	pectoral fin radial decreased amount, abnormal
ZP:0015737	lepidotrichium segment decreased amount, abnormal
ZP:0015738	pectoral fin skeleton has fewer parts of type lepidotrichium, abnormal
ZP:0015739	axial fin skeleton has fewer parts of type lepidotrichium, abnormal
ZP:0015740	pelvic fin has fewer parts of type lepidotrichium, abnormal
ZP:0015741	pelvic fin skeleton has fewer parts of type lepidotrichium, abnormal
ZP:0015742	dorsal fin hypoplastic, abnormal
ZP:0015745	whole organism increased weight, abnormal
ZP:0015777	vertical myoseptum irregular spatial pattern, abnormal
ZP:0015778	somite border somite 11 amorphous, abnormal
ZP:0015779	somite border somite 14 amorphous, abnormal
ZP:0015780	somite border somite 17 amorphous, abnormal
ZP:0015781	somite border somite 12 amorphous, abnormal
ZP:0015782	somite border somite 15 amorphous, abnormal
ZP:0015785	somite border somite 10 amorphous, abnormal
ZP:0015786	somite border somite 13 amorphous, abnormal
ZP:0015787	somite border somite 16 amorphous, abnormal
ZP:0015788	reproductive behavior behavioral quality of a process, abnormal
ZP:0015789	dentary structure, abnormal
ZP:0015790	maxilla structure, abnormal
ZP:0015791	gill malformed, abnormal
ZP:0015792	opercular flap decreased size, abnormal
ZP:0015793	premaxilla structure, abnormal
ZP:0015794	supraorbital bone decreased size, abnormal
ZP:0015795	mandibular arch skeleton increased length, abnormal
ZP:0015796	orbital region decreased size, abnormal
ZP:0015797	neurocranium structure, abnormal
ZP:0015802	otolith physical object quality, abnormal
ZP:0015803	hair cell inner ear decreased functionality, abnormal
ZP:0015804	stereocilia tip link posterior lateral line neuromast absent, abnormal
ZP:0015805	lysosome neuromast support cell increased amount, abnormal
ZP:0015806	lysosome neuromast hair cell increased amount, abnormal
ZP:0015807	stereocilium posterior lateral line neuromast decreased diameter, abnormal
ZP:0015808	posterior lateral line neuromast physical object quality, abnormal
ZP:0015811	apical ectodermal ridge pectoral fin bud absent, abnormal
ZP:0015818	regulation of Notch signaling pathway disrupted, abnormal
ZP:0015822	detection of light stimulus disrupted, abnormal
ZP:0015823	entopterygoid decreased size, abnormal
ZP:0015824	cranium structure, abnormal
ZP:0015826	anterior region lens epithelium structure, abnormal
ZP:0015828	blood cell increased amount, abnormal
ZP:0015830	anterior lateral plate mesoderm decreased width, abnormal
ZP:0015831	dorsal region forebrain aplastic, abnormal
ZP:0015832	cell head undifferentiated, abnormal
ZP:0015840	fast muscle cell myotome disorganized, abnormal
ZP:0015846	response to mechanical stimulus disrupted, abnormal
ZP:0015853	oocyte stage I absent, abnormal
ZP:0015883	testis hypoplastic, abnormal
ZP:0015885	spermatogonium absent, abnormal
ZP:0015887	intracellular mRNA localization process quality, abnormal
ZP:0015888	central nervous system myelination decreased occurrence, abnormal
ZP:0015890	peripheral nervous system myelin maintenance process quality, abnormal
ZP:0015891	oligodendrocyte physical object quality, abnormal
ZP:0015895	cell projection oligodendrocyte mislocalised, abnormal
ZP:0015896	detection of mechanical stimulus involved in sensory perception of touch disrupted, abnormal
ZP:0015899	lapillus absent, abnormal
ZP:0015907	female gonad development process quality, abnormal
ZP:0015938	afferent neuron has extra parts of type dendritic branch afferent neuron, abnormal
ZP:0015950	notochord mislocalised, abnormal
ZP:0015977	central artery decreased amount, abnormal
ZP:0015978	central artery absent, abnormal
ZP:0015992	glomerular basement membrane decreased functionality, abnormal
ZP:0016010	left side dorsal habenular nucleus physical object quality, abnormal
ZP:0016013	leptotene arrested, abnormal
ZP:0016014	meiotic prophase I increased duration, abnormal
ZP:0016015	male meiosis I arrested, abnormal
ZP:0016016	male meiosis I increased duration, abnormal
ZP:0016017	sperm non-functional, abnormal
ZP:0016018	condensed chromosome spermatocyte morphology, abnormal
ZP:0016020	sperm sperm duct absent, abnormal
ZP:0016023	zygotene arrested, abnormal
ZP:0016024	meiotic prophase I non-progressive, abnormal
ZP:0016025	Sertoli cell apoptotic, abnormal
ZP:0016026	chromatin spermatocyte phosphorylation, abnormal
ZP:0016027	Leydig cell apoptotic, abnormal
ZP:0016038	extraocular musculature absent, abnormal
ZP:0016039	median fin fold perforate, abnormal
ZP:0016040	fin hypoplastic, abnormal
ZP:0016041	pelvic fin aplastic, abnormal
ZP:0016042	integument necrotic, abnormal
ZP:0016043	extracellular matrix chondrocyte composition, abnormal
ZP:0016049	otic epithelium decreased thickness, abnormal
ZP:0016050	startle response decreased occurrence, abnormal
ZP:0016051	semicircular canal formation delayed, abnormal
ZP:0016052	motor neuron decreased length, abnormal
ZP:0016070	heart rudiment absent, abnormal
ZP:0016071	heart absent, abnormal
ZP:0016075	whole organism transparent, abnormal
ZP:0016083	liver development delayed, abnormal
ZP:0016084	whole organism lacks parts or has fewer parts of type pharyngeal arch cartilage, abnormal
ZP:0016085	whole organism lacks all parts of type pharyngeal arch 3-7 skeleton, abnormal
ZP:0016086	trunk musculature degenerate, abnormal
ZP:0016087	ceratohyal cartilage oriented, abnormal
ZP:0016092	yolk condensed, abnormal
ZP:0016093	yolk teardrop-shaped, abnormal
ZP:0016094	anterior region trunk decreased thickness, abnormal
ZP:0016095	posterior region trunk increased width, abnormal
ZP:0016096	anterior region trunk kinked, abnormal
ZP:0016097	dorsal-ventral axis head increased height, abnormal
ZP:0016098	posterior region trunk bulbous, abnormal
ZP:0016104	epithelial cell intrahepatic bile duct disorganized, abnormal
ZP:0016121	parasphenoid bent, abnormal
ZP:0016132	hepatocyte spatial pattern, abnormal
ZP:0016133	hepatocyte apical-basal polarity, abnormal
ZP:0016134	skeletal muscle contraction decreased magnitude, abnormal
ZP:0016135	trunk musculature decreased contractility, abnormal
ZP:0016136	trunk decreased angle to anterior-posterior axis whole organism, abnormal
ZP:0016137	post-vent region decreased contractility, abnormal
ZP:0016138	cell communication by electrical coupling arrested, abnormal
ZP:0016139	slow muscle cell electrical conductivity, abnormal
ZP:0016140	retinal rod cell retinal outer nuclear layer increased amount, abnormal
ZP:0016141	ceratohyal cartilage disorganized, abnormal
ZP:0016142	slow-twitch skeletal muscle fiber contraction amplitude, abnormal
ZP:0016145	glucose import in response to insulin stimulus decreased process quality, abnormal
ZP:0016147	cardiac ventricle increased thickness, abnormal
ZP:0016148	interrenal gland hyperplastic, abnormal
ZP:0016152	ventral wall of dorsal aorta has fewer parts of type nucleate erythrocyte, abnormal
ZP:0016158	whole organism lacks all parts of type iridophore, abnormal
ZP:0016159	cardiac muscle progenitor cell migration to the midline involved in heart field formation process quality, abnormal
ZP:0016176	pharyngeal arch cartilage loose, abnormal
ZP:0016177	prechordal plate apoptotic, abnormal
ZP:0016178	hatching gland cell decreased size, abnormal
ZP:0016179	anterior region prechordal plate apoptotic, abnormal
ZP:0016180	regulation of muscle contraction disrupted, abnormal
ZP:0016181	head curved dorsal, abnormal
ZP:0016182	hindbrain neural rod decreased diameter, abnormal
ZP:0016183	hindbrain flat, abnormal
ZP:0016184	hindbrain neural rod flat, abnormal
ZP:0016185	hindbrain neural rod decreased thickness, abnormal
ZP:0016187	blood circulation decreased intensity, abnormal
ZP:0016188	neuroepithelial cell apoptotic, abnormal
ZP:0016189	medial longitudinal fasciculus fasciculation, abnormal
ZP:0016190	hindbrain commissure decreased size, abnormal
ZP:0016191	chromosome brain broken, abnormal
ZP:0016192	chromosome spinal cord broken, abnormal
ZP:0016193	chromosome neuroectoderm broken, abnormal
ZP:0016194	proliferative region tail bud apoptotic, abnormal
ZP:0016195	telencephalon mislocalised anteriorly, abnormal
ZP:0016196	hindbrain has fewer parts of type grey matter, abnormal
ZP:0016197	radial glial cell decreased amount, abnormal
ZP:0016199	post-vent region degenerate, abnormal
ZP:0016200	hypothalamus degenerate, abnormal
ZP:0016201	thalamus degenerate, abnormal
ZP:0016202	immature eye degenerate, abnormal
ZP:0016207	olfactory epithelium hypoplastic, abnormal
ZP:0016211	inner ear distended, abnormal
ZP:0016212	inner ear morphogenesis delayed, abnormal
ZP:0016213	auditory behavior decreased process quality, abnormal
ZP:0016214	equilibrioception decreased process quality, abnormal
ZP:0016218	nucleate erythrocyte colorless, abnormal
ZP:0016228	forebrain hemorrhagic, abnormal
ZP:0016229	chondrocyte structure, abnormal
ZP:0016232	neurocranial trabecula kinked, abnormal
ZP:0016235	palatoquadrate cartilage increased thickness, abnormal
ZP:0016236	Meckel's cartilage kinked, abnormal
ZP:0016237	ventral mandibular arch increased length, abnormal
ZP:0016240	xanthophore increased fluorescence, abnormal
ZP:0016246	xanthophore white, abnormal
ZP:0016249	xanthophore pinnate, abnormal
ZP:0016250	pterinosome xanthophore composition, abnormal
ZP:0016251	xanthophore head desaturated yellow, abnormal
ZP:0016252	xanthophore head granular, abnormal
ZP:0016253	iris decreased size, abnormal
ZP:0016254	xanthophore head brown, abnormal
ZP:0016256	xanthophore brown, abnormal
ZP:0016259	xanthophore shape, abnormal
ZP:0016260	iridophore white, abnormal
ZP:0016261	xanthophore composition, abnormal
ZP:0016262	cell projection melanocyte decreased amount, abnormal
ZP:0016263	central region melanocyte decreased pigmentation, abnormal
ZP:0016264	melanocyte star shaped, abnormal
ZP:0016265	ventral larval melanophore stripe decreased width, abnormal
ZP:0016266	swim bladder lacks all parts of type dorsal region melanocyte, abnormal
ZP:0016267	ventral larval melanophore stripe lacks all parts of type dorsal region melanocyte, abnormal
ZP:0016268	ventral region ventral larval melanophore stripe patchy, abnormal
ZP:0016269	yolk larval melanophore stripe has fewer parts of type iridophore, abnormal
ZP:0016270	iridophore yolk larval melanophore stripe irregular spatial pattern, abnormal
ZP:0016271	trunk increased accumulation ventro-lateral region melanocyte, abnormal
ZP:0016272	trunk increased accumulation ventro-lateral region iridophore, abnormal
ZP:0016273	post-vent region increased accumulation ventro-lateral region melanocyte, abnormal
ZP:0016274	post-vent region increased accumulation ventro-lateral region iridophore, abnormal
ZP:0016279	oral ectoderm mislocalised dorsally, abnormal
ZP:0016280	cilium peripheral olfactory organ absent, abnormal
ZP:0016281	cilium macula absent, abnormal
ZP:0016286	mandibular arch skeleton apoptotic, abnormal
ZP:0016287	pharyngeal arch 2 skeleton apoptotic, abnormal
ZP:0016288	dorsal hyoid arch decreased size, abnormal
ZP:0016289	ventral hyoid arch decreased size, abnormal
ZP:0016290	pharyngeal arch 3-7 fused with pharyngeal arch 3-7, abnormal
ZP:0016291	chondrocyte proliferation increased occurrence, abnormal
ZP:0016294	dorsal hyoid arch shape, abnormal
ZP:0016295	pharyngeal arch cartilage associated with pharyngeal arch cartilage, abnormal
ZP:0016297	oral ectoderm mislocalised laterally, abnormal
ZP:0016302	anterior region trunk bent, abnormal
ZP:0016303	osteoblast cranium mislocalised, abnormal
ZP:0016313	blood vessel increased amount, abnormal
ZP:0016321	head increased accumulation epidermal cell, abnormal
ZP:0016327	retinal cone cell disorganized, abnormal
ZP:0016328	cranial ganglion maturation decreased process quality, abnormal
ZP:0016329	glossopharyngeal ganglion poorly differentiated, abnormal
ZP:0016330	vagal ganglion 1 poorly differentiated, abnormal
ZP:0016331	vagal ganglion 2 poorly differentiated, abnormal
ZP:0016332	vagal ganglion 3 poorly differentiated, abnormal
ZP:0016333	axon upper rhombic lip decreased amount, abnormal
ZP:0016334	cell motility disrupted, abnormal
ZP:0016335	neutrophil decreased cellular motility, abnormal
ZP:0016341	symplectic length, abnormal
ZP:0016355	substrate-dependent cell migration, cell attachment to substrate disrupted, abnormal
ZP:0016356	melanocyte spheroid, abnormal
ZP:0016364	whole organism low brightness, abnormal
ZP:0016365	swimming behavior increased occurrence, abnormal
ZP:0016367	synapse assembly process quality, abnormal
ZP:0016368	brain size, abnormal
ZP:0016375	nucleolus liver increased amount, abnormal
ZP:0016378	actin filament polymerization decreased occurrence, abnormal
ZP:0016379	filamentous actin heart decreased amount, abnormal
ZP:0016380	heart distended, abnormal
ZP:0016381	myofibril myocardium structure, abnormal
ZP:0016382	myofibril myocardium decreased length, abnormal
ZP:0016383	myofibril heart disorganized, abnormal
ZP:0016384	heart increased contractility, abnormal
ZP:0016405	fat cell pleuroperitoneal cavity increased amount, abnormal
ZP:0016407	response to light stimulus increased process quality, abnormal
ZP:0016413	karyomere membrane fusion disrupted, abnormal
ZP:0016414	nucleus blastomere lobate, abnormal
ZP:0016415	karyomere blastomere life span, abnormal
ZP:0016416	karyomere blastomere morphology, abnormal
ZP:0016417	karyomere blastomere increased amount, abnormal
ZP:0016418	pronucleus cell present, abnormal
ZP:0016419	blastodisc morphology, abnormal
ZP:0016434	lens broken, abnormal
ZP:0016435	iris closed, abnormal
ZP:0016436	lens capsule deformed, abnormal
ZP:0016437	retina low brightness, abnormal
ZP:0016438	retina rough, abnormal
ZP:0016439	artery retina sinuous, abnormal
ZP:0016440	retina spotted, abnormal
ZP:0016441	retinal pigmented epithelium detached from pigmented epithelial cell, abnormal
ZP:0016442	pigmented epithelial cell located in retinal inner plexiform layer, abnormal
ZP:0016445	intestine low brightness, abnormal
ZP:0016446	response to oxidative stress process quality, abnormal
ZP:0016451	mRNA export from nucleus disrupted, abnormal
ZP:0016452	chondroblast pharyngeal arch 3-7 skeleton absent, abnormal
ZP:0016453	pharyngeal arch has fewer parts of type chondroblast nuclear pore chondroblast, abnormal
ZP:0016454	chondroblast pharyngeal arch 2 decreased amount, abnormal
ZP:0016455	chondroblast pharyngeal arch 1 decreased amount, abnormal
ZP:0016456	chondrocyte pharyngeal arch 3-7 skeleton absent, abnormal
ZP:0016457	chondrocyte pharyngeal arch 2 decreased amount, abnormal
ZP:0016458	chondrocyte pharyngeal arch 1 decreased amount, abnormal
ZP:0016459	intestine smooth, abnormal
ZP:0016460	nuclear pore intestine aggregated, abnormal
ZP:0016461	nuclear pore retina aggregated, abnormal
ZP:0016462	nuclear pore optic tectum aggregated, abnormal
ZP:0016463	nuclear pore pharyngeal arch aggregated, abnormal
ZP:0016465	hepatocyte detached from liver, abnormal
ZP:0016466	pelvic fin development disrupted, abnormal
ZP:0016470	mesoderm pelvic fin bud present, abnormal
ZP:0016471	pelvic fin skeleton absent, abnormal
ZP:0016472	apical ectodermal ridge pelvic fin bud absent, abnormal
ZP:0016474	peroxidase activity disrupted, abnormal
ZP:0016484	olfactory pit increased size, abnormal
ZP:0016485	adenohypophyseal placode increased size, abnormal
ZP:0016493	head has fewer parts of type melanocyte, abnormal
ZP:0016494	Meckel's cartilage curved ventral, abnormal
ZP:0016495	ethmoid cartilage curved ventral, abnormal
ZP:0016496	dorsal root ganglion lacks parts or has fewer parts of type glial cell (sensu Vertebrata), abnormal
ZP:0016497	posterior lateral line separated from melanocyte, abnormal
ZP:0016498	posterior lateral line has extra parts of type melanocyte, abnormal
ZP:0016499	trunk has extra parts of type melanocyte, abnormal
ZP:0016500	post-vent region has extra parts of type melanocyte, abnormal
ZP:0016501	trunk has fewer parts of type dorsal region iridophore, abnormal
ZP:0016502	retinal rod cell absent, abnormal
ZP:0016508	collateral sprouting in absence of injury process quality, abnormal
ZP:0016514	axon collateral RoP motor neuron mislocalised, abnormal
ZP:0016515	axon collateral CaP motoneuron mislocalised, abnormal
ZP:0016519	vertebral column malformed, abnormal
ZP:0016524	retina hyperplastic, abnormal
ZP:0016526	cell migration involved in heart jogging decreased process quality, abnormal
ZP:0016527	endocardial precursor heart rudiment mislocalised, abnormal
ZP:0016528	myocardial precursor heart rudiment mislocalised, abnormal
ZP:0016533	keratin filament epidermal cell spatial pattern, abnormal
ZP:0016546	habituation decreased process quality, abnormal
ZP:0016550	pigment cell development decreased process quality, abnormal
ZP:0016561	vertebral column morphology, abnormal
ZP:0016567	central nervous system morphogenesis disrupted, abnormal
ZP:0016568	rhombomere 4 morphogenesis disrupted, abnormal
ZP:0016569	cell division absent, abnormal
ZP:0016570	regulation of cell division disrupted, abnormal
ZP:0016571	ectodermal placode development disrupted, abnormal
ZP:0016572	anterior macula has fewer parts of type auditory receptor cell, abnormal
ZP:0016573	anterior macula unstratified, abnormal
ZP:0016574	reticular formation structure, abnormal
ZP:0016575	pharyngeal endoderm decreased size, abnormal
ZP:0016576	optic cup hypoplastic, abnormal
ZP:0016577	solid lens vesicle protruding out of immature eye, abnormal
ZP:0016578	protoneuromast absent, abnormal
ZP:0016579	neuron increased size, abnormal
ZP:0016580	dorsal region hindbrain disorganized, abnormal
ZP:0016581	ventral region forebrain structure, abnormal
ZP:0016582	microtubule neuron molecular quality, abnormal
ZP:0016583	cell floor plate increased size, abnormal
ZP:0016584	floor plate separated from cell cell floor plate, abnormal
ZP:0016585	cell hypochord increased size, abnormal
ZP:0016586	hypochord separated from cell cell hypochord, abnormal
ZP:0016587	neuron central nervous system decreased amount, abnormal
ZP:0016588	cell cycle lacking processual parts cytokinesis, abnormal
ZP:0016589	nucleus whole organism increased size, abnormal
ZP:0016590	cell cycle lacking processual parts DNA replication, abnormal
ZP:0016591	interneuron axon guidance disrupted, abnormal
ZP:0016592	axon hindbrain commissure disorganized, abnormal
ZP:0016593	axon Mauthner neuron decreased amount, abnormal
ZP:0016594	otic placode morphology, abnormal
ZP:0016596	axon CaP motoneuron decreased branchiness, abnormal
ZP:0016609	hepatocyte ballooning, abnormal
ZP:0016626	atrial endocardium mislocalised, abnormal
ZP:0016647	notochord separated from notochord inner cell notochord inner cell, abnormal
ZP:0016648	vertebra immature, abnormal
ZP:0016649	vertebral column discontinuous bone development, abnormal
ZP:0016650	vertebral column disrupted bone development, abnormal
ZP:0016651	notochord has extra parts of type anatomical space, abnormal
ZP:0016652	notochord outer sheath cell proliferative, abnormal
ZP:0016653	notochord inner cell decreased size, abnormal
ZP:0016654	nucleus notochord spherical, abnormal
ZP:0016655	nucleus notochord decondensed, abnormal
ZP:0016656	cytoplasm notochord inner cell increased volume, abnormal
ZP:0016657	notochord inner cell lacks parts or has fewer parts of type cytoplasm intermediate filament notochord inner cell, abnormal
ZP:0016658	intermediate filament notochord inner cell morphology, abnormal
ZP:0016659	anatomical space notochord mislocalised, abnormal
ZP:0016660	cell notochord proliferative, abnormal
ZP:0016668	palate morphology, abnormal
ZP:0016669	palate decreased length, abnormal
ZP:0016671	nucleus notochord increased amount, abnormal
ZP:0016682	integument transparent, abnormal
ZP:0016683	gold iridophore absent, abnormal
ZP:0016684	silver iridophore absent, abnormal
ZP:0016685	melanosome retinal pigmented epithelium absent, abnormal
ZP:0016686	silver iridophore iris stroma absent, abnormal
ZP:0016692	xanthophore color pattern, abnormal
ZP:0016693	iridophore color pattern, abnormal
ZP:0016694	dorsal-most region melanophore stripe color pattern, abnormal
ZP:0016697	type B pancreatic cell proliferation increased occurrence, abnormal
ZP:0016704	neurocranial trabecula morphology, abnormal
ZP:0016711	angiogenic sprout intersegmental vessel decreased length, abnormal
ZP:0016742	pectoral fin exserted, abnormal
ZP:0016743	pectoral fin increased angle to trunk, abnormal
ZP:0016745	exocrine pancreas disrupted cell migration, abnormal
ZP:0016747	intersegmental vessel delayed angiogenesis, abnormal
ZP:0016755	angiogenesis increased process quality, abnormal
ZP:0016758	intersegmental vessel has extra parts of type filopodium endothelial cell, abnormal
ZP:0016759	intersegmental vessel increased process quality sprouting angiogenesis, abnormal
ZP:0016766	liver increased occurrence apoptotic process, abnormal
ZP:0016769	common bile duct dilated, abnormal
ZP:0016773	cranial vasculature absent, abnormal
ZP:0016788	vertebra dysplastic, abnormal
ZP:0016789	vertebra delayed bone mineralization, abnormal
ZP:0016791	macrophage abnormal, abnormal
ZP:0016792	melanocyte eye absent, abnormal
ZP:0016794	photoreceptor cell abnormal, abnormal
ZP:0016807	histone methylation decreased process quality, abnormal
ZP:0016808	heart hypertrophic, abnormal
ZP:0016823	optic vesicle has extra parts of type hair cell, abnormal
ZP:0016824	heart lacks parts or has fewer parts of type mitochondrion heart, abnormal
ZP:0016825	mitochondrion heart degenerate, abnormal
ZP:0016826	mitochondrial crista heart deformed, abnormal
ZP:0016836	ventral region presumptive ectoderm physical object quality, abnormal
ZP:0016837	ventral region ectoderm physical object quality, abnormal
ZP:0016841	melanoma post-vent region present, abnormal
ZP:0016849	microglia development decreased occurrence, abnormal
ZP:0016850	brain lacks all parts of type macrophage, abnormal
ZP:0016851	brain has extra parts of type neutrophil, abnormal
ZP:0016852	neutrophil brain mislocalised, abnormal
ZP:0016853	brain has fewer parts of type microglial cell, abnormal
ZP:0016854	macrophage activation increased process quality, abnormal
ZP:0016855	whole organism has fewer parts of type macrophage, abnormal
ZP:0016856	macrophage ball apoptotic, abnormal
ZP:0016857	macrophage ball vacuolated, abnormal
ZP:0016858	whole organism inflamed, abnormal
ZP:0016859	macrophage ball mislocalised, abnormal
ZP:0016860	macrophage ball aggregated, abnormal
ZP:0016861	neutrophil adjacent to macrophage, abnormal
ZP:0016862	fast muscle cell process quality skeletal myofibril assembly, abnormal
ZP:0016863	T-tubule fast muscle cell disorganized, abnormal
ZP:0016864	slow muscle cell process quality skeletal myofibril assembly, abnormal
ZP:0016866	myofibril skeletal muscle cell irregular spatial pattern, abnormal
ZP:0016879	splanchnocranium absent, abnormal
ZP:0016893	intestinal epithelium hypertrophic, abnormal
ZP:0016901	CaP motoneuron decreased length, abnormal
ZP:0016907	visual behavior decreased occurrence, abnormal
ZP:0016910	locomotion involved in locomotory behavior decreased occurrence, abnormal
ZP:0016919	branchiomotor neuron decreased occurrence neuron migration, abnormal
ZP:0016941	hindbrain neoplastic, abnormal
ZP:0016942	eye increased pigmentation, abnormal
ZP:0016958	intersegmental vein increased branchiness, abnormal
ZP:0016987	glial cell vagal ganglion absent, abnormal
ZP:0017002	cell integument aggregated, abnormal
ZP:0017007	precaudal vertebra condensed, abnormal
ZP:0017011	swim bladder development delayed, abnormal
ZP:0017012	centrum decreased amount, abnormal
ZP:0017013	vertebra decreased length, abnormal
ZP:0017014	vertebra decreased amount, abnormal
ZP:0017015	vertebra has extra parts of type hemal arch, abnormal
ZP:0017016	vertebra has extra parts of type neural arch, abnormal
ZP:0017024	trunk absent blood circulation, abnormal
ZP:0017030	thyroid follicle absent, abnormal
ZP:0017038	forebrain absent, abnormal
ZP:0017046	caudal vein plexus has fewer parts of type endothelial cell, abnormal
ZP:0017055	nucleate erythrocyte accumulation trunk, abnormal
ZP:0017070	mitochondrial cloud oocyte stage I absent, abnormal
ZP:0017075	radial glial cell spinal cord morphology, abnormal
ZP:0017077	pronephric podocyte apoptotic, abnormal
ZP:0017085	ventral wall of dorsal aorta has extra parts of type hematopoietic stem cell, abnormal
ZP:0017087	myelinating Schwann cell posterior lateral line circular, abnormal
ZP:0017097	lymphangiogenesis decreased process quality, abnormal
ZP:0017105	male sex determination increased occurrence, abnormal
ZP:0017108	melanosome localization process quality, abnormal
ZP:0017113	cell cardiac ventricle spatial pattern, abnormal
ZP:0017118	slit diaphragm pronephric glomerulus decreased amount, abnormal
ZP:0017122	cardiac ventricle size, abnormal
ZP:0017123	atrium size, abnormal
ZP:0017127	vascular lymphangioblast increased amount, abnormal
ZP:0017130	mandibular arch skeleton decreased amount, abnormal
ZP:0017134	diencephalon mislocalised, abnormal
ZP:0017145	neural plate apoptotic, abnormal
ZP:0017146	neural crest cell fate specification disrupted, abnormal
ZP:0017147	hindbrain increased width, abnormal
ZP:0017148	neural crest decreased thickness, abnormal
ZP:0017149	midbrain increased width, abnormal
ZP:0017150	neural crest morphology, abnormal
ZP:0017157	blood accumulation atrium, abnormal
ZP:0017159	anatomical margin EVL scalloped, abnormal
ZP:0017160	EVL detached from blastoderm cell blastoderm cell EVL, abnormal
ZP:0017162	anatomical margin EVL disorganized, abnormal
ZP:0017163	involution involved in gastrulation with mouth forming second delayed, abnormal
ZP:0017178	retinoic acid receptor signaling pathway decreased occurrence, abnormal
ZP:0017187	retinal inner nuclear layer lacks all parts of type Muller cell, abnormal
ZP:0017188	retina decreased area, abnormal
ZP:0017189	whole organism lacks parts or has fewer parts of type neuron projection retinal ganglion cell, abnormal
ZP:0017190	photoreceptor cell shortened, abnormal
ZP:0017191	horizontal cell decreased amount, abnormal
ZP:0017192	neuron projection amacrine cell decreased amount, abnormal
ZP:0017193	compartment boundary rhombomere disorganized, abnormal
ZP:0017198	posterior region whole organism decreased size, abnormal
ZP:0017200	vH ionocyte increased amount, abnormal
ZP:0017201	vH ionocyte gill increased amount, abnormal
ZP:0017215	actin filament somite disorganized, abnormal
ZP:0017216	actin filament somite decondensed, abnormal
ZP:0017217	focal adhesion somite decreased amount, abnormal
ZP:0017233	hatching decreased rate, abnormal
ZP:0017234	cardiac muscle cell heart decreased contractility, abnormal
ZP:0017235	cell whole organism low brightness, abnormal
ZP:0017236	cell whole organism spherical, abnormal
ZP:0017238	pharyngeal musculature absent, abnormal
ZP:0017239	levator arcus palatini undifferentiated, abnormal
ZP:0017240	dilatator operculi undifferentiated, abnormal
ZP:0017241	basal plate cartilage decreased length, abnormal
ZP:0017242	basal plate cartilage increased width, abnormal
ZP:0017243	hypobranchial cartilage absent, abnormal
ZP:0017244	head arrested skeletal system development, abnormal
ZP:0017245	cell pharyngeal arch cartilage undifferentiated, abnormal
ZP:0017246	heart valve decreased functionality, abnormal
ZP:0017251	liver hemorrhagic, abnormal
ZP:0017252	liver increased accumulation nucleate erythrocyte, abnormal
ZP:0017253	lateral crista primordium morphology, abnormal
ZP:0017254	posterior crista primordium morphology, abnormal
ZP:0017255	anterior crista primordium morphology, abnormal
ZP:0017256	whole organism semi-fertile, abnormal
ZP:0017258	ciliary marginal zone hypotrophic, abnormal
ZP:0017259	ciliary marginal zone vacuolated, abnormal
ZP:0017260	xanthophore unpigmented, abnormal
ZP:0017263	endocardium absent, abnormal
ZP:0017266	xanthophore whole organism absent, abnormal
ZP:0017267	chondrocyte pharyngeal arch cartilage morphology, abnormal
ZP:0017268	pharyngeal arch cartilage kinked, abnormal
ZP:0017269	trabecula cranii right angle to ethmoid cartilage, abnormal
ZP:0017278	myotome lacks all parts of type myofibril skeletal muscle cell, abnormal
ZP:0017279	caudal fin lower lobe mislocalised, abnormal
ZP:0017280	cerebral spinal fluid ventricular system decreased fluid flow, abnormal
ZP:0017281	pronephric glomerulus distended, abnormal
ZP:0017282	pronephric podocyte has fewer parts of type cell projection pronephric podocyte, abnormal
ZP:0017283	cell pronephric glomerulus distributed, abnormal
ZP:0017284	cell pronephric glomerulus flattened, abnormal
ZP:0017285	cell pronephric glomerular basement membrane distributed, abnormal
ZP:0017286	pronephric glomerulus flattened, abnormal
ZP:0017287	glomerular capillary distended, abnormal
ZP:0017288	pronephric glomerular basement membrane decreased thickness, abnormal
ZP:0017289	pronephric glomerulus loose, abnormal
ZP:0017290	prechordal plate absent, abnormal
ZP:0017291	axial mesoderm absent, abnormal
ZP:0017292	axial chorda mesoderm hypoplastic, abnormal
ZP:0017293	neural keel hypoplastic, abnormal
ZP:0017294	ventral-most region floor plate spinal cord region hypoplastic, abnormal
ZP:0017295	ventral region diencephalon hypoplastic, abnormal
ZP:0017296	ventral region midbrain hypoplastic, abnormal
ZP:0017297	Kupffer's vesicle absent, abnormal
ZP:0017298	midbrain-hindbrain boundary morphogenesis process quality, abnormal
ZP:0017309	retinal inner nuclear layer increased occurrence cell death, abnormal
ZP:0017311	cell ventral fin fold mislocalised, abnormal
ZP:0017313	epithelium pronephric tubule flattened, abnormal
ZP:0017314	retinal outer plexiform layer absent, abnormal
ZP:0017315	pharyngeal endoderm aplastic, abnormal
ZP:0017316	proctodeum absent, abnormal
ZP:0017317	intestine absent, abnormal
ZP:0017318	kidney morphogenesis disrupted, abnormal
ZP:0017319	heart rudiment split, abnormal
ZP:0017320	pronephric duct mislocalised laterally, abnormal
ZP:0017321	erythroblast mislocalised laterally, abnormal
ZP:0017322	forerunner cell group absent, abnormal
ZP:0017325	melanosome melanocyte position, abnormal
ZP:0017326	retinal rod cell decreased length, abnormal
ZP:0017327	photoreceptor outer segment layer apoptotic, abnormal
ZP:0017330	cell brain spherical, abnormal
ZP:0017331	cell spinal cord spherical, abnormal
ZP:0017332	axis condensed, abnormal
ZP:0017333	integument head texture, abnormal
ZP:0017334	cell fin circular, abnormal
ZP:0017335	myotome has fewer parts of type myofibril skeletal muscle cell, abnormal
ZP:0017337	melanocyte dorsal larval melanophore stripe mislocalised laterally, abnormal
ZP:0017338	pharyngeal arch 3-7 skeleton necrotic, abnormal
ZP:0017339	mandibular arch skeleton necrotic, abnormal
ZP:0017340	pharyngeal arch 2 skeleton necrotic, abnormal
ZP:0017341	melanocyte decreased thickness, abnormal
ZP:0017342	melanocyte elongated, abnormal
ZP:0017344	striated muscle thin filament muscle cell striated, abnormal
ZP:0017345	hyoid muscle aplastic/hypoplastic, abnormal
ZP:0017346	cranium dysplastic, abnormal
ZP:0017347	head muscle dysplastic, abnormal
ZP:0017348	interhyoideus displaced, abnormal
ZP:0017349	muscle cell striated, abnormal
ZP:0017350	muscle cell shortened, abnormal
ZP:0017351	striated muscle myosin thick filament muscle cell striated, abnormal
ZP:0017352	anterior commissure disorganized, abnormal
ZP:0017353	chondrocyte Meckel's cartilage neoplastic, abnormal
ZP:0017355	chondrocyte pharyngeal arch cartilage neoplastic, abnormal
ZP:0017356	chondrocyte neurocranium neoplastic, abnormal
ZP:0017358	cardiac ventricle aplastic, abnormal
ZP:0017359	post-vent region has fewer parts of type yolk larval melanophore stripe melanocyte, abnormal
ZP:0017360	ventral side caudal fin aplastic, abnormal
ZP:0017363	diencephalon bilateral, abnormal
ZP:0017364	determination of ventral identity process quality, abnormal
ZP:0017365	ventricular system aplastic, abnormal
ZP:0017366	somite post-vent region increased width, abnormal
ZP:0017368	notochord trunk aplastic, abnormal
ZP:0017369	trunk has fewer parts of type cell notochord, abnormal
ZP:0017374	axon posterior lateral line nerve decreased length, abnormal
ZP:0017376	somite trunk aplastic, abnormal
ZP:0017378	presumptive paraxial mesoderm morphology, abnormal
ZP:0017379	trunk lacks all parts of type somite, abnormal
ZP:0017380	cell accumulation caudal fin, abnormal
ZP:0017381	muscle trunk malformed, abnormal
ZP:0017382	muscle trunk disorganized, abnormal
ZP:0017386	segment polarity determination disrupted, abnormal
ZP:0017390	desmosome assembly disrupted, abnormal
ZP:0017391	desmosome epidermal cell decreased amount, abnormal
ZP:0017392	desmosome epidermal cell malformed, abnormal
ZP:0017393	gut decreased functionality, abnormal
ZP:0017394	atrioventricular valve development arrested, abnormal
ZP:0017395	atrioventricular ring immature, abnormal
ZP:0017396	whole organism contractility, abnormal
ZP:0017397	pronephric proximal straight tubule increased length, abnormal
ZP:0017401	gliogenesis disrupted, abnormal
ZP:0017402	pleuroperitoneal cavity edematous, abnormal
ZP:0017403	anterior-posterior axis whole organism increased width, abnormal
ZP:0017414	pronephric proximal tubule morphogenesis process quality, abnormal
ZP:0017418	pronephric proximal convoluted tubule increased occurrence apoptotic process, abnormal
ZP:0017424	pronephros decreased process quality renal absorption, abnormal
ZP:0017426	eye photoreceptor cell lacks parts or has fewer parts of type photoreceptor outer segment eye photoreceptor cell, abnormal
ZP:0017427	eye photoreceptor cell has fewer parts of type photoreceptor connecting cilium eye photoreceptor cell, abnormal
ZP:0017428	apical region eye photoreceptor cell decreased length, abnormal
ZP:0017429	apical region eye photoreceptor cell decreased area, abnormal
ZP:0017430	eye photoreceptor cell decreased process quality establishment of apical/basal cell polarity, abnormal
ZP:0017432	endosome pronephric duct increased size, abnormal
ZP:0017433	endosome pronephric duct decreased amount, abnormal
ZP:0017434	endocytic vesicle pronephric duct decreased amount, abnormal
ZP:0017435	pronephros decreased process quality endocytosis, abnormal
ZP:0017436	pronephros process quality endocytic recycling, abnormal
ZP:0017441	macrophage activation involved in immune response disrupted, abnormal
ZP:0017445	macrophage morphology, abnormal
ZP:0017446	macrophage whole organism spatial pattern, abnormal
ZP:0017447	macrophage trunk decreased cellular motility, abnormal
ZP:0017448	anatomical region statoacoustic (VIII) ganglion decreased size, abnormal
ZP:0017449	photoreceptor cell morphogenesis decreased process quality, abnormal
ZP:0017450	camera-type eye photoreceptor cell differentiation decreased occurrence, abnormal
ZP:0017452	photoreceptor inner segment photoreceptor cell physical object quality, abnormal
ZP:0017454	blood coagulation, fibrin clot formation decreased occurrence, abnormal
ZP:0017455	thrombocyte cellular adhesivity, abnormal
ZP:0017456	intestine has extra parts of type neutrophil, abnormal
ZP:0017457	neutrophil intestine increased amount, abnormal
ZP:0017458	gut epithelium permeability, abnormal
ZP:0017459	brush border gut epithelium decreased size, abnormal
ZP:0017460	intestinal epithelial cell decreased height, abnormal
ZP:0017461	intestinal epithelial cell cuboid, abnormal
ZP:0017462	intestinal epithelial cell decreased process quality DNA methylation, abnormal
ZP:0017463	intestinal epithelial cell increased process quality apoptotic process, abnormal
ZP:0017464	hypoblast process quality calcium-mediated signaling, abnormal
ZP:0017465	Kupffer's vesicle decreased process quality cilium movement, abnormal
ZP:0017466	lymphoid progenitor cell thymus absent, abnormal
ZP:0017480	cell retina circular, abnormal
ZP:0017481	anatomical axis trunk decreased length, abnormal
ZP:0017482	ventral region whole organism increased thickness, abnormal
ZP:0017483	axis distended, abnormal
ZP:0017484	cilium movement frequency, abnormal
ZP:0017485	fast muscle cell arrested myoblast fusion, abnormal
ZP:0017486	ventricular cardiac muscle cell action potential absent, abnormal
ZP:0017487	ventricular cardiac muscle cell action potential increased duration, abnormal
ZP:0017488	membrane repolarization during cardiac muscle cell action potential decreased process quality, abnormal
ZP:0017489	midbrain hindbrain boundary disorganized, abnormal
ZP:0017490	diencephalon disorganized, abnormal
ZP:0017491	tegmentum disorganized, abnormal
ZP:0017492	hematopoietic stem cell differentiation decreased occurrence, abnormal
ZP:0017494	whole organism has fewer parts of type hematopoietic stem cell, abnormal
ZP:0017495	optic tectum process quality transmission of nerve impulse, abnormal
ZP:0017496	sleep decreased duration, abnormal
ZP:0017506	locomotion involved in locomotory behavior increased process quality, abnormal
ZP:0017507	melanosome assembly process quality, abnormal
ZP:0017508	melanosome retinal pigmented epithelium morphology, abnormal
ZP:0017509	photoreceptor outer segment photoreceptor cell morphology, abnormal
ZP:0017510	photoreceptor outer segment photoreceptor cell structure, abnormal
ZP:0017511	epidermal basal stratum decreased process quality epithelial cell morphogenesis, abnormal
ZP:0017512	ecto-epithelial cell epidermal basal stratum oblong, abnormal
ZP:0017513	spinal cord process quality generation of neurons, abnormal
ZP:0017514	laminin complex median fin fold increased amount, abnormal
ZP:0017515	median fin fold decreased occurrence epithelial cell proliferation, abnormal
ZP:0017516	epidermal basal stratum decreased height, abnormal
ZP:0017517	epidermal basal stratum increased process quality canonical Wnt signaling pathway, abnormal
ZP:0017518	ecto-epithelial cell epidermal basal stratum elongated, abnormal
ZP:0017523	cilium otic vesicle absent, abnormal
ZP:0017532	neutrophil morphology, abnormal
ZP:0017535	telencephalon development decreased process quality, abnormal
ZP:0017537	cerebellum size, abnormal
ZP:0017538	dorsal telencephalon has extra parts of type neuron, abnormal
ZP:0017539	dorsal telencephalon decreased process quality Notch signaling pathway, abnormal
ZP:0017540	dorsal telencephalon increased occurrence neurogenesis, abnormal
ZP:0017541	neuron projection dorsal telencephalon decreased branchiness, abnormal
ZP:0017542	dorsal telencephalon decreased occurrence neuron projection morphogenesis, abnormal
ZP:0017543	neuronal stem cell dorsal telencephalon proliferative, abnormal
ZP:0017544	neuron dorsal telencephalon immature, abnormal
ZP:0017545	ventricular zone decreased process quality Notch signaling pathway, abnormal
ZP:0017546	paraxial mesoderm decreased process quality Notch signaling pathway, abnormal
ZP:0017547	paraxial mesoderm decreased process quality fibroblast growth factor receptor signaling pathway, abnormal
ZP:0017548	axis elongation decreased rate, abnormal
ZP:0017549	anterior region axis decreased thickness, abnormal
ZP:0017550	caudal vein plexus process quality sprouting angiogenesis, abnormal
ZP:0017551	caudal vein plexus has fewer parts of type blood vessel endothelial cell filopodium blood vessel endothelial cell, abnormal
ZP:0017553	retinal ganglion cell layer increased thickness, abnormal
ZP:0017554	retinal ganglion cell process quality asymmetric cell division, abnormal
ZP:0017555	neuron development delayed, abnormal
ZP:0017556	mandibular arch skeleton agenesis, abnormal
ZP:0017557	pharyngeal arch 3-7 decreased amount, abnormal
ZP:0017558	posterior lateral line neuromast primordium migration decreased process quality, abnormal
ZP:0017559	visceral fat decreased volume, abnormal
ZP:0017560	lipid droplet visceral fat morphology, abnormal
ZP:0017561	lipid droplet visceral fat increased amount, abnormal
ZP:0017562	visceral fat increased process quality cell population proliferation, abnormal
ZP:0017563	visceral fat process quality collagen fibril organization, abnormal
ZP:0017564	fat cell increased process quality cell population proliferation, abnormal
ZP:0017565	endothelial cell lateral dorsal aorta increased amount, abnormal
ZP:0017566	endocardial cushion absent, abnormal
ZP:0017567	endocardium proliferative, abnormal
ZP:0017568	subintestinal vein increased branchiness, abnormal
ZP:0017569	anatomical axis trunk bent, abnormal
ZP:0017570	pronephric duct development process quality, abnormal
ZP:0017573	hypochord decreased process quality Notch signaling pathway, abnormal
ZP:0017574	cell ventricular zone amount, abnormal
ZP:0017575	cell ventricular zone decreased amount, abnormal
ZP:0017576	exocrine pancreas fibrillary, abnormal
ZP:0017577	exocrine pancreas lacks all parts of type central region pancreatic acinar cell, abnormal
ZP:0017578	pancreatic duct obstructed, abnormal
ZP:0017579	neuron forebrain increased amount, abnormal
ZP:0017581	neural precursor cell proliferation decreased process quality, abnormal
ZP:0017582	brain lacks parts or has fewer parts of type oligodendrocyte, abnormal
ZP:0017583	peripheral nervous system lacks parts or has fewer parts of type myelinating Schwann cell, abnormal
ZP:0017584	nervous system has fewer parts of type glioblast, abnormal
ZP:0017585	somite border structure, abnormal
ZP:0017586	astrocyte decreased amount, abnormal
ZP:0017587	chondrocyte head maturity, abnormal
ZP:0017588	chondrocyte head decreased amount, abnormal
ZP:0017589	Meckel's cartilage premature endochondral ossification, abnormal
ZP:0017590	mandibular arch skeleton atrophied, abnormal
ZP:0017591	endothelial cell dorsal aorta aplastic, abnormal
ZP:0017598	receptor signaling pathway via JAK-STAT increased occurrence, abnormal
ZP:0017605	ovarian follicle rupture disrupted, abnormal
ZP:0017606	ovulation disrupted, abnormal
ZP:0017607	multi-organism reproductive process disrupted, abnormal
ZP:0017609	oocyte stage V immobile, abnormal
ZP:0017610	oocyte stage V non-functional, abnormal
ZP:0017624	replacement tooth 4V immature, abnormal
ZP:0017625	pronephric proximal tubule development decreased process quality, abnormal
ZP:0017626	pronephros lacks all parts of type corpuscles of Stannius, abnormal
ZP:0017627	pronephros lacks all parts of type pronephric proximal straight tubule, abnormal
ZP:0017628	pronephric proximal convoluted tubule distended, abnormal
ZP:0017629	pronephric proximal convoluted tubule mislocalised posteriorly, abnormal
ZP:0017630	pronephric proximal convoluted tubule straight, abnormal
ZP:0017633	autophagosome maturation arrested, abnormal
ZP:0017634	tooth placode agenesis, abnormal
ZP:0017635	nucleus eye shape, abnormal
ZP:0017636	eye increased occurrence apoptotic process, abnormal
ZP:0017637	eye delayed cell cycle, abnormal
ZP:0017638	cell eye polyploid, abnormal
ZP:0017639	cell eye decreased amount, abnormal
ZP:0017640	behavior decreased occurrence, abnormal
ZP:0017641	response to gravity decreased occurrence, abnormal
ZP:0017642	synapse hindbrain interneuron decreased amount, abnormal
ZP:0017643	Mauthner neuron process quality synapse assembly, abnormal
ZP:0017644	dendrite Mauthner neuron complexity, abnormal
ZP:0017645	synapse Mauthner neuron decreased amount, abnormal
ZP:0017646	sclerotome morphology, abnormal
ZP:0017647	vertebra cuneate, abnormal
ZP:0017648	vertebral column rotated, abnormal
ZP:0017649	posterior lateral line decreased process quality Schwann cell development, abnormal
ZP:0017650	posterior lateral line arrested myelination of posterior lateral line nerve axons, abnormal
ZP:0017651	posterior lateral line decreased occurrence myelination of posterior lateral line nerve axons, abnormal
ZP:0017652	pronephric proximal straight tubule mislocalised posteriorly, abnormal
ZP:0017653	pronephric distal early tubule mislocalised posteriorly, abnormal
ZP:0017656	tooth 5V absent, abnormal
ZP:0017665	blood plasma heart fatty, abnormal
ZP:0017666	posterior lateral line decreased process quality peripheral nervous system myelin formation, abnormal
ZP:0017667	posterior lateral line arrested peripheral nervous system axon ensheathment, abnormal
ZP:0017671	nucleus hepatocyte broken, abnormal
ZP:0017672	microvesicle hepatocyte increased amount, abnormal
ZP:0017673	brain functionality, abnormal
ZP:0017674	cell-cell adhesion involved in gastrulation decreased process quality, abnormal
ZP:0017675	hatching gland mislocalised, abnormal
ZP:0017676	posterior region hindbrain morphology, abnormal
ZP:0017677	anterior region spinal cord morphology, abnormal
ZP:0017678	trigeminal ganglion mislocalised laterally, abnormal
ZP:0017679	neuron trigeminal ganglion disorganized, abnormal
ZP:0017680	neuron trigeminal ganglion distributed, abnormal
ZP:0017681	nervous system flattened, abnormal
ZP:0017682	filopodium axial hypoblast decreased amount, abnormal
ZP:0017683	Rohon-Beard neuron mislocalised, abnormal
ZP:0017684	heart rudiment formation decreased process quality, abnormal
ZP:0017685	pronephric nephron tubule development process quality, abnormal
ZP:0017686	heart increased process quality apoptotic process, abnormal
ZP:0017687	heart decreased process quality cell population proliferation, abnormal
ZP:0017688	cell atrium spatial pattern, abnormal
ZP:0017689	pectoral fin decreased process quality cell population proliferation, abnormal
ZP:0017690	cardiac ventricle decreased process quality sarcomere organization, abnormal
ZP:0017691	olfactory placode development process quality, abnormal
ZP:0017692	hindbrain has extra parts of type dorsal region neuron, abnormal
ZP:0017693	motor neuron hindbrain mislocalised dorsally, abnormal
ZP:0017694	motor neuron hindbrain mislocalised anteriorly, abnormal
ZP:0017695	midbrain has extra parts of type dorsal region neuron, abnormal
ZP:0017696	cell neural tube increased amount, abnormal
ZP:0017697	alar plate midbrain region separated from basal plate midbrain region, abnormal
ZP:0017698	hindbrain interneuron irregular spatial pattern, abnormal
ZP:0017699	hindbrain interneuron mislocalised, abnormal
ZP:0017700	Mauthner neuron irregular spatial pattern, abnormal
ZP:0017702	vascular lymphangioblast malformed, abnormal
ZP:0017704	swimming increased frequency, abnormal
ZP:0017705	swimming increased process quality, abnormal
ZP:0017707	brain process quality transmission of nerve impulse, abnormal
ZP:0017714	phosphatidylinositol 3-kinase signaling process quality, abnormal
ZP:0017715	protein kinase B signaling process quality, abnormal
ZP:0017717	head cellularity, abnormal
ZP:0017718	forebrain increased process quality apoptotic process, abnormal
ZP:0017719	brain increased process quality cell death, abnormal
ZP:0017720	eye increased process quality cell death, abnormal
ZP:0017721	liver decreased rate cell population proliferation, abnormal
ZP:0017728	pronephric proximal tubule development process quality, abnormal
ZP:0017729	pronephric proximal convoluted tubule decreased size, abnormal
ZP:0017730	otic vesicle has fewer parts of type neuroblast (sensu Vertebrata) otic vesicle, abnormal
ZP:0017732	otic vesicle increased process quality Notch signaling pathway, abnormal
ZP:0017733	otic vesicle increased process quality fibroblast growth factor receptor signaling pathway, abnormal
ZP:0017734	otic vesicle decreased occurrence neuroblast fate specification, abnormal
ZP:0017735	otic vesicle decreased occurrence neurogenesis, abnormal
ZP:0017737	statoacoustic (VIII) ganglion has extra parts of type neuroblast (sensu Vertebrata) statoacoustic (VIII) ganglion, abnormal
ZP:0017738	statoacoustic (VIII) ganglion has fewer parts of type neuron statoacoustic (VIII) ganglion, abnormal
ZP:0017739	statoacoustic (VIII) ganglion decreased rate neuron differentiation, abnormal
ZP:0017740	ATP biosynthetic process decreased process quality, abnormal
ZP:0017741	cardiac ventricle position, abnormal
ZP:0017742	mitochondrial chromosome anatomical structure decreased amount, abnormal
ZP:0017743	chondrocyte hypertrophy decreased process quality, abnormal
ZP:0017744	dentary protruding, abnormal
ZP:0017745	basihyal bone position, abnormal
ZP:0017746	Meckel's cartilage increased angle to palatoquadrate cartilage, abnormal
ZP:0017747	chondrocyte Meckel's cartilage increased amount, abnormal
ZP:0017748	polysome head decreased amount, abnormal
ZP:0017750	cytosolic ribosome head increased amount, abnormal
ZP:0017751	intersegmental vessel delayed vasculature development, abnormal
ZP:0017752	liver decreased process quality organ growth, abnormal
ZP:0017753	pancreas decreased process quality organ growth, abnormal
ZP:0017754	white matter optic tectum position, abnormal
ZP:0017755	white matter optic tectum decreased size, abnormal
ZP:0017756	white matter rhombic lip position, abnormal
ZP:0017757	white matter rhombic lip decreased size, abnormal
ZP:0017758	hindbrain decreased area, abnormal
ZP:0017759	optic tectum decreased width, abnormal
ZP:0017760	autophagosome neuron increased amount, abnormal
ZP:0017761	cardioblast cell midline fusion delayed, abnormal
ZP:0017762	mesoderm head absent, abnormal
ZP:0017763	mesoderm trunk absent, abnormal
ZP:0017769	hepatocyte swollen, abnormal
ZP:0017783	neoplasm whole organism increased occurrence, abnormal
ZP:0017788	podocyte disorganized, abnormal
ZP:0017789	cell projection podocyte absent, abnormal
ZP:0017791	barbel increased size, abnormal
ZP:0017793	cilium pronephros curled, abnormal
ZP:0017799	statoacoustic (VIII) ganglion occurrence neuron differentiation, abnormal
ZP:0017803	cardiac muscle cell decreased velocity, abnormal
ZP:0017804	cardiac muscle cell decreased process quality cell migration involved in heart formation, abnormal
ZP:0017815	pharyngeal arch decreased object quality, abnormal
ZP:0017816	pharyngeal arch cartilage has fewer parts of type ceratobranchial cartilage, abnormal
ZP:0017817	pharyngeal arch cartilage lacks all parts of type ceratobranchial 3 cartilage, abnormal
ZP:0017818	pharyngeal arch cartilage lacks all parts of type ceratobranchial 4 cartilage, abnormal
ZP:0017819	pharyngeal arch cartilage lacks all parts of type ceratobranchial 5 cartilage, abnormal
ZP:0017820	pharyngeal arch 3 decreased object quality, abnormal
ZP:0017821	pharyngeal arch 4 decreased object quality, abnormal
ZP:0017822	dorsal aorta in contact with lateral region common cardinal vein, abnormal
ZP:0017823	dorsal aorta in contact with lateral region primary head sinus, abnormal
ZP:0017824	trunk arrested blood circulation, abnormal
ZP:0017825	axon spinal nerve decreased length, abnormal
ZP:0017826	axon spinal nerve increased branchiness, abnormal
ZP:0017828	glomerular filtration decreased functionality, abnormal
ZP:0017829	renal glomerular capsule increased size, abnormal
ZP:0017830	cilium movement process quality, abnormal
ZP:0017831	neuron brain decreased branchiness, abnormal
ZP:0017832	trunk disrupted neuron development, abnormal
ZP:0017833	post-vent region disrupted neuron development, abnormal
ZP:0017837	ceratobranchial 1 cartilage fused with ceratobranchial 2 cartilage, abnormal
ZP:0017841	endocardium hypotrophic, abnormal
ZP:0017842	pronephric nephron tubule development decreased process quality, abnormal
ZP:0017843	distal region pronephros decreased object quality, abnormal
ZP:0017844	melanosome melanocyte decreased size, abnormal
ZP:0017853	pronephric distal early tubule poorly differentiated, abnormal
ZP:0017856	caudal vein decreased thickness, abnormal
ZP:0017857	embryonic organ development decreased rate, abnormal
ZP:0017858	inner ear lacks all parts of type semicircular canal, abnormal
ZP:0017859	whole organism has extra parts of type common myeloid progenitor, abnormal
ZP:0017860	whole organism has fewer parts of type neutrophil, abnormal
ZP:0017861	melanosome retinal pigmented epithelium decreased pigmentation, abnormal
ZP:0017862	melanosome melanocyte unpigmented, abnormal
ZP:0017863	cardiac muscle cell cardiac ventricle degenerate, abnormal
ZP:0017864	collateral sprouting disrupted, abnormal
ZP:0017866	membrane eye photoreceptor cell immature, abnormal
ZP:0017876	neuron locus coeruleus absent, abnormal
ZP:0017877	norepinephrine secreting cell pharyngeal arch absent, abnormal
ZP:0017878	glomerular visceral epithelial cell development decreased process quality, abnormal
ZP:0017879	pronephric glomerulus lacks all parts of type slit diaphragm pronephric podocyte, abnormal
ZP:0017880	pronephric glomerulus lacks all parts of type pronephric glomerular capillary, abnormal
ZP:0017881	stem cell population maintenance decreased occurrence, abnormal
ZP:0017882	inner ear development decreased process quality, abnormal
ZP:0017883	blood has fewer parts of type nucleate erythrocyte, abnormal
ZP:0017884	retina has fewer parts of type somatic stem cell, abnormal
ZP:0017885	skeletal muscle cell myotome malformed, abnormal
ZP:0017886	heart valve morphogenesis disrupted, abnormal
ZP:0017887	heart process quality blood circulation, abnormal
ZP:0017888	heart valve morphology, abnormal
ZP:0017889	pronephric glomerular capillary increased diameter, abnormal
ZP:0017890	pronephros has fewer parts of type cell, abnormal
ZP:0017891	optic chiasma development disrupted, abnormal
ZP:0017892	spinal cord disrupted motor neuron axon guidance, abnormal
ZP:0017893	neuroepithelial cell hindbrain neural tube morphology, abnormal
ZP:0017894	neuroepithelial cell morphology, abnormal
ZP:0017895	glomerular basement membrane morphology, abnormal
ZP:0017902	neuroblast (sensu Vertebrata) ventricular zone increased amount, abnormal
ZP:0017909	leukocyte increased amount, abnormal
ZP:0017912	noradrenergic neuron development disrupted, abnormal
ZP:0017913	trochlear motor nucleus decreased size, abnormal
ZP:0017914	oculomotor nucleus decreased size, abnormal
ZP:0017915	regulation of blood coagulation process quality, abnormal
ZP:0017916	regulation of circulating fibrinogen levels process quality, abnormal
ZP:0017917	heart obstructed, abnormal
ZP:0017918	heart increased process quality blood coagulation, abnormal
ZP:0017919	posterior cardinal vein increased occurrence blood coagulation, fibrin clot formation, abnormal
ZP:0017920	caudal fin development delayed, abnormal
ZP:0017922	locus coeruleus absent, abnormal
ZP:0017923	locus ceruleus development process quality, abnormal
ZP:0017924	ventricular system hydrocephalic, abnormal
ZP:0017925	hematopoietic multipotent progenitor cell ventral wall of dorsal aorta decreased amount, abnormal
ZP:0017932	integument broken, abnormal
ZP:0017934	telencephalon absent, abnormal
ZP:0017951	hematopoietic multipotent progenitor cell ventral wall of dorsal aorta increased amount, abnormal
ZP:0017952	T cell increased amount, abnormal
ZP:0017953	hematopoietic cell intermediate cell mass of mesoderm decreased amount, abnormal
ZP:0017954	Kupffer's vesicle decreased frequency cilium movement, abnormal
ZP:0017958	hematopoietic cell intermediate cell mass of mesoderm increased amount, abnormal
ZP:0017959	primitive erythrocyte differentiation decreased process quality, abnormal
ZP:0017960	nucleus of the caudal commissure decreased amount, abnormal
ZP:0017961	blood island process quality cell cycle, abnormal
ZP:0017962	blood island decreased process quality cell population proliferation, abnormal
ZP:0017963	atrioventricular valve morphogenesis process quality, abnormal
ZP:0017964	atrium decreased process quality heart contraction, abnormal
ZP:0017965	atrioventricular canal constricted, abnormal
ZP:0017966	atrial myocardium absent, abnormal
ZP:0017967	atrioventricular valve process quality blood circulation, abnormal
ZP:0017968	blood atrioventricular valve fluid flow rate, abnormal
ZP:0017969	ventral trunk neural crest cell migration arrested, abnormal
ZP:0017970	eye lacks all parts of type macrophage, abnormal
ZP:0017971	head has fewer parts of type macrophage, abnormal
ZP:0017972	head has fewer parts of type leukocyte, abnormal
ZP:0017973	leukocyte head apoptotic, abnormal
ZP:0017974	caudal vein blistered, abnormal
ZP:0017975	yolk syncytial layer deformed, abnormal
ZP:0017976	trunk colorless, abnormal
ZP:0017980	cranial neural crest decreased amount, abnormal
ZP:0017999	myeloid cell head kidney increased amount, abnormal
ZP:0018013	brain increased process quality cell population proliferation, abnormal
ZP:0018014	caudal fin increased process quality cell population proliferation, abnormal
ZP:0018015	cell cycle rhythm quality, abnormal
ZP:0018016	circadian rhythm disrupted, abnormal
ZP:0018017	developmental growth increased rate, abnormal
ZP:0018018	nucleus skeletal muscle circular, abnormal
ZP:0018019	fin development process quality, abnormal
ZP:0018020	caudal fin increased rate developmental growth, abnormal
ZP:0018021	lepidotrichium segment increased length, abnormal
ZP:0018022	photoreceptor outer segment layer decreased amount, abnormal
ZP:0018023	cilium neuromast hair cell morphology, abnormal
ZP:0018024	cilium neuromast hair cell decreased amount, abnormal
ZP:0018025	thyroid gland development process quality, abnormal
ZP:0018026	hypocretin-secreting neuron decreased amount, abnormal
ZP:0018027	DEL decreased rate cell migration, abnormal
ZP:0018028	DEL process quality cell migration, abnormal
ZP:0018029	skeletal muscle myofibril skeletal muscle absent, abnormal
ZP:0018030	vacuole muscle cell increased amount, abnormal
ZP:0018031	optokinetic behavior amplitude, abnormal
ZP:0018032	optokinetic behavior decreased frequency, abnormal
ZP:0018033	vestibular reflex amplitude, abnormal
ZP:0018047	myelin sheath spinal cord decreased amount, abnormal
ZP:0018049	dorsal longitudinal anastomotic vessel incomplete structure, abnormal
ZP:0018053	nitric oxide production involved in inflammatory response disrupted, abnormal
ZP:0018057	renal system lacks parts or has fewer parts of type podocyte, abnormal
ZP:0018058	GABAergic neuron hindbrain decreased amount, abnormal
ZP:0018059	glutamatergic neuron hindbrain decreased amount, abnormal
ZP:0018060	GABAergic neuron midbrain decreased amount, abnormal
ZP:0018061	outer dynein arm Kupffer's vesicle decreased amount, abnormal
ZP:0018062	motile cilium spinal cord immobile, abnormal
ZP:0018063	hypophysis increased size, abnormal
ZP:0018064	cell hypophysis increased amount, abnormal
ZP:0018066	subintestinal vein decreased length, abnormal
ZP:0018073	neuromast support cell decreased amount, abnormal
ZP:0018081	retinal rod cell physical object quality, abnormal
ZP:0018082	pronephros immature, abnormal
ZP:0018083	renal glomerulus immature, abnormal
ZP:0018084	microvillus glomerular basement membrane crowded, abnormal
ZP:0018085	sarcomere post-vent region disorganized, abnormal
ZP:0018086	slit diaphragm renal glomerulus decreased functionality, abnormal
ZP:0018087	slit diaphragm glomerular basement membrane absent, abnormal
ZP:0018088	podocyte foot glomerular basement membrane protruding, abnormal
ZP:0018089	podocyte foot glomerular basement membrane irregularly shaped, abnormal
ZP:0018091	median fin blistered, abnormal
ZP:0018092	osteoblast differentiation disrupted, abnormal
ZP:0018093	protein N-linked glycosylation disrupted, abnormal
ZP:0018094	cell Meckel's cartilage decreased amount, abnormal
ZP:0018095	mandibular arch skeleton truncated, abnormal
ZP:0018096	cell palatoquadrate cartilage decreased amount, abnormal
ZP:0018097	cell ceratohyal cartilage decreased amount, abnormal
ZP:0018098	brain has extra parts of type neuronal stem cell, abnormal
ZP:0018099	brain has extra parts of type astrocyte, abnormal
ZP:0018100	brain has fewer parts of type neuron, abnormal
ZP:0018101	brain decreased occurrence neuron differentiation, abnormal
ZP:0018102	brain increased occurrence astrocyte differentiation, abnormal
ZP:0018103	brain increased occurrence neural precursor cell proliferation, abnormal
ZP:0018104	neuronal stem cell brain proliferative, abnormal
ZP:0018105	trigeminal ganglion has fewer parts of type motor neuron, abnormal
ZP:0018106	facial ganglion has fewer parts of type motor neuron, abnormal
ZP:0018107	vagal ganglion has fewer parts of type motor neuron, abnormal
ZP:0018108	cerebellum increased occurrence apoptotic process, abnormal
ZP:0018109	carbohydrate metabolic process disrupted, abnormal
ZP:0018110	cellular amino acid metabolic process disrupted, abnormal
ZP:0018111	fatty acid metabolic process disrupted, abnormal
ZP:0018112	cerebellum decreased occurrence cell proliferation in hindbrain, abnormal
ZP:0018113	enteric neuron posterior intestine absent, abnormal
ZP:0018114	enteric neuron intestine decreased amount, abnormal
ZP:0018115	whole organism has extra parts of type posterior pancreatic bud, abnormal
ZP:0018116	pancreatic bud lacks parts or has fewer parts of type cell, abnormal
ZP:0018117	dorsal aorta increased diameter, abnormal
ZP:0018127	photoreceptor outer segment photoreceptor outer segment layer morphology, abnormal
ZP:0018136	Golgi vesicle transport process quality, abnormal
ZP:0018137	brain increased occurrence Notch signaling pathway, abnormal
ZP:0018138	vagal neural crest decreased distance hyoid neural crest, abnormal
ZP:0018139	whole organism lacks parts or has fewer parts of type otic vesicle, abnormal
ZP:0018140	anterior-posterior axis pharyngeal arch decreased length, abnormal
ZP:0018142	pharyngeal arch 3-7 orientation anterior-posterior axis whole organism, abnormal
ZP:0018143	chordoma intestine present, abnormal
ZP:0018144	intestinal epithelium hyperplastic, abnormal
ZP:0018145	chordoma vertebra present, abnormal
ZP:0018146	hemoglobin biosynthetic process decreased process quality, abnormal
ZP:0018147	T cell thymus decreased amount, abnormal
ZP:0018148	posterior lateral line primordium increased occurrence apoptotic process, abnormal
ZP:0018149	posterior lateral line primordium decreased occurrence cell population proliferation, abnormal
ZP:0018150	neuromast posterior lateral line primordium decreased amount, abnormal
ZP:0018151	heart unlumenized, abnormal
ZP:0018152	cardiac jelly increased thickness, abnormal
ZP:0018153	endocardium increased distance myocardium, abnormal
ZP:0018154	semicircular canal development delayed, abnormal
ZP:0018155	posterior lateral line primordium structure, abnormal
ZP:0018156	establishment of blood-brain barrier disrupted, abnormal
ZP:0018157	cranial vasculature porous, abnormal
ZP:0018158	blood accumulation hindbrain, abnormal
ZP:0018159	hair cell semicircular canal decreased amount, abnormal
ZP:0018160	hair cell decreased functionality, abnormal
ZP:0018161	neuromast hair cell degenerate, abnormal
ZP:0018162	stereocilium bundle neuromast hair cell morphology, abnormal
ZP:0018163	kinocilium neuromast hair cell morphology, abnormal
ZP:0018164	neuron differentiation decreased process quality, abnormal
ZP:0018165	head lacks all parts of type cleithrum, abnormal
ZP:0018166	head lacks all parts of type opercle, abnormal
ZP:0018167	head lacks all parts of type pharyngeal arch 3-7, abnormal
ZP:0018168	neurocranial trabecula truncated, abnormal
ZP:0018169	ethmoid cartilage truncated, abnormal
ZP:0018170	brain has fewer parts of type neuronal stem cell, abnormal
ZP:0018171	brain has fewer parts of type astrocyte, abnormal
ZP:0018172	brain has extra parts of type neuron, abnormal
ZP:0018173	brain increased occurrence neuron differentiation, abnormal
ZP:0018174	brain decreased occurrence neural precursor cell proliferation, abnormal
ZP:0018175	hindbrain decreased duration mitotic cell cycle, abnormal
ZP:0018178	hematopoietic multipotent progenitor cell increased amount, abnormal
ZP:0018186	whole organism lacks parts or has fewer parts of type eye, abnormal
ZP:0018187	anatomical margin median fin fold protruding, abnormal
ZP:0018188	cell apical ectodermal ridge median fin fold morphology, abnormal
ZP:0018208	anatomical margin pectoral fin fold increased thickness, abnormal
ZP:0018209	fin fold actinotrichium increased thickness, abnormal
ZP:0018210	fin fold actinotrichium bent, abnormal
ZP:0018211	fin fold actinotrichium mislocalised, abnormal
ZP:0018212	anatomical margin median fin fold increased thickness, abnormal
ZP:0018223	otic vesicle has fewer parts of type cilium otic vesicle, abnormal
ZP:0018224	lateral crista has fewer parts of type kinocilium lateral crista, abnormal
ZP:0018225	spinal cord has fewer parts of type cilium ependymal cell, abnormal
ZP:0018227	angioblastic mesenchymal cell ventral wall of dorsal aorta decreased amount, abnormal
ZP:0018228	endothelial to hematopoietic transition decreased process quality, abnormal
ZP:0018229	trunk vasculature decreased process quality blood vessel lumenization, abnormal
ZP:0018230	Kupffer's vesicle decreased occurrence detection of nodal flow, abnormal
ZP:0018231	dorsal aorta decreased process quality blood vessel lumenization, abnormal
ZP:0018232	blood cell accumulation sinus venosus, abnormal
ZP:0018233	monoamine oxidase activity increased process quality, abnormal
ZP:0018234	central artery hindbrain absent, abnormal
ZP:0018235	central artery hindbrain decreased amount, abnormal
ZP:0018236	brain vasculature absent, abnormal
ZP:0018237	dorsal root ganglion decreased process quality Wnt signaling pathway, abnormal
ZP:0018238	primordial hindbrain channel decreased process quality Wnt signaling pathway, abnormal
ZP:0018239	primordial hindbrain channel decreased process quality sprouting angiogenesis, abnormal
ZP:0018240	primordial hindbrain channel decreased process quality endothelial tip cell fate specification, abnormal
ZP:0018241	angiogenic sprout primordial hindbrain channel absent, abnormal
ZP:0018242	endothelial cell decreased accumulation filamentous actin dorsal region primordial hindbrain channel, abnormal
ZP:0018243	sympathetic neuron absent, abnormal
ZP:0018249	aerobic respiration process quality, abnormal
ZP:0018253	mitochondrial chromosome whole organism increased amount, abnormal
ZP:0018255	lens decreased diameter, abnormal
ZP:0018269	optic tectum decreased process quality generation of neurons, abnormal
ZP:0018270	photoreceptor outer segment retinal cone cell increased length, abnormal
ZP:0018271	photoreceptor outer segment retinal rod cell decreased size, abnormal
ZP:0018272	photoreceptor outer segment retinal rod cell absence due to degeneration, abnormal
ZP:0018273	photoreceptor disc membrane retinal rod cell disorganized, abnormal
ZP:0018274	optic tectum decreased process quality mitotic cell cycle process, abnormal
ZP:0018275	myofibril post-vent region disorganized, abnormal
ZP:0018276	blood island size, abnormal
ZP:0018281	mitochondrion slow muscle cell functionality, abnormal
ZP:0018282	mitochondrion slow muscle cell decreased functionality, abnormal
ZP:0018283	mitochondrial respirasome slow muscle cell decreased functionality, abnormal
ZP:0018284	mitochondrial respirasome fast muscle cell decreased functionality, abnormal
ZP:0018285	ventricular system brain edematous, abnormal
ZP:0018286	germ ring decreased circumference, abnormal
ZP:0018287	collagen network caudal fin disorganized, abnormal
ZP:0018288	epithelium protruding, abnormal
ZP:0018289	neutrophil epithelium increased amount, abnormal
ZP:0018290	mitochondrial fission disrupted, abnormal
ZP:0018291	mitochondrion spinal cord aggregated, abnormal
ZP:0018292	neuron projection spinal cord decreased amount, abnormal
ZP:0018293	mitochondrion motor neuron spatial pattern, abnormal
ZP:0018294	mitochondrion motor neuron aggregated, abnormal
ZP:0018295	motor neuron process quality bleb assembly, abnormal
ZP:0018296	axon retinal ganglion cell shortened, abnormal
ZP:0018297	dendrite retinal ganglion cell decreased amount, abnormal
ZP:0018298	angioblast cell migration from lateral mesoderm to midline arrested, abnormal
ZP:0018299	vascular lymphangioblast posterior cardinal vein absent, abnormal
ZP:0018300	vascular lymphangioblast posterior cardinal vein decreased amount, abnormal
ZP:0018301	thoracic duct aplastic/hypoplastic, abnormal
ZP:0018302	nucleate erythrocyte blood morphology, abnormal
ZP:0018303	nucleate erythrocyte blood circular, abnormal
ZP:0018304	myeloid cell kidney dysplastic, abnormal
ZP:0018305	erythroid lineage cell kidney morphology, abnormal
ZP:0018306	hematopoietic multipotent progenitor cell kidney dysplastic, abnormal
ZP:0018307	common myeloid progenitor head kidney increased amount, abnormal
ZP:0018308	nucleate erythrocyte head kidney decreased amount, abnormal
ZP:0018309	myeloid cell head kidney dysplastic, abnormal
ZP:0018310	erythroid lineage cell head kidney morphology, abnormal
ZP:0018311	hematopoietic multipotent progenitor cell head kidney increased amount, abnormal
ZP:0018312	hematopoietic multipotent progenitor cell head kidney dysplastic, abnormal
ZP:0018313	ribosome nucleate erythrocyte increased amount, abnormal
ZP:0018335	nucleus neutrophil morphology, abnormal
ZP:0018336	glossopharyngeal ganglion decreased size, abnormal
ZP:0018337	glossopharyngeal ganglion lacks parts or has fewer parts of type axon glossopharyngeal ganglion, abnormal
ZP:0018338	axon facial ganglion malformed, abnormal
ZP:0018339	axon glossopharyngeal ganglion malformed, abnormal
ZP:0018340	axon epibranchial ganglion morphology, abnormal
ZP:0018341	axon vagal ganglion malformed, abnormal
ZP:0018342	epibranchial ganglion process quality axon development, abnormal
ZP:0018343	vagal ganglion decreased process quality fasciculation of sensory neuron axon, abnormal
ZP:0018344	forebrain increased process quality cell death, abnormal
ZP:0018345	midbrain increased process quality cell death, abnormal
ZP:0018346	hindbrain decreased process quality mitotic cell cycle, abnormal
ZP:0018347	cerebellum structure, abnormal
ZP:0018348	epidermal cell aggregated, abnormal
ZP:0018349	central nervous system decreased thickness, abnormal
ZP:0018350	ball increased diameter, abnormal
ZP:0018351	pancreas growth quality of occurrent growth, abnormal
ZP:0018352	pancreas increased process quality growth, abnormal
ZP:0018353	subintestinal vein delayed angiogenesis, abnormal
ZP:0018354	cilium hair cell anterior macula decreased length, abnormal
ZP:0018355	histone H3-K9 acetylation increased process quality, abnormal
ZP:0018356	histone H3-K27 acetylation increased process quality, abnormal
ZP:0018357	artery increased size, abnormal
ZP:0018358	anatomical axis whole organism decreased size, abnormal
ZP:0018359	erythrocyte differentiation increased process quality, abnormal
ZP:0018360	respiratory gaseous exchange by respiratory system increased rate, abnormal
ZP:0018361	skeletal muscle collagenous, abnormal
ZP:0018362	muscle cell skeletal muscle disorganized, abnormal
ZP:0018363	mitochondrion muscle cell morphology, abnormal
ZP:0018364	muscle cell detached from mitochondrial outer membrane mitochondrial inner membrane muscle cell, abnormal
ZP:0018365	mitochondrial matrix muscle cell morphology, abnormal
ZP:0018366	vacuole muscle cell present, abnormal
ZP:0018367	sarcoplasm muscle cell composition, abnormal
ZP:0018368	sarcoplasmic reticulum muscle cell increased size, abnormal
ZP:0018369	muscle cell misaligned with sarcomere sarcomere muscle cell, abnormal
ZP:0018370	mitochondrial crista muscle cell morphology, abnormal
ZP:0018371	mitochondrial crista muscle cell swollen, abnormal
ZP:0018372	skeletal muscle myofibril muscle cell disorganized, abnormal
ZP:0018373	lymphangioblast cord decreased length, abnormal
ZP:0018374	heart tube present, abnormal
ZP:0018375	heart tube linear, abnormal
ZP:0018376	myocardium heart tube decreased thickness, abnormal
ZP:0018377	mesenchyme pectoral fin flattened, abnormal
ZP:0018378	mesenchyme pectoral fin absent cell population proliferation, abnormal
ZP:0018379	pectoral fin upturned, abnormal
ZP:0018382	sperm testis absent, abnormal
ZP:0018386	male organism sterile, abnormal
ZP:0018387	Sertoli cell disorganized, abnormal
ZP:0018388	oocyte maturation disrupted, abnormal
ZP:0018390	ovary decreased amount, abnormal
ZP:0018399	female organism sterile, abnormal
ZP:0018408	trunk absent, abnormal
ZP:0018409	central nervous system decreased size, abnormal
ZP:0018410	pericardium decreased size, abnormal
ZP:0018411	trunk increased thickness, abnormal
ZP:0018412	neuron central nervous system irregular spatial pattern, abnormal
ZP:0018414	heart lacks all parts of type atrioventricular valve, abnormal
ZP:0018415	pharyngeal arch 3 increased diameter, abnormal
ZP:0018416	granulocyte intestinal bulb increased amount, abnormal
ZP:0018417	goblet cell intestine increased amount, abnormal
ZP:0018418	intestinal epithelial cell increased rate cell population proliferation, abnormal
ZP:0018419	pectoral fin uncoordinated, abnormal
ZP:0018420	pectoral fin movement quality, abnormal
ZP:0018421	mandibular arch skeleton increased mobility, abnormal
ZP:0018422	slit diaphragm assembly disrupted, abnormal
ZP:0018423	renal glomerulus protruding into microvillus renal capsular space, abnormal
ZP:0018424	podocyte foot glomerular basement membrane morphology, abnormal
ZP:0018425	retinal pigmented epithelium detached from retina, abnormal
ZP:0018426	neuron retina mislocalised, abnormal
ZP:0018427	adherens junction outer limiting membrane absent, abnormal
ZP:0018428	adherens junction outer limiting membrane malformed, abnormal
ZP:0018429	eye photoreceptor cell immature, abnormal
ZP:0018430	green sensitive photoreceptor cell absent, abnormal
