GO:0000012PHENOTYPE	single strand break repair phenotype
GO:0000045PHENOTYPE	autophagosome assembly phenotype
GO:0000050PHENOTYPE	urea cycle phenotype
GO:0000052PHENOTYPE	citrulline metabolic process phenotype
GO:0000070PHENOTYPE	mitotic sister chromatid segregation phenotype
GO:0000077PHENOTYPE	DNA damage checkpoint phenotype
GO:0000079PHENOTYPE	regulation of cyclin-dependent protein serine/threonine kinase activity phenotype
GO:0000082PHENOTYPE	G1/S transition of mitotic cell cycle phenotype
GO:0000086PHENOTYPE	G2/M 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:0000187PHENOTYPE	activation of MAPK activity phenotype
GO:0000226PHENOTYPE	microtubule cytoskeleton organization phenotype
GO:0000237PHENOTYPE	leptotene phenotype
GO:0000271PHENOTYPE	polysaccharide biosynthetic process phenotype
GO:0000278PHENOTYPE	mitotic cell cycle phenotype
GO:0000281PHENOTYPE	mitotic cytokinesis phenotype
GO:0000320PHENOTYPE	re-entry into mitotic cell cycle phenotype
GO:0000381PHENOTYPE	regulation of alternative mRNA splicing, via spliceosome phenotype
GO:0000398PHENOTYPE	mRNA splicing, via spliceosome phenotype
GO:0000578PHENOTYPE	embryonic axis specification phenotype
GO:0000723PHENOTYPE	telomere maintenance phenotype
GO:0000724PHENOTYPE	double-strand break repair via homologous recombination phenotype
GO:0000737PHENOTYPE	DNA catabolic process, endonucleolytic phenotype
GO:0000768PHENOTYPE	syncytium formation by plasma membrane fusion phenotype
GO:0000793PHENOTYPE	condensed chromosome phenotype
GO:0000902PHENOTYPE	cell morphogenesis phenotype
GO:0000904PHENOTYPE	cell morphogenesis involved in differentiation phenotype
GO:0000910PHENOTYPE	cytokinesis phenotype
GO:0001501PHENOTYPE	skeletal system development phenotype
GO:0001502PHENOTYPE	cartilage condensation phenotype
GO:0001503PHENOTYPE	ossification phenotype
GO:0001504PHENOTYPE	neurotransmitter uptake phenotype
GO:0001505PHENOTYPE	regulation of neurotransmitter levels phenotype
GO:0001508PHENOTYPE	action potential phenotype
GO:0001523PHENOTYPE	retinoid metabolic process phenotype
GO:0001525PHENOTYPE	angiogenesis phenotype
GO:0001541PHENOTYPE	ovarian follicle development phenotype
GO:0001542PHENOTYPE	ovulation from ovarian follicle phenotype
GO:0001543PHENOTYPE	ovarian follicle rupture phenotype
GO:0001547PHENOTYPE	antral ovarian follicle growth phenotype
GO:0001553PHENOTYPE	luteinization phenotype
GO:0001556PHENOTYPE	oocyte maturation phenotype
GO:0001558PHENOTYPE	regulation of cell growth phenotype
GO:0001568PHENOTYPE	blood vessel development phenotype
GO:0001569PHENOTYPE	patterning of blood vessels phenotype
GO:0001570PHENOTYPE	vasculogenesis phenotype
GO:0001573PHENOTYPE	ganglioside metabolic process phenotype
GO:0001578PHENOTYPE	microtubule bundle formation phenotype
GO:0001609PHENOTYPE	G-protein coupled adenosine receptor activity phenotype
GO:0001649PHENOTYPE	osteoblast differentiation phenotype
GO:0001654PHENOTYPE	eye development phenotype
GO:0001655PHENOTYPE	urogenital system development phenotype
GO:0001656PHENOTYPE	metanephros development phenotype
GO:0001657PHENOTYPE	ureteric bud development phenotype
GO:0001658PHENOTYPE	branching involved in ureteric bud morphogenesis phenotype
GO:0001659PHENOTYPE	temperature homeostasis phenotype
GO:0001660PHENOTYPE	fever generation phenotype
GO:0001662PHENOTYPE	behavioral fear response phenotype
GO:0001666PHENOTYPE	response to hypoxia phenotype
GO:0001667PHENOTYPE	ameboidal-type cell migration phenotype
GO:0001696PHENOTYPE	gastric acid secretion phenotype
GO:0001701PHENOTYPE	in utero embryonic development phenotype
GO:0001702PHENOTYPE	gastrulation with mouth forming second phenotype
GO:0001704PHENOTYPE	formation of primary germ layer 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:0001755PHENOTYPE	neural crest cell migration phenotype
GO:0001756PHENOTYPE	somitogenesis phenotype
GO:0001763PHENOTYPE	morphogenesis of a branching structure phenotype
GO:0001764PHENOTYPE	neuron migration phenotype
GO:0001774PHENOTYPE	microglial cell activation phenotype
GO:0001775PHENOTYPE	cell activation phenotype
GO:0001776PHENOTYPE	leukocyte homeostasis phenotype
GO:0001779PHENOTYPE	natural killer cell differentiation phenotype
GO:0001780PHENOTYPE	neutrophil homeostasis phenotype
GO:0001783PHENOTYPE	B cell apoptotic process phenotype
GO:0001806PHENOTYPE	type IV hypersensitivity phenotype
GO:0001816PHENOTYPE	cytokine production phenotype
GO:0001817PHENOTYPE	regulation of cytokine production phenotype
GO:0001820PHENOTYPE	serotonin secretion phenotype
GO:0001822PHENOTYPE	kidney development phenotype
GO:0001823PHENOTYPE	mesonephros development phenotype
GO:0001824PHENOTYPE	blastocyst development phenotype
GO:0001832PHENOTYPE	blastocyst growth phenotype
GO:0001833PHENOTYPE	inner cell mass cell proliferation phenotype
GO:0001834PHENOTYPE	trophectodermal cell proliferation phenotype
GO:0001835PHENOTYPE	blastocyst hatching phenotype
GO:0001837PHENOTYPE	epithelial to mesenchymal transition phenotype
GO:0001839PHENOTYPE	neural plate morphogenesis phenotype
GO:0001841PHENOTYPE	neural tube formation phenotype
GO:0001842PHENOTYPE	neural fold formation phenotype
GO:0001843PHENOTYPE	neural tube closure phenotype
GO:0001845PHENOTYPE	phagolysosome assembly phenotype
GO:0001880PHENOTYPE	Mullerian duct regression phenotype
GO:0001881PHENOTYPE	receptor recycling phenotype
GO:0001885PHENOTYPE	endothelial cell development phenotype
GO:0001887PHENOTYPE	selenium compound metabolic process phenotype
GO:0001889PHENOTYPE	liver development phenotype
GO:0001890PHENOTYPE	placenta development phenotype
GO:0001892PHENOTYPE	embryonic placenta development phenotype
GO:0001893PHENOTYPE	maternal placenta development phenotype
GO:0001894PHENOTYPE	tissue homeostasis phenotype
GO:0001895PHENOTYPE	retina homeostasis phenotype
GO:0001909PHENOTYPE	leukocyte mediated cytotoxicity phenotype
GO:0001913PHENOTYPE	T cell mediated cytotoxicity phenotype
GO:0001932PHENOTYPE	regulation of protein phosphorylation phenotype
GO:0001934PHENOTYPE	positive regulation of protein phosphorylation phenotype
GO:0001935PHENOTYPE	endothelial cell proliferation phenotype
GO:0001942PHENOTYPE	hair follicle development 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:0001973PHENOTYPE	adenosine receptor signaling pathway phenotype
GO:0001974PHENOTYPE	blood vessel remodeling phenotype
GO:0001975PHENOTYPE	response to amphetamine phenotype
GO:0001976PHENOTYPE	neurological system process involved in regulation of systemic arterial blood pressure phenotype
GO:0001990PHENOTYPE	regulation of systemic arterial blood pressure by hormone phenotype
GO:0002009PHENOTYPE	morphogenesis of an epithelium phenotype
GO:0002011PHENOTYPE	morphogenesis of an epithelial sheet phenotype
GO:0002016PHENOTYPE	regulation of blood volume by renin-angiotensin phenotype
GO:0002026PHENOTYPE	regulation of the force of heart contraction 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:0002067PHENOTYPE	glandular epithelial cell differentiation 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:0002159PHENOTYPE	desmosome assembly phenotype
GO:0002176PHENOTYPE	male germ cell proliferation phenotype
GO:0002177PHENOTYPE	manchette phenotype
GO:0002218PHENOTYPE	activation of innate immune response phenotype
GO:0002232PHENOTYPE	leukocyte chemotaxis involved in inflammatory response phenotype
GO:0002244PHENOTYPE	hematopoietic progenitor cell differentiation phenotype
GO:0002246PHENOTYPE	wound healing involved in inflammatory response phenotype
GO:0002248PHENOTYPE	connective tissue replacement involved in inflammatory response wound healing phenotype
GO:0002250PHENOTYPE	adaptive immune response phenotype
GO:0002253PHENOTYPE	activation of immune response phenotype
GO:0002260PHENOTYPE	lymphocyte homeostasis phenotype
GO:0002262PHENOTYPE	myeloid cell homeostasis phenotype
GO:0002281PHENOTYPE	macrophage activation involved in immune response phenotype
GO:0002282PHENOTYPE	microglial cell activation involved in immune response phenotype
GO:0002287PHENOTYPE	alpha-beta T cell activation involved in immune response phenotype
GO:0002292PHENOTYPE	T cell differentiation involved in immune response phenotype
GO:0002309PHENOTYPE	T cell proliferation involved in immune response phenotype
GO:0002317PHENOTYPE	plasma cell differentiation phenotype
GO:0002320PHENOTYPE	lymphoid progenitor cell differentiation phenotype
GO:0002322PHENOTYPE	B cell proliferation involved in immune response phenotype
GO:0002328PHENOTYPE	pro-B cell differentiation phenotype
GO:0002335PHENOTYPE	mature B cell differentiation phenotype
GO:0002367PHENOTYPE	cytokine production involved in immune response phenotype
GO:0002376PHENOTYPE	immune system process phenotype
GO:0002377PHENOTYPE	immunoglobulin production phenotype
GO:0002381PHENOTYPE	immunoglobulin production involved in immunoglobulin mediated immune response phenotype
GO:0002432PHENOTYPE	granuloma formation phenotype
GO:0002437PHENOTYPE	inflammatory response to antigenic stimulus phenotype
GO:0002438PHENOTYPE	acute inflammatory response to antigenic stimulus phenotype
GO:0002443PHENOTYPE	leukocyte mediated immunity phenotype
GO:0002446PHENOTYPE	neutrophil mediated immunity phenotype
GO:0002448PHENOTYPE	mast cell mediated immunity phenotype
GO:0002455PHENOTYPE	humoral immune response mediated by circulating immunoglobulin phenotype
GO:0002456PHENOTYPE	T cell mediated immunity phenotype
GO:0002507PHENOTYPE	tolerance induction phenotype
GO:0002520PHENOTYPE	immune system development 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:0002526PHENOTYPE	acute inflammatory response phenotype
GO:0002534PHENOTYPE	cytokine production involved in inflammatory response phenotype
GO:0002536PHENOTYPE	respiratory burst involved in inflammatory response phenotype
GO:0002537PHENOTYPE	nitric oxide production involved in inflammatory response phenotype
GO:0002573PHENOTYPE	myeloid leukocyte differentiation phenotype
GO:0002679PHENOTYPE	respiratory burst involved in defense response phenotype
GO:0002682PHENOTYPE	regulation of immune system process phenotype
GO:0002761PHENOTYPE	regulation of myeloid leukocyte differentiation phenotype
GO:0002790PHENOTYPE	peptide secretion phenotype
GO:0002934PHENOTYPE	desmosome organization phenotype
GO:0003002PHENOTYPE	regionalization phenotype
GO:0003007PHENOTYPE	heart morphogenesis phenotype
GO:0003009PHENOTYPE	skeletal muscle contraction phenotype
GO:0003012PHENOTYPE	muscle system process phenotype
GO:0003014PHENOTYPE	renal system process phenotype
GO:0003016PHENOTYPE	respiratory system process phenotype
GO:0003017PHENOTYPE	lymph circulation phenotype
GO:0003029PHENOTYPE	detection of hypoxic conditions in blood by carotid body chemoreceptor signaling phenotype
GO:0003032PHENOTYPE	detection of oxygen phenotype
GO:0003071PHENOTYPE	renal system process involved in regulation of systemic arterial blood pressure phenotype
GO:0003073PHENOTYPE	regulation of systemic arterial blood pressure phenotype
GO:0003081PHENOTYPE	regulation of systemic arterial blood pressure by renin-angiotensin phenotype
GO:0003091PHENOTYPE	renal water homeostasis phenotype
GO:0003093PHENOTYPE	regulation of glomerular filtration phenotype
GO:0003094PHENOTYPE	glomerular filtration phenotype
GO:0003096PHENOTYPE	renal sodium ion transport phenotype
GO:0003097PHENOTYPE	renal water transport phenotype
GO:0003139PHENOTYPE	secondary heart field specification phenotype
GO:0003151PHENOTYPE	outflow tract morphogenesis phenotype
GO:0003158PHENOTYPE	endothelium development 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:0003197PHENOTYPE	endocardial cushion development phenotype
GO:0003198PHENOTYPE	epithelial to mesenchymal transition involved in endocardial cushion formation phenotype
GO:0003199PHENOTYPE	endocardial cushion to mesenchymal transition involved in heart valve formation phenotype
GO:0003203PHENOTYPE	endocardial cushion morphogenesis phenotype
GO:0003205PHENOTYPE	cardiac chamber development phenotype
GO:0003207PHENOTYPE	cardiac chamber formation phenotype
GO:0003208PHENOTYPE	cardiac ventricle morphogenesis phenotype
GO:0003209PHENOTYPE	cardiac atrium morphogenesis phenotype
GO:0003229PHENOTYPE	ventricular cardiac muscle tissue development phenotype
GO:0003231PHENOTYPE	cardiac ventricle development phenotype
GO:0003253PHENOTYPE	cardiac neural crest cell migration involved in outflow tract morphogenesis phenotype
GO:0003260PHENOTYPE	cardioblast migration phenotype
GO:0003273PHENOTYPE	cell migration involved in endocardial cushion formation phenotype
GO:0003278PHENOTYPE	apoptotic process involved in heart morphogenesis phenotype
GO:0003294PHENOTYPE	atrial ventricular junction remodeling phenotype
GO:0003300PHENOTYPE	cardiac muscle hypertrophy phenotype
GO:0003309PHENOTYPE	type B pancreatic cell differentiation phenotype
GO:0003323PHENOTYPE	type B pancreatic cell development phenotype
GO:0003334PHENOTYPE	keratinocyte development phenotype
GO:0003335PHENOTYPE	corneocyte development phenotype
GO:0003338PHENOTYPE	metanephros morphogenesis phenotype
GO:0003341PHENOTYPE	cilium movement phenotype
GO:0003351PHENOTYPE	epithelial cilium movement phenotype
GO:0003357PHENOTYPE	noradrenergic neuron differentiation phenotype
GO:0003365PHENOTYPE	establishment of cell polarity involved in ameboidal cell migration phenotype
GO:0003382PHENOTYPE	epithelial cell morphogenesis phenotype
GO:0003401PHENOTYPE	axis elongation phenotype
GO:0003402PHENOTYPE	planar cell polarity pathway involved in axis elongation phenotype
GO:0003406PHENOTYPE	retinal pigment epithelium development phenotype
GO:0003407PHENOTYPE	neural retina development phenotype
GO:0003413PHENOTYPE	chondrocyte differentiation involved in endochondral bone morphogenesis phenotype
GO:0003415PHENOTYPE	chondrocyte hypertrophy phenotype
GO:0003416PHENOTYPE	endochondral bone growth phenotype
GO:0003417PHENOTYPE	growth plate cartilage development phenotype
GO:0003677PHENOTYPE	DNA binding phenotype
GO:0003720PHENOTYPE	telomerase activity phenotype
GO:0004089PHENOTYPE	carbonate dehydratase activity phenotype
GO:0004096PHENOTYPE	catalase activity phenotype
GO:0004102PHENOTYPE	choline O-acetyltransferase activity phenotype
GO:0004129PHENOTYPE	cytochrome-c oxidase activity phenotype
GO:0004175PHENOTYPE	endopeptidase activity phenotype
GO:0004340PHENOTYPE	glucokinase activity phenotype
GO:0004345PHENOTYPE	glucose-6-phosphate dehydrogenase activity phenotype
GO:0004347PHENOTYPE	glucose-6-phosphate isomerase activity phenotype
GO:0004365PHENOTYPE	glyceraldehyde-3-phosphate dehydrogenase (NAD+) (phosphorylating) activity phenotype
GO:0004396PHENOTYPE	hexokinase activity phenotype
GO:0004422PHENOTYPE	hypoxanthine phosphoribosyltransferase activity phenotype
GO:0004439PHENOTYPE	phosphatidylinositol-4,5-bisphosphate 5-phosphatase activity phenotype
GO:0004505PHENOTYPE	phenylalanine 4-monooxygenase activity phenotype
GO:0004517PHENOTYPE	nitric-oxide synthase activity phenotype
GO:0004558PHENOTYPE	alpha-1,4-glucosidase activity phenotype
GO:0004601PHENOTYPE	peroxidase activity phenotype
GO:0004602PHENOTYPE	glutathione peroxidase activity phenotype
GO:0004618PHENOTYPE	phosphoglycerate kinase activity phenotype
GO:0004634PHENOTYPE	phosphopyruvate hydratase activity phenotype
GO:0004656PHENOTYPE	procollagen-proline 4-dioxygenase activity phenotype
GO:0004658PHENOTYPE	propionyl-CoA carboxylase activity phenotype
GO:0004672PHENOTYPE	protein kinase activity phenotype
GO:0004674PHENOTYPE	protein serine/threonine kinase activity phenotype
GO:0004708PHENOTYPE	MAP kinase kinase activity phenotype
GO:0004713PHENOTYPE	protein tyrosine kinase activity phenotype
GO:0004731PHENOTYPE	purine-nucleoside phosphorylase activity phenotype
GO:0004806PHENOTYPE	triglyceride lipase activity phenotype
GO:0004853PHENOTYPE	uroporphyrinogen decarboxylase activity phenotype
GO:0004871PHENOTYPE	signal transducer activity phenotype
GO:0004872PHENOTYPE	receptor activity phenotype
GO:0004930PHENOTYPE	G-protein coupled receptor activity phenotype
GO:0004972PHENOTYPE	NMDA glutamate receptor activity phenotype
GO:0005096PHENOTYPE	GTPase activator activity phenotype
GO:0005102PHENOTYPE	receptor binding phenotype
GO:0005179PHENOTYPE	hormone activity phenotype