ZP:0018431	red sensitive photoreceptor cell absent, abnormal
ZP:0018432	ventral region caudal vein decreased diameter, abnormal
ZP:0018433	ventral region caudal vein plexus decreased diameter, abnormal
ZP:0018434	hemangioblast cell differentiation process quality, abnormal
ZP:0018435	photoreceptor inner segment photoreceptor cell absent, abnormal
ZP:0018436	retinal inner nuclear layer apoptotic, abnormal
ZP:0018437	female sex determination decreased process quality, abnormal
ZP:0018441	retinal inner plexiform layer increased thickness, abnormal
ZP:0018442	male organism decreased fecundity, abnormal
ZP:0018447	glomerular basement membrane increased thickness, abnormal
ZP:0018448	nucleate erythrocyte increased fluorescence, abnormal
ZP:0018449	posterior cardinal vein malformed, abnormal
ZP:0018450	blood cell low saturation, abnormal
ZP:0018451	anatomical axis whole organism morphology, abnormal
ZP:0018452	perichondrium edematous, abnormal
ZP:0018453	distal region pronephros disorganized, abnormal
ZP:0018454	cloaca increased width, abnormal
ZP:0018455	epithelium cloaca disorganized, abnormal
ZP:0018456	cell cloaca disconnected, abnormal
ZP:0018457	posterior region caudal fin curled, abnormal
ZP:0018458	posterior region caudal fin malformed, abnormal
ZP:0018462	cilium assembly decreased process quality, abnormal
ZP:0018463	intracellular cholesterol transport disrupted, abnormal
ZP:0018464	cholesterol whole organism increased amount, abnormal
ZP:0018465	spinal cord decreased amount, abnormal
ZP:0018466	glial cell disrupted myelination, abnormal
ZP:0018467	retinal inner plexiform layer circular, abnormal
ZP:0018468	axon peripheral neuron morphology, abnormal
ZP:0018469	Purkinje cell layer corpus cerebelli morphology, abnormal
ZP:0018470	medial longitudinal fasciculus decreased amount, abnormal
ZP:0018471	retinotectal tract morphology, abnormal
ZP:0018472	glial cell central nervous system absent, abnormal
ZP:0018473	axon peripheral neuron branchiness, abnormal
ZP:0018474	peripheral neuron process quality axon guidance, abnormal
ZP:0018475	myelinating Schwann cell posterior lateral line nerve decreased amount, abnormal
ZP:0018476	axon peripheral neuron shape, abnormal
ZP:0018477	retinal ganglion cell layer patchy, abnormal
ZP:0018478	acetylcholine-gated channel complex myotome increased area, abnormal
ZP:0018479	spinal cord decreased process quality motor neuron axon guidance, abnormal
ZP:0018480	neuronal cell body motor neuron mislocalised, abnormal
ZP:0018481	neuromuscular junction of skeletal muscle fiber myotome area, abnormal
ZP:0018482	regulation of synaptic transmission, cholinergic decreased process quality, abnormal
ZP:0018483	acetylcholine-gated channel complex myotome increased distribution, abnormal
ZP:0018484	myotome decreased process quality regulation of synaptic transmission, cholinergic, abnormal
ZP:0018485	pronephric distal late tubule spatial pattern, abnormal
ZP:0018486	pronephros spatial pattern, abnormal
ZP:0018487	pronephric proximal convoluted tubule spatial pattern, abnormal
ZP:0018488	pronephric glomerulus spatial pattern, abnormal
ZP:0018489	heart contraction increased frequency, abnormal
ZP:0018490	vasodilation increased occurrence, abnormal
ZP:0018491	artery increased diameter, abnormal
ZP:0018492	blood circulation increased volume, abnormal
ZP:0018495	mitochondrion skeletal muscle increased amount, abnormal
ZP:0018496	sarcomere skeletal muscle increased thickness, abnormal
ZP:0018497	cranial blood vessel process quality artery morphogenesis, abnormal
ZP:0018498	dorsal aorta increased amount, abnormal
ZP:0018499	optic artery increased amount, abnormal
ZP:0018500	metencephalic artery increased amount, abnormal
ZP:0018501	cell migration involved in heart development decreased occurrence, abnormal
ZP:0018502	caudal division of the internal carotid artery increased width, abnormal
ZP:0018503	endothelial cell caudal division of the internal carotid artery increased amount, abnormal
ZP:0018504	internal carotid artery process quality blood vessel endothelial cell migration, abnormal
ZP:0018505	aortic arch 1 process quality blood vessel development, abnormal
ZP:0018506	endothelial cell internal carotid artery increased amount, abnormal
ZP:0018507	internal carotid artery increased width, abnormal
ZP:0018508	aortic arch 1 decreased occurrence cell migration involved in heart development, abnormal
ZP:0018509	aortic arch 1 constricted, abnormal
ZP:0018510	endothelial cell aortic arch 1 decreased amount, abnormal
ZP:0018511	caudal division of the internal carotid artery process quality blood vessel endothelial cell migration, abnormal
ZP:0018512	caudal division of the internal carotid artery process quality blood vessel development, abnormal
ZP:0018513	aortic arch 1 morphology, abnormal
ZP:0018514	aortic arch 1 process quality blood vessel endothelial cell migration, abnormal
ZP:0018515	internal carotid artery process quality blood vessel development, abnormal
ZP:0018516	caudal division of the internal carotid artery increased occurrence blood vessel endothelial cell migration, abnormal
ZP:0018517	lateral dorsal aorta increased amount, abnormal
ZP:0018518	aortic arch 1 decreased process quality blood vessel endothelial cell migration, abnormal
ZP:0018519	aortic arch 1 increased amount, abnormal
ZP:0018520	internal carotid artery increased amount, abnormal
ZP:0018521	pancreatic B cell decreased area, abnormal
ZP:0018522	endocrine pancreas decreased distribution, abnormal
ZP:0018523	neuron trunk decreased distribution, abnormal
ZP:0018524	melanophore stripe broken, abnormal
ZP:0018525	anterior region spinal cord neural tube decreased distribution, abnormal
ZP:0018526	anterior region spinal cord decreased distribution, abnormal
ZP:0018527	dorsal root ganglion development disrupted, abnormal
ZP:0018528	spinal cord has fewer parts of type ventral region myelin sheath spinal cord, abnormal
ZP:0018529	oligodendrocyte development decreased process quality, abnormal
ZP:0018530	spinal cord increased occurrence central nervous system myelination, abnormal
ZP:0018531	spinal cord decreased occurrence central nervous system myelination, abnormal
ZP:0018532	spinal cord premature central nervous system myelination, abnormal
ZP:0018533	spinal cord premature axon ensheathment in central nervous system, abnormal
ZP:0018534	spinal cord decreased occurrence oligodendrocyte development, abnormal
ZP:0018535	oligodendrocyte progenitor proliferation decreased occurrence, abnormal
ZP:0018536	spinal cord decreased occurrence axon ensheathment in central nervous system, abnormal
ZP:0018537	posterior lateral line nerve decreased amount, abnormal
ZP:0018538	muscle pioneer myotome absent, abnormal
ZP:0018539	fast muscle cell myotome absent, abnormal
ZP:0018540	swim bladder development decreased process quality, abnormal
ZP:0018541	anatomical structure absent, abnormal
ZP:0018542	interneuron absent, abnormal
ZP:0018543	neural tube decreased amount, abnormal
ZP:0018544	skeletal muscle cell increased occurrence apoptotic process, abnormal
ZP:0018545	skeletal muscle myofibril skeletal muscle morphology, abnormal
ZP:0018546	whole organism increased amount, abnormal
ZP:0018547	thymus decreased amount, abnormal
ZP:0018548	retinal cone cell decreased process quality photoreceptor cell outer segment organization, abnormal
ZP:0018549	dorsal region retinal outer nuclear layer decreased thickness, abnormal
ZP:0018550	photoreceptor outer segment retinal cone cell irregular spatial pattern, abnormal
ZP:0018551	posterior pronephric duct lacks all parts of type motile cilium posterior pronephric duct, abnormal
ZP:0018552	pronephric duct decreased occurrence cilium assembly, abnormal
ZP:0018553	retinal cone cell has fewer parts of type photoreceptor outer segment retinal cone cell, abnormal
ZP:0018554	photoreceptor disc membrane retinal cone cell irregular spatial pattern, abnormal
ZP:0018555	retinal outer nuclear layer mislocalised, abnormal
ZP:0018556	photoreceptor connecting cilium eye photoreceptor cell decreased amount, abnormal
ZP:0018557	dorsal region photoreceptor outer segment layer malformed, abnormal
ZP:0018558	anterior lateral plate mesoderm increased distribution, abnormal
ZP:0018559	heart primordium increased distribution, abnormal
ZP:0018560	heart primordium decreased distribution, abnormal
ZP:0018561	hematopoietic progenitor cell differentiation decreased process quality, abnormal
ZP:0018562	hematopoietic system increased process quality apoptotic process, abnormal
ZP:0018563	hematopoietic stem cell differentiation decreased process quality, abnormal
ZP:0018564	blood island increased process quality apoptotic process, abnormal
ZP:0018565	intermediate cell mass of mesoderm increased process quality apoptotic process, abnormal
ZP:0018566	myeloid cell development decreased process quality, abnormal
ZP:0018567	myeloid leukocyte differentiation decreased process quality, abnormal
ZP:0018568	primitive hemopoiesis absent, abnormal
ZP:0018569	myeloid cell development absent, abnormal
ZP:0018570	cilium peripheral olfactory organ morphology, abnormal
ZP:0018571	musculoskeletal movement, spinal reflex action decreased occurrence, abnormal
ZP:0018572	nervous system wholly anterioralized, abnormal
ZP:0018573	retina decreased amount, abnormal
ZP:0018574	pancreatic B cell decreased mass, abnormal
ZP:0018575	whole organism absent, abnormal
ZP:0018576	whole organism decreased amount, abnormal
ZP:0018577	posterior lateral line primordium has extra parts of type cell posterior lateral line primordium, abnormal
ZP:0018578	posterior lateral line primordium has extra parts of type posterior region cell posterior lateral line primordium, abnormal
ZP:0018579	posterior lateral line has extra parts of type posterior lateral line neuromast, abnormal
ZP:0018580	posterior lateral line primordium decreased speed posterior lateral line neuromast primordium migration, abnormal
ZP:0018581	trunk vasculature decreased occurrence blood circulation, abnormal
ZP:0018582	posterior lateral line primordium increased occurrence cell population proliferation, abnormal
ZP:0018583	posterior lateral line primordium increased distribution, abnormal
ZP:0018584	dorsal aorta constricted, abnormal
ZP:0018585	intersegmental vein closed, abnormal
ZP:0018586	dorsal aorta morphogenesis decreased process quality, abnormal
ZP:0018587	dorsal longitudinal anastomotic vessel closed, abnormal
ZP:0018588	endothelial cell increased occurrence apoptotic process, abnormal
ZP:0018589	endocrine pancreas increased distribution, abnormal
ZP:0018590	motile cilium pronephric duct decreased functionality, abnormal
ZP:0018591	pronephric duct decreased process quality epithelial cilium movement involved in extracellular fluid movement, abnormal
ZP:0018592	ventral wall of dorsal aorta decreased amount, abnormal
ZP:0018593	neuromast increased rate mitotic cell cycle, abnormal
ZP:0018594	atrioventricular canal endocardium decreased amount, abnormal
ZP:0018595	heart primordium decreased amount, abnormal
ZP:0018596	establishment of epithelial cell polarity disrupted, abnormal
ZP:0018597	endodermal cell decreased distribution, abnormal
ZP:0018598	heart primordium hypoplastic, abnormal
ZP:0018599	hindbrain decreased amount, abnormal
ZP:0018600	rhombomere 4 morphogenesis process quality, abnormal
ZP:0018601	hindbrain decreased occurrence cell proliferation in hindbrain, abnormal
ZP:0018602	hindbrain increased amount, abnormal
ZP:0018603	hindbrain decreased occurrence neuron differentiation, abnormal
ZP:0018604	hindbrain lacks parts or has fewer parts of type Mauthner neuron, abnormal
ZP:0018605	rhombomere 3 decreased length, abnormal
ZP:0018606	rhombomere 4 decreased length, abnormal
ZP:0018607	rhombomere 3 morphogenesis process quality, abnormal
ZP:0018608	hindbrain increased occurrence Notch signaling pathway, abnormal
ZP:0018609	leukocyte accumulation brain, abnormal
ZP:0018610	brain vasculature increased fragility, abnormal
ZP:0018611	nucleate erythrocyte accumulation brain, abnormal
ZP:0018612	anatomical structure increased amount, abnormal
ZP:0018613	photoreceptor cell cilium photoreceptor cell decreased length, abnormal
ZP:0018614	cilium renal system spatial pattern, abnormal
ZP:0018615	preoptic area absent, abnormal
ZP:0018616	cell body microglial cell increased size, abnormal
ZP:0018617	microglial cell optic tectum morphology, abnormal
ZP:0018618	cell body microglial cell increased volume, abnormal
ZP:0018619	microglial cell increased frequency phagocytosis, abnormal
ZP:0018620	cell projection microglial cell increased amount, abnormal
ZP:0018621	ventral wall of dorsal aorta increased amount, abnormal
ZP:0018622	somite atrophied, abnormal
ZP:0018623	macrophage accumulation lysosome macrophage, abnormal
ZP:0018624	macrophage decreased process quality myeloid leukocyte migration, abnormal
ZP:0018625	macrophage process quality myeloid leukocyte migration, abnormal
ZP:0018626	motor neuron fragile, abnormal
ZP:0018627	neuromuscular junction motor neuron decreased amount, abnormal
ZP:0018628	pancreatic D cell decreased amount, abnormal
ZP:0018629	somatostatin secreting cell decreased distribution, abnormal
ZP:0018630	retinal outer plexiform layer decreased occurrence synapse assembly, abnormal
ZP:0018631	synapse retinal outer plexiform layer morphology, abnormal
ZP:0018632	retina increased occurrence mitotic cell cycle, abnormal
ZP:0018633	autophagosome assembly disrupted, abnormal
ZP:0018634	autophagosome heart decreased amount, abnormal
ZP:0018635	post-vent region increased occurrence cell death, abnormal
ZP:0018636	atrioventricular canal increased distribution, abnormal
ZP:0018637	atrioventricular canal mislocalised, abnormal
ZP:0018638	cell decreased process quality autophagosome assembly, abnormal
ZP:0018639	heart increased distribution, abnormal
ZP:0018640	atrium increased distribution, abnormal
ZP:0018641	cardiac ventricle increased distribution, abnormal
ZP:0018642	epidermis increased occurrence cell death, abnormal
ZP:0018643	basement membrane epidermis decreased distribution, abnormal
ZP:0018644	epidermal cell mislocalised, abnormal
ZP:0018645	peridermal cell aggregated, abnormal
ZP:0018646	fin fold actinotrichium disassembled, abnormal
ZP:0018647	keratinocyte epidermal basal stratum mislocalised, abnormal
ZP:0018648	basement membrane epidermis broken, abnormal
ZP:0018649	keratinocyte epidermal basal stratum increased amount, abnormal
ZP:0018650	epidermal cell epidermis absent, abnormal
ZP:0018651	peridermal cell circular, abnormal
ZP:0018652	epidermis increased amount, abnormal
ZP:0018653	epidermis increased distribution, abnormal
ZP:0018654	thigmotaxis lacking processual parts regulation of twitch skeletal muscle contraction, abnormal
ZP:0018656	thigmotaxis having decreased processual parts relaxation of skeletal muscle, abnormal
ZP:0018657	cell ciliated cell decreased amount, abnormal
ZP:0018658	forerunner cell group decreased occurrence cell population proliferation, abnormal
ZP:0018659	obsolete cell forerunner cell group decreased amount, abnormal
ZP:0018660	plasma membrane EVL decreased amount, abnormal
ZP:0018661	plasma membrane forerunner cell group decreased amount, abnormal
ZP:0018662	mesoderm mislocalised, abnormal
ZP:0018663	plasma membrane cell decreased amount, abnormal
ZP:0018664	right side mesoderm mislocalised, abnormal
ZP:0018665	determination of left/right asymmetry in lateral mesoderm decreased occurrence, abnormal
ZP:0018666	anatomical structure decreased amount, abnormal
ZP:0018667	cytoplasm forerunner cell group decreased acidity, abnormal
ZP:0018668	basal region neuromast hair cell decreased amount, abnormal
ZP:0018669	ciliated olfactory receptor neuron decreased occurrence olfactory bulb development, abnormal
ZP:0018670	non-motile cilium neuromast hair cell absent, abnormal
ZP:0018671	cranium increased amount, abnormal
ZP:0018672	bone mineralization decreased occurrence, abnormal
ZP:0018673	centrum hollow, abnormal
ZP:0018674	determination of pancreatic left/right asymmetry decreased occurrence, abnormal
ZP:0018675	right side lateral plate mesoderm mislocalised, abnormal
ZP:0018676	mitotic cell cycle increased duration, abnormal
ZP:0018677	centrosome duplication decreased occurrence, abnormal
ZP:0018678	right side epithalamus mislocalised, abnormal
ZP:0018679	cilium pronephric tubule decreased mobility, abnormal
ZP:0018680	pancreatic bud decreased amount, abnormal
ZP:0018681	cilium olfactory pit decreased mobility, abnormal
ZP:0018682	cilium cloaca decreased mobility, abnormal
ZP:0018683	pancreatic B cell increased area, abnormal
ZP:0018684	exocrine pancreas decreased area, abnormal
ZP:0018685	atrioventricular valve increased distribution, abnormal
ZP:0018686	tectal ventricle distended, abnormal
ZP:0018687	optic tectum decreased distribution, abnormal
ZP:0018688	retina decreased distribution, abnormal
ZP:0018689	trunk increased amount, abnormal
ZP:0018690	lymphoid progenitor cell differentiation increased occurrence, abnormal
ZP:0018691	myeloid progenitor cell differentiation decreased occurrence, abnormal
ZP:0018692	lymphoid progenitor cell thymus increased amount, abnormal
ZP:0018693	erythroid lineage cell decreased occurrence myeloid progenitor cell differentiation, abnormal
ZP:0018694	female organism increased occurrence male gamete generation, abnormal
ZP:0018695	female organism male, abnormal
ZP:0018696	granulosa cell ovary absent, abnormal
ZP:0018697	female organism has extra parts of type sperm, abnormal
ZP:0018698	oocyte decreased amount, abnormal
ZP:0018699	female organism has extra parts of type spermatogonium, abnormal
ZP:0018700	oocyte maturation arrested, abnormal
ZP:0018701	female organism has extra parts of type spermatocyte, abnormal
ZP:0018702	oocyte degeneration, abnormal
ZP:0018703	Melanin whole organism decreased amount, abnormal
ZP:0018704	apical ectodermal ridge decreased amount, abnormal
ZP:0018705	oocyte stage II spatial pattern, abnormal
ZP:0018706	oocyte stage II increased distribution, abnormal
ZP:0018707	oocyte stage I increased distribution, abnormal
ZP:0018708	oocyte stage I spatial pattern, abnormal
ZP:0018709	orbit constricted, abnormal
ZP:0018710	supraorbital bone protruding out of orbit, abnormal
ZP:0018711	ventral margin supraorbital bone rough, abnormal
ZP:0018712	supraorbital bone distended, abnormal
ZP:0018713	extracellular matrix skeletal muscle cell absent, abnormal
ZP:0018714	muscle tendon junction skeletal muscle cell morphology, abnormal
ZP:0018715	muscle post-vent region structure, abnormal
ZP:0018716	plasma membrane trunk musculature decreased amount, abnormal
ZP:0018717	skeletal muscle detached from muscle tendon junction skeletal muscle cell, abnormal
ZP:0018718	trunk musculature pathological, abnormal
ZP:0018719	cytoplasmic vesicle trunk musculature increased amount, abnormal
ZP:0018720	pronephric duct lacks all parts of type motile cilium outer dynein arm pronephric duct, abnormal
ZP:0018721	pronephric duct decreased occurrence outer dynein arm assembly, abnormal
ZP:0018722	otolith organ absent, abnormal
ZP:0018723	motor neuron activation quality, abnormal
ZP:0018724	Mauthner neuron has fewer parts of type AMPA glutamate receptor complex Mauthner neuron, abnormal
ZP:0018725	Mauthner neuron decreased rate AMPA selective glutamate receptor signaling pathway, abnormal
ZP:0018726	hindbrain decreased occurrence AMPA glutamate receptor clustering, abnormal
ZP:0018727	Mauthner neuron decreased magnitude AMPA selective glutamate receptor signaling pathway, abnormal
ZP:0018728	Mauthner neuron increased rate AMPA selective glutamate receptor signaling pathway, abnormal
ZP:0018729	trigeminal motor nucleus mislocalised, abnormal
ZP:0018730	branchiomotor neuron disorganized, abnormal
ZP:0018731	motor nucleus of vagal nerve mislocalised, abnormal
ZP:0018732	microtubule cytoskeleton brain disorganized, abnormal
ZP:0018733	neuronal cell body facial nerve motor nucleus mislocalised, abnormal
ZP:0018734	extension physical object quality, abnormal
ZP:0018735	endosome skeletal muscle cell increased amount, abnormal
ZP:0018736	membrane skeletal muscle cell convolute, abnormal
ZP:0018737	caveola skeletal muscle cell decreased amount, abnormal
ZP:0018738	caveola assembly disrupted, abnormal
ZP:0018739	skeletal muscle decreased amount, abnormal
ZP:0018740	skeletal muscle occurrence ERK1 and ERK2 cascade, abnormal
ZP:0018741	cytoplasm skeletal muscle cell decreased amount, abnormal
ZP:0018742	male organism decreased mass, abnormal
ZP:0018743	sarcomere skeletal muscle cell spatial pattern, abnormal
ZP:0018744	cytoplasm skeletal muscle cell mislocalised, abnormal
ZP:0018745	cytoplasm skeletal muscle cell increased amount, abnormal
ZP:0018746	skeletal muscle cell decreased process quality T-tubule organization, abnormal
ZP:0018747	skeletal muscle increased amount, abnormal
ZP:0018748	skeletal muscle cell has extra parts of type caveola skeletal muscle cell, abnormal
ZP:0018749	skeletal muscle cell decreased diameter, abnormal
ZP:0018750	female organism decreased length, abnormal
ZP:0018751	male organism decreased length, abnormal
ZP:0018752	skeletal muscle cell irregularly shaped, abnormal
ZP:0018753	female organism decreased mass, abnormal
ZP:0018754	definitive hemopoiesis decreased occurrence, abnormal
ZP:0018755	cytoplasmic vesicle eye photoreceptor cell mislocalised, abnormal
ZP:0018756	shield increased distribution, abnormal
ZP:0018757	ventral region non neural ectoderm decreased distribution, abnormal
ZP:0018758	ventral region whole organism decreased distribution, abnormal
ZP:0018759	posterior region trunk absent, abnormal
ZP:0018760	dorsal/ventral pattern formation decreased occurrence, abnormal
ZP:0018761	dorsal region whole organism increased distribution, abnormal
ZP:0018762	Wnt signaling pathway involved in dorsal/ventral axis specification increased occurrence, abnormal
ZP:0018763	animal-vegetal axis whole organism elongated, abnormal
ZP:0018764	anterior region neuroectoderm increased distribution, abnormal
ZP:0018765	pronephros decreased process quality cilium movement, abnormal
ZP:0018766	fourth ventricle decreased process quality cerebrospinal fluid circulation, abnormal
ZP:0018767	ventral aorta increased diameter, abnormal
ZP:0018768	thymus absent, abnormal
ZP:0018769	pronephric glomerular capillary distended, abnormal
ZP:0018770	protein poly-ADP-ribosylation increased occurrence, abnormal
ZP:0018771	cilium posterior macula length, abnormal
ZP:0018772	hindbrain neural tube increased distribution, abnormal
ZP:0018773	posterior lateral line neuromast far from posterior lateral line neuromast, abnormal
ZP:0018774	stereocilium bundle hair cell splayed, abnormal
ZP:0018775	blood vessel endothelial cell common cardinal vein structure, cavities, abnormal
ZP:0018776	intersegmental vessel disconnected, abnormal
ZP:0018777	mitotic cell cycle decreased occurrence, abnormal
ZP:0018778	cardiac muscle contraction process quality, abnormal
ZP:0018779	cardiac muscle tissue regeneration decreased occurrence, abnormal
ZP:0018780	hematopoietic progenitor cell differentiation decreased occurrence, abnormal
ZP:0018781	granular vesicle neutrophil decreased amount, abnormal
ZP:0018782	neutrophil differentiation decreased occurrence, abnormal
ZP:0018783	neutrophil immature, abnormal
ZP:0018784	liver increased occurrence cell population proliferation, abnormal
ZP:0018785	liver decreased distribution, abnormal
ZP:0018786	macrophage brain absent, abnormal
ZP:0018787	myeloid lineage restricted progenitor cell arrested mitotic S phase, abnormal
ZP:0018788	myeloid lineage restricted progenitor cell decreased occurrence myeloid leukocyte migration, abnormal
ZP:0018789	myeloid lineage restricted progenitor cell rostral blood island decreased distribution, abnormal
ZP:0018790	myeloid lineage restricted progenitor cell accumulation rostral blood island, abnormal
ZP:0018791	DNA damage response, detection of DNA damage process quality, abnormal
ZP:0018792	gut decreased process quality determination of digestive tract left/right asymmetry, abnormal
ZP:0018793	right side posterior lateral plate mesoderm mislocalised, abnormal
ZP:0018794	lateral plate mesoderm spatial pattern, abnormal
ZP:0018795	right side heart rudiment mislocalised, abnormal
ZP:0018796	heart tube decreased process quality heart jogging, abnormal
ZP:0018797	habenula decreased process quality determination of left/right asymmetry in diencephalon, abnormal
ZP:0018798	right side habenula mislocalised, abnormal
ZP:0018799	heart decreased process quality heart looping, abnormal
ZP:0018800	heart rudiment decreased process quality determination of heart left/right asymmetry, abnormal
ZP:0018801	Kupffer's vesicle decreased process quality epithelial cilium movement involved in determination of left/right asymmetry, abnormal
ZP:0018802	heart tube mislocalised medially, abnormal
ZP:0018803	embryonic heart tube left/right pattern formation decreased occurrence, abnormal
ZP:0018804	right side brain mislocalised, abnormal
ZP:0018805	pancreatic centroacinar cell decreased amount, abnormal
ZP:0018806	cell secondary islet decreased amount, abnormal
ZP:0018807	trunk spatial pattern, abnormal
ZP:0018808	migratory neural crest mislocalised, abnormal
ZP:0018809	melanocyte whole organism shape, abnormal
ZP:0018810	neural keel decreased amount, abnormal
ZP:0018811	cranial motor neuron decreased amount, abnormal
ZP:0018812	myelinating Schwann cell increased amount, abnormal
ZP:0018813	myelinating Schwann cell decreased distribution, abnormal
ZP:0018814	melanoblast neural crest increased amount, abnormal
ZP:0018815	neural crest increased amount, abnormal
ZP:0018816	glial cell (sensu Vertebrata) lateral line increased amount, abnormal
ZP:0018817	glial cell (sensu Vertebrata) brain decreased amount, abnormal
ZP:0018818	glial cell (sensu Vertebrata) cranium absent, abnormal
ZP:0018819	iridophore trunk absent, abnormal
ZP:0018820	somite increased amount, abnormal
ZP:0018821	neuroblast epibranchial cartilage decreased amount, abnormal
ZP:0018822	glial cell cranium absent, abnormal
ZP:0018823	neural crest cell pharyngeal arch decreased amount, abnormal
ZP:0018824	neuroblast head decreased amount, abnormal
ZP:0018825	vagal neural crest decreased amount, abnormal
ZP:0018826	glial cell (sensu Vertebrata) lateral line morphology, abnormal
ZP:0018827	melanoblast head increased amount, abnormal
ZP:0018828	neural crest spatial pattern, abnormal
ZP:0018829	olfactory receptor cell decreased amount, abnormal
ZP:0018830	perichondrium disorganized, abnormal
ZP:0018831	neural plate border decreased amount, abnormal
ZP:0018832	myelinating Schwann cell disrupted myelination, abnormal
ZP:0018833	microvillous olfactory receptor neuron disorganized, abnormal
ZP:0018834	chondrocyte pharyngeal arch absent, abnormal
ZP:0018835	perichondrium decreased amount, abnormal
ZP:0018836	esophageal epithelium decreased amount, abnormal
ZP:0018837	detection of mechanical stimulus involved in sensory perception of sound disrupted, abnormal
ZP:0018838	stereocilium neuromast hair cell decreased amount, abnormal
ZP:0018839	neuromast hair cell lacks parts or has fewer parts of type stereocilium bundle neuromast hair cell, abnormal
ZP:0018840	hair cell inner ear decreased amount, abnormal
ZP:0018841	cell intestine apoptotic, abnormal
ZP:0018842	retinal pigmented epithelium atrophied, abnormal
ZP:0018843	intestine malformed, abnormal
ZP:0018844	cytoplasm retina decreased amount, abnormal
ZP:0018845	iridophore eye irregular spatial pattern, abnormal
ZP:0018846	hair cell inner ear non-functional, abnormal
ZP:0018847	retinal pigmented epithelium displaced to pigmented epithelial cell retinal outer nuclear layer, abnormal
ZP:0018848	posterior surface lens degenerate, abnormal
ZP:0018849	kinocilium neuromast hair cell decreased amount, abnormal
ZP:0018850	inclusion body pigmented epithelial cell increased amount, abnormal
ZP:0018851	primitive erythrocyte differentiation increased occurrence, abnormal
ZP:0018852	mesoderm increased amount, abnormal
ZP:0018853	myeloid cell increased distribution, abnormal
ZP:0018854	positive regulation of receptor signaling pathway via JAK-STAT increased occurrence, abnormal
ZP:0018855	lymphocyte thymus increased amount, abnormal
ZP:0018856	common myeloid progenitor increased distribution, abnormal
ZP:0018857	chloride transport process quality, abnormal
ZP:0018858	stereocilium bundle hair cell shortened, abnormal
ZP:0018859	neuromast hair cell decreased process quality action potential, abnormal
ZP:0018860	neuromast hair cell decreased process quality membrane depolarization during action potential, abnormal
ZP:0018861	stereocilium bundle hair cell absent, abnormal
ZP:0018862	neuron increased occurrence cell death, abnormal
ZP:0018863	central region retinal photoreceptor layer degenerate, abnormal
ZP:0018864	photoreceptor cell lacks all parts of type cilium photoreceptor cell, abnormal
ZP:0018865	retina lacks parts or has fewer parts of type central region retinal rod cell, abnormal
ZP:0018866	photoreceptor cell disrupted cilium assembly, abnormal
ZP:0018867	retinal rod cell decreased distribution, abnormal
ZP:0018868	retina lacks parts or has fewer parts of type central region retinal cone cell, abnormal
ZP:0018869	retinal cone cell decreased distribution, abnormal
ZP:0018870	retina lacks all parts of type central region photoreceptor cell, abnormal
ZP:0018871	cilium olfactory pit absent, abnormal
ZP:0018872	retina lacks parts or has fewer parts of type central region photoreceptor cell, abnormal
ZP:0018873	S-adenosyl-L-homocysteine liver decreased amount, abnormal
ZP:0018874	cysteine liver decreased amount, abnormal
ZP:0018876	common bile duct morphology, abnormal
ZP:0018877	S-adenosyl-L-methionine liver decreased amount, abnormal
ZP:0018879	liver and biliary system spatial pattern, abnormal
ZP:0018880	homoserine liver decreased amount, abnormal
ZP:0018882	bile accumulation liver, abnormal
ZP:0018883	common bile duct decreased branchiness, abnormal
ZP:0018884	protein methylation decreased occurrence, abnormal
ZP:0018885	homocysteine liver decreased amount, abnormal
ZP:0018886	serine liver decreased amount, abnormal
ZP:0018887	common bile duct development process quality, abnormal
ZP:0018888	methionine liver decreased amount, abnormal
ZP:0018889	liver male organism decreased amount, abnormal
ZP:0018890	lipid liver increased amount, abnormal
ZP:0018891	triglyceride liver increased amount, abnormal
ZP:0018892	muscle pioneer increased distribution, abnormal
ZP:0018893	secondary motor neuron decreased process quality motor neuron axon guidance, abnormal
ZP:0018894	primary motor neuron decreased process quality motor neuron axon guidance, abnormal
ZP:0018895	medial side myotome absent, abnormal
ZP:0018896	myotome process quality skeletal muscle cell differentiation, abnormal
ZP:0018897	vertical myoseptum absent, abnormal
ZP:0018898	vertical myoseptum decreased amount, abnormal
ZP:0018899	extracellular matrix myotome absent, abnormal
ZP:0018900	myotome decreased process quality skeletal muscle tissue development, abnormal
ZP:0018901	medial side myotome decreased amount, abnormal
ZP:0018902	myotome atrophied, abnormal
ZP:0018903	myotome has extra parts of type muscle pioneer, abnormal
ZP:0018904	slow muscle cell myotome shape, abnormal
ZP:0018905	fast muscle cell myotome decreased area, abnormal
ZP:0018906	fast muscle cell has fewer parts of type skeletal muscle myofibril fast muscle cell, abnormal
ZP:0018907	dorsal aorta increased elasticity, abnormal
ZP:0018908	basement membrane optic tectum spatial pattern, abnormal
ZP:0018909	basement membrane hindbrain irregular spatial pattern, abnormal
ZP:0018910	hindbrain decreased process quality basement membrane organization, abnormal
ZP:0018911	retinal ganglion cell decreased process quality retinal ganglion cell axon guidance, abnormal
ZP:0018912	cerebellar granule cell decreased process quality axon extension involved in axon guidance, abnormal
ZP:0018913	optic tectum decreased process quality basement membrane organization, abnormal
ZP:0018914	basement membrane hindbrain spatial pattern, abnormal
ZP:0018915	basement membrane optic tectum irregular spatial pattern, abnormal
ZP:0018916	basement membrane hindbrain bifurcated, abnormal
ZP:0018917	axon cerebellar granule cell mislocalised, abnormal
ZP:0018918	dorsal region hindbrain decreased amount, abnormal
ZP:0018919	epidermal cell hindbrain decreased amount, abnormal
ZP:0018920	basement membrane hindbrain truncated, abnormal
ZP:0018921	basement membrane hindbrain branched, abnormal
ZP:0018922	vertical myoseptum integument morphology, abnormal
ZP:0018923	nucleus muscle cell increased size, abnormal
ZP:0018924	T-tubule muscle increased size, abnormal
ZP:0018925	sarcoplasm muscle cell undifferentiated, abnormal
ZP:0018926	skeletal muscle myofibril skeletal muscle disorganized, abnormal
ZP:0018927	Z disc muscle morphology, abnormal
ZP:0018928	nucleolus muscle cell increased size, abnormal
ZP:0018929	compartment boundary myotome morphology, abnormal
ZP:0018930	muscle cell vacuolated, abnormal
ZP:0018931	compartment boundary vertical myoseptum irregularly shaped, abnormal
ZP:0018932	optic cup absent, abnormal
ZP:0018933	intermediate cell mass of mesoderm decreased occurrence cell population proliferation, abnormal
ZP:0018934	posterior region hematopoietic system increased amount, abnormal
ZP:0018935	intermediate cell mass of mesoderm increased occurrence apoptotic process, abnormal
ZP:0018936	posterior region trunk decreased amount, abnormal
ZP:0018937	posterior region hematopoietic system decreased amount, abnormal
ZP:0018938	hematopoietic multipotent progenitor cell thymus absent, abnormal
ZP:0018939	somite decreased distribution, abnormal
ZP:0018940	whole organism has fewer parts of type neural crest cell, abnormal
ZP:0018941	pharyngeal arch 3-7 decreased occurrence cell population proliferation, abnormal
ZP:0018942	lens eye opaque, abnormal
ZP:0018943	lens decreased amount, abnormal
ZP:0018944	lens eye decreased size, abnormal
ZP:0018945	macrophage midbrain decreased amount, abnormal
ZP:0018946	macrophage spleen decreased amount, abnormal
ZP:0018947	macrophage liver decreased amount, abnormal
ZP:0018948	macrophage decreased speed, abnormal
ZP:0018949	macrophage pericardium decreased amount, abnormal
ZP:0018950	macrophage caudal fin decreased amount, abnormal
ZP:0018951	macrophage spherical, abnormal
ZP:0018952	neutrophil trunk decreased amount, abnormal
ZP:0018953	retinal inner plexiform layer decreased amount, abnormal
ZP:0018954	portion of tissue broken, abnormal
ZP:0018955	posterior region whole organism malformed, abnormal
ZP:0018956	brain decreased amount, abnormal
ZP:0018957	caudal fin decreased amount, abnormal
ZP:0018958	yolk split, abnormal
ZP:0018959	microtubule external yolk syncytial layer disorganized, abnormal
ZP:0018960	microtubule external yolk syncytial layer absent, abnormal
ZP:0018961	cell EVL elongated, abnormal
ZP:0018962	actin cytoskeleton external yolk syncytial layer disorganized, abnormal
ZP:0018963	cell EVL decreased amount, abnormal
ZP:0018964	whole organism increased occurrence cytolysis, abnormal
ZP:0018965	cell EVL increased size, abnormal
ZP:0018966	convergent extension increased occurrence, abnormal
ZP:0018967	actin cytoskeleton external yolk syncytial layer absent, abnormal
ZP:0018968	microtubule external yolk syncytial layer decreased amount, abnormal
ZP:0018969	actin cytoskeleton external yolk syncytial layer decreased amount, abnormal
ZP:0018970	ventral region whole organism mislocalised, abnormal
ZP:0018971	whole organism mislocalised, abnormal
ZP:0018972	hindbrain neural keel decreased distribution, abnormal
ZP:0018973	ventral region whole organism decreased amount, abnormal
ZP:0018974	paraxial mesoderm spatial pattern, abnormal
ZP:0018975	adaxial cell spatial pattern, abnormal
ZP:0018976	neural plate spatial pattern, abnormal
ZP:0018977	notochord spatial pattern, abnormal
ZP:0018978	blastodisc decreased amount, abnormal
ZP:0018979	segmental plate spatial pattern, abnormal
ZP:0018980	yolk syncytial layer decreased amount, abnormal
ZP:0018981	retinal pigmented epithelium absent, abnormal
ZP:0018982	integument disrupted pigmentation, abnormal
ZP:0018983	whole organism mottled, abnormal
ZP:0018984	iridophore process quality pigmentation, abnormal
ZP:0018985	preural vertebra decreased length, abnormal
ZP:0018986	vertebra 8 decreased length, abnormal
ZP:0018987	precaudal vertebra decreased length, abnormal
ZP:0018988	centrum morphology, abnormal
ZP:0018989	postcranial axial skeleton morphology, abnormal
ZP:0018990	caudal vertebra decreased length, abnormal
ZP:0018991	bone morphogenesis decreased process quality, abnormal
ZP:0018992	bone growth decreased process quality, abnormal
ZP:0018993	vertebra 7 decreased length, abnormal
ZP:0018994	vertebra 9 decreased length, abnormal
ZP:0018995	vertebra 11 decreased length, abnormal
ZP:0018996	vertebra 10 decreased length, abnormal
ZP:0018997	neuromast primordium migration arrested, abnormal
ZP:0018998	cardiac ventricle decreased angle to atrium, abnormal
ZP:0018999	male gamete generation premature, abnormal
ZP:0019000	oocyte premature apoptotic process, abnormal
ZP:0019001	germ line cell increased occurrence apoptotic process, abnormal
ZP:0019002	swimming increased speed, abnormal
ZP:0019003	pronephric proximal straight tubule increased distribution, abnormal
ZP:0019004	pronephros wholly anterioralized, abnormal
ZP:0019005	anterior/posterior pattern specification involved in pronephros development disrupted, abnormal
ZP:0019006	pronephric distal late tubule decreased distribution, abnormal
ZP:0019007	pronephric distal early tubule mislocalised, abnormal
ZP:0019008	pronephric proximal convoluted tubule increased distribution, abnormal
ZP:0019009	retinoic acid whole organism increased amount, abnormal
ZP:0019010	pectoral fin decreased amount, abnormal
ZP:0019011	dendrite morphogenesis disrupted, abnormal
ZP:0019012	dendrite habenula truncated, abnormal
ZP:0019013	neuron projection dorsal habenular nucleus decreased amount, abnormal
ZP:0019014	interpeduncular nucleus tegmentum process quality innervation, abnormal
ZP:0019015	neuron projection terminus dorsal habenular nucleus incomplete structure, abnormal
ZP:0019016	neuron dorsal habenular nucleus morphology, abnormal
ZP:0019017	lipoprotein lipase activity disrupted, abnormal
ZP:0019018	cranial nerve X disorganized, abnormal
ZP:0019019	axon retinal ganglion cell hypoplastic, abnormal
ZP:0019020	cranial nerve X misrouted, abnormal
ZP:0019021	cranial skeletal system development disrupted, abnormal
ZP:0019022	CoPA decreased process quality axon extension involved in axon guidance, abnormal
ZP:0019023	neuron projection CoPA misrouted, abnormal
ZP:0019024	yolk displaced to blastodisc, abnormal
ZP:0019025	cytoplasm organization process quality, abnormal
ZP:0019026	microtubule oocyte stage I decreased amount, abnormal
ZP:0019027	microtubule fertilized egg disoriented, abnormal
ZP:0019028	cytoplasm yolk present, abnormal
ZP:0019029	blastomere increased variability of size, abnormal
ZP:0019030	embryonic cleavage variability, abnormal
ZP:0019031	Spemann organizer formation at the embryonic shield process quality, abnormal
ZP:0019032	cell division increased duration, abnormal
ZP:0019033	medial-lateral axis notochord increased width, abnormal
ZP:0019034	cortical granule exocytosis delayed, abnormal
ZP:0019035	egg activation process quality, abnormal
ZP:0019036	microtubule fertilized egg irregular spatial pattern, abnormal
ZP:0019037	mesoderm formation process quality, abnormal
ZP:0019038	heart disrupted blood circulation, abnormal
ZP:0019039	yolk displaced to blastoderm, abnormal
ZP:0019040	yolk amorphous, abnormal
ZP:0019041	anterior-posterior axis notochord decreased length, abnormal
ZP:0019042	synapse eye photoreceptor cell poorly differentiated, abnormal
ZP:0019043	retina lacks parts or has fewer parts of type photoreceptor outer segment eye photoreceptor cell, abnormal
ZP:0019044	peripheral region retina morphology, abnormal
ZP:0019045	cell projection Muller cell decreased amount, abnormal
ZP:0019046	cell projection Muller cell disorganized, abnormal
ZP:0019047	nucleus photoreceptor cell disorganized, abnormal
ZP:0019048	photoreceptor outer segment photoreceptor cell disorganized, abnormal
ZP:0019049	retinal photoreceptor layer mislocalised, abnormal
ZP:0019050	proliferative region brain decreased amount, abnormal
ZP:0019051	ciliary marginal zone increased occurrence apoptotic process, abnormal
ZP:0019052	optic tectum increased occurrence cell death, abnormal
ZP:0019053	eye increased occurrence cell death, abnormal
ZP:0019054	forebrain increased occurrence cell death, abnormal
ZP:0019055	mouth decreased position, abnormal
ZP:0019056	anterior region head increased length, abnormal
ZP:0019057	regulation of transcription of nucleolar large rRNA by RNA polymerase I decreased process quality, abnormal
ZP:0019058	nucleolar chromatin organization process quality, abnormal
ZP:0019059	trunk curved caudal, abnormal
ZP:0019060	hematopoietic stem cell intermediate cell mass of mesoderm decreased distribution, abnormal
ZP:0019061	mRNA splicing, via spliceosome decreased occurrence, abnormal
ZP:0019062	hematopoietic stem cell ventral wall of dorsal aorta decreased distribution, abnormal
ZP:0019063	hematopoietic stem cell decreased distribution, abnormal
ZP:0019065	skeletal muscle cell structure, abnormal
ZP:0019066	T-tubule skeletal muscle cell bent, abnormal
ZP:0019067	ventricular myocardium spatial pattern, abnormal
ZP:0019068	skeletal muscle cell decreased size, abnormal
ZP:0019069	sarcoplasmic reticulum skeletal muscle dilated, abnormal
ZP:0019070	mitochondrion skeletal muscle cell dilated, abnormal
ZP:0019071	endocrine pancreas decreased amount, abnormal
ZP:0019072	pancreas decreased amount, abnormal
ZP:0019073	anterior pancreatic bud disrupted type B pancreatic cell differentiation, abnormal
ZP:0019074	primary islet has fewer parts of type pancreatic B cell, abnormal
ZP:0019075	hypophysis increased amount, abnormal
ZP:0019076	liver decreased amount, abnormal
ZP:0019077	oviposition disrupted, abnormal
ZP:0019078	swim bladder decreased functionality, abnormal
ZP:0019079	thyroxine 5'-deiodinase activity disrupted, abnormal
ZP:0019080	thyroxine 5'-deiodinase activity decreased process quality, abnormal
ZP:0019081	retinal photoreceptor layer has fewer parts of type green sensitive photoreceptor cell retinal photoreceptor layer, abnormal
ZP:0019082	retinal photoreceptor layer has fewer parts of type retinal cone cell, abnormal
ZP:0019083	retinal photoreceptor layer has fewer parts of type blue sensitive photoreceptor cell retinal photoreceptor layer, abnormal
ZP:0019084	response to light stimulus decreased occurrence, abnormal
ZP:0019085	retinal photoreceptor layer has fewer parts of type red sensitive photoreceptor cell retinal photoreceptor layer, abnormal
ZP:0019086	retinal photoreceptor layer has fewer parts of type UV sensitive photoreceptor cell retinal photoreceptor layer, abnormal
ZP:0019087	neuron nervous system decreased distribution, abnormal
ZP:0019088	neuron trigeminal ganglion decreased branchiness, abnormal
ZP:0019089	trigeminal ganglion development disrupted, abnormal
ZP:0019090	pigmentation increased amount, abnormal
ZP:0019091	whole organism lethargic, abnormal
ZP:0019092	cytoplasm endothelial cell spatial pattern, abnormal
ZP:0019093	endothelial tip cell spatial pattern, abnormal
ZP:0019094	membrane trunk musculature damage, abnormal
ZP:0019095	myotome decreased process quality skeletal myofibril assembly, abnormal
ZP:0019096	skeletal muscle structure, abnormal
ZP:0019097	female organism increased amount, abnormal
ZP:0019098	germ line cell testis decreased amount, abnormal
ZP:0019099	male gonad development arrested, abnormal
ZP:0019100	testis disorganized, abnormal
ZP:0019101	gonad mislocalised, abnormal
ZP:0019102	testis unlumenized, abnormal
ZP:0019103	immature gonad decreased process quality apoptotic process, abnormal
ZP:0019104	neural crest cell xanthoblast aggregated, abnormal
ZP:0019105	neural crest cell melanoblast aggregated, abnormal
ZP:0019106	Kupffer's vesicle decreased process quality epithelial cilium movement involved in extracellular fluid movement, abnormal
ZP:0019107	nucleus lens apoptotic, abnormal
ZP:0019108	cornea degenerate, abnormal
ZP:0019109	nucleus lens present, abnormal
ZP:0019110	lens elongated, abnormal
ZP:0019111	male sex differentiation increased occurrence, abnormal
ZP:0019112	female sex differentiation absent, abnormal
ZP:0019113	testis aplastic/hypoplastic, abnormal
ZP:0019114	gonad primordium lacks all parts of type germ line cell, abnormal
ZP:0019115	germ line cell mislocalised, abnormal
ZP:0019116	skeletal muscle cell increased diameter, abnormal
ZP:0019117	somite hypoplastic, abnormal
ZP:0019118	skeletal muscle cell decreased amount, abnormal
ZP:0019119	podocyte foot pronephric glomerulus morphology, abnormal
ZP:0019120	myeloid cell decreased distribution, abnormal
ZP:0019121	nucleate erythrocyte decreased distribution, abnormal
ZP:0019122	pancreas decreased distribution, abnormal
ZP:0019123	lymphocyte thymus absent, abnormal
ZP:0019124	bile ductule morphology, abnormal
ZP:0019125	hepatocyte decreased distribution, abnormal
ZP:0019126	posterior region hematopoietic system decreased distribution, abnormal
ZP:0019127	nucleate erythrocyte malformed, abnormal
ZP:0019128	blood cell decreased occurrence DNA methylation, abnormal
ZP:0019129	hematopoietic cell head kidney decreased amount, abnormal
ZP:0019130	pronephros decreased process quality cilium assembly, abnormal
ZP:0019131	blood accumulation distal region caudal fin, abnormal
ZP:0019132	caudal artery increased size, abnormal
ZP:0019133	caudal artery fused with caudal vein, abnormal
ZP:0019134	caudal vein increased size, abnormal
ZP:0019135	membrane skeletal muscle damaged, abnormal
ZP:0019136	nucleus whole organism apoptotic, abnormal
ZP:0019137	histone H3-K4 methylation decreased process quality, abnormal
ZP:0019138	blastodisc furrowed, abnormal
ZP:0019140	mitotic spindle pole cell broken, abnormal
ZP:0019141	mitotic spindle cell elongated, abnormal
ZP:0019142	blastomere increased size, abnormal
ZP:0019143	cell division arrested, abnormal
ZP:0019144	blastomere deformed, abnormal
ZP:0019145	nucleus whole organism decreased amount, abnormal
ZP:0019146	mitotic spindle pole cell structure, abnormal
ZP:0019147	non-motile cilium olfactory epithelium decreased length, abnormal
ZP:0019148	Golgi stack eye photoreceptor cell distended, abnormal
ZP:0019149	eye photoreceptor cell has extra parts of type photoreceptor inner segment lysosome eye photoreceptor cell, abnormal
ZP:0019150	eye photoreceptor cell accumulation photoreceptor inner segment vacuole eye photoreceptor cell, abnormal
ZP:0019151	eye photoreceptor cell has extra parts of type photoreceptor outer segment vesicle eye photoreceptor cell, abnormal
ZP:0019152	photoreceptor disc membrane eye photoreceptor cell deformed, abnormal
ZP:0019153	cell body eye photoreceptor cell mislocalised, abnormal
ZP:0019154	eye photoreceptor cell vacuolated, abnormal
ZP:0019155	eye photoreceptor cell accumulation photoreceptor inner segment vesicle eye photoreceptor cell, abnormal
ZP:0019156	Golgi apparatus eye photoreceptor cell swollen, abnormal
ZP:0019157	eye photoreceptor cell decreased distribution, abnormal
ZP:0019158	floor plate has fewer parts of type motile cilium floor plate, abnormal
ZP:0019159	cilium whole organism decreased amount, abnormal
ZP:0019160	cilium whole organism absent, abnormal
ZP:0019161	motile cilium whole organism absent, abnormal
ZP:0019162	whole organism lacks parts or has fewer parts of type ceratobranchial 5 primary tooth, abnormal
ZP:0019163	ventral region pharyngeal arch 1 decreased size, abnormal
ZP:0019164	neural crest cell pharyngeal arch increased amount, abnormal
ZP:0019165	ventral region pharyngeal arch 2 decreased amount, abnormal
ZP:0019166	joint pharyngeal arch 2 absent, abnormal
ZP:0019167	ventral region pharyngeal arch cartilage morphology, abnormal
ZP:0019168	ventral region pharyngeal arch increased amount, abnormal
ZP:0019169	ventral region pharyngeal arch 2 increased amount, abnormal
ZP:0019170	ventral region pharyngeal arch 2 decreased size, abnormal
ZP:0019171	ventral region pharyngeal arch cartilage decreased amount, abnormal
ZP:0019172	pharyngeal arch 2 decreased amount, abnormal
ZP:0019173	ventral region pharyngeal arch 1 decreased amount, abnormal
ZP:0019174	nucleus somite morphology, abnormal
ZP:0019175	filopodium hepatoblast decreased length, abnormal
ZP:0019176	intestinal bulb primordium decreased curvature, abnormal
ZP:0019177	hepatoblast shape, abnormal
ZP:0019178	hepatoblast anterior orientation, abnormal
ZP:0019179	liver primordium malformed, abnormal
ZP:0019180	hepatoblast absent, abnormal
ZP:0019181	apical junction complex mesoderm mislocalised, abnormal
ZP:0019182	hepatocyte cell migration decreased occurrence, abnormal
ZP:0019183	embryonic liver development process quality, abnormal
ZP:0019184	embryonic digestive tract development decreased process quality, abnormal
ZP:0019185	hepatoblast has fewer parts of type filopodium hepatoblast, abnormal
ZP:0019186	lateral plate mesoderm decreased process quality establishment of epithelial cell apical/basal polarity, abnormal
ZP:0019187	hepatoblast mislocalised medially, abnormal
ZP:0019188	hepatoblast mislocalised, abnormal
ZP:0019189	hepatoblast process quality regulation of filopodium assembly, abnormal
ZP:0019190	hepatocyte cell migration process quality, abnormal
ZP:0019191	hepatoblast mislocalised posteriorly, abnormal
ZP:0019192	trabecular layer absent, abnormal
ZP:0019193	heart decreased amount, abnormal
ZP:0019194	commissure of the tract of the commissure of the caudal tuberculum has extra parts of type axon commissure of the tract of the commissure of the caudal tuberculum, abnormal
ZP:0019195	forerunner cell group dispersed, abnormal
ZP:0019196	heart decreased occurrence heart looping, abnormal
ZP:0019197	spinal cord increased occurrence apoptotic process, abnormal
ZP:0019198	spinal cord increased occurrence cell population proliferation, abnormal
ZP:0019199	pharyngeal arch increased occurrence apoptotic process, abnormal
ZP:0019200	brain increased occurrence cell population proliferation, abnormal
ZP:0019201	neuroblast (sensu Vertebrata) increased occurrence apoptotic process, abnormal
ZP:0019202	glial cell spinal cord deformed, abnormal
ZP:0019203	neuroblast (sensu Vertebrata) spinal cord deformed, abnormal
ZP:0019204	closure of optic fissure disrupted, abnormal
ZP:0019205	dorsal-ventral axis head decreased height, abnormal
ZP:0019206	ventral region retina decreased thickness, abnormal
ZP:0019207	central nervous system increased occurrence apoptotic process, abnormal
ZP:0019208	nuclear-transcribed mRNA catabolic process, nonsense-mediated decay increased process quality, abnormal
ZP:0019209	retina increased amount, abnormal
ZP:0019210	nucleus retina decreased amount, abnormal
ZP:0019211	midbrain decreased amount, abnormal
ZP:0019212	pronephric tubule decreased distribution, abnormal
ZP:0019213	pronephric distal early tubule decreased distribution, abnormal
ZP:0019214	pronephric proximal straight tubule decreased distribution, abnormal
ZP:0019215	pronephric duct decreased distribution, abnormal
ZP:0019216	pronephric glomerulus lacks parts or has fewer parts of type podocyte foot pronephric podocyte, abnormal
ZP:0019217	renal glomerulus increased amount, abnormal
ZP:0019218	macula utricle decreased process quality vestibular receptor cell stereocilium organization, abnormal
ZP:0019219	lateral crista decreased process quality vestibular receptor cell stereocilium organization, abnormal
ZP:0019220	lateral crista orientation stereocilium bundle lateral crista, abnormal
ZP:0019221	neuromast hair cell orientation stereocilium bundle neuromast, abnormal
ZP:0019222	macula utricle orientation stereocilium bundle macula utricle, abnormal
ZP:0019223	stereocilium bundle neuromast unidirectional, abnormal
ZP:0019224	posterior lateral line decreased process quality posterior lateral line neuromast development, abnormal
ZP:0019225	posterior lateral line decreased process quality neuromast hair cell development, abnormal
ZP:0019226	stereocilium bundle neuromast bilateral symmetry, abnormal
ZP:0019227	chondrocyte ceratohyal cartilage increased variability of size, abnormal
ZP:0019228	chondrocyte Meckel's cartilage increased variability of size, abnormal
ZP:0019229	filopodium hepatoblast increased branchiness, abnormal
ZP:0019230	pancreas decreased occurrence determination of pancreatic left/right asymmetry, abnormal
ZP:0019231	Kupffer's vesicle loose, abnormal
ZP:0019232	forerunner cell group mislocalised ventrally, abnormal
ZP:0019235	forerunner cell group mislocalised anteriorly, abnormal
ZP:0019236	Kupffer's vesicle irregularly shaped, abnormal
ZP:0019237	liver decreased occurrence determination of liver left/right asymmetry, abnormal
ZP:0019238	margin absent, abnormal
ZP:0019239	heart tube decreased occurrence heart jogging, abnormal
ZP:0019240	margin decreased amount, abnormal
ZP:0019241	afferent neuron defasciculated, abnormal
ZP:0019242	afferent neuron lacks all parts of type axon myelinating Schwann cell, abnormal
ZP:0019243	myelinating Schwann cell posterior lateral line absent, abnormal
ZP:0019244	glial cell (sensu Vertebrata) lateral line disorganized, abnormal
ZP:0019245	photoreceptor inner segment retinal cone cell decreased amount, abnormal
ZP:0019246	mitochondrion retinal cone cell decreased amount, abnormal
ZP:0019247	mitochondrion retinal cone cell decreased size, abnormal
ZP:0019248	retinal cone cell process quality mitochondrion morphogenesis, abnormal
ZP:0019249	sister chromatid cohesion decreased process quality, abnormal
ZP:0019250	mitotic spindle cell rotated, abnormal
ZP:0019251	micronucleus cell increased amount, abnormal
ZP:0019252	chromosome cell distributed, abnormal
ZP:0019253	metaphase plate cell absent, abnormal
ZP:0019254	cell separated from chromosome chromosome cell, abnormal
ZP:0019255	chromosome organization decreased process quality, abnormal
ZP:0019256	chromosome cell amount, abnormal
ZP:0019257	mitotic chromosome decondensation premature, abnormal
ZP:0019258	mitotic cytokinesis decreased occurrence, abnormal
ZP:0019259	mitotic cell cycle increased occurrence, abnormal
ZP:0019260	pharyngeal arch cartilage decreased process quality embryonic viscerocranium morphogenesis, abnormal
ZP:0019261	pharyngeal arch 3-7 decreased process quality cartilage development, abnormal
ZP:0019262	pharyngeal arch cartilage increased amount, abnormal
ZP:0019263	myotome decreased occurrence striated muscle cell differentiation, abnormal
ZP:0019264	pharyngeal arch cartilage decreased process quality cartilage development, abnormal
ZP:0019265	myotome increased amount, abnormal
ZP:0019266	pharyngeal musculature increased amount, abnormal
ZP:0019267	myotome decreased amount, abnormal
ZP:0019268	caudal vein plexus decreased amount, abnormal
ZP:0019269	axial vasculature increased process quality apoptotic process, abnormal
ZP:0019270	blood vasculature lacks parts or has fewer parts of type blood vessel, abnormal
ZP:0019271	pronephros has fewer parts of type multi-ciliated epithelial cell pronephros, abnormal
ZP:0019272	pronephric nephron tubule epithelial cell differentiation process quality, abnormal
ZP:0019273	pronephros decreased occurrence multi-ciliated epithelial cell differentiation, abnormal
ZP:0019274	pronephros decreased distribution, abnormal
ZP:0019275	pronephric proximal straight tubule has fewer parts of type multi-ciliated epithelial cell pronephric proximal straight tubule, abnormal
ZP:0019276	renal system process decreased occurrence, abnormal
ZP:0019277	common lymphoid progenitor increased amount, abnormal
ZP:0019278	intermediate cell mass of mesoderm decreased amount, abnormal
ZP:0019279	whole organism has extra parts of type macrophage, abnormal
ZP:0019280	kidney decreased amount, abnormal
ZP:0019281	whole organism has extra parts of type monocyte, abnormal
ZP:0019282	whole organism has extra parts of type neutrophil, abnormal
ZP:0019283	whole organism has extra parts of type erythroblast, abnormal
ZP:0019284	mitotic spindle midzone assembly process quality, abnormal
ZP:0019285	cerebellar Purkinje cell layer structural organization disrupted, abnormal
ZP:0019286	cranial nerve VII morphology, abnormal
ZP:0019287	Purkinje cell cerebellum distributed, abnormal
ZP:0019288	thymus decreased volume, abnormal
ZP:0019289	thymus decreased distribution, abnormal
ZP:0019290	myocardium decreased amount, abnormal
ZP:0019292	posterior region whole organism increased distribution, abnormal
ZP:0019293	heart jogging decreased occurrence, abnormal
ZP:0019294	heart wholeness, abnormal
ZP:0019295	rhombomere 3 decreased amount, abnormal
ZP:0019296	blood accumulation extension, abnormal
ZP:0019297	presumptive cardiac ventricle heart tube decreased amount, abnormal
ZP:0019298	artery pharyngeal arch absent, abnormal
ZP:0019299	cardiac muscle cell detached from atrium, abnormal
ZP:0019300	gut straight, abnormal
ZP:0019301	cardiac muscle cell detached from cardiac ventricle, abnormal
ZP:0019302	endocardium decreased amount, abnormal
ZP:0019304	rhombomere 5 decreased amount, abnormal
ZP:0019308	heart decreased distribution, abnormal
ZP:0019309	cardiac ventricle decreased amount, abnormal
ZP:0019310	atrium decreased amount, abnormal
ZP:0019311	ciliary basal body pronephric duct mislocalised, abnormal
ZP:0019312	1-phosphatidyl-1D-myo-inositol 4,5-bisphosphate pronephric duct mislocalised, abnormal
ZP:0019313	filamentous actin pronephric duct mislocalised, abnormal
ZP:0019314	pronephric duct has fewer parts of type motile cilium pronephric duct, abnormal
ZP:0019315	pronephric duct decreased process quality ciliary basal body-plasma membrane docking, abnormal
ZP:0019316	pronephric duct decreased process quality actin filament bundle distribution, abnormal
ZP:0019317	1-phosphatidyl-1D-myo-inositol 3,4,5-trisphosphate pronephric duct mislocalised, abnormal
ZP:0019318	apical plasma membrane pronephric duct mislocalised, abnormal
ZP:0019319	epiboly decreased process quality, abnormal
ZP:0019320	blood coagulation, fibrin clot formation delayed, abnormal
ZP:0019321	blood plasma decreased amount, abnormal
ZP:0019322	whole organism has fewer parts of type eye, abnormal
ZP:0019323	motor neuron process quality axon guidance, abnormal
ZP:0019324	thymus increased distribution, abnormal
ZP:0019325	anatomical structure increased distribution, abnormal
ZP:0019326	myofilament skeletal muscle disorganized, abnormal
ZP:0019327	mitochondrion cardiac muscle cell morphology, abnormal
ZP:0019328	heart contraction decreased efficacy, abnormal
ZP:0019329	autophagy disrupted, abnormal
ZP:0019330	mitochondrion skeletal muscle morphology, abnormal
ZP:0019331	skeletal muscle vacuolated, abnormal
ZP:0019332	mitotic cell cycle lacking processual parts cytokinesis, abnormal
ZP:0019333	cell polyploid, abnormal
ZP:0019334	cell cycle lacking processual parts mitotic cell cycle, abnormal
ZP:0019335	oligodendrocyte spinal cord increased amount, abnormal
ZP:0019336	oligodendrocyte increased occurrence TOR signaling, abnormal
ZP:0019337	whole organism increased occurrence TOR signaling, abnormal
ZP:0019338	medial region spinal cord mislocalised, abnormal
ZP:0019339	myelin sheath spinal cord increased thickness, abnormal
ZP:0019340	myelin sheath spinal cord increased amount, abnormal
ZP:0019341	whole organism increased occurrence cholesterol biosynthetic process, abnormal
ZP:0019342	cell adhesion process quality, abnormal
ZP:0019343	pharyngeal arch 4 has fewer parts of type cranial neural crest, abnormal
ZP:0019344	digestive system duct increased distribution, abnormal
ZP:0019345	liver development decreased occurrence, abnormal
ZP:0019346	primary islet increased distribution, abnormal
ZP:0019347	pancreas primordium increased distribution, abnormal
ZP:0019348	insulin secreting cell increased distribution, abnormal
ZP:0019349	insulin secreting cell increased amount, abnormal
ZP:0019350	endoderm increased distribution, abnormal
ZP:0019351	endocrine cell pancreas increased amount, abnormal
ZP:0019352	lateral region endoderm mislocalised, abnormal
ZP:0019353	posterior pancreatic bud increased distribution, abnormal
ZP:0019354	endocrine pancreas increased occurrence pancreas induction, abnormal
ZP:0019355	pancreas induction increased occurrence, abnormal
ZP:0019356	intestine decreased distribution, abnormal
ZP:0019357	somatostatin secreting cell increased amount, abnormal
ZP:0019358	endocrine cell pancreatic bud increased distribution, abnormal
ZP:0019359	endothelial cell medial facial lymph vessel decreased amount, abnormal
ZP:0019360	endothelial cell lateral facial lymph vessel decreased amount, abnormal
ZP:0019361	chondrocyte apoptotic, abnormal
ZP:0019362	protein localization to peroxisome disrupted, abnormal
ZP:0019363	ciliary basal body photoreceptor cell mislocalised, abnormal
ZP:0019364	photoreceptor cell displaced to photoreceptor outer segment lateral surface photoreceptor cell, abnormal
ZP:0019365	retinal cone cell absence due to degeneration, abnormal
ZP:0019366	retinal rod cell absence due to degeneration, abnormal
ZP:0019367	trunk vasculature has extra parts of type dorsal region blood vessel, abnormal
ZP:0019368	vascular sprouts intersegmental vein increased amount, abnormal
ZP:0019369	dorsal region intersegmental vessel increased branchiness, abnormal
ZP:0019370	endothelial cell dorsal aorta increased amount, abnormal
ZP:0019371	vascular sprouts intersegmental vessel increased amount, abnormal
ZP:0019373	endothelial cell dorsal longitudinal anastomotic vessel increased amount, abnormal
ZP:0019374	endothelial cell intersegmental vein increased amount, abnormal
ZP:0019375	intersegmental vessel displaced to vascular sprouts neural tube, abnormal
ZP:0019376	endothelial cell posterior cardinal vein increased amount, abnormal
ZP:0019377	trunk vasculature has extra parts of type dorsal region vascular sprouts, abnormal
ZP:0019378	thoracic duct decreased occurrence lymph vessel development, abnormal
ZP:0019381	primordial hindbrain channel decreased occurrence vasculature development, abnormal
ZP:0019382	swim bladder inflation decreased occurrence, abnormal
ZP:0019383	endothelial cell posterior cardinal vein absent, abnormal
ZP:0019384	anatomical structure decreased distribution, abnormal
ZP:0019385	primordial hindbrain channel malformed, abnormal
ZP:0019386	thoracic duct process quality lymph vessel development, abnormal
ZP:0019387	vascular sprouts posterior caudal vein decreased amount, abnormal
ZP:0019389	lateral facial lymph vessel truncated, abnormal
ZP:0019390	otolithic lymph vessel absent, abnormal
ZP:0019391	lymphangiogenic sprout lateral facial lymph vessel absent, abnormal
ZP:0019392	parachordal vessel decreased occurrence vasculature development, abnormal
ZP:0019393	lateral facial lymph vessel malformed, abnormal
ZP:0019394	posterior cardinal vein decreased amount, abnormal
ZP:0019395	lateral facial lymph vessel process quality lymph vessel development, abnormal
ZP:0019396	otolithic lymph vessel delayed lymph vessel development, abnormal
ZP:0019397	lateral facial lymph vessel closed, abnormal
ZP:0019398	whole organism increased occurrence mRNA modification, abnormal
ZP:0019399	hypocretin-secreting neuron increased occurrence synapse assembly, abnormal
ZP:0019400	cholinergic neuron increased occurrence synapse assembly, abnormal
ZP:0019401	motor neuron increased occurrence collateral sprouting, abnormal
ZP:0019402	brain increased occurrence mRNA modification, abnormal
ZP:0019403	motor neuron increased occurrence synapse assembly, abnormal
ZP:0019404	atrioventricular valve morphogenesis decreased process quality, abnormal
ZP:0019405	cell cardiac jelly decreased amount, abnormal
ZP:0019406	cell atrioventricular canal spatial pattern, abnormal
ZP:0019407	smooth muscle bulbus arteriosus absent, abnormal
ZP:0019408	cardiac ventricle decreased rate cardiac muscle tissue growth, abnormal
ZP:0019409	cardiac ventricle increased rate cardiac muscle tissue growth, abnormal
ZP:0019410	cardiac ventricle hypotrophic growth cardiac muscle tissue growth, abnormal
ZP:0019411	muscle precursor cell bulbus arteriosus increased amount, abnormal
ZP:0019412	pharynx decreased amount, abnormal
ZP:0019413	goblet cell disrupted cell maturation, abnormal
ZP:0019414	aortic arch incomplete structure, abnormal
ZP:0019415	pericyte brain vasculature decreased amount, abnormal
ZP:0019416	vascular smooth muscle brain vasculature decreased amount, abnormal
ZP:0019417	vascular smooth muscle brain vasculature decreased branchiness, abnormal
ZP:0019418	pericyte decreased occurrence cell development, abnormal
ZP:0019419	otic vesicle decreased distribution, abnormal
ZP:0019420	dorsolateral placode decreased distribution, abnormal
ZP:0019421	epibranchial field decreased distribution, abnormal
ZP:0019422	posterior region neurogenic field decreased amount, abnormal
ZP:0019423	otic placode decreased distribution, abnormal
ZP:0019424	Kupffer's vesicle decreased distribution, abnormal
ZP:0019425	posterior region whole organism decreased distribution, abnormal
ZP:0019426	pharyngeal pouch 1 morphology, abnormal
ZP:0019427	posterior pancreatic bud decreased amount, abnormal
ZP:0019428	gut decreased amount, abnormal
ZP:0019429	epiboly decreased rate, abnormal
ZP:0019430	endoderm development decreased occurrence, abnormal
ZP:0019431	embryonic liver development decreased occurrence, abnormal
ZP:0019432	presumptive endoderm decreased amount, abnormal
ZP:0019433	digestive tract development decreased occurrence, abnormal
ZP:0019434	pharynx development decreased occurrence, abnormal
ZP:0019435	liver primordium absent, abnormal
ZP:0019436	pancreas development decreased occurrence, abnormal
ZP:0019437	posterior pancreatic bud absent, abnormal
ZP:0019438	female organism female semi-sterile, abnormal
ZP:0019439	ovarian follicle stage III decreased amount, abnormal
ZP:0019440	ovarian follicle stage IV decreased amount, abnormal
ZP:0019441	ovarian follicle stage I decreased size, abnormal
ZP:0019442	germ line cell decreased size, abnormal
ZP:0019443	ovarian follicle development arrested, abnormal
ZP:0019444	ovarian follicle stage IV absent, abnormal
ZP:0019445	whole organism biological sex, abnormal
ZP:0019446	testis decreased process quality growth, abnormal
ZP:0019447	female organism decreased amount, abnormal
ZP:0019448	testis decreased amount, abnormal
ZP:0019449	testis immature, abnormal
ZP:0019450	ovarian follicle stage II absent, abnormal
ZP:0019451	ovarian follicle stage III absent, abnormal
ZP:0019452	ovarian follicle stage I immature, abnormal
ZP:0019453	male organism increased amount, abnormal
ZP:0019454	brain absent, abnormal
ZP:0019455	axon CoPA misrouted, abnormal
ZP:0019456	CoPA process quality anterior/posterior axon guidance, abnormal
ZP:0019457	axon CoPA mislocalised posteriorly, abnormal
ZP:0019458	CoPA decreased process quality anterior/posterior axon guidance, abnormal
ZP:0019459	planar cell polarity pathway involved in axon guidance decreased process quality, abnormal
ZP:0019460	CoPA decreased process quality dorsal spinal cord interneuron anterior axon guidance, abnormal
ZP:0019461	optic cup increased amount, abnormal
ZP:0019462	solid lens vesicle decreased amount, abnormal
ZP:0019463	mesenchymal cell atrioventricular canal decreased amount, abnormal
ZP:0019464	neuromuscular junction somite decreased area, abnormal
ZP:0019465	neuromuscular junction muscle decreased amount, abnormal
ZP:0019466	myofibril skeletal muscle decreased thickness, abnormal
ZP:0019467	muscle disrupted axonogenesis, abnormal
ZP:0019468	skeletal muscle myofibril skeletal muscle loose, abnormal
ZP:0019469	muscle tendon junction myoseptum morphology, abnormal
ZP:0019470	Z disc muscle decreased length, abnormal
ZP:0019471	blood island mislocalised, abnormal
ZP:0019472	intermediate cell mass of mesoderm mislocalised, abnormal
ZP:0019473	atrioventricular canal increased amount, abnormal
ZP:0019474	atrioventricular canal decreased amount, abnormal
ZP:0019475	solid lens vesicle decreased distribution, abnormal
ZP:0019476	olfactory placode decreased distribution, abnormal
ZP:0019477	neurogenic field decreased amount, abnormal
ZP:0019478	macrophage liver increased amount, abnormal
ZP:0019479	macrophage brain morphology, abnormal
ZP:0019480	microglial cell brain circular, abnormal
ZP:0019482	dopaminergic neuron caudal periventricular hypothalamus decreased amount, abnormal
ZP:0019483	macrophage decreased occurrence endocytic recycling, abnormal
ZP:0019484	microglial cell increased accumulation brain, abnormal
ZP:0019485	macrophage tectal ventricle increased size, abnormal
ZP:0019486	glucosylceramidase activity decreased process quality, abnormal
ZP:0019487	sphingolipid metabolic process disrupted, abnormal
ZP:0019488	macrophage brain increased amount, abnormal
ZP:0019490	glial cell projection brain retracted, abnormal
ZP:0019491	vacuole microglial cell increased amount, abnormal
ZP:0019492	inclusion body CNS neuron (sensu Vertebrata) increased amount, abnormal
ZP:0019493	macrophage increased accumulation tectal ventricle, abnormal
ZP:0019495	microglial cell spherical, abnormal
ZP:0019496	macrophage thymus morphology, abnormal
ZP:0019498	microglial cell activation increased occurrence, abnormal
ZP:0019499	autophagosome brain increased amount, abnormal
ZP:0019500	macrophage liver morphology, abnormal
ZP:0019501	brain increased amount, abnormal
ZP:0019502	mitochondrion brain decreased functionality, abnormal
ZP:0019503	macrophage thymus increased amount, abnormal
ZP:0019504	pancreatic A cell increased rate cell population proliferation, abnormal
ZP:0019505	pancreatic A cell primary islet increased amount, abnormal
ZP:0019506	glucagon secretion increased process quality, abnormal
ZP:0019508	pancreatic A cell hyperplastic, abnormal
ZP:0019509	axon peripheral neuron absent, abnormal
ZP:0019510	ciliary marginal zone decreased amount, abnormal
ZP:0019511	ciliary marginal zone decreased thickness, abnormal
ZP:0019512	ciliary marginal zone decreased distribution, abnormal
ZP:0019513	retinal inner nuclear layer increased distribution, abnormal
ZP:0019514	lens mislocalised ventrally, abnormal
ZP:0019515	retinal inner nuclear layer spatial pattern, abnormal
ZP:0019516	T cell differentiation decreased occurrence, abnormal
ZP:0019517	lymphoid progenitor cell thymus decreased amount, abnormal
ZP:0019518	erythroid lineage cell posterior lateral mesoderm absent, abnormal
ZP:0019519	head kidney decreased amount, abnormal
ZP:0019520	synapse Mauthner neuron absent, abnormal
ZP:0019521	spinal cord increased occurrence cell death, abnormal
ZP:0019522	myelinating Schwann cell posterior lateral line decreased amount, abnormal
ZP:0019523	Kupffer's vesicle decreased rate cilium movement, abnormal
ZP:0019524	whole organism increased occurrence cell death, abnormal
ZP:0019525	posterior lateral line nerve lacks parts or has fewer parts of type axon myelin sheath neuron, abnormal
ZP:0019526	eurydendroid cell absent, abnormal
ZP:0019527	myelinating Schwann cell anterior lateral line absent, abnormal
ZP:0019528	axon posterior lateral line nerve decreased diameter, abnormal
ZP:0019529	retinal pigmented epithelium increased occurrence cell death, abnormal
ZP:0019530	poly(A)+ mRNA export from nucleus decreased occurrence, abnormal
ZP:0019531	oligodendrocyte hindbrain spatial pattern, abnormal
ZP:0019532	immature Schwann cell decreased occurrence cell population proliferation, abnormal
ZP:0019533	anterior region posterior lateral line decreased distribution, abnormal
ZP:0019534	cloaca decreased functionality, abnormal
ZP:0019535	motor neuron spinal cord physical object quality, abnormal
ZP:0019536	pronephric tubule lacks parts or has fewer parts of type multi-ciliated epithelial cell pronephric tubule, abnormal
ZP:0019537	multi-ciliated epithelial cell pronephric duct absent, abnormal
ZP:0019538	extracellular space chondrocyte mislocalised, abnormal
ZP:0019539	chondrocyte ceratohyal cartilage increased amount, abnormal
ZP:0019540	cranial cartilage increased amount, abnormal
ZP:0019541	nucleus chondrocyte increased amount, abnormal
ZP:0019542	nucleus chondrocyte mislocalised, abnormal
ZP:0019543	Meckel's cartilage increased amount, abnormal
ZP:0019545	chondrocyte Meckel's cartilage decreased amount, abnormal
ZP:0019546	opercle decreased amount, abnormal
ZP:0019547	palate increased amount, abnormal
ZP:0019548	endochondral bone decreased occurrence ossification, abnormal
ZP:0019549	cleithrum decreased amount, abnormal
ZP:0019550	dermatocranium decreased amount, abnormal
ZP:0019551	parasphenoid decreased amount, abnormal
ZP:0019552	head decreased amount, abnormal
ZP:0019553	dermatocranium decreased occurrence ossification, abnormal
ZP:0019554	ceratohyal cartilage increased amount, abnormal
ZP:0019555	Collagen Meckel's cartilage increased amount, abnormal
ZP:0019556	cranial cartilage process quality chondrocyte development, abnormal
ZP:0019557	chondrocyte cranial cartilage decreased amount, abnormal
ZP:0019558	chondrocyte palatoquadrate cartilage increased amount, abnormal
ZP:0019559	cranial skeletal system development process quality, abnormal
ZP:0019560	dentary decreased amount, abnormal
ZP:0019561	chondrocyte ceratohyal cartilage decreased amount, abnormal
ZP:0019562	maxilla decreased amount, abnormal
ZP:0019563	chondrocyte cranial cartilage increased amount, abnormal
ZP:0019564	entopterygoid decreased amount, abnormal
ZP:0019566	palatoquadrate cartilage increased amount, abnormal
ZP:0019567	Collagen ceratohyal cartilage increased amount, abnormal
ZP:0019568	transferase activity, transferring phosphorus-containing groups decreased process quality, abnormal
ZP:0019569	head increased amount, abnormal
ZP:0019570	gastrulation decreased speed, abnormal
ZP:0019571	embryonic cleavage decreased occurrence, abnormal
ZP:0019572	glucosidase activity decreased process quality, abnormal
ZP:0019573	developmental process decreased speed, abnormal
ZP:0019574	somite rostral/caudal axis specification process quality, abnormal
ZP:0019575	site of double-strand break whole organism increased amount, abnormal
ZP:0019576	posterior side somite absent, abnormal
ZP:0019577	pronephros increased amount, abnormal
ZP:0019578	posterior side trunk increased amount, abnormal
ZP:0019579	anterior-most region segmental plate absent, abnormal
ZP:0019580	post-vent region increased occurrence apoptotic process, abnormal
ZP:0019581	DNA damage checkpoint increased process quality, abnormal
ZP:0019582	horizontal myoseptum decreased amount, abnormal
ZP:0019583	posterior lateral line primordium mislocalised dorsally, abnormal
ZP:0019584	posterior lateral line primordium mislocalised anteriorly, abnormal
ZP:0019585	posterior lateral line primordium decreased amount, abnormal
ZP:0019586	posterior lateral line primordium increased thickness, abnormal
ZP:0019587	ventral wall of dorsal aorta absent, abnormal
ZP:0019588	ventral wall of dorsal aorta increased occurrence Notch signaling pathway, abnormal
ZP:0019589	cell head kidney decreased amount, abnormal
ZP:0019590	hemopoiesis increased occurrence, abnormal
ZP:0019592	hair cell increased occurrence apoptotic process, abnormal
ZP:0019593	desmosome neuromast hair cell disorganized, abnormal
ZP:0019594	desmosome neuromast hair cell damaged, abnormal
ZP:0019595	margin spatial pattern, abnormal
ZP:0019596	yolk increased distribution, abnormal
ZP:0019597	anterior region axis duplicated, abnormal
ZP:0019598	cortical microtubule cytoskeleton fertilized egg spatial pattern, abnormal
ZP:0019599	head aplastic/hypoplastic, abnormal
ZP:0019600	animal-vegetal axis yolk decreased amount, abnormal
ZP:0019601	fertilized egg has extra parts of type cortical microtubule cytoskeleton aster fertilized egg, abnormal
ZP:0019602	basal region blastodisc mislocalised, abnormal
ZP:0019603	pole plasm oocyte stage II increased distribution, abnormal
ZP:0019604	pole plasm oocyte stage I increased distribution, abnormal
ZP:0019605	motile cilium Kupffer's vesicle increased length, abnormal
ZP:0019606	cone photoresponse recovery decreased efficacy, abnormal
ZP:0019607	acetylcholine-gated channel complex myotome disorganized, abnormal
ZP:0019608	acetylcholine-gated channel complex myotome mislocalised, abnormal
ZP:0019609	otic vesicle decreased occurrence epithelial to mesenchymal transition, abnormal
ZP:0019610	statoacoustic (VIII) ganglion has fewer parts of type neuroblast statoacoustic (VIII) ganglion, abnormal
ZP:0019611	basal part of cell otic epithelium decreased amount, abnormal
ZP:0019612	ventro-medial region otic vesicle increased distribution, abnormal
ZP:0019613	ventro-medial region otic vesicle mislocalised, abnormal
ZP:0019614	ventral region otic vesicle increased amount, abnormal
ZP:0019615	otic vesicle decreased occurrence neuroblast delamination, abnormal
ZP:0019616	neuron optic tectum increased amount, abnormal
ZP:0019617	forebrain decreased amount, abnormal
ZP:0019618	hypothalamus decreased amount, abnormal
ZP:0019619	mitotic cell cycle asynchronous, abnormal
ZP:0019620	embryonic morphogenesis arrested, abnormal
ZP:0019621	iron ion homeostasis decreased occurrence, abnormal
ZP:0019622	caudal fin decreased occurrence bone mineralization, abnormal
ZP:0019623	vertebra decreased occurrence bone mineralization, abnormal
ZP:0019625	pancreatic acinar gland absent, abnormal
ZP:0019626	exocrine pancreas decreased occurrence growth, abnormal
ZP:0019627	exocrine pancreas decreased distribution, abnormal
ZP:0019628	epithelial cell of pancreas exocrine pancreas decreased amount, abnormal
ZP:0019629	exocrine pancreas decreased occurrence cell population proliferation, abnormal
ZP:0019630	protoneuromast decreased amount, abnormal
ZP:0019631	posterior lateral line primordium decreased distribution, abnormal
ZP:0019632	horizontal myoseptum decreased distribution, abnormal
ZP:0019633	posterior lateral line primordium size, abnormal
ZP:0019634	posterior lateral line neuromast decreased distribution, abnormal
ZP:0019635	posterior lateral line primordium absent, abnormal
ZP:0019636	protoneuromast decreased distribution, abnormal
ZP:0019637	neuromast hair cell development disrupted, abnormal
ZP:0019638	artery decreased amount, abnormal
ZP:0019639	primitive hemopoiesis decreased occurrence, abnormal
ZP:0019640	neuron hypothalamus decreased distribution, abnormal
ZP:0019641	neuron hypothalamus absent, abnormal
ZP:0019642	sleep behavioral quality of a process, abnormal
ZP:0019643	histamine brain decreased amount, abnormal
ZP:0019644	gliogenesis decreased process quality, abnormal
ZP:0019645	exocrine pancreas development arrested, abnormal
ZP:0019646	motor neuron decreased process quality axon guidance, abnormal
ZP:0019647	motor neuron trunk increased amount, abnormal
ZP:0019648	goblet cell intestine decreased amount, abnormal
ZP:0019649	whole organism morbidity, abnormal
ZP:0019650	head delayed neural crest cell migration, abnormal
ZP:0019651	neural crest cell trunk decreased distribution, abnormal
ZP:0019652	neural crest cell trunk decreased amount, abnormal
ZP:0019653	neural crest cell head decreased amount, abnormal
ZP:0019654	pharyngeal arch 3 decreased amount, abnormal
ZP:0019655	ventral region brain decreased amount, abnormal
ZP:0019656	neural crest cell head decreased distribution, abnormal
ZP:0019657	pharyngeal arch 4 decreased amount, abnormal
ZP:0019658	pharyngeal arch 1 decreased amount, abnormal
ZP:0019659	oral ectoderm decreased distribution, abnormal
ZP:0019660	ceratohyal cartilage increased angle to left side right side ceratohyal cartilage, abnormal
ZP:0019661	trunk delayed neural crest cell migration, abnormal
ZP:0019662	ethmoid cartilage decreased distribution, abnormal
ZP:0019663	ethmoid cartilage decreased amount, abnormal
ZP:0019664	endoderm pharynx decreased distribution, abnormal
ZP:0019665	presumptive rhombomere 5 mislocalised, abnormal
ZP:0019666	intestinal bulb primordium increased distribution, abnormal
ZP:0019667	presumptive rhombomere 5 decreased distribution, abnormal
ZP:0019668	hindbrain development process quality, abnormal
ZP:0019669	pronephric tubule physical object quality, abnormal
ZP:0019670	presumptive rhombomere 6 decreased distribution, abnormal
ZP:0019671	endocrine pancreas absent, abnormal
ZP:0019672	anterior region intestinal rod decreased distribution, abnormal
ZP:0019673	posterior region intestinal bulb primordium mislocalised, abnormal
ZP:0019674	pronephric glomerulus increased distribution, abnormal
ZP:0019675	hepatocyte undifferentiated, abnormal
ZP:0019676	terminal Schwann cell decreased amount, abnormal
ZP:0019677	motor neuron disrupted axonogenesis, abnormal
ZP:0019678	motor neuron disrupted axon development, abnormal
ZP:0019679	eye decreased circumference, abnormal
ZP:0019680	commissure of the tract of the commissure of the caudal tuberculum decreased process quality commissural neuron axon guidance, abnormal
ZP:0019681	commissure of the tract of the commissure of the caudal tuberculum decreased occurrence axon extension involved in axon guidance, abnormal
ZP:0019682	axon commissure of the tract of the commissure of the caudal tuberculum defasciculated, abnormal
ZP:0019683	hindbrain dilated, abnormal
ZP:0019684	forebrain dilated, abnormal
ZP:0019685	midbrain dilated, abnormal
ZP:0019686	dorsal region cranial vasculature increased branchiness, abnormal
ZP:0019687	angiogenic sprout trunk vasculature increased amount, abnormal
ZP:0019688	angiogenic sprout cranial vasculature increased amount, abnormal
ZP:0019689	cranial vasculature increased branchiness, abnormal
ZP:0019690	cranial vasculature increased occurrence angiogenesis, abnormal
ZP:0019691	trunk vasculature increased occurrence angiogenesis, abnormal
ZP:0019692	amacrine cell differentiation arrested, abnormal
ZP:0019693	retina increased distribution, abnormal
ZP:0019694	eye photoreceptor cell differentiation decreased process quality, abnormal
ZP:0019695	retinal cone cell differentiation arrested, abnormal
ZP:0019696	sinus venosus mislocalised, abnormal
ZP:0019697	endocardial cushion increased distribution, abnormal
ZP:0019698	cell atrioventricular canal endocardium increased distribution, abnormal
ZP:0019699	bulbus arteriosus increased amount, abnormal
ZP:0019700	cell body photoreceptor cell mislocalised, abnormal
ZP:0019701	kinocilium hair cell disorganized, abnormal
ZP:0019702	cilium olfactory pit swollen, abnormal
ZP:0019703	kinocilium hair cell decreased length, abnormal
ZP:0019704	kinocilium neuromast disorganized, abnormal
ZP:0019705	cell body photoreceptor cell decreased size, abnormal
ZP:0019707	cilium photoreceptor cell decreased length, abnormal
ZP:0019708	ciliary tip photoreceptor cell increased amount, abnormal
ZP:0019709	floor plate lacks all parts of type motile cilium floor plate, abnormal
ZP:0019710	retinal photoreceptor layer increased occurrence apoptotic process, abnormal
ZP:0019711	optic tectum has fewer parts of type axon terminus retinal ganglion cell, abnormal
ZP:0019712	optic tectum decreased occurrence innervation, abnormal
ZP:0019713	gonadotrophin-releasing hormone neuronal migration to the hypothalamus decreased occurrence, abnormal
ZP:0019714	hypothalamus gonadotrophin-releasing hormone neuron development decreased occurrence, abnormal
ZP:0019715	mature B cell decreased amount, abnormal
ZP:0019716	pronephros decreased rate renal filtration, abnormal
ZP:0019717	apical plasma membrane pronephric duct absent, abnormal
ZP:0019718	pronephric duct decreased process quality establishment of epithelial cell apical/basal polarity, abnormal
ZP:0019719	ciliary basal body pronephric duct absent, abnormal
ZP:0019720	junctional membrane complex somite decreased size, abnormal
ZP:0019721	muscle cell somite undulate, abnormal
ZP:0019722	I band somite morphology, abnormal
ZP:0019723	muscle cell somite sparse, abnormal
ZP:0019724	A band somite morphology, abnormal
ZP:0019725	eye oblique orientation, abnormal
ZP:0019726	anterior region lens mislocalised, abnormal
ZP:0019727	neuromuscular junction development, skeletal muscle fiber disrupted, abnormal
ZP:0019728	lens has extra parts of type nucleus cell, abnormal
ZP:0019729	somite attachment quality muscle cell myoseptum, abnormal
ZP:0019730	nucleus lens mislocalised, abnormal
ZP:0019731	pancreatic B cell increased distribution, abnormal
ZP:0019732	pancreatic B cell primary islet decreased amount, abnormal
ZP:0019733	caudal artery decreased distance caudal vein, abnormal
ZP:0019734	blood island disorganized, abnormal
ZP:0019735	common myeloid progenitor decreased amount, abnormal
ZP:0019736	podocyte foot glomerular basement membrane increased width, abnormal
ZP:0019738	leukocyte hematopoietic system increased amount, abnormal
ZP:0019739	leukocyte thymus decreased amount, abnormal
ZP:0019740	leukocyte thymus decreased distribution, abnormal
ZP:0019741	macrophage increased distribution, abnormal
ZP:0019742	intermediate cell mass of mesoderm decreased distribution, abnormal
ZP:0019743	thymus decreased occurrence hematopoietic stem cell migration, abnormal
ZP:0019744	leukocyte intermediate cell mass of mesoderm increased amount, abnormal
ZP:0019745	neutrophil intermediate cell mass of mesoderm increased amount, abnormal
ZP:0019746	neutrophil increased distribution, abnormal
ZP:0019747	lymphoid lineage cell migration into thymus decreased process quality, abnormal
ZP:0019748	hematopoietic system increased amount, abnormal
ZP:0019749	thymus primordium absent, abnormal
ZP:0019750	macrophage intermediate cell mass of mesoderm increased amount, abnormal
ZP:0019751	optic tectum decreased occurrence apoptotic cell clearance, abnormal
ZP:0019752	pharyngeal arch 2 skeleton decreased process quality embryonic skeletal joint development, abnormal
ZP:0019753	interhyal-hyosymplectic joint increased process quality cartilage development, abnormal
ZP:0019754	ceratohyal cartilage fused with interhyal cartilage, abnormal
ZP:0019755	chondrocyte ceratohyal-interhyal joint increased amount, abnormal
ZP:0019756	hyosymplectic cartilage fused with interhyal cartilage, abnormal
ZP:0019757	ceratohyal-interhyal joint increased process quality cartilage development, abnormal
ZP:0019758	joint pharyngeal arch 2 skeleton increased amount, abnormal
ZP:0019759	ceratohyal-interhyal joint malformed, abnormal
ZP:0019760	chondrocyte ceratohyal-interhyal joint increased size, abnormal
ZP:0019761	chondrocyte interhyal-hyosymplectic joint increased amount, abnormal
ZP:0019762	chondrocyte interhyal-hyosymplectic joint increased size, abnormal
ZP:0019763	interhyal-hyosymplectic joint malformed, abnormal
ZP:0019764	Z disc ventricular myocardium decreased amount, abnormal
ZP:0019765	striated muscle thin filament ventricular myocardium decreased amount, abnormal
ZP:0019766	Z disc cardiac muscle spatial pattern, abnormal
ZP:0019767	Z disc cardiac muscle cell decreased amount, abnormal
ZP:0019768	neuroectoderm decreased distribution, abnormal
ZP:0019769	pharyngeal arch increased distribution, abnormal
ZP:0019770	hyomandibula morphology, abnormal
ZP:0019771	pharyngeal arch 1 increased distribution, abnormal
ZP:0019772	pharyngeal arch 2 increased distribution, abnormal
ZP:0019773	pronephros increased occurrence multi-ciliated epithelial cell differentiation, abnormal
ZP:0019774	cilium assembly increased occurrence, abnormal
ZP:0019775	pronephric tubule has extra parts of type multi-ciliated epithelial cell pronephric tubule, abnormal
ZP:0019776	engulfment of apoptotic cell disrupted, abnormal
ZP:0019777	apoptotic cell clearance arrested, abnormal
ZP:0019778	anatomical structure spatial pattern, abnormal
ZP:0019779	whole organism spatial pattern, abnormal
ZP:0019780	somite increased occurrence apoptotic process, abnormal
ZP:0019781	heart structure, cavities, abnormal
ZP:0019782	lymph vessel development arrested, abnormal
ZP:0019783	lymph vessel development delayed, abnormal
ZP:0019784	primitive hemopoiesis increased occurrence, abnormal
ZP:0019785	ventricular system brain decreased size, abnormal
ZP:0019786	cell third ventricle mislocalised, abnormal
ZP:0019787	neuroepithelial cell spatial pattern, abnormal
ZP:0019788	neuroepithelial cell increased occurrence cell population proliferation, abnormal
ZP:0019789	neuroepithelial cell third ventricle structure, abnormal
ZP:0019790	neuroepithelial cell third ventricle wholeness, abnormal
ZP:0019791	neuroepithelial cell third ventricle apical-basal polarity, abnormal
ZP:0019792	ventricular system brain increased volume, abnormal
ZP:0019793	neuroepithelial cell increased distribution, abnormal
ZP:0019794	apical plasma membrane third ventricle spatial pattern, abnormal
ZP:0019795	regulation of circadian sleep/wake cycle, sleep decreased process quality, abnormal
ZP:0019796	cardiac muscle cell action potential involved in contraction decreased duration, abnormal
ZP:0019797	atrium process quality cardiac muscle cell action potential, abnormal
ZP:0019798	intersegmental vessel decreased occurrence sprouting angiogenesis, abnormal
ZP:0019799	posterior lateral plate mesoderm decreased amount, abnormal
ZP:0019800	posterior lateral plate mesoderm increased amount, abnormal
ZP:0019801	neuroectoderm increased distribution, abnormal
ZP:0019802	blood island decreased amount, abnormal
ZP:0019803	angioblastic mesenchymal cell increased amount, abnormal
ZP:0019804	hematopoietic system decreased amount, abnormal
ZP:0019805	tegmentum decreased thickness, abnormal
ZP:0019806	optic tectum decreased thickness, abnormal
ZP:0019807	forebrain decreased process quality neuron differentiation, abnormal
ZP:0019808	hypothalamus decreased thickness, abnormal
ZP:0019809	nucleus forebrain elongated, abnormal
ZP:0019810	midbrain decreased process quality neuron differentiation, abnormal
ZP:0019811	medulla oblongata decreased thickness, abnormal
ZP:0019812	nucleus midbrain elongated, abnormal
ZP:0019813	axon neuron increased length, abnormal
ZP:0019814	sensory neuron increased rate axon extension, abnormal
ZP:0019815	motor neuron increased rate axon extension, abnormal
ZP:0019816	filopodium neuron increased length, abnormal
ZP:0019817	neuron decreased branchiness, abnormal
ZP:0019818	efferent axon development in a lateral line nerve disrupted, abnormal
ZP:0019819	photoreceptor connecting cilium photoreceptor cell absent, abnormal
ZP:0019820	cilium hair cell anterior macula absent, abnormal
ZP:0019821	retina has fewer parts of type central region retinal cone cell, abnormal
ZP:0019822	cilium lateral crista decreased length, abnormal
ZP:0019824	cilium posterior crista decreased amount, abnormal
ZP:0019825	cilium lateral line absent, abnormal
ZP:0019826	cilium anterior crista decreased amount, abnormal
ZP:0019827	retinal rod cell structure, abnormal
ZP:0019828	cilium lateral crista decreased amount, abnormal
ZP:0019829	cilium photoreceptor cell absent, abnormal
ZP:0019830	retinal cone cell non-functional, abnormal
ZP:0019831	photoreceptor inner segment retinal rod cell mislocalised, abnormal
ZP:0019832	cilium anterior crista decreased length, abnormal
ZP:0019833	photoreceptor outer segment layer degenerate, abnormal
ZP:0019834	central region retina degenerate, abnormal
ZP:0019835	retinal outer nuclear layer absence due to degeneration, abnormal
ZP:0019836	cilium posterior crista decreased length, abnormal
ZP:0019837	cilium hair cell posterior macula absent, abnormal
ZP:0019838	ciliary basal body photoreceptor cell absent, abnormal
ZP:0019839	cilium central canal absent, abnormal
ZP:0019840	optic tectum increased amount, abnormal
ZP:0019841	optic tectum increased distribution, abnormal
ZP:0019842	retinal ganglion cell layer decreased amount, abnormal
ZP:0019843	melanosome melanocyte distended, abnormal
ZP:0019844	axon terminus retinal ganglion cell increased branchiness, abnormal
ZP:0019845	retinal ganglion cell decreased occurrence anterograde axonal transport of mitochondrion, abnormal
ZP:0019846	cranial nerve II decreased occurrence anterograde axonal transport of mitochondrion, abnormal
ZP:0019847	dendrite optic tectum decreased amount, abnormal
ZP:0019848	retinal ganglion cell has fewer parts of type axon terminus mitochondrion retinal ganglion cell, abnormal
ZP:0019849	axon retinal ganglion cell decreased amount, abnormal
ZP:0019850	axon terminus retinal ganglion cell decreased branchiness, abnormal
ZP:0019851	cranial nerve II decreased occurrence collateral sprouting, abnormal
ZP:0019852	cranial nerve II delayed axonogenesis involved in innervation, abnormal
ZP:0019853	cranial nerve II decreased occurrence anterograde trans-synaptic signaling, abnormal
ZP:0019854	cranial nerve II increased occurrence collateral sprouting, abnormal
ZP:0019855	optic tectum decreased occurrence anterograde trans-synaptic signaling, abnormal
ZP:0019856	germ cell development decreased process quality, abnormal
ZP:0019857	whole organism lacks all parts of type primordial germ cell, abnormal
ZP:0019858	testis lacks all parts of type germ line cell, abnormal
ZP:0019859	posterior region unfertilized egg increased amount, abnormal
ZP:0019860	posterior region unfertilized egg increased distribution, abnormal
ZP:0019861	egg activation decreased process quality, abnormal
ZP:0019862	dorsal/ventral pattern formation decreased process quality, abnormal
ZP:0019863	posterior region unfertilized egg mislocalised, abnormal
ZP:0019864	unfertilized egg increased amount, abnormal
ZP:0019865	unfertilized egg has extra parts of type posterior region cortical granule unfertilized egg, abnormal
ZP:0019866	microtubule unfertilized egg disorganized, abnormal
ZP:0019867	myotome increased distribution, abnormal
ZP:0019868	regulation of protein processing process quality, abnormal
ZP:0019869	cell cardiac jelly disorganized, abnormal
ZP:0019870	podocyte foot podocyte morphology, abnormal
ZP:0019871	myosin II filament chondrocyte position, abnormal
ZP:0019872	filamentous actin chondrocyte position, abnormal
ZP:0019873	ceratohyal cartilage increased width, abnormal
ZP:0019874	MAP kinase kinase activity process quality, abnormal
ZP:0019875	ceratohyal cartilage right angle to anterior-posterior axis whole organism, abnormal
ZP:0019876	Meckel's cartilage distance ethmoid cartilage, abnormal
ZP:0019877	Meckel's cartilage orientation anterior-posterior axis whole organism, abnormal
ZP:0019878	Meckel's cartilage truncated, abnormal
ZP:0019879	pharyngeal arch 1 disorganized, abnormal
ZP:0019880	mouth atretic, abnormal
ZP:0019881	lateral line has fewer parts of type neuromast, abnormal
ZP:0019882	hair cell has extra parts of type neuromast, abnormal
ZP:0019883	hematopoietic stem cell post-vent region decreased amount, abnormal
ZP:0019884	hematopoietic stem cell thymus decreased amount, abnormal
ZP:0019885	hematopoietic stem cell ventral wall of dorsal aorta normal amount, abnormal
ZP:0019886	autophagosome blood island increased amount, abnormal
ZP:0019887	hematopoietic stem cell kidney decreased amount, abnormal
ZP:0019888	cytosolic large ribosomal subunit whole organism increased amount, abnormal
ZP:0019889	focal adhesion optic cup increased amount, abnormal
ZP:0019890	presumptive retinal pigmented epithelium flattened, abnormal
ZP:0019891	optic furrow malformed, abnormal
ZP:0019892	lens ovate, abnormal
ZP:0019893	cell presumptive neural retina decreased length, abnormal
ZP:0019894	basal lamina optic cup spatial pattern, abnormal
ZP:0019895	focal adhesion optic fissure decreased amount, abnormal
ZP:0019896	anterior margin optic cup increased amount, abnormal
ZP:0019897	presumptive neural retina flattened, abnormal
ZP:0019898	cell motility involved in camera-type eye morphogenesis disrupted, abnormal
ZP:0019899	basal lamina optic cup mislocalised, abnormal
ZP:0019900	optic stalk increased diameter, abnormal
ZP:0019901	establishment of epithelial cell apical/basal polarity involved in camera-type eye morphogenesis disrupted, abnormal
ZP:0019902	somite detached from muscle cell somite, abnormal
ZP:0019903	motile cilium Kupffer's vesicle decreased functionality, abnormal
ZP:0019904	microglia development decreased process quality, abnormal
ZP:0019905	ciliary marginal zone increased process quality cell population proliferation, abnormal
ZP:0019906	pancreas has extra parts of type pancreatic B cell, abnormal
ZP:0019907	response to glucose decreased magnitude, abnormal
ZP:0019908	glucose whole organism increased amount, abnormal
ZP:0019909	nodal signaling pathway increased occurrence, abnormal
ZP:0019910	ovulation process quality, abnormal
ZP:0019911	testis decreased weight, abnormal
ZP:0019912	postovulatory follicle absent, abnormal
ZP:0019913	ovary increased size, abnormal
ZP:0019914	ovary increased weight, abnormal
ZP:0019915	ovarian follicle stage IV increased amount, abnormal
ZP:0019916	postovulatory follicle increased amount, abnormal
ZP:0019917	double-strand break repair via alternative nonhomologous end joining decreased process quality, abnormal
ZP:0019918	double-strand break repair via alternative nonhomologous end joining increased process quality, abnormal
ZP:0019919	hindbrain absent, abnormal
ZP:0019920	midbrain absent, abnormal
ZP:0019921	determination of left/right asymmetry in nervous system disrupted, abnormal
ZP:0019922	atrioventricular valve functionality, abnormal
ZP:0019923	atrioventricular valve closure, abnormal
ZP:0019924	endothelial cell proliferation disrupted, abnormal
ZP:0019925	glutamatergic neuron decreased distribution, abnormal
ZP:0019927	spinal cord absent, abnormal
ZP:0019928	anterior pancreatic bud decreased distribution, abnormal
ZP:0019929	exocrine pancreas decreased amount, abnormal
ZP:0019930	pancreas increased distribution, abnormal
ZP:0019931	pancreatic bud increased distribution, abnormal
ZP:0019932	anterior pancreatic bud decreased process quality cell population proliferation, abnormal
ZP:0019933	supramolecular fiber ceratobranchial cartilage increased amount, abnormal
ZP:0019934	supramolecular fiber ceratobranchial cartilage increased thickness, abnormal
ZP:0019935	supramolecular fiber organization decreased process quality, abnormal
ZP:0019936	establishment of synaptic specificity at neuromuscular junction decreased occurrence, abnormal
ZP:0019937	acetylcholine-gated channel complex muscle decreased amount, abnormal
ZP:0019938	midbrain hindbrain boundary decreased distribution, abnormal
ZP:0019939	hindbrain increased distribution, abnormal
ZP:0019940	cranium lacks parts or has fewer parts of type ceratobranchial cartilage, abnormal
ZP:0019941	hindbrain decreased distribution, abnormal
ZP:0019942	cranial neural crest cell decreased process quality neural crest cell migration, abnormal
ZP:0019943	dorsal region hindbrain mislocalised, abnormal
ZP:0019944	cranial neural crest cell decreased distribution, abnormal
ZP:0019945	ceratobranchial 1 cartilage aplastic, abnormal
ZP:0019946	rhombomere 6 mislocalised, abnormal
ZP:0019947	hindbrain decreased process quality canonical Wnt signaling pathway, abnormal
ZP:0019948	cranial neural crest cell decreased process quality canonical Wnt signaling pathway, abnormal
ZP:0019949	tail bud decreased distribution, abnormal
ZP:0019950	ceratobranchial 1 cartilage hypoplastic, abnormal
ZP:0019951	volume-sensitive chloride channel activity decreased process quality, abnormal
ZP:0019952	otic vesicle edematous, abnormal
ZP:0019953	pronephric duct process quality kidney epithelium development, abnormal
ZP:0019954	brain has fewer parts of type dopaminergic neuron, abnormal
ZP:0019955	midbrain increased amount, abnormal
ZP:0019956	apicolateral plasma membrane pronephric duct mislocalised, abnormal
ZP:0019957	lens edematous, abnormal
ZP:0019958	postoptic commissure increased amount, abnormal
ZP:0019959	spinal cord has fewer parts of type neuron, abnormal
ZP:0019960	diencephalon increased amount, abnormal
ZP:0019961	mRNA processing decreased occurrence, abnormal
ZP:0019962	iridophore scale increased amount, abnormal
ZP:0019963	iridophore mislocalised, abnormal
ZP:0019965	iridophore dorsal fin increased amount, abnormal
ZP:0019966	iridophore displaced to dorsal root ganglion, abnormal
ZP:0019967	iridophore displaced to pupil, abnormal
ZP:0019968	iridophore caudal fin increased amount, abnormal
ZP:0019969	iridophore displaced to trunk, abnormal
ZP:0019971	iridophore anal fin increased amount, abnormal
ZP:0019972	melanocyte scale increased amount, abnormal
ZP:0019973	supramolecular fiber corneal stroma increased diameter, abnormal
ZP:0019974	lymph vasculature hypoplastic, abnormal
ZP:0019975	endothelial cell lymph vessel decreased amount, abnormal
ZP:0019976	dorsal longitudinal lymphatic vessel absent, abnormal
ZP:0019977	venous endothelial cell migration involved in lymph vessel development decreased process quality, abnormal
ZP:0019978	venous endothelial cell migration involved in lymph vessel development process quality, abnormal
ZP:0019979	lymphangioblast horizontal myoseptum morphology, abnormal
ZP:0019980	intersegmental lymph vessel absent, abnormal
ZP:0019981	endothelial cell lymphatic branchial arch 1 decreased amount, abnormal
ZP:0019982	lymph vasculature aplastic, abnormal
ZP:0019983	endothelial cell otolithic lymph vessel decreased amount, abnormal
ZP:0019984	neural tube closure delayed, abnormal
ZP:0019985	whole organism has extra parts of type neural tube, abnormal
ZP:0019986	neural plate decreased rate cell migration, abnormal
ZP:0019987	neural tube closure, abnormal
ZP:0019988	cell neural keel morphology, abnormal
ZP:0019989	microtubule cytoskeleton neural keel composition, abnormal
ZP:0019990	ceratobranchial cartilage immature, abnormal
ZP:0019991	hematopoietic progenitor cell differentiation increased occurrence, abnormal
ZP:0019992	definitive hemopoiesis increased occurrence, abnormal
ZP:0019993	ventral region whole organism increased distribution, abnormal
ZP:0019994	neuroectoderm spatial pattern, abnormal
ZP:0019995	dorsal region whole organism increased amount, abnormal
ZP:0019996	prechordal plate spatial pattern, abnormal
ZP:0019997	ventral region whole organism increased amount, abnormal
ZP:0019998	cranial nerve VII decreased amount, abnormal
ZP:0019999	facial nerve formation decreased process quality, abnormal
ZP:0020000	cranial motor neuron trigeminal motor nucleus mislocalised, abnormal
ZP:0020001	cranial nerve VII increased occurrence collateral sprouting in absence of injury, abnormal
ZP:0020002	axon cranial nerve VII defasciculated, abnormal
ZP:0020003	trigeminal motor nucleus development decreased process quality, abnormal
ZP:0020004	trigeminal motor nucleus process quality motor neuron migration, abnormal
ZP:0020005	posterior lateral line decreased amount, abnormal
ZP:0020006	cranial nerve V absent, abnormal
ZP:0020007	hair cell otic vesicle absent, abnormal
ZP:0020008	cranial nerve V decreased amount, abnormal
ZP:0020009	retina decreased occurrence mitotic cell cycle, abnormal
ZP:0020010	head discolored, abnormal
ZP:0020011	cysteine-type endopeptidase activity involved in apoptotic process increased process quality, abnormal
ZP:0020012	epithelial cell pronephric tubule decreased amount, abnormal
ZP:0020013	epithelial cell pronephric tubule apoptotic, abnormal
ZP:0020015	atrioventricular ring morphology, abnormal
ZP:0020016	atrium spatial pattern, abnormal
ZP:0020017	atrioventricular canal absent, abnormal
ZP:0020018	cardiac jelly decreased amount, abnormal
ZP:0020019	endocardial cushion atrioventricular canal absent, abnormal
ZP:0020020	cardiac ventricle spatial pattern, abnormal
ZP:0020025	ventral telencephalon decreased distribution, abnormal
ZP:0020026	hypothalamus decreased distribution, abnormal
ZP:0020027	spinal cord increased amount, abnormal
ZP:0020028	neuron mid intestine decreased amount, abnormal
ZP:0020029	intestinal bulb has fewer parts of type enteric neuron, abnormal
ZP:0020030	electrically responsive cell intestine increased distribution, abnormal
ZP:0020031	neuron intestinal bulb decreased amount, abnormal
ZP:0020032	neuron projection mid intestine decreased distribution, abnormal
ZP:0020033	neuron projection mid intestine decreased amount, abnormal
ZP:0020034	neuron mid intestine decreased distribution, abnormal
ZP:0020035	neuron posterior intestine decreased amount, abnormal
ZP:0020036	interstitial cell of Cajal differentiation delayed, abnormal
ZP:0020037	phasic smooth muscle contraction occurrence, abnormal
ZP:0020038	mid intestine has fewer parts of type enteric neuron, abnormal
ZP:0020039	posterior intestine has fewer parts of type enteric neuron, abnormal
ZP:0020040	neuron projection enteric neuron decreased distribution, abnormal
ZP:0020041	serotonergic neuron mid intestine decreased distribution, abnormal
ZP:0020042	neuron projection enteric neuron decreased amount, abnormal
ZP:0020043	intestine smooth muscle contraction decreased frequency, abnormal
ZP:0020044	phasic smooth muscle contraction frequency, abnormal
ZP:0020045	posterior intestine lacks parts or has fewer parts of type enteric neuron, abnormal
ZP:0020046	branchiostegal ray fused with opercle, abnormal
ZP:0020047	head has extra parts of type bone tissue, abnormal
ZP:0020048	branchiostegal ray increased size, abnormal
ZP:0020049	mesenchyme increased distribution, abnormal
ZP:0020050	fin bud absent, abnormal
ZP:0020052	enteric neuron mid intestine decreased amount, abnormal
ZP:0020053	enteric neuron intestinal bulb decreased amount, abnormal
ZP:0020054	intestinal bulb primordium decreased amount, abnormal
ZP:0020055	neural crest cell migration involved in autonomic nervous system development decreased process quality, abnormal
ZP:0020059	anatomical region vagal ganglion mislocalised, abnormal
ZP:0020060	neural crest cell migration involved in autonomic nervous system development decreased rate, abnormal
ZP:0020061	enteric neuron gut decreased amount, abnormal
ZP:0020064	fin bud decreased amount, abnormal
ZP:0020065	neural crest cell decreased process quality cell population proliferation, abnormal
ZP:0020066	gut endothelial cell absent, abnormal
ZP:0020068	neural crest cell enteric nervous system decreased amount, abnormal
ZP:0020070	right side heart primordium mislocalised, abnormal
ZP:0020071	heart primordium absent, abnormal
ZP:0020072	left/right pattern formation decreased efficacy, abnormal
ZP:0020073	determination of heart left/right asymmetry decreased efficacy, abnormal
ZP:0020074	pineal complex increased distribution, abnormal
ZP:0020075	inner ear increased amount, abnormal
ZP:0020076	pancreas primordium decreased amount, abnormal
ZP:0020077	hematopoietic multipotent progenitor cell absent, abnormal
ZP:0020078	nervous system decreased amount, abnormal
ZP:0020079	nervous system increased amount, abnormal
ZP:0020080	pancreas primordium absent, abnormal
ZP:0020081	pancreas primordium increased amount, abnormal
ZP:0020082	neuroblast increased amount, abnormal
ZP:0020083	pronephric tubule increased distribution, abnormal
ZP:0020084	post-vent region white, abnormal
ZP:0020087	inner ear decreased amount, abnormal
ZP:0020088	cleavage furrow blastomere morphology, abnormal
ZP:0020089	early embryonic cell cellular adhesivity, abnormal
ZP:0020090	blastomere has fewer parts of type actomyosin contractile ring filamentous actin blastomere, abnormal
ZP:0020091	blastomere morphology, abnormal
ZP:0020092	cleavage furrow blastomere decreased amount, abnormal
ZP:0020093	early embryonic cell morphology, abnormal
ZP:0020094	blastomere irregularly shaped, abnormal
ZP:0020095	early embryonic cell multinucleate, abnormal
ZP:0020096	vesicle blastomere increased amount, abnormal
ZP:0020097	lymphangioblast cord broken, abnormal
ZP:0020098	lymphangiogenic sprout posterior cardinal vein decreased amount, abnormal
ZP:0020099	lymphatic endothelial cell migration disrupted, abnormal
ZP:0020100	lymphangiogenic sprout absent, abnormal
ZP:0020101	vascular sprouts posterior cardinal vein decreased distribution, abnormal
ZP:0020102	lymphangiogenic sprout posterior cardinal vein absent, abnormal
ZP:0020103	lymphangioblast cord hypoplastic, abnormal
ZP:0020104	cardiac ventricle decreased magnitude cardiac muscle contraction, abnormal
ZP:0020105	retina development in camera-type eye decreased process quality, abnormal
ZP:0020106	cardiac ventricle increased duration ventricular cardiac muscle cell action potential, abnormal
ZP:0020107	melanocyte melanophore stripe absent, abnormal
ZP:0020108	melanocyte larval melanophore stripe absent, abnormal
ZP:0020109	ventral region caudal fin decreased pigmentation, abnormal
ZP:0020110	stereocilium inner ear decreased width, abnormal
ZP:0020111	stereocilium inner ear decreased length, abnormal
ZP:0020112	neuromast hair cell increased process quality apoptotic process, abnormal
ZP:0020113	endothelial cell common cardinal vein decreased amount, abnormal
ZP:0020114	primordial hindbrain channel decreased occurrence blood vessel development, abnormal
ZP:0020115	primordial hindbrain channel decreased occurrence cell migration involved in sprouting angiogenesis, abnormal
ZP:0020116	primordial hindbrain channel arrested angiogenesis, abnormal
ZP:0020117	intersegmental vessel decreased occurrence blood vessel development, abnormal
ZP:0020118	common cardinal vein decreased occurrence cell population proliferation, abnormal
ZP:0020119	intersegmental vessel arrested angiogenesis, abnormal
ZP:0020120	endothelial cell primordial hindbrain channel decreased amount, abnormal
ZP:0020121	anatomical region primordial hindbrain channel absent, abnormal
ZP:0020122	extension decreased amount, abnormal
ZP:0020123	common cardinal vein decreased occurrence angiogenesis, abnormal
ZP:0020124	common cardinal vein decreased occurrence blood vessel development, abnormal
ZP:0020125	endothelial cell anterior cardinal vein decreased amount, abnormal
ZP:0020126	primordial hindbrain channel arrested cell migration involved in sprouting angiogenesis, abnormal
ZP:0020127	fat cell visceral fat decreased amount, abnormal
ZP:0020128	fat cell differentiation disrupted, abnormal
ZP:0020129	ventral fin fold absence due to degeneration, abnormal
ZP:0020130	T-tubule skeletal muscle broken, abnormal
ZP:0020131	ventral fin fold degenerate, abnormal
ZP:0020132	skeletal muscle lacks all parts of type T-tubule sarcoplasmic reticulum skeletal muscle, abnormal
ZP:0020133	vertical myoseptum increased amount, abnormal
ZP:0020134	ciliary basal body pronephros disorganized, abnormal
ZP:0020135	neutrophil progenitor cell decreased amount, abnormal
ZP:0020136	skeletal muscle trunk increased amount, abnormal
ZP:0020137	skeletal muscle cell decreased thickness, abnormal
ZP:0020138	skeletal muscle increased process quality apoptotic process, abnormal
ZP:0020139	skeletal muscle cell decondensed, abnormal
ZP:0020140	skeletal muscle trunk decreased amount, abnormal
ZP:0020141	actin filament skeletal muscle cell decreased length, abnormal
ZP:0020142	head lacks parts or has fewer parts of type cephalic musculature, abnormal
ZP:0020143	presumptive cephalic mesoderm disrupted gene expression, abnormal
ZP:0020144	pharyngeal arch 6 has fewer parts of type cranial neural crest, abnormal
ZP:0020145	pharyngeal arch 3 has fewer parts of type chondroblast, abnormal
ZP:0020146	neural crest cell neuroectoderm decreased amount, abnormal
ZP:0020147	pharyngeal arch 5 absent, abnormal
ZP:0020148	copula absent, abnormal
ZP:0020149	pharyngeal arch 5 has fewer parts of type cranial neural crest, abnormal
ZP:0020150	chondroblast cranial neural crest decreased amount, abnormal
ZP:0020151	pharyngeal arch 3 has fewer parts of type cranial neural crest, abnormal
ZP:0020152	vasoconstriction increased occurrence, abnormal
ZP:0020153	intestine decreased efficacy peristalsis, abnormal
ZP:0020154	basement membrane intestinal epithelium spatial pattern, abnormal
ZP:0020155	artery decreased diameter, abnormal
ZP:0020157	mid intestine increased occurrence epithelial cell migration, abnormal
ZP:0020158	posterior intestine increased occurrence epithelial cell migration, abnormal
ZP:0020159	basement membrane intestine discontinuous, abnormal
ZP:0020160	blood circulation decreased volume, abnormal
ZP:0020161	invadopodium intestinal epithelium increased amount, abnormal
ZP:0020162	nucleus fast muscle cell decreased amount, abnormal
ZP:0020163	somite patchy, abnormal
ZP:0020164	muscle cell detached from myotome, abnormal
ZP:0020165	muscle cell misaligned with somite, abnormal
ZP:0020166	muscle cell detached from somite border, abnormal
ZP:0020167	interhyoideus spatial pattern, abnormal
ZP:0020168	fast muscle cell spatial pattern, abnormal
ZP:0020170	skeletal muscle myofibril cephalic musculature decreased amount, abnormal
ZP:0020171	blood accumulation pericardial cavity, abnormal
ZP:0020172	Z disc fast muscle cell irregular spatial pattern, abnormal
ZP:0020173	Z disc myotome absent, abnormal
ZP:0020174	somite border decreased distribution, abnormal
ZP:0020175	striated muscle thin filament myotome disorganized, abnormal
ZP:0020176	myofilament skeletal muscle cell decreased amount, abnormal
ZP:0020177	sarcomere myotome absent, abnormal
ZP:0020178	skeletal muscle myofibril cephalic musculature undulate, abnormal
ZP:0020179	ventral intermandibularis posterior spatial pattern, abnormal
ZP:0020180	fast muscle cell trunk musculature morphology, abnormal
ZP:0020181	M band skeletal muscle cell absent, abnormal
ZP:0020182	myofilament skeletal muscle cell disorganized, abnormal
ZP:0020183	inferior hyohyoid spatial pattern, abnormal
ZP:0020184	Z disc skeletal muscle cell absent, abnormal
ZP:0020185	skeletal muscle myofibril cephalic musculature disorganized, abnormal
ZP:0020186	fast muscle cell decreased distribution, abnormal
ZP:0020187	sarcomere muscle cell absent, abnormal
ZP:0020188	mitochondrion skeletal muscle cell increased size, abnormal
ZP:0020189	microvillus intestine morphology, abnormal
ZP:0020190	inclusion body enterocyte increased amount, abnormal
ZP:0020191	enterocyte increased height, abnormal
ZP:0020192	microvillus enterocyte mislocalised, abnormal
ZP:0020193	enterocyte columnar, abnormal
ZP:0020194	enterocyte morphology, abnormal
ZP:0020195	enterocyte accumulation secretory granule apical side enterocyte, abnormal
ZP:0020196	enterocyte gut decreased amount, abnormal
ZP:0020197	anatomical axis whole organism bent, abnormal
ZP:0020198	epiblast increased thickness, abnormal
ZP:0020199	embryonic skeletal system development disrupted, abnormal
ZP:0020200	CaP motoneuron increased occurrence collateral sprouting, abnormal
ZP:0020201	ocular blood vessel decreased area, abnormal
ZP:0020202	pineal complex split, abnormal
ZP:0020203	pineal complex elongated, abnormal
ZP:0020204	floor plate decreased amount, abnormal
ZP:0020205	paraxial mesoderm head decreased amount, abnormal
ZP:0020206	hypochord decreased amount, abnormal
ZP:0020207	notochord decreased amount, abnormal
ZP:0020208	paraxial mesoderm head aplastic/hypoplastic, abnormal
ZP:0020209	hatching gland cell decreased amount, abnormal
ZP:0020210	synaptic vesicle posterior lateral line nerve aggregated, abnormal
ZP:0020211	axon posterior lateral line nerve decreased distribution, abnormal
ZP:0020212	synaptic vesicle posterior lateral line nerve spatial pattern, abnormal
ZP:0020213	neuron posterior lateral line ganglion decreased distribution, abnormal
ZP:0020214	posterior lateral line ganglion decreased distribution, abnormal
ZP:0020215	otolith non-functional, abnormal
ZP:0020216	dorsal region whole organism decreased amount, abnormal
ZP:0020217	shield decreased distribution, abnormal
ZP:0020218	dorsal/ventral axis specification decreased process quality, abnormal
ZP:0020219	dorsal region neuroectoderm decreased amount, abnormal
ZP:0020220	ventro-lateral region presumptive mesoderm decreased amount, abnormal
ZP:0020221	dorsal region whole organism decreased distribution, abnormal
ZP:0020222	ventro-lateral region presumptive mesoderm decreased distribution, abnormal
ZP:0020223	ventral region non neural ectoderm increased distribution, abnormal
ZP:0020224	dorsal region neuroectoderm decreased distribution, abnormal
ZP:0020225	efferent axon development in a lateral line nerve decreased process quality, abnormal
ZP:0020226	synaptic ribbon neuromast hair cell increased amount, abnormal
ZP:0020227	synaptic ribbon neuromast hair cell mislocalised, abnormal
ZP:0020228	efferent neuron posterior lateral line nerve aplastic, abnormal
ZP:0020229	neuromast hair cell increased distance synaptic ribbon synaptic ribbon neuromast hair cell, abnormal
ZP:0020230	posterior lateral line neuromast has fewer parts of type synaptic ribbon neuromast hair cell, abnormal
ZP:0020231	afferent neuron posterior lateral line nerve aplastic, abnormal
ZP:0020232	afferent axon development in posterior lateral line nerve decreased process quality, abnormal
ZP:0020233	synaptic ribbon neuromast hair cell decreased size, abnormal
ZP:0020234	cell superior cervical ganglion increased amount, abnormal
ZP:0020235	common bile duct cystic, abnormal
ZP:0020236	gall bladder dilated, abnormal
ZP:0020237	hepatocyte increased distance hepatocyte, abnormal
ZP:0020238	swim bladder inflation delayed, abnormal
ZP:0020239	photoreceptor outer segment eye photoreceptor cell structure, abnormal
ZP:0020240	eye photoreceptor cell accumulation vesicle eye photoreceptor cell, abnormal
ZP:0020241	eye photoreceptor cell disrupted protein localization, abnormal
ZP:0020242	eye photoreceptor cell accumulation vacuole eye photoreceptor cell, abnormal
ZP:0020243	neural tube increased occurrence apoptotic process, abnormal
ZP:0020244	pharyngeal arch 2 decreased distribution, abnormal
ZP:0020245	pharyngeal arch 1 decreased distribution, abnormal
ZP:0020246	pharyngeal arch decreased distribution, abnormal
ZP:0020247	aortic arch 6 decreased occurrence blood vessel lumenization, abnormal
ZP:0020248	pharyngeal arch 2 absent, abnormal
ZP:0020249	ventral region pharyngeal arch decreased distribution, abnormal
ZP:0020250	pharyngeal arch 4 decreased distribution, abnormal
ZP:0020251	aortic arch 3 decreased amount, abnormal
ZP:0020252	pharyngeal arch 3 decreased distribution, abnormal
ZP:0020253	aortic arch 5 decreased occurrence blood vessel lumenization, abnormal
ZP:0020254	pancreatic bud absent, abnormal
ZP:0020255	endothelial cell caudal vein swollen, abnormal
ZP:0020257	zymogen granule exocrine pancreas decreased size, abnormal
ZP:0020258	pancreatic duct absent, abnormal
ZP:0020259	erythroid progenitor cell post-vent region decreased amount, abnormal
ZP:0020261	hematopoietic multipotent progenitor cell post-vent region decreased amount, abnormal
ZP:0020262	zymogen granule exocrine pancreas decreased amount, abnormal
ZP:0020264	nucleate erythrocyte blood island decreased amount, abnormal
ZP:0020265	nucleate erythrocyte hematopoietic system absent, abnormal
ZP:0020266	rough endoplasmic reticulum exocrine pancreas absent, abnormal
ZP:0020267	mitochondrion exocrine pancreas morphology, abnormal
ZP:0020268	mitochondrion exocrine pancreas increased size, abnormal
ZP:0020270	ribosomal small subunit biogenesis decreased occurrence, abnormal
ZP:0020271	choroid plexus fourth ventricle shape, abnormal
ZP:0020272	hindbrain has extra parts of type Mauthner neuron, abnormal
ZP:0020273	Notch signaling involved in heart development decreased occurrence, abnormal
ZP:0020274	parapineal organ has extra parts of type neuron parapineal organ, abnormal
ZP:0020275	parapineal organ increased occurrence neuron fate specification, abnormal
ZP:0020276	left side habenula decreased amount, abnormal
ZP:0020277	pineal complex absent, abnormal
ZP:0020278	habenula bilateral symmetry, abnormal
ZP:0020279	right side habenula increased amount, abnormal
ZP:0020280	epiphysis decreased amount, abnormal
ZP:0020281	cardiovascular system decreased amount, abnormal
ZP:0020282	posterior lateral plate mesoderm decreased distribution, abnormal
ZP:0020283	basement membrane optic furrow present, abnormal
ZP:0020284	heart spatial pattern, abnormal
ZP:0020285	lateral plate mesoderm decreased size, abnormal
ZP:0020286	posterior lateral mesoderm decreased amount, abnormal
ZP:0020287	hematopoietic system absent, abnormal
ZP:0020288	optic furrow delayed basement membrane disassembly, abnormal
ZP:0020289	cardiovascular system decreased distribution, abnormal
ZP:0020290	locomotor rhythm delayed, abnormal
ZP:0020291	intestine decreased amount, abnormal
ZP:0020292	autophagosome liver increased amount, abnormal
ZP:0020293	eye increased amount, abnormal
ZP:0020294	autolysosome hindbrain increased amount, abnormal
ZP:0020295	pineal complex decreased amount, abnormal
ZP:0020296	pineal complex has fewer parts of type photoreceptor cell pineal complex, abnormal
ZP:0020297	pineal complex decreased occurrence photoreceptor cell fate specification, abnormal
ZP:0020298	cell intersegmental vessel decreased amount, abnormal
ZP:0020299	intersegmental vessel incomplete structure, abnormal
ZP:0020300	vein decreased distribution, abnormal
ZP:0020301	angioblast cell migration decreased process quality, abnormal
ZP:0020302	cell vein decreased amount, abnormal
ZP:0020303	ceratohyal cartilage disoriented, abnormal
ZP:0020304	circadian behavior disrupted, abnormal
ZP:0020305	sleep light phase, abnormal
ZP:0020306	larval behavior decreased process quality, abnormal
ZP:0020307	pancreatic bud decreased distribution, abnormal
ZP:0020308	acinar cell absent, abnormal
ZP:0020309	cell exocrine pancreas decreased amount, abnormal
ZP:0020310	pancreas morphogenesis process quality, abnormal
ZP:0020311	blood vessel endothelium common cardinal vein patchy, abnormal
ZP:0020312	actin filament bundle common cardinal vein disoriented, abnormal
ZP:0020313	venous blood vessel morphogenesis decreased process quality, abnormal
ZP:0020314	cell-cell junction common cardinal vein decreased length, abnormal
ZP:0020315	common cardinal vein decreased process quality actin filament bundle organization, abnormal
ZP:0020316	mid cerebral vein absent, abnormal
ZP:0020317	mid cerebral vein decreased length, abnormal
ZP:0020318	retinal pigmented epithelium has fewer parts of type melanosome melanocyte, abnormal
ZP:0020319	pronephric duct process quality epithelial cilium movement involved in extracellular fluid movement, abnormal
ZP:0020320	anterior region pronephric duct dilated, abnormal
ZP:0020321	cilium pronephric duct decreased coordination, abnormal
ZP:0020322	podocyte foot renal glomerulus shape, abnormal
ZP:0020323	glomerular capillary collapsed, abnormal
ZP:0020324	renal glomerulus hypoplastic, abnormal
ZP:0020325	intersegmental vessel decreased process quality angiogenesis, abnormal
ZP:0020326	retina arrested mitotic cell cycle, abnormal
ZP:0020327	retina increased duration mitotic cell cycle, abnormal
ZP:0020328	peripheral olfactory organ increased size, abnormal
ZP:0020329	peripheral olfactory organ increased distribution, abnormal
ZP:0020330	synapse horizontal cell amount, abnormal
ZP:0020331	optic tectum increased process quality mitotic cell cycle, abnormal
ZP:0020332	brain increased process quality mitotic cell cycle, abnormal
ZP:0020333	fourth ventricle increased process quality mitotic cell cycle, abnormal
ZP:0020334	male mating behavior decreased occurrence, abnormal
ZP:0020335	response to pheromone decreased occurrence, abnormal
ZP:0020336	male courtship behavior decreased occurrence, abnormal
ZP:0020337	pronephric glomerulus morphogenesis disrupted, abnormal
ZP:0020338	glomerular visceral epithelial cell differentiation disrupted, abnormal
ZP:0020339	pronephric proximal tubule development disrupted, abnormal
ZP:0020340	pronephric podocyte mislocalised, abnormal
ZP:0020341	pronephric podocyte absent, abnormal
ZP:0020342	anterior region pronephric duct absent, abnormal
ZP:0020343	anterior region intermediate mesoderm absent, abnormal
ZP:0020344	neurosecretory neuron preoptic area increased distribution, abnormal
ZP:0020345	caudal tuberculum decreased amount, abnormal
ZP:0020346	social behavior process quality, abnormal
ZP:0020347	response to stress behavioral quality of a process, abnormal
ZP:0020348	caudal tuberculum decreased distribution, abnormal
ZP:0020349	caudal tuberculum increased amount, abnormal
ZP:0020350	neurosecretory neuron preoptic area increased amount, abnormal
ZP:0020351	intersegmental vessel decreased distribution, abnormal
ZP:0020352	nucleate erythrocyte spatial pattern, abnormal
ZP:0020353	telencephalon decreased distribution, abnormal
ZP:0020354	vasculature spatial pattern, abnormal
ZP:0020355	caudal vein plexus irregularly shaped, abnormal
ZP:0020356	tegmentum decreased distribution, abnormal
ZP:0020357	hindbrain spatial pattern, abnormal
ZP:0020358	diencephalon decreased distribution, abnormal
ZP:0020359	tegmentum spatial pattern, abnormal
ZP:0020360	caudal vein plexus hemorrhagic, abnormal
ZP:0020361	posterior cardinal vein decreased distribution, abnormal
ZP:0020362	central nervous system decreased distribution, abnormal
ZP:0020363	dorsal aorta decreased distribution, abnormal
ZP:0020364	ventro-lateral region otic vesicle increased distribution, abnormal
ZP:0020365	otic vesicle decreased occurrence neuroblast proliferation, abnormal
ZP:0020366	otic vesicle increased occurrence neuroblast delamination, abnormal
ZP:0020367	cardioblast migration to the midline involved in heart rudiment formation decreased occurrence, abnormal
ZP:0020368	anterior lateral plate mesoderm decreased amount, abnormal
ZP:0020369	cardiac muscle cell anterior lateral plate mesoderm decreased amount, abnormal
ZP:0020370	secondary heart field specification decreased occurrence, abnormal
ZP:0020371	heart tube increased distribution, abnormal
ZP:0020372	blood accumulation anatomical region atrium, abnormal
ZP:0020373	lateral plate mesoderm increased distribution, abnormal
ZP:0020374	proepicardium development decreased occurrence, abnormal
ZP:0020375	heart tube decreased amount, abnormal
ZP:0020376	smooth muscle bulbus arteriosus spatial pattern, abnormal
ZP:0020377	neuron optic tectum morphology, abnormal
ZP:0020378	optic tectum has extra parts of type neuron, abnormal
ZP:0020380	embryonic viscerocranium morphogenesis delayed, abnormal
ZP:0020381	head muscle delayed muscle fiber development, abnormal
ZP:0020382	splanchnocranium delayed ossification, abnormal
ZP:0020383	energy coupled proton transmembrane transport, against electrochemical gradient decreased process quality, abnormal
ZP:0020384	retinal rod cell increased volume, abnormal
ZP:0020385	chondrocranium cartilage decreased occurrence neural crest cell migration, abnormal
ZP:0020386	cardiac muscle cell spatial pattern, abnormal
ZP:0020387	cardioblast cell midline fusion decreased occurrence, abnormal
ZP:0020388	cardiac muscle cell decreased speed, abnormal
ZP:0020389	anterior lateral plate mesoderm far from anterior lateral plate mesoderm, abnormal
ZP:0020390	anterior lateral plate mesoderm spatial pattern, abnormal
ZP:0020391	roof of mouth development decreased process quality, abnormal
ZP:0020392	heart primordium separated from heart primordium, abnormal
ZP:0020393	cardiac muscle progenitor cell migration to the midline involved in heart field formation decreased efficacy, abnormal
ZP:0020394	cardioblast migration to the midline involved in heart rudiment formation process quality, abnormal
ZP:0020395	anterior lateral plate mesoderm separated from anterior lateral plate mesoderm, abnormal
ZP:0020396	exocrine pancreas polarity, abnormal
ZP:0020397	pancreatic acinar cell absent, abnormal
ZP:0020398	secondary islet absent, abnormal
ZP:0020399	secondary islet decreased amount, abnormal
ZP:0020400	pancreatic B cell decreased distribution, abnormal
ZP:0020401	dorsal aorta dilated, abnormal
ZP:0020402	intersegmental vessel trunk disorganized, abnormal
ZP:0020403	caudal artery dilated, abnormal
ZP:0020404	hepatic portal vein disorganized, abnormal
ZP:0020406	ceratobranchial 5 cartilage lacks parts or has fewer parts of type ceratobranchial 5 primary tooth, abnormal
ZP:0020407	anterior segment eye malformed, abnormal
ZP:0020408	odontogenesis disrupted, abnormal
ZP:0020409	aqueous humor decreased volume, abnormal
ZP:0020410	female sex determination disrupted, abnormal
ZP:0020411	tooth 4V incomplete structure, abnormal
ZP:0020412	cytoplasm Kupffer's vesicle decreased amount, abnormal
ZP:0020413	Kolmer-Agduhr neuron decreased process quality response to muscle activity, abnormal
ZP:0020414	Kolmer-Agduhr neuron decreased process quality response to mechanical stimulus, abnormal
ZP:0020415	response to muscle activity decreased process quality, abnormal
ZP:0020416	angiogenic sprout dorsal aorta decreased amount, abnormal
ZP:0020417	cilium retinal photoreceptor layer decreased amount, abnormal
ZP:0020418	mitotic spindle cell morphology, abnormal
ZP:0020420	mitotic cell cycle process disrupted, abnormal
ZP:0020421	centriole cell decreased amount, abnormal
ZP:0020422	bone tissue surrounding notochord, abnormal
ZP:0020423	hemal arch morphology, abnormal
ZP:0020424	vertebra condensed, abnormal
ZP:0020425	hypural curved, abnormal
ZP:0020426	epithelium notochord deformed, abnormal
ZP:0020427	bone tissue increased amount, abnormal
ZP:0020428	centrum increased thickness, abnormal
ZP:0020429	skeletal muscle cell horizontal myoseptum dense, abnormal
ZP:0020430	parhypural curved, abnormal
ZP:0020431	vertebra protruding, abnormal
ZP:0020432	centrum decreased length, abnormal
ZP:0020433	collagen fibril organization disrupted, abnormal
ZP:0020434	rib curved, abnormal
ZP:0020435	epithelium notochord proliferative, abnormal
ZP:0020436	elastic fiber notochord morphology, abnormal
ZP:0020437	neural arch morphology, abnormal
ZP:0020438	epithelium notochord increased thickness, abnormal
ZP:0020439	procollagen-lysine 5-dioxygenase activity disrupted, abnormal
ZP:0020440	skeletal muscle cell horizontal myoseptum decreased diameter, abnormal
ZP:0020441	collagen type I trimer notochord disorganized, abnormal
ZP:0020442	rib kinked, abnormal
ZP:0020443	trunk process quality motor neuron axon guidance, abnormal
ZP:0020444	opercular flap mineralized, abnormal
ZP:0020445	axon primary motor neuron spatial pattern, abnormal
ZP:0020446	ventral root mislocalised, abnormal
ZP:0020447	photoreceptor connecting cilium retina decreased length, abnormal
ZP:0020448	photoreceptor connecting cilium retina decreased amount, abnormal
ZP:0020449	neuron retina disorganized, abnormal
ZP:0020450	photoreceptor outer segment retinal cone cell aplastic/hypoplastic, abnormal
ZP:0020451	mitochondrial chromosome compound organ decreased amount, abnormal
ZP:0020452	mitochondrial chromosome caudal fin decreased amount, abnormal
ZP:0020453	mitochondrial DNA replication decreased occurrence, abnormal
ZP:0020454	mitochondrial chromosome central nervous system decreased amount, abnormal
ZP:0020455	central nervous system decreased process quality cellular respiration, abnormal
ZP:0020456	ceratobranchial 5 tooth hypoplastic, abnormal
ZP:0020457	rRNA transcription disrupted, abnormal
ZP:0020458	ventral mandibular arch apoptotic, abnormal
ZP:0020459	pharyngeal arch 1 decreased occurrence cell population proliferation, abnormal
ZP:0020460	ceratohyal cartilage polarity, abnormal
ZP:0020461	neural crest cell pharyngeal arch decreased distribution, abnormal
ZP:0020462	neural crest cell pharyngeal arch spatial pattern, abnormal
ZP:0020463	opercle hypoplastic, abnormal
ZP:0020464	cranium increased occurrence apoptotic process, abnormal
ZP:0020465	pharyngeal arch 2 decreased occurrence cell population proliferation, abnormal
ZP:0020466	cranium necrotic, abnormal
ZP:0020467	preoptic area decreased amount, abnormal
ZP:0020468	fin decreased amount, abnormal
ZP:0020469	trunk decreased distribution, abnormal
ZP:0020470	anatomical margin dorsal aorta shape, abnormal
ZP:0020471	anatomical margin posterior cardinal vein shape, abnormal
ZP:0020472	cell body CaP motoneuron mislocalised anteriorly, abnormal
ZP:0020473	motor neuron increased occurrence bleb assembly, abnormal
ZP:0020474	CaP motoneuron process quality axonogenesis, abnormal
ZP:0020475	axon CaP motoneuron morphology, abnormal
ZP:0020476	membrane motor neuron decreased amount, abnormal
ZP:0020477	retinal neural layer increased occurrence apoptotic process, abnormal
ZP:0020478	negative regulation of hh target transcription factor activity disrupted, abnormal
ZP:0020479	dendrite Purkinje cell decreased amount, abnormal
ZP:0020480	dendrite Purkinje cell decreased branchiness, abnormal
ZP:0020481	midbrain hindbrain boundary edematous, abnormal
ZP:0020482	intracellular DEL mislocalised, abnormal
ZP:0020483	endocytosis increased occurrence, abnormal
ZP:0020484	cytosol DEL mislocalised, abnormal
ZP:0020485	lateral plate mesoderm decreased distribution, abnormal
ZP:0020486	lateral plate mesoderm decreased occurrence cell migration, abnormal
ZP:0020487	caudal fin increased pigmentation, abnormal
ZP:0020488	pronephric proximal convoluted tubule shape, abnormal
ZP:0020489	ceratobranchial cartilage increased angle to anterior-posterior axis whole organism, abnormal
ZP:0020490	mRNA destabilization decreased occurrence, abnormal
ZP:0020491	Meckel's cartilage decreased distribution, abnormal
ZP:0020492	integument has fewer parts of type NaK ionocyte, abnormal
ZP:0020493	Meckel's cartilage decreased amount, abnormal
ZP:0020494	branchiostegal ray decreased distribution, abnormal
ZP:0020495	integument decreased amount, abnormal
ZP:0020496	integument has fewer parts of type vH ionocyte, abnormal
ZP:0020497	epidermis has fewer parts of type somatic stem cell, abnormal
ZP:0020498	somatic stem cell epidermis decreased distribution, abnormal
ZP:0020499	calcium ion import decreased rate, abnormal
ZP:0020500	hindbrain has fewer parts of type ependymal cell motile cilium ependymal cell, abnormal
ZP:0020501	vertebral column asymmetrically curved, abnormal
ZP:0020502	ependymal cell decreased occurrence motile cilium assembly, abnormal
ZP:0020503	vertebral column decreased process quality skeletal system morphogenesis, abnormal
ZP:0020504	mitochondrial matrix skeletal muscle composition, abnormal
ZP:0020505	mitochondrial membrane skeletal muscle broken, abnormal
ZP:0020506	mitochondrial intermembrane space skeletal muscle increased size, abnormal
ZP:0020507	mitochondrial crista skeletal muscle morphology, abnormal
ZP:0020508	skeletal muscle accumulation mitochondrial matrix vesicle skeletal muscle, abnormal
ZP:0020509	retina increased process quality mitotic cell cycle, abnormal
ZP:0020510	locomotory behavior increased occurrence, abnormal
ZP:0020511	sleep decreased occurrence, abnormal
ZP:0020512	whole organism behavioural activity, abnormal
ZP:0020513	neutrophil pericardium increased amount, abnormal
ZP:0020514	fin broken, abnormal
ZP:0020515	neutrophil otic vesicle decreased amount, abnormal
ZP:0020516	neutrophil head decreased amount, abnormal
ZP:0020517	cell binucleate, abnormal
ZP:0020518	spinal cord motor neuron differentiation arrested, abnormal
ZP:0020519	trunk increased distribution, abnormal
ZP:0020520	mitotic cytokinesis checkpoint disrupted, abnormal
ZP:0020521	proliferative region decreased amount, abnormal
ZP:0020522	axon Rohon-Beard neuron disorganized, abnormal
ZP:0020523	head increased distribution, abnormal
ZP:0020524	axon sensory neuron spatial pattern, abnormal
ZP:0020525	tail bud increased distribution, abnormal
ZP:0020526	trigeminal sensory neuron disrupted spinal sensory neuron axon guidance, abnormal
ZP:0020527	whole organism has extra parts of type nucleus embryonic structure, abnormal
ZP:0020528	cytokinesis lacking processual parts membrane fission, abnormal
ZP:0020529	blastoderm increased occurrence apoptotic process, abnormal
ZP:0020530	axon microtubule bundle Rohon-Beard neuron disorganized, abnormal
ZP:0020531	nucleus nucleate erythrocyte increased amount, abnormal
ZP:0020532	cell decreased amount mitotic cell cycle, abnormal
ZP:0020533	nucleate erythrocyte increased duration mitotic cell cycle, abnormal
ZP:0020534	cell multinucleate, abnormal
ZP:0020535	whole organism opacity, abnormal
ZP:0020536	Rohon-Beard neuron disrupted spinal sensory neuron axon guidance, abnormal
ZP:0020537	blood cell increased size, abnormal
ZP:0020538	proliferative region decreased distribution, abnormal
ZP:0020539	macrophage decreased distribution, abnormal
ZP:0020540	primary motor neuron spatial pattern, abnormal
ZP:0020541	CoSA spatial pattern, abnormal
ZP:0020542	mitotic cell cycle has extra parts of type nuclear division, abnormal
ZP:0020543	cell knobbled, abnormal
ZP:0020544	spinal cord commissural neuron specification arrested, abnormal
ZP:0020545	neutrophil decreased distribution, abnormal
ZP:0020546	axon sensory neuron distended, abnormal
ZP:0020547	intermediate cell mass of mesoderm spatial pattern, abnormal
ZP:0020548	spinal cord interneuron spatial pattern, abnormal
ZP:0020549	Rohon-Beard neuron spatial pattern, abnormal
ZP:0020550	neuroblast decreased distribution, abnormal
ZP:0020551	cardiac neural crest heart decreased amount, abnormal
ZP:0020552	melanocyte epidermis position, abnormal
ZP:0020553	cardiac neural crest accumulation posterior region otic vesicle, abnormal
ZP:0020554	atrioventricular valve orientation ventriculo bulbo valve, abnormal
ZP:0020555	blood cardiac ventricle decreased amount, abnormal
ZP:0020556	cranial cartilage disrupted cartilage development, abnormal
ZP:0020557	cardiac neural crest mislocalised, abnormal
ZP:0020558	nucleate erythrocyte increased accumulation heart, abnormal
ZP:0020559	atrioventricular valve decreased size, abnormal
ZP:0020560	neural tube increased occurrence pigmentation, abnormal
ZP:0020561	blood atrium decreased amount, abnormal
ZP:0020562	developmental growth disrupted, abnormal
ZP:0020563	ventriculo bulbo valve aplastic, abnormal
ZP:0020564	ventriculo bulbo valve decreased size, abnormal
ZP:0020565	kidney increased amount, abnormal
ZP:0020566	eye decreased distribution, abnormal
ZP:0020567	eye decreased occurrence cell population proliferation, abnormal
ZP:0020568	ciliary marginal zone absent, abnormal
ZP:0020569	acetylcholine-gated channel complex skeletal muscle distributed, abnormal
ZP:0020570	CaP motoneuron decreased process quality synaptic vesicle exocytosis, abnormal
ZP:0020571	CaP motoneuron decreased process quality action potential, abnormal
ZP:0020572	CaP motoneuron process quality synaptic signaling, abnormal
ZP:0020573	synapse CaP motoneuron decreased amount, abnormal
ZP:0020574	CaP motoneuron decreased occurrence synaptic vesicle exocytosis, abnormal
ZP:0020575	CaP motoneuron process quality regulation of synaptic plasticity, abnormal
ZP:0020576	fast muscle cell process quality transmission of nerve impulse, abnormal
ZP:0020577	muscle adaptation decreased process quality, abnormal
ZP:0020578	heart process quality alternative mRNA splicing, via spliceosome, abnormal
ZP:0020579	skeletal muscle contraction decreased efficacy, abnormal
ZP:0020580	motor nucleus of vagal nerve shortened, abnormal
ZP:0020581	nucleate erythrocyte intermediate cell mass of mesoderm decreased amount, abnormal
ZP:0020582	ocular blood vessel disrupted blood vessel lumenization, abnormal
ZP:0020583	eye disrupted vasculature development, abnormal
ZP:0020584	ocular blood vessel decreased thickness, abnormal
ZP:0020585	cone photoresponse recovery increased efficacy, abnormal
ZP:0020586	brain vasculature lacks all parts of type central artery, abnormal
ZP:0020587	primordial hindbrain channel decreased process quality establishment of endothelial blood-brain barrier, abnormal
ZP:0020588	central artery decreased process quality vasculature development, abnormal
ZP:0020589	primordial hindbrain channel has extra parts of type blood vessel endothelial cell, abnormal
ZP:0020590	primordial hindbrain channel decreased process quality canonical Wnt signaling pathway, abnormal
ZP:0020591	peripheral nervous system lacks all parts of type dorsal root ganglion, abnormal
ZP:0020592	central artery decreased process quality canonical Wnt signaling pathway, abnormal
ZP:0020593	dorsal root ganglion morphogenesis decreased process quality, abnormal
ZP:0020594	brain vasculature lacks parts or has fewer parts of type central artery, abnormal
ZP:0020595	brain vasculature has extra parts of type atrioventricular canal, abnormal
ZP:0020596	primordial hindbrain channel mislocalised, abnormal
ZP:0020597	hindbrain mislocalised, abnormal
ZP:0020598	primary motor neuron increased amount, abnormal
ZP:0020599	gut lacks all parts of type distal region enteric neuron, abnormal
ZP:0020600	enteric nervous system absent, abnormal
ZP:0020601	enteric nervous system development process quality, abnormal
ZP:0020602	enteric nervous system decreased distribution, abnormal
ZP:0020603	intestine decreased process quality peristalsis, abnormal
ZP:0020604	enteric neuron absent, abnormal
ZP:0020605	neuron neural crest derived gut absent, abnormal
ZP:0020606	neuron neural crest derived gut decreased distribution, abnormal
ZP:0020607	neural crest increased distribution, abnormal
ZP:0020608	migratory neural crest increased amount, abnormal
ZP:0020609	ectomesenchyme decreased amount, abnormal
ZP:0020610	migratory neural crest increased occurrence cell population proliferation, abnormal
ZP:0020611	migratory neural crest increased distribution, abnormal
ZP:0020612	extension hypotrophic, abnormal
ZP:0020613	whole organism bulbous, abnormal
ZP:0020614	melanocyte larval melanophore stripe decreased amount, abnormal
ZP:0020615	eye lacks all parts of type iridophore, abnormal
ZP:0020616	convergent extension decreased process quality, abnormal
ZP:0020617	photoreceptor outer segment photoreceptor outer segment layer shortened, abnormal
ZP:0020618	retinal photoreceptor layer decreased amount, abnormal
ZP:0020619	photoreceptor outer segment layer decreased distribution, abnormal
ZP:0020621	nucleate erythrocyte irregularly shaped, abnormal
ZP:0020622	central side anatomical structure mislocalised, abnormal
ZP:0020623	erythrocyte maturation decreased occurrence, abnormal
ZP:0020624	right side anatomical structure mislocalised, abnormal
ZP:0020625	hindbrain inflated, abnormal
ZP:0020626	microglial cell process quality lysosome organization, abnormal
ZP:0020627	optic tectum has extra parts of type microglial cell phagolysosome microglial cell, abnormal
ZP:0020628	microglial cell morphology, abnormal
ZP:0020629	brain decreased occurrence apoptotic cell clearance, abnormal
ZP:0020630	phagolysosome microglial cell increased size, abnormal
ZP:0020631	microglial cell decreased occurrence lysosomal protein catabolic process, abnormal
ZP:0020632	lysosome microglial cell increased size, abnormal
ZP:0020633	retinal inner plexiform layer absent, abnormal
ZP:0020634	intermediate cell mass of mesoderm absent, abnormal
ZP:0020635	hypothalamus increased occurrence apoptotic process, abnormal
ZP:0020636	hypothalamus spatial pattern, abnormal
ZP:0020637	hypothalamus increased amount, abnormal
ZP:0020638	hypothalamus increased occurrence mitotic cell cycle process, abnormal
ZP:0020639	caudal hypothalamic zone absent, abnormal
ZP:0020640	anterior region hypothalamus decreased amount, abnormal
ZP:0020641	anterior region caudal hypothalamic zone mislocalised, abnormal
ZP:0020643	hypothalamus decreased occurrence cell population proliferation, abnormal
ZP:0020644	anterior region hypothalamus absent, abnormal
ZP:0020645	anterior region caudal hypothalamic zone absent, abnormal
ZP:0020646	telencephalon mislocalised, abnormal
ZP:0020647	skeletal muscle myofibril skeletal muscle broken, abnormal
ZP:0020648	sarcomere skeletal muscle structure, abnormal
ZP:0020649	Z disc skeletal muscle broken, abnormal
ZP:0020650	mitochondrion skeletal muscle infiltrative, abnormal
ZP:0020651	splanchnocranium disrupted bone mineralization, abnormal
ZP:0020652	epithelium post-vent region blistered, abnormal
ZP:0020653	embryonic heart tube formation decreased occurrence, abnormal
ZP:0020654	cell migration to the midline involved in heart development decreased occurrence, abnormal
ZP:0020655	anterior-posterior axis ventral mandibular arch decreased length, abnormal
ZP:0020656	heart contraction decreased efficiency, abnormal
ZP:0020657	blood has fewer parts of type hemoglobin complex nucleate erythrocyte, abnormal
ZP:0020658	granulocyte migration disrupted, abnormal
ZP:0020659	medial region exocrine pancreas aplastic, abnormal
ZP:0020660	basement membrane notochord malformed, abnormal
ZP:0020661	vacuole notochord malformed, abnormal
ZP:0020662	basement membrane notochord vacuolated, abnormal
ZP:0020663	posterior region notochord absent, abnormal
ZP:0020664	vacuole notochord position, abnormal
ZP:0020665	vesicle chondrocyte mislocalised, abnormal
ZP:0020666	goblet cell absent, abnormal
ZP:0020667	chondrocyte mandibular arch skeleton decreased amount, abnormal
ZP:0020668	forebrain process quality neuronal action potential, abnormal
ZP:0020669	brain ictal synaptic signaling, abnormal
ZP:0020670	posterior lateral plate mesoderm morphology, abnormal
ZP:0020671	posterior lateral mesoderm decreased distribution, abnormal
ZP:0020672	supramolecular fiber organization disrupted, abnormal
ZP:0020673	pronephric glomerulus lacks parts or has fewer parts of type glomerular endothelium fenestra glomerular basement membrane, abnormal
ZP:0020674	pronephric tubule atrophied, abnormal
ZP:0020675	posterior lateral line primordium malformed, abnormal
ZP:0020676	blood vessel endothelial cell common cardinal vein shape, abnormal
ZP:0020677	common cardinal vein decreased process quality blood vessel endothelial cell migration, abnormal
ZP:0020678	blood vessel endothelial cell common cardinal vein disorganized, abnormal
ZP:0020679	cell-cell junction common cardinal vein irregular spatial pattern, abnormal
ZP:0020680	cell-cell junction common cardinal vein spatial pattern, abnormal