GO:0005216PHENOTYPE	ion channel activity phenotype
GO:0005245PHENOTYPE	voltage-gated calcium channel activity phenotype
GO:0005248PHENOTYPE	voltage-gated sodium channel activity phenotype
GO:0005249PHENOTYPE	voltage-gated potassium channel activity phenotype
GO:0005261PHENOTYPE	cation channel activity phenotype
GO:0005262PHENOTYPE	calcium channel activity phenotype
GO:0005267PHENOTYPE	potassium channel activity phenotype
GO:0005391PHENOTYPE	sodium:potassium-exchanging ATPase activity phenotype
GO:0005576PHENOTYPE	extracellular region phenotype
GO:0005581PHENOTYPE	collagen trimer phenotype
GO:0005584PHENOTYPE	collagen type I trimer phenotype
GO:0005585PHENOTYPE	collagen type II trimer phenotype
GO:0005615PHENOTYPE	extracellular space phenotype
GO:0005622PHENOTYPE	intracellular phenotype
GO:0005634PHENOTYPE	nucleus phenotype
GO:0005635PHENOTYPE	nuclear envelope phenotype
GO:0005737PHENOTYPE	cytoplasm phenotype
GO:0005739PHENOTYPE	mitochondrion phenotype
GO:0005764PHENOTYPE	lysosome phenotype
GO:0005768PHENOTYPE	endosome phenotype
GO:0005777PHENOTYPE	peroxisome phenotype
GO:0005829PHENOTYPE	cytosol phenotype
GO:0005833PHENOTYPE	hemoglobin complex phenotype
GO:0005858PHENOTYPE	axonemal dynein complex phenotype
GO:0005886PHENOTYPE	plasma membrane phenotype
GO:0005887PHENOTYPE	integral component of plasma membrane phenotype
GO:0005891PHENOTYPE	voltage-gated calcium channel complex phenotype
GO:0005912PHENOTYPE	adherens junction phenotype
GO:0005977PHENOTYPE	glycogen metabolic process phenotype
GO:0005980PHENOTYPE	glycogen catabolic process phenotype
GO:0006000PHENOTYPE	fructose metabolic process phenotype
GO:0006006PHENOTYPE	glucose metabolic process phenotype
GO:0006007PHENOTYPE	glucose catabolic process phenotype
GO:0006012PHENOTYPE	galactose metabolic process phenotype
GO:0006024PHENOTYPE	glycosaminoglycan biosynthetic process phenotype
GO:0006029PHENOTYPE	proteoglycan metabolic process phenotype
GO:0006082PHENOTYPE	organic acid metabolic process phenotype
GO:0006089PHENOTYPE	lactate metabolic process phenotype
GO:0006091PHENOTYPE	generation of precursor metabolites and energy phenotype
GO:0006094PHENOTYPE	gluconeogenesis phenotype
GO:0006096PHENOTYPE	glycolytic process phenotype
GO:0006112PHENOTYPE	energy reserve metabolic process phenotype
GO:0006116PHENOTYPE	NADH oxidation phenotype
GO:0006119PHENOTYPE	oxidative phosphorylation phenotype
GO:0006120PHENOTYPE	mitochondrial electron transport, NADH to ubiquinone phenotype
GO:0006122PHENOTYPE	mitochondrial electron transport, ubiquinol to cytochrome c phenotype
GO:0006164PHENOTYPE	purine nucleotide biosynthetic process phenotype
GO:0006183PHENOTYPE	GTP biosynthetic process phenotype
GO:0006259PHENOTYPE	DNA metabolic process phenotype
GO:0006260PHENOTYPE	DNA replication phenotype
GO:0006270PHENOTYPE	DNA replication initiation phenotype
GO:0006281PHENOTYPE	DNA repair phenotype
GO:0006284PHENOTYPE	base-excision repair phenotype
GO:0006298PHENOTYPE	mismatch repair phenotype
GO:0006302PHENOTYPE	double-strand break repair phenotype
GO:0006303PHENOTYPE	double-strand break repair via nonhomologous end joining phenotype
GO:0006306PHENOTYPE	DNA methylation phenotype
GO:0006308PHENOTYPE	DNA catabolic process phenotype
GO:0006309PHENOTYPE	apoptotic DNA fragmentation phenotype
GO:0006310PHENOTYPE	DNA recombination phenotype
GO:0006325PHENOTYPE	chromatin organization phenotype
GO:0006349PHENOTYPE	regulation of gene expression by genetic imprinting 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:0006383PHENOTYPE	transcription from RNA polymerase III promoter phenotype
GO:0006396PHENOTYPE	RNA processing 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:0006461PHENOTYPE	protein complex assembly phenotype
GO:0006468PHENOTYPE	protein phosphorylation phenotype
GO:0006479PHENOTYPE	protein methylation phenotype
GO:0006486PHENOTYPE	protein glycosylation phenotype
GO:0006487PHENOTYPE	protein N-linked glycosylation phenotype
GO:0006493PHENOTYPE	protein O-linked glycosylation phenotype
GO:0006497PHENOTYPE	protein lipidation phenotype
GO:0006508PHENOTYPE	proteolysis phenotype
GO:0006511PHENOTYPE	ubiquitin-dependent protein catabolic process phenotype
GO:0006520PHENOTYPE	cellular amino acid metabolic process phenotype
GO:0006534PHENOTYPE	cysteine metabolic process phenotype
GO:0006541PHENOTYPE	glutamine metabolic process phenotype
GO:0006544PHENOTYPE	glycine metabolic process phenotype
GO:0006549PHENOTYPE	isoleucine metabolic process phenotype
GO:0006551PHENOTYPE	leucine metabolic process phenotype
GO:0006555PHENOTYPE	methionine metabolic process phenotype
GO:0006558PHENOTYPE	L-phenylalanine metabolic process phenotype
GO:0006563PHENOTYPE	L-serine metabolic process phenotype
GO:0006566PHENOTYPE	threonine metabolic process phenotype
GO:0006568PHENOTYPE	tryptophan metabolic process phenotype
GO:0006570PHENOTYPE	tyrosine metabolic process phenotype
GO:0006573PHENOTYPE	valine metabolic process phenotype
GO:0006576PHENOTYPE	cellular biogenic amine metabolic process phenotype
GO:0006582PHENOTYPE	melanin metabolic process phenotype
GO:0006584PHENOTYPE	catecholamine metabolic process phenotype
GO:0006585PHENOTYPE	dopamine biosynthetic process from tyrosine phenotype
GO:0006590PHENOTYPE	thyroid hormone generation phenotype
GO:0006629PHENOTYPE	lipid metabolic process phenotype
GO:0006631PHENOTYPE	fatty acid metabolic process phenotype
GO:0006635PHENOTYPE	fatty acid beta-oxidation phenotype
GO:0006638PHENOTYPE	neutral lipid metabolic process phenotype
GO:0006644PHENOTYPE	phospholipid metabolic process phenotype
GO:0006650PHENOTYPE	glycerophospholipid metabolic process phenotype
GO:0006665PHENOTYPE	sphingolipid metabolic process phenotype
GO:0006672PHENOTYPE	ceramide metabolic process phenotype
GO:0006687PHENOTYPE	glycosphingolipid metabolic process phenotype
GO:0006693PHENOTYPE	prostaglandin metabolic process phenotype
GO:0006694PHENOTYPE	steroid biosynthetic process phenotype
GO:0006695PHENOTYPE	cholesterol biosynthetic process phenotype
GO:0006704PHENOTYPE	glucocorticoid biosynthetic process phenotype
GO:0006725PHENOTYPE	cellular aromatic compound metabolic process phenotype
GO:0006749PHENOTYPE	glutathione metabolic process phenotype
GO:0006754PHENOTYPE	ATP biosynthetic process phenotype
GO:0006777PHENOTYPE	Mo-molybdopterin cofactor biosynthetic process phenotype
GO:0006778PHENOTYPE	porphyrin-containing compound metabolic process phenotype
GO:0006779PHENOTYPE	porphyrin-containing compound biosynthetic process phenotype
GO:0006783PHENOTYPE	heme biosynthetic process phenotype
GO:0006801PHENOTYPE	superoxide metabolic process phenotype
GO:0006807PHENOTYPE	nitrogen compound metabolic process phenotype
GO:0006809PHENOTYPE	nitric oxide biosynthetic process phenotype
GO:0006811PHENOTYPE	ion transport phenotype
GO:0006812PHENOTYPE	cation transport phenotype
GO:0006813PHENOTYPE	potassium ion 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:0006833PHENOTYPE	water transport phenotype
GO:0006836PHENOTYPE	neurotransmitter transport phenotype
GO:0006839PHENOTYPE	mitochondrial transport phenotype
GO:0006851PHENOTYPE	mitochondrial calcium ion transport phenotype
GO:0006865PHENOTYPE	amino acid transport phenotype
GO:0006869PHENOTYPE	lipid transport phenotype
GO:0006874PHENOTYPE	cellular calcium ion homeostasis phenotype
GO:0006878PHENOTYPE	cellular copper ion homeostasis phenotype
GO:0006879PHENOTYPE	cellular iron ion homeostasis phenotype
GO:0006882PHENOTYPE	cellular zinc ion homeostasis phenotype
GO:0006883PHENOTYPE	cellular sodium ion homeostasis phenotype
GO:0006885PHENOTYPE	regulation of pH phenotype
GO:0006886PHENOTYPE	intracellular protein transport phenotype
GO:0006887PHENOTYPE	exocytosis 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:0006910PHENOTYPE	phagocytosis, recognition 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:0006924PHENOTYPE	activation-induced cell death of T cells phenotype
GO:0006928PHENOTYPE	movement of cell or subcellular component phenotype
GO:0006931PHENOTYPE	substrate-dependent cell migration, cell attachment to substrate phenotype
GO:0006933PHENOTYPE	negative regulation of cell adhesion involved in substrate-bound cell migration phenotype
GO:0006935PHENOTYPE	chemotaxis phenotype
GO:0006936PHENOTYPE	muscle contraction phenotype
GO:0006937PHENOTYPE	regulation of muscle contraction phenotype
GO:0006939PHENOTYPE	smooth muscle contraction phenotype
GO:0006940PHENOTYPE	regulation of smooth muscle contraction phenotype
GO:0006941PHENOTYPE	striated muscle contraction phenotype
GO:0006942PHENOTYPE	regulation of striated muscle contraction phenotype
GO:0006949PHENOTYPE	syncytium formation phenotype
GO:0006950PHENOTYPE	response to stress phenotype
GO:0006952PHENOTYPE	defense response phenotype
GO:0006954PHENOTYPE	inflammatory response phenotype
GO:0006955PHENOTYPE	immune response phenotype
GO:0006956PHENOTYPE	complement activation phenotype
GO:0006957PHENOTYPE	complement activation, alternative pathway phenotype
GO:0006958PHENOTYPE	complement activation, classical pathway phenotype
GO:0006959PHENOTYPE	humoral immune response phenotype
GO:0006968PHENOTYPE	cellular defense response phenotype
GO:0006974PHENOTYPE	cellular response to DNA damage stimulus phenotype
GO:0006979PHENOTYPE	response to oxidative stress phenotype
GO:0006983PHENOTYPE	ER overload response phenotype
GO:0006996PHENOTYPE	organelle organization phenotype
GO:0006997PHENOTYPE	nucleus organization phenotype
GO:0006998PHENOTYPE	nuclear envelope organization phenotype
GO:0007004PHENOTYPE	telomere maintenance via telomerase phenotype
GO:0007005PHENOTYPE	mitochondrion organization phenotype
GO:0007006PHENOTYPE	mitochondrial membrane organization phenotype
GO:0007009PHENOTYPE	plasma membrane organization phenotype
GO:0007010PHENOTYPE	cytoskeleton organization phenotype
GO:0007015PHENOTYPE	actin filament organization phenotype
GO:0007016PHENOTYPE	cytoskeletal anchoring at plasma membrane phenotype
GO:0007017PHENOTYPE	microtubule-based process phenotype
GO:0007026PHENOTYPE	negative regulation of microtubule depolymerization phenotype
GO:0007028PHENOTYPE	cytoplasm organization phenotype
GO:0007030PHENOTYPE	Golgi organization phenotype
GO:0007033PHENOTYPE	vacuole organization phenotype
GO:0007035PHENOTYPE	vacuolar acidification phenotype
GO:0007040PHENOTYPE	lysosome organization phenotype
GO:0007042PHENOTYPE	lysosomal lumen acidification phenotype
GO:0007043PHENOTYPE	cell-cell junction assembly phenotype
GO:0007050PHENOTYPE	cell cycle arrest phenotype
GO:0007052PHENOTYPE	mitotic spindle organization phenotype
GO:0007059PHENOTYPE	chromosome segregation phenotype
GO:0007060PHENOTYPE	male meiosis chromosome segregation phenotype
GO:0007088PHENOTYPE	regulation of mitotic nuclear division phenotype
GO:0007091PHENOTYPE	metaphase/anaphase transition of mitotic cell cycle phenotype
GO:0007093PHENOTYPE	mitotic cell cycle checkpoint phenotype
GO:0007094PHENOTYPE	mitotic spindle assembly checkpoint phenotype
GO:0007095PHENOTYPE	mitotic G2 DNA damage checkpoint phenotype
GO:0007097PHENOTYPE	nuclear migration phenotype
GO:0007099PHENOTYPE	centriole replication phenotype
GO:0007100PHENOTYPE	mitotic centrosome separation phenotype
GO:0007127PHENOTYPE	meiosis I phenotype
GO:0007128PHENOTYPE	meiotic prophase I phenotype
GO:0007129PHENOTYPE	synapsis phenotype
GO:0007131PHENOTYPE	reciprocal meiotic recombination phenotype
GO:0007140PHENOTYPE	male meiosis phenotype
GO:0007141PHENOTYPE	male meiosis I phenotype
GO:0007143PHENOTYPE	female meiotic division phenotype
GO:0007154PHENOTYPE	cell communication phenotype
GO:0007155PHENOTYPE	cell adhesion phenotype
GO:0007158PHENOTYPE	neuron cell-cell adhesion phenotype
GO:0007162PHENOTYPE	negative regulation of cell adhesion phenotype
GO:0007163PHENOTYPE	establishment or maintenance of cell polarity phenotype
GO:0007165PHENOTYPE	signal transduction phenotype
GO:0007166PHENOTYPE	cell surface receptor signaling pathway phenotype
GO:0007169PHENOTYPE	transmembrane receptor protein tyrosine kinase signaling pathway phenotype
GO:0007179PHENOTYPE	transforming growth factor beta receptor signaling pathway phenotype
GO:0007182PHENOTYPE	common-partner SMAD protein phosphorylation phenotype
GO:0007186PHENOTYPE	G-protein coupled receptor signaling pathway phenotype
GO:0007204PHENOTYPE	positive regulation of cytosolic calcium ion concentration phenotype
GO:0007215PHENOTYPE	glutamate receptor signaling pathway phenotype
GO:0007219PHENOTYPE	Notch signaling pathway phenotype
GO:0007224PHENOTYPE	smoothened signaling pathway phenotype
GO:0007249PHENOTYPE	I-kappaB kinase/NF-kappaB signaling phenotype
GO:0007250PHENOTYPE	activation of NF-kappaB-inducing kinase activity phenotype
GO:0007259PHENOTYPE	JAK-STAT cascade phenotype
GO:0007267PHENOTYPE	cell-cell signaling phenotype
GO:0007268PHENOTYPE	synaptic transmission phenotype
GO:0007269PHENOTYPE	neurotransmitter secretion phenotype
GO:0007270PHENOTYPE	neuron-neuron synaptic transmission phenotype
GO:0007271PHENOTYPE	synaptic transmission, cholinergic phenotype
GO:0007274PHENOTYPE	neuromuscular synaptic transmission phenotype
GO:0007276PHENOTYPE	gamete generation phenotype
GO:0007281PHENOTYPE	germ cell development phenotype
GO:0007283PHENOTYPE	spermatogenesis phenotype
GO:0007284PHENOTYPE	spermatogonial cell division phenotype
GO:0007286PHENOTYPE	spermatid development phenotype
GO:0007289PHENOTYPE	spermatid nucleus differentiation phenotype
GO:0007292PHENOTYPE	female gamete generation phenotype
GO:0007296PHENOTYPE	vitellogenesis phenotype
GO:0007320PHENOTYPE	insemination phenotype
GO:0007338PHENOTYPE	single fertilization phenotype
GO:0007340PHENOTYPE	acrosome reaction phenotype
GO:0007346PHENOTYPE	regulation of mitotic cell cycle phenotype
GO:0007368PHENOTYPE	determination of left/right symmetry phenotype
GO:0007369PHENOTYPE	gastrulation phenotype
GO:0007379PHENOTYPE	segment specification phenotype
GO:0007389PHENOTYPE	pattern specification process 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: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:0007522PHENOTYPE	visceral muscle development phenotype
GO:0007528PHENOTYPE	neuromuscular junction development phenotype
GO:0007530PHENOTYPE	sex determination phenotype
GO:0007548PHENOTYPE	sex differentiation phenotype
GO:0007565PHENOTYPE	female pregnancy phenotype
GO:0007566PHENOTYPE	embryo implantation phenotype
GO:0007567PHENOTYPE	parturition phenotype
GO:0007568PHENOTYPE	aging phenotype
GO:0007569PHENOTYPE	cell aging phenotype
GO:0007585PHENOTYPE	respiratory gaseous exchange phenotype
GO:0007586PHENOTYPE	digestion phenotype
GO:0007588PHENOTYPE	excretion phenotype
GO:0007589PHENOTYPE	body fluid secretion phenotype
GO:0007595PHENOTYPE	lactation phenotype
GO:0007596PHENOTYPE	blood coagulation phenotype
GO:0007599PHENOTYPE	hemostasis phenotype
GO:0007600PHENOTYPE	sensory perception phenotype
GO:0007601PHENOTYPE	visual perception phenotype
GO:0007602PHENOTYPE	phototransduction phenotype
GO:0007603PHENOTYPE	phototransduction, visible light phenotype
GO:0007605PHENOTYPE	sensory perception of sound phenotype
GO:0007608PHENOTYPE	sensory perception of smell phenotype
GO:0007610PHENOTYPE	behavior phenotype
GO:0007611PHENOTYPE	learning or memory phenotype
GO:0007612PHENOTYPE	learning phenotype
GO:0007613PHENOTYPE	memory phenotype
GO:0007617PHENOTYPE	mating behavior phenotype
GO:0007622PHENOTYPE	rhythmic behavior phenotype
GO:0007623PHENOTYPE	circadian rhythm phenotype
GO:0007626PHENOTYPE	locomotory behavior phenotype
GO:0007631PHENOTYPE	feeding behavior phenotype
GO:0007632PHENOTYPE	visual 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:0008045PHENOTYPE	motor neuron axon guidance phenotype
GO:0008046PHENOTYPE	axon guidance receptor activity phenotype
GO:0008047PHENOTYPE	enzyme activator activity phenotype
GO:0008078PHENOTYPE	mesodermal cell migration phenotype
GO:0008088PHENOTYPE	axon cargo transport phenotype
GO:0008089PHENOTYPE	anterograde axon cargo transport phenotype
GO:0008090PHENOTYPE	retrograde axon cargo transport phenotype
GO:0008092PHENOTYPE	cytoskeletal protein binding phenotype
GO:0008104PHENOTYPE	protein localization phenotype
GO:0008105PHENOTYPE	asymmetric protein localization phenotype
GO:0008156PHENOTYPE	negative regulation of DNA replication phenotype