ZP:0020681	intestinal epithelial cell development disrupted, abnormal
ZP:0020682	DNA damage response, signal transduction by p53 class mediator process quality, abnormal
ZP:0020683	whole organism disrupted cell redox homeostasis, abnormal
ZP:0020684	whole organism process quality cell cycle, abnormal
ZP:0020685	neural tube process quality cilium assembly, abnormal
ZP:0020686	fin regeneration decreased efficacy, abnormal
ZP:0020687	regenerating fin decreased occurrence cell population proliferation, abnormal
ZP:0020688	post-vent region decreased distribution, abnormal
ZP:0020689	head decreased distribution, abnormal
ZP:0020690	lateral line system development disrupted, abnormal
ZP:0020691	trunk decreased occurrence cell population proliferation, abnormal
ZP:0020692	head decreased occurrence cell population proliferation, abnormal
ZP:0020693	hematopoietic progenitor cell differentiation disrupted, abnormal
ZP:0020694	posterior lateral line neuromast deposition decreased occurrence, abnormal
ZP:0020695	chondrocyte pectoral fin decreased amount, abnormal
ZP:0020696	cerebellum shape, abnormal
ZP:0020697	cilium neural tube absent, abnormal
ZP:0020698	hepatocyte proliferation decreased rate, abnormal
ZP:0020699	corpuscles of Stannius absent, abnormal
ZP:0020700	pronephric proximal convoluted tubule mislocalised, abnormal
ZP:0020701	pronephric proximal straight tubule absent, abnormal
ZP:0020702	retinal outer nuclear layer temporally extended cell population proliferation, abnormal
ZP:0020703	retinal outer nuclear layer increased occurrence apoptotic process, abnormal
ZP:0020704	retinal rod cell increased occurrence cell population proliferation, abnormal
ZP:0020705	retinal ganglion cell layer increased occurrence apoptotic process, abnormal
ZP:0020706	retinal inner nuclear layer increased occurrence apoptotic process, abnormal
ZP:0020707	oligodendrocyte brain decreased amount, abnormal
ZP:0020708	oligodendrocyte midbrain decreased amount, abnormal
ZP:0020709	cell projection oligodendrocyte decreased length, abnormal
ZP:0020710	noradrenaline brain decreased amount, abnormal
ZP:0020711	serotonin brain decreased amount, abnormal
ZP:0020712	(5-hydroxyindol-3-yl)acetic acid brain increased amount, abnormal
ZP:0020713	dopamine brain decreased amount, abnormal
ZP:0020714	melanocyte caudal fin decreased pigmentation, abnormal
ZP:0020715	mitochondrial inner membrane skeletal muscle broken, abnormal
ZP:0020716	mitochondrial membrane skeletal muscle swollen, abnormal
ZP:0020717	Mauthner neuron amplitude excitatory postsynaptic potential, abnormal
ZP:0020718	neuromast hair cell disorganized, abnormal
ZP:0020719	stereocilium auditory receptor cell decreased amount, abnormal
ZP:0020720	neuromast hair cell posterior lateral line apoptotic, abnormal
ZP:0020721	neuromast hair cell lateral line decreased amount, abnormal
ZP:0020722	neuromast hair cell anterior lateral line apoptotic, abnormal
ZP:0020723	whole organism decreased process quality manganese ion homeostasis, abnormal
ZP:0020724	brain decreased process quality manganese ion homeostasis, abnormal
ZP:0020725	hemoglobin biosynthetic process decreased occurrence, abnormal
ZP:0020726	statoacoustic (VIII) ganglion decreased amount, abnormal
ZP:0020727	dorsal region diencephalon decreased amount, abnormal
ZP:0020728	anterior lateral line ganglion absent, abnormal
ZP:0020729	interneuromast cell spatial pattern, abnormal
ZP:0020730	midbrain hindbrain boundary decreased amount, abnormal
ZP:0020731	telencephalon decreased amount, abnormal
ZP:0020732	otic vesicle lacks parts or has fewer parts of type cilium otic epithelium, abnormal
ZP:0020733	gall bladder hypoplastic, abnormal
ZP:0020734	pharyngeal arch 3-7 delayed embryonic viscerocranium morphogenesis, abnormal
ZP:0020735	heart tube decreased distribution, abnormal
ZP:0020736	fast muscle cell increased distribution, abnormal
ZP:0020737	slow muscle cell increased distribution, abnormal
ZP:0020738	presumptive cardiac ventricle heart tube decreased distribution, abnormal
ZP:0020739	embryonic cranial skeleton morphogenesis decreased process quality, abnormal
ZP:0020740	terminal nerve decreased length, abnormal
ZP:0020741	fast muscle cell decreased process quality neuromuscular synaptic transmission, abnormal
ZP:0020742	synaptic cleft fast muscle cell decreased width, abnormal
ZP:0020743	CaP motoneuron decreased process quality axon extension involved in axon guidance, abnormal
ZP:0020744	neuromuscular junction fast muscle cell decreased width, abnormal
ZP:0020745	fast muscle cell decreased process quality neuromuscular junction development, abnormal
ZP:0020746	neural tube absent, abnormal
ZP:0020747	dorso-lateral region hindbrain decreased distribution, abnormal
ZP:0020748	ventral region diencephalon decreased amount, abnormal
ZP:0020749	axial region hindbrain decreased amount, abnormal
ZP:0020750	ventral region diencephalon decreased distribution, abnormal
ZP:0020751	ventral region spinal cord absent, abnormal
ZP:0020752	chondrocyte absent, abnormal
ZP:0020753	spermine biosynthetic process decreased occurrence, abnormal
ZP:0020754	skeletal muscle spatial pattern, abnormal
ZP:0020755	common myeloid progenitor increased amount, abnormal
ZP:0020756	lysosome macrophage increased size, abnormal
ZP:0020757	macrophage increased size, abnormal
ZP:0020758	lateral plate mesoderm increased amount, abnormal
ZP:0020759	subcutaneous fat decreased amount, abnormal
ZP:0020760	regulation of protein kinase B signaling disrupted, abnormal
ZP:0020761	blood plasma increased amount, abnormal
ZP:0020762	male organism has extra parts of type lipid droplet liver, abnormal
ZP:0020763	whole organism increased rate growth, abnormal
ZP:0020764	blood plasma decreased process quality response to insulin, abnormal
ZP:0020765	liver decreased process quality cellular response to insulin stimulus, abnormal
ZP:0020766	liver decreased process quality cellular response to glucagon stimulus, abnormal
ZP:0020767	female organism has extra parts of type lipid droplet liver, abnormal
ZP:0020768	whole organism decreased rate growth, abnormal
ZP:0020769	liver disrupted regulation of tyrosine phosphorylation of STAT protein, abnormal
ZP:0020770	chondrocyte pharyngeal arch decreased amount, abnormal
ZP:0020771	blood vessel endothelium posterior cardinal vein decreased amount, abnormal
ZP:0020772	blood vessel endothelium dorsal aorta decreased amount, abnormal
ZP:0020773	left-right axis roof plate rhombomere region decreased width, abnormal
ZP:0020774	adipose tissue development decreased process quality, abnormal
ZP:0020775	nucleus fast muscle cell absent, abnormal
ZP:0020776	lipid droplet pleuroperitoneal cavity decreased amount, abnormal
ZP:0020777	fast muscle cell process quality calcium-mediated signaling, abnormal
ZP:0020778	lipid droplet pleuroperitoneal cavity decreased size, abnormal
ZP:0020779	rib broken, abnormal
ZP:0020780	parasphenoid deformed, abnormal
ZP:0020781	ossification involved in bone maturation process quality, abnormal
ZP:0020782	cleithrum decreased distribution, abnormal
ZP:0020783	skeletal system decreased process quality bone mineralization, abnormal
ZP:0020784	nucleus osteoblast composition, abnormal
ZP:0020785	cranium decreased process quality bone mineralization, abnormal
ZP:0020786	ceratobranchial 5 primary tooth decreased process quality tooth mineralization, abnormal
ZP:0020787	cranium has extra parts of type bone element, abnormal
ZP:0020788	cranial suture morphogenesis disrupted, abnormal
ZP:0020789	bone development delayed, abnormal
ZP:0020790	vertebral column decreased process quality bone mineralization, abnormal
ZP:0020791	cranial vault morphology, abnormal
ZP:0020792	vertebra size, abnormal
ZP:0020793	fibrous joint cranium increased amount, abnormal
ZP:0020794	cranium domed, abnormal
ZP:0020795	nucleus osteoblast circular, abnormal
ZP:0020796	spinal cord disrupted microtubule cytoskeleton organization, abnormal
ZP:0020797	primary motor neuron process quality axonogenesis, abnormal
ZP:0020798	whole organism arched, abnormal
ZP:0020799	axon microtubule bundle motor neuron decreased diameter, abnormal
ZP:0020800	microtubule cytoskeleton spinal cord disorganized, abnormal
ZP:0020801	lateral plate mesoderm absent, abnormal
ZP:0020802	neural crest cell decreased occurrence cell population proliferation, abnormal
ZP:0020803	palate shortened, abnormal
ZP:0020804	anatomical structure apoptotic, abnormal
ZP:0020805	DNA damage response, detection of DNA damage disrupted, abnormal
ZP:0020806	xanthophore integument mislocalised, abnormal
ZP:0020807	spermidine biosynthetic process decreased occurrence, abnormal
ZP:0020808	tooth placode absent, abnormal
ZP:0020809	tooth placode spatial pattern, abnormal
ZP:0020810	tooth placode decreased amount, abnormal
ZP:0020811	mitotic cell cycle, embryonic decreased occurrence, abnormal
ZP:0020813	bone tissue decreased volume, abnormal
ZP:0020814	anterior-posterior axis somite decreased length, abnormal
ZP:0020815	cell whole organism decreased distribution, abnormal
ZP:0020816	cell notochord increased area, abnormal
ZP:0020817	cell notochord decreased length, abnormal
ZP:0020818	cell notochord increased width, abnormal
ZP:0020820	spinal cord increased occurrence mitotic cell cycle, abnormal
ZP:0020821	lactate biosynthetic process increased occurrence, abnormal
ZP:0020822	vasculature increased size, abnormal
ZP:0020823	blood vessel dilated, abnormal
ZP:0020824	anterior region head shortened, abnormal
ZP:0020825	whole organism decreased process quality metabolic process, abnormal
ZP:0020826	locomotor rhythm disrupted, abnormal
ZP:0020827	forebrain electric potential, abnormal
ZP:0020828	hematopoietic multipotent progenitor cell decreased occurrence cell population proliferation, abnormal
ZP:0020829	thrombocyte intermediate cell mass of mesoderm decreased amount, abnormal
ZP:0020830	late endosome retinal cone cell morphology, abnormal
ZP:0020831	autophagosome retinal cone cell increased amount, abnormal
ZP:0020832	late endosome retinal cone cell increased size, abnormal
ZP:0020833	optic tectum decreased area, abnormal
ZP:0020834	cranial neural crest cell disorganized, abnormal
ZP:0020835	splanchnocranium immature, abnormal
ZP:0020836	chondrocyte ceratobranchial cartilage absent, abnormal
ZP:0020837	ceratobranchial cartilage disorganized, abnormal
ZP:0020838	branching involved in blood vessel morphogenesis increased occurrence, abnormal
ZP:0020839	brain vasculature increased branchiness, abnormal
ZP:0020840	vasculature aortic arch dilated, abnormal
ZP:0020841	whole organism lacks all parts of type heart, abnormal
ZP:0020842	whole organism lacks all parts of type head, abnormal
ZP:0020843	heart primordium anterior lateral plate mesoderm decreased amount, abnormal
ZP:0020844	branchiomotor neuron decreased amount, abnormal
ZP:0020845	heart tube decreased size, abnormal
ZP:0020846	hypophysis decreased amount, abnormal
ZP:0020847	corpuscles of Stannius increased distribution, abnormal
ZP:0020848	cell corpuscles of Stannius increased amount, abnormal
ZP:0020849	posterior region pronephros decreased distribution, abnormal
ZP:0020850	blue sensitive photoreceptor cell retina decreased amount, abnormal
ZP:0020851	parapineal organ has fewer parts of type neuron parapineal organ, abnormal
ZP:0020852	foraging behavior decreased efficacy, abnormal
ZP:0020853	UV sensitive photoreceptor cell retina increased amount, abnormal
ZP:0020854	parapineal organ decreased occurrence neuron fate specification, abnormal
ZP:0020855	embryonic pelvic fin morphogenesis arrested, abnormal
ZP:0020856	pelvic fin bud arrested apical ectodermal ridge formation, abnormal
ZP:0020857	hindlimb morphogenesis arrested, abnormal
ZP:0020858	pelvic fin morphogenesis arrested, abnormal
ZP:0020859	pelvic fin bud lacks all parts of type apical ectodermal ridge pelvic fin bud, abnormal
ZP:0020860	embryonic hindlimb morphogenesis arrested, abnormal
ZP:0020861	whole organism lacks all parts of type pelvic fin, abnormal
ZP:0020862	mesenchyme pelvic fin bud absent, abnormal
ZP:0020863	mesenchyme pelvic fin bud increased distribution, abnormal
ZP:0020864	somite irregularly shaped, abnormal
ZP:0020865	trunk has fewer parts of type central region dermomyotome, abnormal
ZP:0020866	paraxial mesoderm decreased amount, abnormal
ZP:0020867	head muscle aplastic/hypoplastic, abnormal
ZP:0020868	hypobranchial artery detached from lateral dorsal aorta, abnormal
ZP:0020869	hypobranchial artery shape, abnormal
ZP:0020870	interhyoideus hypoplastic, abnormal
ZP:0020871	intermandibularis hypoplastic, abnormal
ZP:0020872	hypobranchial artery absent, abnormal
ZP:0020873	aortic arch 4 decreased occurrence blood vessel lumenization, abnormal
ZP:0020874	aortic arch 3 decreased occurrence blood vessel lumenization, abnormal
ZP:0020875	pharyngeal vasculature absent, abnormal
ZP:0020876	aortic arch 4 decreased amount, abnormal
ZP:0020877	aortic arch 6 decreased amount, abnormal
ZP:0020878	aortic arch 6 arrested blood vessel lumenization, abnormal
ZP:0020879	aortic arch 5 decreased amount, abnormal
ZP:0020880	nucleus thalamus absent, abnormal
ZP:0020881	neuron thalamus absent, abnormal
ZP:0020882	germ ring absent, abnormal
ZP:0020883	dorsal region margin absent, abnormal
ZP:0020884	larval heart development decreased process quality, abnormal
ZP:0020885	neural tube closure decreased occurrence, abnormal
ZP:0020886	lens fused with lens, abnormal
ZP:0020887	pineal complex shape, abnormal
ZP:0020888	pineal complex split bilaterally, abnormal
ZP:0020889	neural plate process quality cell migration, abnormal
ZP:0020890	axon notochord morphology, abnormal
ZP:0020891	peripheral nervous system disrupted axonogenesis involved in innervation, abnormal
ZP:0020892	muscle increased amount, abnormal
ZP:0020893	head kidney increased amount, abnormal
ZP:0020894	chromosome, telomeric region muscle decreased length, abnormal
ZP:0020895	age-dependent general metabolic decline physiological state, abnormal
ZP:0020896	chromosome, telomeric region gut decreased length, abnormal
ZP:0020897	intestinal lamina propria mucosa increased occurrence leukocyte migration involved in inflammatory response, abnormal
ZP:0020899	muscle cell atrophied, abnormal
ZP:0020900	testis decreased occurrence cell population proliferation, abnormal
ZP:0020901	chromosome, telomeric region testis decreased length, abnormal
ZP:0020902	gut increased amount, abnormal
ZP:0020903	neoplasm whole organism increased amount, abnormal
ZP:0020904	muscle cell degeneration, abnormal
ZP:0020905	whole organism degeneration, abnormal
ZP:0020906	head kidney decreased occurrence cell population proliferation, abnormal
ZP:0020907	gut decreased occurrence cell population proliferation, abnormal
ZP:0020908	trunk decreased amount, abnormal
ZP:0020909	circulating cell decreased amount, abnormal
ZP:0020910	posterior lateral line neuromast irregular spatial pattern, abnormal
ZP:0020911	endothelial cell trunk increased amount, abnormal
ZP:0020912	caudal vein plexus increased occurrence apoptotic process, abnormal
ZP:0020913	dorsal longitudinal anastomotic vessel decreased occurrence blood vessel development, abnormal
ZP:0020914	ventral region somite absent, abnormal
ZP:0020915	somite border blurry, abnormal
ZP:0020916	proximal region pronephric duct absent, abnormal
ZP:0020917	hypophysis increased distribution, abnormal
ZP:0020918	pronephric duct decreased amount, abnormal
ZP:0020919	cell hypophysis decreased volume, abnormal
ZP:0020920	whole organism has fewer parts of type thyroid follicle, abnormal
ZP:0020921	cell thyroid follicle decreased volume, abnormal
ZP:0020922	thyroid follicle decreased distribution, abnormal
ZP:0020923	mandibular arch skeleton has fewer parts of type cartilage element, abnormal
ZP:0020924	thyroid follicle increased amount, abnormal
ZP:0020925	cell thyroid follicle increased amount, abnormal
ZP:0020926	thyroid follicle hyperplastic, abnormal
ZP:0020927	thyroid follicle increased distribution, abnormal
ZP:0020928	thyroid follicle increased size, abnormal
ZP:0020929	cell hypophysis increased volume, abnormal
ZP:0020930	UV sensitive photoreceptor cell increased amount, abnormal
ZP:0020931	whole organism lacks parts or has fewer parts of type semicircular canal, abnormal
ZP:0020932	synapse horizontal cell increased amount, abnormal
ZP:0020933	cell thyroid follicle increased volume, abnormal
ZP:0020934	whole organism has extra parts of type thyroid follicle, abnormal
ZP:0020935	whole organism lacks parts or has fewer parts of type otolith, abnormal
ZP:0020936	axon RoP motor neuron absent, abnormal
ZP:0020937	RoP motor neuron decreased occurrence axon development, abnormal
ZP:0020938	parachordal vessel decreased occurrence angiogenesis, abnormal
ZP:0020939	cell projection endothelial tip cell morphology, abnormal
ZP:0020940	MiP motor neuron process quality axon development, abnormal
ZP:0020941	axon MiP motor neuron morphology, abnormal
ZP:0020942	axon RoP motor neuron morphology, abnormal
ZP:0020943	secondary motor neuron process quality axon development, abnormal
ZP:0020944	xanthophore displaced to melanophore stripe, abnormal
ZP:0020945	iridophore behavioral quality, abnormal
ZP:0020946	iridophore displaced to melanophore stripe, abnormal
ZP:0020947	iridophore structure, abnormal
ZP:0020948	endocardium separated from myocardium, abnormal
ZP:0020949	optic furrow disrupted basement membrane disassembly, abnormal
ZP:0020951	filamentous actin vascular endothelium decreased amount, abnormal
ZP:0020952	heart decreased volume, abnormal
ZP:0020953	basement membrane optic furrow increased distribution, abnormal
ZP:0020954	hyaloid vessel decreased distribution, abnormal
ZP:0020955	hyaloid vessel hypotrophic, abnormal
ZP:0020956	subintestinal vein disrupted blood vessel morphogenesis, abnormal
ZP:0020957	muscle tendon junction skeletal muscle decreased amount, abnormal
ZP:0020958	hyaluronic acid posterior cardinal vein increased amount, abnormal
ZP:0020959	muscle tendon junction skeletal muscle disorganized, abnormal
ZP:0020960	extracellular matrix skeletal muscle disorganized, abnormal
ZP:0020961	fast muscle cell detached from muscle tendon junction trunk musculature, abnormal
ZP:0020962	skeletal muscle cell detached from trunk musculature, abnormal
ZP:0020963	muscle tendon junction skeletal muscle spatial pattern, abnormal
ZP:0020964	protein complex involved in cell-matrix adhesion skeletal muscle disorganized, abnormal
ZP:0020965	slow muscle cell detached from trunk musculature, abnormal
ZP:0020966	endothelial cell dorsal aorta decreased distribution, abnormal
ZP:0020967	hyaluronic acid dorsal aorta increased amount, abnormal
ZP:0020968	extracellular matrix myocardium spatial pattern, abnormal
ZP:0020969	skeletal muscle cell detached from muscle tendon junction trunk musculature, abnormal
ZP:0020970	dystroglycan complex skeletal muscle disorganized, abnormal
ZP:0020971	fast muscle cell detached from trunk musculature, abnormal
ZP:0020972	myocardium spatial pattern, abnormal
ZP:0020973	extracellular matrix myocardium disorganized, abnormal
ZP:0020974	slow muscle cell detached from muscle tendon junction trunk musculature, abnormal
ZP:0020975	endothelial cell posterior cardinal vein decreased distribution, abnormal
ZP:0020976	cell pronephric glomerulus decreased amount, abnormal
ZP:0020977	podocyte foot pronephric podocyte decreased amount, abnormal
ZP:0020978	proximal convoluted tubule morphology, abnormal
ZP:0020979	neuron intertectal commissure decreased amount, abnormal
ZP:0020980	sarcolemma myotome broken, abnormal
ZP:0020981	regulation of tyrosine phosphorylation of STAT protein disrupted, abnormal
ZP:0020982	melanocyte stimulating hormone secreting cell pars intermedia decreased amount, abnormal
ZP:0020983	trabecular layer cardiac ventricle absent, abnormal
ZP:0020984	heart decreased process quality Notch signaling pathway, abnormal
ZP:0020985	cardiac muscle cell decreased process quality Notch signaling pathway, abnormal
ZP:0020986	endothelial cell decreased accumulation atrioventricular valve, abnormal
ZP:0020987	hematopoietic stem cell homeostasis decreased process quality, abnormal
ZP:0020988	double-strand break repair via nonhomologous end joining increased frequency, abnormal
ZP:0020989	double-strand break repair via single-strand annealing increased frequency, abnormal
ZP:0020990	eye ovate, abnormal
ZP:0020991	anatomical surface retina decreased area, abnormal
ZP:0020992	microtubule polymerization decreased rate, abnormal
ZP:0020993	response to endoplasmic reticulum stress increased occurrence, abnormal
ZP:0020994	N-glycan whole organism decreased amount, abnormal
ZP:0020995	liver increased accumulation lipid droplet liver, abnormal
ZP:0020996	cholesterol homeostasis disrupted, abnormal
ZP:0020997	lipooligosaccharide whole organism decreased amount, abnormal
ZP:0020998	endoplasmic reticulum hepatocyte distended, abnormal
ZP:0020999	Golgi apparatus hepatocyte broken, abnormal
ZP:0021000	tRNA processing disrupted, abnormal
ZP:0021001	serotonergic neuron pretectum increased amount, abnormal
ZP:0021002	sarcomere myotome spatial pattern, abnormal
ZP:0021003	Z disc somite disorganized, abnormal
ZP:0021004	sarcomere somite disorganized, abnormal
ZP:0021005	sarcomere cardiac muscle disorganized, abnormal
ZP:0021006	sarcomere somite decreased length, abnormal
ZP:0021007	sarcomere somite spatial pattern, abnormal
ZP:0021008	myofibril slow muscle cell damaged, abnormal
ZP:0021009	Z disc somite spatial pattern, abnormal
ZP:0021010	melanocyte whole organism absent, abnormal
ZP:0021011	whole organism has extra parts of type Rohon-Beard neuron, abnormal
ZP:0021012	epithelium optic vesicle disorganized, abnormal
ZP:0021013	epithelium optic vesicle morphology, abnormal
ZP:0021014	retinal cone cell photoreceptor outer segment layer decreased amount, abnormal
ZP:0021015	artery trunk vasculature increased amount, abnormal
ZP:0021016	trunk vasculature decreased amount, abnormal
ZP:0021017	endothelial tip cell decreased rate blood vessel endothelial cell migration, abnormal
ZP:0021018	hindbrain atrophied, abnormal
ZP:0021019	motile cilium floor plate disoriented, abnormal
ZP:0021020	pronephric podocyte decreased length, abnormal
ZP:0021021	protein blood decreased amount, abnormal
ZP:0021022	pronephric podocyte increased width, abnormal
ZP:0021023	squamous epithelial cell epicardium morphology, abnormal
ZP:0021024	cell epicardium decreased size, abnormal
ZP:0021025	epicardium increased amount, abnormal
ZP:0021026	pleuroperitoneal cavity fluid-filled, abnormal
ZP:0021027	blood vessel heart vasculature disorganized, abnormal
ZP:0021028	endothelial cell endocardium increased amount, abnormal
ZP:0021029	endocardium increased amount, abnormal
ZP:0021030	squamous epithelial cell epicardium ovate, abnormal
ZP:0021031	heart vasculature increased amount, abnormal
ZP:0021032	fibroblast accumulation epicardium, abnormal
ZP:0021033	epicardium hemorrhagic, abnormal
ZP:0021034	cardiac ventricle spherical, abnormal
ZP:0021036	blood vessel heart vasculature increased amount, abnormal
ZP:0021037	blood vessel heart vasculature disconnected, abnormal
ZP:0021038	epicardium increased occurrence cell population proliferation, abnormal
ZP:0021039	membrane epicardium smooth, abnormal
ZP:0021040	endocardium increased occurrence cell population proliferation, abnormal
ZP:0021041	myocardium increased occurrence cell population proliferation, abnormal
ZP:0021042	motor behavior disrupted, abnormal
ZP:0021043	vasculature decreased amount, abnormal
ZP:0021044	whole organism lacks all parts of type anterior mesencephalic central artery, abnormal
ZP:0021045	whole organism lacks all parts of type central artery, abnormal
ZP:0021046	cardiac ventricle increased amount, abnormal
ZP:0021047	dorsal aorta decreased amount, abnormal
ZP:0021048	basilar artery morphology, abnormal
ZP:0021049	whole organism lacks all parts of type cerebellar central artery, abnormal
ZP:0021050	whole organism lacks all parts of type posterior mesencephalic central artery, abnormal
ZP:0021051	heart decreased process quality regeneration, abnormal
ZP:0021052	whole organism lacks all parts of type axial blood vessel, abnormal
ZP:0021053	whole organism lacks all parts of type intersegmental vessel, abnormal
ZP:0021054	whole organism lacks all parts of type middle mesencephalic central artery, abnormal
ZP:0021055	whole organism lacks all parts of type basilar artery, abnormal
ZP:0021056	nucleate erythrocyte brain aggregated, abnormal
ZP:0021057	hindbrain disrupted vasculature development, abnormal
ZP:0021058	midbrain disrupted vasculature development, abnormal
ZP:0021059	thoracic duct decreased amount, abnormal
ZP:0021060	facial lymphatic vessel decreased occurrence lymphangiogenesis, abnormal
ZP:0021061	lymphangioblast cord decreased occurrence lymph vessel development, abnormal
ZP:0021062	pronephric proximal straight tubule increased diameter, abnormal
ZP:0021063	ciliated epithelial cell pronephric proximal straight tubule disorganized, abnormal
ZP:0021064	epithelial cell pronephric proximal straight tubule decreased amount, abnormal
ZP:0021065	pronephric proximal straight tubule increased occurrence cell population proliferation, abnormal
ZP:0021066	pronephric duct curved, abnormal
ZP:0021067	pronephric glomerulus swollen, abnormal
ZP:0021068	subintestinal vein spatial pattern, abnormal
ZP:0021069	pronephric proximal convoluted tubule increased occurrence cell population proliferation, abnormal
ZP:0021070	pronephric tubule curved, abnormal
ZP:0021071	cytoplasmic vesicle pronephric proximal straight tubule increased amount, abnormal
ZP:0021072	ciliated epithelial cell pronephric proximal convoluted tubule disorganized, abnormal
ZP:0021073	bicellular tight junction pronephric glomerulus decreased amount, abnormal
ZP:0021074	pronephric proximal straight tubule apical-basal polarity, abnormal
ZP:0021075	pronephric glomerulus atrophied, abnormal
ZP:0021076	pronephric proximal straight tubule increased occurrence apoptotic process, abnormal
ZP:0021077	podocyte increased amount, abnormal
ZP:0021078	respiratory gaseous exchange by respiratory system increased occurrence, abnormal
ZP:0021079	regulation of respiratory gaseous exchange increased occurrence, abnormal
ZP:0021080	epithelial cell pronephric proximal convoluted tubule decreased amount, abnormal
ZP:0021081	pronephric proximal convoluted tubule apical-basal polarity, abnormal
ZP:0021082	cytoplasmic vesicle pronephric proximal convoluted tubule increased amount, abnormal
ZP:0021083	pronephros shape, abnormal
ZP:0021084	oligodendrocyte hindbrain decreased distribution, abnormal
ZP:0021085	lysosome hepatocyte decreased amount, abnormal
ZP:0021086	bile canaliculus distended, abnormal
ZP:0021087	bile canaliculus obstructed, abnormal
ZP:0021088	vacuole hepatocyte increased amount, abnormal
ZP:0021089	microvillus bile canaliculus decreased length, abnormal
ZP:0021090	pigment granule retina sparse, abnormal
ZP:0021091	pigment granule integument sparse, abnormal
ZP:0021092	microvillus bile canaliculus sparse, abnormal
ZP:0021093	regulation of odontogenesis disrupted, abnormal
ZP:0021094	telencephalon diencephalon boundary malformed, abnormal
ZP:0021095	ventral thalamus decreased process quality forebrain morphogenesis, abnormal
ZP:0021096	ventral telencephalon mislocalised, abnormal
ZP:0021097	forebrain lacks all parts of type supraoptic tract, abnormal
ZP:0021098	dorsal telencephalon decreased process quality forebrain morphogenesis, abnormal
ZP:0021099	brain increased occurrence BMP signaling pathway, abnormal
ZP:0021100	brain increased occurrence astrocyte development, abnormal
ZP:0021101	brain decreased occurrence oligodendrocyte development, abnormal
ZP:0021102	ventral thalamus decreased amount, abnormal
ZP:0021103	ventral telencephalon decreased amount, abnormal
ZP:0021104	dorsal region brain increased amount, abnormal
ZP:0021105	ventral telencephalon decreased process quality forebrain morphogenesis, abnormal
ZP:0021106	forebrain decreased process quality GABAergic neuron differentiation, abnormal
ZP:0021107	postoptic commissure decreased occurrence central nervous system projection neuron axonogenesis, abnormal
ZP:0021108	forebrain lacks all parts of type postoptic commissure, abnormal
ZP:0021109	diencephalon decreased amount, abnormal
ZP:0021110	anterior commissure decreased occurrence central nervous system projection neuron axonogenesis, abnormal
ZP:0021111	supraoptic tract decreased occurrence central nervous system projection neuron axonogenesis, abnormal
ZP:0021112	ventral thalamus increased amount, abnormal
ZP:0021113	GABAergic neuron ventral telencephalon decreased amount, abnormal
ZP:0021114	GABAergic neuron diencephalon decreased amount, abnormal
ZP:0021115	telencephalon increased amount, abnormal
ZP:0021116	GABAergic neuron nucleus of the tract of the postoptic commissure decreased amount, abnormal
ZP:0021117	astrocyte brain increased amount, abnormal
ZP:0021118	diencephalon absent, abnormal
ZP:0021119	epithalamus decreased distribution, abnormal
ZP:0021120	habenula decreased amount, abnormal
ZP:0021121	pharyngeal pouch 2 decreased object quality, abnormal
ZP:0021122	pharyngeal pouch 1 decreased object quality, abnormal
ZP:0021123	ventral habenular nucleus absent, abnormal
ZP:0021124	pharyngeal arch decreased process quality cartilage development, abnormal
ZP:0021125	dorsal habenular nucleus decreased distribution, abnormal
ZP:0021126	habenula decreased distribution, abnormal
ZP:0021127	dorsal habenular nucleus decreased amount, abnormal
ZP:0021128	dorsal region diencephalon absent, abnormal
ZP:0021129	Meckel's cartilage dislocated, abnormal
ZP:0021130	pharyngeal arch decreased occurrence Wnt protein secretion, abnormal
ZP:0021131	ceratohyal cartilage dislocated, abnormal
ZP:0021132	hematopoietic stem cell arrested mitotic G1 phase, abnormal
ZP:0021133	response to mechanical stimulus decreased occurrence, abnormal
ZP:0021134	hair cell has fewer parts of type cytoskeleton of presynaptic active zone synaptic vesicle hair cell, abnormal
ZP:0021135	neuromast decreased distribution, abnormal
ZP:0021136	hair cell decreased process quality presynaptic active zone organization, abnormal
ZP:0021137	basolateral plasma membrane neuromast hair cell decreased amount, abnormal
ZP:0021138	cytoskeleton of presynaptic active zone retinal cone cell decreased amount, abnormal
ZP:0021139	cytoskeleton of presynaptic active zone retinal cone cell decreased size, abnormal
ZP:0021140	ON-bipolar cell decreased process quality synaptic transmission, glutamatergic, abnormal
ZP:0021141	detection of mechanical stimulus involved in sensory perception of sound decreased occurrence, abnormal
ZP:0021142	retinal outer plexiform layer decreased process quality modulation of chemical synaptic transmission, abnormal
ZP:0021143	macula saccule has fewer parts of type hair cell synaptic vesicle hair cell, abnormal
ZP:0021144	response to auditory stimulus decreased occurrence, abnormal
ZP:0021145	retinal cone cell decreased process quality synaptic transmission, glutamatergic, abnormal
ZP:0021146	lateral crista has fewer parts of type hair cell ribbon synapse hair cell, abnormal
ZP:0021147	detection of light stimulus involved in sensory perception decreased process quality, abnormal
ZP:0021148	hair cell has fewer parts of type ribbon synapse synaptic vesicle hair cell, abnormal
ZP:0021149	retinal outer plexiform layer decreased amount, abnormal
ZP:0021150	retinal photoreceptor layer has fewer parts of type eye photoreceptor cell, abnormal
ZP:0021151	hair cell inner ear decreased distribution, abnormal
ZP:0021152	basolateral plasma membrane hair cell decreased amount, abnormal
ZP:0021153	proepicardial cluster decreased amount, abnormal
ZP:0021154	podocyte foot podocyte flattened, abnormal
ZP:0021155	somite mislocalised, abnormal
ZP:0021156	pronephric glomerulus decreased amount, abnormal
ZP:0021157	cell atrioventricular canal morphology, abnormal
ZP:0021158	determination of heart left/right asymmetry decreased occurrence, abnormal
ZP:0021159	ciliary basal body proepicardial cluster absent, abnormal
ZP:0021160	atrial myocardium separated from ventricular endocardium, abnormal
ZP:0021161	atrioventricular valve development decreased occurrence, abnormal
ZP:0021162	atrial myocardium decreased thickness, abnormal
ZP:0021163	atrioventricular canal development decreased process quality, abnormal
ZP:0021164	atrial myocardium separated from ventricular myocardium, abnormal
ZP:0021165	posterior lateral line primordium has fewer parts of type cell posterior lateral line primordium, abnormal
ZP:0021166	posterior pronephric duct morphology, abnormal
ZP:0021167	dorsal longitudinal anastomotic vessel constricted, abnormal
ZP:0021168	distal region pronephric tubule dilated, abnormal
ZP:0021169	cerebellar central artery constricted, abnormal
ZP:0021170	eye closure incomplete, abnormal
ZP:0021171	single ciliated epithelial cell pronephric duct decreased amount, abnormal
ZP:0021172	pronephric duct broken, abnormal
ZP:0021173	angiogenic sprout lateral dorsal aorta increased amount, abnormal
ZP:0021174	cloaca disorganized, abnormal
ZP:0021175	proximal region pronephric tubule dilated, abnormal
ZP:0021176	pronephric duct decreased process quality establishment or maintenance of cell polarity, abnormal
ZP:0021177	cloaca atretic, abnormal
ZP:0021178	embryo development increased duration, abnormal
ZP:0021179	deoxyribonucleic acid whole organism increased amount, abnormal
ZP:0021180	RNA catabolic process process quality, abnormal
ZP:0021181	apoptotic cell clearance disrupted, abnormal
ZP:0021182	heart increased length, abnormal
ZP:0021183	whole organism decreased distribution, abnormal
ZP:0021184	brain decreased distribution, abnormal
ZP:0021185	atrium absent, abnormal
ZP:0021186	cortical granule oocyte increased size, abnormal
ZP:0021188	oocyte growth arrested, abnormal
ZP:0021190	ovary increased process quality apoptotic process, abnormal
ZP:0021191	cortical granule oocyte decreased amount, abnormal
ZP:0021192	ventral fin fold decreased thickness, abnormal
ZP:0021193	presumptive ventral mesoderm decreased distribution, abnormal
ZP:0021194	somite distended, abnormal
ZP:0021195	ventral region presumptive ectoderm decreased distribution, abnormal
ZP:0021196	dorsal region mesoderm increased distribution, abnormal
ZP:0021197	central nervous system decreased amount, abnormal
ZP:0021198	oligodendrocyte decreased distribution, abnormal
ZP:0021199	central region retina mislocalised, abnormal
ZP:0021200	multi fate stem cell retina spatial pattern, abnormal
ZP:0021201	retinal bipolar neuron increased distribution, abnormal
ZP:0021202	nucleus retinal bipolar neuron absent, abnormal
ZP:0021203	central region retina spatial pattern, abnormal
ZP:0021204	midbrain mislocalised, abnormal
ZP:0021205	neuron hindbrain spatial pattern, abnormal
ZP:0021206	neuroblast retina spatial pattern, abnormal
ZP:0021207	cell ciliary marginal zone spatial pattern, abnormal
ZP:0021208	cell ciliary marginal zone increased distribution, abnormal
ZP:0021209	neuroblast retina increased amount, abnormal
ZP:0021210	multi fate stem cell retina increased amount, abnormal
ZP:0021211	regulation of gene silencing disrupted, abnormal
ZP:0021212	midbrain spatial pattern, abnormal
ZP:0021213	retinal bipolar neuron spatial pattern, abnormal
ZP:0021214	Kupffer's vesicle lacks all parts of type motile cilium Kupffer's vesicle, abnormal
ZP:0021215	forerunner cell group decreased distribution, abnormal
ZP:0021216	motile cilium pronephros decreased amount, abnormal
ZP:0021217	pronephric glomerulus absent, abnormal
ZP:0021221	skeletal muscle cell spatial pattern, abnormal
ZP:0021269	otic vesicle decreased area, abnormal
ZP:0021272	sagitta decreased area, abnormal
ZP:0021278	swim bladder increased amount, abnormal
ZP:0021301	male organism decreased life span, abnormal
ZP:0021305	glucose blood increased amount, abnormal
ZP:0021307	scale increased occurrence bone resorption, abnormal
ZP:0021312	blood island decreased distribution, abnormal
ZP:0021321	neutrophil chemotaxis decreased occurrence, abnormal
ZP:0021328	otic vesicle increased distribution, abnormal
ZP:0021329	solid lens vesicle absent, abnormal
ZP:0021337	otic placode increased distribution, abnormal
ZP:0021345	neurocranial trabecula decreased distribution, abnormal
ZP:0021346	male organism decreased amount, abnormal
ZP:0021358	otic vesicle process quality cilium assembly, abnormal
ZP:0021359	whole organism decreased occurrence cholesterol biosynthetic process, abnormal
ZP:0021360	whole organism decreased occurrence TOR signaling, abnormal
ZP:0021361	myelin sheath spinal cord decreased thickness, abnormal
ZP:0021363	segmental plate decreased amount, abnormal
ZP:0021389	sleep occurrence, abnormal
ZP:0021390	corpuscles of Stannius decreased distribution, abnormal
ZP:0021393	hematopoietic stem cell intermediate cell mass of mesoderm increased amount, abnormal
ZP:0021406	macrophage head increased amount, abnormal
ZP:0021437	female organism female fertility, abnormal
ZP:0021440	vertebral column curvature, abnormal
ZP:0021443	posterior lateral line primordium increased amount, abnormal
ZP:0021445	gill increased amount, abnormal
ZP:0021446	intestine increased amount, abnormal
ZP:0021478	neural crest cell aggregated, abnormal
ZP:0021479	endosome neural crest cell immature, abnormal
ZP:0021480	early endosome neural crest cell increased amount, abnormal
ZP:0021481	early endosome neural crest cell increased size, abnormal
ZP:0021482	early endosome neural crest cell aggregated, abnormal
ZP:0021483	late endosome neural crest cell decreased size, abnormal
ZP:0021484	late endosome neural crest cell decreased amount, abnormal
ZP:0021485	neural crest cell process quality endocytosis, abnormal
ZP:0021492	parasphenoid absent, abnormal
ZP:0021496	calcium-mediated signaling decreased process quality, abnormal
ZP:0021502	embryonic viscerocranium morphogenesis decreased occurrence, abnormal
ZP:0021503	cranial skeletal system development decreased occurrence, abnormal
ZP:0021514	liver spatial pattern, abnormal
ZP:0021517	oligodendrocyte decreased occurrence TOR signaling, abnormal
ZP:0021553	forebrain increased amount, abnormal
ZP:0021573	microtubule yolk irregular spatial pattern, abnormal
ZP:0021574	microtubule yolk disoriented, abnormal
ZP:0021580	visual perception increased process quality, abnormal
ZP:0021589	scale increased amount, abnormal
ZP:0021601	thigmotaxis increased occurrence, abnormal
ZP:0021629	DNA methylation increased occurrence, abnormal
ZP:0021632	digestive system increased amount, abnormal
ZP:0021651	glucose blood plasma increased amount, abnormal
ZP:0021659	intermediate cell mass of mesoderm increased amount, abnormal
ZP:0021663	myeloid cell increased occurrence cell population proliferation, abnormal
ZP:0021666	lymphocyte head kidney decreased amount, abnormal
ZP:0021671	myeloblast blood increased amount, abnormal
ZP:0021672	myeloblast head kidney increased amount, abnormal
ZP:0021674	granulocyte kidney increased amount, abnormal
ZP:0021715	vasculature increased amount, abnormal
ZP:0021716	female organism viability, abnormal
ZP:0021725	adipose tissue increased amount, abnormal
ZP:0021731	myocardium increased amount, abnormal
ZP:0021740	muscle decreased amount, abnormal
ZP:0021746	lateral dorsal aorta decreased amount, abnormal
ZP:0021757	anterior neural plate decreased amount, abnormal
ZP:0021768	spermatogonium decreased amount, abnormal
ZP:0021795	notochord decreased distribution, abnormal
ZP:0021800	swimming increased occurrence, abnormal
ZP:0021815	gill decreased amount, abnormal
ZP:0021835	brain female organism increased amount, abnormal
ZP:0021836	ovary female organism increased amount, abnormal
ZP:0021837	testis male organism increased amount, abnormal
ZP:0021838	testis male organism decreased amount, abnormal
ZP:0021841	optic tectum decreased amount, abnormal
ZP:0021843	retinal inner nuclear layer increased amount, abnormal
ZP:0021844	whole organism increased distribution, abnormal
ZP:0021845	DNA methylation process quality, abnormal
ZP:0021865	aggressive behavior decreased occurrence, abnormal
ZP:0021892	ventricular endocardium mislocalised, abnormal
ZP:0021893	ventricular myocardium mislocalised, abnormal
ZP:0021900	ovarian follicle stage III increased amount, abnormal
ZP:0021904	adult locomotory behavior process quality, abnormal
ZP:0021916	response to absence of light decreased process quality, abnormal
ZP:0021922	potassium(1+) whole organism decreased amount, abnormal
ZP:0021939	triglyceride whole organism increased amount, abnormal
ZP:0021941	lipid whole organism increased amount, abnormal
ZP:0021992	blood vessel trunk vasculature decreased amount, abnormal
ZP:0022023	presumptive atrium heart tube increased amount, abnormal
ZP:0022029	atrium increased amount, abnormal
ZP:0022049	photoreceptor outer segment retinal rod cell decreased amount, abnormal
ZP:0022067	digestive system decreased amount, abnormal
ZP:0022082	neurofibrosarcoma whole organism increased amount, abnormal
ZP:0022083	atrioventricular valve shape, abnormal
ZP:0022092	startle response increased occurrence, abnormal
ZP:0022094	habenula increased amount, abnormal
ZP:0022106	microglial cell optic tectum decreased amount, abnormal
ZP:0022139	cardiac ventricle decreased velocity cardiac conduction, abnormal
ZP:0022140	atrium decreased velocity cardiac conduction, abnormal
ZP:0022141	atrial myocardium increased duration action potential, abnormal
ZP:0022142	ventricular myocardium increased duration action potential, abnormal
ZP:0022176	hematopoietic multipotent progenitor cell intermediate cell mass of mesoderm increased amount, abnormal
ZP:0022179	pharyngeal arch 5 has fewer parts of type chondroblast, abnormal
ZP:0022180	pharyngeal arch 6 has fewer parts of type chondroblast, abnormal
ZP:0022183	retinal pigmented epithelium decreased amount, abnormal
ZP:0022190	sperm cellular motility, abnormal
ZP:0022206	whole organism has fewer parts of type swim bladder, abnormal
ZP:0022207	ceratohyal bone mislocalised, abnormal
ZP:0022233	muscle pioneer decreased distribution, abnormal
ZP:0022272	exocrine pancreas spatial pattern, abnormal
ZP:0022282	intramembranous ossification decreased process quality, abnormal
ZP:0022283	perichondral ossification decreased process quality, abnormal
ZP:0022284	opercle decreased process quality intramembranous ossification, abnormal
ZP:0022285	branchiostegal ray decreased process quality intramembranous ossification, abnormal
ZP:0022286	parasphenoid decreased process quality intramembranous ossification, abnormal
ZP:0022287	ceratohyal bone decreased process quality perichondral ossification, abnormal
ZP:0022288	hyomandibula decreased process quality perichondral ossification, abnormal
ZP:0022289	ceratobranchial 5 bone decreased process quality perichondral ossification, abnormal
ZP:0022290	osteoblast differentiation delayed, abnormal
ZP:0022291	opercle decreased distribution, abnormal
ZP:0022292	parasphenoid decreased distribution, abnormal
ZP:0022293	osteoblast decreased distribution, abnormal
ZP:0022294	osteoblast absent, abnormal
ZP:0022297	developmental growth arrested, abnormal
ZP:0022318	integument increased amount, abnormal
ZP:0022319	intestinal epithelium increased amount, abnormal
ZP:0022321	sleep increased occurrence, abnormal
ZP:0022323	swimming behavior occurrence, abnormal
ZP:0022324	response to light stimulus increased behavioural activity, abnormal
ZP:0022325	sleep delayed, abnormal
ZP:0022331	brain increased distribution, abnormal
ZP:0022352	segmental plate absent, abnormal
ZP:0022356	somite increased distribution, abnormal
ZP:0022357	paraxial mesoderm increased amount, abnormal
ZP:0022359	posterior region trunk increased distribution, abnormal
ZP:0022360	posterior region trunk mislocalised, abnormal
ZP:0022361	paraxial mesoderm increased distribution, abnormal
ZP:0022362	segmental plate increased distribution, abnormal
ZP:0022363	slow muscle myoblast increased amount, abnormal
ZP:0022381	optic stalk increased amount, abnormal
ZP:0022394	podocyte decreased amount, abnormal
ZP:0022395	pronephric tubule increased amount, abnormal
ZP:0022416	myotome mislocalised, abnormal
ZP:0022434	hematopoietic multipotent progenitor cell increased occurrence apoptotic process, abnormal
ZP:0022439	macrophage chemotaxis decreased occurrence, abnormal
ZP:0022440	macrophage accumulation apoptotic body lysosome macrophage, abnormal
ZP:0022464	pancreatic bud position, abnormal
ZP:0022511	extension shape, abnormal
ZP:0022512	spinal cord decreased distribution, abnormal
ZP:0022534	endoderm decreased distribution, abnormal
ZP:0022548	fin increased amount, abnormal
ZP:0022572	regenerating tissue increased occurrence cell population proliferation, abnormal
ZP:0022579	macrophage trunk decreased amount, abnormal
ZP:0022581	granulocyte monocyte progenitor cell decreased amount, abnormal
ZP:0022641	stereocilium bundle neuromast hair cell decreased amount, abnormal
ZP:0022649	proximal convoluted tubule decreased area, abnormal
ZP:0022661	multi-ciliated epithelial cell pronephric tubule absent, abnormal
ZP:0022691	segmental plate mislocalised, abnormal
ZP:0022718	tail bud immature, abnormal
ZP:0022719	epithelial to mesenchymal transition delayed, abnormal
ZP:0022720	feeding behavior process quality, abnormal
ZP:0022731	margin decreased distribution, abnormal
ZP:0022747	whole organism has fewer parts of type dorsal region melanocyte, abnormal
ZP:0022796	epidermis disrupted cell adhesion, abnormal
ZP:0022800	cardiac ventricle truncated, abnormal
ZP:0022801	cardiac muscle fiber development disrupted, abnormal
ZP:0022802	cardiac muscle cell vacuolated, abnormal
ZP:0022803	autophagosome cardiac muscle cell present, abnormal
ZP:0022804	Z disc heart disorganized, abnormal
ZP:0022841	spermatogenesis decreased occurrence, abnormal
ZP:0022842	hypophysis absent, abnormal
ZP:0022845	blood cell morphology, abnormal
ZP:0022847	lens reflectivity, abnormal
ZP:0022867	cardiac muscle cell increased occurrence cell population proliferation, abnormal
ZP:0022876	eye photoreceptor cell mislocalised, abnormal
ZP:0022893	axon primary motor neuron branchiness, abnormal
ZP:0022920	neoplasm brain increased amount, abnormal
ZP:0022969	brain process quality vasculature development, abnormal
ZP:0022972	microglial cell hindbrain increased amount, abnormal
ZP:0022974	retina mislocalised, abnormal
ZP:0022977	striated muscle cell trunk musculature decreased amount, abnormal
ZP:0022979	ceratohyal cartilage curved ventral, abnormal
ZP:0022980	basihyal cartilage curved ventral, abnormal
ZP:0022981	ceratobranchial 1 cartilage absent, abnormal
ZP:0022983	cardiac muscle cell decreased occurrence cell population proliferation, abnormal
ZP:0023050	endothelial cell dorsal aorta absent, abnormal
ZP:0023061	cardiac ventricle decreased distribution, abnormal
ZP:0100002	choroid plexus increased distribution, abnormal
ZP:0100009	whole organism quality, abnormal
ZP:0100010	anatomical system quality, abnormal
ZP:0100013	cartilage element pharyngeal arch cartilage mislocalised, abnormal
ZP:0100017	pronephric duct decreased occurrence autophagy, abnormal
ZP:0100021	vent malformed, abnormal
ZP:0100027	intermediate cell mass of mesoderm increased occurrence cell population proliferation, abnormal
ZP:0100031	T cell thymus increased amount, abnormal
ZP:0100037	optic vesicle decreased amount, abnormal
ZP:0100038	anterior neural plate decreased distribution, abnormal
ZP:0100039	posterior neural plate increased distribution, abnormal
ZP:0100040	presumptive telencephalon decreased distribution, abnormal
ZP:0100042	ventral wall of dorsal aorta has fewer parts of type hematopoietic multipotent progenitor cell, abnormal
ZP:0100043	ventral wall of dorsal aorta has extra parts of type hematopoietic multipotent progenitor cell, abnormal
ZP:0100044	hematopoietic multipotent progenitor cell ventral wall of dorsal aorta spatial pattern, abnormal
ZP:0100045	neutrophil kidney decreased amount, abnormal
ZP:0100047	cilium inner ear morphology, abnormal
ZP:0100048	photoreceptor connecting cilium photoreceptor cell decreased amount, abnormal
ZP:0100053	central region retina increased amount, abnormal
ZP:0100058	Kupffer's vesicle decreased fluid flow, abnormal
ZP:0100060	cell body Muller cell displaced, abnormal
ZP:0100062	primordial germ cell aggregated, abnormal
ZP:0100063	calcium carbonate caudal fin increased amount, abnormal
ZP:0100065	axon retinal neural layer truncated, abnormal
ZP:0100066	axon retinal neural layer decreased branchiness, abnormal
ZP:0100067	heparan sulfate 6-O-sulfotransferase activity process quality, abnormal
ZP:0100071	otolith development decreased process quality, abnormal
ZP:0100075	hypochord spatial pattern, abnormal
ZP:0100076	intermediate mesoderm spatial pattern, abnormal
ZP:0100077	angioblastic mesenchymal cell spatial pattern, abnormal
ZP:0100078	pronephric proximal convoluted tubule has extra parts of type cytoplasm vesicle pronephric proximal convoluted tubule, abnormal
ZP:0100082	vesicle pronephric proximal convoluted tubule increased variability of size, abnormal
ZP:0100083	cell pronephric proximal convoluted tubule botryoidal, abnormal
ZP:0100084	cell pronephric proximal straight tubule botryoidal, abnormal
ZP:0100085	pronephros development decreased process quality, abnormal
ZP:0100086	pronephric podocyte increased amount, abnormal
ZP:0100087	pronephric capsular space increased width, abnormal
ZP:0100088	capillary loop nephron increased amount, abnormal
ZP:0100089	capillary loop nephron dilated, abnormal
ZP:0100095	trunk neural crest cell migration arrested, abnormal
ZP:0100096	neural crest separated from dorsal aorta, abnormal
ZP:0100097	midbrain lacks all parts of type lymph vessel endothelial cell, abnormal
ZP:0100099	dorsal region spinal cord increased amount, abnormal
ZP:0100100	ventral region spinal cord increased amount, abnormal
ZP:0100101	ventricular zone hindbrain increased amount, abnormal
ZP:0100102	ventricular zone forebrain increased amount, abnormal
ZP:0100103	ventricular zone midbrain increased amount, abnormal
ZP:0100104	neuronal stem cell increased amount, abnormal
ZP:0100105	actin-based cell projection peridermal cell increased length, abnormal
ZP:0100106	actin-based cell projection peridermal cell decreased length, abnormal
ZP:0100107	posterior lateral line primordium spatial pattern, abnormal
ZP:0100113	post-vent vasculature increased amount, abnormal
ZP:0100115	paired fin morphology, abnormal
ZP:0100116	paired fin absent, abnormal
ZP:0100117	paired fin decreased size, abnormal
ZP:0100118	thyroid follicle spatial pattern, abnormal
ZP:0100119	aortic arch dysplastic, abnormal
ZP:0100120	thyroid follicle decreased diameter, abnormal
ZP:0100121	thyroid primordium increased amount, abnormal
ZP:0100122	protein localization to plasma membrane disrupted, abnormal
ZP:0100123	apical side peridermal cell increased amount, abnormal
ZP:0100124	apical side peridermal cell decreased amount, abnormal
ZP:0100126	actin-based cell projection peridermal cell increased amount, abnormal
ZP:0100127	actin-based cell projection peridermal cell decreased amount, abnormal
ZP:0100128	endothelial cell decreased distribution, abnormal
ZP:0100129	skeletal muscle decreased occurrence skeletal myofibril assembly, abnormal
ZP:0100130	skeletal muscle myofibril skeletal muscle cell decreased amount, abnormal
ZP:0100131	myotome has fewer parts of type skeletal muscle cell skeletal muscle myofibril skeletal muscle cell, abnormal
ZP:0100137	muscle tendon junction myotome spatial pattern, abnormal
ZP:0100138	muscle tendon junction myotome increased amount, abnormal
ZP:0100139	muscle tendon junction fast muscle cell increased amount, abnormal
ZP:0100140	slow muscle cell degenerate, abnormal
ZP:0100141	slow muscle cell detached from slow muscle cell, abnormal
ZP:0100142	muscle tendon junction myotome decreased amount, abnormal
ZP:0100143	olfactory pit arrested epithelial cilium movement involved in extracellular fluid movement, abnormal
ZP:0100146	rhombomere 2 mislocalised, abnormal
ZP:0100147	rhombomere 4 mislocalised, abnormal
ZP:0100148	erythroblast premature mitophagy, abnormal
ZP:0100149	erythroblast increased occurrence mitophagy, abnormal
ZP:0100151	mitochondrion erythroblast decreased amount, abnormal
ZP:0100152	erythroblast has extra parts of type lysosome mitochondrion erythroblast, abnormal
ZP:0100154	nucleate erythrocyte decreased occurrence hemoglobin biosynthetic process, abnormal
ZP:0100158	otolith amount, abnormal
ZP:0100160	branchiomotor neuron rhombomere 4 mislocalised anteriorly, abnormal
ZP:0100165	myofibril muscle patchy, abnormal
ZP:0100166	trunk musculature increased duration relaxation of muscle, abnormal
ZP:0100167	twitch skeletal muscle contraction increased duration, abnormal
ZP:0100168	twitch skeletal muscle contraction decreased intensity, abnormal
ZP:0100169	sarcomere trunk musculature increased diameter, abnormal
ZP:0100170	sarcomere trunk musculature decreased length, abnormal
ZP:0100171	tonic skeletal muscle contraction decreased intensity, abnormal
ZP:0100172	skeletal muscle adaptation disrupted, abnormal
ZP:0100173	sarcomere trunk musculature decreased diameter, abnormal
ZP:0100174	sarcomere myotome malformed, abnormal
ZP:0100175	skeletal muscle cell myotome spatial pattern, abnormal
ZP:0100176	whole organism process quality respiratory gaseous exchange by respiratory system, abnormal
ZP:0100178	mitochondrion fast muscle cell swollen, abnormal
ZP:0100179	mitochondrial matrix muscle decreased mass density, abnormal
ZP:0100181	skeletal muscle detached from myofibril muscle tendon junction skeletal muscle, abnormal
ZP:0100183	mitochondrial crista muscle decreased amount, abnormal
ZP:0100184	skeletal muscle cell damaged, abnormal
ZP:0100199	skeletal muscle cell increased amount, abnormal
ZP:0100201	chromosome, telomeric region cell decreased length, abnormal
ZP:0100205	retina increased occurrence Notch signaling pathway, abnormal
ZP:0100209	retinal outer nuclear layer increased amount, abnormal
ZP:0100218	spinal cord spatial pattern, abnormal
ZP:0100219	posterior cardinal vein increased amount, abnormal
ZP:0100220	primordial hindbrain channel hypoplastic, abnormal
ZP:0100221	optic cup decreased amount, abnormal
ZP:0100222	basement membrane notochord absent, abnormal
ZP:0100223	posterior region neuroectoderm increased distribution, abnormal
ZP:0100229	sodium ion export across plasma membrane increased process quality, abnormal
ZP:0100230	sodium ion import across plasma membrane increased process quality, abnormal
ZP:0100231	integument decreased occurrence proton export across plasma membrane, abnormal
ZP:0100232	proton export across plasma membrane decreased occurrence, abnormal
ZP:0100234	vertebral artery absent, abnormal
ZP:0100246	determination of digestive tract left/right asymmetry decreased occurrence, abnormal
ZP:0100247	determination of liver left/right asymmetry decreased occurrence, abnormal
ZP:0100248	digestive system spatial pattern, abnormal
ZP:0100250	myofibril slow muscle cell increased length, abnormal
ZP:0100251	myofibril slow muscle cell decreased width, abnormal
ZP:0100252	anterior region whole organism decreased amount, abnormal
ZP:0100253	neural crest increased occurrence apoptotic process, abnormal
ZP:0100254	neural crest decreased occurrence cell population proliferation, abnormal
ZP:0100255	neural crest cell development decreased occurrence, abnormal
ZP:0100256	neural crest decreased amount, abnormal
ZP:0100258	pronephric distal early tubule increased size, abnormal
ZP:0100259	pronephric distal early tubule increased distribution, abnormal
ZP:0100262	telencephalon increased occurrence apoptotic process, abnormal
ZP:0100264	distal region pronephric tubule decreased distribution, abnormal
ZP:0100265	distal region pronephric tubule decreased amount, abnormal
ZP:0100266	pronephric tubule increased distance cell cell pronephric tubule, abnormal
ZP:0100267	pronephric tubule has fewer parts of type proximal region cell, abnormal
ZP:0100271	pronephric tubule decreased amount, abnormal
ZP:0100272	lactate whole organism decreased amount, abnormal
ZP:0100273	nucleate erythrocyte heart absent, abnormal
ZP:0100276	cell cortex oocyte stage I absent, abnormal
ZP:0100277	oocyte stage I decreased occurrence organelle disassembly, abnormal
ZP:0100278	cortisol whole organism increased amount, abnormal
ZP:0100282	anatomical region third ventricle absent, abnormal
ZP:0100283	otic vesicle spatial pattern, abnormal
ZP:0100284	otic vesicle increased amount, abnormal
ZP:0100285	basement membrane retinal pigmented epithelium aplastic, abnormal
ZP:0100286	pharyngeal arch 3-7 aplastic/hypoplastic, abnormal
ZP:0100287	skeletal muscle myofibril fast muscle cell absent, abnormal
ZP:0100288	vacuole slow muscle cell increased amount, abnormal
ZP:0100289	vacuole fast muscle cell increased amount, abnormal
ZP:0100290	sarcomere fast muscle cell absent, abnormal
ZP:0100291	dorsal longitudinal vein morphology, abnormal
ZP:0100292	dorsal longitudinal vein increased amount, abnormal
ZP:0100293	mesencephalic vein absent, abnormal
ZP:0100296	ciliary shaft lateral crista spatial pattern, abnormal
ZP:0100297	ciliary shaft lateral crista increased amount, abnormal
ZP:0100298	lateral crista has extra parts of type ciliary shaft intraciliary transport particle lateral crista, abnormal
ZP:0100299	ciliary shaft olfactory epithelium spatial pattern, abnormal
ZP:0100300	ciliary shaft olfactory epithelium increased amount, abnormal
ZP:0100301	posterior region whole organism absent, abnormal
ZP:0100302	neuroectoderm decreased amount, abnormal
ZP:0100305	myocardium increased distribution, abnormal
ZP:0100307	presumptive endoderm increased amount, abnormal
ZP:0100308	presumptive ectoderm decreased distribution, abnormal
ZP:0100309	presumptive ectoderm decreased amount, abnormal
ZP:0100313	primordial germ cell decreased occurrence establishment of cell polarity, abnormal
ZP:0100314	primordial germ cell process quality regulation of intracellular pH, abnormal
ZP:0100319	liver increased occurrence cell death, abnormal
ZP:0100321	retinal neural layer disrupted axon guidance, abnormal
ZP:0100322	axon retinal neural layer mislocalised, abnormal
ZP:0100328	anatomical region myoseptum increased distribution, abnormal
ZP:0100329	posterior lateral line primordium has extra parts of type filopodium posterior lateral line primordium, abnormal
ZP:0100330	secondary motor neuron amount, abnormal
ZP:0100332	sperm increased cellular motility, abnormal
ZP:0100333	sperm increased velocity, abnormal
ZP:0100338	neuromast hair cell decreased process quality endocytosis, abnormal
ZP:0100339	cuticular plate neuromast hair cell mislocalised, abnormal
ZP:0100340	neuromast hair cell decreased process quality intraciliary transport, abnormal
ZP:0100341	neuromast hair cell decreased process quality cilium assembly, abnormal
ZP:0100342	kinociliary basal body neuromast hair cell spatial pattern, abnormal
ZP:0100343	neuromast hair cell morphogenesis decreased process quality, abnormal
ZP:0100346	Kupffer's vesicle spatial pattern, abnormal
ZP:0100352	pronephric tubule decreased occurrence cell population proliferation, abnormal
ZP:0100354	pronephros decreased amount, abnormal
ZP:0100356	presumptive ventral mesoderm decreased amount, abnormal
ZP:0100357	utricle arrested otolith formation, abnormal
ZP:0100361	utricle lacks all parts of type lapillus, abnormal
ZP:0100366	utricle delayed otolith formation, abnormal
ZP:0100368	utricle has fewer parts of type lapillus, abnormal
ZP:0100371	blood accumulation pharyngeal arch 3-7, abnormal
ZP:0100374	margin increased distribution, abnormal
ZP:0100376	whole organism dorsalized, abnormal
ZP:0100380	inflammatory response to antigenic stimulus decreased efficacy, abnormal
ZP:0100382	whole organism lacks parts or has fewer parts of type IgM immunoglobulin complex blood, abnormal
ZP:0100383	whole organism lacks parts or has fewer parts of type thymus, abnormal
ZP:0100384	mature B cell absent, abnormal
ZP:0100385	lymphocyte absent, abnormal
ZP:0100388	gut increased occurrence cell population proliferation, abnormal
ZP:0100389	neutrophil gut increased amount, abnormal
ZP:0100390	intestinal motility process quality, abnormal
ZP:0100391	glutathione disulfide anatomical structure increased amount, abnormal
ZP:0100392	glutathione oxidoreductase activity increased occurrence, abnormal
ZP:0100393	glutathione disulfide anatomical structure decreased amount, abnormal
ZP:0100394	glutathione oxidoreductase activity decreased occurrence, abnormal
ZP:0100397	gonad primordium decreased size, abnormal
ZP:0100399	primary motor neuron disrupted axonogenesis, abnormal
ZP:0100401	axon terminus primary motor neuron swollen, abnormal
ZP:0100402	spinal cord lacks parts or has fewer parts of type postero-ventral region axon reticulospinal neuron, abnormal
ZP:0100403	spinal cord lacks parts or has fewer parts of type posterior region axon reticulospinal neuron, abnormal
ZP:0100404	spinal cord lacks parts or has fewer parts of type ventral region axon reticulospinal neuron, abnormal
ZP:0100405	axon reticulospinal neuron decreased perimeter, abnormal
ZP:0100406	epithalamus absent, abnormal
ZP:0100407	habenula absent, abnormal
ZP:0100408	optic furrow closure incomplete, abnormal
ZP:0100410	central nervous system increased amount, abnormal
ZP:0100412	cardiac conduction rate, abnormal
ZP:0100413	cell-cell adhesion decreased process quality, abnormal
ZP:0100414	anterior region neuroectoderm decreased amount, abnormal
ZP:0100415	posterior region neuroectoderm decreased distribution, abnormal
ZP:0100416	cranial nerve VIII process quality axon guidance, abnormal
ZP:0100422	pupil irregularly shaped, abnormal
ZP:0100424	nucleus brain increased amount, abnormal
ZP:0100425	nucleus optic vesicle increased amount, abnormal
ZP:0100426	sodium ion import across plasma membrane increased occurrence, abnormal
ZP:0100428	caudal hematopoietic tissue increased amount, abnormal
ZP:0100429	glutathione anatomical structure decreased amount, abnormal
ZP:0100431	neuromuscular junction pectoral fin nerve decreased amount, abnormal
ZP:0100432	axon terminus pectoral fin nerve decreased amount, abnormal
ZP:0100433	pectoral fin decreased mobility, abnormal
ZP:0100434	non neural ectoderm increased amount, abnormal
ZP:0100435	endocardium unfused from endocardium, abnormal
ZP:0100438	endothelial cell absent, abnormal
ZP:0100439	cerebellum hemorrhagic, abnormal
ZP:0100443	ventral wall of dorsal aorta lacks parts or has fewer parts of type hematopoietic multipotent progenitor cell, abnormal
ZP:0100448	posterior region midbrain increased amount, abnormal
ZP:0100449	axial hypoblast absent, abnormal
ZP:0100465	hematopoietic stem cell caudal hematopoietic tissue decreased amount, abnormal
ZP:0100470	slow muscle cell trunk disorganized, abnormal
ZP:0100471	synaptic transmission, glycinergic process quality, abnormal
ZP:0100473	filopodium intersegmental vessel decreased amount, abnormal
ZP:0100478	antero-dorsal region whole organism absent, abnormal
ZP:0100479	postero-dorsal region whole organism absent, abnormal
ZP:0100480	posterior region neuroectoderm absent, abnormal
ZP:0100481	lateral region shield absent, abnormal
ZP:0100482	midbrain hindbrain boundary neural rod absent, abnormal
ZP:0100484	anatomical region Kupffer's vesicle absent, abnormal
ZP:0100485	skeletal muscle myofibril somite disorganized, abnormal
ZP:0100486	water transport decreased process quality, abnormal
ZP:0100487	carbon dioxide transport decreased process quality, abnormal
ZP:0100488	oxygen transport decreased process quality, abnormal
ZP:0100489	pectoral artery decreased amount, abnormal
ZP:0100491	feeding behavior decreased occurrence, abnormal
ZP:0100494	site of DNA damage whole organism increased amount, abnormal
ZP:0100495	response to stress process quality, abnormal
ZP:0100498	motor neuron disrupted axon extension, abnormal
ZP:0100499	superior ocular sulcus morphology, abnormal
ZP:0100500	superior ocular sulcus closure incomplete, abnormal
ZP:0100502	heart functionality, abnormal
ZP:0100503	dorsal aorta mislocalised, abnormal
ZP:0100504	basal region peridermal cell decreased amount, abnormal
ZP:0100505	peridermal cell has fewer parts of type basal region filamentous actin peridermal cell, abnormal
ZP:0100506	aggressive behavior increased occurrence, abnormal
ZP:0100508	pharyngeal arch 3-7 increased amount, abnormal
ZP:0100510	basement membrane epidermis absent, abnormal
ZP:0100511	basement membrane epidermis decreased thickness, abnormal
ZP:0100513	pancreatic B cell decreased occurrence cell population proliferation, abnormal
ZP:0100514	whole organism decreased process quality glucose homeostasis, abnormal
ZP:0100515	striated muscle myosin thick filament heart disorganized, abnormal
ZP:0100516	striated muscle thin filament heart disorganized, abnormal
ZP:0100517	striated muscle thin filament heart decreased amount, abnormal
ZP:0100518	muscle tendon junction muscle absent, abnormal
ZP:0100519	Z disc heart structure, abnormal
ZP:0100520	Z disc heart absent, abnormal
ZP:0100522	cardiac ventricle absent, abnormal
ZP:0100527	trunk vasculature increased amount, abnormal
ZP:0100528	cell-cell junction dorsal aorta structure, abnormal
ZP:0100529	cell-cell junction dorsal aorta decreased length, abnormal
ZP:0100530	cell-cell junction dorsal aorta hypoplastic, abnormal
ZP:0100531	dorsal region eye absent, abnormal
ZP:0100532	dorsal region optic cup absent, abnormal
ZP:0100534	facial nerve motor nucleus arrested motor neuron migration, abnormal
ZP:0100535	motor neuron facial nerve motor nucleus increased amount, abnormal
ZP:0100536	facial nerve motor nucleus displaced to motor neuron rhombomere 4, abnormal
ZP:0100537	facial nerve motor nucleus decreased occurrence motor neuron migration, abnormal
ZP:0100538	facial nerve motor nucleus displaced to motor neuron rhombomere 5, abnormal
ZP:0100539	rhombomere 6 has fewer parts of type motor neuron facial nerve motor nucleus, abnormal
ZP:0100541	chondrocyte ceratohyal cartilage circular, abnormal
ZP:0100542	symplectic decreased volume, abnormal
ZP:0100543	Meckel's cartilage condensed, abnormal
ZP:0100544	Meckel's cartilage perpendicular to anterior-posterior axis whole organism, abnormal
ZP:0100545	ceratohyal cartilage decreased volume, abnormal
ZP:0100546	ceratohyal cartilage condensed, abnormal
ZP:0100547	ceratohyal cartilage perpendicular to anterior-posterior axis whole organism, abnormal
ZP:0100548	chondrocyte mandibular arch skeleton morphology, abnormal
ZP:0100549	chondrocyte mandibular arch skeleton position, abnormal
ZP:0100567	anatomical margin caudal fin increased distribution, abnormal
ZP:0100573	caudal fin actinotrichium increased length, abnormal
ZP:0100577	cholesterol blood plasma increased amount, abnormal
ZP:0100580	lipid vasculature increased amount, abnormal
ZP:0100589	nucleus intestinal epithelial cell pleomorphic, abnormal
ZP:0100590	microvillus intestinal bulb decreased length, abnormal
ZP:0100591	microvillus mid intestine decreased length, abnormal
ZP:0100592	goblet cell mid intestine immature, abnormal
ZP:0100593	enteroendocrine cell decreased amount, abnormal
ZP:0100594	enterocyte cuboid, abnormal
ZP:0100595	microvillus intestinal bulb decreased amount, abnormal
ZP:0100596	microvillus mid intestine decreased amount, abnormal
ZP:0100599	intestinal bulb increased process quality cell population proliferation, abnormal
ZP:0100600	mid intestine increased process quality cell population proliferation, abnormal
ZP:0100601	enterocyte intestinal bulb decreased height, abnormal
ZP:0100602	enterocyte mid intestine decreased height, abnormal
ZP:0100603	regenerating fin increased occurrence apoptotic process, abnormal
ZP:0100616	spinal cord neural tube decreased distribution, abnormal
ZP:0100617	glial cell morphology, abnormal
ZP:0100618	glial cell disorganized, abnormal
ZP:0100630	lateral plate mesoderm decreased occurrence tissue migration, abnormal
ZP:0100631	lateral plate mesoderm decreased process quality tissue migration, abnormal
ZP:0100633	slow muscle cell decreased process quality skeletal myofibril assembly, abnormal
ZP:0100636	microtubule yolk structure, abnormal
ZP:0100637	epiblast decreased amount, abnormal
ZP:0100638	yolk process quality microtubule cytoskeleton organization, abnormal
ZP:0100639	yolk process quality microtubule bundle formation, abnormal
ZP:0100640	microtubule yolk area density, abnormal
ZP:0100641	microtubule yolk syncytial layer area density, abnormal
ZP:0100642	yolk process quality microtubule polymerization, abnormal
ZP:0100643	pregnenolone whole organism increased amount, abnormal
ZP:0100644	progesterone whole organism decreased amount, abnormal
ZP:0100645	melanophore stripe decreased size, abnormal
ZP:0100648	glycolytic process decreased process quality, abnormal
ZP:0100649	heart has extra parts of type anatomical region muscle, abnormal
ZP:0100650	atrioventricular canal morphogenesis decreased occurrence, abnormal
ZP:0100651	sinus venosus absent, abnormal
ZP:0100653	axis spatial pattern, abnormal
ZP:0100654	axis decreased distribution, abnormal
ZP:0100655	axis decreased amount, abnormal
ZP:0100659	presumptive atrium heart tube spatial pattern, abnormal
ZP:0100660	presumptive atrium heart tube increased distribution, abnormal
ZP:0100661	pronephric proximal convoluted tubule increased amount, abnormal
ZP:0100669	basement membrane caudal fin disorganized, abnormal
ZP:0100670	basement membrane caudal fin distributed, abnormal
ZP:0100679	dorsal aorta increased distribution, abnormal
ZP:0100682	sclerotome decreased amount, abnormal
ZP:0100686	chondrocyte palate irregular spatial pattern, abnormal
ZP:0100687	palate increased width, abnormal
ZP:0100689	chondrocyte interhyal cartilage decreased amount, abnormal
ZP:0100690	retroarticular malformed, abnormal
ZP:0100691	retroarticular shortened, abnormal
ZP:0100692	quadrate-anguloarticular joint morphology, abnormal
ZP:0100696	centrum delayed ossification, abnormal
ZP:0100697	collagen type I trimer bone tissue physical quality, abnormal
ZP:0100698	endoplasmic reticulum lumen osteoblast increased size, abnormal
ZP:0100699	rib deformed, abnormal
ZP:0100700	pelvic fin atrophied, abnormal
ZP:0100701	pelvic fin kinked, abnormal
ZP:0100702	neural spine sloped, abnormal
ZP:0100704	optic cup decreased occurrence cell population proliferation, abnormal
ZP:0100705	centrum increased process quality bone mineralization, abnormal
ZP:0100706	hemal arch increased process quality bone mineralization, abnormal
ZP:0100707	neural arch increased process quality bone mineralization, abnormal
ZP:0100708	centrum increased mass density, abnormal
ZP:0100709	hemal arch increased mass density, abnormal
ZP:0100710	neural arch decreased volume, abnormal
ZP:0100711	neural arch increased mass density, abnormal
ZP:0100712	primordial germ cell absent, abnormal
ZP:0100713	longitudinal sarcoplasmic reticulum skeletal muscle cell increased amount, abnormal
ZP:0100714	T-tubule skeletal muscle cell decreased amount, abnormal
ZP:0100718	forebrain spatial pattern, abnormal
ZP:0100723	pretectum decreased amount, abnormal
ZP:0100726	oligodendrocyte decreased occurrence MAPK cascade, abnormal
ZP:0100728	heart trabecula formation decreased occurrence, abnormal
ZP:0100732	triglyceride whole organism decreased amount, abnormal
ZP:0100733	lactate whole organism increased amount, abnormal
ZP:0100736	sarcomere cardiac muscle cell disassembled, abnormal
ZP:0100739	cardiac muscle cell decreased length, abnormal
ZP:0100740	rhombomere 5 has extra parts of type facial nerve motor nucleus neuron projection motor neuron, abnormal
ZP:0100741	rhombomere 4 has extra parts of type facial nerve motor nucleus neuron projection motor neuron, abnormal
ZP:0100742	response to absence of light decreased behavioural activity, abnormal
ZP:0100743	response to absence of light behavioral quality of a process, abnormal
ZP:0100744	regulation of action potential firing pattern disrupted, abnormal
ZP:0100745	optic tectum spatial pattern, abnormal
ZP:0100751	vasculature liver decreased branchiness, abnormal
ZP:0100759	integument decreased process quality proton export across plasma membrane, abnormal
ZP:0100774	pyridoxamine 5'-phosphate whole organism decreased amount, abnormal
ZP:0100776	whole organism decreased fecundity, abnormal
ZP:0100777	lipid caudal vein increased amount, abnormal
ZP:0100780	male organism increased weight, abnormal
ZP:0100782	female organism increased weight, abnormal
ZP:0100789	glutathione whole organism decreased amount, abnormal
ZP:0100796	visceral fat increased amount, abnormal
ZP:0100797	triglyceride blood plasma increased amount, abnormal
ZP:0100799	rhombomere 1 decreased amount, abnormal
ZP:0100800	central nervous system increased occurrence cell death, abnormal
ZP:0100809	glucose blood decreased amount, abnormal
ZP:0100822	male organism decreased weight, abnormal
ZP:0100823	oogenesis arrested, abnormal
ZP:0100824	oocyte stage III decreased amount, abnormal
ZP:0100825	oocyte stage I increased amount, abnormal
ZP:0100826	oocyte stage IV decreased amount, abnormal
ZP:0100829	whole organism increased mass, abnormal
ZP:0100838	noradrenergic neuron locus coeruleus decreased amount, abnormal
ZP:0100841	swim bladder immature, abnormal
ZP:0100848	visual perception decreased sensitivity of a process response to light stimulus, abnormal
ZP:0100849	retinal inner nuclear layer has fewer parts of type dopaminergic neuron, abnormal
ZP:0100863	superoxide dismutase activity decreased efficacy, abnormal
ZP:0100869	regenerating fin decreased area, abnormal
ZP:0100872	reactive oxygen species whole organism increased amount, abnormal
ZP:0100880	learning or memory disrupted, abnormal
ZP:0100903	cholesterol liver increased amount, abnormal
ZP:0100911	presumptive mesoderm increased distribution, abnormal
ZP:0100912	endodermal cell increased amount, abnormal
ZP:0100913	endoderm formation decreased occurrence, abnormal
ZP:0100914	mesoderm formation decreased occurrence, abnormal
ZP:0100916	presumptive rhombomere 3 decreased distribution, abnormal
ZP:0100917	forebrain neural plate increased distribution, abnormal
ZP:0100918	midbrain hindbrain boundary neural plate decreased distribution, abnormal
ZP:0100919	rhombomere 5 decreased distribution, abnormal
ZP:0100920	rhombomere 3 decreased distribution, abnormal
ZP:0100921	midbrain hindbrain boundary neural keel absent, abnormal
ZP:0100923	posterior region hindbrain spatial pattern, abnormal
ZP:0100924	posterior region hindbrain increased distribution, abnormal
ZP:0100925	posterior region mesoderm spatial pattern, abnormal
ZP:0100926	posterior region mesoderm increased distribution, abnormal
ZP:0100927	anterior margin paraxial mesoderm spatial pattern, abnormal
ZP:0100928	anterior margin paraxial mesoderm decreased distribution, abnormal
ZP:0100929	anterior margin spinal cord neural tube spatial pattern, abnormal
ZP:0100930	anterior margin spinal cord neural tube decreased distribution, abnormal
ZP:0100931	tail bud decreased amount, abnormal
ZP:0100932	paraxial mesoderm decreased distribution, abnormal
ZP:0100933	otic epithelium decreased distribution, abnormal
ZP:0100935	presumptive rhombomere 5 decreased amount, abnormal
ZP:0100936	presumptive rhombomere 3 decreased amount, abnormal
ZP:0100939	joint Meckel's cartilage morphology, abnormal
ZP:0100940	joint palatoquadrate cartilage morphology, abnormal
ZP:0100941	joint decreased occurrence cell population proliferation, abnormal
ZP:0100942	joint decreased occurrence cell migration, abnormal
ZP:0100943	embryonic skeletal joint development decreased process quality, abnormal
ZP:0100944	hematopoietic stem cell caudal hematopoietic tissue increased amount, abnormal
ZP:0100945	myeloid lineage restricted progenitor cell caudal hematopoietic tissue increased amount, abnormal
ZP:0100946	thymus epithelium morphogenesis disrupted, abnormal
ZP:0100947	thymus decreased process quality cell population proliferation, abnormal
ZP:0100948	thymus increased process quality apoptotic process, abnormal
ZP:0100949	macrophage caudal hematopoietic tissue increased amount, abnormal
ZP:0100950	neutrophil caudal hematopoietic tissue increased amount, abnormal
ZP:0100952	pharynx decreased process quality cell population proliferation, abnormal
ZP:0100953	pro-T cell caudal hematopoietic tissue increased amount, abnormal
ZP:0100954	lymphoid progenitor cell thymus primordium decreased amount, abnormal
ZP:0100955	pharynx hypotrophic, abnormal
ZP:0100956	thymus primordium decreased amount, abnormal
ZP:0100957	pharyngeal pouch 2 decreased amount, abnormal
ZP:0100958	pharyngeal pouch 3 decreased amount, abnormal
ZP:0100959	pharyngeal pouch 5 decreased amount, abnormal
ZP:0100960	pharyngeal pouch 4 decreased amount, abnormal
ZP:0100961	pharyngeal arch 5 decreased amount, abnormal
ZP:0100962	cell liver fatty, abnormal
ZP:0100971	hypothalamus increased distribution, abnormal
ZP:0100973	forebrain increased occurrence action potential, abnormal
ZP:0100974	optic tectum increased occurrence action potential, abnormal
ZP:0100994	vertical myoseptum spatial pattern, abnormal
ZP:0101011	glucose whole organism decreased amount, abnormal
ZP:0101019	oocyte stage III increased amount, abnormal
ZP:0101049	hemoglobin biosynthetic process increased occurrence, abnormal
ZP:0101050	ovarian follicle increased amount, abnormal
ZP:0101051	cysteine-type endopeptidase activity involved in apoptotic process increased occurrence, abnormal
ZP:0101052	cysteine-type endopeptidase activity involved in apoptotic process decreased occurrence, abnormal
ZP:0101070	primordial germ cell spatial pattern, abnormal
ZP:0101081	blood vessel development decreased process quality, abnormal
ZP:0101091	triglyceride liver decreased amount, abnormal
ZP:0101097	liver male organism increased amount, abnormal
ZP:0101100	midbrain hindbrain boundary increased amount, abnormal
ZP:0101107	cerebellum increased amount, abnormal
ZP:0101108	cerebellum decreased amount, abnormal
ZP:0101115	photoreceptor outer segment retinal photoreceptor layer decreased amount, abnormal
ZP:0101119	striated muscle cell increased length, abnormal
ZP:0101120	striated muscle cell decreased width, abnormal
ZP:0101125	hematopoietic stem cell migration decreased occurrence, abnormal
ZP:0101130	dorsal telencephalon increased distribution, abnormal
ZP:0101133	fatty acid blood plasma increased amount, abnormal
ZP:0101135	dorsal longitudinal anastomotic vessel decreased amount, abnormal
ZP:0101168	brain increased occurrence cell death, abnormal
ZP:0101170	microglial cell brain increased amount, abnormal
ZP:0101174	manganese(2+) brain increased amount, abnormal
ZP:0101175	manganese(2+) liver increased amount, abnormal
ZP:0101177	chondrocyte increased amount, abnormal
ZP:0101183	hematopoietic multipotent progenitor cell decreased distribution, abnormal
ZP:0101189	dentary absent, abnormal
ZP:0101195	auditory receptor cell decreased amount, abnormal
ZP:0101214	BMP signaling pathway decreased occurrence, abnormal
ZP:0101215	margin increased amount, abnormal
ZP:0101226	yolk hourglass-shaped, abnormal
ZP:0101230	dopamine whole organism decreased amount, abnormal
ZP:0101231	serotonin whole organism decreased amount, abnormal
ZP:0101233	hematopoietic cell increased amount, abnormal
ZP:0101238	glial cell projection oligodendrocyte decreased amount, abnormal
ZP:0101239	neuromast trunk decreased amount, abnormal
ZP:0101252	presumptive bulbus arteriosus absent, abnormal
ZP:0101266	rhombomere 5 absent, abnormal
ZP:0101280	skeletal tissue decreased area, abnormal
ZP:0101290	gut hemorrhagic, abnormal
ZP:0101297	myocardial precursor anterior lateral plate mesoderm decreased amount, abnormal
ZP:0101298	proton transmembrane transport disrupted, abnormal
ZP:0101299	pharyngeal mesoderm decreased amount, abnormal
ZP:0101302	dorsal region forebrain increased amount, abnormal
ZP:0101303	ventral region forebrain increased amount, abnormal
ZP:0101307	forebrain increased occurrence asymmetric stem cell division, abnormal
ZP:0101308	response to chemical behavioral quality of a process, abnormal
ZP:0101309	lysosome pronephric duct increased diameter, abnormal
ZP:0101310	pectoral fin bud increased amount, abnormal
ZP:0101314	diencephalon has fewer parts of type dopaminergic neuron diencephalon, abnormal
ZP:0101317	endocardium increased distribution, abnormal
ZP:0101318	ventricular endocardium increased occurrence Notch signaling involved in heart development, abnormal
ZP:0101320	optic stalk decreased amount, abnormal
ZP:0101321	prechordal plate decreased distribution, abnormal
ZP:0101322	involuntary skeletal muscle contraction increased occurrence, abnormal
ZP:0101325	posterior region whole organism decreased amount, abnormal
ZP:0101329	retina layer formation decreased occurrence, abnormal
ZP:0101333	medial longitudinal fasciculus decreased occurrence axonal fasciculation, abnormal
ZP:0101334	neuron nucleus of the medial longitudinal fasciculus medulla oblongata loose, abnormal
ZP:0101336	anterior margin neuroectoderm spatial pattern, abnormal
ZP:0101337	anterior margin neuroectoderm decreased distribution, abnormal
ZP:0101338	pancreatic D cell differentiation disrupted, abnormal
ZP:0101339	pancreatic D cell absent, abnormal
ZP:0101340	presumptive telencephalon increased distribution, abnormal
ZP:0101343	estradiol whole organism decreased amount, abnormal
ZP:0101345	intersegmental vessel trunk branchiness, abnormal
ZP:0101348	vasculature increased permeability, abnormal
ZP:0101350	lens fiber cell disorganized, abnormal
ZP:0101351	nucleus lens swollen, abnormal
ZP:0101352	posterior region whole organism increased amount, abnormal
ZP:0101357	forebrain process quality transmission of nerve impulse, abnormal
ZP:0101358	T cell receptor V(D)J recombination disrupted, abnormal
ZP:0101359	T cell head kidney decreased amount, abnormal
ZP:0101360	mature B cell head kidney decreased amount, abnormal
ZP:0101361	photoreceptor outer segment layer decreased height, abnormal
ZP:0101362	whole organism decreased efficacy ATP generation from ADP, abnormal
ZP:0101363	whole organism decreased efficacy aerobic respiration, abnormal
ZP:0101366	rhombomere 3 increased distribution, abnormal
ZP:0101368	presumptive rhombomere 3 increased distribution, abnormal
ZP:0101369	multi fate stem cell epidermis normal amount, abnormal
ZP:0101370	skin development cellular spatiotemporal quality, abnormal
ZP:0101371	NaK ionocyte increased amount, abnormal
ZP:0101372	basement membrane pronephric tubule decreased width, abnormal
ZP:0101373	convergent extension involved in gastrulation decreased occurrence, abnormal
ZP:0101374	cell notochord position, abnormal
ZP:0101378	glycolytic process decreased rate, abnormal
ZP:0101380	oxidative phosphorylation decreased rate, abnormal
ZP:0101383	swimming behavior increased magnitude, abnormal
ZP:0101384	regulation of locomotor rhythm disrupted, abnormal
ZP:0101386	atrium irregular rhythm heart contraction, abnormal
ZP:0101387	cardiac conduction decreased process quality, abnormal
ZP:0101388	cardiac muscle cell membrane repolarization decreased rate, abnormal
ZP:0101391	nerve degeneration, abnormal
ZP:0101392	blood spatial pattern, abnormal
ZP:0101393	blood decreased distribution, abnormal
ZP:0101394	endothelial cell atrioventricular canal mislocalised, abnormal
ZP:0101395	pericardium decreased thickness, abnormal
ZP:0101396	bulbus arteriosus shortened, abnormal
ZP:0101397	atrioventricular canal spatial pattern, abnormal
ZP:0101398	lateral plate mesoderm decreased amount, abnormal
ZP:0101399	ventral region pharyngeal arch decreased amount, abnormal
ZP:0101401	radical lens increased amount, abnormal
ZP:0101402	lens disrupted cellular oxidant detoxification, abnormal
ZP:0101403	retinal pigmented epithelium reflectivity, abnormal
ZP:0101404	presumptive endoderm absent, abnormal
ZP:0101405	mesendoderm development decreased process quality, abnormal
ZP:0101406	hypoblast decreased amount, abnormal
ZP:0101407	mitochondrial chromosome integument decreased amount, abnormal
ZP:0101408	dorsal region midbrain decreased amount, abnormal
ZP:0101411	liver decreased process quality intrahepatic bile duct development, abnormal
ZP:0101413	bile ductule decreased occurrence morphogenesis of a branching epithelium, abnormal
ZP:0101421	bile ductule decreased branchiness, abnormal
ZP:0101422	mandibular arch skeleton increased amount, abnormal
ZP:0101430	pronephric duct has extra parts of type anatomical region leukocyte, abnormal
ZP:0101433	pronephric duct increased occurrence epithelial cell proliferation, abnormal
ZP:0101434	atrioventricular canal functionality, abnormal
ZP:0101435	posterior side midbrain increased distribution, abnormal
ZP:0101436	posterior region midbrain absent, abnormal
ZP:0101437	posterior region midbrain mislocalised, abnormal
ZP:0101440	ventral telencephalon increased distribution, abnormal
ZP:0101441	adenohypophyseal placode absent, abnormal
ZP:0101442	optic fissure absent, abnormal
ZP:0101444	pyruvate whole organism increased amount, abnormal
ZP:0101447	cell-cell adhesion increased occurrence, abnormal
ZP:0101453	ventral region forebrain decreased amount, abnormal
ZP:0101454	brain decreased occurrence gamma-aminobutyric acid signaling pathway, abnormal
ZP:0101455	interneuron hypothalamus decreased amount, abnormal
ZP:0101456	interneuron telencephalon decreased amount, abnormal
ZP:0101457	swimming behavior irregular duration, abnormal
ZP:0101458	olfactory bulb decreased amount, abnormal
ZP:0101459	locus coeruleus decreased amount, abnormal
ZP:0101463	heart decreased occurrence cardiac muscle cell proliferation, abnormal
ZP:0101464	basement membrane liver aplastic, abnormal
ZP:0101472	blood vessel superior ocular sulcus morphology, abnormal
ZP:0101474	blood vessel superior ocular sulcus mislocalised, abnormal
ZP:0101475	circulating cell common cardinal vein decreased amount, abnormal
ZP:0101481	dopamine head decreased amount, abnormal
ZP:0101483	optic vesicle increased distribution, abnormal
ZP:0101485	hematopoietic stem cell migration delayed, abnormal
ZP:0101486	dorsal longitudinal anastomotic vessel increased size, abnormal
ZP:0101489	cartilage element pharyngeal arch cartilage decreased length, abnormal
ZP:0101490	cell symplectic decreased amount, abnormal
ZP:0101492	whole organism process quality larval locomotory behavior, abnormal
ZP:0101493	sarcoplasmic reticulum skeletal muscle increased size, abnormal
ZP:0101494	contractile fiber skeletal muscle decreased amount, abnormal
ZP:0101496	(R)-adrenaline head decreased amount, abnormal
ZP:0101497	noradrenaline head decreased amount, abnormal
ZP:0101498	histamine head increased amount, abnormal
ZP:0101501	neuron caudal hypothalamic zone increased amount, abnormal
ZP:0101502	neuron caudal hypothalamic zone increased distribution, abnormal
ZP:0101518	cholesterol anatomical structure increased amount, abnormal
ZP:0101519	triglyceride anatomical structure increased amount, abnormal
ZP:0101520	high-density lipoprotein blood plasma decreased amount, abnormal
ZP:0101521	low-density lipoprotein blood plasma increased amount, abnormal
ZP:0101522	very-low-density lipoprotein blood plasma increased amount, abnormal
ZP:0101523	lipid trunk vasculature increased amount, abnormal
ZP:0101524	lipid macrophage increased amount, abnormal
ZP:0101525	skeletal muscle cell skeletal muscle disorganized, abnormal
ZP:0101527	sphingosine oocyte increased amount, abnormal
ZP:0101529	sphingoid 1-phosphate oocyte absent, abnormal
ZP:0101530	oocyte increased amount, abnormal
ZP:0101531	sphingosine whole organism increased amount, abnormal
ZP:0101532	sphingosine 1-phosphate whole organism decreased amount, abnormal
ZP:0101536	yolk syncytial layer increased width, abnormal
ZP:0101538	glutamic acid head increased amount, abnormal
ZP:0101542	anatomical region intestinal bulb increased distribution, abnormal
ZP:0101543	intestinal bulb lacks all parts of type anatomical region neural crest cell, abnormal
ZP:0101544	anatomical region intestinal bulb primordium absent, abnormal
ZP:0101545	gut has fewer parts of type anatomical region neural crest cell, abnormal
ZP:0101546	determination of intestine left/right asymmetry decreased occurrence, abnormal
ZP:0101547	right side lateral plate mesoderm spatial pattern, abnormal
ZP:0101551	proximal region caudal fin increased amount, abnormal
ZP:0101552	proximal region caudal fin decreased amount, abnormal
ZP:0101553	distal region caudal fin increased amount, abnormal
ZP:0101554	distal region caudal fin decreased amount, abnormal
ZP:0101555	medial region caudal fin increased amount, abnormal
ZP:0101556	medial region caudal fin decreased amount, abnormal
ZP:0101558	anatomical region eye edematous, abnormal
ZP:0101562	anatomical region heart tube mislocalised, abnormal
ZP:0101563	anatomical region heart mislocalised, abnormal
ZP:0101564	anatomical region atrioventricular canal mislocalised, abnormal
ZP:0101565	anatomical region presumptive atrium heart tube mislocalised, abnormal
ZP:0101566	anatomical region presumptive cardiac ventricle heart tube mislocalised, abnormal
ZP:0101567	whole organism has extra parts of type iridophore, abnormal
ZP:0101570	ectoderm increased amount, abnormal
ZP:0101572	anatomical region heart edematous, abnormal
ZP:0101573	anatomical region digestive system edematous, abnormal
ZP:0101577	integument has extra parts of type NCC ionocyte, abnormal
ZP:0101578	endothelial cell atrial endocardium increased amount, abnormal
ZP:0101579	endothelial cell atrial endocardium decreased amount, abnormal
ZP:0101580	endothelial cell atrioventricular canal endocardium decreased amount, abnormal
ZP:0101582	retinal ganglion cell layer broken, abnormal
ZP:0101583	retinal ganglion cell layer separated from retinal neural layer, abnormal
ZP:0101587	hatching decreased process quality, abnormal
ZP:0101590	spinal cord has fewer parts of type anatomical region angiogenic sprout, abnormal
ZP:0101591	centrum increased volume, abnormal
ZP:0101592	hemal arch decreased thickness, abnormal
ZP:0101593	hemal arch decreased volume, abnormal
ZP:0101594	neural arch decreased thickness, abnormal
ZP:0101600	epicardium increased accumulation cell anatomical region heart vasculature, abnormal
ZP:0101601	Meckel's cartilage increased distance ceratohyal cartilage, abnormal
ZP:0101605	spinal cord has fewer parts of type glutamatergic neuron, abnormal
ZP:0101606	spinal cord has extra parts of type glycinergic neuron, abnormal
ZP:0101607	spinal cord interneuron absent, abnormal
ZP:0101608	spinal cord interneuron decreased distribution, abnormal
ZP:0101611	slow muscle cell spatial pattern, abnormal
ZP:0101612	trigeminal ganglion disrupted axon arborization, abnormal
ZP:0101613	gut discolored, abnormal
ZP:0101615	pronephric proximal convoluted tubule increased occurrence blood vessel morphogenesis, abnormal
ZP:0101617	pronephric proximal straight tubule increased occurrence blood vessel morphogenesis, abnormal
ZP:0101619	pronephric proximal convoluted tubule increased occurrence renal system vasculature morphogenesis, abnormal
ZP:0101621	pronephric proximal straight tubule increased occurrence renal system vasculature morphogenesis, abnormal
ZP:0101622	pronephric proximal convoluted tubule increased occurrence endocytosis, abnormal
ZP:0101623	pronephric proximal straight tubule increased occurrence endocytosis, abnormal
ZP:0101624	midbrain has fewer parts of type lymph vessel endothelial cell, abnormal
ZP:0101625	somite 1 has fewer parts of type lateral region cell notochord, abnormal
ZP:0101626	somite 2 has fewer parts of type lateral region cell notochord, abnormal
ZP:0101628	olfactory placode increased amount, abnormal
ZP:0101633	osteoblast operculohyoid ligament mislocalised, abnormal
ZP:0101634	ligamentous ossification increased occurrence, abnormal
ZP:0101635	portion of connective tissue decreased amount, abnormal
ZP:0101636	operculohyoid ligament ossified, abnormal
ZP:0101641	vertebral column variability bone mineralization, abnormal
ZP:0101642	apatite parietal bone decreased amount, abnormal
ZP:0101643	extracellular matrix osteoblast composition, abnormal
ZP:0101644	fibrous joint cranial vault morphology, abnormal
ZP:0101645	osteoblast parietal bone morphology, abnormal
ZP:0101646	orbitosphenoid poorly ossified, abnormal
ZP:0101647	pterosphenoid poorly ossified, abnormal
ZP:0101648	parasphenoid increased angle to frontal bone, abnormal
ZP:0101649	anterior region cranial vault truncated, abnormal
ZP:0101650	palatoquadrate arch truncated, abnormal
ZP:0101651	bone element cranial vault irregularly shaped, abnormal
ZP:0101652	cranial vault closure incomplete, abnormal
ZP:0101653	osteoblast replacement bone mislocalised, abnormal
ZP:0101661	epiphyseal bar increased width, abnormal
ZP:0101662	inter-ventral hypohyal joint increased width, abnormal
ZP:0101663	neural tube trunk decreased amount, abnormal
ZP:0101664	neural tube post-vent region decreased amount, abnormal
ZP:0101668	regulation of canonical Wnt signaling pathway involved in heart development disrupted, abnormal
ZP:0101670	atrioventricular valve disorganized, abnormal
ZP:0101671	hepaticobiliary system development decreased occurrence, abnormal
ZP:0101672	liver has fewer parts of type intrahepatic bile duct, abnormal
ZP:0101673	liver morphogenesis decreased occurrence, abnormal
ZP:0101674	liver malformed, abnormal
ZP:0101677	L-type voltage-gated calcium channel complex muscle cell decreased amount, abnormal
ZP:0101678	muscle cell decreased process quality release of sequestered calcium ion into cytosol by sarcoplasmic reticulum, abnormal
ZP:0101679	L-type voltage-gated calcium channel complex muscle cell structure, abnormal
ZP:0101684	lateral recess decreased distribution, abnormal
ZP:0101685	hypothalamus process quality neuron differentiation, abnormal
ZP:0101686	neuron hypothalamus irregular spatial pattern, abnormal
ZP:0101687	preoptic area decreased distribution, abnormal
ZP:0101688	caudal hypothalamic zone decreased distribution, abnormal
ZP:0101689	preoptic area increased distribution, abnormal
ZP:0101690	caudal hypothalamic zone increased distribution, abnormal
ZP:0101692	brain physical object quality, abnormal
ZP:0101694	whole organism lacks parts or has fewer parts of type thoracic duct, abnormal
ZP:0101696	vascular lymphangioblast position, abnormal
ZP:0101697	anatomical region dorsal aorta absent, abnormal
ZP:0101698	vascular associated smooth muscle cell dorsal aorta absent, abnormal
ZP:0101699	vascular associated smooth muscle cell dorsal aorta decreased amount, abnormal
ZP:0101702	gonad primordium decreased amount, abnormal
ZP:0101703	immature gonad decreased occurrence germ cell development, abnormal
ZP:0101704	immature gonad increased occurrence male gonad development, abnormal
ZP:0101705	immature gonad decreased occurrence female gonad development, abnormal
ZP:0101706	immature gonad decreased occurrence female somatic sex determination, abnormal
ZP:0101707	immature gonad increased occurrence male somatic sex determination, abnormal
ZP:0101708	somatic cell immature gonad increased amount, abnormal
ZP:0101709	somatic cell immature gonad increased distribution, abnormal
ZP:0101710	somatic cell immature gonad decreased distribution, abnormal
ZP:0101711	somatic cell immature gonad decreased amount, abnormal
ZP:0101712	immature gonad increased amount, abnormal
ZP:0101713	immature gonad decreased amount, abnormal
ZP:0101714	immature gonad has fewer parts of type germ line cell, abnormal
ZP:0101715	gonad decreased occurrence cell population proliferation, abnormal
ZP:0101716	germ line cell decreased occurrence cell population proliferation, abnormal
ZP:0101717	somatic cell decreased occurrence cell population proliferation, abnormal
ZP:0101720	smooth muscle intestine decreased amount, abnormal
ZP:0101721	female sex determination decreased occurrence, abnormal
ZP:0101723	female sex determination increased occurrence, abnormal
ZP:0101725	male sex determination decreased occurrence, abnormal
ZP:0101726	olfactory bulb process quality response to odorant, abnormal
ZP:0101727	ciliated olfactory receptor neuron process quality response to odorant, abnormal
ZP:0101728	blood vessel endothelial cell proliferation involved in sprouting angiogenesis decreased process quality, abnormal
ZP:0101729	blood vessel endothelial cell migration decreased process quality, abnormal
ZP:0101730	smooth muscle cell intestine decreased amount, abnormal
ZP:0101731	gut decreased occurrence peristalsis, abnormal
ZP:0101732	smooth muscle intestine increased amount, abnormal
ZP:0101733	cardiac conduction system mislocalised, abnormal
ZP:0101734	sinoatrial node increased distribution, abnormal
ZP:0101735	sinoatrial node increased area, abnormal
ZP:0101738	anatomical region gut spatial pattern, abnormal
ZP:0101739	anatomical region gut decreased amount, abnormal
ZP:0101740	lateral plate mesoderm decreased occurrence cell population proliferation, abnormal
ZP:0101741	smooth muscle cell intestine disorganized, abnormal
ZP:0101742	smooth muscle cell decreased occurrence cell maturation, abnormal
ZP:0101743	smooth muscle cell intestine shape, abnormal
ZP:0101744	brain aplastic/hypoplastic, abnormal
ZP:0101747	reactive oxygen species metabolic process increased occurrence, abnormal
ZP:0101748	myelinating Schwann cell lateral line decreased amount, abnormal
ZP:0101749	myelinating Schwann cell lateral line absent, abnormal
ZP:0101750	telencephalon decreased occurrence cell population proliferation, abnormal
ZP:0101751	telencephalon decreased occurrence commitment of multipotent stem cells to neuronal lineage in forebrain, abnormal
ZP:0101752	telencephalon aplastic/hypoplastic, abnormal
ZP:0101754	ERK1 and ERK2 cascade decreased process quality, abnormal
ZP:0101755	presumptive neural plate decreased distribution, abnormal
ZP:0101756	presumptive neural plate decreased amount, abnormal
ZP:0101757	anterior neural plate aplastic/hypoplastic, abnormal
ZP:0101758	presumptive telencephalon aplastic/hypoplastic, abnormal
ZP:0101759	presumptive telencephalon decreased amount, abnormal
ZP:0101764	axon terminus posterior lateral line nerve swollen, abnormal
ZP:0101765	axon terminus posterior lateral line neuromast swollen, abnormal
ZP:0101766	posterior lateral line nerve decreased process quality anterograde axonal transport, abnormal
ZP:0101767	axon terminus posterior lateral line nerve increased amount, abnormal
ZP:0101768	axon terminus posterior lateral line neuromast increased amount, abnormal
ZP:0101770	myoseptum spatial pattern, abnormal
ZP:0101771	cell junction pronephric glomerulus decreased amount, abnormal
ZP:0101772	podocyte foot pronephric podocyte decreased thickness, abnormal
ZP:0101773	pronephric glomerular basement membrane decreased functionality, abnormal
ZP:0101774	whole organism lacks all parts of type thoracic duct, abnormal
ZP:0101776	leukocyte integument increased amount, abnormal
ZP:0101777	leukocyte muscle increased amount, abnormal
ZP:0101780	posterior lateral line nerve decreased occurrence retrograde axonal transport of mitochondrion, abnormal
ZP:0101781	mitochondrion posterior lateral line nerve mislocalised, abnormal
ZP:0101782	posterior lateral line nerve has extra parts of type axon terminus mitochondrion posterior lateral line nerve, abnormal
ZP:0101783	posterior lateral line neuromast has extra parts of type axon terminus mitochondrion posterior lateral line neuromast, abnormal
ZP:0101790	posterior lateral line nerve decreased diameter, abnormal
ZP:0101798	spinal cord has fewer parts of type postero-dorsal region oligodendrocyte, abnormal
ZP:0101799	spinal cord has fewer parts of type postero-ventral region oligodendrocyte, abnormal
ZP:0101800	spinal cord has fewer parts of type posterior region oligodendrocyte, abnormal
ZP:0101801	Mauthner neuron has fewer parts of type posterior region myelin sheath Mauthner neuron, abnormal
ZP:0101802	oligodendrocyte increased occurrence cell death, abnormal
ZP:0101803	oligodendrocyte decreased occurrence cell population proliferation, abnormal
ZP:0101804	mesenchymal cell decreased amount, abnormal
ZP:0101805	perineuronal satellite cell decreased amount, abnormal
ZP:0101806	circadian regulation of gene expression rhythm quality, abnormal
ZP:0101807	melanin biosynthetic process rhythm quality, abnormal
ZP:0101808	presumptive mesoderm decreased amount, abnormal
ZP:0101809	ventral mesoderm decreased amount, abnormal
ZP:0101810	axial mesoderm decreased amount, abnormal
ZP:0101811	cardiac neural crest increased amount, abnormal
ZP:0101812	Meckel's cartilage dysplastic, abnormal
ZP:0101813	palatoquadrate cartilage dysplastic, abnormal
ZP:0101814	anterior segment eye edematous, abnormal
ZP:0101816	neuromuscular junction ventral root structure, abnormal
ZP:0101817	synapse ventral root decreased amount, abnormal
ZP:0101818	presynapse assembly disrupted, abnormal
ZP:0101819	swimming decreased duration, abnormal
ZP:0101821	retina decreased occurrence Notch signaling pathway, abnormal
ZP:0101822	myotome development decreased process quality, abnormal
ZP:0101823	anterior side mesoderm decreased amount, abnormal
ZP:0101824	erythroid lineage cell delayed cell cycle G1/S phase transition, abnormal
ZP:0101855	pronephric tubule orientation anterior-posterior axis whole organism, abnormal
ZP:0101858	retinal cone cell increased occurrence apoptotic process, abnormal
ZP:0101859	retinal rod cell increased occurrence apoptotic process, abnormal
ZP:0101860	retinal cone cell optical quality, abnormal
ZP:0101866	Meckel's cartilage misaligned with palatoquadrate cartilage, abnormal
ZP:0101867	oocyte increased occurrence reproductive senescence, abnormal
ZP:0101868	oogenesis process quality, abnormal
ZP:0101869	ovary senescent, abnormal
ZP:0101870	gonad increased amount, abnormal
ZP:0101871	ovary increased occurrence spermatogenesis, abnormal
ZP:0101872	ovary disrupted maintenance of animal organ identity, abnormal
ZP:0101874	photoreceptor outer segment layer has fewer parts of type photoreceptor disc membrane photoreceptor cell, abnormal
ZP:0101875	photoreceptor outer segment layer has extra parts of type axoneme photoreceptor cell, abnormal
ZP:0101877	pronephros decreased length, abnormal
ZP:0101878	autophagosome trunk increased amount, abnormal
ZP:0101881	3',5'-cyclic AMP whole organism decreased amount, abnormal
ZP:0101882	pectoral fin motor nerve 3 process quality motor neuron axon guidance, abnormal
ZP:0101883	axon pectoral fin motor nerve 4 decreased branchiness, abnormal
ZP:0101884	sclerotome structure, abnormal
ZP:0101885	gonadotrophin-releasing hormone neuronal migration to the hypothalamus disrupted, abnormal
ZP:0101886	olfactory bulb spatial pattern, abnormal
ZP:0101887	primary motor neuron process quality axon guidance, abnormal
ZP:0101888	pectoral fin motor nerve 1 process quality motor neuron axon guidance, abnormal
ZP:0101889	pectoral fin motor nerve 2 process quality motor neuron axon guidance, abnormal
ZP:0101890	pectoral fin motor nerve 4 process quality motor neuron axon guidance, abnormal
ZP:0101891	axon pectoral fin motor nerve 2 defasciculated, abnormal
ZP:0101892	axon pectoral fin motor nerve 3 defasciculated, abnormal
ZP:0101893	axon terminus pectoral fin motor nerve 2 mislocalised, abnormal
ZP:0101894	axon terminus pectoral fin motor nerve 3 mislocalised, abnormal
ZP:0101895	facial nerve motor nucleus premature neuron maturation, abnormal
ZP:0101896	neuron projection facial nerve motor nucleus increased length, abnormal
ZP:0101897	motor neuron facial nerve motor nucleus circular, abnormal
ZP:0101898	facial nerve motor nucleus has extra parts of type neuron projection motor neuron, abnormal
ZP:0101899	neuron projection facial nerve motor nucleus increased amount, abnormal
ZP:0101900	motor neuron facial nerve motor nucleus increased volume, abnormal
ZP:0101901	facial nerve motor nucleus rhombomere 6 increased volume, abnormal
ZP:0101902	facial nerve motor nucleus rhombomere 5 increased volume, abnormal
ZP:0101903	facial nerve motor nucleus rhombomere 4 increased volume, abnormal
ZP:0101909	intestine lacks all parts of type distal region enteric neuron, abnormal
ZP:0101910	hematopoietic multipotent progenitor cell ventral wall of dorsal aorta decreased distribution, abnormal
ZP:0101911	germ cell migration decreased occurrence, abnormal
ZP:0101912	primordial germ cell increased occurrence bleb assembly, abnormal
ZP:0101913	primordial germ cell decreased occurrence actin filament polymerization, abnormal
ZP:0101916	retina decreased occurrence cell proliferation involved in compound eye morphogenesis, abnormal
ZP:0101917	intersegmental vein decreased branchiness, abnormal
ZP:0101924	dorsal longitudinal anastomotic vessel aplastic/hypoplastic, abnormal
ZP:0101925	cell projection oligodendrocyte absent, abnormal
ZP:0101926	lamellipodium intersegmental vessel decreased amount, abnormal
ZP:0101928	forebrain neural keel increased size, abnormal
ZP:0101929	spinal cord neural keel decreased size, abnormal
ZP:0101930	spinal cord neural keel decreased distribution, abnormal
ZP:0101931	posterior region neuroectoderm decreased size, abnormal
ZP:0101932	nucleosome positioning process quality, abnormal
ZP:0101935	ventro-lateral region mesoderm decreased amount, abnormal
ZP:0101936	dorsal region diencephalon increased amount, abnormal
ZP:0101937	trunk increased occurrence cell death, abnormal
ZP:0101938	ionocyte decreased process quality proton export across plasma membrane, abnormal
ZP:0101939	vH ionocyte decreased process quality proton export across plasma membrane, abnormal
ZP:0101940	dendrite habenula decreased branchiness, abnormal
ZP:0101941	habenula process quality dendrite arborization, abnormal
ZP:0101942	whole organism disrupted thigmotaxis, abnormal
ZP:0101943	mitochondrion eye morphology, abnormal
ZP:0101944	lysosome brain hypertrophic, abnormal
ZP:0101945	lysosome whole organism increased size, abnormal
ZP:0101946	axon brain disorganized, abnormal
ZP:0101947	axon brain aggregated, abnormal
ZP:0101948	axon optic tectum absent, abnormal
ZP:0101949	apoptotic body forebrain increased amount, abnormal
ZP:0101950	optic tectum disrupted regulation of neuronal action potential, abnormal
ZP:0101951	astrocyte spinal cord increased amount, abnormal
ZP:0101952	regulation of mitochondrial membrane potential disrupted, abnormal
ZP:0101953	sleep decreased process quality, abnormal
ZP:0101954	neuromast hair cell decreased process quality response to mechanical stimulus, abnormal
ZP:0101955	stereocilium neuromast hair cell decreased functionality, abnormal
ZP:0101956	hair cell lateral crista decreased functionality, abnormal
ZP:0101961	anterior region pronephros increased amount, abnormal
ZP:0101962	posterior region vasculature increased amount, abnormal
ZP:0101963	post-vent vasculature decreased process quality vasculature development, abnormal
ZP:0101964	primordial germ cell increased amount, abnormal
ZP:0101965	cardiac ventricle decreased process quality regulation of cardiac muscle contraction by calcium ion signaling, abnormal
ZP:0101966	cilium ventricular zone decreased amount, abnormal
ZP:0101967	retina broken, abnormal
ZP:0101968	ventricular zone ciliatedness, abnormal
ZP:0101970	neuron morphology, abnormal
ZP:0101974	nucleus fast muscle cell undistributed, abnormal
ZP:0101978	lateral crista decreased process quality inner ear receptor cell stereocilium organization, abnormal
ZP:0101992	cranial vasculature decreased amount, abnormal
ZP:0101993	motile cilium multi-ciliated epithelial cell decreased amount, abnormal
ZP:0101996	fast muscle cell disrupted myoblast fusion, abnormal
ZP:0101997	fast muscle myoblast nucleate quality, abnormal
ZP:0101998	fast muscle cell decreased size, abnormal
ZP:0102000	pharyngeal arch 3-7 skeleton lacks parts or has fewer parts of type ceratobranchial cartilage, abnormal
ZP:0102001	ceratohyal cartilage posterior orientation, abnormal
ZP:0102002	Meckel's cartilage physical object quality, abnormal
ZP:0102003	ceratobranchial cartilage agenesis, abnormal
ZP:0102004	photoreceptor outer segment photoreceptor cell degenerate, abnormal
ZP:0102005	eye photoreceptor cell detached from photoreceptor outer segment photoreceptor inner segment eye photoreceptor cell, abnormal
ZP:0102006	photoreceptor outer segment retinal cone cell degenerate, abnormal
ZP:0102007	retinal photoreceptor layer has extra parts of type vesicle retinal photoreceptor layer, abnormal
ZP:0102008	retina process quality regulation of apoptotic cell clearance, abnormal
ZP:0102011	photoreceptor outer segment retinal rod cell disorganized, abnormal
ZP:0102014	posterior region midbrain hindbrain boundary decreased distribution, abnormal
ZP:0102015	mesoderm disorganized, abnormal
ZP:0102016	gut decreased distribution, abnormal
ZP:0102017	spinal cord interneuron mislocalised, abnormal
ZP:0102018	hindbrain interneuron spatial pattern, abnormal
ZP:0102019	retinal ganglion cell decreased distribution, abnormal
ZP:0102020	whole organism decreased occurrence apoptotic process, abnormal
ZP:0102021	endothelial cell intersegmental vessel increased amount, abnormal
ZP:0102022	hematopoietic stem cell proliferation disrupted, abnormal
ZP:0102024	proliferative region retina increased amount, abnormal
ZP:0102025	proliferative region retina mislocalised, abnormal
ZP:0102026	dorsal longitudinal anastomotic vessel arrested angiogenic sprout fusion, abnormal
ZP:0102036	neuromast hair cell process quality innervation, abnormal
ZP:0102042	anterior region whole organism decreased size, abnormal
ZP:0102043	endoderm increased amount, abnormal
ZP:0102048	type B pancreatic cell differentiation premature, abnormal
ZP:0102049	pancreatic A cell differentiation decreased occurrence, abnormal
ZP:0102050	myelin sheath oligodendrocyte increased length, abnormal
ZP:0102055	cell projection xanthophore decreased amount, abnormal
ZP:0102059	thrombocyte decreased occurrence cell population proliferation, abnormal
ZP:0102060	thrombocyte blood decreased amount, abnormal
ZP:0102061	thrombocyte head kidney decreased amount, abnormal
ZP:0102062	hematopoietic multipotent progenitor cell head kidney decreased amount, abnormal
ZP:0102063	thromboblast decreased occurrence cell population proliferation, abnormal
ZP:0102066	hemin whole organism decreased amount, abnormal
ZP:0102067	axon hindbrain commissure decreased amount, abnormal
ZP:0102068	neuron cerebellum spatial pattern, abnormal
ZP:0102069	midbrain hindbrain boundary increased thickness, abnormal
ZP:0102070	midbrain structure, abnormal
ZP:0102071	supraoptic commissure absent, abnormal
ZP:0102072	compartment boundary rhombomere absent, abnormal
ZP:0102073	hindbrain lacks all parts of type compartment boundary rhombomere, abnormal
ZP:0102074	post-vent region immobile, abnormal
ZP:0102075	hindbrain increased process quality neurogenesis, abnormal
ZP:0102078	neuroblast (sensu Vertebrata) decreased amount, abnormal
ZP:0102079	dopaminergic neuron differentiation disrupted, abnormal
ZP:0102080	endocardium process quality cardioblast cell midline fusion, abnormal
ZP:0102081	medial region whole organism absent, abnormal
ZP:0102082	anterior lateral plate mesoderm absent, abnormal
ZP:0102083	cardioblast cell midline fusion arrested, abnormal
ZP:0102084	cardioblast cell midline fusion process quality, abnormal
ZP:0102085	presumptive atrium heart tube increased width, abnormal
ZP:0102086	presumptive atrium heart tube distended, abnormal
ZP:0102087	presumptive cardiac ventricle heart tube increased width, abnormal
ZP:0102088	anterior-posterior axis whole organism decreased size, abnormal
ZP:0102089	swim bladder inflation process quality, abnormal
ZP:0102090	heart collapsed, abnormal
ZP:0102091	oral region process quality neural crest cell migration, abnormal
ZP:0102092	dopaminergic neuron midbrain decreased amount, abnormal
ZP:0102093	ATP whole organism decreased amount, abnormal
ZP:0102094	slow muscle cell process quality calcium-mediated signaling, abnormal
ZP:0102099	blood cell accumulation heart, abnormal
ZP:0102104	axon cranial motor neuron decreased amount, abnormal
ZP:0102106	motor neuron migration decreased process quality, abnormal
ZP:0102110	notochord increased fragility, abnormal
ZP:0102111	notochord inner cell collapsed, abnormal
ZP:0102118	notochord outer sheath cell displaced to central region notochord, abnormal
ZP:0102120	notochord outer sheath cell metaplastic, abnormal
ZP:0102121	notochord inner cell metaplastic, abnormal
ZP:0102122	notochord outer sheath cell increased amount, abnormal
ZP:0102123	chondrocyte palatoquadrate cartilage decreased area, abnormal
ZP:0102124	cleithrum length, abnormal
ZP:0102125	branchiostegal ray length, abnormal
ZP:0102126	entopterygoid length, abnormal
ZP:0102127	palatoquadrate cartilage decreased area, abnormal
ZP:0102128	brain decreased occurrence endothelial cell development, abnormal
ZP:0102129	brain vasculature decreased amount, abnormal
ZP:0102131	blood vessel brain morphology, abnormal
ZP:0102132	endothelial cell brain decreased amount, abnormal
ZP:0102133	endothelial cell brain absent, abnormal
ZP:0102136	hematopoietic cell decreased amount, abnormal
ZP:0102139	epicardium increased size, abnormal
ZP:0102140	blood accumulation yolk syncytial layer, abnormal
ZP:0102141	erythroid progenitor cell dysplastic, abnormal
ZP:0102142	plasma membrane notochord inner cell broken, abnormal
ZP:0102144	notochord development decreased process quality, abnormal
ZP:0102145	caveola notochord inner cell malformed, abnormal
ZP:0102146	notochord inner cell malformed, abnormal
ZP:0102147	notochord inner cell has fewer parts of type plasma membrane caveola notochord inner cell, abnormal
ZP:0102148	caveola neck notochord inner cell increased width, abnormal
ZP:0102149	caveola bulb notochord inner cell decreased depth, abnormal
ZP:0102153	thymus development decreased process quality, abnormal
ZP:0102154	immune response decreased process quality, abnormal
ZP:0102155	T cell receptor V(D)J recombination arrested, abnormal
ZP:0102156	T cell activation arrested, abnormal
ZP:0102157	B cell activation arrested, abnormal
ZP:0102158	immunoglobulin heavy chain V-D-J recombination arrested, abnormal
ZP:0102159	spleen absent, abnormal
ZP:0102160	kidney absent, abnormal
ZP:0102161	kidney decreased thickness, abnormal
ZP:0102162	kidney decreased mass density, abnormal
ZP:0102171	anal fin development process quality, abnormal
ZP:0102172	caudal fin development process quality, abnormal
ZP:0102173	dorsal fin development process quality, abnormal
ZP:0102174	dorsal fin morphogenesis process quality, abnormal
ZP:0102175	caudal fin morphogenesis process quality, abnormal
ZP:0102176	anal fin morphogenesis process quality, abnormal
ZP:0102181	autophagy decreased occurrence, abnormal
ZP:0102184	dorsal aorta has extra parts of type circulating cell neutrophil, abnormal
ZP:0102186	hypobranchial artery increased variability of size, abnormal
ZP:0102187	hematopoietic multipotent progenitor cell thymus increased amount, abnormal
ZP:0102192	post-vent region decreased amount, abnormal
ZP:0102195	filopodium intersegmental vessel variability of count, abnormal
ZP:0102198	cytoskeleton muscle cell disorganized, abnormal
ZP:0102199	defense response to Gram-positive bacterium decreased process quality, abnormal
ZP:0102200	somite amount, abnormal
ZP:0102201	endothelial cell trabecular layer decreased amount, abnormal
ZP:0102202	angiogenesis involved in coronary vascular morphogenesis disrupted, abnormal
ZP:0102203	cell-cell junction DEL decreased amount, abnormal
ZP:0102204	DEL delayed cell migration involved in gastrulation, abnormal
ZP:0102205	DEL process quality cell migration involved in gastrulation, abnormal
ZP:0102206	blastomere organization quality, abnormal
ZP:0102210	CaP motoneuron disrupted axonogenesis, abnormal
ZP:0102211	axon secondary motor neuron decreased branchiness, abnormal
ZP:0102212	neuromuscular junction myotome increased distribution, abnormal
ZP:0102213	presynaptic density myotome increased amount, abnormal
ZP:0102215	peripheral nervous system has fewer parts of type myelinating Schwann cell, abnormal
ZP:0102216	motor neuron has fewer parts of type myelinating Schwann cell, abnormal
ZP:0102218	glial cell decreased thickness, abnormal
ZP:0102220	manganese(2+) whole organism increased amount, abnormal
ZP:0102222	manganese atom whole organism increased amount, abnormal
ZP:0102224	manganese atom whole organism decreased amount, abnormal
ZP:0102226	vertebra process quality bone mineralization, abnormal
ZP:0102227	neural arch increased area, abnormal
ZP:0102228	neural arch decreased angle to vertebra, abnormal
ZP:0102229	vertebra increased size, abnormal
ZP:0102230	fourth ventricle absent, abnormal
ZP:0102231	fourth ventricle decreased amount, abnormal
ZP:0102232	tegmentum decreased amount, abnormal
ZP:0102234	blood vessel lumenization decreased occurrence, abnormal
ZP:0102235	artery malformed, abnormal
ZP:0102236	vein malformed, abnormal
ZP:0102239	whole organism decreased mass, abnormal
ZP:0102246	orbital region edematous, abnormal
ZP:0102247	pronephric duct kinked, abnormal
ZP:0102250	vasculature hematopoietic system increased amount, abnormal
ZP:0102251	endoderm spatial pattern, abnormal
ZP:0102252	cilium ependymal cell increased length, abnormal
ZP:0102254	skeletal tissue disrupted tissue homeostasis, abnormal
ZP:0102255	vertebra decreased distance vertebra, abnormal
ZP:0102256	ventral mandibular arch decreased width, abnormal
ZP:0102257	skeletal tissue decreased amount, abnormal
ZP:0102258	pericardial cavity process quality bone mineralization, abnormal
ZP:0102259	cilium neural tube increased length, abnormal
ZP:0102260	neural tube has fewer parts of type cilium neural tube, abnormal
ZP:0102261	olfactory pit process quality cilium assembly, abnormal
ZP:0102262	9+2 non-motile cilium ciliated olfactory receptor neuron malformed, abnormal
ZP:0102263	myotome process quality cilium assembly, abnormal
ZP:0102264	non-motile cilium myotome increased length, abnormal
ZP:0102265	brainstem decreased size, abnormal
ZP:0102266	brainstem morphology, abnormal
ZP:0102267	vascular associated smooth muscle cell cerebellar central artery decreased amount, abnormal
ZP:0102268	actin filament bundle keratinocyte decreased amount, abnormal
ZP:0102269	epidermal superficial stratum morphology, abnormal
ZP:0102270	keratinocyte increased size, abnormal
ZP:0102271	spinal cord interneuron arrested synapse assembly, abnormal
ZP:0102272	Mauthner neuron arrested synapse assembly, abnormal
ZP:0102273	afferent neuron arrested synapse assembly, abnormal
ZP:0102274	synapse cranial nerve VIII absent, abnormal
ZP:0102275	synapse spinal cord interneuron absent, abnormal
ZP:0102276	synapse Mauthner neuron non-functional, abnormal
ZP:0102277	synapse afferent neuron absent, abnormal
ZP:0102278	startle response latency, abnormal
ZP:0102279	Meckel's cartilage immature, abnormal
ZP:0102280	ceratohyal cartilage immature, abnormal
ZP:0102281	hypothalamus disrupted axon extension, abnormal
ZP:0102282	cerebellum disrupted axon extension, abnormal
ZP:0102283	neuroblast differentiation disrupted, abnormal
ZP:0102284	regulation of neuroblast proliferation disrupted, abnormal
ZP:0102285	posterior side whole organism absent, abnormal
ZP:0102286	iridophore eye disorganized, abnormal
ZP:0102287	ventral mandibular arch immature, abnormal
ZP:0102289	hematopoietic system increased occurrence cell death, abnormal
ZP:0102290	stromal cell caudal vein plexus apoptotic, abnormal
ZP:0102291	granulocyte differentiation decreased process quality, abnormal
ZP:0102292	thymus lacks all parts of type lymphoid progenitor cell, abnormal
ZP:0102293	caudal vein plexus has fewer parts of type hematopoietic stem cell, abnormal
ZP:0102294	neuronal stem cell disrupted cell population proliferation, abnormal
ZP:0102295	afferent neuron decreased occurrence synapse assembly, abnormal
ZP:0102296	synapse cranial nerve VIII decreased amount, abnormal
ZP:0102297	synapse afferent neuron decreased amount, abnormal
ZP:0102298	maturation of SSU-rRNA from tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA) disrupted, abnormal
ZP:0102299	sympathetic nervous system development disrupted, abnormal
ZP:0102300	superior cervical ganglion decreased size, abnormal
ZP:0102301	superior cervical ganglion hypoplastic, abnormal
ZP:0102302	superior cervical ganglion decreased distribution, abnormal
ZP:0102303	sarcomere somite absent, abnormal
ZP:0102304	superior cervical ganglion decreased amount, abnormal
ZP:0102317	pharynx inflamed, abnormal
ZP:0102318	gill inflamed, abnormal
ZP:0102319	integument inflamed, abnormal
ZP:0102320	olfactory epithelium inflamed, abnormal
ZP:0102321	gill filament swollen, abnormal
ZP:0102322	intestine swollen, abnormal
ZP:0102323	T cell pharynx increased amount, abnormal
ZP:0102324	T cell integument increased amount, abnormal
ZP:0102325	T cell olfactory epithelium increased amount, abnormal
ZP:0102326	T cell gill filament increased amount, abnormal
ZP:0102327	T cell intestine increased amount, abnormal
ZP:0102328	pharynx has extra parts of type T cell, abnormal
ZP:0102329	gill has extra parts of type T cell, abnormal
ZP:0102330	integument has extra parts of type T cell, abnormal
ZP:0102331	olfactory epithelium has extra parts of type T cell, abnormal
ZP:0102332	intestine has extra parts of type T cell, abnormal
ZP:0102334	intestine lumen decreased volume, abnormal
ZP:0102336	intestinal epithelium decreased amount, abnormal
ZP:0102351	calcium ion import increased occurrence, abnormal
ZP:0102353	epidermis rough, abnormal
ZP:0102354	keratinocyte morphology, abnormal
ZP:0102355	Wnt signaling pathway, calcium modulating pathway decreased occurrence, abnormal
ZP:0102357	blood vessel endothelial cell intersegmental vessel apoptotic, abnormal
ZP:0102358	blood vessel endothelial cell trunk vasculature apoptotic, abnormal
ZP:0102360	whole organism decreased velocity, abnormal
ZP:0102361	intersegmental vessel hemorrhagic, abnormal
ZP:0102362	basal side cardiac muscle cell absent, abnormal
ZP:0102366	caudal fin lepidotrichium spatial pattern, abnormal
ZP:0102367	caudal fin lepidotrichium broken, abnormal
ZP:0102368	caudal fin lepidotrichium lacks parts or has fewer parts of type lepidotrichium joint, abnormal
ZP:0102369	trigeminal ganglion absent, abnormal
ZP:0102370	trigeminal ganglion increased amount, abnormal
ZP:0102371	posterior lateral line neuromast hair cell morphogenesis disrupted, abnormal
ZP:0102372	neuromast spatial pattern, abnormal
ZP:0102374	posterior lateral line primordium disrupted cell population proliferation, abnormal
ZP:0102375	myoseptum decreased amount, abnormal
ZP:0102382	cell pancreas apoptotic, abnormal
ZP:0102383	intestinal bulb epithelium morphology, abnormal
ZP:0102384	histone H3-K27 methylation disrupted, abnormal
ZP:0102386	posterior lateral line neuromast deposition decreased rate, abnormal
ZP:0102396	growth decreased efficacy, abnormal
ZP:0102397	carotenoid integument decreased amount, abnormal
ZP:0102398	carotenoid vesicle xanthophore aggregated, abnormal
ZP:0102401	intersegmental vessel trunk increased branchiness, abnormal
ZP:0102407	intersegmental vessel detached from dorsal longitudinal anastomotic vessel, abnormal
ZP:0102410	mesodermal cell tail bud increased distribution, abnormal
ZP:0102413	myofilament cardiac muscle cell disorganized, abnormal
ZP:0102414	myofilament cardiac muscle cell decreased thickness, abnormal
ZP:0102415	cardiac muscle cell misaligned with myofilament myofilament cardiac muscle cell, abnormal
ZP:0102416	cardiac muscle cell separated from myofilament myofilament cardiac muscle cell, abnormal
ZP:0102417	cardiac muscle cell has extra parts of type plasma membrane cell projection cardiac muscle cell, abnormal
ZP:0102421	yolk syncytial layer mislocalised, abnormal
ZP:0102422	muscle pioneer disorganized, abnormal
ZP:0102423	pharyngeal arch 3-7 decreased distribution, abnormal
ZP:0102424	somite border incomplete structure, abnormal
ZP:0102428	cell migration involved in heart development process quality, abnormal
ZP:0102429	melanoma eye present, abnormal
ZP:0102430	melanoma trunk present, abnormal
ZP:0102431	melanoma in situ whole organism increased amount, abnormal
ZP:0102432	sex determination disrupted, abnormal
ZP:0102433	fertilization disrupted, abnormal
ZP:0102434	oogenesis disrupted, abnormal
ZP:0102435	oocyte female organism viability, abnormal
ZP:0102436	cell division asynchronous, abnormal
ZP:0102437	blastomere asymmetrical, abnormal
ZP:0102438	pharyngeal arch decreased process quality embryonic viscerocranium morphogenesis, abnormal
ZP:0102439	pharyngeal arch cartilage decreased occurrence chondrocyte differentiation, abnormal
ZP:0102440	pectoral fin decreased process quality cartilage development, abnormal
ZP:0102442	pectoral girdle lacks all parts of type cleithrum, abnormal
ZP:0102443	pectoral girdle lacks all parts of type scapulocoracoid, abnormal
ZP:0102446	erythroblast decreased occurrence mitophagy, abnormal
ZP:0102447	blood cell increased accumulation ventricular system, abnormal
ZP:0102448	cell-cell junction blood vessel decreased amount, abnormal
ZP:0102449	blood vasculature brain decreased amount, abnormal
ZP:0102450	blood vessel brain broken, abnormal
ZP:0102451	brain separated from blood vessel endothelial cell blood vessel endothelial cell, abnormal
ZP:0102452	aerobic respiration decreased process quality, abnormal
ZP:0102454	cholangiocyte increased amount, abnormal
ZP:0102455	liver increased occurrence Wnt signaling pathway, abnormal
ZP:0102456	cholangiocyte increased occurrence Wnt signaling pathway, abnormal
ZP:0102468	epithelial cell regenerating fin apoptotic, abnormal
ZP:0102469	epithelial cell protruding out of regenerating fin, abnormal
ZP:0102471	actin-based cell projection peridermal cell decreased size, abnormal
ZP:0102472	photoreceptor outer segment photoreceptor outer segment layer disorganized, abnormal
ZP:0102473	cilium retina absent, abnormal
ZP:0102474	regulation of hippo signaling disrupted, abnormal
ZP:0102475	angioblastic mesenchymal cell posterior lateral mesoderm spatial pattern, abnormal
ZP:0102476	angioblastic mesenchymal cell irregular spatial pattern, abnormal
ZP:0102477	medial region pharyngeal arch 2 decreased amount, abnormal
ZP:0102478	medial region pharyngeal arch 1 decreased amount, abnormal
ZP:0102479	ventral region pharyngeal arch 2 absent, abnormal
ZP:0102480	ventral region pharyngeal arch 1 absent, abnormal
ZP:0102481	ventral hyoid arch mislocalised, abnormal
ZP:0102482	intersegmental artery decreased process quality sprouting angiogenesis, abnormal
ZP:0102492	atrioventricular canal process quality blood circulation, abnormal
ZP:0102495	notochord post-vent region bent, abnormal
ZP:0102498	nucleus optic vesicle decreased amount, abnormal
ZP:0102499	brain decreased process quality regulation of cell cycle, abnormal
ZP:0102500	retina decreased process quality regulation of cell cycle, abnormal
ZP:0102503	locomotory exploration behavior decreased process quality, abnormal
ZP:0102504	optic tectum process quality microglial cell migration, abnormal
ZP:0102509	midbrain increased distribution, abnormal
ZP:0102512	axoneme anterior neural tube structure, abnormal
ZP:0102513	axoneme spinal cord neural tube structure, abnormal
ZP:0102514	motile cilium assembly process quality, abnormal
ZP:0102515	9+2 motile cilium olfactory epithelium absent, abnormal
ZP:0102516	9+2 motile cilium olfactory epithelium decreased mobility, abnormal
ZP:0102517	epithelial cilium movement involved in extracellular fluid movement decreased process quality, abnormal
ZP:0102520	spinal cord process quality cilium movement, abnormal
ZP:0102521	hindbrain arrested mitotic cell cycle, abnormal
ZP:0102522	centrosome hindbrain size, abnormal
ZP:0102523	hindbrain adjacent to centrosome centrosome hindbrain, abnormal
ZP:0102524	spindle hindbrain spatial pattern, abnormal
ZP:0102525	spindle hindbrain decreased amount, abnormal
ZP:0102526	centrosome cycle process quality, abnormal
ZP:0102527	mitotic centrosome separation decreased occurrence, abnormal
ZP:0102528	monocyte ventral wall of dorsal aorta decreased amount, abnormal
ZP:0102529	nucleate erythrocyte ventral wall of dorsal aorta decreased amount, abnormal
ZP:0102535	pronephric podocyte decreased process quality glomerular visceral epithelial cell development, abnormal
ZP:0102536	pronephros decreased occurrence renal filtration, abnormal
ZP:0102537	podocyte foot pronephric podocyte malformed, abnormal
ZP:0102538	podocyte foot pronephric podocyte dystrophic, abnormal
ZP:0102539	pronephric glomerulus increased width, abnormal
ZP:0102540	pronephric tubule decreased length, abnormal
ZP:0102541	centrosome somite border spatial pattern, abnormal
ZP:0102542	somite border decreased occurrence mesenchymal to epithelial transition, abnormal
ZP:0102543	epithelial cell somite border morphology, abnormal
ZP:0102544	actin filament somite border morphology, abnormal
ZP:0102545	actin filament somite border malformed, abnormal
ZP:0102546	cardiac ventricle decreased process quality cardiac muscle cell proliferation, abnormal
ZP:0102548	pronephros increased occurrence apoptotic process, abnormal
ZP:0102549	podocyte foot pronephric podocyte immature, abnormal
ZP:0102552	neuron spinal cord decreased distribution, abnormal
ZP:0102553	tail bud spatial pattern, abnormal
ZP:0102554	post-vent region increased process quality cell death, abnormal
ZP:0102555	midbrain hindbrain boundary spatial pattern, abnormal
ZP:0102557	lateral line ganglion decreased distribution, abnormal
ZP:0102558	midbrain hindbrain boundary neural rod decreased distribution, abnormal
ZP:0102561	posterior region caudal fin absent, abnormal
ZP:0102562	ventral region caudal fin absent, abnormal
ZP:0102563	ventral region trunk absent, abnormal
ZP:0102564	ventral region margin decreased distribution, abnormal
ZP:0102565	ventral region margin decreased amount, abnormal
ZP:0102566	ventral mesoderm mislocalised, abnormal
ZP:0102567	axial mesoderm increased amount, abnormal
ZP:0102568	axial mesoderm increased distribution, abnormal
ZP:0102569	nucleus presumptive mesoderm absent, abnormal
ZP:0102570	nucleus ectodermal cell absent, abnormal
ZP:0102571	male courtship behavior decreased process quality, abnormal
ZP:0102574	pancreas decreased occurrence pancreatic A cell differentiation, abnormal
ZP:0102575	endocrine pancreas has fewer parts of type pancreatic A cell, abnormal
ZP:0102576	islet decreased process quality cell differentiation, abnormal
ZP:0102577	exocrine pancreas malformed, abnormal
ZP:0102585	gut epithelium mislocalised, abnormal
ZP:0102586	intrapancreatic duct mislocalised, abnormal
ZP:0102587	axon cranial motor neuron decreased length, abnormal
ZP:0102588	otic vesicle decreased occurrence cell population proliferation, abnormal
ZP:0102589	stereocilium neuromast hair cell decreased length, abnormal
ZP:0102590	stereocilium neuromast hair cell decreased thickness, abnormal
ZP:0102591	autophagosome skeletal muscle increased amount, abnormal
ZP:0102592	glycogen granule heart increased amount, abnormal
ZP:0102593	glycogen granule liver increased amount, abnormal
ZP:0102594	glycogen granule skeletal muscle increased amount, abnormal
ZP:0102595	alpha-glucosidase activity decreased efficacy, abnormal
ZP:0102597	heart increased occurrence apoptotic process, abnormal
ZP:0102598	vasculature aortic arch hypoplastic, abnormal
ZP:0102603	ceratohyal cartilage process quality cartilage morphogenesis, abnormal
ZP:0102614	retroarticular decreased occurrence cell population proliferation, abnormal
ZP:0102616	axon cranial nerve VIII mislocalised, abnormal
ZP:0102617	cranial nerve VIII defasciculated, abnormal
ZP:0102622	cholesteryl ester blood plasma increased amount, abnormal
ZP:0102623	cardiac ventricle process quality action potential, abnormal
ZP:0102624	mitochondrion chondrocyte position, abnormal
ZP:0102625	endoplasmic reticulum chondrocyte position, abnormal
ZP:0102626	extracellular matrix chondrocyte spatial pattern, abnormal
ZP:0102627	chondrocyte decreased occurrence secretion, abnormal
ZP:0102647	dentary morphology, abnormal
ZP:0102650	ceratobranchial 5 bone absent, abnormal
ZP:0102651	endochondral bone absent, abnormal
ZP:0102652	head muscle decreased length, abnormal
ZP:0102653	microtubule organizing center chondrocyte disorganized, abnormal
ZP:0102654	Meckel's cartilage process quality cartilage morphogenesis, abnormal
ZP:0102655	chondrocyte Meckel's cartilage morphology, abnormal
ZP:0102656	chondrocyte Meckel's cartilage positional polarity, abnormal
ZP:0102657	chondrocyte palate decreased size, abnormal
ZP:0102659	maxilla absent, abnormal
ZP:0102660	quadrate absent, abnormal
ZP:0102662	branchiostegal ray absent, abnormal
ZP:0102664	chondrocyte proliferation disrupted, abnormal
ZP:0102665	epidermis decreased rate mitotic cell cycle, abnormal
ZP:0102676	muscle pioneer process quality skeletal muscle cell differentiation, abnormal
ZP:0102677	Z disc fast muscle cell increased thickness, abnormal
ZP:0102678	fast muscle cell decreased process quality skeletal muscle fiber development, abnormal
ZP:0102679	MiP motor neuron decreased process quality axon extension involved in axon guidance, abnormal
ZP:0102680	RoP motor neuron decreased process quality axon extension involved in axon guidance, abnormal
ZP:0102681	fast muscle cell myotome loose, abnormal
ZP:0102682	anatomical region Kupffer's vesicle decreased volume, abnormal
ZP:0102683	Kupffer's vesicle decreased occurrence tube formation, abnormal
ZP:0102684	anatomical space Kupffer's vesicle decreased volume, abnormal
ZP:0102685	Kupffer's vesicle shape, abnormal
ZP:0102686	right side diencephalon spatial pattern, abnormal
ZP:0102696	taurine whole organism decreased amount, abnormal
ZP:0102699	methionine whole organism decreased amount, abnormal
ZP:0102700	gamma-aminobutyric acid whole organism decreased amount, abnormal
ZP:0102702	L-saccharopine whole organism increased amount, abnormal
ZP:0102703	beta-alanine whole organism increased amount, abnormal
ZP:0102704	allysine whole organism increased amount, abnormal
ZP:0102705	pyridoxal whole organism decreased amount, abnormal
ZP:0102706	serine whole organism increased amount, abnormal
ZP:0102707	tyrosine whole organism increased amount, abnormal
ZP:0102708	alpha-aminobutyric acid whole organism decreased amount, abnormal
ZP:0102709	pipecolate whole organism increased amount, abnormal
ZP:0102710	1-piperideine-6-carboxylic acid whole organism increased amount, abnormal
ZP:0102715	optic tectum electric potential, abnormal
ZP:0102716	segmental plate increased amount, abnormal
ZP:0102717	neuron projection terminal nerve disorganized, abnormal
ZP:0102718	neuron projection terminal nerve decreased branchiness, abnormal
ZP:0102719	cell retinal inner nuclear layer swollen, abnormal
ZP:0102720	retinal inner nuclear layer hollow, abnormal
ZP:0102723	axoneme neural tube structure, abnormal
ZP:0102728	lateral dorsal aorta absent, abnormal
ZP:0102731	trunk vasculature absent, abnormal
ZP:0102737	lens decreased frequency autophagy, abnormal
ZP:0102738	spinal cord decreased frequency autophagy, abnormal
ZP:0102739	myotome decreased frequency autophagy, abnormal
ZP:0102740	optic cup decreased frequency autophagy, abnormal
ZP:0102741	lymphocyte thymus decreased amount, abnormal
ZP:0102742	cranial neural crest process quality neural crest cell differentiation, abnormal
ZP:0102743	ceratohyal cartilage decreased amount, abnormal
ZP:0102744	posterior region intermediate cell mass of mesoderm decreased amount, abnormal
ZP:0102745	caudal hematopoietic tissue decreased occurrence hematopoietic stem cell proliferation, abnormal
ZP:0102750	caudal vein plexus decreased volume, abnormal
ZP:0102751	blood island decreased rate hematopoietic stem cell proliferation, abnormal
ZP:0102752	head kidney increased rate hematopoietic stem cell proliferation, abnormal
ZP:0102753	sex differentiation process quality, abnormal
ZP:0102754	blood island increased occurrence hepatoblast apoptotic process, abnormal
ZP:0102755	pronephric distal late tubule decreased amount, abnormal
ZP:0102756	hematopoietic multipotent progenitor cell caudal hematopoietic tissue decreased amount, abnormal
ZP:0102771	thromboblast head kidney increased amount, abnormal
ZP:0102782	cranial neural crest cell increased occurrence cell death, abnormal
ZP:0102783	migratory cranial neural crest cell pharyngeal arch decreased amount, abnormal
ZP:0102784	raphe nucleus process quality neuronal action potential, abnormal
ZP:0102786	filopodium cranial neural crest cell decreased length, abnormal
ZP:0102787	filopodium cranial neural crest cell decreased amount, abnormal
ZP:0102788	pharyngeal pouch process quality neural crest cell migration, abnormal
ZP:0102789	pharyngeal pouch decreased occurrence neural crest cell migration, abnormal
ZP:0102790	macrophage migration decreased process quality, abnormal
ZP:0102791	blood island lacks all parts of type erythroid progenitor cell, abnormal
ZP:0102792	heart lacks all parts of type nucleate erythrocyte, abnormal
ZP:0102793	common cardinal vein lacks all parts of type nucleate erythrocyte, abnormal
ZP:0102794	optic tectum lacks parts or has fewer parts of type microglial cell, abnormal
ZP:0102795	macrophage retina decreased amount, abnormal
ZP:0102796	macrophage migration decreased rate, abnormal
ZP:0102797	macrophage retina mislocalised, abnormal
ZP:0102803	macrophage yolk increased amount, abnormal
ZP:0102806	neutrophil aggregated, abnormal
ZP:0102807	macrophage eye decreased amount, abnormal
ZP:0102808	macrophage vitreous decreased amount, abnormal
ZP:0102812	otic vesicle absent, abnormal
ZP:0102829	CaP motoneuron distance CaP motoneuron, abnormal
ZP:0102830	neuron undifferentiated, abnormal
ZP:0102831	trabecular layer of ventricle decreased object quality, abnormal
ZP:0102832	subcutaneous fat increased amount, abnormal
ZP:0102838	hematopoietic stem cell increased occurrence cell population proliferation, abnormal
ZP:0102840	cell-cell junction epidermis decreased amount, abnormal
ZP:0102841	nucleate erythrocyte increased accumulation pericardium, abnormal
ZP:0102842	actin cytoskeleton epidermis structure, abnormal
ZP:0102843	epidermal cell integument decreased area, abnormal
ZP:0102844	dorsal aorta disrupted blood vessel lumenization, abnormal
ZP:0102845	telomerase activity decreased process quality, abnormal
ZP:0102846	nucleate erythrocyte radius, abnormal
ZP:0102847	lipid male organism increased amount, abnormal
ZP:0102848	lipid female organism increased amount, abnormal
ZP:0102851	D3 vitamins liver decreased amount, abnormal
ZP:0102852	D3 vitamins blood plasma decreased amount, abnormal
ZP:0102853	D3 vitamins visceral fat decreased amount, abnormal
ZP:0102856	mitochondrion visceral fat membrane potential, abnormal
ZP:0102857	mitochondrion visceral fat decreased functionality, abnormal
ZP:0102858	mitochondrion visceral fat decreased amount, abnormal
ZP:0102861	visceral fat decreased amount, abnormal
ZP:0102863	swimming behavior increased rate, abnormal
ZP:0102864	eye increased height, abnormal
ZP:0102866	whole organism increased velocity, abnormal
ZP:0102867	head increased height, abnormal
ZP:0102871	eye increased width, abnormal
ZP:0102872	head increased length, abnormal
ZP:0102875	left side Kupffer's vesicle mislocalised, abnormal
ZP:0102878	very-low-density lipoprotein blood plasma decreased amount, abnormal
ZP:0102881	lipid blood plasma increased amount, abnormal
ZP:0102883	myeloid cell head kidney decreased amount, abnormal
ZP:0102884	optic primordium decreased distribution, abnormal
ZP:0102885	forebrain neural plate decreased distribution, abnormal
ZP:0102886	forebrain neural rod decreased distribution, abnormal
ZP:0102891	heart process rhythm quality, abnormal
ZP:0102893	photoreceptor outer segment blue sensitive photoreceptor cell decreased amount, abnormal
ZP:0102894	photoreceptor outer segment green sensitive photoreceptor cell decreased thickness, abnormal
ZP:0102896	photoreceptor outer segment red sensitive photoreceptor cell decreased amount, abnormal
ZP:0102897	photoreceptor outer segment retinal rod cell decreased thickness, abnormal
ZP:0102898	photoreceptor inner segment retina mislocalised, abnormal
ZP:0102899	filamentous actin retina disorganized, abnormal
ZP:0102902	axon trigeminal ganglion branchiness, abnormal
ZP:0102905	olfactory receptor cell absent, abnormal
ZP:0102906	germ line cell seminiferous tubule absent, abnormal
ZP:0102907	lymphocyte testis increased amount, abnormal
ZP:0102910	gonad decreased amount, abnormal
ZP:0102911	vacuole primordial germ cell increased amount, abnormal
ZP:0102912	primordial germ cell gonad decreased amount, abnormal
ZP:0102913	meiosis I arrested, abnormal
ZP:0102914	germ cell development arrested, abnormal
ZP:0102915	meiotic cell cycle arrested, abnormal
ZP:0102916	gonad spatial pattern, abnormal
ZP:0102919	melatonin whole organism decreased amount, abnormal
ZP:0102921	triglyceride skeletal muscle increased amount, abnormal
ZP:0102922	lipid skeletal muscle increased amount, abnormal
ZP:0102923	regulation of lipid metabolic process process quality, abnormal
ZP:0102924	muscle hyperplastic, abnormal
ZP:0102925	adipose tissue decreased amount, abnormal
ZP:0102926	muscle cell hyperplastic, abnormal
ZP:0102929	retinal pigmented epithelium has extra parts of type inclusion body retinal pigmented epithelium, abnormal
ZP:0102931	ciliary marginal zone increased occurrence apoptotic chromosome condensation, abnormal
ZP:0102932	cell ciliary marginal zone apoptotic, abnormal
ZP:0102933	digestion decreased rate, abnormal
ZP:0102935	digestive system delayed G1/S transition of mitotic cell cycle, abnormal
ZP:0102937	digestive system disrupted cell population proliferation, abnormal
ZP:0102938	whole organism decreased duration swimming, abnormal
ZP:0102939	spinal cord process quality ossification, abnormal
ZP:0102940	anatomical region Kupffer's vesicle spatial pattern, abnormal
ZP:0102941	Kupffer's vesicle structure, cavities, abnormal
ZP:0102942	Kupffer's vesicle uninflated, abnormal
ZP:0102945	pharyngeal arch 3 absent, abnormal
ZP:0102946	pharyngeal arch 4 absent, abnormal
ZP:0102948	lens increased occurrence cell death, abnormal
ZP:0102949	lens development in camera-type eye arrested, abnormal
ZP:0102952	lens epithelium mislocalised, abnormal
ZP:0102964	swim bladder flattened, abnormal
ZP:0102970	pronephric glomerular capillary collapsed, abnormal
ZP:0102971	blood plasma blood vasculature decreased amount, abnormal
ZP:0102972	glomerular filtration decreased occurrence, abnormal
ZP:0102974	anterior margin ethmoid cartilage emarginate, abnormal
ZP:0102975	pharyngeal arch 3-7 has fewer parts of type ectomesenchyme, abnormal
ZP:0102981	neuron projection cranial nerve II physical object quality, abnormal
ZP:0102982	cranial nerve II optic chiasm malformed, abnormal
ZP:0102983	NCC ionocyte gill decreased amount, abnormal
ZP:0102984	corpuscles of Stannius decreased amount, abnormal
ZP:0102986	chloride whole organism decreased amount, abnormal
ZP:0102987	sodium(1+) gill decreased amount, abnormal
ZP:0102988	sodium(1+) whole organism decreased amount, abnormal
ZP:0102991	vH ionocyte pronephric duct decreased amount, abnormal
ZP:0102992	vH ionocyte pronephric proximal convoluted tubule decreased amount, abnormal
ZP:0102993	vH ionocyte pronephric proximal straight tubule decreased amount, abnormal
ZP:0102999	glycosaminoglycan cornea increased amount, abnormal
ZP:0103020	nucleus lens fiber cell present, abnormal
ZP:0103021	early endosome lens fiber cell present, abnormal
ZP:0103022	late endosome lens fiber cell present, abnormal
ZP:0103023	late endosome lens fiber cell mislocalised, abnormal
ZP:0103024	organelle lens fiber cell present, abnormal
ZP:0103025	epithelial cell lens epithelium increased amount, abnormal
ZP:0103026	activation of cysteine-type endopeptidase activity involved in apoptotic process decreased process quality, abnormal
ZP:0103027	lens fiber cell increased amount, abnormal
ZP:0103028	estradiol blood decreased amount, abnormal
ZP:0103029	11-oxotestosterone blood decreased amount, abnormal
ZP:0103030	oocyte stage IV disrupted oocyte maturation, abnormal
ZP:0103036	female organism decreased rate ovulation, abnormal
ZP:0103037	oocyte stage IV disrupted meiosis II nuclear envelope disassembly, abnormal
ZP:0103038	hypophysis male organism decreased amount, abnormal
ZP:0103039	hypophysis female organism decreased amount, abnormal
ZP:0103040	flagellated sperm motility decreased process quality, abnormal
ZP:0103041	female organism proportionality to male organism, abnormal
ZP:0103042	female organism decreased female fertility, abnormal
ZP:0103043	female organism has fewer parts of type oocyte stage V, abnormal
ZP:0103044	ovary has fewer parts of type ovarian follicle stage IV, abnormal
ZP:0103045	testis lacks parts or has fewer parts of type sperm, abnormal
ZP:0103046	testis has extra parts of type spermatocyte, abnormal
ZP:0103047	testis has extra parts of type spermatogonium, abnormal
ZP:0103049	atrioventricular canal arrested endocardial cushion formation, abnormal
ZP:0103050	atrioventricular canal lacks all parts of type endocardial cushion atrioventricular canal, abnormal
ZP:0103051	atrioventricular canal endocardium absent, abnormal
ZP:0103052	whole organism ventralized, abnormal
ZP:0103053	anterior region neuroectoderm decreased distribution, abnormal
ZP:0103054	optic vesicle decreased distribution, abnormal
ZP:0103055	cilium lateral crista increased length, abnormal
ZP:0103056	cilium olfactory epithelium increased length, abnormal
ZP:0103057	ciliary base macula absent, abnormal
ZP:0103059	ciliary base macula decreased amount, abnormal
ZP:0103060	head decreased diameter, abnormal