GO:0008203PHENOTYPE	cholesterol metabolic process phenotype
GO:0008211PHENOTYPE	glucocorticoid metabolic process phenotype
GO:0008217PHENOTYPE	regulation of blood pressure phenotype
GO:0008233PHENOTYPE	peptidase activity phenotype
GO:0008237PHENOTYPE	metallopeptidase activity phenotype
GO:0008276PHENOTYPE	protein methyltransferase activity phenotype
GO:0008277PHENOTYPE	regulation of G-protein coupled receptor protein signaling pathway phenotype
GO:0008283PHENOTYPE	cell proliferation phenotype
GO:0008285PHENOTYPE	negative regulation of cell proliferation phenotype
GO:0008298PHENOTYPE	intracellular mRNA localization phenotype
GO:0008306PHENOTYPE	associative learning phenotype
GO:0008331PHENOTYPE	high voltage-gated calcium channel activity phenotype
GO:0008340PHENOTYPE	determination of adult lifespan phenotype
GO:0008344PHENOTYPE	adult locomotory behavior phenotype
GO:0008347PHENOTYPE	glial cell migration phenotype
GO:0008354PHENOTYPE	germ cell migration phenotype
GO:0008361PHENOTYPE	regulation of cell size phenotype
GO:0008366PHENOTYPE	axon ensheathment phenotype
GO:0008375PHENOTYPE	acetylglucosaminyltransferase activity phenotype
GO:0008380PHENOTYPE	RNA splicing phenotype
GO:0008406PHENOTYPE	gonad development phenotype
GO:0008455PHENOTYPE	alpha-1,6-mannosylglycoprotein 2-beta-N-acetylglucosaminyltransferase activity phenotype
GO:0008474PHENOTYPE	palmitoyl-(protein) hydrolase 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:0008630PHENOTYPE	intrinsic apoptotic signaling pathway in response to DNA damage phenotype
GO:0008637PHENOTYPE	apoptotic mitochondrial changes phenotype
GO:0009048PHENOTYPE	dosage compensation by inactivation of X chromosome phenotype
GO:0009060PHENOTYPE	aerobic respiration phenotype
GO:0009062PHENOTYPE	fatty acid catabolic process phenotype
GO:0009081PHENOTYPE	branched-chain amino acid metabolic process phenotype
GO:0009100PHENOTYPE	glycoprotein metabolic process phenotype
GO:0009101PHENOTYPE	glycoprotein biosynthetic process phenotype
GO:0009117PHENOTYPE	nucleotide metabolic process phenotype
GO:0009259PHENOTYPE	ribonucleotide metabolic process phenotype
GO:0009266PHENOTYPE	response to temperature stimulus phenotype
GO:0009267PHENOTYPE	cellular response to starvation phenotype
GO:0009303PHENOTYPE	rRNA transcription phenotype
GO:0009306PHENOTYPE	protein secretion phenotype
GO:0009308PHENOTYPE	amine metabolic process phenotype
GO:0009313PHENOTYPE	oligosaccharide catabolic process phenotype
GO:0009314PHENOTYPE	response to radiation phenotype
GO:0009405PHENOTYPE	pathogenesis 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:0009437PHENOTYPE	carnitine metabolic process phenotype
GO:0009566PHENOTYPE	fertilization phenotype
GO:0009583PHENOTYPE	detection of light stimulus phenotype
GO:0009584PHENOTYPE	detection of visible light phenotype
GO:0009590PHENOTYPE	detection of gravity phenotype
GO:0009593PHENOTYPE	detection of chemical stimulus 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:0009620PHENOTYPE	response to fungus phenotype
GO:0009629PHENOTYPE	response to gravity phenotype
GO:0009636PHENOTYPE	response to toxic substance phenotype
GO:0009649PHENOTYPE	entrainment of circadian clock phenotype
GO:0009651PHENOTYPE	response to salt stress phenotype
GO:0009712PHENOTYPE	catechol-containing compound metabolic process phenotype
GO:0009743PHENOTYPE	response to carbohydrate phenotype
GO:0009749PHENOTYPE	response to glucose phenotype
GO:0009790PHENOTYPE	embryo development phenotype
GO:0009791PHENOTYPE	post-embryonic development 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:0009855PHENOTYPE	determination of bilateral symmetry phenotype
GO:0009880PHENOTYPE	embryonic pattern specification phenotype
GO:0009887PHENOTYPE	organ morphogenesis phenotype
GO:0009888PHENOTYPE	tissue development 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:0009967PHENOTYPE	positive regulation of signal transduction phenotype
GO:0009968PHENOTYPE	negative regulation of signal transduction phenotype
GO:0009994PHENOTYPE	oocyte differentiation phenotype
GO:0010001PHENOTYPE	glial cell differentiation phenotype
GO:0010002PHENOTYPE	cardioblast differentiation phenotype
GO:0010033PHENOTYPE	response to organic substance phenotype
GO:0010035PHENOTYPE	response to inorganic substance phenotype
GO:0010070PHENOTYPE	zygote asymmetric cell division phenotype
GO:0010092PHENOTYPE	specification of organ identity 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:0010224PHENOTYPE	response to UV-B phenotype
GO:0010243PHENOTYPE	response to organonitrogen compound phenotype
GO:0010259PHENOTYPE	multicellular organismal aging phenotype
GO:0010310PHENOTYPE	regulation of hydrogen peroxide metabolic process phenotype
GO:0010332PHENOTYPE	response to gamma radiation 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:0010453PHENOTYPE	regulation of cell fate commitment phenotype
GO:0010458PHENOTYPE	exit from mitosis phenotype
GO:0010459PHENOTYPE	negative regulation of heart rate phenotype
GO:0010463PHENOTYPE	mesenchymal cell proliferation 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:0010608PHENOTYPE	posttranscriptional regulation of gene expression phenotype
GO:0010628PHENOTYPE	positive regulation of gene expression phenotype
GO:0010629PHENOTYPE	negative regulation of gene expression phenotype
GO:0010631PHENOTYPE	epithelial cell migration phenotype
GO:0010646PHENOTYPE	regulation of cell communication phenotype
GO:0010668PHENOTYPE	ectodermal cell differentiation phenotype
GO:0010669PHENOTYPE	epithelial structure maintenance phenotype
GO:0010712PHENOTYPE	regulation of collagen metabolic process phenotype
GO:0010717PHENOTYPE	regulation of epithelial to mesenchymal transition phenotype
GO:0010719PHENOTYPE	negative regulation of epithelial to mesenchymal transition phenotype
GO:0010721PHENOTYPE	negative regulation of cell development phenotype
GO:0010761PHENOTYPE	fibroblast migration phenotype
GO:0010769PHENOTYPE	regulation of cell morphogenesis involved in differentiation phenotype
GO:0010817PHENOTYPE	regulation of hormone levels phenotype
GO:0010833PHENOTYPE	telomere maintenance via telomere lengthening phenotype
GO:0010837PHENOTYPE	regulation of keratinocyte proliferation phenotype
GO:0010839PHENOTYPE	negative regulation of keratinocyte proliferation phenotype
GO:0010842PHENOTYPE	retina layer formation phenotype
GO:0010906PHENOTYPE	regulation of glucose metabolic process phenotype
GO:0010934PHENOTYPE	macrophage cytokine production phenotype
GO:0010954PHENOTYPE	positive regulation of protein processing phenotype
GO:0010955PHENOTYPE	negative regulation of protein processing phenotype
GO:0010960PHENOTYPE	magnesium ion homeostasis phenotype
GO:0010975PHENOTYPE	regulation of neuron projection development phenotype
GO:0010996PHENOTYPE	response to auditory stimulus phenotype
GO:0012501PHENOTYPE	programmed cell death phenotype
GO:0014002PHENOTYPE	astrocyte development phenotype
GO:0014003PHENOTYPE	oligodendrocyte development phenotype
GO:0014005PHENOTYPE	microglia development phenotype
GO:0014012PHENOTYPE	peripheral nervous system axon regeneration phenotype
GO:0014013PHENOTYPE	regulation of gliogenesis phenotype
GO:0014028PHENOTYPE	notochord formation phenotype
GO:0014031PHENOTYPE	mesenchymal cell development phenotype
GO:0014032PHENOTYPE	neural crest cell development phenotype
GO:0014034PHENOTYPE	neural crest cell fate commitment phenotype
GO:0014037PHENOTYPE	Schwann cell differentiation phenotype
GO:0014044PHENOTYPE	Schwann cell development phenotype
GO:0014047PHENOTYPE	glutamate secretion phenotype
GO:0014061PHENOTYPE	regulation of norepinephrine secretion phenotype
GO:0014065PHENOTYPE	phosphatidylinositol 3-kinase signaling phenotype
GO:0014066PHENOTYPE	regulation of phosphatidylinositol 3-kinase signaling phenotype
GO:0014070PHENOTYPE	response to organic cyclic compound phenotype
GO:0014706PHENOTYPE	striated muscle tissue development phenotype
GO:0014707PHENOTYPE	branchiomeric skeletal muscle development phenotype
GO:0014812PHENOTYPE	muscle cell migration phenotype
GO:0014832PHENOTYPE	urinary bladder smooth muscle contraction phenotype
GO:0014835PHENOTYPE	myoblast differentiation involved in skeletal muscle regeneration phenotype
GO:0014902PHENOTYPE	myotube differentiation phenotype
GO:0014904PHENOTYPE	myotube cell development phenotype
GO:0014905PHENOTYPE	myoblast fusion involved in skeletal muscle regeneration phenotype
GO:0015012PHENOTYPE	heparan sulfate proteoglycan biosynthetic process phenotype
GO:0015031PHENOTYPE	protein transport phenotype
GO:0015078PHENOTYPE	hydrogen ion transmembrane transporter activity phenotype
GO:0015267PHENOTYPE	channel activity phenotype
GO:0015269PHENOTYPE	calcium-activated potassium channel activity phenotype
GO:0015379PHENOTYPE	potassium:chloride symporter activity phenotype
GO:0015671PHENOTYPE	oxygen transport phenotype
GO:0015672PHENOTYPE	monovalent inorganic cation transport phenotype
GO:0015696PHENOTYPE	ammonium transport phenotype
GO:0015721PHENOTYPE	bile acid and bile salt transport phenotype
GO:0015758PHENOTYPE	glucose transport phenotype
GO:0015833PHENOTYPE	peptide transport phenotype
GO:0015840PHENOTYPE	urea transport phenotype
GO:0015844PHENOTYPE	monoamine transport phenotype
GO:0015918PHENOTYPE	sterol transport phenotype
GO:0016020PHENOTYPE	membrane phenotype
GO:0016042PHENOTYPE	lipid catabolic process phenotype
GO:0016049PHENOTYPE	cell growth phenotype
GO:0016050PHENOTYPE	vesicle organization phenotype
GO:0016055PHENOTYPE	Wnt signaling pathway phenotype
GO:0016064PHENOTYPE	immunoglobulin mediated immune response phenotype
GO:0016071PHENOTYPE	mRNA metabolic process phenotype
GO:0016079PHENOTYPE	synaptic vesicle exocytosis phenotype
GO:0016125PHENOTYPE	sterol metabolic process phenotype
GO:0016126PHENOTYPE	sterol biosynthetic process phenotype
GO:0016188PHENOTYPE	synaptic vesicle maturation phenotype
GO:0016192PHENOTYPE	vesicle-mediated transport phenotype
GO:0016197PHENOTYPE	endosomal transport phenotype
GO:0016198PHENOTYPE	axon choice point recognition phenotype
GO:0016199PHENOTYPE	axon midline choice point recognition phenotype
GO:0016206PHENOTYPE	catechol O-methyltransferase activity phenotype
GO:0016236PHENOTYPE	macroautophagy phenotype
GO:0016246PHENOTYPE	RNA interference phenotype
GO:0016308PHENOTYPE	1-phosphatidylinositol-4-phosphate 5-kinase activity phenotype
GO:0016321PHENOTYPE	female meiosis chromosome segregation phenotype
GO:0016322PHENOTYPE	neuron remodeling phenotype
GO:0016323PHENOTYPE	basolateral plasma membrane phenotype
GO:0016331PHENOTYPE	morphogenesis of embryonic epithelium phenotype
GO:0016339PHENOTYPE	calcium-dependent cell-cell adhesion via plasma membrane cell adhesion molecules phenotype
GO:0016358PHENOTYPE	dendrite development phenotype
GO:0016409PHENOTYPE	palmitoyltransferase activity phenotype
GO:0016445PHENOTYPE	somatic diversification of immunoglobulins phenotype
GO:0016446PHENOTYPE	somatic hypermutation of immunoglobulin genes phenotype
GO:0016447PHENOTYPE	somatic recombination of immunoglobulin gene segments phenotype
GO:0016458PHENOTYPE	gene silencing phenotype
GO:0016462PHENOTYPE	pyrophosphatase activity phenotype
GO:0016477PHENOTYPE	cell migration phenotype
GO:0016485PHENOTYPE	protein processing phenotype
GO:0016486PHENOTYPE	peptide hormone processing phenotype
GO:0016491PHENOTYPE	oxidoreductase activity phenotype
GO:0016525PHENOTYPE	negative regulation of angiogenesis phenotype
GO:0016567PHENOTYPE	protein ubiquitination phenotype
GO:0016571PHENOTYPE	histone methylation phenotype
GO:0016573PHENOTYPE	histone acetylation phenotype
GO:0016757PHENOTYPE	transferase activity, transferring glycosyl groups phenotype
GO:0016791PHENOTYPE	phosphatase activity phenotype
GO:0016798PHENOTYPE	hydrolase activity, acting on glycosyl bonds phenotype
GO:0016887PHENOTYPE	ATPase activity phenotype
GO:0016925PHENOTYPE	protein sumoylation phenotype
GO:0017145PHENOTYPE	stem cell division phenotype
GO:0017148PHENOTYPE	negative regulation of translation phenotype
GO:0017156PHENOTYPE	calcium ion-dependent exocytosis phenotype
GO:0017157PHENOTYPE	regulation of exocytosis phenotype
GO:0017158PHENOTYPE	regulation of calcium ion-dependent exocytosis phenotype
GO:0018023PHENOTYPE	peptidyl-lysine trimethylation phenotype
GO:0018026PHENOTYPE	peptidyl-lysine monomethylation phenotype
GO:0018105PHENOTYPE	peptidyl-serine phosphorylation phenotype
GO:0018108PHENOTYPE	peptidyl-tyrosine phosphorylation phenotype
GO:0018158PHENOTYPE	protein oxidation phenotype
GO:0018205PHENOTYPE	peptidyl-lysine modification phenotype
GO:0018344PHENOTYPE	protein geranylgeranylation phenotype
GO:0019098PHENOTYPE	reproductive behavior phenotype
GO:0019216PHENOTYPE	regulation of lipid metabolic process phenotype
GO:0019217PHENOTYPE	regulation of fatty acid metabolic process phenotype
GO:0019221PHENOTYPE	cytokine-mediated signaling pathway phenotype
GO:0019222PHENOTYPE	regulation of metabolic process phenotype
GO:0019226PHENOTYPE	transmission of nerve impulse phenotype
GO:0019228PHENOTYPE	neuronal action potential phenotype
GO:0019230PHENOTYPE	proprioception phenotype
GO:0019236PHENOTYPE	response to pheromone phenotype
GO:0019538PHENOTYPE	protein metabolic process phenotype
GO:0019637PHENOTYPE	organophosphate metabolic process phenotype
GO:0019722PHENOTYPE	calcium-mediated signaling phenotype
GO:0019724PHENOTYPE	B cell mediated immunity phenotype
GO:0019725PHENOTYPE	cellular homeostasis phenotype
GO:0019827PHENOTYPE	stem cell population maintenance phenotype
GO:0019835PHENOTYPE	cytolysis phenotype
GO:0019852PHENOTYPE	L-ascorbic acid metabolic process phenotype
GO:0019882PHENOTYPE	antigen processing and presentation phenotype
GO:0019896PHENOTYPE	axon transport of mitochondrion phenotype
GO:0019915PHENOTYPE	lipid storage phenotype
GO:0019953PHENOTYPE	sexual reproduction phenotype
GO:0020027PHENOTYPE	hemoglobin metabolic process phenotype
GO:0021502PHENOTYPE	neural fold elevation formation phenotype
GO:0021503PHENOTYPE	neural fold bending phenotype
GO:0021506PHENOTYPE	anterior neuropore closure 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:0021533PHENOTYPE	cell differentiation in hindbrain phenotype
GO:0021535PHENOTYPE	cell migration in hindbrain phenotype
GO:0021537PHENOTYPE	telencephalon development phenotype
GO:0021543PHENOTYPE	pallium development phenotype
GO:0021544PHENOTYPE	subpallium development phenotype
GO:0021545PHENOTYPE	cranial nerve development phenotype
GO:0021549PHENOTYPE	cerebellum development phenotype
GO:0021553PHENOTYPE	olfactory nerve development phenotype
GO:0021554PHENOTYPE	optic nerve development phenotype
GO:0021555PHENOTYPE	midbrain-hindbrain boundary morphogenesis phenotype
GO:0021559PHENOTYPE	trigeminal 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:0021587PHENOTYPE	cerebellum morphogenesis phenotype
GO:0021589PHENOTYPE	cerebellum structural organization phenotype
GO:0021591PHENOTYPE	ventricular system development phenotype
GO:0021592PHENOTYPE	fourth ventricle development phenotype
GO:0021602PHENOTYPE	cranial nerve morphogenesis phenotype
GO:0021631PHENOTYPE	optic nerve morphogenesis phenotype
GO:0021636PHENOTYPE	trigeminal nerve morphogenesis phenotype
GO:0021675PHENOTYPE	nerve development phenotype
GO:0021680PHENOTYPE	cerebellar Purkinje cell layer development phenotype
GO:0021683PHENOTYPE	cerebellar granular layer morphogenesis phenotype
GO:0021692PHENOTYPE	cerebellar Purkinje cell layer morphogenesis phenotype
GO:0021695PHENOTYPE	cerebellar cortex development phenotype
GO:0021696PHENOTYPE	cerebellar cortex morphogenesis phenotype
GO:0021697PHENOTYPE	cerebellar cortex formation phenotype
GO:0021702PHENOTYPE	cerebellar Purkinje cell differentiation phenotype
GO:0021703PHENOTYPE	locus ceruleus development phenotype
GO:0021707PHENOTYPE	cerebellar granule cell differentiation phenotype
GO:0021761PHENOTYPE	limbic system development phenotype
GO:0021766PHENOTYPE	hippocampus development phenotype
GO:0021772PHENOTYPE	olfactory bulb development phenotype
GO:0021775PHENOTYPE	smoothened signaling pathway involved in ventral spinal cord interneuron specification phenotype
GO:0021776PHENOTYPE	smoothened signaling pathway involved in spinal cord motor neuron cell fate specification phenotype
GO:0021778PHENOTYPE	oligodendrocyte cell fate specification phenotype
GO:0021779PHENOTYPE	oligodendrocyte cell fate commitment phenotype
GO:0021781PHENOTYPE	glial cell fate commitment phenotype
GO:0021782PHENOTYPE	glial cell development phenotype
GO:0021785PHENOTYPE	branchiomotor neuron axon guidance phenotype
GO:0021793PHENOTYPE	chemorepulsion of branchiomotor axon 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:0021871PHENOTYPE	forebrain regionalization phenotype
GO:0021872PHENOTYPE	forebrain generation of neurons phenotype
GO:0021877PHENOTYPE	forebrain neuron fate commitment phenotype
GO:0021879PHENOTYPE	forebrain neuron differentiation phenotype
GO:0021882PHENOTYPE	regulation of transcription from RNA polymerase II promoter involved in forebrain neuron fate commitment phenotype
GO:0021884PHENOTYPE	forebrain neuron development phenotype
GO:0021885PHENOTYPE	forebrain cell migration phenotype
GO:0021903PHENOTYPE	rostrocaudal neural tube patterning phenotype
GO:0021904PHENOTYPE	dorsal/ventral neural tube patterning phenotype
GO:0021910PHENOTYPE	smoothened signaling pathway involved in ventral spinal cord patterning phenotype
GO:0021913PHENOTYPE	regulation of transcription from RNA polymerase II promoter involved in ventral spinal cord interneuron specification phenotype
GO:0021914PHENOTYPE	negative regulation of smoothened signaling pathway involved in ventral spinal cord patterning phenotype
GO:0021915PHENOTYPE	neural tube development phenotype
GO:0021930PHENOTYPE	cerebellar granule cell precursor proliferation phenotype
GO:0021933PHENOTYPE	radial glia guided migration of cerebellar granule cell 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:0021979PHENOTYPE	hypothalamus cell differentiation phenotype
GO:0021983PHENOTYPE	pituitary gland development phenotype
GO:0021984PHENOTYPE	adenohypophysis development phenotype
GO:0021985PHENOTYPE	neurohypophysis development phenotype
GO:0021986PHENOTYPE	habenula development phenotype
GO:0021988PHENOTYPE	olfactory lobe development phenotype
GO:0021990PHENOTYPE	neural plate formation phenotype
GO:0022007PHENOTYPE	convergent extension involved in neural plate elongation phenotype
GO:0022008PHENOTYPE	neurogenesis phenotype
GO:0022010PHENOTYPE	central nervous system myelination phenotype
GO:0022011PHENOTYPE	myelination in peripheral nervous system phenotype
GO:0022013PHENOTYPE	pallium cell proliferation in forebrain phenotype
GO:0022027PHENOTYPE	interkinetic nuclear migration phenotype
GO:0022029PHENOTYPE	telencephalon cell migration phenotype
GO:0022037PHENOTYPE	metencephalon development phenotype
GO:0022405PHENOTYPE	hair cycle process phenotype
GO:0022407PHENOTYPE	regulation of cell-cell adhesion phenotype
GO:0022408PHENOTYPE	negative regulation of cell-cell adhesion phenotype
GO:0022414PHENOTYPE	reproductive process phenotype
GO:0022602PHENOTYPE	ovulation cycle process phenotype
GO:0022604PHENOTYPE	regulation of cell morphogenesis phenotype
GO:0022605PHENOTYPE	oogenesis stage phenotype
GO:0022612PHENOTYPE	gland morphogenesis phenotype
GO:0022617PHENOTYPE	extracellular matrix disassembly phenotype
GO:0022839PHENOTYPE	ion gated channel activity phenotype
GO:0022904PHENOTYPE	respiratory electron transport chain phenotype
GO:0030010PHENOTYPE	establishment of cell polarity phenotype
GO:0030030PHENOTYPE	cell projection organization phenotype
GO:0030036PHENOTYPE	actin cytoskeleton organization phenotype
GO:0030041PHENOTYPE	actin filament polymerization phenotype
GO:0030048PHENOTYPE	actin filament-based movement phenotype
GO:0030057PHENOTYPE	desmosome phenotype
GO:0030070PHENOTYPE	insulin processing phenotype
GO:0030072PHENOTYPE	peptide hormone secretion phenotype
GO:0030073PHENOTYPE	insulin secretion phenotype
GO:0030097PHENOTYPE	hemopoiesis phenotype
GO:0030098PHENOTYPE	lymphocyte differentiation phenotype
GO:0030099PHENOTYPE	myeloid cell differentiation phenotype
GO:0030101PHENOTYPE	natural killer cell activation phenotype
GO:0030103PHENOTYPE	vasopressin secretion phenotype
GO:0030104PHENOTYPE	water homeostasis phenotype
GO:0030111PHENOTYPE	regulation of Wnt signaling pathway phenotype
GO:0030141PHENOTYPE	secretory granule phenotype
GO:0030148PHENOTYPE	sphingolipid biosynthetic process phenotype
GO:0030154PHENOTYPE	cell differentiation phenotype
GO:0030155PHENOTYPE	regulation of cell adhesion phenotype
GO:0030163PHENOTYPE	protein catabolic process 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:0030193PHENOTYPE	regulation of blood coagulation phenotype
GO:0030198PHENOTYPE	extracellular matrix organization phenotype
GO:0030199PHENOTYPE	collagen fibril organization phenotype
GO:0030203PHENOTYPE	glycosaminoglycan metabolic process phenotype
GO:0030204PHENOTYPE	chondroitin sulfate metabolic process 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:0030219PHENOTYPE	megakaryocyte differentiation phenotype
GO:0030220PHENOTYPE	platelet formation phenotype
GO:0030223PHENOTYPE	neutrophil differentiation phenotype
GO:0030224PHENOTYPE	monocyte differentiation phenotype
GO:0030225PHENOTYPE	macrophage differentiation phenotype
GO:0030238PHENOTYPE	male sex determination phenotype
GO:0030239PHENOTYPE	myofibril assembly phenotype
GO:0030240PHENOTYPE	skeletal muscle thin filament assembly phenotype
GO:0030252PHENOTYPE	growth hormone secretion phenotype
GO:0030258PHENOTYPE	lipid modification phenotype
GO:0030262PHENOTYPE	apoptotic nuclear changes phenotype
GO:0030277PHENOTYPE	maintenance of gastrointestinal epithelium phenotype
GO:0030278PHENOTYPE	regulation of ossification phenotype
GO:0030279PHENOTYPE	negative regulation of ossification phenotype
GO:0030282PHENOTYPE	bone mineralization phenotype
GO:0030299PHENOTYPE	intestinal cholesterol absorption phenotype
GO:0030301PHENOTYPE	cholesterol transport phenotype
GO:0030308PHENOTYPE	negative regulation of cell growth phenotype
GO:0030316PHENOTYPE	osteoclast differentiation phenotype
GO:0030317PHENOTYPE	sperm motility phenotype
GO:0030318PHENOTYPE	melanocyte differentiation phenotype
GO:0030323PHENOTYPE	respiratory tube development phenotype
GO:0030324PHENOTYPE	lung development phenotype
GO:0030325PHENOTYPE	adrenal gland development phenotype
GO:0030330PHENOTYPE	DNA damage response, signal transduction by p53 class mediator 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:0030540PHENOTYPE	female genitalia development phenotype
GO:0030575PHENOTYPE	nuclear body organization phenotype
GO:0030593PHENOTYPE	neutrophil chemotaxis phenotype
GO:0030595PHENOTYPE	leukocyte chemotaxis phenotype
GO:0030641PHENOTYPE	regulation of cellular pH phenotype
GO:0030718PHENOTYPE	germ-line stem cell population maintenance phenotype
GO:0030728PHENOTYPE	ovulation phenotype
GO:0030823PHENOTYPE	regulation of cGMP metabolic process phenotype
GO:0030850PHENOTYPE	prostate gland development phenotype
GO:0030851PHENOTYPE	granulocyte differentiation phenotype
GO:0030855PHENOTYPE	epithelial cell differentiation phenotype
GO:0030856PHENOTYPE	regulation of epithelial cell differentiation phenotype
GO:0030857PHENOTYPE	negative regulation of 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:0030879PHENOTYPE	mammary gland development phenotype
GO:0030889PHENOTYPE	negative regulation of B cell proliferation 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: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:0031034PHENOTYPE	myosin filament assembly phenotype
GO:0031069PHENOTYPE	hair follicle morphogenesis phenotype
GO:0031076PHENOTYPE	embryonic camera-type eye development phenotype
GO:0031100PHENOTYPE	organ regeneration phenotype
GO:0031102PHENOTYPE	neuron projection regeneration phenotype
GO:0031103PHENOTYPE	axon regeneration phenotype
GO:0031110PHENOTYPE	regulation of microtubule polymerization or depolymerization phenotype
GO:0031122PHENOTYPE	cytoplasmic microtubule organization phenotype
GO:0031128PHENOTYPE	developmental induction phenotype
GO:0031129PHENOTYPE	inductive cell-cell signaling phenotype
GO:0031146PHENOTYPE	SCF-dependent proteasomal ubiquitin-dependent protein catabolic process phenotype
GO:0031175PHENOTYPE	neuron projection development phenotype
GO:0031223PHENOTYPE	auditory behavior phenotype
GO:0031290PHENOTYPE	retinal ganglion cell axon guidance phenotype
GO:0031323PHENOTYPE	regulation of cellular metabolic process phenotype
GO:0031396PHENOTYPE	regulation of protein ubiquitination phenotype
GO:0031397PHENOTYPE	negative regulation of protein ubiquitination phenotype
GO:0031424PHENOTYPE	keratinization phenotype
GO:0031443PHENOTYPE	fast-twitch skeletal muscle fiber contraction phenotype
GO:0031514PHENOTYPE	motile cilium phenotype
GO:0031532PHENOTYPE	actin cytoskeleton reorganization phenotype
GO:0031571PHENOTYPE	mitotic G1 DNA damage checkpoint phenotype
GO:0031573PHENOTYPE	intra-S DNA damage checkpoint phenotype
GO:0031579PHENOTYPE	membrane raft organization phenotype
GO:0031589PHENOTYPE	cell-substrate adhesion phenotype
GO:0031638PHENOTYPE	zymogen activation phenotype
GO:0031645PHENOTYPE	negative regulation of neurological system process phenotype
GO:0031647PHENOTYPE	regulation of protein stability phenotype
GO:0031668PHENOTYPE	cellular response to extracellular stimulus phenotype
GO:0031946PHENOTYPE	regulation of glucocorticoid biosynthetic process phenotype
GO:0031947PHENOTYPE	negative regulation of glucocorticoid biosynthetic process phenotype
GO:0031987PHENOTYPE	locomotion involved in locomotory behavior phenotype
GO:0032006PHENOTYPE	regulation of TOR signaling phenotype
GO:0032007PHENOTYPE	negative regulation of TOR signaling phenotype
GO:0032053PHENOTYPE	ciliary basal body organization phenotype
GO:0032060PHENOTYPE	bleb assembly phenotype
GO:0032094PHENOTYPE	response to food phenotype
GO:0032098PHENOTYPE	regulation of appetite phenotype
GO:0032147PHENOTYPE	activation of protein kinase activity phenotype
GO:0032259PHENOTYPE	methylation phenotype
GO:0032286PHENOTYPE	central nervous system myelin maintenance phenotype
GO:0032287PHENOTYPE	peripheral nervous system myelin maintenance phenotype
GO:0032288PHENOTYPE	myelin assembly phenotype
GO:0032289PHENOTYPE	central nervous system myelin formation phenotype
GO:0032324PHENOTYPE	molybdopterin cofactor biosynthetic process phenotype
GO:0032330PHENOTYPE	regulation of chondrocyte differentiation phenotype
GO:0032331PHENOTYPE	negative regulation of chondrocyte differentiation phenotype
GO:0032350PHENOTYPE	regulation of hormone metabolic process phenotype
GO:0032353PHENOTYPE	negative regulation of hormone biosynthetic process phenotype
GO:0032387PHENOTYPE	negative regulation of intracellular transport phenotype
GO:0032400PHENOTYPE	melanosome localization phenotype
GO:0032402PHENOTYPE	melanosome transport phenotype
GO:0032434PHENOTYPE	regulation of proteasomal ubiquitin-dependent protein catabolic process phenotype
GO:0032435PHENOTYPE	negative 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:0032525PHENOTYPE	somite rostral/caudal axis specification phenotype
GO:0032526PHENOTYPE	response to retinoic acid phenotype
GO:0032607PHENOTYPE	interferon-alpha production phenotype
GO:0032609PHENOTYPE	interferon-gamma production phenotype
GO:0032610PHENOTYPE	interleukin-1 alpha production phenotype
GO:0032611PHENOTYPE	interleukin-1 beta production phenotype
GO:0032613PHENOTYPE	interleukin-10 production phenotype
GO:0032615PHENOTYPE	interleukin-12 production phenotype
GO:0032618PHENOTYPE	interleukin-15 production phenotype
GO:0032620PHENOTYPE	interleukin-17 production phenotype
GO:0032621PHENOTYPE	interleukin-18 production phenotype
GO:0032623PHENOTYPE	interleukin-2 production phenotype
GO:0032632PHENOTYPE	interleukin-3 production phenotype
GO:0032633PHENOTYPE	interleukin-4 production phenotype
GO:0032635PHENOTYPE	interleukin-6 production phenotype
GO:0032776PHENOTYPE	DNA methylation on cytosine phenotype
GO:0032782PHENOTYPE	bile acid secretion phenotype
GO:0032796PHENOTYPE	uropod organization phenotype
GO:0032808PHENOTYPE	lacrimal gland development phenotype
GO:0032835PHENOTYPE	glomerulus development phenotype
GO:0032844PHENOTYPE	regulation of homeostatic process phenotype
GO:0032868PHENOTYPE	response to insulin phenotype
GO:0032869PHENOTYPE	cellular response to insulin stimulus phenotype
GO:0032870PHENOTYPE	cellular response to hormone stimulus phenotype
GO:0032880PHENOTYPE	regulation of protein localization phenotype
GO:0032922PHENOTYPE	circadian regulation of gene expression phenotype
GO:0032925PHENOTYPE	regulation of activin receptor signaling pathway phenotype
GO:0032940PHENOTYPE	secretion by cell phenotype
GO:0032943PHENOTYPE	mononuclear cell proliferation phenotype
GO:0032956PHENOTYPE	regulation of actin cytoskeleton organization phenotype
GO:0032963PHENOTYPE	collagen metabolic process phenotype
GO:0032964PHENOTYPE	collagen biosynthetic process phenotype
GO:0032990PHENOTYPE	cell part morphogenesis phenotype
GO:0033028PHENOTYPE	myeloid cell apoptotic process phenotype
GO:0033044PHENOTYPE	regulation of chromosome organization phenotype
GO:0033077PHENOTYPE	T cell differentiation in thymus phenotype
GO:0033151PHENOTYPE	V(D)J recombination phenotype
GO:0033152PHENOTYPE	immunoglobulin V(D)J recombination phenotype
GO:0033153PHENOTYPE	T cell receptor V(D)J recombination phenotype
GO:0033157PHENOTYPE	regulation of intracellular protein transport phenotype
GO:0033209PHENOTYPE	tumor necrosis factor-mediated signaling pathway phenotype
GO:0033292PHENOTYPE	T-tubule organization phenotype
GO:0033316PHENOTYPE	meiotic spindle assembly checkpoint phenotype
GO:0033327PHENOTYPE	Leydig cell differentiation phenotype
GO:0033344PHENOTYPE	cholesterol efflux phenotype
GO:0033363PHENOTYPE	secretory granule organization phenotype
GO:0033364PHENOTYPE	mast cell secretory granule organization phenotype
GO:0033365PHENOTYPE	protein localization to organelle phenotype
GO:0033484PHENOTYPE	nitric oxide homeostasis phenotype
GO:0033504PHENOTYPE	floor plate development phenotype
GO:0033505PHENOTYPE	floor plate morphogenesis phenotype
GO:0033555PHENOTYPE	multicellular organismal response to stress phenotype
GO:0033561PHENOTYPE	regulation of water loss via skin phenotype
GO:0033563PHENOTYPE	dorsal/ventral axon guidance phenotype
GO:0033598PHENOTYPE	mammary gland epithelial cell proliferation phenotype
GO:0034097PHENOTYPE	response to cytokine phenotype
GO:0034101PHENOTYPE	erythrocyte homeostasis phenotype
GO:0034103PHENOTYPE	regulation of tissue remodeling phenotype
GO:0034220PHENOTYPE	ion transmembrane transport phenotype
GO:0034332PHENOTYPE	adherens junction organization phenotype
GO:0034334PHENOTYPE	adherens junction maintenance phenotype
GO:0034349PHENOTYPE	glial cell apoptotic process phenotype
GO:0034435PHENOTYPE	cholesterol esterification phenotype
GO:0034504PHENOTYPE	protein localization to nucleus phenotype
GO:0034595PHENOTYPE	phosphatidylinositol phosphate 5-phosphatase activity phenotype
GO:0034599PHENOTYPE	cellular response to oxidative stress phenotype
GO:0034612PHENOTYPE	response to tumor necrosis factor phenotype
GO:0034613PHENOTYPE	cellular protein localization phenotype
GO:0034629PHENOTYPE	cellular protein complex localization phenotype
GO:0034644PHENOTYPE	cellular response to UV phenotype
GO:0034765PHENOTYPE	regulation of ion transmembrane transport phenotype
GO:0034976PHENOTYPE	response to endoplasmic reticulum stress phenotype
GO:0035050PHENOTYPE	embryonic heart tube development phenotype
GO:0035082PHENOTYPE	axoneme assembly phenotype
GO:0035088PHENOTYPE	establishment or maintenance of apical/basal cell polarity phenotype
GO:0035089PHENOTYPE	establishment of apical/basal cell polarity phenotype
GO:0035090PHENOTYPE	maintenance of apical/basal cell polarity phenotype
GO:0035094PHENOTYPE	response to nicotine phenotype
GO:0035095PHENOTYPE	behavioral response to nicotine phenotype
GO:0035108PHENOTYPE	limb morphogenesis phenotype
GO:0035148PHENOTYPE	tube formation phenotype
GO:0035150PHENOTYPE	regulation of tube size phenotype
GO:0035162PHENOTYPE	embryonic hemopoiesis phenotype
GO:0035176PHENOTYPE	social behavior phenotype
GO:0035195PHENOTYPE	gene silencing by miRNA phenotype
GO:0035196PHENOTYPE	production of miRNAs involved in gene silencing by miRNA phenotype
GO:0035235PHENOTYPE	ionotropic glutamate receptor signaling pathway phenotype