ZP:0103064	atrioventricular canal endocardium increased occurrence Notch signaling involved in heart development, abnormal
ZP:0103065	ventricular endocardium increased distribution, abnormal
ZP:0103066	atrioventricular canal endocardium increased distribution, abnormal
ZP:0103068	germ line cell gonad absent, abnormal
ZP:0103069	germ line cell testis absent, abnormal
ZP:0103071	oogonia absent, abnormal
ZP:0103072	testis increased occurrence apoptotic process, abnormal
ZP:0103073	spermatogonium apoptotic, abnormal
ZP:0103074	spermatogonium deformed, abnormal
ZP:0103077	male organism proportionality to female organism, abnormal
ZP:0103078	estradiol blood absent, abnormal
ZP:0103079	immature gonad absent, abnormal
ZP:0103080	testosterone male organism increased amount, abnormal
ZP:0103082	estradiol female organism decreased amount, abnormal
ZP:0103083	11-oxotestosterone male organism increased amount, abnormal
ZP:0103088	bulbus arteriosus decreased amount, abnormal
ZP:0103089	cleithrum decreased process quality bone mineralization, abnormal
ZP:0103090	mouth shape, abnormal
ZP:0103092	chondrocyte palate circular, abnormal
ZP:0103093	chondrocyte palate size, abnormal
ZP:0103094	palate increased length, abnormal
ZP:0103095	palate decreased width, abnormal
ZP:0103096	palate process quality cell migration, abnormal
ZP:0103097	vertebra split, abnormal
ZP:0103098	vertebra curved, abnormal
ZP:0103099	mouth position, abnormal
ZP:0103100	caudal fin principal ray morphology, abnormal
ZP:0103101	caudal fin principal ray deformed, abnormal
ZP:0103102	caudal fin principal ray decreased amount, abnormal
ZP:0103103	nasal bone morphology, abnormal
ZP:0103104	caudal fin principal ray shortened, abnormal
ZP:0103105	vertebra caudal peduncle deformed, abnormal
ZP:0103106	caudal peduncle deformed, abnormal
ZP:0103107	horizontal plane cranium morphology, abnormal
ZP:0103108	dermis fin absent, abnormal
ZP:0103109	pelvic fin deformed, abnormal
ZP:0103110	lepidotrichium shortened, abnormal
ZP:0103111	paired fin shortened, abnormal
ZP:0103112	median fin shortened, abnormal
ZP:0103113	lepidotrichium segment shortened, abnormal
ZP:0103114	melanophore stripe increased distance melanophore stripe, abnormal
ZP:0103115	vertebra composition, abnormal
ZP:0103116	germ line cell gonad primordium decreased amount, abnormal
ZP:0103117	somatic cell gonad primordium morphology, abnormal
ZP:0103118	somatic cell gonad primordium absent, abnormal
ZP:0103119	somatic cell gonad primordium decreased amount, abnormal
ZP:0103120	gonad primordium absent, abnormal
ZP:0103121	germ line cell immature gonad decreased amount, abnormal
ZP:0103122	gonad primordium decreased process quality cell population proliferation, abnormal
ZP:0103123	germ line cell gonad decreased amount, abnormal
ZP:0103124	gonad disorganized, abnormal
ZP:0103125	Sertoli cell absent, abnormal
ZP:0103126	pericardium increased area, abnormal
ZP:0103127	atrium increased area, abnormal
ZP:0103128	17alpha-hydroxyprogesterone whole organism present, abnormal
ZP:0103129	cortisol whole organism decreased amount, abnormal
ZP:0103130	21-deoxycortisol whole organism present, abnormal
ZP:0103132	steroid biosynthetic process process quality, abnormal
ZP:0103134	neurohypophysis increased distribution, abnormal
ZP:0103135	adenohypophysis increased distribution, abnormal
ZP:0103136	interrenal gland increased size, abnormal
ZP:0103137	interrenal gland increased distribution, abnormal
ZP:0103139	thromboblast caudal hematopoietic tissue decreased amount, abnormal
ZP:0103140	chondrocyte neurocranial trabecula morphology, abnormal
ZP:0103141	mouth decreased width, abnormal
ZP:0103142	mesenchyme pharyngeal arch 1 decreased amount, abnormal
ZP:0103144	retinal rod cell decreased process quality photoreceptor cell outer segment organization, abnormal
ZP:0103145	cell body retinal rod cell mislocalised, abnormal
ZP:0103146	photoreceptor cell cilium retinal rod cell decreased length, abnormal
ZP:0103148	retinal rod cell lacks all parts of type photoreceptor outer segment retinal rod cell, abnormal
ZP:0103149	melanosome melanocyte mislocalised, abnormal
ZP:0103150	photoreceptor inner segment retinal cone cell mislocalised, abnormal
ZP:0103151	cell body retinal cone cell mislocalised, abnormal
ZP:0103152	synapse retinal cone cell mislocalised, abnormal
ZP:0103153	retinal cone cell decreased process quality retinal cone cell development, abnormal
ZP:0103154	ciliary base eye photoreceptor cell decreased amount, abnormal
ZP:0103156	yolk color, abnormal
ZP:0103161	fertilization increased occurrence, abnormal
ZP:0103162	whole organism increased fertility, abnormal
ZP:0103165	ethmoid cartilage cleft, abnormal
ZP:0103166	ethmoid cartilage circular, abnormal
ZP:0103167	axon spinal cord swollen, abnormal
ZP:0103168	axon posterior lateral line swollen, abnormal
ZP:0103174	axis elongation decreased occurrence, abnormal
ZP:0103175	embryonic structure decreased amount, abnormal
ZP:0103176	intersegmental vessel has fewer parts of type endothelial tip cell filopodium endothelial tip cell, abnormal
ZP:0103177	dorsal longitudinal anastomotic vessel decreased occurrence blood vessel morphogenesis, abnormal
ZP:0103178	photoreceptor outer segment retina decreased amount, abnormal
ZP:0103179	photoreceptor outer segment photoreceptor outer segment layer disoriented, abnormal
ZP:0103180	photoreceptor outer segment retinal cone cell mislocalised, abnormal
ZP:0103181	photoreceptor outer segment retinal rod cell mislocalised, abnormal
ZP:0103182	retinal inner nuclear layer incomplete structure, abnormal
ZP:0103183	retinal outer nuclear layer incomplete structure, abnormal
ZP:0103184	endothelial tip cell decreased rate cell migration involved in sprouting angiogenesis, abnormal
ZP:0103185	endothelial tip cell decreased occurrence cell division, abnormal
ZP:0103186	filamentous actin epidermal cell increased distribution, abnormal
ZP:0103187	spinal cord has fewer parts of type glioblast spinal cord, abnormal
ZP:0103190	spinal cord decreased rate mitotic cell cycle, abnormal
ZP:0103191	spinal cord decreased rate oligodendrocyte progenitor proliferation, abnormal
ZP:0103192	epidermal cell decreased size, abnormal
ZP:0103195	neuron projection terminus afferent neuron decreased amount, abnormal
ZP:0103196	posterior lateral line neuromast decreased occurrence innervation, abnormal
ZP:0103201	heart decreased process quality heart morphogenesis, abnormal
ZP:0103202	otic vesicle decreased process quality otolith development, abnormal
ZP:0103203	Kupffer's vesicle decreased occurrence motile cilium assembly, abnormal
ZP:0103204	pronephros decreased process quality epithelial cilium movement involved in extracellular fluid movement, abnormal
ZP:0103205	pancreatic A cell differentiation process quality, abnormal
ZP:0103210	left side lateral plate mesoderm absent, abnormal
ZP:0103212	left side lateral plate mesoderm decreased amount, abnormal
ZP:0103213	determination of intestine left/right asymmetry arrested, abnormal
ZP:0103214	pancreas bilateral, abnormal
ZP:0103217	pronephric proximal convoluted tubule decreased distribution, abnormal
ZP:0103218	pronephric proximal convoluted tubule decreased area, abnormal
ZP:0103219	endocrine pancreas spatial pattern, abnormal
ZP:0103220	whole organism has fewer parts of type forerunner cell group, abnormal
ZP:0103221	muscle cell structure, abnormal
ZP:0103222	skeletal muscle myofibril muscle cell structure, abnormal
ZP:0103223	myotome increased occurrence apoptotic process, abnormal
ZP:0103224	skeletal muscle fiber development decreased process quality, abnormal
ZP:0103225	muscle cell detached from myoseptum, abnormal
ZP:0103227	rhombomere decreased size, abnormal
ZP:0103228	presumptive neural retina increased amount, abnormal
ZP:0103229	presumptive neural retina decreased amount, abnormal
ZP:0103230	posterior lateral line ganglion decreased amount, abnormal
ZP:0103231	dopamine retina decreased amount, abnormal
ZP:0103232	dopaminergic neuron retinal inner nuclear layer decreased distribution, abnormal
ZP:0103235	pronephric tubule has fewer parts of type motile cilium inner dynein arm pronephric tubule, abnormal
ZP:0103236	pronephric tubule has fewer parts of type motile cilium outer dynein arm pronephric tubule, abnormal
ZP:0103237	motile cilium peripheral olfactory organ immobile, abnormal
ZP:0103238	motile cilium pronephric tubule immobile, abnormal
ZP:0103239	cytoplasm pronephric tubule decreased amount, abnormal
ZP:0103246	cardiac ventricle decreased process quality trabecula formation, abnormal
ZP:0103247	ventricular trabecula myocardium morphogenesis decreased process quality, abnormal
ZP:0103248	trabecular layer of ventricle malformed, abnormal
ZP:0103249	trabecular layer of ventricle lacks parts or has fewer parts of type cardiac muscle cell, abnormal
ZP:0103258	cell surface whole organism shape, abnormal
ZP:0103259	cranial motor neuron absent, abnormal
ZP:0103260	cortical actin cytoskeleton compact layer of ventricle spatial pattern, abnormal
ZP:0103261	cortical actin cytoskeleton compact layer of ventricle malformed, abnormal
ZP:0103263	focal adhesion heart absent, abnormal
ZP:0103265	liver decreased occurrence canonical Wnt signaling pathway, abnormal
ZP:0103266	exocrine pancreas decreased occurrence canonical Wnt signaling pathway, abnormal
ZP:0103272	endodermal cell liver decreased amount, abnormal
ZP:0103273	endodermal cell exocrine pancreas decreased amount, abnormal
ZP:0103279	anterior-posterior axis whole organism size, abnormal
ZP:0103280	angiogenic sprout intersegmental vessel morphology, abnormal
ZP:0103281	endothelial cell angiogenic sprout morphology, abnormal
ZP:0103282	cerebellar central artery process quality angiogenesis, abnormal
ZP:0103283	middle mesencephalic central artery process quality angiogenesis, abnormal
ZP:0103284	intersegmental vessel disrupted blood circulation, abnormal
ZP:0103285	nasal ciliary artery separated from angiogenic sprout dorsal ciliary vein, abnormal
ZP:0103286	angiogenic sprout mesencephalic vein morphology, abnormal
ZP:0103288	nucleate erythrocyte dorsal aorta decreased velocity, abnormal
ZP:0103296	parachordal vessel intersegmental vessel decreased amount, abnormal
ZP:0103301	notochord development process quality, abnormal
ZP:0103302	photoreceptor outer segment retinal cone cell decreased volume, abnormal
ZP:0103303	RoP motor neuron decreased amount, abnormal
ZP:0103304	CaP motoneuron increased branchiness, abnormal
ZP:0103305	primary motor neuron shape, abnormal
ZP:0103309	hemal arch increased thickness, abnormal
ZP:0103310	hemal arch increased volume, abnormal
ZP:0103311	neural arch increased thickness, abnormal
ZP:0103315	circadian sleep/wake cycle, wakefulness increased duration, abnormal
ZP:0103325	neuroectoderm increased amount, abnormal
ZP:0103327	presumptive rhombomere 4 decreased amount, abnormal
ZP:0103334	cranium decreased amount, abnormal
ZP:0103346	retinal ganglion cell axon guidance decreased process quality, abnormal
ZP:0103367	pronephric glomerulus increased occurrence apoptotic process, abnormal
ZP:0103383	central nervous system absent, abnormal
ZP:0103390	migratory neural crest cell increased amount, abnormal
ZP:0103414	pectoral fin bud decreased amount, abnormal
ZP:0103424	autophagosome heart increased amount, abnormal
ZP:0103425	eye photoreceptor cell increased occurrence apoptotic process, abnormal
ZP:0103426	ciliary basal body eye photoreceptor cell mislocalised, abnormal
ZP:0103427	perikaryon eye photoreceptor cell mislocalised, abnormal
ZP:0103428	ciliary basal body eye photoreceptor cell decreased amount, abnormal
ZP:0103429	retinal photoreceptor layer has fewer parts of type photoreceptor outer segment eye photoreceptor cell, abnormal
ZP:0103438	11-oxotestosterone whole organism increased amount, abnormal
ZP:0103439	lipid droplet muscle increased amount, abnormal
ZP:0103440	brain female organism decreased amount, abnormal
ZP:0103441	liver female organism decreased amount, abnormal
ZP:0103442	testis male organism increased size, abnormal
ZP:0103444	oocyte stage II increased amount, abnormal
ZP:0103445	unfertilized egg decreased amount, abnormal
ZP:0103446	Sertoli cell increased amount, abnormal
ZP:0103447	granulosa cell absent, abnormal
ZP:0103448	breeding tubercle male organism deformed, abnormal
ZP:0103449	breeding tubercle male organism decreased amount, abnormal
ZP:0103450	wound healing decreased occurrence, abnormal
ZP:0103451	angiogenic sprout central artery complexity, abnormal
ZP:0103452	angiogenic sprout central artery decreased amount, abnormal
ZP:0103453	angiogenic sprout central artery decreased branchiness, abnormal
ZP:0103454	nucleus cell increased amount, abnormal
ZP:0103455	EVL fused with nucleus nucleus EVL, abnormal
ZP:0103456	cell detached from cell, abnormal
ZP:0103457	cleavage furrow blastomere blurry, abnormal
ZP:0103458	cleavage furrow cell decreased amount, abnormal
ZP:0103460	acetylcholine-gated channel complex skeletal muscle decreased size, abnormal
ZP:0103461	neuromuscular junction skeletal muscle morphology, abnormal
ZP:0103462	skeletal muscle myofibril skeletal muscle structure, abnormal
ZP:0103463	liver primordium decreased amount, abnormal
ZP:0103464	posterior side neural plate T-shaped, abnormal
ZP:0103465	cell brain mislocalised, abnormal
ZP:0103466	neural tube duplicated, abnormal
ZP:0103467	retinal ganglion cell aplastic/hypoplastic, abnormal
ZP:0103468	myotome decreased magnitude skeletal muscle contraction, abnormal
ZP:0103469	sarcoplasm skeletal muscle cell increased size, abnormal
ZP:0103474	Z disc skeletal muscle cell malformed, abnormal
ZP:0103475	optic tectum decreased occurrence neuron projection development, abnormal
ZP:0103476	skeletal muscle cell decreased process quality sarcomere organization, abnormal
ZP:0103477	optic tectum has fewer parts of type neuron projection optic tectum, abnormal
ZP:0103478	oocyte stage I decreased occurrence establishment of cell polarity, abnormal
ZP:0103479	mitochondrial cloud oocyte stage I increased life span, abnormal
ZP:0103480	oocyte stage I polarity, abnormal
ZP:0103485	hematopoietic cell anterior lateral mesoderm decreased amount, abnormal
ZP:0103486	hematopoietic cell posterior lateral mesoderm decreased amount, abnormal
ZP:0103487	capillary endocrine pancreas decreased diameter, abnormal
ZP:0103488	capillary endocrine pancreas decreased amount, abnormal
ZP:0103492	dorsal telencephalon increased amount, abnormal
ZP:0103493	medial region ventral thalamus absent, abnormal
ZP:0103494	neuron projection ventral thalamus spatial pattern, abnormal
ZP:0103495	neuron projection ventral thalamus disorganized, abnormal
ZP:0103496	lateral region ventral thalamus increased amount, abnormal
ZP:0103498	pancreatic acinar cell exocrine pancreas disorganized, abnormal
ZP:0103499	pancreatic acinar cell exocrine pancreas dispersed, abnormal
ZP:0103501	macrophage head increased distribution, abnormal
ZP:0103503	intestine male organism increased amount, abnormal
ZP:0103504	intestine male organism decreased amount, abnormal
ZP:0103505	intestine female organism increased amount, abnormal
ZP:0103511	liver female organism increased amount, abnormal
ZP:0103512	caudal vein plexus increased permeability, abnormal
ZP:0103513	cranial vasculature decreased size, abnormal
ZP:0103514	neutrophil head increased distribution, abnormal
ZP:0103515	macrophage head decreased distribution, abnormal
ZP:0103516	neutrophil head decreased distribution, abnormal
ZP:0103518	nucleate erythrocyte caudal hematopoietic tissue increased amount, abnormal
ZP:0103519	monocyte pronephros increased amount, abnormal
ZP:0103520	myeloid cell caudal hematopoietic tissue increased amount, abnormal
ZP:0103521	basophilic erythroblast increased amount, abnormal
ZP:0103529	caudal hematopoietic tissue decreased amount, abnormal
ZP:0103530	myosin filament skeletal muscle disorganized, abnormal
ZP:0103531	pineal complex decreased distribution, abnormal
ZP:0103532	pineal complex decreased process quality animal organ formation, abnormal
ZP:0103533	left side habenula absent, abnormal
ZP:0103534	left side habenula increased amount, abnormal
ZP:0103535	pinealocyte decreased process quality pineal gland development, abnormal
ZP:0103536	pineal complex decreased occurrence cell differentiation, abnormal
ZP:0103537	pinealocyte decreased occurrence cell differentiation, abnormal
ZP:0103538	epiphysis process quality photoreceptor cell differentiation, abnormal
ZP:0103539	parapineal organ decreased process quality animal organ formation, abnormal
ZP:0103540	photoreceptor cell epiphysis absent, abnormal
ZP:0103541	photoreceptor cell epiphysis decreased amount, abnormal
ZP:0103542	pineal complex lacks all parts of type parapineal organ, abnormal
ZP:0103543	pineal complex lacks all parts of type pinealocyte, abnormal
ZP:0103544	parapineal organ absent, abnormal
ZP:0103545	pinealocyte absent, abnormal
ZP:0103546	whole organism decreased process quality DNA methylation, abnormal
ZP:0103547	estrogen female organism decreased amount, abnormal
ZP:0103548	3,3',5-triiodo-L-thyronine whole organism decreased amount, abnormal
ZP:0103549	epiphysis decreased distribution, abnormal
ZP:0103550	epiphysis increased occurrence neuron projection development, abnormal
ZP:0103551	visible light photoreceptor cell epiphysis absent, abnormal
ZP:0103552	median fin decreased size, abnormal
ZP:0103561	cell roof plate amount, abnormal
ZP:0103562	cell roof plate disorganized, abnormal
ZP:0103563	floor plate spatial pattern, abnormal
ZP:0103564	floor plate spinal cord region decreased amount, abnormal
ZP:0103565	dorsal side spinal cord increased amount, abnormal
ZP:0103585	gut cystic, abnormal
ZP:0103586	microvillus pronephros decreased amount, abnormal
ZP:0103589	ciliary basal body pronephros mislocalised, abnormal
ZP:0103591	ciliary membrane pronephros absent, abnormal
ZP:0103592	ciliary basal body-plasma membrane docking disrupted, abnormal
ZP:0103593	microvillus brush border epithelial cell absent, abnormal
ZP:0103594	peptidylglycine monooxygenase activity disrupted, abnormal
ZP:0103595	swim bladder arrested surfactant homeostasis, abnormal
ZP:0103596	swim bladder decreased occurrence surfactant homeostasis, abnormal
ZP:0103597	swim bladder decreased amount, abnormal
ZP:0103598	Melanin melanocyte decreased amount, abnormal
ZP:0103599	retinal pigmented epithelium decreased process quality melanosome organization, abnormal
ZP:0103600	melanocyte decreased occurrence cellular pigmentation, abnormal
ZP:0103601	eye decreased occurrence iridophore differentiation, abnormal
ZP:0103603	optic tectum has extra parts of type posterior region lysosome optic tectum, abnormal
ZP:0103604	optic tectum decreased process quality lysosome localization, abnormal
ZP:0103605	iridophore decreased process quality pigment granule organization, abnormal
ZP:0103606	iridophore differentiation decreased process quality, abnormal
ZP:0103607	iridophore lacks all parts of type iridosome iridophore, abnormal
ZP:0103608	integument decreased occurrence melanocyte differentiation, abnormal
ZP:0103609	integument decreased occurrence iridophore differentiation, abnormal
ZP:0103610	mesenchyme swim bladder decreased amount, abnormal
ZP:0103611	epithelium swim bladder decreased amount, abnormal
ZP:0103612	neuroblast brain decreased amount, abnormal
ZP:0103613	neuroblast hindbrain decreased amount, abnormal
ZP:0103614	neuroblast spinal cord decreased amount, abnormal
ZP:0103615	neuroblast forebrain decreased amount, abnormal
ZP:0103616	glioblast decreased amount, abnormal
ZP:0103617	homocysteine brain increased amount, abnormal
ZP:0103618	B cell head kidney decreased amount, abnormal
ZP:0103620	cell projection posterior lateral line neuromast direction, abnormal
ZP:0103630	central artery hindbrain increased branchiness, abnormal
ZP:0103631	transverse plane eye decreased length, abnormal
ZP:0103632	retinal neural layer folded, abnormal
ZP:0103633	retinal pigmented epithelium folded, abnormal
ZP:0103634	optic furrow increased amount, abnormal
ZP:0103635	closure of optic fissure decreased occurrence, abnormal
ZP:0103636	enteric nervous system decreased amount, abnormal
ZP:0103637	neuron projection intestine increased thickness, abnormal
ZP:0103638	neuron projection intestine disorganized, abnormal
ZP:0103639	neuron projection intestine shortened, abnormal
ZP:0103641	hatching behavior decreased rate, abnormal
ZP:0103643	presumptive rhombomere 4 increased amount, abnormal
ZP:0103644	presumptive rhombomere 3 increased amount, abnormal
ZP:0103645	hindbrain hemorrhagic, abnormal
ZP:0103646	muscle hemorrhagic, abnormal
ZP:0103647	gill filament hemorrhagic, abnormal
ZP:0103648	hemostasis disrupted, abnormal
ZP:0103651	presumptive rhombomere 4 mislocalised, abnormal
ZP:0103652	striated muscle myosin thick filament slow muscle cell decreased length, abnormal
ZP:0103653	striated muscle thin filament slow muscle cell decreased length, abnormal
ZP:0103664	intersegmental vein process quality sprouting angiogenesis, abnormal
ZP:0103665	angiogenic sprout intersegmental vein decreased length, abnormal
ZP:0103666	vascular lymphangioblast morphology, abnormal
ZP:0103671	cysteine-type endopeptidase activity involved in apoptotic process decreased process quality, abnormal
ZP:0103672	slow muscle cell somite 7 spatial pattern, abnormal
ZP:0103676	post-vent vasculature hemorrhagic, abnormal
ZP:0103677	startle response increased sensitivity of a process sensory perception of sound, abnormal
ZP:0103678	xanthophore disrupted pigment biosynthetic process, abnormal
ZP:0103685	testis increased occurrence cell population proliferation, abnormal
ZP:0103686	caudal fin decreased process quality male pigmentation, abnormal
ZP:0103687	pleuroperitoneal cavity male organism increased size, abnormal
ZP:0103688	pleuroperitoneal cavity female organism increased size, abnormal
ZP:0103689	developmental process involved in reproduction process quality, abnormal
ZP:0103690	male gonad development increased duration, abnormal
ZP:0103691	male gonad development peramorphic growth, abnormal
ZP:0103692	development of primary sexual characteristics process quality, abnormal
ZP:0103693	development of primary male sexual characteristics process quality, abnormal
ZP:0103694	oocyte development process quality, abnormal
ZP:0103695	ovary hypertrophic, abnormal
ZP:0103696	spermatid decreased amount, abnormal
ZP:0103697	oogonia increased amount, abnormal
ZP:0103698	testis spatial pattern, abnormal
ZP:0103699	testis increased distribution, abnormal
ZP:0103700	actin filament forerunner cell group structure, abnormal
ZP:0103701	somatic cell testis disorganized, abnormal
ZP:0103702	testis vacuolated, abnormal
ZP:0103703	oocyte stage I present, abnormal
ZP:0103704	Leydig cell testis increased amount, abnormal
ZP:0103705	heart tube spatial pattern, abnormal
ZP:0103706	axis increased amount, abnormal
ZP:0103707	axis increased distribution, abnormal
ZP:0103708	anatomical margin blastodisc increased amount, abnormal
ZP:0103709	cilium inner ear absent, abnormal
ZP:0103710	membrane photoreceptor cell irregularly shaped, abnormal
ZP:0103711	optic cup decreased rate cell population proliferation, abnormal
ZP:0103712	basement membrane optic cup morphology, abnormal
ZP:0103713	basement membrane disassembly disrupted, abnormal
ZP:0103715	brain decreased process quality cell population proliferation, abnormal
ZP:0103716	plasma membrane retinal rod cell mislocalised, abnormal
ZP:0103717	retinal photoreceptor layer retinal rod cell decreased thickness, abnormal
ZP:0103718	apical region photoreceptor cell mislocalised, abnormal
ZP:0103719	copper-63 liver decreased amount, abnormal
ZP:0103720	copper-63 midbrain decreased amount, abnormal
ZP:0103721	copper-63 retina absent, abnormal
ZP:0103722	copper-63 nervous system decreased amount, abnormal
ZP:0103723	copper-63 kidney increased amount, abnormal
ZP:0103724	copper-63 retinal outer nuclear layer decreased amount, abnormal
ZP:0103740	mRNA cis splicing, via spliceosome process quality, abnormal
ZP:0103748	convergent extension involved in axis elongation decreased occurrence, abnormal
ZP:0103751	photoreceptor outer segment layer spatial pattern, abnormal
ZP:0103752	cell midbrain degenerate, abnormal
ZP:0103753	cell midbrain vacuolated, abnormal
ZP:0103754	dorsal region midbrain increased amount, abnormal
ZP:0103755	dorsal region midbrain mislocalised, abnormal
ZP:0103756	epiboly increased duration, abnormal
ZP:0103757	mitotic G2 phase increased duration, abnormal
ZP:0103758	scale disrupted growth, abnormal
ZP:0103759	scale fin decreased size, abnormal
ZP:0103763	pronephric duct process quality regulation of autophagy, abnormal
ZP:0103765	endoplasmic reticulum lumen liver increased width, abnormal
ZP:0103766	endoplasmic reticulum lumen liver dilated, abnormal
ZP:0103767	endoplasmic reticulum lumen enterocyte increased width, abnormal
ZP:0103768	lipid droplet enterocyte increased amount, abnormal
ZP:0103769	low-density lipoprotein particle whole organism decreased amount, abnormal
ZP:0103771	retina decreased process quality transmission of nerve impulse, abnormal
ZP:0103772	retinal bipolar neuron decreased process quality transmission of nerve impulse, abnormal
ZP:0103773	cell hindbrain apoptotic, abnormal
ZP:0103774	ventricular zone spatial pattern, abnormal
ZP:0103775	dorso-lateral region hindbrain increased amount, abnormal
ZP:0103776	cell forebrain apoptotic, abnormal
ZP:0103777	cell third ventricle apoptotic, abnormal
ZP:0103778	tegmentum increased amount, abnormal
ZP:0103779	medulla oblongata decreased amount, abnormal
ZP:0103780	hindbrain nucleus decreased amount, abnormal
ZP:0103783	female organism decreased fecundity, abnormal
ZP:0103784	frontal bone morphology, abnormal
ZP:0103785	opercular flap morphology, abnormal
ZP:0103786	anal fin morphology, abnormal
ZP:0103787	dorsal fin morphology, abnormal
ZP:0103788	ovarian follicle stage IV degenerate, abnormal
ZP:0103791	exploration behavior decreased process quality, abnormal
ZP:0103803	musculoskeletal movement decreased frequency, abnormal
ZP:0103804	cell yolk syncytial layer position, abnormal
ZP:0103805	yolk syncytial layer absent, abnormal
ZP:0103806	DEL increased amount, abnormal
ZP:0103807	actin filament yolk syncytial layer structure, abnormal
ZP:0103808	blastoderm detached from yolk, abnormal
ZP:0103809	epiblast absent, abnormal
ZP:0103810	centrosome cell absent, abnormal
ZP:0103811	olfactory bulb absent, abnormal
ZP:0103814	shield spatial pattern, abnormal
ZP:0103828	mesodermal cell migration decreased process quality, abnormal
ZP:0103829	blastoderm spatial pattern, abnormal
ZP:0103830	caudal fin decreased occurrence blood circulation, abnormal
ZP:0103831	mesenchyme caudal fin morphology, abnormal
ZP:0103832	mesenchyme ventral fin fold morphology, abnormal
ZP:0103833	blood increased accumulation caudal fin, abnormal
ZP:0103834	endodermal cell apoptotic, abnormal
ZP:0103835	central artery increased branchiness, abnormal
ZP:0103836	endothelial cell cranial blood vessel spatial pattern, abnormal
ZP:0103838	optic tectum process quality neuronal action potential, abnormal
ZP:0103839	endoderm process quality cell migration involved in gastrulation, abnormal
ZP:0103840	blood accumulation blood vessel, abnormal
ZP:0103842	cardiac atrium morphogenesis decreased process quality, abnormal
ZP:0103843	atrial myocardium increased occurrence cell population proliferation, abnormal
ZP:0103844	atrium decreased process quality cardiac conduction, abnormal
ZP:0103848	retinal cone cell retinal outer nuclear layer decreased amount, abnormal
ZP:0103850	ciliary marginal zone mislocalised, abnormal
ZP:0103852	nucleus nucleate erythrocyte size, abnormal
ZP:0103856	hyoid muscle decreased process quality tendon formation, abnormal
ZP:0103857	skeletal muscle cell interhyoideus mislocalised, abnormal
ZP:0103858	ventral intermandibularis posterior decreased process quality determination of muscle attachment site, abnormal
ZP:0103859	interhyoideus decreased process quality determination of muscle attachment site, abnormal
ZP:0103860	skeletal muscle cell sternohyoid mislocalised medially, abnormal
ZP:0103861	skeletal muscle cell ventral intermandibularis anterior mislocalised, abnormal
ZP:0103862	skeletal muscle cell ventral intermandibularis posterior mislocalised, abnormal
ZP:0103863	skeletal muscle cell hyohyoideus mislocalised, abnormal
ZP:0103864	ventral intermandibularis posterior increased length, abnormal
ZP:0103865	anterior region basihyal cartilage hypoplastic, abnormal
ZP:0103866	medial region Meckel's cartilage malformed, abnormal
ZP:0103867	medial region ceratohyal cartilage malformed, abnormal
ZP:0103869	mandibular muscle decreased process quality tendon development, abnormal
ZP:0103870	hyoid muscle decreased process quality tendon development, abnormal
ZP:0103871	anterior region basihyal cartilage decreased width, abnormal
ZP:0103872	parasphenoid decreased width, abnormal
ZP:0103873	adenohypophyseal placode decreased amount, abnormal
ZP:0103874	thymus primordium has fewer parts of type lymphocyte, abnormal
ZP:0103880	paired fin decreased amount, abnormal
ZP:0103881	ventral region iris morphology, abnormal
ZP:0103882	ethmoid cartilage size, abnormal
ZP:0103883	anterior chamber eye decreased size, abnormal
ZP:0103884	integument anterior segment eye mislocalised, abnormal
ZP:0103885	cartilage tissue eye mislocalised, abnormal
ZP:0103886	cartilage tissue anterior segment eye mislocalised, abnormal
ZP:0103887	eye opacity, abnormal
ZP:0103888	iris absent, abnormal
ZP:0103889	iris hypoplastic, abnormal
ZP:0103890	corneal epithelium mislocalised, abnormal
ZP:0103891	corneal epithelium vacuolated, abnormal
ZP:0103892	corneal epithelium decreased amount, abnormal
ZP:0103893	corneal stroma morphology, abnormal
ZP:0103894	corneal stroma spatial pattern, abnormal
ZP:0103895	corneal stroma position, abnormal
ZP:0103896	corneal stroma increased thickness, abnormal
ZP:0103897	corneal stroma decreased thickness, abnormal
ZP:0103898	corneal stroma undulate, abnormal
ZP:0103899	corneal endothelium morphology, abnormal
ZP:0103900	corneal endothelium increased thickness, abnormal
ZP:0103901	corneal endothelium disorganized, abnormal
ZP:0103902	iris stroma morphology, abnormal
ZP:0103903	lens capsule morphology, abnormal
ZP:0103904	anterior chamber eye morphology, abnormal
ZP:0103905	anterior chamber eye absent, abnormal
ZP:0103906	cornea abutting lens capsule, abnormal
ZP:0103907	annular ligament morphology, abnormal
ZP:0103908	corneal epithelium irregular thickness, abnormal
ZP:0103909	corneal stroma irregular thickness, abnormal
ZP:0103911	vasculature decreased functionality, abnormal
ZP:0103912	dorsal region whole organism absent, abnormal
ZP:0103913	axial mesoderm decreased process quality mediolateral intercalation, abnormal
ZP:0103914	lateral margin notochord irregularly shaped, abnormal
ZP:0103915	whole organism decreased occurrence cell population proliferation, abnormal
ZP:0103916	notochord process quality cell-cell adhesion, abnormal
ZP:0103917	cell Kupffer's vesicle morphology, abnormal
ZP:0103918	left/right pattern formation decreased occurrence, abnormal
ZP:0103919	palate disrupted cell population proliferation, abnormal
ZP:0103920	cranial neural crest cell disrupted cell population proliferation, abnormal
ZP:0103921	splanchnocranium process quality skeletal muscle tissue development, abnormal
ZP:0103922	sarcomere interhyoideus disorganized, abnormal
ZP:0103923	Z disc interhyoideus absent, abnormal
ZP:0103924	A band interhyoideus absent, abnormal
ZP:0103925	I band interhyoideus absent, abnormal
ZP:0103926	anterior region central nervous system malformed, abnormal
ZP:0103927	ventro-medial region brain absent, abnormal
ZP:0103928	neuron spinal cord absent, abnormal
ZP:0103929	floor plate spinal cord region absent, abnormal
ZP:0103930	pharyngeal endoderm absent, abnormal
ZP:0103931	pharyngeal mesoderm absent, abnormal
ZP:0103932	dorsal region germ ring decreased amount, abnormal
ZP:0103933	germ ring spatial pattern, abnormal
ZP:0103934	anterior region axial mesoderm absent, abnormal
ZP:0103935	posterior region axial mesoderm absent, abnormal
ZP:0103936	axial chorda mesoderm absent, abnormal
ZP:0103937	hypoblast absent, abnormal
ZP:0103938	neuroectoderm absent, abnormal
ZP:0103947	glycogen hepatocyte decreased amount, abnormal
ZP:0103948	cytoplasm hepatocyte mislocalised, abnormal
ZP:0103949	mitochondrion hepatocyte malformed, abnormal
ZP:0103950	hepatocyte increased occurrence autophagy, abnormal
ZP:0103951	intracellular canaliculus hepatocyte spatial pattern, abnormal
ZP:0103953	bile acid secretion decreased occurrence, abnormal
ZP:0103954	bile canaliculus spatial pattern, abnormal
ZP:0103955	hepatocyte has extra parts of type autophagosome hepatocyte, abnormal
ZP:0103956	bile canaliculus malformed, abnormal
ZP:0103957	mitochondrion hepatocyte swollen, abnormal
ZP:0103958	plasma membrane hepatocyte degenerate, abnormal
ZP:0103959	mitochondrial crista hepatocyte degenerate, abnormal
ZP:0103960	posterior region gut epithelium absent, abnormal
ZP:0103961	intracellular canaliculus hepatocyte absent, abnormal
ZP:0103962	bile canaliculus absent, abnormal
ZP:0103965	EVL broken, abnormal
ZP:0103967	midbrain hindbrain boundary neural tube morphology, abnormal
ZP:0103970	cell periderm increased size, abnormal
ZP:0103972	neuron projection cranial nerve X decreased amount, abnormal
ZP:0103973	intestinal motility disrupted, abnormal
ZP:0103977	ventricular epicardium absent, abnormal
ZP:0103978	hindbrain decreased height, abnormal
ZP:0103980	head kidney decreased volume, abnormal
ZP:0103981	microglial cell retina increased amount, abnormal
ZP:0103983	lymph vessel trunk absent, abnormal
ZP:0103984	facial lymphatic vessel decreased amount, abnormal
ZP:0103985	posterior cardinal vein disrupted sprouting angiogenesis, abnormal
ZP:0103986	primordial hindbrain channel immature, abnormal
ZP:0103988	intersegmental vein somite decreased amount, abnormal
ZP:0103989	intersegmental vessel thoracic duct absent, abnormal
ZP:0103990	primordial germ cell morphology, abnormal
ZP:0103991	primordial germ cell decreased occurrence cell migration, abnormal
ZP:0103993	cardiac muscle cell bulbus arteriosus decreased amount, abnormal
ZP:0103994	closure of optic fissure delayed, abnormal
ZP:0103995	optic cup mislocalised, abnormal
ZP:0103996	optic cup increased distribution, abnormal
ZP:0103997	retina delayed cell cycle arrest, abnormal
ZP:0103999	retina decreased occurrence cell division, abnormal
ZP:0104000	retinal cell apoptotic process increased occurrence, abnormal
ZP:0104001	retina degree of pigmentation, abnormal
ZP:0104002	retinal ganglion cell layer increased width, abnormal
ZP:0104003	retinal inner nuclear layer increased width, abnormal
ZP:0104004	cardiac muscle myoblast disrupted cell population proliferation, abnormal
ZP:0104005	MAP kinase kinase activity increased rate, abnormal
ZP:0104007	lens morphogenesis in camera-type eye decreased process quality, abnormal
ZP:0104008	lens fiber cell differentiation increased occurrence, abnormal
ZP:0104021	cysteine whole organism increased amount, abnormal
ZP:0104022	cystine whole organism increased amount, abnormal
ZP:0104023	glutathione disulfide whole organism increased amount, abnormal
ZP:0104027	cystine brain increased amount, abnormal
ZP:0104028	cystine heart increased amount, abnormal
ZP:0104029	cystine liver increased amount, abnormal
ZP:0104030	cystine kidney increased amount, abnormal
ZP:0104031	neutrophilic myelocyte blood increased amount, abnormal
ZP:0104032	neutrophilic metamyelocyte blood increased amount, abnormal
ZP:0104033	memory process quality, abnormal
ZP:0104035	response to misfolded protein increased occurrence, abnormal
ZP:0104036	female organism process quality oocyte maturation, abnormal
ZP:0104038	male organism arrested sperm ejaculation, abnormal
ZP:0104039	male organism increased occurrence development of secondary female sexual characteristics, abnormal
ZP:0104041	male organism decreased occurrence development of secondary male sexual characteristics, abnormal
ZP:0104043	ovary female organism decreased amount, abnormal
ZP:0104044	female organism has fewer parts of type ovary oocyte stage III, abnormal
ZP:0104045	female organism has extra parts of type ovary oocyte stage I, abnormal
ZP:0104046	trunk male organism obtuse, abnormal
ZP:0104050	anal fin male organism white, abnormal
ZP:0104052	seminiferous tubule male organism malformed, abnormal
ZP:0104053	seminiferous tubule male organism disorganized, abnormal
ZP:0104054	spermatogenic cyst male organism malformed, abnormal
ZP:0104055	spermatogenic cyst male organism disorganized, abnormal
ZP:0104057	ovary delayed oocyte maturation, abnormal
ZP:0104058	testis delayed spermatid development, abnormal
ZP:0104060	female organism lacks all parts of type ovary oocyte stage III, abnormal
ZP:0104061	testis lacks all parts of type spermatid, abnormal
ZP:0104063	retina decreased process quality detection of light stimulus involved in visual perception, abnormal
ZP:0104065	synapse eye photoreceptor cell mislocalised, abnormal
ZP:0104066	photoreceptor inner segment layer mislocalised, abnormal
ZP:0104068	positive regulation of NIK/NF-kappaB signaling disrupted, abnormal
ZP:0104073	atrial cardiac muscle cell action potential decreased duration, abnormal
ZP:0104074	whole organism has fewer parts of type pectoral fin, abnormal
ZP:0104075	lymphoid progenitor cell caudal hematopoietic tissue increased amount, abnormal
ZP:0104076	T cell migration decreased process quality, abnormal
ZP:0104077	cartilage tissue decreased amount, abnormal
ZP:0104078	pectoral fin cartilage decreased amount, abnormal
ZP:0104079	pharyngeal pouch 1 decreased amount, abnormal
ZP:0104083	anatomical region thymus increased amount, abnormal
ZP:0104084	anatomical region thymus decreased amount, abnormal
ZP:0104085	T cell increased occurrence apoptotic process, abnormal
ZP:0104086	T cell decreased occurrence cell maturation, abnormal
ZP:0104088	ventral telencephalon increased amount, abnormal
ZP:0104089	facial ganglion decreased distribution, abnormal
ZP:0104090	facial ganglion decreased amount, abnormal
ZP:0104091	glossopharyngeal ganglion decreased amount, abnormal
ZP:0104092	vagal ganglion 1 decreased distribution, abnormal
ZP:0104093	vagal ganglion 1 decreased amount, abnormal
ZP:0104094	vagal ganglion 2 decreased distribution, abnormal
ZP:0104095	vagal ganglion 2 decreased amount, abnormal
ZP:0104096	vagal ganglion 1 spatial pattern, abnormal
ZP:0104097	vagal ganglion 2 spatial pattern, abnormal
ZP:0104098	otic placode increased amount, abnormal
ZP:0104106	ectoderm absent, abnormal
ZP:0104107	yolk syncytial layer decreased thickness, abnormal
ZP:0104116	notochord decreased distance prechordal plate, abnormal
ZP:0104117	forerunner cell group process quality cell migration, abnormal
ZP:0104118	presumptive paraxial mesoderm spatial pattern, abnormal
ZP:0104119	presumptive ventral mesoderm increased distribution, abnormal
ZP:0104120	obsolete cell notochord cuboid, abnormal
ZP:0104121	mediolateral intercalation decreased process quality, abnormal
ZP:0104122	anterior-posterior axis somite decreased width, abnormal
ZP:0104128	trabecular layer of ventricle increased thickness, abnormal
ZP:0104131	cell migration involved in mesendoderm migration process quality, abnormal
ZP:0104132	extracellular matrix endoderm decreased amount, abnormal
ZP:0104133	extracellular matrix organization process quality, abnormal
ZP:0104134	fibronectin fibril organization decreased process quality, abnormal
ZP:0104135	antero-dorsal region rhombomere 1 absent, abnormal
ZP:0104136	antero-dorsal region rhombomere 1 increased amount, abnormal
ZP:0104137	anterior margin hindbrain increased amount, abnormal
ZP:0104138	anterior margin hindbrain mislocalised, abnormal
ZP:0104139	cerebellar granule cell differentiation decreased process quality, abnormal
ZP:0104140	corpus cerebelli has fewer parts of type parallel fiber, abnormal
ZP:0104141	cerebellar granule cell precursor tangential migration decreased process quality, abnormal
ZP:0104146	cardioblast migration to the midline involved in heart field formation decreased occurrence, abnormal
ZP:0104149	compact layer of ventricle increased occurrence cardiac muscle cell proliferation, abnormal
ZP:0104150	compact layer of ventricle increased thickness, abnormal
ZP:0104151	corpus cerebelli decreased occurrence cerebellar granule cell differentiation, abnormal
ZP:0104152	granular eminence decreased occurrence cerebellar granule cell differentiation, abnormal
ZP:0104153	medial caudal lobe decreased occurrence cerebellar granule cell differentiation, abnormal
ZP:0104154	cerebellar granule cell corpus cerebelli decreased amount, abnormal
ZP:0104155	cerebellar granule cell granular eminence decreased amount, abnormal
ZP:0104156	cerebellar granule cell medial caudal lobe decreased amount, abnormal
ZP:0104157	glutamatergic neuron cerebellum decreased amount, abnormal
ZP:0104158	corpus cerebelli has fewer parts of type cerebellar granule cell, abnormal
ZP:0104159	granular eminence has fewer parts of type cerebellar granule cell, abnormal
ZP:0104160	medial caudal lobe increased amount, abnormal
ZP:0104161	medial caudal lobe mislocalised, abnormal
ZP:0104162	medial caudal lobe has fewer parts of type cerebellar granule cell, abnormal
ZP:0104165	mitochondrion whole organism decreased amount, abnormal
ZP:0104166	mandibular arch skeleton disrupted bone mineralization, abnormal
ZP:0104167	ceratobranchial 5 tooth detached from mandibular arch skeleton, abnormal
ZP:0104168	palatoquadrate arch decreased thickness, abnormal
ZP:0104170	ceratobranchial 5 tooth disrupted tooth mineralization, abnormal
ZP:0104172	dentinogenesis disrupted, abnormal
ZP:0104174	tooth placode disoriented, abnormal
ZP:0104175	tooth pulp disorganized, abnormal
ZP:0104176	tooth pulp increased mass density, abnormal
ZP:0104177	odontoblast shape, abnormal
ZP:0104179	iron(3+) whole organism increased amount, abnormal
ZP:0104181	iron(3+) brain increased amount, abnormal
ZP:0104183	iron(3+) gut increased amount, abnormal
ZP:0104184	iron(3+) liver increased amount, abnormal
ZP:0104187	iron(3+) muscle increased amount, abnormal
ZP:0104188	cartilage tissue palate shortened, abnormal
ZP:0104189	ceratobranchial 5 cartilage morphology, abnormal
ZP:0104190	ventral region hypothalamus increased amount, abnormal
ZP:0104191	ventral region hypothalamus increased distribution, abnormal
ZP:0104192	hypocretin-secreting neuron hypothalamus increased amount, abnormal
ZP:0104193	insulin-like growth factor receptor signaling pathway increased occurrence, abnormal
ZP:0104194	superior raphe nucleus increased amount, abnormal
ZP:0104195	locus coeruleus increased amount, abnormal
ZP:0104196	vertebra decreased occurrence ossification, abnormal
ZP:0104197	Melanin eye decreased amount, abnormal
ZP:0104199	neuron development disrupted, abnormal
ZP:0104201	magnesium(2+) whole organism decreased amount, abnormal
ZP:0104202	post-vent region disrupted blood circulation, abnormal
ZP:0104203	yolk disrupted metabolic process, abnormal
ZP:0104206	axon Mauthner neuron absent, abnormal
ZP:0104208	posterior lateral line delayed myelination in peripheral nervous system, abnormal
ZP:0104209	posterior lateral line delayed myelination of posterior lateral line nerve axons, abnormal
ZP:0104210	myelinating Schwann cell posterior lateral line decreased distribution, abnormal
ZP:0104212	immature Schwann cell posterior lateral line decreased distribution, abnormal
ZP:0104213	immature Schwann cell posterior lateral line decreased amount, abnormal
ZP:0104215	caudal fin increased process quality I-kappaB kinase/NF-kappaB signaling, abnormal
ZP:0104216	ceratohyal cartilage decreased distance Meckel's cartilage, abnormal
ZP:0104217	post-vent vasculature fused with post-vent vasculature, abnormal
ZP:0104221	dorsal region eye decreased distribution, abnormal
ZP:0104222	dorsal region eye decreased amount, abnormal
ZP:0104227	blood vessel compact layer of ventricle increased amount, abnormal
ZP:0104230	blood vessel superior ocular sulcus decreased size, abnormal
ZP:0104231	blood vessel superior ocular sulcus decreased branchiness, abnormal
ZP:0104233	blood vessel superior ocular sulcus degenerate, abnormal
ZP:0104235	statoacoustic (VIII) ganglion absent, abnormal
ZP:0104236	anterior lateral line ganglion decreased amount, abnormal
ZP:0104237	caudal vein plexus decreased occurrence sprouting angiogenesis, abnormal
ZP:0104238	blood increased accumulation caudal vein plexus, abnormal
ZP:0104240	epidermis increased occurrence apoptotic process, abnormal
ZP:0104243	trunk decreased occurrence startle response, abnormal
ZP:0104245	trunk decreased occurrence thigmotaxis, abnormal
ZP:0104246	corpus cerebelli decreased size, abnormal
ZP:0104247	diffuse nucleus inferior lobe increased amount, abnormal
ZP:0104248	ventral hypothalamic zone decreased amount, abnormal
ZP:0104249	nucleate erythrocyte vasculature absent, abnormal
ZP:0104251	cell dorsal aorta increased area, abnormal
ZP:0104252	iridophore opercular flap decreased amount, abnormal
ZP:0104253	opercular flap has fewer parts of type iridophore, abnormal
ZP:0104256	regenerating fin process quality blood circulation, abnormal
ZP:0104257	artery regenerating fin increased diameter, abnormal
ZP:0104258	artery regenerating fin increased area, abnormal
ZP:0104259	vein regenerating fin increased diameter, abnormal
ZP:0104260	vein regenerating fin increased area, abnormal
ZP:0104261	blood vessel brain irregular spatial pattern, abnormal
ZP:0104262	blood vessel brain dilated, abnormal
ZP:0104263	blood vessel brain kinked, abnormal
ZP:0104264	endothelial cell artery decreased mass density, abnormal
ZP:0104265	endothelial cell vein increased amount, abnormal
ZP:0104266	blood accumulation vasculature regenerating fin, abnormal
ZP:0104267	intersegmental vein decreased process quality blood circulation, abnormal
ZP:0104268	vein intersegmental vein decreased diameter, abnormal
ZP:0104270	arteriole intersegmental vein dilated, abnormal
ZP:0104271	blood cell dorsal aorta increased velocity, abnormal
ZP:0104272	blood cell posterior cardinal vein increased velocity, abnormal
ZP:0104273	nucleate erythrocyte intersegmental vein absent, abnormal
ZP:0104277	gap junction spinal cord interneuron absent, abnormal
ZP:0104278	gap junction Mauthner neuron absent, abnormal
ZP:0104279	spinal cord interneuron decreased occurrence gap junction assembly, abnormal
ZP:0104280	Mauthner neuron decreased occurrence gap junction assembly, abnormal
ZP:0104281	spinal cord interneuron arrested gap junction-mediated intercellular transport, abnormal
ZP:0104282	Mauthner neuron arrested gap junction-mediated intercellular transport, abnormal
ZP:0104286	rhombomere 4 decreased amount, abnormal
ZP:0104287	rhombomere 3 spatial pattern, abnormal
ZP:0104288	rhombomere 4 absent, abnormal
ZP:0104289	rhombomere 4 decreased distribution, abnormal
ZP:0104290	anterior/posterior compartment boundary rhombomere 2 morphology, abnormal
ZP:0104291	anterior/posterior compartment boundary rhombomere 2 absent, abnormal
ZP:0104292	anterior/posterior compartment boundary rhombomere 5 spatial pattern, abnormal
ZP:0104293	anterior/posterior compartment boundary rhombomere 5 decreased distribution, abnormal
ZP:0104294	anterior/posterior compartment boundary rhombomere 3 morphology, abnormal
ZP:0104295	anterior/posterior compartment boundary rhombomere 3 spatial pattern, abnormal
ZP:0104296	anterior/posterior compartment boundary rhombomere 3 absent, abnormal
ZP:0104297	anterior/posterior compartment boundary rhombomere 3 decreased distribution, abnormal
ZP:0104298	anterior/posterior compartment boundary rhombomere 4 morphology, abnormal
ZP:0104299	anterior/posterior compartment boundary rhombomere 4 spatial pattern, abnormal
ZP:0104300	anterior/posterior compartment boundary rhombomere 4 absent, abnormal
ZP:0104301	anterior/posterior compartment boundary rhombomere 4 decreased distribution, abnormal
ZP:0104302	migratory cranial neural crest rhombomere 2 morphology, abnormal
ZP:0104303	migratory cranial neural crest rhombomere 2 spatial pattern, abnormal
ZP:0104304	rhombomere 2 fused with migratory cranial neural crest migratory cranial neural crest rhombomere 4, abnormal
ZP:0104305	migratory cranial neural crest rhombomere 4 morphology, abnormal
ZP:0104306	migratory cranial neural crest rhombomere 4 spatial pattern, abnormal
ZP:0104307	MiD3cm absent, abnormal
ZP:0104317	hemoglobin whole organism decreased amount, abnormal
ZP:0104318	retina process quality transmission of nerve impulse, abnormal
ZP:0104319	periciliary membrane compartment photoreceptor cell absent, abnormal
ZP:0104320	periciliary membrane compartment photoreceptor cell decreased amount, abnormal
ZP:0104321	cranial division of the internal carotid artery dysplastic, abnormal
ZP:0104322	basal communicating artery fused with primordial midbrain channel, abnormal
ZP:0104323	basal communicating artery dilated, abnormal
ZP:0104324	basal communicating artery deformed, abnormal
ZP:0104325	posterior communicating artery dilated, abnormal
ZP:0104326	posterior communicating artery deformed, abnormal
ZP:0104327	basilar artery fused with primordial hindbrain channel, abnormal
ZP:0104329	central canal decreased occurrence detection of mechanical stimulus, abnormal
ZP:0104331	olfactory receptor cell process quality axon guidance, abnormal
ZP:0104332	olfactory receptor cell displaced to neuron projection central zone olfactory bulb, abnormal
ZP:0104333	dorsal zone olfactory bulb has fewer parts of type neuron projection olfactory receptor cell, abnormal
ZP:0104334	olfactory receptor cell displaced to neuron projection dorsal zone olfactory bulb, abnormal
ZP:0104335	central zone olfactory bulb has fewer parts of type neuron projection olfactory receptor cell, abnormal
ZP:0104336	maG1 has extra parts of type neuron projection olfactory receptor cell, abnormal
ZP:0104337	spinal cord decreased occurrence epithelial cilium movement involved in extracellular fluid movement, abnormal
ZP:0104338	spinal cord decreased occurrence cerebrospinal fluid circulation, abnormal
ZP:0104339	mechanoreceptor cell central canal decreased functionality, abnormal
ZP:0104340	mechanoreceptor cell central canal absent, abnormal
ZP:0104341	vertebral column decreased process quality skeletal system development, abnormal
ZP:0104342	vertebral column convex, abnormal
ZP:0104343	glucagon blood plasma decreased amount, abnormal
ZP:0104344	branchiomotor neuron rhombomere 6 absent, abnormal
ZP:0104345	motor neuron migration decreased occurrence, abnormal
ZP:0104346	branchiomotor neuron rhombomere 6 decreased amount, abnormal
ZP:0104348	whole organism decreased occurrence double-strand break repair, abnormal
ZP:0104351	pronephric glomerulus development decreased occurrence, abnormal
ZP:0104352	interrenal primordium increased amount, abnormal
ZP:0104353	interrenal primordium increased distribution, abnormal
ZP:0104355	cardiac muscle cell polyploid, abnormal
ZP:0104356	pancreatic A cell primary islet decreased amount, abnormal
ZP:0104360	neuromuscular junction trunk musculature malformed, abnormal
ZP:0104361	skeletal muscle cell trunk musculature irregular spatial pattern, abnormal
ZP:0104362	skeletal muscle cell trunk musculature sparse, abnormal
ZP:0104363	motor neuron malformed, abnormal
ZP:0104367	anatomical space Kupffer's vesicle increased permeability, abnormal
ZP:0104368	tight junction Kupffer's vesicle structure, abnormal
ZP:0104369	blood cell accumulation anatomical region caudal fin, abnormal
ZP:0104370	blood cell accumulation yolk, abnormal
ZP:0104382	dorsal aorta decreased efficacy blood circulation, abnormal
ZP:0104383	caudal vein decreased efficacy blood circulation, abnormal
ZP:0104384	intersegmental vessel decreased efficacy blood circulation, abnormal
ZP:0104386	caudal artery increased distribution, abnormal
ZP:0104387	caudal vein plexus increased amount, abnormal
ZP:0104388	caudal vein plexus mislocalised, abnormal
ZP:0104389	caudal vein plexus increased distribution, abnormal
ZP:0104395	caudal artery decreased distribution, abnormal
ZP:0104396	caudal artery decreased amount, abnormal
ZP:0104411	pronephros lacks parts or has fewer parts of type pronephric podocyte, abnormal
ZP:0104412	pancreatic B cell exocrine pancreas increased amount, abnormal
ZP:0104418	dark adaptation increased process quality, abnormal
ZP:0104422	head lacks parts or has fewer parts of type eye, abnormal
ZP:0104424	GABAergic neuron decreased occurrence axon arborization, abnormal
ZP:0104425	optic tectum increased occurrence neuronal action potential, abnormal
ZP:0104426	optic tectum decreased occurrence negative regulation of neuronal action potential, abnormal
ZP:0104436	vertebral column curved dorsal, abnormal
ZP:0104441	filamentous actin lens disorganized, abnormal
ZP:0104442	pharyngeal arch 2 spatial pattern, abnormal
ZP:0104455	dorsal region VeLD absent, abnormal
ZP:0104456	dorsal region VeLD decreased amount, abnormal
ZP:0104457	medial region Kolmer-Agduhr neuron absent, abnormal
ZP:0104458	medial region Kolmer-Agduhr neuron decreased amount, abnormal
ZP:0104459	Kolmer-Agduhr neuron lacks parts or has fewer parts of type medial region GABAergic neuron, abnormal
ZP:0104460	ventral region VeLD absent, abnormal
ZP:0104461	ventral region VeLD decreased amount, abnormal
ZP:0104462	ventro-medial region Kolmer-Agduhr neuron absent, abnormal
ZP:0104463	ventro-medial region Kolmer-Agduhr neuron decreased amount, abnormal
ZP:0104464	Kolmer-Agduhr neuron lacks parts or has fewer parts of type ventro-medial region GABAergic neuron, abnormal
ZP:0104465	primary motor neuron increased occurrence cell division, abnormal
ZP:0104466	VeLD has fewer parts of type GABAergic neuron, abnormal
ZP:0104468	ventral-most region Kolmer-Agduhr neuron absent, abnormal
ZP:0104469	epiphysis absent, abnormal
ZP:0104470	somite development decreased occurrence, abnormal
ZP:0104471	auditory behavior process quality, abnormal
ZP:0104472	iridoblast absent, abnormal
ZP:0104473	whole organism has fewer parts of type iridophore, abnormal
ZP:0104474	basement membrane eye spatial pattern, abnormal
ZP:0104479	ribonucleoprotein complex blastomere mislocalised, abnormal
ZP:0104480	blastomere displaced to ribonucleoprotein complex peripheral region blastodisc, abnormal
ZP:0104487	proximal pars anterior decreased amount, abnormal
ZP:0104491	copper-63 brain decreased amount, abnormal
ZP:0104496	skeletal muscle myotome malformed, abnormal
ZP:0104497	proteasome-mediated ubiquitin-dependent protein catabolic process decreased occurrence, abnormal
ZP:0104498	anterior lateral plate mesoderm decreased distribution, abnormal
ZP:0104508	anterior region lens increased amount, abnormal
ZP:0104509	anterior region lens increased distribution, abnormal
ZP:0104513	lens fiber cell absent, abnormal
ZP:0104514	angioblastic mesenchymal cell pharyngeal arch absent, abnormal
ZP:0104515	pharyngeal arch has fewer parts of type angioblastic mesenchymal cell, abnormal
ZP:0104516	levator arcus palatini absent, abnormal
ZP:0104517	adductor operculi absent, abnormal
ZP:0104518	dilatator operculi absent, abnormal
ZP:0104519	levator operculi absent, abnormal
ZP:0104520	ventral intermandibularis anterior absent, abnormal
ZP:0104521	ventral intermandibularis posterior absent, abnormal
ZP:0104522	adductor mandibulae absent, abnormal
ZP:0104523	interhyoideus absent, abnormal
ZP:0104524	adductor hyomandibulae absent, abnormal
ZP:0104527	cilium Kupffer's vesicle anterior orientation, abnormal
ZP:0104528	ciliary basal body Kupffer's vesicle mislocalised anteriorly, abnormal
ZP:0104529	Kupffer's vesicle process quality epithelial cilium movement involved in determination of left/right asymmetry, abnormal
ZP:0104530	endodermal cell displaced, abnormal
ZP:0104532	enteric smooth muscle cell differentiation process quality, abnormal
ZP:0104533	pharynx development process quality, abnormal
ZP:0104538	ventral-most region Kolmer-Agduhr neuron increased amount, abnormal
ZP:0104539	ventral-most region Kolmer-Agduhr neuron decreased amount, abnormal
ZP:0104540	Kolmer-Agduhr neuron has fewer parts of type ventral-most region GABAergic neuron, abnormal
ZP:0104542	Kolmer-Agduhr neuron has extra parts of type medial region GABAergic neuron, abnormal
ZP:0104543	Kolmer-Agduhr neuron has fewer parts of type ventro-medial region GABAergic neuron, abnormal
ZP:0104544	glutamatergic neuron differentiation increased occurrence, abnormal
ZP:0104546	radial glial cell process quality cell quiescence, abnormal
ZP:0104548	ceratohyal-interhyal joint absent, abnormal
ZP:0104549	interhyal-hyosymplectic joint absent, abnormal
ZP:0104551	posterior lateral line neuromast decreased occurrence synapse assembly, abnormal
ZP:0104552	posterior lateral line neuromast orientation stereocilium bundle posterior lateral line neuromast, abnormal
ZP:0104553	symplectic articulated with hyomandibula, abnormal
ZP:0104554	hyosymplectic cartilage has extra parts of type joint, abnormal
ZP:0104555	presumptive rhombomere 2 spatial pattern, abnormal
ZP:0104556	midbrain hindbrain boundary neural keel spatial pattern, abnormal
ZP:0104557	rhombomere 2 morphology, abnormal
ZP:0104558	presumptive rhombomere 4 morphology, abnormal
ZP:0104559	presumptive rhombomere 4 spatial pattern, abnormal
ZP:0104560	presumptive rhombomere 4 decreased size, abnormal
ZP:0104561	presumptive rhombomere 4 decreased distribution, abnormal
ZP:0104562	presumptive rhombomere 3 spatial pattern, abnormal
ZP:0104563	presumptive rhombomere 3 mislocalised, abnormal
ZP:0104564	hindbrain neural plate spatial pattern, abnormal
ZP:0104565	rhombomere 6 decreased distribution, abnormal
ZP:0104571	chorion deformed, abnormal
ZP:0104573	ovarian follicle degenerate, abnormal
ZP:0104574	thyroid follicle aplastic/hypoplastic, abnormal
ZP:0104577	Kolmer-Agduhr neuron lacks all parts of type medial region GABAergic neuron, abnormal
ZP:0104578	Kolmer-Agduhr neuron has fewer parts of type medial region GABAergic neuron, abnormal
ZP:0104588	otic vesicle increased occurrence otolith formation, abnormal
ZP:0104589	sagitta increased size, abnormal
ZP:0104590	sagitta ovate, abnormal
ZP:0104591	otic vesicle decreased frequency epithelial cilium movement involved in extracellular fluid movement, abnormal
ZP:0104592	otic vesicle process quality otolith formation, abnormal
ZP:0104595	anatomical region dorsal aorta disorganized, abnormal
ZP:0104596	dorsal aorta decreased occurrence sprouting angiogenesis, abnormal
ZP:0104607	whole organism lacks parts or has fewer parts of type anterior region nucleate erythrocyte, abnormal
ZP:0104608	nucleate erythrocyte trunk increased amount, abnormal
ZP:0104609	blood island increased distribution, abnormal
ZP:0104610	nucleate erythrocyte increased accumulation posterior region intermediate cell mass of mesoderm, abnormal
ZP:0104611	whole organism lacks parts or has fewer parts of type posterior region nucleate erythrocyte, abnormal
ZP:0104612	anatomical region posterior cardinal vein disorganized, abnormal
ZP:0104613	hematopoietic cell decreased occurrence blood circulation, abnormal
ZP:0104614	axoneme sperm decreased amount, abnormal
ZP:0104615	inner dynein arm sperm decreased amount, abnormal
ZP:0104616	axoneme sperm absent, abnormal
ZP:0104617	sperm flagellum sperm absent, abnormal
ZP:0104618	outer dynein arm sperm absent, abnormal
ZP:0104619	flagellated sperm motility process quality, abnormal
ZP:0104620	anatomical region midbrain necrotic, abnormal
ZP:0104621	retina arrested neurogenesis, abnormal
ZP:0104622	optic tectum arrested neurogenesis, abnormal
ZP:0104623	mitotic S phase process quality, abnormal
ZP:0104624	central nervous system decreased volume, abnormal
ZP:0104625	hypothalamus disorganized, abnormal
ZP:0104626	eye decreased volume, abnormal
ZP:0104627	ventral telencephalon disorganized, abnormal
ZP:0104628	nucleus optic tectum increased diameter, abnormal
ZP:0104629	central zone of the optic tectum arrested neurogenesis, abnormal
ZP:0104630	proliferative region optic tectum increased thickness, abnormal
ZP:0104631	ball shape, abnormal
ZP:0104634	artery pharyngeal arch morphology, abnormal
ZP:0104635	CaP motoneuron occurrence release of sequestered calcium ion into cytosol, abnormal
ZP:0104636	CaP motoneuron asynchronous release of sequestered calcium ion into cytosol, abnormal
ZP:0104637	involuntary skeletal muscle contraction decreased occurrence, abnormal
ZP:0104639	myotome has extra parts of type skeletal muscle cell vesicle skeletal muscle cell, abnormal
ZP:0104640	mitochondrion skeletal muscle malformed, abnormal
ZP:0104641	skeletal muscle decreased process quality skeletal myofibril assembly, abnormal
ZP:0104643	skeletal muscle decreased process quality sarcomere organization, abnormal
ZP:0104646	skeletal muscle cell has fewer parts of type skeletal muscle myofibril skeletal muscle cell, abnormal
ZP:0104651	Kupffer's vesicle physical quality of a process epithelial cilium movement involved in determination of left/right asymmetry, abnormal
ZP:0104652	Kupffer's vesicle elliptic, abnormal
ZP:0104653	gut decreased occurrence determination of digestive tract left/right asymmetry, abnormal
ZP:0104654	nucleus Kupffer's vesicle broken, abnormal
ZP:0104655	vacuole Kupffer's vesicle increased volume, abnormal
ZP:0104656	Kupffer's vesicle decreased rate vacuolar transport, abnormal
ZP:0104658	Kupffer's vesicle has extra parts of type posterior region vacuole Kupffer's vesicle, abnormal
ZP:0104659	Kupffer's vesicle process quality epithelial cell morphogenesis, abnormal
ZP:0104660	epithelial cell Kupffer's vesicle columnar, abnormal
ZP:0104666	leukocyte spatial pattern, abnormal
ZP:0104667	sphingolipid liver increased amount, abnormal
ZP:0104668	skeletal muscle satellite cell decreased amount, abnormal
ZP:0104669	skeletal muscle decreased distribution, abnormal
ZP:0104671	very long-chain fatty acid whole organism increased amount, abnormal
ZP:0104672	very long-chain fatty acid metabolic process disrupted, abnormal
ZP:0104673	oligodendrocyte brain spatial pattern, abnormal
ZP:0104674	oligodendrocyte spinal cord spatial pattern, abnormal
ZP:0104675	optic tectum increased occurrence cellular response to light stimulus, abnormal
ZP:0104676	optic tectum increased occurrence membrane depolarization during action potential, abnormal
ZP:0104677	cephalic mesoderm absent, abnormal
ZP:0104678	axial blood vessel absent, abnormal
ZP:0104679	axial blood vessel increased distribution, abnormal
ZP:0104683	blood vessel endothelial cell posterior cardinal vein increased amount, abnormal
ZP:0104684	angiogenic sprout cerebellar central artery decreased amount, abnormal
ZP:0104685	mesencephalic artery absent, abnormal
ZP:0104688	cerebellar central artery decreased amount, abnormal
ZP:0104691	metencephalic artery absent, abnormal
ZP:0104692	GABAergic neuron decreased occurrence inhibitory synapse assembly, abnormal
ZP:0104693	hindbrain has fewer parts of type inhibitory synapse hindbrain, abnormal
ZP:0104694	spinal cord has fewer parts of type inhibitory synapse spinal cord, abnormal
ZP:0104695	telencephalon has fewer parts of type inhibitory synapse telencephalon, abnormal
ZP:0104697	optic tectum has fewer parts of type inhibitory synapse optic tectum, abnormal
ZP:0104698	startle response increased magnitude, abnormal
ZP:0104699	response to light stimulus increased magnitude, abnormal
ZP:0104700	postsynaptic density hindbrain decreased distribution, abnormal
ZP:0104701	postsynaptic density hindbrain decreased amount, abnormal
ZP:0104702	GABA-ergic synapse hindbrain decreased distribution, abnormal
ZP:0104703	GABA-ergic synapse hindbrain decreased amount, abnormal
ZP:0104704	GABAergic neuron hindbrain decreased distribution, abnormal
ZP:0104705	GABAergic neuron spinal cord decreased distribution, abnormal
ZP:0104706	GABAergic neuron telencephalon decreased distribution, abnormal
ZP:0104707	GABAergic neuron telencephalon decreased amount, abnormal
ZP:0104708	GABAergic neuron optic tectum decreased distribution, abnormal
ZP:0104709	GABAergic neuron optic tectum decreased amount, abnormal
ZP:0104716	lens fiber cell differentiation decreased occurrence, abnormal
ZP:0104719	lens epithelium increased amount, abnormal
ZP:0104721	lens epithelium increased distribution, abnormal
ZP:0104722	lens epithelium decreased amount, abnormal
ZP:0104723	lens epithelium decreased occurrence early endosome to late endosome transport, abnormal
ZP:0104724	lens epithelium decreased occurrence early endosome to recycling endosome transport, abnormal
ZP:0104725	heart decreased occurrence tube formation, abnormal
ZP:0104726	endocardium accumulation endothelial cell anatomical space heart, abnormal
ZP:0104727	atrium hypotrophic, abnormal
ZP:0104728	heart valve malformed, abnormal
ZP:0104729	heart hypotrophic, abnormal
ZP:0104730	heart valve trabecular, abnormal
ZP:0104731	presumptive cardiac ventricle primitive heart tube delayed cardioblast migration to the midline involved in heart field formation, abnormal
ZP:0104732	cardioblast migration to the midline involved in heart field formation delayed, abnormal
ZP:0104734	determination of left/right asymmetry in nervous system process quality, abnormal
ZP:0104735	cilium Kupffer's vesicle posterior orientation, abnormal
ZP:0104736	gut process quality determination of digestive tract left/right asymmetry, abnormal
ZP:0104740	cilium Kupffer's vesicle decreased size, abnormal
ZP:0104748	female mating behavior process quality, abnormal
ZP:0104750	ovarian follicle stage I increased amount, abnormal
ZP:0104751	ovarian follicle stage II decreased amount, abnormal
ZP:0104752	peripheral region blastodisc mislocalised, abnormal
ZP:0104753	blastomere has fewer parts of type cleavage furrow ribonucleoprotein complex blastodisc, abnormal
ZP:0104754	filamentous actin blastomere spatial pattern, abnormal
ZP:0104755	paraxial mesoderm irregular spatial pattern, abnormal
ZP:0104756	myoblast disorganized, abnormal
ZP:0104768	serotonin hindbrain increased amount, abnormal
ZP:0104769	noradrenaline hindbrain decreased amount, abnormal
ZP:0104770	(3,4-dihydroxyphenyl)acetic acid hindbrain decreased amount, abnormal
ZP:0104771	(3,4-dihydroxyphenyl)acetic acid telencephalon decreased amount, abnormal
ZP:0104772	(3,4-dihydroxyphenyl)acetic acid diencephalon decreased amount, abnormal
ZP:0104773	(3,4-dihydroxyphenyl)acetic acid optic tectum decreased amount, abnormal
ZP:0104774	brain decreased occurrence nitric oxide mediated signal transduction, abnormal
ZP:0104776	response to environmental enrichment occurrence, abnormal
ZP:0104777	radial glial cell increased occurrence neuron differentiation, abnormal
ZP:0104779	neuronal stem cell radial glial cell decreased amount, abnormal
ZP:0104780	cell body Mauthner neuron increased area, abnormal
ZP:0104781	establishment of left/right asymmetry disrupted, abnormal
ZP:0104784	thigmotaxis delayed, abnormal
ZP:0104788	CaP motoneuron has fewer parts of type neuronal cell body membrane glutamatergic synapse CaP motoneuron, abnormal
ZP:0104791	CaP motoneuron decreased occurrence excitatory synapse assembly, abnormal
ZP:0104794	vertical myoseptum skeletal muscle mislocalised, abnormal
ZP:0104795	skeletal muscle mislocalised, abnormal
ZP:0104796	primitive heart tube increased distribution, abnormal
ZP:0104797	skeletal muscle cell accumulation actin cytoskeleton vertical myoseptum, abnormal
ZP:0105640	neutrophil decreased process quality peroxidase activity, abnormal
ZP:0105641	corpuscles of Stannius increased occurrence specification of animal organ identity, abnormal
ZP:0105642	corpuscles of Stannius decreased occurrence specification of animal organ identity, abnormal
ZP:0105643	pronephric distal early tubule decreased amount, abnormal
ZP:0105644	corpuscles of Stannius decreased process quality embryonic organ development, abnormal
ZP:0105645	podocyte foot pronephric podocyte flattened, abnormal
ZP:0105646	lamina rara interna structure, cavities, abnormal
ZP:0105647	ependymal cell decreased occurrence epithelial cilium movement involved in extracellular fluid movement, abnormal
ZP:0105648	motile cilium ependymal cell inactive, abnormal
ZP:0105649	central canal decreased occurrence cerebrospinal fluid circulation, abnormal
ZP:0105651	midsagittal plane brain absent, abnormal
ZP:0105652	polster decreased amount, abnormal
ZP:0105653	intermediate mesoderm decreased amount, abnormal
ZP:0105657	retinal ganglion cell decreased occurrence cysteine-type endopeptidase activity, abnormal
ZP:0105659	melanocyte decreased process quality catechol oxidase activity, abnormal
ZP:0105660	midsagittal plane neural tube absent, abnormal
ZP:0105662	neural rod spatial pattern, abnormal
ZP:0105663	neural rod mislocalised, abnormal
ZP:0105664	neural tube decreased occurrence specification of symmetry, abnormal
ZP:0105665	plasma membrane region neural tube mislocalised, abnormal
ZP:0105666	ciliary basal body Kupffer's vesicle position, abnormal
ZP:0105667	determination of left/right asymmetry in lateral mesoderm occurrence, abnormal
ZP:0105668	determination of heart left/right asymmetry occurrence, abnormal
ZP:0105669	determination of digestive tract left/right asymmetry occurrence, abnormal
ZP:0105671	myocardium mislocalised medially, abnormal
ZP:0105673	olfactory bulb decreased process quality olfactory receptor activity, abnormal
ZP:0105674	microtubule blastomere spatial pattern, abnormal
ZP:0105675	microtubule blastomere mislocalised, abnormal
ZP:0105682	hypophysis male organism increased amount, abnormal
ZP:0105699	presumptive rhombomere 5 absent, abnormal
ZP:0105700	presumptive rhombomere 4 absent, abnormal
ZP:0105701	presumptive rhombomere 3 absent, abnormal
ZP:0105702	forebrain neural keel decreased amount, abnormal
ZP:0105703	negative regulation of convergent extension involved in axis elongation delayed, abnormal
ZP:0105706	Reissner's fiber spatial pattern, abnormal
ZP:0105707	Reissner's fiber malformed, abnormal
ZP:0105708	Reissner's fiber decreased amount, abnormal
ZP:0105709	brain increased process quality acetylcholinesterase activity, abnormal
ZP:0105711	anterior region posterior lateral line primordium mislocalised, abnormal
ZP:0105713	central region posterior lateral line primordium mislocalised, abnormal
ZP:0105714	posterior lateral line primordium decreased process quality posterior lateral line development, abnormal
ZP:0105715	central region posterior lateral line primordium increased amount, abnormal
ZP:0105716	posterior lateral line primordium decreased rate posterior lateral line neuromast primordium migration, abnormal
ZP:0105717	posterior lateral line ganglion fused with posterior lateral line placode, abnormal
ZP:0105728	neuromast hair cell decreased occurrence detection of mechanical stimulus involved in sensory perception of sound, abnormal
ZP:0105733	opercle absent, abnormal
ZP:0105735	intrahepatic bile duct epithelial cell decreased amount, abnormal
ZP:0105739	dorsal aorta decreased occurrence alkaline phosphatase activity, abnormal
ZP:0105740	oligodendrocyte abutting myelin sheath cell body neuron, abnormal
ZP:0105742	basolateral plasma membrane posterior lateral line neuromast decreased amount, abnormal
ZP:0105745	chromatin organization process quality, abnormal
ZP:0105746	rhombomere 6 absent, abnormal
ZP:0105747	centrum decreased process quality bone mineralization, abnormal
ZP:0105748	hemal arch decreased process quality bone mineralization, abnormal
ZP:0105749	neural arch decreased process quality bone mineralization, abnormal
ZP:0105750	centrum decreased volume, abnormal
ZP:0105751	osteoblast increased accumulation rib, abnormal
ZP:0105752	hematopoietic stem cell dorsal aorta absent, abnormal
ZP:0105753	vascular cord decreased amount, abnormal
ZP:0105754	mesoderm trunk decreased amount, abnormal
ZP:0105755	vH ionocyte rate proton transmembrane transport, abnormal
ZP:0105756	vH ionocyte decreased rate proton transmembrane transport, abnormal
ZP:0105758	posterior lateral line neuromast decreased process quality detection of mechanical stimulus involved in sensory perception of sound, abnormal
ZP:0105760	motile cilium ependymal cell decreased length, abnormal
ZP:0105761	spinal cord decreased occurrence motile cilium assembly, abnormal
ZP:0105762	spinal cord has fewer parts of type ependymal cell motile cilium ependymal cell, abnormal
ZP:0105767	optic vesicle process quality cell migration, abnormal
ZP:0105768	optic stalk process quality cell migration, abnormal
ZP:0105769	optic cup process quality cell migration, abnormal
ZP:0105770	optic fissure process quality cell migration, abnormal
ZP:0105771	optic fissure increased amount, abnormal
ZP:0105772	optic fissure increased distribution, abnormal
ZP:0105773	optic vesicle increased amount, abnormal
ZP:0105777	pronephric duct increased distribution, abnormal