GO:0035239PHENOTYPE	tube morphogenesis phenotype
GO:0035249PHENOTYPE	synaptic transmission, glutamatergic phenotype
GO:0035253PHENOTYPE	ciliary rootlet 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:0035441PHENOTYPE	cell migration involved in vasculogenesis phenotype
GO:0035483PHENOTYPE	gastric emptying phenotype
GO:0035556PHENOTYPE	intracellular signal transduction phenotype
GO:0035567PHENOTYPE	non-canonical Wnt signaling pathway phenotype
GO:0035622PHENOTYPE	intrahepatic bile duct development phenotype
GO:0035630PHENOTYPE	bone mineralization involved in bone maturation phenotype
GO:0035640PHENOTYPE	exploration behavior phenotype
GO:0035641PHENOTYPE	locomotory exploration behavior phenotype
GO:0035701PHENOTYPE	hematopoietic stem cell migration phenotype
GO:0035809PHENOTYPE	regulation of urine volume phenotype
GO:0035845PHENOTYPE	photoreceptor cell outer segment organization phenotype
GO:0035878PHENOTYPE	nail development phenotype
GO:0035883PHENOTYPE	enteroendocrine cell differentiation phenotype
GO:0035898PHENOTYPE	parathyroid hormone secretion phenotype
GO:0035904PHENOTYPE	aorta development phenotype
GO:0035909PHENOTYPE	aorta morphogenesis phenotype
GO:0035934PHENOTYPE	corticosterone secretion phenotype
GO:0035987PHENOTYPE	endodermal cell differentiation phenotype
GO:0035988PHENOTYPE	chondrocyte proliferation phenotype
GO:0035994PHENOTYPE	response to muscle stretch phenotype
GO:0036064PHENOTYPE	ciliary basal body phenotype
GO:0036065PHENOTYPE	fucosylation phenotype
GO:0036093PHENOTYPE	germ cell proliferation phenotype
GO:0036158PHENOTYPE	outer dynein arm assembly phenotype
GO:0036159PHENOTYPE	inner dynein arm assembly phenotype
GO:0036269PHENOTYPE	swimming behavior phenotype
GO:0036302PHENOTYPE	atrioventricular canal development phenotype
GO:0036303PHENOTYPE	lymph vessel morphogenesis phenotype
GO:0036336PHENOTYPE	dendritic cell migration phenotype
GO:0036342PHENOTYPE	post-anal tail morphogenesis phenotype
GO:0036344PHENOTYPE	platelet morphogenesis phenotype
GO:0036465PHENOTYPE	synaptic vesicle recycling phenotype
GO:0038066PHENOTYPE	p38MAPK cascade phenotype
GO:0040007PHENOTYPE	growth phenotype
GO:0040008PHENOTYPE	regulation of growth phenotype
GO:0040009PHENOTYPE	regulation of growth rate phenotype
GO:0040011PHENOTYPE	locomotion phenotype
GO:0040012PHENOTYPE	regulation of locomotion phenotype
GO:0040013PHENOTYPE	negative regulation of locomotion phenotype
GO:0040016PHENOTYPE	embryonic cleavage phenotype
GO:0040020PHENOTYPE	regulation of meiotic nuclear division phenotype
GO:0040029PHENOTYPE	regulation of gene expression, epigenetic phenotype
GO:0040036PHENOTYPE	regulation of fibroblast growth factor receptor signaling pathway phenotype
GO:0040040PHENOTYPE	thermosensory behavior phenotype
GO:0042048PHENOTYPE	olfactory behavior phenotype
GO:0042060PHENOTYPE	wound healing phenotype
GO:0042063PHENOTYPE	gliogenesis phenotype
GO:0042073PHENOTYPE	intraciliary transport phenotype
GO:0042074PHENOTYPE	cell migration involved in gastrulation phenotype
GO:0042088PHENOTYPE	T-helper 1 type immune response phenotype
GO:0042092PHENOTYPE	type 2 immune response phenotype
GO:0042093PHENOTYPE	T-helper cell differentiation phenotype
GO:0042098PHENOTYPE	T cell proliferation phenotype
GO:0042100PHENOTYPE	B cell proliferation phenotype
GO:0042110PHENOTYPE	T cell activation phenotype
GO:0042113PHENOTYPE	B cell activation phenotype
GO:0042116PHENOTYPE	macrophage activation phenotype
GO:0042127PHENOTYPE	regulation of cell proliferation phenotype
GO:0042133PHENOTYPE	neurotransmitter metabolic process phenotype
GO:0042136PHENOTYPE	neurotransmitter biosynthetic process phenotype
GO:0042157PHENOTYPE	lipoprotein metabolic process phenotype
GO:0042158PHENOTYPE	lipoprotein biosynthetic process phenotype
GO:0042159PHENOTYPE	lipoprotein catabolic process phenotype
GO:0042168PHENOTYPE	heme metabolic process phenotype
GO:0042176PHENOTYPE	regulation of protein catabolic process phenotype
GO:0042177PHENOTYPE	negative regulation of protein catabolic process phenotype
GO:0042182PHENOTYPE	ketone catabolic process phenotype
GO:0042246PHENOTYPE	tissue regeneration phenotype
GO:0042249PHENOTYPE	establishment of planar polarity of embryonic epithelium phenotype
GO:0042254PHENOTYPE	ribosome biogenesis phenotype
GO:0042267PHENOTYPE	natural killer cell mediated cytotoxicity phenotype
GO:0042273PHENOTYPE	ribosomal large subunit biogenesis phenotype
GO:0042278PHENOTYPE	purine nucleoside metabolic process phenotype
GO:0042310PHENOTYPE	vasoconstriction phenotype
GO:0042311PHENOTYPE	vasodilation phenotype
GO:0042327PHENOTYPE	positive regulation of phosphorylation phenotype
GO:0042335PHENOTYPE	cuticle development phenotype
GO:0042359PHENOTYPE	vitamin D metabolic process phenotype
GO:0042360PHENOTYPE	vitamin E metabolic process phenotype
GO:0042391PHENOTYPE	regulation of membrane potential phenotype
GO:0042403PHENOTYPE	thyroid hormone metabolic process phenotype
GO:0042414PHENOTYPE	epinephrine metabolic process phenotype
GO:0042416PHENOTYPE	dopamine biosynthetic process phenotype
GO:0042417PHENOTYPE	dopamine metabolic process phenotype
GO:0042420PHENOTYPE	dopamine catabolic process phenotype
GO:0042428PHENOTYPE	serotonin metabolic process phenotype
GO:0042438PHENOTYPE	melanin biosynthetic process phenotype
GO:0042445PHENOTYPE	hormone metabolic process phenotype
GO:0042446PHENOTYPE	hormone biosynthetic process phenotype
GO:0042462PHENOTYPE	eye photoreceptor cell development phenotype
GO:0042471PHENOTYPE	ear morphogenesis phenotype
GO:0042472PHENOTYPE	inner ear morphogenesis phenotype
GO:0042473PHENOTYPE	outer ear morphogenesis phenotype
GO:0042475PHENOTYPE	odontogenesis of dentin-containing tooth phenotype
GO:0042476PHENOTYPE	odontogenesis phenotype
GO:0042490PHENOTYPE	mechanoreceptor differentiation phenotype
GO:0042491PHENOTYPE	auditory receptor cell differentiation phenotype
GO:0042493PHENOTYPE	response to drug phenotype
GO:0042509PHENOTYPE	regulation of tyrosine phosphorylation of STAT protein phenotype
GO:0042541PHENOTYPE	hemoglobin biosynthetic process phenotype
GO:0042551PHENOTYPE	neuron maturation 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:0042594PHENOTYPE	response to starvation phenotype
GO:0042596PHENOTYPE	fear response phenotype
GO:0042632PHENOTYPE	cholesterol homeostasis phenotype
GO:0042633PHENOTYPE	hair cycle phenotype
GO:0042637PHENOTYPE	catagen phenotype
GO:0042640PHENOTYPE	anagen phenotype
GO:0042659PHENOTYPE	regulation of cell fate specification phenotype
GO:0042663PHENOTYPE	regulation of endodermal cell fate specification phenotype
GO:0042667PHENOTYPE	auditory receptor cell fate specification phenotype
GO:0042692PHENOTYPE	muscle cell differentiation phenotype
GO:0042693PHENOTYPE	muscle cell fate commitment phenotype
GO:0042698PHENOTYPE	ovulation cycle phenotype
GO:0042701PHENOTYPE	progesterone secretion phenotype
GO:0042713PHENOTYPE	sperm ejaculation phenotype
GO:0042730PHENOTYPE	fibrinolysis phenotype
GO:0042742PHENOTYPE	defense response to bacterium phenotype
GO:0042743PHENOTYPE	hydrogen peroxide metabolic process phenotype
GO:0042745PHENOTYPE	circadian sleep/wake cycle phenotype
GO:0042755PHENOTYPE	eating behavior phenotype
GO:0042756PHENOTYPE	drinking behavior phenotype
GO:0042771PHENOTYPE	intrinsic apoptotic signaling pathway in response to DNA damage by p53 class mediator phenotype
GO:0042775PHENOTYPE	mitochondrial ATP synthesis coupled electron transport phenotype
GO:0042787PHENOTYPE	protein ubiquitination involved in ubiquitin-dependent protein catabolic process phenotype
GO:0042981PHENOTYPE	regulation of apoptotic process phenotype
GO:0043009PHENOTYPE	chordate embryonic development phenotype
GO:0043010PHENOTYPE	camera-type eye development phenotype
GO:0043029PHENOTYPE	T cell homeostasis phenotype
GO:0043045PHENOTYPE	DNA methylation involved in embryo development phenotype
GO:0043046PHENOTYPE	DNA methylation involved in gamete generation 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:0043068PHENOTYPE	positive regulation of programmed cell death phenotype
GO:0043069PHENOTYPE	negative regulation of programmed cell death phenotype
GO:0043084PHENOTYPE	penile erection phenotype
GO:0043085PHENOTYPE	positive regulation of catalytic activity phenotype
GO:0043086PHENOTYPE	negative regulation of catalytic activity phenotype
GO:0043087PHENOTYPE	regulation of GTPase activity phenotype
GO:0043112PHENOTYPE	receptor metabolic process phenotype
GO:0043113PHENOTYPE	receptor clustering phenotype
GO:0043143PHENOTYPE	regulation of translation by machinery localization phenotype
GO:0043153PHENOTYPE	entrainment of circadian clock by photoperiod phenotype
GO:0043161PHENOTYPE	proteasome-mediated ubiquitin-dependent protein catabolic process phenotype
GO:0043200PHENOTYPE	response to amino acid phenotype
GO:0043249PHENOTYPE	erythrocyte maturation phenotype
GO:0043277PHENOTYPE	apoptotic cell clearance phenotype
GO:0043279PHENOTYPE	response to alkaloid 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:0043297PHENOTYPE	apical junction assembly phenotype
GO:0043303PHENOTYPE	mast cell degranulation phenotype
GO:0043320PHENOTYPE	natural killer cell degranulation phenotype
GO:0043331PHENOTYPE	response to dsRNA phenotype
GO:0043367PHENOTYPE	CD4-positive, alpha-beta T cell differentiation phenotype
GO:0043368PHENOTYPE	positive T cell selection phenotype
GO:0043374PHENOTYPE	CD8-positive, alpha-beta T cell differentiation phenotype
GO:0043393PHENOTYPE	regulation of protein binding phenotype
GO:0043403PHENOTYPE	skeletal muscle tissue regeneration phenotype
GO:0043408PHENOTYPE	regulation of MAPK cascade phenotype
GO:0043410PHENOTYPE	positive regulation of MAPK cascade phenotype
GO:0043434PHENOTYPE	response to peptide hormone phenotype
GO:0043462PHENOTYPE	regulation of ATPase activity phenotype
GO:0043473PHENOTYPE	pigmentation phenotype
GO:0043487PHENOTYPE	regulation of RNA stability phenotype
GO:0043491PHENOTYPE	protein kinase B signaling phenotype
GO:0043523PHENOTYPE	regulation of neuron apoptotic process phenotype
GO:0043534PHENOTYPE	blood vessel endothelial cell migration phenotype
GO:0043542PHENOTYPE	endothelial cell migration phenotype
GO:0043547PHENOTYPE	positive regulation of GTPase activity phenotype
GO:0043549PHENOTYPE	regulation of kinase activity phenotype
GO:0043576PHENOTYPE	regulation of respiratory gaseous exchange phenotype
GO:0043583PHENOTYPE	ear development phenotype
GO:0043584PHENOTYPE	nose development phenotype
GO:0043586PHENOTYPE	tongue development phenotype
GO:0043587PHENOTYPE	tongue morphogenesis phenotype
GO:0043588PHENOTYPE	skin development phenotype
GO:0043589PHENOTYPE	skin morphogenesis phenotype
GO:0043616PHENOTYPE	keratinocyte proliferation phenotype
GO:0043623PHENOTYPE	cellular protein complex assembly phenotype
GO:0043652PHENOTYPE	engulfment of apoptotic cell phenotype
GO:0043931PHENOTYPE	ossification involved in bone maturation phenotype
GO:0043932PHENOTYPE	ossification involved in bone remodeling phenotype
GO:0043954PHENOTYPE	cellular component maintenance phenotype
GO:0043966PHENOTYPE	histone H3 acetylation phenotype
GO:0043967PHENOTYPE	histone H4 acetylation phenotype
GO:0044030PHENOTYPE	regulation of DNA methylation phenotype
GO:0044062PHENOTYPE	regulation of excretion phenotype
GO:0044236PHENOTYPE	multicellular organismal metabolic process phenotype
GO:0044237PHENOTYPE	cellular metabolic process phenotype
GO:0044241PHENOTYPE	lipid digestion phenotype
GO:0044242PHENOTYPE	cellular lipid catabolic process phenotype
GO:0044255PHENOTYPE	cellular lipid metabolic process phenotype
GO:0044257PHENOTYPE	cellular protein catabolic process phenotype
GO:0044265PHENOTYPE	cellular macromolecule catabolic process phenotype
GO:0044267PHENOTYPE	cellular protein metabolic process phenotype
GO:0044342PHENOTYPE	type B pancreatic cell proliferation phenotype
GO:0044458PHENOTYPE	motile cilium assembly phenotype
GO:0044537PHENOTYPE	regulation of circulating fibrinogen levels phenotype
GO:0044773PHENOTYPE	mitotic DNA damage checkpoint phenotype
GO:0044782PHENOTYPE	cilium organization phenotype
GO:0044853PHENOTYPE	plasma membrane raft phenotype
GO:0045026PHENOTYPE	plasma membrane fusion phenotype
GO:0045063PHENOTYPE	T-helper 1 cell differentiation phenotype
GO:0045064PHENOTYPE	T-helper 2 cell differentiation phenotype
GO:0045087PHENOTYPE	innate immune response phenotype
GO:0045088PHENOTYPE	regulation of innate immune response phenotype
GO:0045089PHENOTYPE	positive regulation of innate immune response phenotype
GO:0045123PHENOTYPE	cellular extravasation phenotype
GO:0045132PHENOTYPE	meiotic chromosome segregation phenotype
GO:0045136PHENOTYPE	development of secondary sexual characteristics phenotype
GO:0045165PHENOTYPE	cell fate commitment phenotype
GO:0045176PHENOTYPE	apical protein localization phenotype
GO:0045184PHENOTYPE	establishment of protein localization phenotype
GO:0045190PHENOTYPE	isotype switching phenotype
GO:0045197PHENOTYPE	establishment or maintenance of epithelial cell apical/basal polarity phenotype
GO:0045198PHENOTYPE	establishment of epithelial cell apical/basal polarity phenotype
GO:0045202PHENOTYPE	synapse phenotype
GO:0045214PHENOTYPE	sarcomere organization phenotype
GO:0045216PHENOTYPE	cell-cell junction organization phenotype
GO:0045217PHENOTYPE	cell-cell junction maintenance phenotype
GO:0045271PHENOTYPE	respiratory chain complex I phenotype
GO:0045299PHENOTYPE	otolith mineralization phenotype
GO:0045333PHENOTYPE	cellular respiration phenotype
GO:0045428PHENOTYPE	regulation of nitric oxide biosynthetic process phenotype
GO:0045444PHENOTYPE	fat cell differentiation phenotype
GO:0045446PHENOTYPE	endothelial cell differentiation phenotype
GO:0045453PHENOTYPE	bone resorption phenotype
GO:0045471PHENOTYPE	response to ethanol phenotype
GO:0045475PHENOTYPE	locomotor rhythm phenotype
GO:0045494PHENOTYPE	photoreceptor cell maintenance phenotype
GO:0045576PHENOTYPE	mast cell activation phenotype
GO:0045577PHENOTYPE	regulation of B cell differentiation phenotype
GO:0045578PHENOTYPE	negative regulation of B cell differentiation phenotype
GO:0045580PHENOTYPE	regulation of T cell differentiation phenotype
GO:0045581PHENOTYPE	negative regulation of T cell differentiation phenotype
GO:0045595PHENOTYPE	regulation of cell differentiation phenotype
GO:0045596PHENOTYPE	negative regulation of cell differentiation phenotype
GO:0045604PHENOTYPE	regulation of epidermal cell differentiation phenotype
GO:0045605PHENOTYPE	negative regulation of epidermal cell differentiation phenotype
GO:0045616PHENOTYPE	regulation of keratinocyte differentiation phenotype
GO:0045617PHENOTYPE	negative regulation of keratinocyte differentiation phenotype
GO:0045619PHENOTYPE	regulation of lymphocyte differentiation 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:0045744PHENOTYPE	negative regulation of G-protein coupled receptor protein signaling pathway 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:0045793PHENOTYPE	positive regulation of cell size phenotype
GO:0045822PHENOTYPE	negative regulation of heart contraction phenotype
GO:0045859PHENOTYPE	regulation of protein kinase activity phenotype
GO:0045860PHENOTYPE	positive regulation of protein kinase activity phenotype
GO:0045861PHENOTYPE	negative regulation of proteolysis 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:0045926PHENOTYPE	negative regulation of growth phenotype
GO:0045927PHENOTYPE	positive regulation of growth phenotype
GO:0045930PHENOTYPE	negative regulation of mitotic cell cycle phenotype
GO:0045944PHENOTYPE	positive regulation of transcription from RNA polymerase II promoter phenotype
GO:0045986PHENOTYPE	negative regulation of smooth muscle contraction phenotype
GO:0045988PHENOTYPE	negative regulation of striated muscle contraction phenotype
GO:0046031PHENOTYPE	ADP metabolic process phenotype
GO:0046034PHENOTYPE	ATP metabolic process phenotype
GO:0046058PHENOTYPE	cAMP metabolic process phenotype
GO:0046148PHENOTYPE	pigment biosynthetic process phenotype
GO:0046323PHENOTYPE	glucose import phenotype
GO:0046425PHENOTYPE	regulation of JAK-STAT cascade phenotype
GO:0046483PHENOTYPE	heterocycle metabolic process phenotype
GO:0046488PHENOTYPE	phosphatidylinositol metabolic process phenotype
GO:0046541PHENOTYPE	saliva secretion phenotype
GO:0046543PHENOTYPE	development of secondary female sexual characteristics phenotype
GO:0046544PHENOTYPE	development of secondary male sexual characteristics 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:0046631PHENOTYPE	alpha-beta T cell activation phenotype
GO:0046632PHENOTYPE	alpha-beta T cell differentiation phenotype
GO:0046649PHENOTYPE	lymphocyte activation phenotype
GO:0046651PHENOTYPE	lymphocyte proliferation phenotype
GO:0046661PHENOTYPE	male sex differentiation phenotype
GO:0046666PHENOTYPE	retinal cell programmed cell death phenotype
GO:0046676PHENOTYPE	negative regulation of insulin secretion phenotype
GO:0046686PHENOTYPE	response to cadmium ion phenotype
GO:0046697PHENOTYPE	decidualization phenotype
GO:0046716PHENOTYPE	muscle cell cellular homeostasis phenotype
GO:0046777PHENOTYPE	protein autophosphorylation phenotype
GO:0046835PHENOTYPE	carbohydrate phosphorylation phenotype
GO:0046849PHENOTYPE	bone remodeling phenotype
GO:0046850PHENOTYPE	regulation of bone remodeling phenotype
GO:0046856PHENOTYPE	phosphatidylinositol dephosphorylation phenotype
GO:0046879PHENOTYPE	hormone secretion phenotype
GO:0046883PHENOTYPE	regulation of hormone secretion phenotype
GO:0046888PHENOTYPE	negative regulation of hormone secretion phenotype
GO:0046890PHENOTYPE	regulation of lipid biosynthetic process phenotype
GO:0046903PHENOTYPE	secretion phenotype
GO:0046921PHENOTYPE	alpha-(1->6)-fucosyltransferase activity phenotype
GO:0046951PHENOTYPE	ketone body biosynthetic process phenotype
GO:0046959PHENOTYPE	habituation phenotype
GO:0047496PHENOTYPE	vesicle transport along microtubule phenotype
GO:0047497PHENOTYPE	mitochondrion transport along microtubule phenotype
GO:0048002PHENOTYPE	antigen processing and presentation of peptide antigen phenotype
GO:0048010PHENOTYPE	vascular endothelial growth factor receptor signaling pathway phenotype
GO:0048015PHENOTYPE	phosphatidylinositol-mediated signaling phenotype
GO:0048048PHENOTYPE	embryonic eye morphogenesis phenotype
GO:0048066PHENOTYPE	developmental pigmentation phenotype
GO:0048069PHENOTYPE	eye pigmentation phenotype
GO:0048137PHENOTYPE	spermatocyte division phenotype
GO:0048143PHENOTYPE	astrocyte activation phenotype
GO:0048144PHENOTYPE	fibroblast proliferation phenotype
GO:0048149PHENOTYPE	behavioral response to ethanol phenotype
GO:0048167PHENOTYPE	regulation of synaptic plasticity phenotype
GO:0048168PHENOTYPE	regulation of neuronal synaptic plasticity phenotype
GO:0048193PHENOTYPE	Golgi vesicle transport phenotype
GO:0048240PHENOTYPE	sperm capacitation phenotype
GO:0048242PHENOTYPE	epinephrine secretion phenotype
GO:0048246PHENOTYPE	macrophage chemotaxis phenotype
GO:0048255PHENOTYPE	mRNA stabilization phenotype
GO:0048286PHENOTYPE	lung alveolus development phenotype
GO:0048318PHENOTYPE	axial mesoderm development phenotype
GO:0048319PHENOTYPE	axial mesoderm morphogenesis phenotype
GO:0048320PHENOTYPE	axial mesoderm formation phenotype
GO:0048333PHENOTYPE	mesodermal cell differentiation phenotype
GO:0048339PHENOTYPE	paraxial mesoderm development phenotype
GO:0048340PHENOTYPE	paraxial mesoderm morphogenesis phenotype
GO:0048341PHENOTYPE	paraxial mesoderm formation phenotype
GO:0048343PHENOTYPE	paraxial mesodermal cell fate commitment phenotype
GO:0048368PHENOTYPE	lateral mesoderm development phenotype
GO:0048371PHENOTYPE	lateral mesodermal cell differentiation phenotype
GO:0048382PHENOTYPE	mesendoderm development phenotype
GO:0048384PHENOTYPE	retinoic acid receptor signaling pathway phenotype
GO:0048389PHENOTYPE	intermediate mesoderm development phenotype
GO:0048468PHENOTYPE	cell development phenotype
GO:0048469PHENOTYPE	cell maturation phenotype
GO:0048477PHENOTYPE	oogenesis phenotype
GO:0048483PHENOTYPE	autonomic nervous system development phenotype
GO:0048484PHENOTYPE	enteric nervous system development phenotype
GO:0048485PHENOTYPE	sympathetic nervous system development phenotype
GO:0048486PHENOTYPE	parasympathetic nervous system development phenotype
GO:0048488PHENOTYPE	synaptic vesicle endocytosis phenotype
GO:0048489PHENOTYPE	synaptic vesicle transport phenotype
GO:0048511PHENOTYPE	rhythmic process phenotype
GO:0048512PHENOTYPE	circadian behavior phenotype
GO:0048513PHENOTYPE	organ development phenotype
GO:0048514PHENOTYPE	blood vessel morphogenesis phenotype
GO:0048515PHENOTYPE	spermatid differentiation phenotype
GO:0048532PHENOTYPE	anatomical structure arrangement phenotype
GO:0048534PHENOTYPE	hematopoietic or lymphoid organ development phenotype
GO:0048535PHENOTYPE	lymph node development phenotype
GO:0048536PHENOTYPE	spleen development phenotype
GO:0048538PHENOTYPE	thymus development phenotype
GO:0048539PHENOTYPE	bone marrow 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:0048608PHENOTYPE	reproductive structure development phenotype
GO:0048609PHENOTYPE	multicellular organismal reproductive process phenotype
GO:0048638PHENOTYPE	regulation of developmental growth phenotype
GO:0048644PHENOTYPE	muscle organ morphogenesis phenotype
GO:0048645PHENOTYPE	organ formation phenotype
GO:0048663PHENOTYPE	neuron fate commitment phenotype
GO:0048664PHENOTYPE	neuron fate determination phenotype
GO:0048665PHENOTYPE	neuron fate specification phenotype
GO:0048666PHENOTYPE	neuron development phenotype
GO:0048667PHENOTYPE	cell morphogenesis involved in neuron differentiation phenotype
GO:0048675PHENOTYPE	axon extension phenotype
GO:0048677PHENOTYPE	axon extension involved in regeneration phenotype
GO:0048678PHENOTYPE	response to axon 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:0048704PHENOTYPE	embryonic skeletal system 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:0048729PHENOTYPE	tissue morphogenesis phenotype
GO:0048730PHENOTYPE	epidermis morphogenesis phenotype
GO:0048732PHENOTYPE	gland development phenotype
GO:0048733PHENOTYPE	sebaceous gland development 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:0048754PHENOTYPE	branching morphogenesis of an epithelial tube phenotype
GO:0048755PHENOTYPE	branching morphogenesis of a nerve phenotype
GO:0048762PHENOTYPE	mesenchymal cell differentiation phenotype
GO:0048771PHENOTYPE	tissue remodeling phenotype
GO:0048812PHENOTYPE	neuron projection morphogenesis phenotype
GO:0048813PHENOTYPE	dendrite morphogenesis phenotype
GO:0048814PHENOTYPE	regulation of dendrite morphogenesis phenotype
GO:0048820PHENOTYPE	hair follicle maturation phenotype
GO:0048821PHENOTYPE	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:0048850PHENOTYPE	hypophysis morphogenesis phenotype
GO:0048852PHENOTYPE	diencephalon morphogenesis phenotype
GO:0048853PHENOTYPE	forebrain morphogenesis phenotype
GO:0048854PHENOTYPE	brain morphogenesis phenotype
GO:0048855PHENOTYPE	adenohypophysis morphogenesis phenotype
GO:0048857PHENOTYPE	neural nucleus development phenotype
GO:0048859PHENOTYPE	formation of anatomical boundary phenotype
GO:0048863PHENOTYPE	stem cell differentiation phenotype
GO:0048864PHENOTYPE	stem cell development phenotype
GO:0048870PHENOTYPE	cell motility phenotype
GO:0048871PHENOTYPE	multicellular organismal homeostasis phenotype
GO:0048872PHENOTYPE	homeostasis of number of cells phenotype
GO:0048873PHENOTYPE	homeostasis of number of cells within a tissue phenotype
GO:0048878PHENOTYPE	chemical homeostasis phenotype
GO:0048894PHENOTYPE	efferent axon development in a lateral line nerve phenotype
GO:0048934PHENOTYPE	peripheral nervous system neuron differentiation phenotype
GO:0048935PHENOTYPE	peripheral nervous system neuron development phenotype
GO:0048936PHENOTYPE	peripheral nervous system neuron axonogenesis phenotype
GO:0050432PHENOTYPE	catecholamine secretion phenotype
GO:0050433PHENOTYPE	regulation of catecholamine secretion phenotype
GO:0050663PHENOTYPE	cytokine secretion phenotype
GO:0050665PHENOTYPE	hydrogen peroxide biosynthetic process phenotype
GO:0050667PHENOTYPE	homocysteine metabolic process phenotype
GO:0050672PHENOTYPE	negative 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:0050684PHENOTYPE	regulation of mRNA processing phenotype
GO:0050688PHENOTYPE	regulation of defense response to virus phenotype
GO:0050701PHENOTYPE	interleukin-1 secretion phenotype
GO:0050708PHENOTYPE	regulation of protein secretion 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:0050770PHENOTYPE	regulation of axonogenesis phenotype
GO:0050773PHENOTYPE	regulation of dendrite development phenotype
GO:0050776PHENOTYPE	regulation of immune response phenotype
GO:0050777PHENOTYPE	negative regulation of immune response phenotype
GO:0050778PHENOTYPE	positive regulation of immune response phenotype
GO:0050790PHENOTYPE	regulation of catalytic activity phenotype
GO:0050796PHENOTYPE	regulation of insulin secretion phenotype
GO:0050798PHENOTYPE	activated T cell proliferation phenotype
GO:0050801PHENOTYPE	ion homeostasis phenotype
GO:0050803PHENOTYPE	regulation of synapse structure or activity phenotype
GO:0050804PHENOTYPE	modulation of synaptic transmission phenotype
GO:0050805PHENOTYPE	negative regulation of synaptic transmission phenotype
GO:0050806PHENOTYPE	positive regulation of synaptic transmission phenotype
GO:0050807PHENOTYPE	regulation of synapse organization phenotype
GO:0050808PHENOTYPE	synapse organization phenotype
GO:0050810PHENOTYPE	regulation of steroid biosynthetic process phenotype
GO:0050821PHENOTYPE	protein stabilization phenotype
GO:0050829PHENOTYPE	defense response to Gram-negative bacterium phenotype
GO:0050832PHENOTYPE	defense response to fungus phenotype
GO:0050848PHENOTYPE	regulation of calcium-mediated signaling phenotype
GO:0050863PHENOTYPE	regulation of T cell activation phenotype
GO:0050864PHENOTYPE	regulation of B cell activation phenotype
GO:0050865PHENOTYPE	regulation of cell activation phenotype
GO:0050868PHENOTYPE	negative regulation of T cell activation phenotype
GO:0050869PHENOTYPE	negative regulation of B cell activation phenotype
GO:0050872PHENOTYPE	white fat cell differentiation phenotype
GO:0050873PHENOTYPE	brown fat cell differentiation phenotype
GO:0050877PHENOTYPE	neurological system process phenotype
GO:0050878PHENOTYPE	regulation of body fluid levels phenotype
GO:0050880PHENOTYPE	regulation of blood vessel size phenotype
GO:0050881PHENOTYPE	musculoskeletal movement phenotype
GO:0050882PHENOTYPE	voluntary musculoskeletal movement phenotype
GO:0050883PHENOTYPE	musculoskeletal movement, spinal reflex action phenotype
GO:0050884PHENOTYPE	neuromuscular process controlling posture phenotype
GO:0050885PHENOTYPE	neuromuscular process controlling balance phenotype
GO:0050890PHENOTYPE	cognition phenotype
GO:0050892PHENOTYPE	intestinal absorption phenotype
GO:0050900PHENOTYPE	leukocyte migration phenotype
GO:0050901PHENOTYPE	leukocyte tethering or rolling phenotype
GO:0050905PHENOTYPE	neuromuscular process phenotype
GO:0050907PHENOTYPE	detection of chemical stimulus involved in sensory perception phenotype
GO:0050908PHENOTYPE	detection of light stimulus involved in visual perception phenotype
GO:0050909PHENOTYPE	sensory perception of taste phenotype
GO:0050910PHENOTYPE	detection of mechanical stimulus involved in sensory perception of sound phenotype
GO:0050913PHENOTYPE	sensory perception of bitter taste phenotype
GO:0050916PHENOTYPE	sensory perception of sweet taste phenotype
GO:0050917PHENOTYPE	sensory perception of umami taste phenotype
GO:0050919PHENOTYPE	negative chemotaxis phenotype
GO:0050951PHENOTYPE	sensory perception of temperature stimulus phenotype
GO:0050953PHENOTYPE	sensory perception of light stimulus phenotype
GO:0050954PHENOTYPE	sensory perception of mechanical stimulus phenotype
GO:0050955PHENOTYPE	thermoception phenotype
GO:0050957PHENOTYPE	equilibrioception phenotype
GO:0050973PHENOTYPE	detection of mechanical stimulus involved in equilibrioception phenotype
GO:0050974PHENOTYPE	detection of mechanical stimulus involved in sensory perception phenotype
GO:0050975PHENOTYPE	sensory perception of touch phenotype
GO:0050982PHENOTYPE	detection of mechanical stimulus phenotype
GO:0050994PHENOTYPE	regulation of lipid catabolic process phenotype
GO:0050996PHENOTYPE	positive regulation of lipid catabolic process phenotype
GO:0051026PHENOTYPE	chiasma assembly phenotype
GO:0051055PHENOTYPE	negative regulation of lipid biosynthetic process phenotype
GO:0051081PHENOTYPE	nuclear envelope disassembly phenotype
GO:0051090PHENOTYPE	regulation of sequence-specific DNA binding transcription factor activity phenotype
GO:0051092PHENOTYPE	positive regulation of NF-kappaB transcription factor activity phenotype
GO:0051124PHENOTYPE	synaptic growth at neuromuscular junction phenotype
GO:0051128PHENOTYPE	regulation of cellular component organization phenotype
GO:0051145PHENOTYPE	smooth muscle cell differentiation phenotype
GO:0051146PHENOTYPE	striated muscle cell differentiation phenotype
GO:0051156PHENOTYPE	glucose 6-phosphate metabolic process phenotype
GO:0051171PHENOTYPE	regulation of nitrogen compound metabolic process phenotype
GO:0051209PHENOTYPE	release of sequestered calcium ion into cytosol phenotype
GO:0051216PHENOTYPE	cartilage development phenotype
GO:0051223PHENOTYPE	regulation of protein transport phenotype
GO:0051225PHENOTYPE	spindle assembly phenotype
GO:0051232PHENOTYPE	meiotic spindle elongation phenotype
GO:0051246PHENOTYPE	regulation of protein metabolic process phenotype
GO:0051252PHENOTYPE	regulation of RNA metabolic process phenotype
GO:0051276PHENOTYPE	chromosome organization phenotype
GO:0051282PHENOTYPE	regulation of sequestering of calcium ion phenotype
GO:0051298PHENOTYPE	centrosome duplication phenotype
GO:0051301PHENOTYPE	cell division phenotype
GO:0051302PHENOTYPE	regulation of cell division phenotype
GO:0051306PHENOTYPE	mitotic sister chromatid separation phenotype
GO:0051321PHENOTYPE	meiotic cell cycle phenotype
GO:0051347PHENOTYPE	positive regulation of transferase activity phenotype
GO:0051348PHENOTYPE	negative regulation of transferase activity phenotype
GO:0051355PHENOTYPE	proprioception involved in equilibrioception phenotype
GO:0051402PHENOTYPE	neuron apoptotic process phenotype
GO:0051445PHENOTYPE	regulation of meiotic cell cycle phenotype
GO:0051447PHENOTYPE	negative regulation of meiotic cell cycle phenotype
GO:0051450PHENOTYPE	myoblast proliferation phenotype
GO:0051458PHENOTYPE	corticotropin secretion phenotype
GO:0051480PHENOTYPE	cytosolic calcium ion homeostasis phenotype
GO:0051546PHENOTYPE	keratinocyte migration phenotype
GO:0051567PHENOTYPE	histone H3-K9 methylation phenotype
GO:0051602PHENOTYPE	response to electrical stimulus phenotype
GO:0051604PHENOTYPE	protein maturation phenotype
GO:0051607PHENOTYPE	defense response to virus phenotype
GO:0051642PHENOTYPE	centrosome localization phenotype
GO:0051645PHENOTYPE	Golgi localization phenotype
GO:0051647PHENOTYPE	nucleus localization phenotype
GO:0051648PHENOTYPE	vesicle localization phenotype
GO:0051651PHENOTYPE	maintenance of location in cell phenotype
GO:0051654PHENOTYPE	establishment of mitochondrion localization phenotype
GO:0051656PHENOTYPE	establishment of organelle localization phenotype
GO:0051707PHENOTYPE	response to other organism phenotype
GO:0051726PHENOTYPE	regulation of cell cycle phenotype
GO:0051782PHENOTYPE	negative regulation of cell division phenotype
GO:0051873PHENOTYPE	killing by host of symbiont cells phenotype
GO:0051875PHENOTYPE	pigment granule localization phenotype
GO:0051899PHENOTYPE	membrane depolarization phenotype
GO:0051904PHENOTYPE	pigment granule transport phenotype
GO:0051923PHENOTYPE	sulfation phenotype
GO:0051932PHENOTYPE	synaptic transmission, GABAergic phenotype
GO:0051963PHENOTYPE	regulation of synapse assembly phenotype
GO:0051964PHENOTYPE	negative regulation of synapse assembly phenotype
GO:0051966PHENOTYPE	regulation of synaptic transmission, glutamatergic phenotype
GO:0051971PHENOTYPE	positive regulation of transmission of nerve impulse phenotype
GO:0051983PHENOTYPE	regulation of chromosome segregation phenotype
GO:0051985PHENOTYPE	negative regulation of chromosome segregation phenotype
GO:0052547PHENOTYPE	regulation of peptidase activity phenotype
GO:0052689PHENOTYPE	carboxylic ester hydrolase activity phenotype