ZP:0105779	posterior caudal vein decreased amount, abnormal
ZP:0105781	Mauthner neuron decreased duration NMDA glutamate receptor activity, abnormal
ZP:0105782	Mauthner neuron decreased process quality NMDA glutamate receptor activity, abnormal
ZP:0105783	whole organism decreased occurrence phosphodiesterase I activity, abnormal
ZP:0105785	cardiac muscle cell process quality establishment of animal organ orientation, abnormal
ZP:0105786	cardiac muscle cell orientation heart tube, abnormal
ZP:0105790	neutrophil intestine decreased amount, abnormal
ZP:0105791	photoreceptor cell accumulation vesicle apical region photoreceptor cell, abnormal
ZP:0105792	photoreceptor outer segment eye photoreceptor cell mislocalised, abnormal
ZP:0105793	vesicle eye photoreceptor cell mislocalised, abnormal
ZP:0105794	whole organism decreased occurrence laminin binding, abnormal
ZP:0105795	tectal neuropile decreased amount, abnormal
ZP:0105796	intestine lumen decreased occurrence chitin synthase activity, abnormal
ZP:0105801	rhombomere 4 increased distribution, abnormal
ZP:0105802	heme whole organism increased amount, abnormal
ZP:0105803	secretory granule neutrophil absent, abnormal
ZP:0105804	rhombomere 3 mislocalised, abnormal
ZP:0105805	rhombomere 1 mislocalised, abnormal
ZP:0105806	Mauthner neuron rhombomere 4 decreased amount, abnormal
ZP:0105809	anterior region central nervous system decreased amount, abnormal
ZP:0105810	pronephric duct opening decreased amount, abnormal
ZP:0105812	central artery decreased process quality blood vessel lumenization, abnormal
ZP:0105813	pharyngeal arch 2 increased amount, abnormal
ZP:0105814	pharyngeal arch 1 increased amount, abnormal
ZP:0105821	ribonucleoprotein granule blastomere position, abnormal
ZP:0105822	blastomere decreased accumulation ribonucleoprotein granule cleavage furrow blastomere, abnormal
ZP:0105827	pericardial region edematous, abnormal
ZP:0105835	lipid intestine increased amount, abnormal
ZP:0105838	thyroxine thyroid follicle absent, abnormal
ZP:0105839	melanophore stripe has extra parts of type melanocyte, abnormal
ZP:0105840	anterior region posterior lateral line primordium increased amount, abnormal
ZP:0105865	locomotory exploration behavior decreased occurrence, abnormal
ZP:0105866	telencephalon has fewer parts of type dopaminergic neuron, abnormal
ZP:0105880	brain decreased occurrence monoamine oxidase activity, abnormal
ZP:0105881	regulation of neuronal action potential disrupted, abnormal
ZP:0105892	oocyte stage IV increased amount, abnormal
ZP:0105901	swimming behavior frequency, abnormal
ZP:0105902	circadian behavior process quality, abnormal
ZP:0105903	regulation of locomotor rhythm process quality, abnormal
ZP:0105911	retinal outer plexiform layer increased thickness, abnormal
ZP:0105913	oocyte stage V decreased amount, abnormal
ZP:0105920	multi-ciliated epithelial cell pronephros decreased distribution, abnormal
ZP:0105921	corpuscles of Stannius spatial pattern, abnormal
ZP:0105922	corpuscles of Stannius mislocalised, abnormal
ZP:0105925	hemoglobin blood decreased amount, abnormal
ZP:0105931	vertebral column decreased length, abnormal
ZP:0105932	ovarian follicle stage III has extra parts of type micropylar cell, abnormal
ZP:0105933	micropylar cell mislocalised, abnormal
ZP:0105934	brain increased occurrence protein serine/threonine kinase activity, abnormal
ZP:0105935	spinal cord increased occurrence protein serine/threonine kinase activity, abnormal
ZP:0105936	eye increased occurrence protein serine/threonine kinase activity, abnormal
ZP:0105937	liver increased occurrence protein serine/threonine kinase activity, abnormal
ZP:0105938	kidney increased occurrence protein serine/threonine kinase activity, abnormal
ZP:0105939	intestine increased occurrence protein serine/threonine kinase activity, abnormal
ZP:0105940	whole organism decreased occurrence NADH dehydrogenase (ubiquinone) activity, abnormal
ZP:0105941	adipose tissue decreased size, abnormal
ZP:0105945	floor plate increased distribution, abnormal
ZP:0105953	macrophage trunk absent, abnormal
ZP:0105967	sterol trunk spatial pattern, abnormal
ZP:0105968	cholesterol transport process quality, abnormal
ZP:0105986	optic tectum has fewer parts of type dorso-lateral region microglial cell, abnormal
ZP:0105988	microvillous olfactory receptor neuron decreased process quality olfactory receptor activity, abnormal
ZP:0105989	eye disrupted catechol oxidase activity, abnormal
ZP:0105990	melanocyte disrupted catechol oxidase activity, abnormal
ZP:0105992	medial region trunk absent, abnormal
ZP:0105996	central artery decreased occurrence angiogenesis, abnormal
ZP:0106000	central artery decreased occurrence blood vessel morphogenesis, abnormal
ZP:0106003	neuronal stem cell brain decreased amount, abnormal
ZP:0106004	neuronal stem cell spinal cord decreased amount, abnormal
ZP:0106005	spinal cord neural tube increased amount, abnormal
ZP:0106006	melanocyte hypodermal cell decreased amount, abnormal
ZP:0106007	iridophore peritoneum absent, abnormal
ZP:0106008	iridophore hypodermal cell decreased amount, abnormal
ZP:0106010	optic choroid vascular plexus decreased amount, abnormal
ZP:0106013	central nervous system decreased process quality central nervous system myelination, abnormal
ZP:0106014	peripheral nervous system decreased process quality myelination in peripheral nervous system, abnormal
ZP:0106015	oligodendrocyte central nervous system decreased amount, abnormal
ZP:0106016	myelinating Schwann cell peripheral nervous system decreased amount, abnormal
ZP:0106017	dorsal region trunk increased distribution, abnormal
ZP:0106018	neural crest cell trunk absent, abnormal
ZP:0106019	dorsal region trunk absent, abnormal
ZP:0106022	midbrain hindbrain boundary notched, abnormal
ZP:0106023	neural crest cell pharyngeal arch disorganized, abnormal
ZP:0106024	Rohon-Beard neuron decreased process quality voltage-gated sodium channel activity, abnormal
ZP:0106025	brain decreased process quality cytochrome-c oxidase activity, abnormal
ZP:0106026	brain increased process quality chitinase activity, abnormal
ZP:0106027	brain decreased process quality ubiquinol-cytochrome-c reductase activity, abnormal
ZP:0106028	brain increased process quality hexosaminidase activity, abnormal
ZP:0106029	alanine whole organism decreased amount, abnormal
ZP:0106030	ADP whole organism increased amount, abnormal
ZP:0106031	guanosine 5'-monophosphate whole organism increased amount, abnormal
ZP:0106032	histidine whole organism decreased amount, abnormal
ZP:0106033	glutamine whole organism increased amount, abnormal
ZP:0106034	glutathione metabolic process process quality, abnormal
ZP:0106038	macrophage increased occurrence phagocytosis, abnormal
ZP:0106039	renal albumin absorption decreased occurrence, abnormal
ZP:0106040	peritoneum edematous, abnormal
ZP:0106041	lateral side peripheral olfactory organ absent, abnormal
ZP:0106042	posterior lateral mesoderm increased distribution, abnormal
ZP:0106043	vascular endothelium increased distribution, abnormal
ZP:0106045	brain vasculature process quality angiogenic sprout fusion, abnormal
ZP:0106048	gall bladder absent lipase activity, abnormal
ZP:0106049	intestine decreased occurrence lipase activity, abnormal
ZP:0106052	myotome decreased occurrence neuromuscular junction development, abnormal
ZP:0106057	dorsal region pharyngeal arch 2 absent, abnormal
ZP:0106058	dorsal region pharyngeal arch 2 decreased amount, abnormal
ZP:0106059	dorsal region pharyngeal arch 1 absent, abnormal
ZP:0106060	dorsal region pharyngeal arch 1 decreased amount, abnormal
ZP:0106061	ventral-most region pharyngeal arch 1 absent, abnormal
ZP:0106062	medial region pharyngeal arch 2 spatial pattern, abnormal
ZP:0106063	medial region pharyngeal arch 2 increased distribution, abnormal
ZP:0106064	medial region pharyngeal arch 1 spatial pattern, abnormal
ZP:0106065	medial region pharyngeal arch 1 increased distribution, abnormal
ZP:0106066	ventral region pharyngeal arch 2 increased distribution, abnormal
ZP:0106067	ventral region pharyngeal arch 1 increased distribution, abnormal
ZP:0106070	opercle aplastic/hypoplastic, abnormal
ZP:0106073	brain decreased occurrence mRNA (2'-O-methyladenosine-N6-)-methyltransferase activity, abnormal
ZP:0106074	liver decreased occurrence mRNA (2'-O-methyladenosine-N6-)-methyltransferase activity, abnormal
ZP:0106075	ovary decreased occurrence mRNA (2'-O-methyladenosine-N6-)-methyltransferase activity, abnormal
ZP:0106076	testis decreased occurrence mRNA (2'-O-methyladenosine-N6-)-methyltransferase activity, abnormal
ZP:0106077	muscle decreased occurrence mRNA (2'-O-methyladenosine-N6-)-methyltransferase activity, abnormal
ZP:0106078	anterior-most region cranium decreased size, abnormal
ZP:0106079	vertebral column condensed, abnormal
ZP:0106080	cranial vault decreased thickness, abnormal
ZP:0106089	optic furrow morphology, abnormal
ZP:0106090	whole organism decreased process quality glutathione transferase activity, abnormal
ZP:0106092	cerebellum atrophied, abnormal
ZP:0106093	trabecular layer increased occurrence cardiac muscle cell proliferation, abnormal
ZP:0106094	whole organism decreased process quality protein N-linked glycosylation, abnormal
ZP:0106095	podocyte absent, abnormal
ZP:0106096	anterior crista process quality innervation, abnormal
ZP:0106097	occipital lateral line neuromast process quality innervation, abnormal
ZP:0106098	nerve anterior crista absent, abnormal
ZP:0106099	basal region cardiac muscle cell deformed, abnormal
ZP:0106100	cardiac muscle cell smooth, abnormal
ZP:0106101	noradrenaline whole organism decreased amount, abnormal
ZP:0106102	norepinephrine biosynthetic process process quality, abnormal
ZP:0106103	ovary process quality progesterone receptor binding, abnormal
ZP:0106104	heart rudiment increased distribution, abnormal
ZP:0106106	immature eye increased amount, abnormal
ZP:0106107	anterior lateral plate mesoderm increased amount, abnormal
ZP:0106108	spinal cord has fewer parts of type ventral region myelin sheath oligodendrocyte, abnormal
ZP:0106113	Z disc atrium blurry, abnormal
ZP:0106114	sarcomere cardiac ventricle decreased length, abnormal
ZP:0106115	sarcomere cardiac ventricle increased width, abnormal
ZP:0106116	sarcomere atrium decreased length, abnormal
ZP:0106117	sarcomere atrium increased width, abnormal
ZP:0106118	sarcomere atrium disorganized, abnormal
ZP:0106119	Z disc cardiac ventricle increased thickness, abnormal
ZP:0106120	M band cardiac ventricle absent, abnormal
ZP:0106121	I band cardiac ventricle absent, abnormal
ZP:0106122	I band atrium absent, abnormal
ZP:0106123	cardiac conduction irregular rhythm, abnormal
ZP:0106124	cardiac muscle cell presumptive sinus venosus absent, abnormal
ZP:0106125	posterior lateral line neuromast has fewer parts of type hair cell, abnormal
ZP:0106126	blood absent, abnormal
ZP:0106128	fusion of sperm to egg plasma membrane involved in single fertilization disrupted, abnormal
ZP:0106130	sperm-egg recognition disrupted, abnormal
ZP:0106131	unfertilized egg absent, abnormal
ZP:0106132	heart tube heterotaxic, abnormal
ZP:0106133	post-vent vasculature swollen, abnormal
ZP:0106134	oligodendrocyte central nervous system increased amount, abnormal
ZP:0106138	posterior lateral line primordium has fewer parts of type cell, abnormal
ZP:0106139	whole organism has fewer parts of type posterior lateral line neuromast, abnormal
ZP:0106140	peripheral region heart rudiment absent, abnormal
ZP:0106142	whole organism decreased process quality galactose metabolic process, abnormal
ZP:0106143	brain arrested UDP-glucose:hexose-1-phosphate uridylyltransferase activity, abnormal
ZP:0106144	ovary arrested UDP-glucose:hexose-1-phosphate uridylyltransferase activity, abnormal
ZP:0106145	skeletal muscle arrested UDP-glucose:hexose-1-phosphate uridylyltransferase activity, abnormal
ZP:0106146	raphe nucleus decreased distribution, abnormal
ZP:0106148	specification of pronephric distal tubule identity process quality, abnormal
ZP:0106152	anal fin male organism decreased pigmentation, abnormal
ZP:0106153	pectoral fin breeding tubercle male organism absent, abnormal
ZP:0106154	fertilization decreased rate, abnormal
ZP:0106155	germ cell proliferation decreased occurrence, abnormal
ZP:0106156	female organism has fewer parts of type oocyte, abnormal
ZP:0106157	ovary transparent, abnormal
ZP:0106158	ovary lacks all parts of type oocyte, abnormal
ZP:0106159	ovary has fewer parts of type oocyte, abnormal
ZP:0106160	testis transparent, abnormal
ZP:0106161	testis has fewer parts of type sperm, abnormal
ZP:0106162	testis has extra parts of type Sertoli cell, abnormal
ZP:0106163	ovarian follicle atretic, abnormal
ZP:0106164	spermatogenic cyst decreased size, abnormal
ZP:0106165	spermatogonium increased size, abnormal
ZP:0106166	caudal fin has number of regenerating fin regeneration epithelium, abnormal
ZP:0106167	rhombomere 6 increased distribution, abnormal
ZP:0106168	rhombomere 2 increased distribution, abnormal
ZP:0106169	paraxial mesoderm condensed, abnormal
ZP:0106170	centriole notochord mislocalised, abnormal
ZP:0106171	centriole neuroectoderm mislocalised, abnormal
ZP:0106172	microtubule organizing center localization disrupted, abnormal
ZP:0106173	convergent extension involved in notochord morphogenesis process quality, abnormal
ZP:0106174	spinal cord has extra parts of type dorsal region myelin sheath oligodendrocyte, abnormal
ZP:0106176	cell body oligodendrocyte mislocalised, abnormal
ZP:0106177	cell body oligodendrocyte increased distribution, abnormal
ZP:0106181	dorsal longitudinal vein truncated, abnormal
ZP:0106182	mesencephalic vein truncated, abnormal
ZP:0106183	lysosome neuromast increased amount, abnormal
ZP:0106184	cholesterol neuromast increased amount, abnormal
ZP:0106185	liver opaque, abnormal
ZP:0106186	axon hindbrain structure, abnormal
ZP:0106187	Purkinje cell disorganized, abnormal
ZP:0106188	cholesterol trunk increased amount, abnormal
ZP:0106189	lysosome peripheral olfactory organ increased amount, abnormal
ZP:0106190	cholesterol yolk syncytial layer increased amount, abnormal
ZP:0106191	cholesterol extension increased amount, abnormal
ZP:0106192	microglial cell brain absent, abnormal
ZP:0106193	trunk lacks all parts of type iridophore, abnormal
ZP:0106194	caudal fin lacks all parts of type iridophore, abnormal
ZP:0106197	central canal lacks all parts of type Reissner's fiber, abnormal
ZP:0106198	ventricular system lacks all parts of type Reissner's fiber, abnormal
ZP:0106199	Reissner's fiber absent, abnormal
ZP:0106201	third ventricle lacks all parts of type Reissner's fiber, abnormal
ZP:0106202	subcommissural organ absent, abnormal
ZP:0106203	neural tube spinal cord duplicated, abnormal
ZP:0106204	neural tube split bilaterally, abnormal
ZP:0106211	retinal cone cell structure, abnormal
ZP:0106212	retinal cone cell decreased functionality, abnormal
ZP:0106213	cilium pronephros dispersed, abnormal
ZP:0106214	pronephros decreased rate cilium movement, abnormal
ZP:0106215	pronephros decreased occurrence cilium movement, abnormal
ZP:0106221	tail bud lacks all parts of type Kupffer's vesicle, abnormal
ZP:0106222	photoreceptor cell decreased occurrence synaptic vesicle docking, abnormal
ZP:0106223	synaptic ribbon photoreceptor cell position, abnormal
ZP:0106224	OFF-bipolar cell process quality synaptic signaling, abnormal
ZP:0106225	retinal outer plexiform layer spatial pattern, abnormal
ZP:0106228	centrum decreased thickness, abnormal
ZP:0106229	ligament vertebral column composition, abnormal
ZP:0106230	bone tissue vertebra morphology, abnormal
ZP:0106231	dermis decreased thickness, abnormal
ZP:0106232	notochord inner cell morphology, abnormal
ZP:0106233	notochord inner cell has fewer parts of type vacuole notochord inner cell, abnormal
ZP:0106234	neuromuscular junction skeletal muscle cell spatial pattern, abnormal
ZP:0106237	pleuroperitoneal region increased process quality cell population proliferation, abnormal
ZP:0106238	neoplasm pleuroperitoneal cavity increased amount, abnormal
ZP:0106239	cardiac muscle decreased amount, abnormal
ZP:0106240	pleuroperitoneal region neoplastic, abnormal
ZP:0106241	whole organism decreased process quality histone H3-K36 trimethylation, abnormal
ZP:0106242	whole organism decreased process quality histone H3-K36 dimethylation, abnormal
ZP:0106243	medial side somite increased distribution, abnormal
ZP:0106244	somite trunk decreased amount, abnormal
ZP:0106245	yolk mislocalised, abnormal
ZP:0106246	immature eye decreased distribution, abnormal
ZP:0106247	primordial vasculature spatial pattern, abnormal
ZP:0106248	primordial vasculature decreased amount, abnormal
ZP:0106249	anterior side whole organism decreased amount, abnormal
ZP:0106250	ventral side somite mislocalised, abnormal
ZP:0106251	immature eye absent, abnormal
ZP:0106252	anatomical region pronephros mislocalised, abnormal
ZP:0106253	periderm decreased amount, abnormal
ZP:0106256	yolk syncytial layer increased amount, abnormal
ZP:0106257	brain decreased occurrence MAPK cascade, abnormal
ZP:0106258	whole organism decreased occurrence MAPK cascade, abnormal
ZP:0106259	central artery decreased occurrence MAPK cascade, abnormal
ZP:0106260	whole organism decreased occurrence protein kinase B signaling, abnormal
ZP:0106264	central artery decreased occurrence vasculature development, abnormal
ZP:0106265	central artery hindbrain malformed, abnormal
ZP:0106270	central artery decreased rate blood vessel endothelial cell migration, abnormal
ZP:0106272	central artery decreased occurrence vascular endothelial cell proliferation, abnormal
ZP:0106273	prechordal plate process quality cell migration involved in gastrulation, abnormal
ZP:0106275	chorion attached to fertilized egg, abnormal
ZP:0106276	blastodisc hypoplastic, abnormal
ZP:0106277	midbrain neoplastic, abnormal
ZP:0106278	nucleus optic tectum increased size, abnormal
ZP:0106279	nucleus optic tectum broken, abnormal
ZP:0106280	retinal inner nuclear layer mislocalised, abnormal
ZP:0106281	optic tectum mislocalised, abnormal
ZP:0106282	thalamus mislocalised, abnormal
ZP:0106283	thalamus increased distribution, abnormal
ZP:0106284	retinal outer nuclear layer increased distribution, abnormal
ZP:0106285	brain increased occurrence mitotic cell cycle, abnormal
ZP:0106286	ceratohyal cartilage increased distance Meckel's cartilage, abnormal
ZP:0106287	ceratohyal cartilage angle palatoquadrate cartilage, abnormal
ZP:0106288	ceratohyal cartilage angle ceratohyal cartilage, abnormal
ZP:0106289	ceratohyal cartilage increased angle to palatoquadrate cartilage, abnormal
ZP:0106290	precaudal vertebra fused with hemal arch hemal arch precaudal vertebra, abnormal
ZP:0106291	caudal vertebra fused with neural arch neural arch caudal vertebra, abnormal
ZP:0106292	Weberian vertebra fused with neural arch centrum Weberian vertebra, abnormal
ZP:0106293	pectoral girdle asymmetrical, abnormal
ZP:0106294	postcleithrum anterior orientation, abnormal
ZP:0106295	hemal arch unfused from hemal arch, abnormal
ZP:0106296	exoccipital decreased size, abnormal
ZP:0106297	neural arch asymmetrical, abnormal
ZP:0106298	neural arch unfused from neural arch, abnormal
ZP:0106299	Weberian vertebra fused with Weberian vertebra, abnormal
ZP:0106300	oocyte stage II arrested chorion micropyle formation, abnormal
ZP:0106301	oocyte stage III arrested chorion micropyle formation, abnormal
ZP:0106304	oocyte development decreased occurrence, abnormal
ZP:0106305	ovarian follicle stage II lacks all parts of type micropylar cell, abnormal
ZP:0106306	ovarian follicle stage III lacks all parts of type micropylar cell, abnormal
ZP:0106307	unfertilized egg arrested chorion micropyle formation, abnormal
ZP:0106308	unfertilized egg lacks all parts of type micropyle unfertilized egg, abnormal
ZP:0106309	median fin fold ruffled, abnormal
ZP:0106310	pelvic fin musculature absent, abnormal
ZP:0106311	abdominal musculature absent, abnormal
ZP:0106312	microtubule cytoskeleton yolk increased amount, abnormal
ZP:0106313	cleavage furrow blastomere mislocalised radially, abnormal
ZP:0106314	calcium-mediated signaling cellular spatiotemporal quality, abnormal
ZP:0106315	embryonic cleavage process efficacy, abnormal
ZP:0106316	chromosome movement towards spindle pole disrupted, abnormal
ZP:0106328	ventral mandibular arch decreased amount, abnormal
ZP:0106329	interopercular-mandibular ligament mislocalised, abnormal
ZP:0106335	brain opaque, abnormal
ZP:0106336	1-piperideine-6-carboxylate whole organism increased amount, abnormal
ZP:0106337	pipecolic acid whole organism increased amount, abnormal
ZP:0106338	aortic arch 3 decreased length, abnormal
ZP:0106339	aortic arch 3 constricted, abnormal
ZP:0106340	aortic arch 4 decreased length, abnormal
ZP:0106341	aortic arch 4 constricted, abnormal
ZP:0106342	aortic arch 5 decreased length, abnormal
ZP:0106343	aortic arch 5 constricted, abnormal
ZP:0106344	aortic arch 6 decreased length, abnormal
ZP:0106345	aortic arch 6 constricted, abnormal
ZP:0106346	embryonic blood vessel endothelial progenitor cell aortic arch decreased amount, abnormal
ZP:0106347	aortic arch 3 decreased occurrence angioblast cell differentiation, abnormal
ZP:0106348	aortic arch 4 decreased occurrence angioblast cell differentiation, abnormal
ZP:0106349	aortic arch 5 decreased occurrence angioblast cell differentiation, abnormal
ZP:0106350	aortic arch 6 decreased occurrence angioblast cell differentiation, abnormal
ZP:0106351	angioblastic mesenchymal cell aortic arch 3 decreased amount, abnormal
ZP:0106352	angioblastic mesenchymal cell aortic arch 4 decreased amount, abnormal
ZP:0106353	angioblastic mesenchymal cell aortic arch 5 decreased amount, abnormal
ZP:0106354	angioblastic mesenchymal cell aortic arch 6 decreased amount, abnormal
ZP:0106355	aortic arch 3 decreased occurrence vasculogenesis, abnormal
ZP:0106356	aortic arch 4 decreased occurrence vasculogenesis, abnormal
ZP:0106357	aortic arch 5 decreased occurrence vasculogenesis, abnormal
ZP:0106358	aortic arch 6 decreased occurrence vasculogenesis, abnormal
ZP:0106359	angioblastic mesenchymal cell aortic arch decreased amount, abnormal
ZP:0106361	pharynx atrophied, abnormal
ZP:0106362	aortic arch 3 arrested blood circulation, abnormal
ZP:0106363	aortic arch 4 arrested blood circulation, abnormal
ZP:0106364	aortic arch 5 arrested blood circulation, abnormal
ZP:0106365	aortic arch 6 arrested blood circulation, abnormal
ZP:0106366	aortic arch 3 has fewer parts of type blood vessel endothelial cell aortic arch 3, abnormal
ZP:0106367	aortic arch 4 has fewer parts of type blood vessel endothelial cell aortic arch 4, abnormal
ZP:0106368	aortic arch 5 lacks all parts of type blood vessel endothelium aortic arch 5, abnormal
ZP:0106369	aortic arch 6 has fewer parts of type blood vessel endothelial cell aortic arch 6, abnormal
ZP:0106370	migratory cranial neural crest decreased amount, abnormal
ZP:0106371	migratory cranial neural crest pharyngeal arch decreased amount, abnormal
ZP:0106372	dorsal region neurocranium absent, abnormal
ZP:0106376	aortic arch 3 decreased occurrence cell population proliferation, abnormal
ZP:0106377	aortic arch 4 decreased occurrence cell population proliferation, abnormal
ZP:0106378	aortic arch 5 decreased occurrence cell population proliferation, abnormal
ZP:0106379	aortic arch 6 decreased occurrence cell population proliferation, abnormal
ZP:0106381	stereocilium otic sensory epithelium decreased length, abnormal
ZP:0106382	stereocilium otic sensory epithelium decreased amount, abnormal
ZP:0106383	photoreceptor outer segment eye photoreceptor cell degenerate, abnormal
ZP:0106384	photoreceptor disc membrane eye photoreceptor cell disorganized, abnormal
ZP:0106385	auditory behavior decreased occurrence, abnormal
ZP:0106386	retinal rod cell position, abnormal
ZP:0106387	macula position, abnormal
ZP:0106388	statoacoustic (VIII) ganglion position, abnormal
ZP:0106390	neurocranial trabecula deformed, abnormal
ZP:0106391	pterygoid process decreased size, abnormal
ZP:0106392	dentary increased amount, abnormal
ZP:0106393	ceratobranchial 2 cartilage decreased amount, abnormal
ZP:0106394	ceratobranchial 3 cartilage decreased amount, abnormal
ZP:0106395	ceratobranchial 4 cartilage decreased amount, abnormal
ZP:0106396	ceratobranchial 1 cartilage decreased amount, abnormal
ZP:0106397	ceratobranchial 5 cartilage decreased amount, abnormal
ZP:0106398	neurocranium decreased amount, abnormal
ZP:0106405	optic tectum has fewer parts of type ventral region microglial cell, abnormal
ZP:0106420	adipose tissue increased size, abnormal
ZP:0106422	cleavage furrow ingression process quality, abnormal
ZP:0106423	cleavage furrow ingression decreased occurrence, abnormal
ZP:0106424	calcium(2+) blastomere amount, abnormal
ZP:0106425	blastomere process quality actin filament-based process, abnormal
ZP:0106426	blastomere increased frequency release of sequestered calcium ion into cytosol, abnormal
ZP:0106427	blastomere process quality release of sequestered calcium ion into cytosol, abnormal
ZP:0106428	blastomere decreased accumulation mitochondrion cleavage furrow blastomere, abnormal
ZP:0106429	blastomere decreased accumulation lysosome cleavage furrow blastomere, abnormal
ZP:0106430	blastomere decreased accumulation endoplasmic reticulum cleavage furrow blastomere, abnormal
ZP:0106431	cerebellum morphogenesis decreased process quality, abnormal
ZP:0106432	cerebellum decreased area, abnormal
ZP:0106433	cerebellum has fewer parts of type cerebellar granule cell, abnormal
ZP:0106434	cerebellum has fewer parts of type Purkinje cell, abnormal
ZP:0106435	unfertilized egg decreased occurrence pseudocleavage, abnormal
ZP:0106436	blastomere process quality microtubule cytoskeleton organization, abnormal
ZP:0106437	lateral rectus absent, abnormal
ZP:0106438	ventral transverse absent, abnormal
ZP:0106439	dorsal oblique extraocular muscle absent, abnormal
ZP:0106440	hypaxial myotome region absent, abnormal
ZP:0106441	brain segmentation decreased process quality, abnormal
ZP:0106443	parachordal vessel decreased occurrence lymph vessel development, abnormal
ZP:0106444	lymphangiogenic sprout process quality lymphangiogenesis, abnormal
ZP:0106445	fatty acid beta-oxidation decreased process quality, abnormal
ZP:0106446	docosahexaenoic acid whole organism decreased amount, abnormal
ZP:0106449	blood cell caudal vein decreased amount, abnormal
ZP:0106450	hemoglobin blood cell decreased amount, abnormal
ZP:0106451	erythroblast caudal hematopoietic tissue decreased amount, abnormal
ZP:0106454	rhombomere 6 vestigial, abnormal
ZP:0106455	rhombomere 5 vestigial, abnormal
ZP:0106456	abducens motor nucleus rhombomere 6 absent, abnormal
ZP:0106457	abducens motor nucleus rhombomere 5 absent, abnormal
ZP:0106458	abducens motor nucleus process quality axon guidance, abnormal
ZP:0106459	abducens motor nucleus decreased occurrence axon extension, abnormal
ZP:0106460	neuronal cell body abducens motor nucleus mislocalised dorsally, abnormal
ZP:0106465	primordial germ cell decreased process quality microtubule organizing center organization, abnormal
ZP:0106466	primordial germ cell has extra parts of type microtubule organizing center primordial germ cell, abnormal
ZP:0106467	primordial germ cell decreased rate cell division, abnormal
ZP:0106468	pharyngeal arch 2 decreased occurrence cartilage development, abnormal
ZP:0106469	pharyngeal arch 1 decreased occurrence cartilage development, abnormal
ZP:0106472	palatoquadrate cartilage decreased amount, abnormal
ZP:0106477	ventral wall of dorsal aorta decreased distribution, abnormal
ZP:0106478	endothelial cell decreased occurrence cell population proliferation, abnormal
ZP:0106479	mitochondrion endothelial cell decreased amount, abnormal
ZP:0106480	endothelial cell increased process quality mitochondrial ATP synthesis coupled electron transport, abnormal
ZP:0106490	right side lateral mesoderm mislocalised, abnormal
ZP:0106497	grey matter hindbrain physical object quality, abnormal
ZP:0106498	response to external stimulus process quality, abnormal
ZP:0106499	axoneme sperm malformed, abnormal
ZP:0106500	sperm decreased process quality sperm axoneme assembly, abnormal
ZP:0106501	sperm flagellum sperm decreased length, abnormal
ZP:0106502	sperm head sperm increased size, abnormal
ZP:0106503	sperm head sperm vacuolated, abnormal
ZP:0106504	spermatocyte decreased occurrence regulation of meiotic cell cycle phase transition, abnormal
ZP:0106505	sperm head plasma membrane sperm dislocated, abnormal
ZP:0106509	neuromast hair cell process quality establishment of planar polarity, abnormal
ZP:0106510	neuromast hair cell process quality establishment of animal organ orientation, abnormal
ZP:0106513	3',5'-cyclic AMP thrombocyte increased amount, abnormal
ZP:0106514	cardiac muscle cell cardiac ventricle disorganized, abnormal
ZP:0106515	cardiac muscle cell cardiac ventricle condensed, abnormal
ZP:0106516	cardiac muscle cell atrium disorganized, abnormal
ZP:0106517	cardiac muscle cell atrium condensed, abnormal
ZP:0106518	anatomical region atrioventricular canal cellular quality, abnormal
ZP:0106519	filamentous actin endothelial cell spatial pattern, abnormal
ZP:0106520	cell endocardium 3-D shape, abnormal
ZP:0106521	endocardial cushion formation decreased occurrence, abnormal
ZP:0106523	cell presumptive atrioventricular canal 3-D shape, abnormal
ZP:0106524	atrioventricular canal aplastic/hypoplastic, abnormal
ZP:0106525	heart process quality determination of heart left/right asymmetry, abnormal
ZP:0106526	intersegmental vessel decreased efficacy cell migration involved in sprouting angiogenesis, abnormal
ZP:0106527	intersegmental vessel process quality blood vessel development, abnormal
ZP:0106528	trunk vasculature decreased process quality blood circulation, abnormal
ZP:0106529	endothelial cell endocardium mislocalised, abnormal
ZP:0106530	endocardium morphogenesis decreased occurrence, abnormal
ZP:0106531	endocardium formation decreased occurrence, abnormal
ZP:0106532	heart arrested heart looping, abnormal
ZP:0106533	ventral mandibular arch mislocalised posteriorly, abnormal
ZP:0106534	photoreceptor inner segment layer decreased thickness, abnormal
ZP:0106535	anterior region posterior lateral line primordium decreased amount, abnormal
ZP:0106536	central region posterior lateral line primordium decreased amount, abnormal
ZP:0106537	posterior lateral line primordium arrested posterior lateral line neuromast primordium migration, abnormal
ZP:0106538	anterior region posterior lateral line primordium decreased distribution, abnormal
ZP:0106539	posterior region posterior lateral line primordium increased amount, abnormal
ZP:0106540	posterior region posterior lateral line primordium increased distribution, abnormal
ZP:0106541	posterior region posterior lateral line primordium decreased amount, abnormal
ZP:0106542	posterior region posterior lateral line primordium mislocalised, abnormal
ZP:0106543	posterior lateral line primordium delayed posterior lateral line neuromast deposition, abnormal
ZP:0106545	protein blood plasma increased amount, abnormal
ZP:0106546	high-density lipoprotein cholesterol blood plasma increased amount, abnormal
ZP:0106549	regulation of appetite decreased process quality, abnormal
ZP:0106550	eating behavior increased occurrence, abnormal
ZP:0106551	nucleus of the medial longitudinal fasciculus synencephalon absent, abnormal
ZP:0106553	ocular blood vessel hemorrhagic, abnormal
ZP:0106556	lateral dorsal aorta increased diameter, abnormal
ZP:0106559	myelinating Schwann cell scale absent, abnormal
ZP:0106560	axon scale decreased amount, abnormal
ZP:0106565	integument orientation axon integument, abnormal
ZP:0106566	integument process quality innervation, abnormal
ZP:0106567	integument orientation blood vessel integument, abnormal
ZP:0106568	blood vessel integument decreased amount, abnormal
ZP:0106569	trunk lacks all parts of type epidermis axon sensory neuron, abnormal
ZP:0106570	trunk has fewer parts of type epidermis axon sensory neuron, abnormal
ZP:0106571	scale decreased occurrence innervation, abnormal
ZP:0106573	ependymal cell absent, abnormal
ZP:0106574	ependymal cell decreased amount, abnormal
ZP:0106581	mandibular lateral line neuromast decreased occurrence detection of mechanical stimulus involved in sensory perception of sound, abnormal
ZP:0106582	otic lateral line neuromast decreased occurrence detection of mechanical stimulus involved in sensory perception of sound, abnormal
ZP:0106584	opercular lateral line neuromast decreased occurrence detection of mechanical stimulus involved in sensory perception of sound, abnormal
ZP:0106585	middle lateral line neuromast decreased occurrence detection of mechanical stimulus involved in sensory perception of sound, abnormal
ZP:0106586	posterior lateral line neuromast decreased occurrence detection of mechanical stimulus involved in sensory perception of sound, abnormal
ZP:0106588	epiboly involved in gastrulation with mouth forming second onset quality, abnormal
ZP:0106589	epiboly involved in gastrulation with mouth forming second increased duration, abnormal
ZP:0106590	external yolk syncytial layer decreased occurrence actomyosin structure organization, abnormal
ZP:0106591	actomyosin external yolk syncytial layer decreased width, abnormal
ZP:0106592	marginal blastomere external yolk syncytial layer shape, abnormal
ZP:0106593	EVL shape, abnormal
ZP:0106601	blastomere absent, abnormal
ZP:0106603	multi-ciliated epithelial cell olfactory placode decreased amount, abnormal
ZP:0106604	glucose-6-phosphate dehydrogenase activity decreased occurrence, abnormal
ZP:0106606	ceratohyal cartilage rotated, abnormal
ZP:0106608	mitochondrial cloud oocyte morphology, abnormal
ZP:0106609	mitochondrial cloud oocyte decreased size, abnormal
ZP:0106624	cardiac ventricle arrested cardiac muscle contraction, abnormal
ZP:0106625	atrium arrested cardiac muscle contraction, abnormal
ZP:0106626	endothelial cell pronephric glomerulus swollen, abnormal
ZP:0106630	macrophage optic tectum decreased amount, abnormal
ZP:0106647	microglial cell optic tectum increased amount, abnormal
ZP:0106652	pronephros hypoplastic, abnormal
ZP:0106653	proximal convoluted tubule increased size, abnormal
ZP:0106654	proximal straight tubule increased diameter, abnormal
ZP:0106655	forebrain midbrain boundary increased occurrence apoptotic process, abnormal
ZP:0106656	brain disrupted mitotic cell cycle process, abnormal
ZP:0106661	compartment boundary myotome broken, abnormal
ZP:0106662	muscle cell myotome position, abnormal
ZP:0106663	muscle cell spatial pattern, abnormal
ZP:0106666	anatomical line increased amount, abnormal
ZP:0106667	endoderm increased width, abnormal
ZP:0106668	endoderm decreased efficacy cell migration involved in gastrulation, abnormal
ZP:0106669	endoderm process quality convergent extension involved in gastrulation, abnormal
ZP:0106670	endoderm decreased efficacy convergent extension involved in gastrulation, abnormal
ZP:0106671	granulocyte ventral wall of dorsal aorta decreased amount, abnormal
ZP:0106672	granulocyte rostral blood island decreased amount, abnormal
ZP:0106673	granulocyte blood island decreased amount, abnormal
ZP:0106674	hypermethylation of CpG island increased occurrence, abnormal
ZP:0106676	lateral plate mesoderm decreased occurrence determination of left/right asymmetry in lateral mesoderm, abnormal
ZP:0106677	endocrine pancreas decreased occurrence determination of pancreatic left/right asymmetry, abnormal
ZP:0106678	whole organism decreased occurrence smoothened signaling pathway, abnormal
ZP:0106685	melanocyte melanophore stripe decreased pigmentation, abnormal
ZP:0106686	whole organism color pattern, abnormal
ZP:0106690	cytosol myocardium mislocalised, abnormal
ZP:0106691	cytosol myocardium increased distribution, abnormal
ZP:0106692	Z disc myocardium disorganized, abnormal
ZP:0106693	myocardium decreased process quality sarcomere organization, abnormal
ZP:0106697	cardiac ventricle decreased occurrence heart contraction, abnormal
ZP:0106698	male organism decreased process quality heart contraction, abnormal
ZP:0106699	female organism decreased process quality heart contraction, abnormal
ZP:0106701	atrium female organism increased area, abnormal
ZP:0106703	female organism decreased weight, abnormal
ZP:0106704	atrial myocardium has fewer parts of type sarcomere atrial myocardium, abnormal
ZP:0106705	ventricular myocardium has fewer parts of type sarcomere ventricular myocardium, abnormal
ZP:0106706	melanocyte caudal fin increased amount, abnormal
ZP:0106707	melanocyte caudal fin increased area, abnormal
ZP:0106708	pigment cell increased amount, abnormal
ZP:0106712	retinal cone cell delayed cone photoresponse recovery, abnormal
ZP:0106713	retinal cone cell decreased occurrence cone photoresponse recovery, abnormal
ZP:0106717	blood dorsal aorta decreased velocity, abnormal
ZP:0106718	blood posterior cardinal vein decreased velocity, abnormal
ZP:0106719	skeletal muscle myofibril myotome bent, abnormal
ZP:0106720	myoseptum irregularly shaped, abnormal
ZP:0106721	sarcoplasmic reticulum skeletal muscle disorganized, abnormal
ZP:0106722	A band skeletal muscle disorganized, abnormal
ZP:0106723	I band skeletal muscle disorganized, abnormal
ZP:0106724	heart valve formation delayed, abnormal
ZP:0106725	skeletal muscle malformed, abnormal
ZP:0106726	glucose blood molecular quality, abnormal
ZP:0106727	ionocyte yolk increased amount, abnormal
ZP:0106729	double-stranded DNA fragment whole organism decreased amount, abnormal
ZP:0106730	translation increased occurrence, abnormal
ZP:0106731	nucleus blastomere broken, abnormal
ZP:0106732	plasma membrane blastomere structure, abnormal
ZP:0106733	tubulin complex assembly decreased occurrence, abnormal
ZP:0106734	cleavage furrow formation decreased occurrence, abnormal
ZP:0106735	oocyte stage V decreased occurrence proteolysis, abnormal
ZP:0106736	blastomere shape, abnormal
ZP:0106737	blastomere position, abnormal
ZP:0106738	cortical granule fertilized egg increased amount, abnormal
ZP:0106739	cortical granule exocytosis decreased occurrence, abnormal
ZP:0106740	chorion decreased elevation, abnormal
ZP:0106741	chorion decreased diameter, abnormal
ZP:0106742	nuclear pore blastomere absent, abnormal
ZP:0106743	oocyte stage V opaque, abnormal
ZP:0106744	oocyte stage V immature, abnormal
ZP:0106745	cytoplasm pronephric distal early tubule mislocalised, abnormal
ZP:0106746	epithelial cell pronephric proximal straight tubule increased length, abnormal
ZP:0106747	epithelial cell pronephric distal late tubule increased length, abnormal
ZP:0106748	pronephric proximal straight tubule decreased width, abnormal
ZP:0106749	pronephric distal late tubule increased width, abnormal
ZP:0106752	caudal commissure has fewer parts of type axon caudal commissure, abnormal
ZP:0106753	rhombomere disorganized, abnormal
ZP:0106754	supraoptic tract has fewer parts of type axon supraoptic tract, abnormal
ZP:0106755	white matter morphology, abnormal
ZP:0106756	whole organism process quality social behavior, abnormal
ZP:0106757	cranial neural crest cell delayed cell migration, abnormal
ZP:0106758	cranial neural crest cell decreased process quality cell migration, abnormal
ZP:0106759	migratory cranial neural crest cell hindbrain mislocalised, abnormal
ZP:0106760	migratory cranial neural crest increased distribution, abnormal
ZP:0106761	basal communicating artery increased curvature, abnormal
ZP:0106762	basal communicating artery kinked, abnormal
ZP:0106763	posterior communicating artery increased curvature, abnormal
ZP:0106764	posterior communicating artery kinked, abnormal
ZP:0106767	ventral region eye increased amount, abnormal
ZP:0106768	ventral region eye increased distribution, abnormal
ZP:0106769	optic furrow increased distribution, abnormal
ZP:0106770	retinal cone cell process quality cellular response to light stimulus, abnormal
ZP:0106771	retinal cone cell decreased process quality regulation of calcium ion transmembrane transport, abnormal
ZP:0106774	primordial midbrain channel increased amount, abnormal
ZP:0106775	ventricular zone decreased size, abnormal
ZP:0106776	endothelial cell primordial midbrain channel increased amount, abnormal
ZP:0106784	dorsal region trunk decreased distribution, abnormal
ZP:0106785	dorsal region trunk decreased amount, abnormal
ZP:0106786	medial region trunk decreased amount, abnormal
ZP:0106787	ventral region trunk decreased amount, abnormal
ZP:0106788	melanocyte ball decreased amount, abnormal
ZP:0106800	ovulation arrested, abnormal
ZP:0106801	opercular flap protruding, abnormal
ZP:0106802	cranium decreased height, abnormal
ZP:0106803	caudal fin broken, abnormal
ZP:0106804	head has fewer parts of type barbel, abnormal
ZP:0106805	anal fin broken, abnormal
ZP:0106806	dorsal fin broken, abnormal
ZP:0106807	head lacks all parts of type barbel, abnormal
ZP:0106817	epidermal cell head morphology, abnormal
ZP:0106818	epidermal cell trunk morphology, abnormal
ZP:0106819	lysosome peridermal cell increased amount, abnormal
ZP:0106820	peridermal cell increased occurrence endocytosis, abnormal
ZP:0106821	epidermis increased occurrence cell population proliferation, abnormal
ZP:0106822	peridermal cell increased occurrence cell population proliferation, abnormal
ZP:0106823	perinucleolar compartment peridermal cell increased amount, abnormal
ZP:0106827	heme neutrophil decreased amount, abnormal
ZP:0106829	neutrophil arrested peroxidase activity, abnormal
ZP:0106830	desmosome heart disorganized, abnormal
ZP:0106831	desmosome integument disorganized, abnormal
ZP:0106832	heme nucleate erythrocyte increased amount, abnormal
ZP:0106833	floor plate increased amount, abnormal
ZP:0106839	caudal hematopoietic tissue absent, abnormal
ZP:0106840	heme whole organism absent, abnormal
ZP:0106843	blood island edematous, abnormal
ZP:0106844	nucleate erythrocyte circulating cell decreased amount, abnormal
ZP:0106845	central region lens refractivity, abnormal
ZP:0106846	lens decreased process quality lens development in camera-type eye, abnormal
ZP:0106847	anterior region lens opaque, abnormal
ZP:0106848	lens decreased process quality lens morphogenesis in camera-type eye, abnormal
ZP:0106849	lens fiber cell decreased process quality lens fiber cell morphogenesis, abnormal
ZP:0106850	lens refractivity, abnormal
ZP:0106851	central region lens opaque, abnormal
ZP:0106854	epiboly involved in gastrulation with mouth forming second decreased occurrence, abnormal
ZP:0106855	embryonic structure detached from yolk, abnormal
ZP:0106856	periderm broken, abnormal
ZP:0106857	melanin biosynthetic process decreased occurrence, abnormal
ZP:0106861	myofilament muscle disorganized, abnormal
ZP:0106862	lens fiber cell shape, abnormal
ZP:0106863	lens fiber cell convex 3-D shape, abnormal
ZP:0106864	sarcomere heart tube disorganized, abnormal
ZP:0106865	immature eye increased distribution, abnormal
ZP:0106866	diencephalon has fewer parts of type ventral region dopaminergic neuron diencephalon, abnormal
ZP:0106867	caudal periventricular hypothalamus has fewer parts of type serotonergic neuron caudal periventricular hypothalamus, abnormal
ZP:0106868	paraventricular organ has fewer parts of type serotonergic neuron paraventricular organ, abnormal
ZP:0106869	ventral region caudal tuberculum absent, abnormal
ZP:0106870	raphe nucleus decreased amount, abnormal
ZP:0106871	vasculature decreased distribution, abnormal
ZP:0106875	fear response increased process quality, abnormal
ZP:0106879	hyaluronic acid heart decreased amount, abnormal
ZP:0106880	cardiac jelly atrioventricular canal absent, abnormal
ZP:0106881	endocardial cushion development decreased occurrence, abnormal
ZP:0106882	cardiac jelly development decreased occurrence, abnormal
ZP:0106888	scale primordium absent, abnormal
ZP:0106890	dermis absent, abnormal
ZP:0106891	pronephric tubule decreased occurrence lysosomal protein catabolic process, abnormal
ZP:0106897	autophagosome pronephric tubule increased size, abnormal
ZP:0106898	pronephric tubule has extra parts of type autophagosome pronephric tubule, abnormal
ZP:0106899	renal tubule occurrence autophagy, abnormal
ZP:0106900	cortical granule oocyte stage II increased amount, abnormal
ZP:0106901	cortical granule oocyte stage II decreased size, abnormal
ZP:0106902	skeletal muscle has extra parts of type mitochondrion inclusion body skeletal muscle, abnormal
ZP:0106905	swim bladder increased variability of size, abnormal
ZP:0106907	Kupffer's vesicle orientation cilium Kupffer's vesicle, abnormal
ZP:0106908	stereocilium bundle posterior lateral line neuromast decreased functionality, abnormal
ZP:0106909	inner ear arrested detection of mechanical stimulus involved in sensory perception of sound, abnormal
ZP:0106912	neutrophil decreased occurrence cell maturation, abnormal
ZP:0106916	stereocilium bundle hair cell anterior macula decreased amount, abnormal
ZP:0106918	axon midbrain mislocalised, abnormal
ZP:0106919	axon spinal cord defasciculated, abnormal
ZP:0106920	post-vent region lacks all parts of type posterior lateral line neuromast, abnormal
ZP:0106922	hematopoietic stem cell decreased occurrence maintenance of location, abnormal
ZP:0106923	granulocyte caudal hematopoietic tissue decreased amount, abnormal
ZP:0106924	macrophage caudal hematopoietic tissue decreased amount, abnormal
ZP:0106925	erythroid lineage cell caudal hematopoietic tissue decreased amount, abnormal
ZP:0106926	macrophage caudal hematopoietic tissue absent, abnormal
ZP:0106928	dorsal convergence decreased occurrence, abnormal
ZP:0106929	endodermal cell decreased occurrence dorsal convergence, abnormal
ZP:0106932	anterior region trunk musculature decreased amount, abnormal
ZP:0106933	anterior region trunk decreased amount, abnormal
ZP:0106934	nucleus blastomere absent, abnormal
ZP:0106935	plasma membrane blastomere absent, abnormal
ZP:0106936	ectoderm increased distribution, abnormal
ZP:0106937	axis increased thickness, abnormal
ZP:0106938	medial region whole organism increased amount, abnormal
ZP:0106939	medial region whole organism increased distribution, abnormal
ZP:0106940	left side lateral plate mesoderm mislocalised, abnormal
ZP:0106941	notochord increased distribution, abnormal
ZP:0106942	anatomical region Kupffer's vesicle decreased amount, abnormal
ZP:0106950	apical side cardiac muscle cell constricted, abnormal
ZP:0106951	cardiac muscle cell has extra parts of type basal region cell projection cardiac muscle cell, abnormal
ZP:0106952	actomyosin cardiac ventricle spatial pattern, abnormal
ZP:0106953	actomyosin cardiac ventricle polarity, abnormal
ZP:0106954	actomyosin heart spatial pattern, abnormal
ZP:0106955	actomyosin myocardium increased distribution, abnormal
ZP:0106956	cytoplasm whole organism decreased amount, abnormal
ZP:0106957	blastomere increased occurrence apoptotic process, abnormal
ZP:0106958	blastomere arrested cell population proliferation, abnormal
ZP:0106959	microtubule cytoskeleton organization process quality, abnormal
ZP:0106960	cytoplasm blastomere mislocalised, abnormal
ZP:0106961	gamma-tubulin small complex blastomere absent, abnormal
ZP:0106962	perinuclear region of cytoplasm blastomere mislocalised, abnormal
ZP:0106965	thrombocyte activation process quality, abnormal
ZP:0106966	thromboblast head kidney decreased amount, abnormal
ZP:0106967	axon extension accelerated growth, abnormal
ZP:0106968	neuron projection CaP motoneuron increased length, abnormal
ZP:0106969	vein caudal fin tangled, abnormal
ZP:0106970	intersegmental vein caudal fin morphology, abnormal
ZP:0106971	intersegmental vein caudal fin dilated, abnormal
ZP:0106972	subintestinal vein caudal fin morphology, abnormal
ZP:0106973	subintestinal vein caudal fin dilated, abnormal
ZP:0106974	vein protruding out of intersegmental vein caudal fin, abnormal
ZP:0106975	vein protruding out of subintestinal vein caudal fin, abnormal
ZP:0106976	aggressive behavior process quality, abnormal
ZP:0106977	forebrain decreased occurrence axonal fasciculation, abnormal
ZP:0106978	midbrain decreased occurrence axonal fasciculation, abnormal
ZP:0106979	axon forebrain defasciculated, abnormal
ZP:0106980	axon midbrain defasciculated, abnormal
ZP:0106981	peripheral nervous system has fewer parts of type peripheral neuron, abnormal
ZP:0106982	trigeminal ganglion increased length, abnormal
ZP:0106983	trigeminal ganglion increased width, abnormal
ZP:0106984	trigeminal ganglion decondensed, abnormal
ZP:0106985	posterior region hypothalamus decreased amount, abnormal
ZP:0106986	hindbrain has fewer parts of type dopaminergic neuron, abnormal
ZP:0106987	midbrain has fewer parts of type dopaminergic neuron, abnormal
ZP:0106988	endohypothalamic tract decreased amount, abnormal
ZP:0106989	statoacoustic (VIII) ganglion increased amount, abnormal
ZP:0106990	posterior lateral line ganglion increased amount, abnormal
ZP:0106991	anterior region trunk apoptotic, abnormal
ZP:0106992	neuromuscular junction of skeletal muscle fiber fast muscle cell morphology, abnormal
ZP:0106993	cholinergic synapse fast muscle cell spatial pattern, abnormal
ZP:0106994	hindbrain has fewer parts of type cranial motor neuron, abnormal
ZP:0106995	midbrain has fewer parts of type cranial motor neuron, abnormal
ZP:0106996	cholesterol caudal vein increased amount, abnormal
ZP:0106997	low-density lipoprotein cholesterol whole organism increased amount, abnormal
ZP:0106998	intestine lumen distended, abnormal
ZP:0107000	mitochondrion retinal pigmented epithelium increased amount, abnormal
ZP:0107001	mitochondrion retinal pigmented epithelium increased area, abnormal
ZP:0107002	mitochondrion retinal cone cell morphology, abnormal
ZP:0107003	mitochondrion retinal cone cell circular, abnormal
ZP:0107004	mitochondrion retinal cone cell increased size, abnormal
ZP:0107006	cell projection Muller cell increased distribution, abnormal
ZP:0107007	phagocytic vesicle retinal pigmented epithelium increased amount, abnormal
ZP:0107008	cranial neural crest pharyngeal arch decreased amount, abnormal
ZP:0107009	neural crest pharyngeal arch decreased amount, abnormal
ZP:0107010	ceratobranchial 2 cartilage morphology, abnormal
ZP:0107011	ceratobranchial 2 cartilage decreased size, abnormal
ZP:0107012	ceratobranchial 3 cartilage morphology, abnormal
ZP:0107013	ceratobranchial 3 cartilage decreased size, abnormal
ZP:0107014	ceratobranchial 4 cartilage morphology, abnormal
ZP:0107015	ceratobranchial 1 cartilage morphology, abnormal
ZP:0107016	ceratobranchial 1 cartilage decreased size, abnormal
ZP:0107017	ceratobranchial 5 cartilage decreased size, abnormal
ZP:0107018	pharyngeal pouch increased amount, abnormal
ZP:0107019	Non-Lymphoid leukaemias whole organism increased amount, abnormal
ZP:0107020	sarcoma whole organism increased amount, abnormal
ZP:0107021	vasculature neoplastic, abnormal
ZP:0107022	germ line cell neoplastic, abnormal
ZP:0107023	B cell spleen decreased amount, abnormal
ZP:0107026	spinal cord has extra parts of type anterior region axon Mauthner neuron, abnormal
ZP:0107028	neural crest pharyngeal arch 3 decreased amount, abnormal
ZP:0107029	neural crest pharyngeal arch 4 decreased amount, abnormal
ZP:0107030	neural crest pharyngeal arch 5 decreased amount, abnormal
ZP:0107031	neural crest pharyngeal arch 6 decreased amount, abnormal
ZP:0107032	neural crest pharyngeal arch 2 decreased amount, abnormal
ZP:0107033	neural crest pharyngeal arch 1 decreased amount, abnormal
ZP:0107034	(R)-lactate blood plasma increased amount, abnormal
ZP:0107036	B cell increased occurrence apoptotic process, abnormal
ZP:0107037	T cell head kidney increased amount, abnormal
ZP:0107041	spinal cord has fewer parts of type anterior region axon reticulospinal neuron, abnormal
ZP:0107042	spinal cord has fewer parts of type posterior region axon reticulospinal neuron, abnormal
ZP:0107043	reticulospinal neuron decreased occurrence axon extension, abnormal
ZP:0107044	cranial neural crest ceratohyal cartilage decreased amount, abnormal
ZP:0107045	ATP cell decreased amount, abnormal
ZP:0107046	subcutaneous fat dorsal fin increased amount, abnormal
ZP:0107047	calcium import into the mitochondrion disrupted, abnormal
ZP:0107049	caudal fin fat increased amount, abnormal
ZP:0107051	proctodeum decreased amount, abnormal
ZP:0107052	skeletal element head morphology, abnormal
ZP:0107053	pectoral fin increased amount, abnormal
ZP:0107054	cell pharyngeal arch 2 decreased amount, abnormal
ZP:0107055	cell pharyngeal arch 1 decreased amount, abnormal
ZP:0107056	anatomical margin median fin fold irregularly shaped, abnormal
ZP:0107057	anatomical margin pectoral fin irregularly shaped, abnormal
ZP:0107058	proximal region fin fold pectoral fin bud absent, abnormal
ZP:0107059	renal system development process quality, abnormal
ZP:0107060	renal system morphology, abnormal
ZP:0107061	pectoral fin blistered, abnormal
ZP:0107062	nephron morphology, abnormal
ZP:0107063	blood vasculature misrouted, abnormal
ZP:0107064	intersegmental vessel has extra parts of type angiogenic sprout, abnormal
ZP:0107065	dorsal longitudinal vein attached to mesencephalic artery, abnormal
ZP:0107066	dorsal longitudinal vein attached to mesencephalic vein, abnormal
ZP:0107067	lateral dorsal aorta shape, abnormal
ZP:0107068	neural crest cell pharyngeal arch 2 shape, abnormal
ZP:0107069	germ line cell testis spatial pattern, abnormal
ZP:0107070	testis translucent, abnormal
ZP:0107071	condensed nuclear chromosome ovary spatial pattern, abnormal
ZP:0107072	condensed nuclear chromosome testis spatial pattern, abnormal
ZP:0107073	synaptonemal structure spermatocyte absent, abnormal
ZP:0107074	meiotic sister chromatid cohesion process quality, abnormal
ZP:0107075	chromosome organization involved in meiotic cell cycle process quality, abnormal
ZP:0107076	synaptonemal complex organization process quality, abnormal
ZP:0107077	anterior-posterior axis vertebral column increased curvature, abnormal
ZP:0107081	cone photoreceptor disc membrane retinal cone cell broken, abnormal
ZP:0107082	vertebral column deformed, abnormal
ZP:0107083	nuclear chromosome segregation disrupted, abnormal
ZP:0107084	hindbrain decreased magnitude axonogenesis, abnormal
ZP:0107086	cranial nerve X decreased occurrence axon arborization, abnormal
ZP:0107087	cranial nerve IX decreased occurrence axon arborization, abnormal
ZP:0107088	cranial nerve X decreased amount, abnormal
ZP:0107089	cranial nerve VII misrouted, abnormal
ZP:0107090	cranial nerve VII defasciculated, abnormal
ZP:0107091	cranial nerve IX decreased amount, abnormal
ZP:0107093	vestibular reflex decreased process quality, abnormal
ZP:0107097	cranial nerve IX misrouted, abnormal
ZP:0107098	pronephric glomerulus increased diameter, abnormal
ZP:0107099	cytoskeleton intestinal epithelium mislocalised, abnormal
ZP:0107102	pharyngeal arch 3 increased amount, abnormal
ZP:0107103	pharyngeal arch 4 increased amount, abnormal
ZP:0107104	pharyngeal arch 5 increased amount, abnormal
ZP:0107105	pharyngeal arch 6 increased amount, abnormal
ZP:0107106	pharyngeal arch 7 increased amount, abnormal
ZP:0107107	periocular mesenchyme decreased amount, abnormal
ZP:0107110	central region oocyte stage II mislocalised, abnormal
ZP:0107111	cytoplasm oocyte stage II mislocalised, abnormal
ZP:0107112	basement membrane epidermis morphology, abnormal
ZP:0107114	dorsal aorta decreased occurrence Notch signaling pathway, abnormal
ZP:0107115	posterior region whole organism curved ventral, abnormal
ZP:0107124	pillar of the semicircular canal malformed, abnormal
ZP:0107128	dorsal region spinal cord neural keel decreased amount, abnormal
ZP:0107130	dorsal longitudinal anastomotic vessel decreased occurrence sprouting angiogenesis, abnormal
ZP:0107131	dorsal longitudinal anastomotic vessel split, abnormal
ZP:0107133	neural crest cell spatial pattern, abnormal
ZP:0107140	photoreceptor ribbon synapse eye morphology, abnormal
ZP:0107141	extraocular musculature morphology, abnormal
ZP:0107142	extraocular musculature increased amount, abnormal
ZP:0107143	extraocular musculature increased distribution, abnormal
ZP:0107144	muscle pharyngeal arch morphology, abnormal
ZP:0107145	medial rectus morphology, abnormal
ZP:0107146	medial rectus decreased amount, abnormal
ZP:0107147	dorsal rectus decreased amount, abnormal
ZP:0107148	lateral rectus morphology, abnormal
ZP:0107149	lateral rectus decreased amount, abnormal
ZP:0107150	ventral rectus decreased amount, abnormal
ZP:0107151	dorsal oblique extraocular muscle decreased amount, abnormal
ZP:0107152	ventral oblique extraocular muscle decreased amount, abnormal
ZP:0107153	ventral region retina absent, abnormal
ZP:0107154	pharyngeal arch 6 decreased amount, abnormal
ZP:0107155	pharyngeal arch 7 decreased amount, abnormal
ZP:0107156	periocular mesenchyme absent, abnormal
ZP:0107158	neural keel spatial pattern, abnormal
ZP:0107159	neural keel increased distribution, abnormal
ZP:0107160	optic primordium decreased amount, abnormal
ZP:0107161	anterior neural keel decreased amount, abnormal
ZP:0107162	optic vesicle delayed neurogenesis, abnormal
ZP:0107163	neural plate increased distribution, abnormal
ZP:0107164	cellular anatomical entity myoseptum aggregated, abnormal
ZP:0107165	cellular anatomical entity skeletal muscle aggregated, abnormal
ZP:0107166	intersegmental vessel decreased occurrence cell migration involved in sprouting angiogenesis, abnormal
ZP:0107167	blood vessel endothelial cell accumulation intersegmental vessel, abnormal
ZP:0107169	xanthophore disrupted cell migration, abnormal
ZP:0107170	head decreased occurrence macrophage migration, abnormal
ZP:0107171	head decreased duration macrophage migration, abnormal
ZP:0107172	cell projection melanocyte increased amount, abnormal
ZP:0107173	mRNA splicing, via spliceosome process efficacy, abnormal
ZP:0107174	mRNA splice site selection disrupted, abnormal
ZP:0107175	cornea edematous, abnormal
ZP:0107177	anterior region spinal cord decreased size, abnormal
ZP:0107178	dorsal region neural keel decreased amount, abnormal
ZP:0107179	anatomical region common cardinal vein increased amount, abnormal
ZP:0107180	metallopeptidase activity increased occurrence, abnormal
ZP:0107183	pronephric distal early tubule increased volume, abnormal
ZP:0107184	pronephric distal late tubule decreased volume, abnormal
ZP:0107185	male organism decreased size, abnormal
ZP:0107188	pronephric duct increased area, abnormal
ZP:0107189	melanocyte migration process quality, abnormal
ZP:0107190	myeloid cell decreased process quality cell migration, abnormal
ZP:0107191	neutrophil circulating cell decreased amount, abnormal
ZP:0107193	myeloid cell kidney decreased amount, abnormal
ZP:0107194	dihydroceramide whole organism increased amount, abnormal
ZP:0107195	Collagen semicircular canal present, abnormal
ZP:0107199	semicircular canal aplastic/hypoplastic, abnormal
ZP:0107202	otic vesicle ventral protrusion present, abnormal
ZP:0107203	pillar of the lateral semicircular canal absent, abnormal
ZP:0107204	inner ear lacks parts or has fewer parts of type semicircular canal, abnormal
ZP:0107205	proteoglycan otic vesicle protrusion decreased amount, abnormal
ZP:0107206	Collagen otic vesicle protrusion decreased amount, abnormal
ZP:0107207	otic vesicle lacks parts or has fewer parts of type otic vesicle protrusion, abnormal
ZP:0107209	heart decreased process quality cardiac muscle tissue growth involved in heart morphogenesis, abnormal
ZP:0107210	cell cortex cardiac muscle cell spatial pattern, abnormal
ZP:0107211	cell cortex cardiac muscle cell increased amount, abnormal
ZP:0107212	cell cortex cardiac muscle cell mislocalised, abnormal
ZP:0107213	cardiac muscle cell decreased process quality actin filament organization, abnormal
ZP:0107214	filamentous actin cardiac muscle cell mislocalised radially, abnormal
ZP:0107215	cardiac muscle cell decreased occurrence endocytic recycling, abnormal
ZP:0107216	cardiac muscle cell has extra parts of type recycling endosome cardiac muscle cell, abnormal
ZP:0107218	cardiac ventricle decreased occurrence cardiac chamber ballooning, abnormal
ZP:0107219	atrium decreased occurrence cardiac chamber ballooning, abnormal
ZP:0107220	cardiac muscle cell process quality regulation of embryonic cell shape, abnormal
ZP:0107221	dorsal fin fold decreased process quality embryonic dorsal fin morphogenesis, abnormal
ZP:0107222	ventral fin fold decreased process quality embryonic anal fin morphogenesis, abnormal
ZP:0107223	recycling endosome cardiac muscle cell increased amount, abnormal
ZP:0107224	recycling endosome cardiac muscle cell increased size, abnormal
ZP:0107225	epithelial cell dorsal fin fold protruding, abnormal
ZP:0107226	epithelial cell ventral fin fold protruding, abnormal
ZP:0107227	dorsal fin fold malformed, abnormal
ZP:0107228	cardiac muscle cell obtuse, abnormal
ZP:0107229	cardiac muscle cell protruding out of myocardium, abnormal
ZP:0107230	anterior neural plate absent, abnormal
ZP:0107232	postero-medial margin ceratohyal cartilage increased amount, abnormal
ZP:0107233	ceratohyal cartilage premature ossification, abnormal
ZP:0107235	ceratohyal bone irregularly shaped, abnormal
ZP:0107236	anterior region palatoquadrate cartilage decreased size, abnormal
ZP:0107237	ventral hypohyal bone premature ossification, abnormal
ZP:0107238	anguloarticular premature ossification, abnormal
ZP:0107239	quadrate premature ossification, abnormal
ZP:0107240	symplectic premature ossification, abnormal
ZP:0107241	ceratobranchial 2 cartilage premature ossification, abnormal
ZP:0107242	ceratobranchial 1 cartilage premature ossification, abnormal
ZP:0107245	ventral mandibular arch lacks parts or has fewer parts of type Meckel's cartilage, abnormal
ZP:0107248	neurocranium hypertrophic, abnormal
ZP:0107249	endothelial tip cell intersegmental vessel spade-shaped, abnormal
ZP:0107250	lymph vessel development decreased occurrence, abnormal
ZP:0107251	cardiovascular system lacks all parts of type thoracic duct, abnormal
ZP:0107252	cardiovascular system lacks all parts of type vascular lymphangioblast, abnormal
ZP:0107253	endothelial tip cell decreased occurrence calcium-mediated signaling, abnormal
ZP:0107254	endothelial tip cell decreased occurrence regulation of cytosolic calcium ion concentration, abnormal
ZP:0107255	endothelial tip cell decreased occurrence regulation of store-operated calcium channel activity, abnormal
ZP:0107256	endothelial tip cell intersegmental vessel decreased amount, abnormal
ZP:0107257	intersegmental vessel decreased occurrence Notch signaling pathway, abnormal
ZP:0107258	intersegmental vessel decreased occurrence endothelial tip cell filopodium assembly, abnormal
ZP:0107259	intersegmental vessel decreased occurrence MAPK cascade, abnormal
ZP:0107261	dorsal longitudinal anastomotic vessel increased diameter, abnormal
ZP:0107269	eye growth quality of occurrent organ growth, abnormal
ZP:0107270	eye circular, abnormal
ZP:0107271	ciliary marginal zone decreased occurrence cell population proliferation, abnormal
ZP:0107272	retinal ganglion cell layer decreased distribution, abnormal
ZP:0107275	progesterone blood plasma increased amount, abnormal
ZP:0107276	estradiol blood plasma decreased amount, abnormal
ZP:0107277	(20R)-17,20-dihydroxypregn-4-en-3-one testis increased amount, abnormal
ZP:0107278	blood male organism increased amount, abnormal
ZP:0107279	sperm increased amount, abnormal
ZP:0107281	chorion micropyle formation decreased occurrence, abnormal
ZP:0107283	micropylar cell absent, abnormal
ZP:0107284	pronucleus fertilized egg decreased amount, abnormal
ZP:0107285	micropyle fertilized egg absent, abnormal
ZP:0107286	pronephric proximal straight tubule increased occurrence pronephric nephron tubule epithelial cell differentiation, abnormal
ZP:0107287	pronephric distal late tubule decreased occurrence pronephric nephron tubule epithelial cell differentiation, abnormal
ZP:0107288	pronephric tubule decreased occurrence multi-ciliated epithelial cell differentiation, abnormal
ZP:0107289	pronephric tubule has fewer parts of type multi-ciliated epithelial cell pronephric tubule, abnormal
ZP:0107290	neurohypophysis absent, abnormal
ZP:0107291	intrahepatic bile duct aggregated, abnormal
ZP:0107292	intrahepatic bile duct epithelial cell spatial pattern, abnormal
ZP:0110336	pronephric tubule mislocalised, abnormal
ZP:0110337	mitochondrion neuromast hair cell functionality, abnormal
ZP:0110338	neuromast hair cell process quality regulation of mitochondrial membrane potential, abnormal
ZP:0110340	multi-ciliated epithelial cell malformed, abnormal
ZP:0110341	mitochondrion neuromast hair cell spatial pattern, abnormal
ZP:0110348	apical region pronephric duct decreased amount, abnormal
ZP:0110349	apical side pronephric glomerular capsule epithelium mislocalised, abnormal
ZP:0110350	cilium pronephric tubule malformed, abnormal
ZP:0110351	filamentous actin pronephric tubule malformed, abnormal
ZP:0110352	pronephric tubule decreased occurrence ciliary basal body-plasma membrane docking, abnormal
ZP:0110353	pronephric glomerular capsule epithelium apical-basal polarity, abnormal
ZP:0130672	ventral region diencephalon increased amount, abnormal
ZP:0130673	ventral region spinal cord decreased size, abnormal
ZP:0130675	adherens junction EVL structure, abnormal
ZP:0130677	trunk has extra parts of type ventral region melanocyte, abnormal
ZP:0130678	trunk has extra parts of type ventral region iridophore, abnormal
ZP:0130679	adherens junction neural tube morphology, abnormal
ZP:0130682	hypochord absent, abnormal
ZP:0130683	dorsoventral diencephalic tract process quality axon guidance, abnormal
ZP:0130684	Rohon-Beard neuron process quality axon guidance, abnormal
ZP:0130685	roof plate spinal cord region absent, abnormal
ZP:0130688	atrioventricular canal endocardium process quality tissue morphogenesis, abnormal
ZP:0130689	atrioventricular valve process quality tissue morphogenesis, abnormal
ZP:0130690	atrioventricular valve morphogenesis decreased occurrence, abnormal
ZP:0130701	cytosolic large ribosomal subunit whole organism decreased amount, abnormal
ZP:0130702	anatomical region whole organism absent, abnormal
ZP:0130704	cilium ependymal cell decreased amount, abnormal
ZP:0130705	fourth ventricle increased area, abnormal
ZP:0130706	tectal ventricle increased area, abnormal
ZP:0130707	telencephalic ventricle dilated, abnormal
ZP:0130709	neuromast increased occurrence cell population proliferation, abnormal
ZP:0130712	rhombomere 6 increased distance somite 1, abnormal
ZP:0130713	basement membrane pronephric glomerulus increased thickness, abnormal
ZP:0130714	basement membrane pronephric glomerulus disorganized, abnormal
ZP:0130715	pronephric glomerulus collapsed, abnormal
ZP:0130716	adherens junction median fin fold composition, abnormal
ZP:0130717	adherens junction Meckel's cartilage increased amount, abnormal
ZP:0130718	adherens junction chondrocyte increased amount, abnormal
ZP:0130719	melanocyte accumulation posterior-most region otic vesicle, abnormal
ZP:0130720	melanocyte accumulation lateral margin pharyngeal arch, abnormal
ZP:0130725	axon anterior commissure mislocalised, abnormal
ZP:0130726	postoptic commissure decreased amount, abnormal
ZP:0130727	anterior commissure decreased amount, abnormal
ZP:0130728	axon postoptic commissure mislocalised, abnormal
ZP:0130729	neuron projection eye absent, abnormal
ZP:0130730	neuron projection eye disorganized, abnormal
ZP:0130731	neuron projection eye decreased amount, abnormal
ZP:0130732	neuron projection optic tectum absent, abnormal
ZP:0130733	neuron eye decreased amount, abnormal
ZP:0130734	caudal commissure decreased amount, abnormal
ZP:0130735	tectal neuropile decreased size, abnormal
ZP:0130736	posterior side midbrain hindbrain boundary irregularly shaped, abnormal
ZP:0130738	blastoderm decreased occurrence cell-cell adhesion, abnormal
ZP:0130739	blastoderm decreased viscosity, abnormal
ZP:0130740	cilium cloaca decreased length, abnormal
ZP:0130741	cilium cloaca decreased amount, abnormal
ZP:0130744	posterior region inner ear anterioralized, abnormal
ZP:0130745	inner ear lacks all parts of type posterior macula, abnormal
ZP:0130746	inner ear has extra parts of type lateral crista, abnormal
ZP:0130747	sagitta mislocalised ventrally, abnormal
ZP:0130750	forebrain increased occurrence transmission of nerve impulse, abnormal
ZP:0130752	cardiac ventricle increased occurrence cell population proliferation, abnormal
ZP:0130755	ceratohyal cartilage angle basihyal cartilage, abnormal
ZP:0130768	cilium cloaca increased length, abnormal
ZP:0130770	muscle cell decreased diameter, abnormal
ZP:0130783	intestine increased occurrence apoptotic process, abnormal
ZP:0130790	intestinal motility decreased process quality, abnormal
ZP:0130795	brain decreased occurrence phagocytosis, abnormal
ZP:0130801	vasculature increased distribution, abnormal
ZP:0130802	basement membrane pronephric glomerulus morphology, abnormal
ZP:0130803	adherens junction posterior lateral line primordium decreased object quality, abnormal
ZP:0130807	left side intestinal bulb mislocalised, abnormal
ZP:0130808	left side mid intestine absent, abnormal
ZP:0130809	right side intestinal bulb mislocalised, abnormal
ZP:0130810	right side mid intestine absent, abnormal
ZP:0130812	stereocilium bundle lateral crista malformed, abnormal
ZP:0130818	brain vasculature hindbrain decreased amount, abnormal
ZP:0130819	neural crest patchy, abnormal
ZP:0130821	neural crest cell cellular adhesivity, abnormal
ZP:0130822	cleavage furrow blastomere incomplete structure, abnormal
ZP:0130823	cortical granule blastomere mislocalised, abnormal
ZP:0130824	cortical granule early embryonic cell mislocalised, abnormal
ZP:0130825	cortical actin cytoskeleton organization process quality, abnormal
ZP:0130826	cortical actin cytoskeleton organization decreased occurrence, abnormal
ZP:0130827	cortical granule exocytosis process quality, abnormal
ZP:0130828	chorion decreased size, abnormal
ZP:0130829	chorion increased fragility, abnormal
ZP:0130830	blastodisc decreased height, abnormal
ZP:0130831	left side diencephalon absent, abnormal
ZP:0130837	mouth movement quality, abnormal
ZP:0130838	Meckel's cartilage-palatoquadrate cartilage joint morphology, abnormal
ZP:0130839	Meckel's cartilage-palatoquadrate cartilage joint decreased size, abnormal
ZP:0130840	Meckel's cartilage-palatoquadrate cartilage joint movement quality, abnormal
ZP:0130841	opercle inflexible, abnormal
ZP:0130842	mandibular arch skeleton inflexible, abnormal
ZP:0130843	chondrocyte Meckel's cartilage hypertrophic, abnormal
ZP:0130844	chondrocyte mandibular arch skeleton immature, abnormal
ZP:0130845	Meckel's cartilage-palatoquadrate cartilage joint decreased amount, abnormal
ZP:0130846	post-vent vasculature decreased occurrence blood circulation, abnormal
ZP:0130847	caudal fin accumulation blood caudal fin, abnormal
ZP:0130848	blood vessel retina decreased amount, abnormal
ZP:0130849	blood plasma retina decreased amount, abnormal
ZP:0130850	neurosecretory neuron hypothalamus absent, abnormal
ZP:0130851	anatomical region pronephric glomerulus cystic, abnormal
ZP:0130852	axon lateral line increased amount, abnormal
ZP:0130858	podocyte foot pronephric podocyte morphology, abnormal
ZP:0130860	pronephric glomerulus increased volume, abnormal
ZP:0130862	bulbus arteriosus decreased functionality, abnormal
ZP:0130863	blood vasculature increased permeability, abnormal
ZP:0130864	blood brain mislocalised, abnormal
ZP:0130866	thigmotaxis decreased duration, abnormal
ZP:0130867	caudal vertebra fused with caudal vertebra, abnormal
ZP:0130868	caudal vertebra malformed, abnormal
ZP:0130869	non-Weberian precaudal vertebra malformed, abnormal
ZP:0130870	non-Weberian precaudal vertebra increased curvature, abnormal
ZP:0130872	axon spinal cord decreased thickness, abnormal
ZP:0130873	axon spinal cord truncated, abnormal
ZP:0130876	atrioventricular canal morphogenesis decreased process quality, abnormal
ZP:0130877	atrioventricular canal decreased process quality cardiac muscle cell development, abnormal
ZP:0130878	myocardium atrioventricular canal decreased amount, abnormal
ZP:0130879	hematopoietic cell increased distribution, abnormal
ZP:0130880	thrombocyte thymus absent, abnormal
ZP:0130881	lymphoid lineage cell migration into thymus decreased occurrence, abnormal
ZP:0130882	spinal cord curved dorsal, abnormal
ZP:0130883	spinal cord kinked, abnormal
ZP:0130884	axis curved dorsal, abnormal
ZP:0130885	axis kinked, abnormal
ZP:0130887	slit diaphragm pronephros decreased amount, abnormal
ZP:0130888	pronephric glomerulus retracted, abnormal
ZP:0130890	olfactory placode process quality cilium assembly, abnormal
ZP:0130892	ceratobranchial 5 tooth decreased efficacy tooth mineralization, abnormal
ZP:0130893	ceratobranchial 5 tooth composition, abnormal
ZP:0130894	ceratobranchial 5 tooth rough, abnormal