GO:0052866PHENOTYPE	phosphatidylinositol phosphate phosphatase activity 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:0055009PHENOTYPE	atrial cardiac muscle tissue morphogenesis phenotype
GO:0055010PHENOTYPE	ventricular cardiac muscle tissue morphogenesis 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:0055062PHENOTYPE	phosphate ion homeostasis phenotype
GO:0055069PHENOTYPE	zinc ion homeostasis phenotype
GO:0055070PHENOTYPE	copper ion homeostasis phenotype
GO:0055072PHENOTYPE	iron ion homeostasis phenotype
GO:0055074PHENOTYPE	calcium ion homeostasis phenotype
GO:0055075PHENOTYPE	potassium ion homeostasis phenotype
GO:0055078PHENOTYPE	sodium ion homeostasis phenotype
GO:0055082PHENOTYPE	cellular chemical homeostasis phenotype
GO:0055088PHENOTYPE	lipid homeostasis phenotype
GO:0055092PHENOTYPE	sterol homeostasis phenotype
GO:0055114PHENOTYPE	oxidation-reduction process phenotype
GO:0055123PHENOTYPE	digestive system development phenotype
GO:0060004PHENOTYPE	reflex phenotype
GO:0060005PHENOTYPE	vestibular reflex phenotype
GO:0060007PHENOTYPE	linear vestibuloocular reflex phenotype
GO:0060008PHENOTYPE	Sertoli cell differentiation phenotype
GO:0060009PHENOTYPE	Sertoli cell development phenotype
GO:0060012PHENOTYPE	synaptic transmission, glycinergic phenotype
GO:0060014PHENOTYPE	granulosa cell differentiation phenotype
GO:0060017PHENOTYPE	parathyroid gland development phenotype
GO:0060020PHENOTYPE	Bergmann glial cell differentiation phenotype
GO:0060021PHENOTYPE	palate development phenotype
GO:0060026PHENOTYPE	convergent extension phenotype
GO:0060028PHENOTYPE	convergent extension involved in axis elongation phenotype
GO:0060029PHENOTYPE	convergent extension involved in organogenesis phenotype
GO:0060033PHENOTYPE	anatomical structure regression phenotype
GO:0060035PHENOTYPE	notochord cell development phenotype
GO:0060037PHENOTYPE	pharyngeal system development phenotype
GO:0060038PHENOTYPE	cardiac muscle cell proliferation phenotype
GO:0060040PHENOTYPE	retinal bipolar neuron differentiation 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:0060056PHENOTYPE	mammary gland involution phenotype
GO:0060059PHENOTYPE	embryonic retina morphogenesis in camera-type eye phenotype
GO:0060065PHENOTYPE	uterus development phenotype
GO:0060068PHENOTYPE	vagina development phenotype
GO:0060070PHENOTYPE	canonical Wnt signaling pathway phenotype
GO:0060071PHENOTYPE	Wnt signaling pathway, planar cell polarity pathway phenotype
GO:0060073PHENOTYPE	micturition phenotype
GO:0060075PHENOTYPE	regulation of resting membrane potential phenotype
GO:0060078PHENOTYPE	regulation of postsynaptic membrane potential phenotype
GO:0060080PHENOTYPE	inhibitory postsynaptic potential phenotype
GO:0060081PHENOTYPE	membrane hyperpolarization phenotype
GO:0060082PHENOTYPE	eye blink reflex phenotype
GO:0060083PHENOTYPE	smooth muscle contraction involved in micturition phenotype
GO:0060084PHENOTYPE	synaptic transmission involved in micturition phenotype
GO:0060113PHENOTYPE	inner ear receptor cell differentiation phenotype
GO:0060117PHENOTYPE	auditory receptor cell development phenotype
GO:0060119PHENOTYPE	inner ear receptor cell development phenotype
GO:0060122PHENOTYPE	inner ear receptor stereocilium organization phenotype
GO:0060123PHENOTYPE	regulation of growth hormone secretion phenotype
GO:0060126PHENOTYPE	somatotropin secreting cell differentiation phenotype
GO:0060129PHENOTYPE	thyroid-stimulating hormone-secreting cell differentiation phenotype
GO:0060134PHENOTYPE	prepulse inhibition phenotype
GO:0060135PHENOTYPE	maternal process involved in female pregnancy phenotype
GO:0060136PHENOTYPE	embryonic process involved in female pregnancy phenotype
GO:0060156PHENOTYPE	milk ejection phenotype
GO:0060157PHENOTYPE	urinary bladder development phenotype
GO:0060159PHENOTYPE	regulation of dopamine receptor signaling pathway phenotype
GO:0060173PHENOTYPE	limb development phenotype
GO:0060179PHENOTYPE	male mating behavior phenotype
GO:0060197PHENOTYPE	cloacal septation phenotype
GO:0060206PHENOTYPE	estrous cycle phase phenotype
GO:0060214PHENOTYPE	endocardium formation 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:0060235PHENOTYPE	lens induction in camera-type eye phenotype
GO:0060259PHENOTYPE	regulation of feeding behavior phenotype
GO:0060271PHENOTYPE	cilium morphogenesis phenotype
GO:0060272PHENOTYPE	embryonic skeletal joint morphogenesis phenotype
GO:0060284PHENOTYPE	regulation of cell development phenotype
GO:0060291PHENOTYPE	long-term synaptic potentiation phenotype
GO:0060292PHENOTYPE	long term synaptic depression phenotype
GO:0060294PHENOTYPE	cilium movement involved in cell motility phenotype
GO:0060307PHENOTYPE	regulation of ventricular cardiac muscle cell membrane repolarization phenotype
GO:0060317PHENOTYPE	cardiac epithelial to mesenchymal transition phenotype
GO:0060318PHENOTYPE	definitive erythrocyte differentiation 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:0060350PHENOTYPE	endochondral bone morphogenesis phenotype
GO:0060351PHENOTYPE	cartilage development involved in endochondral bone morphogenesis phenotype
GO:0060363PHENOTYPE	cranial suture morphogenesis phenotype
GO:0060384PHENOTYPE	innervation phenotype
GO:0060385PHENOTYPE	axonogenesis involved in innervation phenotype
GO:0060386PHENOTYPE	synapse assembly involved in innervation phenotype
GO:0060395PHENOTYPE	SMAD protein signal transduction phenotype
GO:0060401PHENOTYPE	cytosolic calcium ion transport phenotype
GO:0060407PHENOTYPE	negative regulation of penile erection phenotype
GO:0060415PHENOTYPE	muscle tissue morphogenesis phenotype
GO:0060419PHENOTYPE	heart growth phenotype
GO:0060425PHENOTYPE	lung morphogenesis phenotype
GO:0060428PHENOTYPE	lung epithelium development phenotype
GO:0060429PHENOTYPE	epithelium development phenotype
GO:0060433PHENOTYPE	bronchus development phenotype
GO:0060434PHENOTYPE	bronchus morphogenesis phenotype
GO:0060438PHENOTYPE	trachea development phenotype
GO:0060439PHENOTYPE	trachea morphogenesis phenotype
GO:0060441PHENOTYPE	epithelial tube branching involved in lung morphogenesis phenotype
GO:0060442PHENOTYPE	branching involved in prostate gland morphogenesis phenotype
GO:0060443PHENOTYPE	mammary gland morphogenesis phenotype
GO:0060444PHENOTYPE	branching involved in mammary gland duct morphogenesis phenotype
GO:0060455PHENOTYPE	negative regulation of gastric acid secretion phenotype
GO:0060463PHENOTYPE	lung lobe morphogenesis phenotype
GO:0060464PHENOTYPE	lung lobe formation phenotype
GO:0060468PHENOTYPE	prevention of polyspermy phenotype
GO:0060484PHENOTYPE	lung-associated mesenchyme development phenotype
GO:0060485PHENOTYPE	mesenchyme development phenotype
GO:0060512PHENOTYPE	prostate gland morphogenesis phenotype
GO:0060536PHENOTYPE	cartilage morphogenesis phenotype
GO:0060538PHENOTYPE	skeletal muscle organ development phenotype
GO:0060539PHENOTYPE	diaphragm development phenotype
GO:0060541PHENOTYPE	respiratory system development phenotype
GO:0060548PHENOTYPE	negative regulation of cell death phenotype
GO:0060560PHENOTYPE	developmental growth involved in morphogenesis phenotype
GO:0060561PHENOTYPE	apoptotic process involved in morphogenesis phenotype
GO:0060563PHENOTYPE	neuroepithelial cell differentiation phenotype
GO:0060571PHENOTYPE	morphogenesis of an epithelial fold phenotype
GO:0060575PHENOTYPE	intestinal epithelial cell differentiation phenotype
GO:0060603PHENOTYPE	mammary gland duct morphogenesis phenotype
GO:0060606PHENOTYPE	tube closure phenotype
GO:0060612PHENOTYPE	adipose tissue development phenotype
GO:0060615PHENOTYPE	mammary gland bud formation phenotype
GO:0060644PHENOTYPE	mammary gland epithelial cell differentiation phenotype
GO:0060648PHENOTYPE	mammary gland bud morphogenesis phenotype
GO:0060649PHENOTYPE	mammary gland bud elongation phenotype
GO:0060658PHENOTYPE	nipple morphogenesis phenotype
GO:0060659PHENOTYPE	nipple sheath formation phenotype
GO:0060677PHENOTYPE	ureteric bud elongation phenotype
GO:0060688PHENOTYPE	regulation of morphogenesis of a branching structure phenotype
GO:0060706PHENOTYPE	cell differentiation involved in embryonic placenta development phenotype
GO:0060711PHENOTYPE	labyrinthine layer development phenotype
GO:0060722PHENOTYPE	cell proliferation involved in embryonic placenta development phenotype
GO:0060729PHENOTYPE	intestinal epithelial structure maintenance phenotype
GO:0060740PHENOTYPE	prostate gland epithelium morphogenesis phenotype
GO:0060742PHENOTYPE	epithelial cell differentiation involved in prostate gland development phenotype
GO:0060744PHENOTYPE	mammary gland branching involved in thelarche phenotype
GO:0060745PHENOTYPE	mammary gland branching involved in pregnancy phenotype
GO:0060764PHENOTYPE	cell-cell signaling involved in mammary gland development phenotype
GO:0060828PHENOTYPE	regulation of canonical Wnt signaling pathway phenotype
GO:0060831PHENOTYPE	smoothened signaling pathway involved in dorsal/ventral neural tube patterning phenotype
GO:0060836PHENOTYPE	lymphatic endothelial cell differentiation phenotype
GO:0060837PHENOTYPE	blood vessel endothelial cell differentiation phenotype
GO:0060840PHENOTYPE	artery development phenotype
GO:0060847PHENOTYPE	endothelial cell fate specification phenotype
GO:0060854PHENOTYPE	patterning of lymph vessels phenotype
GO:0060872PHENOTYPE	semicircular canal development phenotype
GO:0060875PHENOTYPE	lateral semicircular canal development phenotype
GO:0060879PHENOTYPE	semicircular canal fusion phenotype
GO:0060896PHENOTYPE	neural plate pattern specification phenotype
GO:0060912PHENOTYPE	cardiac cell fate specification phenotype
GO:0060914PHENOTYPE	heart formation phenotype
GO:0060916PHENOTYPE	mesenchymal cell proliferation involved in lung development phenotype
GO:0060964PHENOTYPE	regulation of gene silencing by miRNA phenotype
GO:0060971PHENOTYPE	embryonic heart tube left/right pattern formation phenotype
GO:0060972PHENOTYPE	left/right pattern formation phenotype
GO:0060993PHENOTYPE	kidney morphogenesis phenotype
GO:0060994PHENOTYPE	regulation of transcription from RNA polymerase II promoter involved in kidney development phenotype
GO:0061005PHENOTYPE	cell differentiation involved in kidney 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:0061024PHENOTYPE	membrane organization phenotype
GO:0061025PHENOTYPE	membrane fusion phenotype
GO:0061031PHENOTYPE	endodermal digestive tract morphogenesis phenotype
GO:0061037PHENOTYPE	negative regulation of cartilage development phenotype
GO:0061045PHENOTYPE	negative regulation of wound healing phenotype
GO:0061053PHENOTYPE	somite development phenotype
GO:0061055PHENOTYPE	myotome development phenotype
GO:0061061PHENOTYPE	muscle structure development phenotype
GO:0061113PHENOTYPE	pancreas morphogenesis phenotype
GO:0061114PHENOTYPE	branching involved in pancreas morphogenesis phenotype
GO:0061136PHENOTYPE	regulation of proteasomal protein catabolic process phenotype
GO:0061138PHENOTYPE	morphogenesis of a branching epithelium phenotype
GO:0061180PHENOTYPE	mammary gland epithelium development phenotype
GO:0061181PHENOTYPE	regulation of chondrocyte development phenotype
GO:0061193PHENOTYPE	taste bud development 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:0061308PHENOTYPE	cardiac neural crest cell development involved in heart development phenotype
GO:0061309PHENOTYPE	cardiac neural crest cell development involved in outflow tract morphogenesis phenotype
GO:0061310PHENOTYPE	canonical Wnt signaling pathway involved in cardiac neural crest cell differentiation involved in heart development phenotype
GO:0061326PHENOTYPE	renal tubule development phenotype
GO:0061337PHENOTYPE	cardiac conduction phenotype
GO:0061346PHENOTYPE	planar cell polarity pathway involved in heart morphogenesis phenotype
GO:0061347PHENOTYPE	planar cell polarity pathway involved in outflow tract morphogenesis phenotype
GO:0061351PHENOTYPE	neural precursor cell proliferation phenotype
GO:0061371PHENOTYPE	determination of heart left/right asymmetry phenotype
GO:0061384PHENOTYPE	heart trabecula morphogenesis phenotype
GO:0061448PHENOTYPE	connective tissue development phenotype
GO:0061458PHENOTYPE	reproductive system development phenotype
GO:0061484PHENOTYPE	hematopoietic stem cell homeostasis phenotype
GO:0061502PHENOTYPE	early endosome to recycling endosome transport phenotype
GO:0061512PHENOTYPE	protein localization to cilium phenotype
GO:0061548PHENOTYPE	ganglion development phenotype
GO:0061564PHENOTYPE	axon development phenotype
GO:0061626PHENOTYPE	pharyngeal arch artery morphogenesis phenotype
GO:0070050PHENOTYPE	neuron cellular homeostasis phenotype
GO:0070059PHENOTYPE	intrinsic apoptotic signaling pathway in response to endoplasmic reticulum stress phenotype
GO:0070166PHENOTYPE	enamel mineralization phenotype
GO:0070192PHENOTYPE	chromosome organization involved in meiosis phenotype
GO:0070231PHENOTYPE	T cell apoptotic process phenotype
GO:0070242PHENOTYPE	thymocyte apoptotic process phenotype
GO:0070255PHENOTYPE	regulation of mucus secretion phenotype
GO:0070256PHENOTYPE	negative regulation of mucus secretion phenotype
GO:0070294PHENOTYPE	renal sodium ion absorption phenotype
GO:0070295PHENOTYPE	renal water absorption phenotype
GO:0070306PHENOTYPE	lens fiber cell differentiation phenotype
GO:0070307PHENOTYPE	lens fiber cell development phenotype
GO:0070309PHENOTYPE	lens fiber cell morphogenesis phenotype
GO:0070314PHENOTYPE	G1 to G0 transition phenotype
GO:0070328PHENOTYPE	triglyceride homeostasis phenotype
GO:0070365PHENOTYPE	hepatocyte differentiation phenotype
GO:0070371PHENOTYPE	ERK1 and ERK2 cascade phenotype
GO:0070372PHENOTYPE	regulation of ERK1 and ERK2 cascade phenotype
GO:0070374PHENOTYPE	positive regulation of ERK1 and ERK2 cascade phenotype
GO:0070384PHENOTYPE	Harderian gland development phenotype
GO:0070527PHENOTYPE	platelet aggregation phenotype
GO:0070586PHENOTYPE	cell-cell adhesion involved in gastrulation phenotype
GO:0070588PHENOTYPE	calcium ion transmembrane transport phenotype
GO:0070613PHENOTYPE	regulation of protein processing phenotype
GO:0070831PHENOTYPE	basement membrane assembly phenotype
GO:0070947PHENOTYPE	neutrophil mediated killing of fungus phenotype
GO:0070970PHENOTYPE	interleukin-2 secretion phenotype
GO:0070986PHENOTYPE	left/right axis specification phenotype
GO:0071174PHENOTYPE	mitotic spindle checkpoint phenotype
GO:0071260PHENOTYPE	cellular response to mechanical stimulus phenotype
GO:0071310PHENOTYPE	cellular response to organic substance phenotype
GO:0071340PHENOTYPE	skeletal muscle acetylcholine-gated channel clustering phenotype
GO:0071345PHENOTYPE	cellular response to cytokine stimulus phenotype
GO:0071359PHENOTYPE	cellular response to dsRNA phenotype
GO:0071361PHENOTYPE	cellular response to ethanol phenotype
GO:0071363PHENOTYPE	cellular response to growth factor stimulus phenotype
GO:0071407PHENOTYPE	cellular response to organic cyclic compound phenotype
GO:0071425PHENOTYPE	hematopoietic stem cell proliferation phenotype
GO:0071478PHENOTYPE	cellular response to radiation phenotype
GO:0071480PHENOTYPE	cellular response to gamma radiation phenotype
GO:0071482PHENOTYPE	cellular response to light stimulus phenotype
GO:0071514PHENOTYPE	genetic imprinting phenotype
GO:0071539PHENOTYPE	protein localization to centrosome phenotype
GO:0071542PHENOTYPE	dopaminergic neuron differentiation phenotype
GO:0071560PHENOTYPE	cellular response to transforming growth factor beta stimulus phenotype
GO:0071599PHENOTYPE	otic vesicle development phenotype
GO:0071600PHENOTYPE	otic vesicle morphogenesis phenotype
GO:0071625PHENOTYPE	vocalization behavior phenotype
GO:0071679PHENOTYPE	commissural neuron axon guidance phenotype
GO:0071707PHENOTYPE	immunoglobulin heavy chain V-D-J recombination phenotype
GO:0071711PHENOTYPE	basement membrane organization phenotype
GO:0071763PHENOTYPE	nuclear membrane organization phenotype
GO:0071805PHENOTYPE	potassium ion transmembrane transport phenotype
GO:0071896PHENOTYPE	protein localization to adherens junction phenotype
GO:0071902PHENOTYPE	positive regulation of protein serine/threonine kinase activity phenotype
GO:0071907PHENOTYPE	determination of digestive tract left/right asymmetry phenotype
GO:0071929PHENOTYPE	alpha-tubulin acetylation phenotype