ZP:0130895	ceratobranchial 5 tooth porous, abnormal
ZP:0130896	ceratobranchial 5 bone lacks parts or has fewer parts of type tooth 5V, abnormal
ZP:0130897	ceratobranchial 5 bone lacks parts or has fewer parts of type tooth 4V, abnormal
ZP:0130898	ceratobranchial 5 bone lacks parts or has fewer parts of type tooth 3V, abnormal
ZP:0130899	ceratohyal cartilage decreased distance palatoquadrate cartilage, abnormal
ZP:0130900	ceratohyal cartilage increased variability of size, abnormal
ZP:0130901	basihyal cartilage oblique orientation, abnormal
ZP:0130902	brain disrupted cellular macromolecule catabolic process, abnormal
ZP:0130903	pharyngeal arch 1 disrupted cellular macromolecule catabolic process, abnormal
ZP:0130904	dental epithelium absent, abnormal
ZP:0130905	dental mesenchyme absent, abnormal
ZP:0130906	ameloblast absent, abnormal
ZP:0130907	ameloblast decreased amount, abnormal
ZP:0130908	odontoblast decreased amount, abnormal
ZP:0130910	centrum increased amount, abnormal
ZP:0130911	neutrophil gut decreased amount, abnormal
ZP:0130913	lipid heart increased amount, abnormal
ZP:0130914	blood vessel liver and biliary system fatty, abnormal
ZP:0130915	glutathione disulfide whole organism decreased amount, abnormal
ZP:0130916	organosulfur compound whole organism decreased amount, abnormal
ZP:0130917	mitochondrion hepatocyte distended, abnormal
ZP:0130918	mitochondrial crista hepatocyte damaged, abnormal
ZP:0130919	mitochondrial crista hepatocyte swollen, abnormal
ZP:0130920	postero-medial region otic vesicle mislocalised, abnormal
ZP:0130921	anterior region otic vesicle decreased amount, abnormal
ZP:0130922	neuroblast statoacoustic (VIII) ganglion decreased amount, abnormal
ZP:0130925	posterior macula fused with anterior macula, abnormal
ZP:0130938	collagen trimer Meckel's cartilage-palatoquadrate cartilage joint irregular spatial pattern, abnormal
ZP:0130939	collagen trimer Meckel's cartilage-palatoquadrate cartilage joint increased thickness, abnormal
ZP:0130940	branchiomotor neuron morphology, abnormal
ZP:0130942	L-alanine:2-oxoglutarate aminotransferase activity increased occurrence, abnormal
ZP:0130943	nucleus germ line cell physical object quality, abnormal
ZP:0130945	axoneme ependymal cell decreased amount, abnormal
ZP:0130946	scale has extra parts of type ventral region melanocyte, abnormal
ZP:0130947	scale has extra parts of type ventral region xanthophore, abnormal
ZP:0130948	scale has extra parts of type ventral region iridophore, abnormal
ZP:0130949	ventral region scale dorsalized, abnormal
ZP:0130950	head has extra parts of type ventral surface melanocyte, abnormal
ZP:0130951	trunk has fewer parts of type ventral surface iridophore, abnormal
ZP:0130952	trunk has extra parts of type ventral surface melanocyte, abnormal
ZP:0130953	trunk has extra parts of type ventral surface xanthophore, abnormal
ZP:0130954	ventral mandibular arch has extra parts of type melanocyte, abnormal
ZP:0130955	melanophore stripe dorsalized, abnormal
ZP:0130967	whole organism symmetry, abnormal
ZP:0130968	myofibril skeletal muscle degenerate, abnormal
ZP:0130970	blood accumulation coelom, abnormal
ZP:0130971	cranial cartilage immature, abnormal
ZP:0130972	cartilage tissue decreased size, abnormal
ZP:0130973	lateral dorsal aorta disconnected, abnormal
ZP:0130974	lateral dorsal aorta structurally discontinuous, abnormal
ZP:0130975	angiogenic sprout intersegmental vessel mislocalised, abnormal
ZP:0130976	intersegmental vessel misrouted, abnormal
ZP:0130977	late endosome microglial cell increased size, abnormal
ZP:0130978	late endosome to lysosome transport decreased occurrence, abnormal
ZP:0130979	microglial cell has extra parts of type late endosome microglial cell, abnormal
ZP:0130985	microglial cell decreased process quality vacuolar calcium ion homeostasis, abnormal
ZP:0130986	lysosome microglial cell decreased functionality, abnormal
ZP:0130987	microglial cell optic tectum circular, abnormal
ZP:0130988	optic tectum has extra parts of type microglial cell vacuole microglial cell, abnormal
ZP:0130990	microglial cell has extra parts of type vacuole microglial cell, abnormal
ZP:0130991	optic tectum separated from neuron microglial cell optic tectum, abnormal
ZP:0130994	Meckel's cartilage increased angle to ceratohyal cartilage, abnormal
ZP:0130996	neuron decreased occurrence chromosome organization, abnormal
ZP:0130999	muscle physical object quality, abnormal
ZP:0131001	caudal vein plexus decreased occurrence cell population proliferation, abnormal
ZP:0131002	caudal vein plexus decreased efficacy developmental growth, abnormal
ZP:0131003	myelin sheath dorsal funiculus increased amount, abnormal
ZP:0131004	myelin sheath ventral funiculus increased amount, abnormal
ZP:0131005	myelin sheath oligodendrocyte increased amount, abnormal
ZP:0131006	dorsal funiculus increased width, abnormal
ZP:0131007	ventral funiculus increased width, abnormal
ZP:0131008	cholesterol blood plasma decreased amount, abnormal
ZP:0131009	phospholipid blood plasma decreased amount, abnormal
ZP:0131010	triglyceride blood plasma decreased amount, abnormal
ZP:0131011	lipid liver decreased amount, abnormal
ZP:0131012	fatty acid blood plasma decreased amount, abnormal
ZP:0131013	feeding behavior increased rate, abnormal
ZP:0131014	phospholipid blood plasma increased amount, abnormal
ZP:0131015	lipid biosynthetic process increased occurrence, abnormal
ZP:0131017	phagocytic vesicle microglial cell increased diameter, abnormal
ZP:0131018	6-phospho-D-gluconate head increased amount, abnormal
ZP:0131019	microglial cell increased duration phagocytosis, engulfment, abnormal
ZP:0131020	microglial cell decreased occurrence microglial cell migration, abnormal
ZP:0131021	microglial cell increased size, abnormal
ZP:0131027	trunk has extra parts of type ventral region pigment cell, abnormal
ZP:0131029	angiogenic sprout central artery increased amount, abnormal
ZP:0131030	nucleus skeletal muscle cell decreased amount, abnormal
ZP:0131031	skeletal muscle has extra parts of type adipose tissue, abnormal
ZP:0131032	fat cell mislocalised, abnormal
ZP:0131033	skeletal muscle cell decreased length, abnormal
ZP:0131034	neural crest cell increased occurrence cell population proliferation, abnormal
ZP:0131037	pectoral fin lepidotrichium decreased length, abnormal
ZP:0131042	pronephros lacks all parts of type multi-ciliated epithelial cell cilium multi-ciliated epithelial cell, abnormal
ZP:0131043	Meckel's cartilage decreased distance pharyngeal arch 2, abnormal
ZP:0131044	intersegmental vein increased occurrence endothelial cell proliferation, abnormal
ZP:0131045	intersegmental vein increased occurrence cell population proliferation, abnormal
ZP:0131050	intestinal bulb decreased distribution, abnormal
ZP:0131051	axon retinal ganglion cell decreased length, abnormal
ZP:0131052	retinal ganglion cell process quality axon extension, abnormal
ZP:0131054	digestive system decreased process quality cell population proliferation, abnormal
ZP:0131057	podocyte foot pronephric podocyte irregularly shaped, abnormal
ZP:0131058	pronephric podocyte pronephric capsular space morphology, abnormal
ZP:0131059	JNK cascade decreased occurrence, abnormal
ZP:0131060	myeloid cell differentiation decreased occurrence, abnormal
ZP:0131061	lymphoid progenitor cell differentiation decreased occurrence, abnormal
ZP:0131062	caudal hematopoietic tissue decreased distribution, abnormal
ZP:0131063	cloacal chamber increased occurrence inflammatory response, abnormal
ZP:0131064	posterior intestine decreased amount, abnormal
ZP:0131065	lymphocyte spleen increased amount, abnormal
ZP:0131067	11-oxotestosterone whole organism decreased amount, abnormal
ZP:0131068	blood plasma male organism decreased amount, abnormal
ZP:0131070	hematopoietic stem cell decreased occurrence cell population proliferation, abnormal
ZP:0131071	intersegmental vessel post-vent vasculature morphology, abnormal
ZP:0131072	blood plasma post-vent vasculature decreased amount, abnormal
ZP:0131073	sperm process quality DNA methylation, abnormal
ZP:0131075	epithelial cell protruding out of epidermal superficial stratum, abnormal
ZP:0131076	epidermal basal stratum increased occurrence cell motility, abnormal
ZP:0131077	epidermal basal stratum decreased process quality cell-cell adhesion, abnormal
ZP:0131079	epidermal superficial stratum increased occurrence cell population proliferation, abnormal
ZP:0131081	cytoplasm epidermal basal stratum mislocalised, abnormal
ZP:0131082	axon habenula decreased amount, abnormal
ZP:0131083	axon telencephalon decreased amount, abnormal
ZP:0131084	skeletal muscle myofibril skeletal muscle undulate, abnormal
ZP:0131086	myoseptum increased distribution, abnormal
ZP:0131089	atrioventricular canal endocardium decreased occurrence cell migration, abnormal
ZP:0131100	microglial cell decreased occurrence phagosome maturation, abnormal
ZP:0131106	insulin (human) blood plasma increased amount, abnormal
ZP:0131107	liver increased occurrence glucose-6-phosphatase activity, abnormal
ZP:0131108	liver decreased occurrence glucose-6-phosphatase activity, abnormal
ZP:0131109	liver increased occurrence phosphoenolpyruvate carboxykinase activity, abnormal
ZP:0131110	liver increased occurrence pyruvate kinase activity, abnormal
ZP:0131111	liver decreased occurrence pyruvate kinase activity, abnormal
ZP:0131112	muscle decreased occurrence pyruvate kinase activity, abnormal
ZP:0131113	glucose-6-phosphatase activity increased occurrence, abnormal
ZP:0131114	phosphoenolpyruvate carboxykinase activity increased occurrence, abnormal
ZP:0131115	liver decreased occurrence phosphoenolpyruvate carboxykinase activity, abnormal
ZP:0131118	reactive oxygen species skeletal muscle increased amount, abnormal
ZP:0131124	G1 to G0 transition involved in cell differentiation decreased occurrence, abnormal
ZP:0131125	microglial cell head decreased amount, abnormal
ZP:0131129	macrophage spinal cord increased amount, abnormal
ZP:0131131	migratory cranial neural crest disrupted establishment of cell polarity, abnormal
ZP:0131132	migratory neural crest irregular spatial pattern, abnormal
ZP:0131134	migratory neural crest patchy, abnormal
ZP:0131135	migratory neural crest positional polarity, abnormal
ZP:0131136	migratory neural crest ovate, abnormal
ZP:0131137	migratory neural crest mislocalised dorsally, abnormal
ZP:0131138	migratory neural crest mislocalised anteriorly, abnormal
ZP:0131139	migratory neural crest mislocalized adaxially, abnormal
ZP:0131141	CaP motoneuron arrested neuron projection extension, abnormal
ZP:0131144	iridophore eye decreased area, abnormal
ZP:0131145	iridophore trunk decreased area, abnormal
ZP:0131159	female organism size, abnormal
ZP:0131160	ovarian follicle absence due to degeneration, abnormal
ZP:0131162	cardiac ventricle increased occurrence cardiac muscle cell proliferation, abnormal
ZP:0131164	skeletal muscle myofibril skeletal muscle spatial pattern, abnormal
ZP:0131167	primary neuron forebrain decreased amount, abnormal
ZP:0131169	head increased frequency apoptotic process, abnormal
ZP:0131170	Meckel's cartilage increased angle to Meckel's cartilage, abnormal
ZP:0131171	lamellipodium migratory neural crest cell absent, abnormal
ZP:0131172	filopodium migratory neural crest cell absent, abnormal
ZP:0131173	bleb migratory neural crest cell increased amount, abnormal
ZP:0131174	migratory neural crest lobed, abnormal
ZP:0131175	male organism increased duration swimming, abnormal
ZP:0131176	muscle cell decreased amount, abnormal
ZP:0131177	cranial nerve IX disrupted axon guidance, abnormal
ZP:0131180	compartment boundary rhombomere decreased amount, abnormal
ZP:0131181	retinal ganglion cell layer process quality neuron differentiation, abnormal
ZP:0131183	sleep latency, abnormal
ZP:0131192	cilium neural tube decreased amount, abnormal
ZP:0131193	whole organism decreased occurrence developmental process, abnormal
ZP:0131194	neural tube decreased occurrence cilium assembly, abnormal
ZP:0131195	lens development in camera-type eye decreased process quality, abnormal
ZP:0131196	cilium retina decreased amount, abnormal
ZP:0131199	cerebellar white matter cerebellum decreased amount, abnormal
ZP:0131200	corpus cerebelli morphology, abnormal
ZP:0131201	corpus cerebelli hypoplastic, abnormal
ZP:0131203	skeletal muscle myofibril skeletal muscle decreased width, abnormal
ZP:0131204	heart primordium mislocalised, abnormal
ZP:0131207	Golgi apparatus hair cell anterior macula functionality, abnormal
ZP:0131208	locomotory behavior decreased spatial extent of a process, abnormal
ZP:0131209	hair cell anterior macula morphology, abnormal
ZP:0131210	hair cell anterior macula increased height, abnormal
ZP:0131211	hair cell anterior macula decreased width, abnormal
ZP:0131212	hair cell anterior macula splayed, abnormal
ZP:0131213	premigratory neural crest cell increased amount, abnormal
ZP:0131214	migratory neural crest cell decreased amount, abnormal
ZP:0131225	head decreased occurrence mitophagy, abnormal
ZP:0131226	dorsal region neural tube absent, abnormal
ZP:0131227	dorsal region neural tube decreased amount, abnormal
ZP:0131232	neural crest cell increased occurrence apoptotic process, abnormal
ZP:0131233	nucleus skeletal muscle cell absent, abnormal
ZP:0131234	skeletal muscle cell myotome absent, abnormal
ZP:0131240	myotome decreased height, abnormal
ZP:0131241	migratory neural crest cell mislocalised, abnormal
ZP:0131242	migratory neural crest cell aggregated, abnormal
ZP:0131243	neural crest cell trunk increased distribution, abnormal
ZP:0131244	cranial ganglion increased distribution, abnormal
ZP:0131245	intestinal villus hypoplastic, abnormal
ZP:0131246	ovarian follicle development disrupted, abnormal
ZP:0131247	female organism decreased size, abnormal
ZP:0131250	estradiol female organism increased amount, abnormal
ZP:0131251	11-oxotestosterone female organism decreased amount, abnormal
ZP:0131252	ovarian follicle decreased occurrence vitellogenesis, abnormal
ZP:0131253	ovary degenerate, abnormal
ZP:0131254	ovarian follicle stage IV absence due to degeneration, abnormal
ZP:0131256	seminiferous tubule development delayed, abnormal
ZP:0131257	seminiferous tubule lumen hypoplastic, abnormal
ZP:0131258	male organism occurrence social behavior, abnormal
ZP:0131259	male organism disrupted interspecies interaction between organisms, abnormal
ZP:0131262	bile alcohol whole organism decreased amount, abnormal
ZP:0131265	forebrain decreased occurrence cell population proliferation, abnormal
ZP:0131267	myotome has extra parts of type fast muscle cell, abnormal
ZP:0131270	cerebellum formation disrupted, abnormal
ZP:0131271	motor neuron notochord morphology, abnormal
ZP:0131272	3-dehydrosphinganine whole organism increased amount, abnormal
ZP:0131273	thrombocyte post-vent region decreased amount, abnormal
ZP:0131277	microvillus intestinal epithelium absent, abnormal
ZP:0131278	adherens junction intestinal epithelium incomplete structure, abnormal
ZP:0131279	digestion decreased efficacy, abnormal
ZP:0131280	mid intestine lacks parts or has fewer parts of type intestinal villus, abnormal
ZP:0131283	cell rhombomere mislocalised, abnormal
ZP:0137210	caudal vein plexus fused with caudal vein plexus, abnormal
ZP:0137211	nucleolus cell increased amount, abnormal
ZP:0137214	posterior lateral plate mesoderm absent, abnormal
ZP:0137225	CaP motoneuron amplitude neuromuscular synaptic transmission, abnormal
ZP:0137226	neuron projection CaP motoneuron decreased size, abnormal
ZP:0137227	neuron projection CaP motoneuron decreased amount, abnormal
ZP:0137228	synapse CaP motoneuron morphology, abnormal
ZP:0137229	synapse CaP motoneuron decreased size, abnormal
ZP:0137231	neuromuscular junction of skeletal muscle fiber CaP motoneuron increased width, abnormal
ZP:0137233	filopodium CaP motoneuron decreased length, abnormal
ZP:0137235	caudal vein plexus decreased distribution, abnormal
ZP:0137237	Collagen chondrocyte spatial pattern, abnormal
ZP:0137238	chondrocyte process quality protein targeting, abnormal
ZP:0137239	vacuole notochord inner cell obtuse, abnormal
ZP:0137240	notochord inner cell irregular spatial pattern, abnormal
ZP:0137241	floor plate decreased occurrence establishment or maintenance of cell polarity, abnormal
ZP:0137242	trunk vasculature increased occurrence sprouting angiogenesis, abnormal
ZP:0137243	myoseptum absent, abnormal
ZP:0137244	primitive heart tube spatial pattern, abnormal
ZP:0137252	axon collateral Mauthner neuron decreased amount, abnormal
ZP:0137260	posterior region trunk shortened, abnormal
ZP:0137261	ventral region caudal fin aplastic/hypoplastic, abnormal
ZP:0137262	multi-ciliated epithelial cell pronephric duct decreased amount, abnormal
ZP:0137263	ionocyte progenitor cell spatial pattern, abnormal
ZP:0137264	ionocyte progenitor cell irregular spatial pattern, abnormal
ZP:0137265	ionocyte progenitor cell aggregated, abnormal
ZP:0137267	angiogenic sprout intersegmental vessel spatial pattern, abnormal
ZP:0137268	circulatory system development disrupted, abnormal
ZP:0137275	cytoskeleton organization decreased process quality, abnormal
ZP:0137276	pronephric glomerular basement membrane structure, abnormal
ZP:0137277	poly(ethylene imine) cranial cartilage spatial pattern, abnormal
ZP:0137288	compartment boundary brain amorphous, abnormal
ZP:0137289	lateral longitudinal fasciculus decreased process quality axonal fasciculation, abnormal
ZP:0137290	medial longitudinal fasciculus decreased process quality axonal fasciculation, abnormal
ZP:0137291	white matter disorganized, abnormal
ZP:0137292	integument pectoral fin fold increased amount, abnormal
ZP:0137293	neural plate process quality dorsal convergence, abnormal
ZP:0137294	neural plate decreased occurrence dorsal convergence, abnormal
ZP:0137295	neural keel formation process quality, abnormal
ZP:0137296	NaK ionocyte absent, abnormal
ZP:0137297	vH ionocyte absent, abnormal
ZP:0137298	cell yolk syncytial layer absent, abnormal
ZP:0137299	ionocyte progenitor cell decreased amount, abnormal
ZP:0137300	epidermal cell absent, abnormal
ZP:0137302	nitric oxide yolk syncytial layer increased amount, abnormal
ZP:0137303	caudal fin neoplastic, abnormal
ZP:0137306	chondroitin sulfate whole organism amount, abnormal
ZP:0137311	epibranchial field absent, abnormal
ZP:0137312	peptide hormone secreting cell intestinal bulb decreased amount, abnormal
ZP:0137315	peripheral region heart rudiment increased distribution, abnormal
ZP:0137316	midbrain hindbrain boundary constriction process quality epithelial cell morphogenesis, abnormal
ZP:0137317	midbrain hindbrain boundary constriction process quality midbrain-hindbrain boundary morphogenesis, abnormal
ZP:0137322	inferior raphe nucleus absent, abnormal
ZP:0137323	pretectum absent, abnormal
ZP:0137324	superior raphe nucleus absent, abnormal
ZP:0137325	medulla oblongata absent, abnormal
ZP:0137326	raphe nucleus absent, abnormal
ZP:0137327	primitive neurectodermal tumor whole organism increased amount, abnormal
ZP:0137336	epiphysis increased amount, abnormal
ZP:0137355	endoplasmic reticulum calcium ion homeostasis process quality, abnormal
ZP:0137369	epibranchial field decreased amount, abnormal
ZP:0137372	cell midbrain hindbrain boundary constriction increased length, abnormal
ZP:0137373	cell midbrain hindbrain boundary constriction decreased length, abnormal
ZP:0137375	midbrain hindbrain boundary constriction increased angle to midbrain hindbrain boundary constriction, abnormal
ZP:0137405	intermediate cell mass of mesoderm increased distribution, abnormal
ZP:0137411	lymph vessel decreased distribution, abnormal
ZP:0137414	ciliary marginal zone increased occurrence cell population proliferation, abnormal
ZP:0137415	retinal outer nuclear layer decreased amount, abnormal
ZP:0137422	swimming decreased linear velocity, abnormal
ZP:0137423	blastoderm increased amount, abnormal
ZP:0137424	anatomical compartment boundary rhombomere decreased amount, abnormal
ZP:0137427	blood viscosity, abnormal
ZP:0137428	ventriculo bulbo valve malformed, abnormal
ZP:0137430	ventral region optic cup increased distribution, abnormal
ZP:0137431	optic stalk increased distribution, abnormal
ZP:0137432	optic cup unfused from optic cup, abnormal
ZP:0137433	posterior region optic vesicle mislocalised, abnormal
ZP:0137434	posterior segment eye lacks parts or has fewer parts of type proximal side retinal pigmented epithelium, abnormal
ZP:0137435	proximal side posterior segment eye irregularly shaped, abnormal
ZP:0137436	photoreceptor inner segment photoreceptor cell malformed, abnormal
ZP:0137437	retinal neural layer protruding into brain, abnormal
ZP:0137438	retinal pigmented epithelium decreased area, abnormal
ZP:0137439	histone modification disrupted, abnormal
ZP:0137440	retina spatial pattern, abnormal
ZP:0137441	endothelial cell lateral dorsal aorta elongated, abnormal
ZP:0137442	endothelial cell lateral dorsal aorta increased area, abnormal
ZP:0137444	trunk vasculature decreased occurrence sprouting angiogenesis, abnormal
ZP:0137445	dorsal longitudinal anastomotic vessel truncated, abnormal
ZP:0137446	vascular lymphangioblast spatial pattern, abnormal
ZP:0137447	vascular lymphangioblast decreased distribution, abnormal
ZP:0137448	vascular lymphangioblast aplastic/hypoplastic, abnormal
ZP:0137455	semicircular canal fusion disrupted, abnormal
ZP:0137456	peripheral nervous system decreased distribution, abnormal
ZP:0137457	pillar of the anterior semicircular canal increased amount, abnormal
ZP:0137458	pillar of the anterior semicircular canal swollen, abnormal
ZP:0137459	pillar of the lateral semicircular canal increased amount, abnormal
ZP:0137460	pillar of the lateral semicircular canal swollen, abnormal
ZP:0137461	pillar of the posterior semicircular canal increased amount, abnormal
ZP:0137462	pillar of the posterior semicircular canal swollen, abnormal
ZP:0137463	caudal fin increased distribution, abnormal
ZP:0137464	axon cranial nerve II decreased branchiness, abnormal
ZP:0137465	cranial nerve II decreased occurrence axon extension, abnormal
ZP:0137466	cranial nerve II decreased occurrence axon arborization, abnormal
ZP:0137469	ventral side somite spatial pattern, abnormal
ZP:0137474	atrioventricular valve spatial pattern, abnormal
ZP:0137478	goblet cell posterior intestine increased amount, abnormal
ZP:0137483	cytoskeleton organization increased process quality, abnormal
ZP:0137485	heart decreased process quality blood circulation, abnormal
ZP:0137486	head arrested blood circulation, abnormal
ZP:0137487	post-vent region arrested blood circulation, abnormal
ZP:0137488	blood accumulation vasculature, abnormal
ZP:0137489	snout circular, abnormal
ZP:0137490	snout shortened, abnormal
ZP:0137491	eye increased distance otic vesicle, abnormal
ZP:0137495	germ ring mislocalised, abnormal
ZP:0137496	germ ring increased distribution, abnormal
ZP:0137497	anatomical margin blastodisc spatial pattern, abnormal
ZP:0137498	anatomical margin blastodisc increased distribution, abnormal
ZP:0137505	glycogen liver decreased amount, abnormal
ZP:0137506	secondary motor neuron process quality axon guidance, abnormal
ZP:0137509	erythroid progenitor cell arrested mitotic cell cycle, abnormal
ZP:0137510	ventriculo bulbo valve morphogenesis delayed, abnormal
ZP:0137512	apical region endolymphatic sac closed, abnormal
ZP:0137513	endolymphatic sac lacks parts or has fewer parts of type basal region cell projection endolymphatic sac, abnormal
ZP:0137514	cell projection endolymphatic sac decreased amount, abnormal
ZP:0137515	endolymphatic sac increased size, abnormal
ZP:0137518	nucleus liver decreased amount, abnormal
ZP:0137519	endocardial cushion bulbus arteriosus decreased amount, abnormal
ZP:0137520	ventriculo bulbo valve development decreased process quality, abnormal
ZP:0137522	cell endocardium increased amount, abnormal
ZP:0137524	cell junction compact layer of ventricle oblique orientation, abnormal
ZP:0137526	pronephric duct has fewer parts of type multi-ciliated epithelial cell cilium multi-ciliated epithelial cell, abnormal
ZP:0137527	multi-ciliated epithelial cell pronephric proximal convoluted tubule decreased amount, abnormal
ZP:0137528	multi-ciliated epithelial cell pronephric proximal straight tubule decreased distribution, abnormal
ZP:0137530	common myeloid progenitor cell proliferation process quality, abnormal
ZP:0137531	myeloid cell increased occurrence apoptotic process, abnormal
ZP:0137532	common myeloid progenitor cell proliferation disrupted, abnormal
ZP:0137534	cell projection tendon cell decreased length, abnormal
ZP:0137536	otolithic lymph vessel decreased amount, abnormal
ZP:0137537	vasculature hindbrain decreased amount, abnormal
ZP:0137539	retina hemorrhagic, abnormal
ZP:0137541	ovulation from ovarian follicle decreased occurrence, abnormal
ZP:0137545	NADPH whole organism decreased amount, abnormal
ZP:0137547	ventricular myocardium decreased occurrence ATP-activated inward rectifier potassium channel activity, abnormal
ZP:0137548	cardiac muscle cell decreased occurrence ATP-activated inward rectifier potassium channel activity, abnormal
ZP:0137549	cardiac ventricle increased occurrence apoptotic process, abnormal
ZP:0137550	atrium increased occurrence apoptotic process, abnormal
ZP:0137553	histone H3-K27 methylation decreased occurrence, abnormal
ZP:0137554	histone H3-K27 trimethylation decreased occurrence, abnormal
ZP:0137555	glycosphingolipid whole organism decreased amount, abnormal
ZP:0137556	Golgi apparatus anterior macula structure, abnormal
ZP:0137559	water whole organism decreased amount, abnormal
ZP:0137561	L-tyrosine muscle decreased amount, abnormal
ZP:0137562	L-lysine muscle increased amount, abnormal
ZP:0137563	protein whole organism increased amount, abnormal
ZP:0137564	hexokinase activity increased occurrence, abnormal
ZP:0137565	adult feeding behavior decreased occurrence, abnormal
ZP:0137566	fat cell skeletal muscle increased amount, abnormal
ZP:0137568	skeletal muscle cell somite decreased amount, abnormal
ZP:0137572	intestinal epithelial cell spatial pattern, abnormal
ZP:0137573	intestinal epithelium has extra parts of type neutrophil, abnormal
ZP:0137574	vesicle intestinal epithelium decreased amount, abnormal
ZP:0137575	vesicle myotome decreased amount, abnormal
ZP:0137576	sternohyoid decreased thickness, abnormal
ZP:0137577	sternohyoid decreased area, abnormal
ZP:0137582	contractile fiber primitive pectoral fin adductor decreased amount, abnormal
ZP:0137583	contractile fiber primitive pectoral fin abductor decreased amount, abnormal
ZP:0137584	pelvic fin musculature decreased amount, abnormal
ZP:0137585	pectoral fin musculature structure, abnormal
ZP:0137586	pectoral fin musculature asymmetrical, abnormal
ZP:0137587	adductor muscle decreased amount, abnormal
ZP:0137588	abductor muscle decreased amount, abnormal
ZP:0137589	adductor muscle pectoral fin decreased amount, abnormal
ZP:0137590	abductor muscle pectoral fin decreased amount, abnormal
ZP:0137591	whole organism lacks parts or has fewer parts of type primitive pectoral fin abductor, abnormal
ZP:0137592	primitive pectoral fin adductor decreased amount, abnormal
ZP:0137593	primitive pectoral fin abductor decreased amount, abnormal
ZP:0137599	pectoral fin decreased functionality, abnormal
ZP:0137600	pectoral fin bud decreased process quality cell population proliferation, abnormal
ZP:0137601	http://purl.obolibrary.org/obo/ZFA_0005921 decreased amount, abnormal
ZP:0137602	pectoral fin clavate, abnormal
ZP:0137603	cardiac ventricle inverted, abnormal
ZP:0137604	regulation of termination of RNA polymerase II transcription disrupted, abnormal
ZP:0137605	neural crest cell migration involved in heart formation disrupted, abnormal
ZP:0137606	cardiac neural crest spatial pattern, abnormal
ZP:0137607	cardiac muscle cell decondensed, abnormal
ZP:0137608	skeletal muscle myofibril trunk musculature increased length, abnormal
ZP:0137609	muscle cell trunk musculature morphology, abnormal
ZP:0137610	muscle cell trunk musculature decondensed, abnormal
ZP:0137611	larval feeding behavior disrupted, abnormal
ZP:0137612	neuromuscular process decreased efficacy, abnormal
ZP:0137613	adherens junction epidermal cell malformed, abnormal
ZP:0137614	periderm decreased thickness, abnormal
ZP:0137615	scale primordium morphology, abnormal
ZP:0137616	peridermal cell elongated, abnormal
ZP:0137617	nucleus chondrocyte decreased amount, abnormal
ZP:0137618	sarcomere fast muscle cell morphology, abnormal
ZP:0137619	myosin filament fast muscle cell decreased amount, abnormal
ZP:0137620	Z disc fast muscle cell decreased amount, abnormal
ZP:0137621	M band fast muscle cell decreased amount, abnormal
ZP:0137622	neuron projection motor neuron branchiness, abnormal
ZP:0137623	cell trigeminal motor nucleus decreased amount, abnormal
ZP:0137624	motor neuron trunk musculature branchiness, abnormal
ZP:0137625	neuron projection motor neuron increased amount, abnormal
ZP:0137626	neuron projection motor neuron truncated, abnormal
ZP:0137627	angiogenic sprout disorganized, abnormal
ZP:0137628	dorsal longitudinal anastomotic vessel agenesis, abnormal
ZP:0137631	sinoatrial ring absent, abnormal
ZP:0137632	blood vessel endothelial cell disrupted endothelial cell migration, abnormal
ZP:0137633	gonad male organism distended, abnormal
ZP:0137634	male organism has fewer parts of type gonad spermatogenic cyst, abnormal
ZP:0137635	male organism has extra parts of type gonad ovarian follicle, abnormal
ZP:0137636	male organism color pattern, abnormal
ZP:0137637	ovary has fewer parts of type ovarian follicle stage III, abnormal
ZP:0137638	ovary has extra parts of type ovarian follicle stage I, abnormal
ZP:0137639	ovary has extra parts of type anatomical space, abnormal
ZP:0137640	hindbrain granular, abnormal
ZP:0137641	midbrain granular, abnormal
ZP:0137644	distal region pronephros decreased distribution, abnormal
ZP:0137645	distal region pronephros decreased amount, abnormal
ZP:0137646	nucleus pronephric distal early tubule absent, abnormal
ZP:0137649	pronephric distal early tubule decreased occurrence pronephric nephron tubule epithelial cell differentiation, abnormal
ZP:0137650	apical part of cell pronephric distal early tubule absent, abnormal
ZP:0137651	pronephric distal early tubule decreased occurrence early distal convoluted tubule development, abnormal
ZP:0137652	nucleus pronephric distal early tubule decreased size, abnormal
ZP:0137653	notochord increased occurrence apoptotic process, abnormal
ZP:0137656	kidney epithelial cell pronephric distal early tubule decreased size, abnormal
ZP:0137672	centrosome branchiomotor neuron position, abnormal
ZP:0137673	neuron projection branchiomotor neuron amount, abnormal
ZP:0137674	neuron projection branchiomotor neuron length, abnormal
ZP:0137675	branchiomotor neuron orientation neuron projection rhombomere 4, abnormal
ZP:0137676	cell body branchiomotor neuron shape, abnormal
ZP:0137677	branchiomotor neuron orientation cell body axon branchiomotor neuron, abnormal
ZP:0137678	branchiomotor neuron process quality motor neuron migration, abnormal
ZP:0137679	rhombomere 6 branchiomotor neuron absent, abnormal
ZP:0137680	rhombomere 5 branchiomotor neuron absent, abnormal
ZP:0137681	branchiomotor neuron accumulation rhombomere 4, abnormal
ZP:0137682	branchiomotor neuron decreased speed, abnormal
ZP:0137684	eye photoreceptor cell alignment eye photoreceptor cell, abnormal
ZP:0137687	pathway-restricted SMAD protein phosphorylation decreased occurrence, abnormal
ZP:0137688	ventral region ventral fin fold decreased distribution, abnormal
ZP:0137689	pathway-restricted SMAD protein phosphorylation increased occurrence, abnormal
ZP:0137690	ventral region ventral fin fold increased distribution, abnormal
ZP:0137691	cell retinal inner nuclear layer mislocalised, abnormal
ZP:0137692	outer limiting membrane morphology, abnormal
ZP:0137693	pronephric proximal straight tubule occurrence pronephric nephron tubule epithelial cell differentiation, abnormal
ZP:0137694	pronephric distal late tubule occurrence pronephric nephron tubule epithelial cell differentiation, abnormal
ZP:0137697	lens capsule increased thickness, abnormal
ZP:0137700	anterior side segmental plate absent, abnormal
ZP:0137703	posterior region postcranial axial skeleton morphology, abnormal
ZP:0137704	keratinocyte decreased amount, abnormal
ZP:0137705	ionocyte decreased amount, abnormal
ZP:0137706	NaK ionocyte extension decreased amount, abnormal
ZP:0137707	vH ionocyte extension decreased amount, abnormal
ZP:0137708	ectoderm decreased occurrence stem cell proliferation, abnormal
ZP:0137709	NaK ionocyte ball decreased amount, abnormal
ZP:0137710	vH ionocyte ball decreased amount, abnormal
ZP:0137711	axon MiP motor neuron bifurcated, abnormal
ZP:0137712	axon CaP motoneuron bifurcated, abnormal
ZP:0137714	trunk neural crest cell migration disrupted, abnormal
ZP:0137715	VaP motor neuron increased amount, abnormal
ZP:0137716	CaP motoneuron increased amount, abnormal
ZP:0137718	neuron dorsal root ganglion increased amount, abnormal
ZP:0137719	MiD3cm increased amount, abnormal
ZP:0137724	glutamate(1-) whole organism decreased amount, abnormal
ZP:0137725	glycine whole organism increased amount, abnormal
ZP:0137726	sarcosine whole organism increased amount, abnormal
ZP:0137727	cystathionine whole organism increased amount, abnormal
ZP:0137729	leucine whole organism increased amount, abnormal
ZP:0137730	proline whole organism increased amount, abnormal
ZP:0137731	valine whole organism increased amount, abnormal
ZP:0137733	arginine whole organism increased amount, abnormal
ZP:0137747	primary ovarian follicle growth non-progressive, abnormal
ZP:0137748	ovarian follicle stage I disrupted ovarian follicle development, abnormal
ZP:0137749	cell gonad decreased size, abnormal
ZP:0137751	gonad has fewer parts of type ovarian follicle stage II, abnormal
ZP:0137757	CaP motoneuron arrested axon extension, abnormal
ZP:0137758	Rohon-Beard neuron decreased occurrence innervation, abnormal
ZP:0137759	axon secondary motor neuron defasciculated, abnormal
ZP:0137760	secondary motor neuron arrested axon extension, abnormal
ZP:0137761	growth cone secondary motor neuron increased size, abnormal
ZP:0137763	hematopoietic system physical object quality, abnormal
ZP:0137764	adaxial-abaxial axis whole organism decreased size, abnormal
ZP:0137765	anatomical boundary hepatocyte amorphous, abnormal
ZP:0137766	nucleus intestine irregular spatial pattern, abnormal
ZP:0137767	nucleus muscle circular, abnormal
ZP:0137768	intestinal villus truncated, abnormal
ZP:0137769	muscle atrophied, abnormal
ZP:0137770	hepatocyte crowded, abnormal
ZP:0137772	erythroid lineage cell blood decreased amount, abnormal
ZP:0137774	thigmotaxis latency, abnormal
ZP:0137780	basement membrane vertical myoseptum increased amount, abnormal
ZP:0137781	myotome decreased occurrence cell adhesion, abnormal
ZP:0137782	muscle cell myotome morphology, abnormal
ZP:0137783	myotome detached from muscle cell myotome, abnormal
ZP:0137784	muscle cell myotome sinuous, abnormal
ZP:0137785	muscle cell myotome decreased amount, abnormal
ZP:0137786	myotome extends beyond muscle cell vertical myoseptum, abnormal
ZP:0137787	connective tissue cell myotome increased amount, abnormal
ZP:0137788	pericardium increased amount, abnormal
ZP:0137789	caudal vein increased amount, abnormal
ZP:0137790	myotome spatial pattern, abnormal
ZP:0137791	multicellular organismal movement decreased occurrence, abnormal
ZP:0137792	muscle cell inflexible, abnormal
ZP:0137793	banded collagen fibril vertical myoseptum decreased amount, abnormal
ZP:0137794	myotome detached from muscle cell basement membrane myotome, abnormal
ZP:0137795	myotome structurally discontinuous, abnormal
ZP:0137796	liver decreased occurrence fatty acid beta-oxidation, abnormal
ZP:0137797	muscle decreased occurrence fatty acid beta-oxidation, abnormal
ZP:0137799	intersegmental vessel decreased occurrence angiogenesis, abnormal
ZP:0137800	trunk vasculature process quality vasculature development, abnormal
ZP:0137801	blood vessel trunk vasculature decreased length, abnormal
ZP:0137803	primitive heart tube shape, abnormal
ZP:0137804	cardiac muscle cell bulbus arteriosus increased amount, abnormal
ZP:0137805	blood cell accumulation trunk vasculature, abnormal
ZP:0137806	bulbus arteriosus increased occurrence cell population proliferation, abnormal
ZP:0137807	atrium increased occurrence cell population proliferation, abnormal
ZP:0137808	pharyngeal mesoderm increased amount, abnormal
ZP:0137809	pharyngeal mesoderm increased distribution, abnormal
ZP:0137814	pronephros asynchronous epithelial cilium movement involved in extracellular fluid movement, abnormal
ZP:0137815	Kupffer's vesicle asynchronous epithelial cilium movement involved in determination of left/right asymmetry, abnormal
ZP:0137816	spinal cord asynchronous epithelial cilium movement involved in extracellular fluid movement, abnormal
ZP:0137817	cilium spinal cord movement quality, abnormal
ZP:0137822	hematopoietic cell thymus decreased amount, abnormal
ZP:0137823	hematopoietic cell caudal hematopoietic tissue decreased amount, abnormal
ZP:0137824	hematopoietic cell caudal hematopoietic tissue increased amount, abnormal
ZP:0137825	caudal hematopoietic tissue increased distribution, abnormal
ZP:0137826	insulin whole organism increased amount, abnormal
ZP:0137827	photoreceptor activity process quality, abnormal
ZP:0137828	detection of light stimulus involved in sensory perception process quality, abnormal
ZP:0137830	kidney interstitial cell morphology, abnormal
ZP:0137831	pronephric duct increased width, abnormal
ZP:0137832	pronephric duct opening obstructed, abnormal
ZP:0137833	pronephric proximal convoluted tubule cystic, abnormal
ZP:0137834	neural tube increased occurrence cell population proliferation, abnormal
ZP:0137835	pronephric duct increased occurrence apoptotic process, abnormal
ZP:0137836	cloaca increased occurrence apoptotic process, abnormal
ZP:0137839	epithelium endolymphatic sac increased thickness, abnormal
ZP:0137840	epithelium endolymphatic sac thickness, abnormal
ZP:0137841	basal region midbrain hindbrain boundary constriction structure, abnormal
ZP:0137842	basal region midbrain hindbrain boundary constriction increased width, abnormal
ZP:0137843	pharyngeal arch cartilage decreased occurrence canonical Wnt signaling pathway, abnormal
ZP:0137844	bulbus arteriosus decreased occurrence canonical Wnt signaling pathway involved in heart development, abnormal
ZP:0137845	atrioventricular valve process quality canonical Wnt signaling pathway involved in heart development, abnormal
ZP:0137846	pharyngeal arch cartilage decreased amount, abnormal
ZP:0137847	endothelial cell lymphatic system increased distribution, abnormal
ZP:0137848	vascular lymphangioblast horizontal myoseptum immature, abnormal
ZP:0137849	nucleus posterior cardinal vein elliptic, abnormal
ZP:0137850	vascular lymphangioblast horizontal myoseptum increased cellular motility, abnormal
ZP:0137851	endothelial cell normal amount, abnormal
ZP:0137857	cerebrospinal fluid contacting neuron process quality cell morphogenesis, abnormal
ZP:0137858	cell projection cerebrospinal fluid contacting neuron decreased size, abnormal
ZP:0137859	cerebrospinal fluid contacting neuron process quality cellular response to mechanical stimulus, abnormal
ZP:0137861	cone telodendria UV sensitive photoreceptor cell morphology, abnormal
ZP:0137862	cone telodendria UV sensitive photoreceptor cell branched, abnormal
ZP:0137863	cone telodendria UV sensitive photoreceptor cell decreased amount, abnormal
ZP:0137864	heart trabecula morphogenesis disrupted, abnormal
ZP:0137865	H3K4Me3 whole organism decreased amount, abnormal
ZP:0137867	histone modification process quality, abnormal
ZP:0137868	blood accumulation ventral aorta, abnormal
ZP:0137869	endothelial cell somite decreased amount, abnormal
ZP:0137871	endoderm development arrested, abnormal
ZP:0137872	cell body Muller cell spatial pattern, abnormal
ZP:0137873	cell body Muller cell position, abnormal
ZP:0137874	cell body Muller cell mislocalised, abnormal
ZP:0137875	glial cell projection Muller cell mislocalised, abnormal
ZP:0137876	glial cell projection Muller cell decreased amount, abnormal
ZP:0137877	inner limiting membrane morphology, abnormal
ZP:0137878	outer limiting membrane broken, abnormal
ZP:0137879	Muller cell physical object quality, abnormal
ZP:0137880	Muller cell irregularly shaped, abnormal
ZP:0137881	glial cell projection Muller cell increased thickness, abnormal
ZP:0137882	outer limiting membrane irregular thickness, abnormal
ZP:0137883	glial cell projection Muller cell morphology, abnormal
ZP:0137884	retinal inner plexiform layer irregular thickness, abnormal
ZP:0137885	Muller cell overlap with glial cell projection glial cell projection Muller cell, abnormal
ZP:0137886	glial limiting end-foot Muller cell absent, abnormal
ZP:0137887	retinal neural layer lacks parts or has fewer parts of type inner limiting membrane, abnormal
ZP:0137888	glial cell projection Muller cell position, abnormal
ZP:0137889	glial limiting end-foot Muller cell decreased amount, abnormal
ZP:0137890	glial cell projection Muller cell spatial pattern, abnormal
ZP:0137891	glial cell projection Muller cell structure, abnormal
ZP:0137893	dermatan sulfate whole organism decreased amount, abnormal
ZP:0137894	hydroxyproline whole organism decreased amount, abnormal
ZP:0137896	neurotransmitter trunk decreased amount, abnormal
ZP:0137897	proline whole organism decreased amount, abnormal
ZP:0137898	heparan sulfate whole organism decreased amount, abnormal
ZP:0137899	chondroitin sulfate whole organism decreased amount, abnormal
ZP:0137901	coenzyme Q10 whole organism decreased amount, abnormal
ZP:0137902	keratan sulfate whole organism decreased amount, abnormal
ZP:0137903	behavioral defense response disrupted, abnormal
ZP:0137904	telomerase activity decreased efficacy, abnormal
ZP:0137905	catalase activity decreased efficacy, abnormal
ZP:0137907	antioxidant activity decreased efficacy, abnormal
ZP:0137908	social behavior disrupted, abnormal
ZP:0137909	exploration behavior decreased occurrence, abnormal
ZP:0137910	creatininase activity decreased efficacy, abnormal
ZP:0137911	retinal inner nuclear layer has fewer parts of type interneuron, abnormal
ZP:0137912	whole organism senescent, abnormal
ZP:0137913	intestine increased permeability, abnormal
ZP:0137914	retinal outer nuclear layer has fewer parts of type eye photoreceptor cell, abnormal
ZP:0137915	pleuroperitoneal region decreased size, abnormal
ZP:0137916	muscle tendon junction vertical myoseptum decreased amount, abnormal
ZP:0137917	vertical myoseptum increased distribution, abnormal
ZP:0137918	tendon cell decondensed, abnormal
ZP:0137922	Kupffer's vesicle process quality epithelial cilium movement involved in extracellular fluid movement, abnormal
ZP:0137923	forerunner cell group arrested cell cycle G1/S phase transition, abnormal
ZP:0137924	forerunner cell group increased distribution, abnormal
ZP:0137927	head misaligned with condensed chromosome mitotic spindle microtubule head, abnormal
ZP:0137928	mitotic spindle head disorganized, abnormal
ZP:0137934	endothelial cell ventral wall of dorsal aorta decreased amount, abnormal
ZP:0137935	cilium blood vessel decreased length, abnormal
ZP:0137936	cilium blood vessel decreased amount, abnormal
ZP:0137937	splanchnocranium decreased process quality skeletal muscle tissue development, abnormal
ZP:0137938	splanchnocranium decreased process quality tendon development, abnormal
ZP:0137939	tendon ceratohyal cartilage malformed, abnormal
ZP:0137940	tendon ventral intermandibularis posterior malformed, abnormal
ZP:0137941	tendon interhyoideus malformed, abnormal
ZP:0137942	skeletal muscle cell adductor mandibulae mislocalised, abnormal
ZP:0137945	rib decreased process quality bone mineralization, abnormal
ZP:0137947	rib decreased process quality bone morphogenesis, abnormal
ZP:0137950	dentary composition, abnormal
ZP:0137951	dentary decreased mass density, abnormal
ZP:0137954	skeletal system lacks all parts of type rib, abnormal
ZP:0137956	intervertebral ligament malformed, abnormal
ZP:0137958	rib of vertebra 5 absent, abnormal
ZP:0137959	rib of vertebra 6 absent, abnormal
ZP:0137960	skeletal system lacks parts or has fewer parts of type rib, abnormal
ZP:0137961	ligament Meckel's cartilage decreased amount, abnormal
ZP:0137962	ligament palatoquadrate cartilage decreased amount, abnormal
ZP:0137963	tendon sternohyoid decreased amount, abnormal
ZP:0137967	Mauthner neuron process quality axon regeneration, abnormal
ZP:0137969	Mauthner neuron process quality axon extension involved in regeneration, abnormal
ZP:0137980	blood cardinal system absent, abnormal
ZP:0137991	dorsal aorta decreased occurrence endothelial tube lumen extension, abnormal
ZP:0137992	posterior cardinal vein decreased occurrence endothelial tube lumen extension, abnormal
ZP:0137993	endothelial tube lumen extension decreased occurrence, abnormal
ZP:0137994	dorsal aorta attached to posterior cardinal vein, abnormal
ZP:0137995	dorsal aorta decreased length, abnormal
ZP:0137996	posterior cardinal vein decreased length, abnormal
ZP:0137997	blood vessel endothelium artery decreased amount, abnormal
ZP:0137998	epiphysis disrupted cellular response to UV, abnormal
ZP:0137999	epiphysis disrupted cellular response to blue light, abnormal
ZP:0138000	epiphysis disrupted cellular response to red light, abnormal
ZP:0138003	blastoderm segmentation delayed, abnormal
ZP:0138004	blastoderm cell decreased adhesivity, abnormal
ZP:0138005	vascular cord decreased occurrence Notch signaling pathway, abnormal
ZP:0138006	posterior lateral plate mesoderm process quality cell migration involved in vasculogenesis, abnormal
ZP:0138007	cell posterior lateral plate mesoderm morphology, abnormal
ZP:0138008	cell posterior lateral plate mesoderm decreased adhesivity, abnormal
ZP:0138009	angiogenic sprout vascular cord decreased amount, abnormal
ZP:0138010	angioblast cell migration from lateral mesoderm to midline decreased occurrence, abnormal
ZP:0138016	central region centrum calcified, abnormal
ZP:0138017	phosphate vertebral body end plate decreased amount, abnormal
ZP:0138018	carbonate vertebral body end plate increased amount, abnormal
ZP:0138019	apatite vertebral body end plate crystal configuration, abnormal
ZP:0138020	collagen network vertebral body end plate immature, abnormal
ZP:0138021	centrum dysplastic, abnormal
ZP:0138022	rib fragile, abnormal
ZP:0138023	rib scarred, abnormal
ZP:0138024	vertebra collapsed, abnormal
ZP:0138025	lepidotrichium deformed, abnormal
ZP:0138026	lacunocanalicular system decreased volume, abnormal
ZP:0138028	vertebral body end plate decreased elasticity, abnormal
ZP:0138029	osteocyte proportionality to bone tissue, abnormal
ZP:0138030	bone mineralization involved in bone maturation decreased rate, abnormal
ZP:0138031	centrum poorly ossified, abnormal
ZP:0138041	neuron mislocalised, abnormal
ZP:0138042	hypothalamus shape, abnormal
ZP:0138043	serotonergic neuron hypothalamus decreased amount, abnormal
ZP:0138044	hypothalamus increased occurrence cell death, abnormal
ZP:0138045	lateral mesoderm disrupted determination of heart left/right asymmetry, abnormal
ZP:0138049	response to absence of light increased process quality, abnormal
ZP:0138050	swimming decreased frequency, abnormal
ZP:0138051	swimming increased linear velocity, abnormal
ZP:0138052	swimming increased spatial extent of a process, abnormal
ZP:0138053	habituation decreased rate, abnormal
ZP:0138054	prepulse inhibition decreased magnitude, abnormal
ZP:0138060	startle response decreased magnitude, abnormal
ZP:0138061	prepulse inhibition increased magnitude, abnormal
ZP:0138062	swimming decreased spatial extent of a process, abnormal
ZP:0138063	habituation increased rate, abnormal
ZP:0138065	tendon decreased process quality collagen fibril organization, abnormal
ZP:0138066	tendon sternohyoid composition, abnormal
ZP:0138067	nucleus fast muscle cell disorganized, abnormal
ZP:0138068	actin filament fast muscle cell decreased thickness, abnormal
ZP:0138069	myotome fast muscle cell morphology, abnormal
ZP:0138070	optic tectum has fewer parts of type axon retinal ganglion cell, abnormal
ZP:0138071	retinal ganglion cell delayed axon extension, abnormal
ZP:0138074	cell body MiD3cl position, abnormal
ZP:0138075	MiD2cm decreased occurrence commissural neuron axon guidance, abnormal
ZP:0138076	MiD3cl decreased occurrence commissural neuron axon guidance, abnormal
ZP:0138077	MiD3cm decreased occurrence commissural neuron axon guidance, abnormal
ZP:0138078	RoL2 decreased occurrence commissural neuron axon guidance, abnormal
ZP:0138079	hindbrain interneuron decreased occurrence commissural neuron axon guidance, abnormal
ZP:0138094	spermatocyte decreased occurrence meiosis II, abnormal
ZP:0138095	mitochondrion myocardium swollen, abnormal
ZP:0138096	intercalated disc myocardium morphology, abnormal
ZP:0138097	Z disc myocardium irregular thickness, abnormal
ZP:0138098	desmosome myocardium morphology, abnormal
ZP:0138099	I band cardiac muscle absent, abnormal
ZP:0138100	myocardium edematous, abnormal
ZP:0138102	vertebra increased process quality bone mineralization, abnormal
ZP:0138103	vacuole notochord inner cell broken, abnormal
ZP:0138104	notochord inner cell decreased process quality notochord cell vacuolation, abnormal
ZP:0138106	notochord inner cell decreased volume, abnormal
ZP:0138107	notochord inner cell irregularly shaped, abnormal
ZP:0138108	notochord inner cell decreased occurrence vesicle fusion with vacuole, abnormal
ZP:0138113	cardiac chamber development disrupted, abnormal
ZP:0138115	nucleus notochord inner cell spheroid, abnormal
ZP:0138116	nucleus notochord inner cell mislocalised medially, abnormal
ZP:0138125	sprouting angiogenesis increased process quality, abnormal
ZP:0138130	atrium process quality cardiac conduction system development, abnormal
ZP:0138131	cardiac muscle process quality macroautophagy, abnormal
ZP:0138132	skeletal muscle increased process quality TOR signaling, abnormal
ZP:0138134	cardiac ventricle increased process quality cardiac muscle cell contraction, abnormal
ZP:0138135	cardiac myofibril cardiac ventricle increased contractility, abnormal
ZP:0138136	regulation of heart contraction decreased process quality, abnormal
ZP:0138137	heart obtuse, abnormal
ZP:0138138	trabecular layer has extra parts of type cardiac muscle cell, abnormal
ZP:0138139	trabecular layer of the atrium increased thickness, abnormal
ZP:0138140	cardiac muscle cell has extra parts of type autophagosome cardiac muscle cell, abnormal
ZP:0138141	apical side pronephric tubule absent, abnormal
ZP:0138145	omega-9 fatty acid whole organism increased amount, abnormal
ZP:0138146	methylglyoxal whole organism increased amount, abnormal
ZP:0138147	omega-3 fatty acid whole organism increased amount, abnormal
ZP:0138148	saturated fatty acid whole organism increased amount, abnormal
ZP:0138149	whole organism arrested lactoylglutathione lyase activity, abnormal
ZP:0138162	otolith formation arrested, abnormal
ZP:0138163	rod photoreceptor outer segment retinal rod cell increased length, abnormal
ZP:0138164	retinal photoreceptor layer has fewer parts of type UV sensitive photoreceptor cell, abnormal
ZP:0138165	retinal photoreceptor layer has fewer parts of type blue sensitive photoreceptor cell, abnormal
ZP:0138166	retinal photoreceptor layer has fewer parts of type green sensitive photoreceptor cell, abnormal
ZP:0138167	retinal photoreceptor layer has fewer parts of type red sensitive photoreceptor cell, abnormal
ZP:0138168	eye photoreceptor cell decreased process quality photoreceptor cell outer segment organization, abnormal
ZP:0138169	photoreceptor disc membrane eye photoreceptor cell malformed, abnormal
ZP:0138172	eye photoreceptor cell retinal outer nuclear layer sparse, abnormal
ZP:0138174	cone photoreceptor outer segment red sensitive photoreceptor cell spatial pattern, abnormal
ZP:0138175	cone photoreceptor outer segment red sensitive photoreceptor cell mislocalised, abnormal
ZP:0138176	rod photoreceptor outer segment retinal rod cell spatial pattern, abnormal
ZP:0138186	neutrophil disrupted voltage-gated ion channel activity, abnormal
ZP:0138187	reactive oxygen species neutrophil decreased amount, abnormal
ZP:0138188	neutrophil disrupted calcium-mediated signaling, abnormal
ZP:0138197	cerebellar Purkinje cell layer morphogenesis decreased occurrence, abnormal
ZP:0138200	granular layer corpus cerebelli has extra parts of type Purkinje cell, abnormal
ZP:0138201	Purkinje cell layer corpus cerebelli has fewer parts of type Purkinje cell, abnormal
ZP:0138202	Purkinje cell inserted into granular layer corpus cerebelli, abnormal
ZP:0138203	granule cell torus longitudinalis absent, abnormal
ZP:0138204	neuron optic tectum mislocalised radially, abnormal
ZP:0138205	molecular layer corpus cerebelli absent, abnormal
ZP:0138206	cerebellar crest absent, abnormal
ZP:0138207	stratum marginale absent, abnormal
ZP:0138208	stratum opticum absent, abnormal
ZP:0138209	cerebellar granule cell absent, abnormal
ZP:0138210	neuron projection Purkinje cell disoriented, abnormal
ZP:0138213	granular layer corpus cerebelli has extra parts of type eurydendroid cell, abnormal
ZP:0138214	Purkinje cell layer corpus cerebelli has fewer parts of type eurydendroid cell, abnormal
ZP:0138215	eurydendroid cell inserted into granular layer corpus cerebelli, abnormal
ZP:0138216	granular layer corpus cerebelli has extra parts of type Bergmann glial cell, abnormal
ZP:0138217	Bergmann glial cell inserted into granular layer corpus cerebelli, abnormal
ZP:0138219	calcium import into the mitochondrion decreased occurrence, abnormal
ZP:0138223	ventral aorta decreased length, abnormal
ZP:0138224	pericyte decreased amount, abnormal
ZP:0138225	vascular associated smooth muscle cell decreased amount, abnormal
ZP:0138226	regulation of mitochondrial membrane potential decreased process quality, abnormal
ZP:0138227	mitochondrion dopaminergic neuron decreased area, abnormal
ZP:0138233	posterior lateral line primordium decreased rate cell migration, abnormal
ZP:0138235	cell posterior lateral line primordium normal amount, abnormal
ZP:0138237	mitochondrion skeletal muscle cell decreased volume, abnormal
ZP:0138238	mitochondrion skeletal muscle cell deformed, abnormal
ZP:0138239	cell-cell junction blood vessel endothelial cell decreased distribution, abnormal
ZP:0138241	intersegmental vessel process quality cell-cell junction organization, abnormal
ZP:0138242	intersegmental vessel process quality blood vessel morphogenesis, abnormal
ZP:0138244	somatic stem cell intestine decreased amount, abnormal
ZP:0138245	intestinal stem cell homeostasis disrupted, abnormal
ZP:0138246	goblet cell decreased area, abnormal
ZP:0138247	chordoma intestine increased amount, abnormal
ZP:0138248	testis fibrotic, abnormal
ZP:0138249	oocyte atretic, abnormal
ZP:0138250	myocardium condensed, abnormal
ZP:0138251	oocyte stage II decreased amount, abnormal
ZP:0138252	intestinal mucosa morphology, abnormal
ZP:0138253	seminiferous tubule morphology, abnormal
ZP:0138254	mitochondrion intestine swollen, abnormal
ZP:0138255	mitochondrial outer membrane skeletal muscle dilated, abnormal
ZP:0138256	mucin granule goblet cell dense, abnormal
ZP:0138257	mitotic cell cycle phase transition disrupted, abnormal
ZP:0138258	cortical actin cytoskeleton blastoderm cell increased thickness, abnormal
ZP:0138259	cell projection blastoderm increased amount, abnormal
ZP:0138260	basal surface ceratobranchial 5 tooth osseous, abnormal
ZP:0138261	centrum increased diameter, abnormal
ZP:0138262	integument lacks all parts of type xanthophore, abnormal
ZP:0138263	integument has fewer parts of type melanocyte, abnormal
ZP:0138264	neural arch dorsal orientation, abnormal
ZP:0138267	scale decreased occurrence bone resorption, abnormal
ZP:0138285	autophagosome-lysosome fusion disrupted, abnormal
ZP:0138286	lysosome whole organism increased amount, abnormal
ZP:0138287	endosome whole organism increased amount, abnormal
ZP:0138288	caudal hematopoietic tissue increased occurrence cell death, abnormal
ZP:0138289	podocyte foot pronephric glomerulus absent, abnormal
ZP:0138290	dorsal aorta decreased linear velocity blood circulation, abnormal
ZP:0138291	intercalated disc heart structure, abnormal
ZP:0138292	cardiac myofibril heart structure, abnormal
ZP:0138294	otic epithelium decreased size, abnormal
ZP:0138295	skeletal muscle myoblast decreased occurrence cell population proliferation, abnormal
ZP:0138296	ribosomal RNA skeletal muscle myoblast decreased amount, abnormal
ZP:0138297	fibrillar center skeletal muscle cell spatial pattern, abnormal
ZP:0138298	nucleolus skeletal muscle cell spatial pattern, abnormal
ZP:0138299	nucleolus skeletal muscle cell increased size, abnormal
ZP:0138300	skeletal muscle myoblast decreased occurrence rRNA processing, abnormal
ZP:0138301	skeletal muscle myoblast decreased occurrence rRNA transcription, abnormal
ZP:0138302	sarcomere skeletal muscle decreased amount, abnormal
ZP:0138303	skeletal muscle myoblast decreased occurrence ribosome biogenesis, abnormal
ZP:0138304	skeletal muscle contraction process quality, abnormal
ZP:0138306	primitive pectoral fin adductor decreased size, abnormal
ZP:0138314	axis elongation delayed, abnormal
ZP:0138316	male courtship behavior behavioral quality of a process, abnormal
ZP:0138317	convergent extension involved in neural plate elongation delayed, abnormal
ZP:0138320	yolk extension decreased length, abnormal
ZP:0138331	pharyngeal arch protruding, abnormal
ZP:0138336	nucleus yolk syncytial layer distributed, abnormal
ZP:0138337	yolk syncytial layer decreased width, abnormal
ZP:0138338	yolk syncytial layer decreased occurrence actin filament organization, abnormal
ZP:0138339	filamentous actin yolk syncytial layer mislocalised, abnormal
ZP:0138340	actin cytoskeleton organization decreased occurrence, abnormal
ZP:0138341	EVL increased distance DEL, abnormal
ZP:0138342	optic stalk increased occurrence cell death, abnormal
ZP:0138343	lens decreased occurrence cell population proliferation, abnormal
ZP:0138344	lens epithelium absent, abnormal
ZP:0138345	lens fiber cell decreased amount, abnormal
ZP:0138346	vascular lymphangioblast cranial vasculature decreased amount, abnormal
ZP:0138348	lateral facial lymph vessel lacks parts or has fewer parts of type endothelial cell, abnormal
ZP:0138349	lateral facial lymph vessel has fewer parts of type endothelial cell, abnormal
ZP:0138350	otolithic lymph vessel lacks parts or has fewer parts of type endothelial cell, abnormal
ZP:0138351	otolithic lymph vessel has fewer parts of type endothelial cell, abnormal
ZP:0138352	medial facial lymph vessel lacks parts or has fewer parts of type endothelial cell, abnormal
ZP:0138353	medial facial lymph vessel has fewer parts of type endothelial cell, abnormal
ZP:0138357	left side dorsal habenular nucleus increased amount, abnormal
ZP:0138358	left side dorsal habenular nucleus decreased amount, abnormal
ZP:0138359	dorsal habenular nucleus decreased process quality neurogenesis, abnormal
ZP:0138362	neuron projection parapineal organ decreased length, abnormal
ZP:0138363	neuron projection parapineal organ decreased amount, abnormal
ZP:0138364	neuron projection parapineal organ decreased branchiness, abnormal
ZP:0138365	efferent neuron parapineal organ morphology, abnormal
ZP:0138366	motor neuron process quality neuron projection development, abnormal
ZP:0138368	lateral facial lymph vessel absent, abnormal
ZP:0138369	medial facial lymph vessel absent, abnormal
ZP:0138370	optic vesicle decreased occurrence cell population proliferation, abnormal
ZP:0138371	axon sensory neuron branchiness, abnormal
ZP:0138372	hypochord increased amount, abnormal
ZP:0138373	hypochord increased distribution, abnormal
ZP:0138375	pronephric tubule decreased occurrence endocytosis, abnormal
ZP:0138384	lysosome microglial cell morphology, abnormal
ZP:0138385	head decreased process quality hexosaminidase activity, abnormal
ZP:0138387	oligosaccharide brain increased amount, abnormal
ZP:0138388	oligosaccharide liver increased amount, abnormal
ZP:0138389	oligosaccharide pancreas increased amount, abnormal
ZP:0138390	oligosaccharide gonad increased amount, abnormal
ZP:0138391	oligosaccharide spleen increased amount, abnormal
ZP:0138392	oligosaccharide intestine increased amount, abnormal
ZP:0138393	brain decreased process quality hexosaminidase activity, abnormal
ZP:0138394	liver decreased process quality hexosaminidase activity, abnormal
ZP:0138395	pancreas decreased process quality hexosaminidase activity, abnormal
ZP:0138396	gonad decreased process quality hexosaminidase activity, abnormal
ZP:0138397	spleen decreased process quality hexosaminidase activity, abnormal
ZP:0138398	intestine decreased process quality hexosaminidase activity, abnormal
ZP:0138400	caudal hematopoietic tissue has fewer parts of type neutrophil, abnormal
ZP:0138401	macrophage decreased occurrence phagocytosis, abnormal
ZP:0138402	pronephric podocyte retracted, abnormal
ZP:0138403	hexosaminidase activity decreased process quality, abnormal
ZP:0138404	parasphenoid decreased occurrence ossification, abnormal
ZP:0138405	splanchnocranium disrupted ossification, abnormal
ZP:0138406	branchiostegal ray 1 decreased occurrence ossification, abnormal
ZP:0138407	branchiostegal ray 2 decreased occurrence ossification, abnormal
ZP:0138408	nucleus nucleate erythrocyte decreased size, abnormal
ZP:0138409	blood has fewer parts of type cell, abnormal
ZP:0138410	pupil increased distance pupil, abnormal
ZP:0138411	vertebral column decreased width, abnormal
ZP:0138412	nucleate erythrocyte decreased volume, abnormal
ZP:0138413	ceratobranchial 5 bone poorly ossified, abnormal
ZP:0138414	lateral larval melanophore stripe increased pigmentation, abnormal
ZP:0138415	scale increased occurrence tissue remodeling, abnormal
ZP:0138416	scale increased occurrence bone remodeling, abnormal
ZP:0138417	scale increased occurrence bone development, abnormal
ZP:0138418	infraorbital increased occurrence bone development, abnormal
ZP:0138419	neural arch angle centrum, abnormal
ZP:0138420	aerobic respiration decreased occurrence, abnormal
ZP:0138425	ventral region cranial vault decreased width, abnormal
ZP:0138426	cranial vault male organism decreased width, abnormal
ZP:0138427	cranial vault female organism decreased width, abnormal
ZP:0138428	subintestinal vein has extra parts of type vascular sprouts, abnormal
ZP:0138429	nerve sheath tumor muscle increased amount, abnormal
ZP:0138430	nerve sheath tumor bone tissue increased amount, abnormal
ZP:0138431	retinal pigmented epithelium incomplete structure, abnormal
ZP:0138432	vagal ganglion decreased amount, abnormal
ZP:0138433	pigment cell organization quality, abnormal
ZP:0138434	cranial nerve II disrupted axon guidance, abnormal
ZP:0138435	cranial nerve II disrupted axonal fasciculation, abnormal
ZP:0138436	optic nerve head fasciculation, abnormal
ZP:0138439	posterior lateral line nerve absent, abnormal
ZP:0138452	synapse neurohypophysis decreased amount, abnormal
ZP:0138455	actin filament neurohypophysis increased stability, abnormal
ZP:0138457	hypophyseal capillary process quality pore complex assembly, abnormal
ZP:0138458	hypophyseal capillary decreased process quality pore complex assembly, abnormal
ZP:0138460	hypophyseal capillary decreased process quality regulation of vascular permeability, abnormal
ZP:0138462	CaP motoneuron frequency calcium-mediated signaling, abnormal
ZP:0138463	CaP motoneuron spatial pattern, abnormal
ZP:0138464	neuromast lacks all parts of type neuromast hair cell, abnormal
ZP:0138465	muscle cell myotome disorganized, abnormal
ZP:0138468	CaP motoneuron decreased occurrence axon guidance, abnormal
ZP:0138469	CaP motoneuron arrested axon extension involved in axon guidance, abnormal
ZP:0138470	growth cone filopodium CaP motoneuron decreased amount, abnormal
ZP:0138471	optic vesicle increased variability of size, abnormal
ZP:0138472	head bilateral symmetry, abnormal
ZP:0138473	apical surface optic vesicle spatial pattern, abnormal
ZP:0138474	basal surface optic vesicle spatial pattern, abnormal
ZP:0138475	epithelium disrupted adherens junction organization, abnormal
ZP:0138476	optic vesicle disrupted establishment of apical/basal cell polarity, abnormal
ZP:0138477	optic vesicle displaced to neuroepithelial cell anatomical space posterior segment eye, abnormal
ZP:0138478	pronephric tubule malformed, abnormal
ZP:0138479	optic vesicle elongation disrupted, abnormal
ZP:0138480	optic vesicle asymmetrical, abnormal
ZP:0138485	yolk agenesis, abnormal
ZP:0138486	cell body secondary motor neuron mislocalised, abnormal
ZP:0138495	central nervous system increased process quality apoptotic process, abnormal
ZP:0138496	optic cup increased process quality apoptotic process, abnormal
ZP:0138498	fourth ventricle lacks parts or has fewer parts of type apical side cilium fourth ventricle, abnormal
ZP:0138499	apical side ventricular system absent, abnormal
ZP:0138500	ventricular system lacks parts or has fewer parts of type apical side gamma-tubulin complex ventricular system, abnormal
ZP:0138501	ventricular system has fewer parts of type apical side microtubule organizing center ventricular system, abnormal
ZP:0138502	ventricular system has fewer parts of type apical side microtubule ventricular system, abnormal
ZP:0138503	gamma-tubulin complex ventricular system absent, abnormal
ZP:0138504	cilium fourth ventricle mislocalised, abnormal
ZP:0138505	cilium fourth ventricle decreased amount, abnormal
ZP:0138506	fourth ventricle decreased occurrence epithelial tube formation, abnormal
ZP:0138507	tectal ventricle decreased occurrence epithelial tube formation, abnormal
ZP:0138508	pronephric duct decreased occurrence nephric duct formation, abnormal
ZP:0138509	apical side gut absent, abnormal
ZP:0138510	gut lacks parts or has fewer parts of type apical side gamma-tubulin complex gut, abnormal
ZP:0138511	gamma-tubulin complex gut absent, abnormal
ZP:0138512	gut has fewer parts of type apical side microtubule gut, abnormal
ZP:0138513	pancreatic duct decreased occurrence epithelial tube formation, abnormal
ZP:0138514	gut decreased occurrence epithelial tube formation, abnormal
ZP:0138515	gut spatial pattern, abnormal
ZP:0138516	gut shortened, abnormal
ZP:0138517	exocrine pancreas position, abnormal
ZP:0138518	brain decreased occurrence DNA methylation, abnormal
ZP:0138519	fin decreased occurrence DNA methylation, abnormal
ZP:0138520	integument decreased occurrence DNA methylation, abnormal
ZP:0138521	muscle decreased occurrence DNA methylation, abnormal
ZP:0138522	IgD immunoglobulin complex whole organism decreased amount, abnormal
ZP:0138523	IgM immunoglobulin complex whole organism decreased amount, abnormal
ZP:0138524	IgZ immunoglobulin complex whole organism decreased amount, abnormal
ZP:0138525	filopodium intersegmental vessel absent, abnormal
ZP:0138526	slit diaphragm pronephric podocyte morphology, abnormal
ZP:0138527	ventriculo bulbo valve morphogenesis decreased process quality, abnormal
ZP:0138532	posterior macula decreased occurrence succinate dehydrogenase activity, abnormal
ZP:0138536	posterior macula decreased occurrence cytochrome-c oxidase activity, abnormal
ZP:0138538	swimming behavioral quality of a process, abnormal
ZP:0138539	posterior macula has fewer parts of type mitochondrion hair cell posterior macula, abnormal
ZP:0138540	neuromast hair cell anterior lateral line neuromast decreased amount, abnormal
ZP:0138541	aerobic respiration disrupted, abnormal
ZP:0138542	mitochondrial tRNA thio-modification disrupted, abnormal
ZP:0138543	tRNA-specific 2-thiouridylase activity disrupted, abnormal
ZP:0138544	macula lagena has fewer parts of type hair cell, abnormal
ZP:0138545	cerebral spinal fluid fourth ventricle increased amount, abnormal
ZP:0138546	cerebral spinal fluid ventricular system increased amount, abnormal
ZP:0138547	dorsal spinal nerve decreased occurrence myelination, abnormal
ZP:0138548	ventral spinal nerve decreased occurrence myelination, abnormal
ZP:0138555	dorsal spinal nerve morphology, abnormal
ZP:0138558	ventral aorta decreased amount, abnormal
ZP:0138559	migrasome whole organism decreased amount, abnormal
ZP:0138560	determination of left/right symmetry decreased occurrence, abnormal
ZP:0138561	forerunner cell group irregular spatial pattern, abnormal
ZP:0138562	migrasome shield decreased amount, abnormal
ZP:0138563	endocardial cushion bulbus arteriosus spatial pattern, abnormal
ZP:0138564	bulbus arteriosus lacks all parts of type ventriculo bulbo valve, abnormal
ZP:0138565	bulbus arteriosus decreased process quality smooth muscle tissue development, abnormal
ZP:0138566	vascular smooth muscle bulbus arteriosus decreased amount, abnormal
ZP:0138567	bulbus arteriosus decreased diameter, abnormal
ZP:0138568	ventriculo bulbo valve decreased process quality Notch signaling involved in heart development, abnormal
ZP:0138569	posterior region ventriculo bulbo valve decreased amount, abnormal
ZP:0138570	intersegmental vessel decreased efficacy angiogenesis, abnormal
ZP:0138571	liver increased occurrence cellular response to DNA damage stimulus, abnormal
ZP:0138573	pronephric tubule decreased occurrence determination of left/right symmetry, abnormal
ZP:0138574	pronephric tubule decreased size, abnormal
ZP:0138575	brain disrupted cell communication by electrical coupling, abnormal
ZP:0138576	endocardial cushion bulbus arteriosus increased amount, abnormal
ZP:0138577	nucleus pronephric duct increased amount, abnormal
ZP:0138578	cytoplasm pronephric duct decreased amount, abnormal
ZP:0138579	caudal fin increased frequency striated muscle contraction, abnormal
ZP:0138580	VeLD decreased process quality action potential, abnormal
ZP:0138584	lipid yolk increased amount, abnormal
ZP:0138590	phenylalanine whole organism increased amount, abnormal
ZP:0138591	spinal cord has fewer parts of type axon myelin sheath spinal cord, abnormal
ZP:0138592	spinal cord process quality central nervous system myelin formation, abnormal
ZP:0138593	myelin sheath spinal cord decreased length, abnormal
ZP:0138594	spinal cord surrounding myelin sheath neuronal cell body spinal cord, abnormal
ZP:0138599	spinal cord decreased rate central nervous system myelin formation, abnormal
ZP:0138600	17beta-estradiol ovary decreased amount, abnormal
ZP:0138601	17beta-estradiol testis decreased amount, abnormal
ZP:0138602	oocyte stage III increased occurrence apoptotic process, abnormal
ZP:0138603	oocyte stage IV increased occurrence apoptotic process, abnormal
ZP:0138604	granulosa cell increased occurrence apoptotic process, abnormal
ZP:0138605	theca cell increased occurrence apoptotic process, abnormal
ZP:0138606	http://purl.obolibrary.org/obo/ZFA_0005926 decreased length, abnormal
ZP:0138609	muscle absent, abnormal
ZP:0138615	http://purl.obolibrary.org/obo/ZFA_0005921 delayed cell migration, abnormal
ZP:0138622	http://purl.obolibrary.org/obo/ZFA_0005926 decreased size, abnormal
ZP:0138623	http://purl.obolibrary.org/obo/ZFA_0005922 hypoplastic, abnormal
ZP:0138624	xanthophore head discolored, abnormal
ZP:0138625	xanthophore caudal fin decreased amount, abnormal
ZP:0138627	xanthophore trunk discolored, abnormal
ZP:0138637	http://purl.obolibrary.org/obo/ZFA_0005923 hypoplastic, abnormal
ZP:0138638	http://purl.obolibrary.org/obo/ZFA_0005925 hypoplastic, abnormal
ZP:0138639	primitive pectoral fin adductor absent, abnormal
ZP:0138640	primitive pectoral fin abductor absent, abnormal
ZP:0138651	immature neutrophil increased amount, abnormal
ZP:0138654	sarcomere slow muscle cell increased size, abnormal
ZP:0138655	slow muscle cell somite increased length, abnormal
ZP:0138663	eye increased process quality cell population proliferation, abnormal
ZP:0138667	pronephric duct deformed, abnormal
ZP:0138668	pronephric duct irregularly shaped, abnormal
ZP:0138669	pronephric duct structurally discontinuous, abnormal
ZP:0138670	pronephric duct opening structure, abnormal
ZP:0138671	locomotion involved in locomotory behavior rhythm quality, abnormal
ZP:0138672	reproduction decreased efficacy, abnormal
ZP:0138673	oocyte maturation decreased process quality, abnormal
ZP:0138674	oviposition decreased frequency, abnormal
ZP:0138676	hindbrain shortened, abnormal
ZP:0138686	liver primordium mislocalised, abnormal
ZP:0138687	intestinal bulb primordium spatial pattern, abnormal
ZP:0138688	intestinal bulb primordium absent, abnormal
ZP:0138689	duct gall bladder absent, abnormal
ZP:0138690	intestine lumen intrahepatic bile duct mislocalised, abnormal
ZP:0138691	left side intestine mislocalised, abnormal
ZP:0138692	intestinal bulb spatial pattern, abnormal
ZP:0138693	hepatic duct absent, abnormal