GO:0072001PHENOTYPE	renal system development phenotype
GO:0072006PHENOTYPE	nephron development phenotype
GO:0072014PHENOTYPE	proximal tubule development phenotype
GO:0072015PHENOTYPE	glomerular visceral epithelial cell development phenotype
GO:0072028PHENOTYPE	nephron morphogenesis phenotype
GO:0072033PHENOTYPE	renal vesicle formation 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:0072092PHENOTYPE	ureteric bud invasion phenotype
GO:0072102PHENOTYPE	glomerulus morphogenesis phenotype
GO:0072111PHENOTYPE	cell proliferation involved in kidney development phenotype
GO:0072112PHENOTYPE	glomerular visceral epithelial cell differentiation phenotype
GO:0072148PHENOTYPE	epithelial cell fate commitment phenotype
GO:0072164PHENOTYPE	mesonephric tubule development phenotype
GO:0072176PHENOTYPE	nephric duct development phenotype
GO:0072178PHENOTYPE	nephric duct morphogenesis phenotype
GO:0072189PHENOTYPE	ureter development phenotype
GO:0072201PHENOTYPE	negative regulation of mesenchymal cell proliferation phenotype
GO:0072203PHENOTYPE	cell proliferation involved in metanephros development phenotype
GO:0072210PHENOTYPE	metanephric nephron development phenotype
GO:0072273PHENOTYPE	metanephric nephron morphogenesis phenotype
GO:0072358PHENOTYPE	cardiovascular system development phenotype
GO:0072359PHENOTYPE	circulatory system development phenotype
GO:0072378PHENOTYPE	blood coagulation, fibrin clot formation phenotype
GO:0072498PHENOTYPE	embryonic skeletal joint development phenotype
GO:0072574PHENOTYPE	hepatocyte proliferation phenotype
GO:0072576PHENOTYPE	liver morphogenesis phenotype
GO:0072579PHENOTYPE	glycine receptor clustering phenotype
GO:0072583PHENOTYPE	clathrin-mediated endocytosis phenotype
GO:0072592PHENOTYPE	oxygen metabolic process phenotype
GO:0072593PHENOTYPE	reactive oxygen species metabolic process phenotype
GO:0072602PHENOTYPE	interleukin-4 secretion phenotype
GO:0072607PHENOTYPE	interleukin-9 secretion phenotype
GO:0072619PHENOTYPE	interleukin-21 secretion phenotype
GO:0072643PHENOTYPE	interferon-gamma secretion phenotype
GO:0072657PHENOTYPE	protein localization to membrane phenotype
GO:0072659PHENOTYPE	protein localization to plasma membrane phenotype
GO:0072676PHENOTYPE	lymphocyte migration phenotype
GO:0072677PHENOTYPE	eosinophil migration phenotype
GO:0072678PHENOTYPE	T cell migration phenotype
GO:0085029PHENOTYPE	extracellular matrix assembly phenotype
GO:0086004PHENOTYPE	regulation of cardiac muscle cell contraction phenotype
GO:0086005PHENOTYPE	ventricular cardiac muscle cell action potential phenotype
GO:0086006PHENOTYPE	voltage-gated sodium channel activity involved in cardiac muscle cell action potential phenotype
GO:0086014PHENOTYPE	atrial cardiac muscle cell action potential phenotype
GO:0086064PHENOTYPE	cell communication by electrical coupling involved in cardiac conduction phenotype
GO:0086065PHENOTYPE	cell communication involved in cardiac conduction phenotype
GO:0090009PHENOTYPE	primitive streak formation phenotype
GO:0090030PHENOTYPE	regulation of steroid hormone biosynthetic process phenotype
GO:0090032PHENOTYPE	negative regulation of steroid hormone biosynthetic process phenotype
GO:0090090PHENOTYPE	negative regulation of canonical Wnt signaling pathway phenotype
GO:0090134PHENOTYPE	cell migration involved in mesendoderm migration phenotype
GO:0090150PHENOTYPE	establishment of protein localization to membrane phenotype
GO:0090177PHENOTYPE	establishment of planar polarity involved in neural tube closure phenotype
GO:0090178PHENOTYPE	regulation of establishment of planar polarity involved in neural tube closure phenotype
GO:0090179PHENOTYPE	planar cell polarity pathway involved in neural tube closure phenotype
GO:0090244PHENOTYPE	Wnt signaling pathway involved in somitogenesis phenotype
GO:0090245PHENOTYPE	axis elongation involved in somitogenesis phenotype
GO:0090273PHENOTYPE	regulation of somatostatin secretion phenotype
GO:0090276PHENOTYPE	regulation of peptide hormone secretion phenotype
GO:0090307PHENOTYPE	mitotic spindle assembly phenotype
GO:0090327PHENOTYPE	negative regulation of locomotion involved in locomotory behavior phenotype
GO:0090521PHENOTYPE	glomerular visceral epithelial cell migration phenotype
GO:0097009PHENOTYPE	energy homeostasis phenotype
GO:0097028PHENOTYPE	dendritic cell differentiation phenotype
GO:0097150PHENOTYPE	neuronal stem cell population maintenance phenotype
GO:0097154PHENOTYPE	GABAergic neuron differentiation phenotype
GO:0097186PHENOTYPE	amelogenesis phenotype
GO:0097190PHENOTYPE	apoptotic signaling pathway phenotype
GO:0097191PHENOTYPE	extrinsic apoptotic signaling pathway phenotype
GO:0097193PHENOTYPE	intrinsic apoptotic signaling pathway phenotype
GO:0097194PHENOTYPE	execution phase of apoptosis phenotype
GO:0097284PHENOTYPE	hepatocyte apoptotic process phenotype
GO:0097352PHENOTYPE	autophagosome maturation phenotype
GO:0097376PHENOTYPE	interneuron axon guidance phenotype
GO:0097401PHENOTYPE	synaptic vesicle lumen acidification phenotype
GO:0097421PHENOTYPE	liver regeneration phenotype
GO:0097484PHENOTYPE	dendrite extension phenotype
GO:0097485PHENOTYPE	neuron projection guidance phenotype
GO:0098542PHENOTYPE	defense response to other organism phenotype
GO:0098609PHENOTYPE	cell-cell adhesion phenotype
GO:0098727PHENOTYPE	maintenance of cell number phenotype
GO:0098781PHENOTYPE	ncRNA transcription phenotype
GO:1900407PHENOTYPE	regulation of cellular response to oxidative stress phenotype
GO:1900408PHENOTYPE	negative regulation of cellular response to oxidative stress phenotype
GO:1900746PHENOTYPE	regulation of vascular endothelial growth factor signaling pathway phenotype
GO:1901142PHENOTYPE	insulin metabolic process phenotype
GO:1901222PHENOTYPE	regulation of NIK/NF-kappaB signaling phenotype
GO:1901224PHENOTYPE	positive regulation of NIK/NF-kappaB signaling phenotype
GO:1901653PHENOTYPE	cellular response to peptide phenotype
GO:1901799PHENOTYPE	negative regulation of proteasomal protein catabolic process phenotype
GO:1901990PHENOTYPE	regulation of mitotic cell cycle phase transition phenotype
GO:1901994PHENOTYPE	negative regulation of meiotic cell cycle phase transition 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:1902600PHENOTYPE	hydrogen ion transmembrane transport phenotype
GO:1902742PHENOTYPE	apoptotic process involved in development phenotype
GO:1903010PHENOTYPE	regulation of bone development phenotype
GO:1903053PHENOTYPE	regulation of extracellular matrix organization phenotype
GO:1903232PHENOTYPE	melanosome assembly phenotype
GO:1903699PHENOTYPE	tarsal gland development phenotype
GO:1903709PHENOTYPE	uterine gland development phenotype
GO:1903828PHENOTYPE	negative regulation of cellular protein localization phenotype
GO:1990523PHENOTYPE	bone regeneration phenotype
GO:2000021PHENOTYPE	regulation of ion homeostasis phenotype
GO:2000027PHENOTYPE	regulation of organ morphogenesis phenotype
GO:2000035PHENOTYPE	regulation of stem cell division phenotype
GO:2000045PHENOTYPE	regulation of G1/S transition of mitotic cell cycle phenotype
GO:2000134PHENOTYPE	negative regulation of G1/S transition of mitotic cell cycle phenotype
GO:2000146PHENOTYPE	negative regulation of cell motility phenotype
GO:2000177PHENOTYPE	regulation of neural precursor cell proliferation phenotype
GO:2000194PHENOTYPE	regulation of female gonad development phenotype
GO:2000252PHENOTYPE	negative regulation of feeding behavior phenotype
GO:2000278PHENOTYPE	regulation of DNA biosynthetic process phenotype
GO:2000377PHENOTYPE	regulation of reactive oxygen species metabolic process phenotype
GO:2000647PHENOTYPE	negative regulation of stem cell proliferation phenotype
GO:2000736PHENOTYPE	regulation of stem cell differentiation phenotype
GO:2000828PHENOTYPE	regulation of parathyroid hormone secretion phenotype
GO:2001234PHENOTYPE	negative regulation of apoptotic signaling pathway phenotype
GO:2001235PHENOTYPE	positive regulation of apoptotic signaling pathway phenotype
GO:2001243PHENOTYPE	negative regulation of intrinsic apoptotic signaling pathway phenotype
HP:0000003	Multicystic kidney dysplasia
HP:0000008	Abnormality of female internal genitalia
HP:0000009	Functional abnormality of the bladder
HP:0000011	Neurogenic bladder
HP:0000013	Hypoplasia of the uterus
HP:0000016	Urinary retention
HP:0000020	Urinary incontinence
HP:0000021	Megacystis
HP:0000022	Abnormality of male internal genitalia
HP:0000023	Inguinal hernia
HP:0000024	Prostatitis
HP:0000027	Azoospermia
HP:0000028	Cryptorchidism
HP:0000029	Testicular atrophy
HP:0000032	Abnormality of male external genitalia
HP:0000035	Abnormality of the testis
HP:0000036	Abnormality of the penis
HP:0000037	Male pseudohermaphroditism
HP:0000045	Abnormality of the scrotum
HP:0000046	Scrotal hypoplasia
HP:0000047	Hypospadias
HP:0000053	Macroorchidism
HP:0000060	Clitoral hypoplasia
HP:0000068	Urethral atresia
HP:0000069	Abnormality of the ureter
HP:0000072	Hydroureter
HP:0000074	Ureteropelvic junction obstruction
HP:0000076	Vesicoureteral reflux
HP:0000080	Abnormality of reproductive system physiology
HP:0000083	Renal insufficiency
HP:0000085	Horseshoe kidney
HP:0000086	Ectopic kidney
HP:0000089	Renal hypoplasia
HP:0000092	Tubular atrophy
HP:0000093	Proteinuria
HP:0000096	Glomerulosclerosis
HP:0000099	Glomerulonephritis
HP:0000103	Polyuria
HP:0000104	Renal agenesis
HP:0000105	Enlarged kidney
HP:0000107	Renal cyst
HP:0000108	Renal corticomedullary cysts
HP:0000121	Nephrocalcinosis
HP:0000122	Unilateral renal agenesis
HP:0000123	Nephritis
HP:0000125	Pelvic kidney
HP:0000126	Hydronephrosis
HP:0000134	Female hypogonadism
HP:0000135	Hypogonadism
HP:0000137	Abnormality of the ovary
HP:0000138	Ovarian cyst
HP:0000139	Uterine prolapse
HP:0000143	Rectovaginal fistula
HP:0000144	Decreased fertility
HP:0000148	Vaginal atresia
HP:0000151	Aplasia of the uterus
HP:0000153	Abnormality of the mouth
HP:0000158	Macroglossia
HP:0000160	Narrow mouth
HP:0000171	Microglossia
HP:0000175	Cleft palate
HP:0000185	Cleft soft palate
HP:0000204	Cleft upper lip
HP:0000217	Xerostomia
HP:0000218	High palate
HP:0000233	Thin vermilion border
HP:0000234	Abnormality of the head
HP:0000238	Hydrocephalus
HP:0000240	Abnormality of skull size
HP:0000246	Sinusitis
HP:0000248	Brachycephaly
HP:0000252	Microcephaly
HP:0000260	Wide anterior fontanel
HP:0000267	Cranial asymmetry
HP:0000272	Malar flattening
HP:0000278	Retrognathia
HP:0000303	Mandibular prognathia
HP:0000315	Abnormality of the orbital region
HP:0000316	Hypertelorism
HP:0000325	Triangular face
HP:0000327	Hypoplasia of the maxilla
HP:0000347	Micrognathia
HP:0000348	High forehead
HP:0000362	Otosclerosis
HP:0000365	Hearing impairment
HP:0000369	Low-set ears
HP:0000377	Abnormality of the pinna
HP:0000378	Cupped ear
HP:0000385	Small earlobe
HP:0000400	Macrotia
HP:0000405	Conductive hearing impairment
HP:0000411	Protruding ear
HP:0000413	Atresia of the external auditory canal
HP:0000421	Epistaxis
HP:0000431	Wide nasal bridge
HP:0000433	Abnormality of the nasal mucosa
HP:0000453	Choanal atresia
HP:0000458	Anosmia
HP:0000470	Short neck
HP:0000472	Long neck
HP:0000480	Retinal coloboma
HP:0000481	Abnormality of the cornea
HP:0000490	Deeply set eye
HP:0000492	Abnormality of the eyelid
HP:0000496	Abnormality of eye movement
HP:0000498	Blepharitis
HP:0000502	Abnormality of the conjunctiva
HP:0000504	Abnormality of vision
HP:0000508	Ptosis
HP:0000509	Conjunctivitis
HP:0000517	Abnormality of the lens
HP:0000518	Cataract
HP:0000520	Proptosis
HP:0000523	Subcapsular cataract
HP:0000525	Abnormality of the iris
HP:0000526	Aniridia
HP:0000528	Anophthalmia
HP:0000531	Corneal crystals
HP:0000541	Retinal detachment
HP:0000545	Myopia
HP:0000546	Retinal degeneration
HP:0000554	Uveitis
HP:0000557	Buphthalmos
HP:0000559	Corneal scarring
HP:0000568	Microphthalmia
HP:0000573	Retinal hemorrhage
HP:0000581	Blepharophimosis
HP:0000586	Shallow orbits
HP:0000588	Optic nerve coloboma
HP:0000589	Coloboma
HP:0000592	Blue sclerae
HP:0000601	Hypotelorism
HP:0000609	Optic nerve hypoplasia
HP:0000612	Iris coloboma
HP:0000613	Photophobia
HP:0000615	Abnormality of the pupil
HP:0000618	Blindness
HP:0000621	Entropion
HP:0000632	Lacrimation abnormality
HP:0000633	Decreased lacrimation
HP:0000647	Sclerocornea
HP:0000648	Optic atrophy
HP:0000649	Abnormality of visual evoked potentials
HP:0000656	Ectropion
HP:0000662	Nyctalopia
HP:0000667	Phthisis bulbi
HP:0000684	Delayed eruption of teeth
HP:0000689	Dental malocclusion
HP:0000706	Unerupted tooth
HP:0000708	Behavioral abnormality
HP:0000718	Aggressive behavior
HP:0000733	Stereotypy
HP:0000735	Impaired social interactions
HP:0000739	Anxiety
HP:0000752	Hyperactivity
HP:0000762	Decreased nerve conduction velocity
HP:0000764	Peripheral axonal degeneration
HP:0000767	Pectus excavatum
HP:0000772	Abnormality of the ribs
HP:0000773	Short ribs
HP:0000776	Congenital diaphragmatic hernia
HP:0000778	Hypoplasia of the thymus
HP:0000782	Abnormality of the scapula
HP:0000787	Nephrolithiasis
HP:0000789	Infertility
HP:0000790	Hematuria
HP:0000795	Abnormality of the urethra
HP:0000796	Urethral obstruction
HP:0000798	Oligospermia
HP:0000803	Renal cortical cysts
HP:0000816	Abnormality of Krebs cycle metabolism
HP:0000821	Hypothyroidism
HP:0000822	Hypertension
HP:0000823	Delayed puberty
HP:0000826	Precocious puberty
HP:0000828	Abnormality of the parathyroid gland
HP:0000829	Hypoparathyroidism
HP:0000833	Glucose intolerance
HP:0000835	Adrenal hypoplasia
HP:0000836	Hyperthyroidism
HP:0000842	Hyperinsulinemia
HP:0000843	Hyperparathyroidism
HP:0000845	Growth hormone excess
HP:0000848	Increased circulating renin level
HP:0000853	Goiter
HP:0000855	Insulin resistance
HP:0000859	Hyperaldosteronism
HP:0000860	Parathyroid hypoplasia
HP:0000870	Prolactin excess
HP:0000872	Hashimoto thyroiditis
HP:0000879	Short sternum
HP:0000882	Hypoplastic scapulae
HP:0000883	Thin ribs
HP:0000885	Broad ribs
HP:0000892	Bifid ribs
HP:0000894	Short clavicles
HP:0000902	Rib fusion
HP:0000921	Missing ribs
HP:0000926	Platyspondyly
HP:0000938	Osteopenia
HP:0000939	Osteoporosis
HP:0000952	Jaundice
HP:0000958	Dry skin
HP:0000961	Cyanosis
HP:0000962	Hyperkeratosis
HP:0000963	Thin skin
HP:0000966	Hypohidrosis
HP:0000967	Petechiae
HP:0000969	Edema
HP:0000970	Anhidrosis
HP:0000971	Abnormality of the sweat gland
HP:0000973	Cutis laxa
HP:0000978	Bruising susceptibility
HP:0000979	Purpura
HP:0000980	Pallor
HP:0000998	Hypertrichosis
HP:0001000	Abnormality of skin pigmentation
HP:0001004	Lymphedema
HP:0001006	Hypotrichosis
HP:0001009	Telangiectasia
HP:0001010	Hypopigmentation of the skin
HP:0001012	Multiple lipomas
HP:0001019	Erythroderma
HP:0001028	Hemangioma
HP:0001036	Parakeratosis
HP:0001045	Vitiligo
HP:0001051	Seborrheic dermatitis
HP:0001059	Pterygium
HP:0001067	Neurofibromas
HP:0001081	Cholelithiasis
HP:0001082	Cholecystitis
HP:0001083	Ectopia lentis
HP:0001089	Iris atrophy
HP:0001090	Large eyes
HP:0001093	Optic nerve dysplasia
HP:0001096	Keratoconjunctivitis
HP:0001097	Keratoconjunctivitis sicca
HP:0001107	Ocular albinism
HP:0001114	Xanthelasma
HP:0001126	Cryptophthalmos
HP:0001134	Anterior polar cataract
HP:0001138	Optic neuropathy
HP:0001142	Lenticonus
HP:0001156	Brachydactyly
HP:0001159	Syndactyly
HP:0001166	Arachnodactyly
HP:0001191	Abnormality of the carpal bones
HP:0001196	Short umbilical cord
HP:0001250	Seizures
HP:0001251	Ataxia
HP:0001252	Muscular hypotonia
HP:0001254	Lethargy
HP:0001257	Spasticity
HP:0001272	Cerebellar atrophy
HP:0001274	Agenesis of corpus callosum
HP:0001288	Gait disturbance
HP:0001291	Abnormality of the cranial nerves
HP:0001310	Dysmetria
HP:0001311	Abnormal nervous system electrophysiology
HP:0001320	Cerebellar vermis hypoplasia
HP:0001321	Cerebellar hypoplasia
HP:0001322	Brain very small
HP:0001324	Muscle weakness
HP:0001332	Dystonia
HP:0001334	Communicating hydrocephalus
HP:0001336	Myoclonus
HP:0001337	Tremor
HP:0001342	Cerebral hemorrhage
HP:0001357	Plagiocephaly
HP:0001360	Holoprosencephaly
HP:0001363	Craniosynostosis
HP:0001367	Abnormal joint morphology
HP:0001369	Arthritis
HP:0001370	Rheumatoid arthritis
HP:0001386	Joint swelling
HP:0001392	Abnormality of the liver
HP:0001394	Cirrhosis
HP:0001395	Hepatic fibrosis
HP:0001396	Cholestasis
HP:0001397	Hepatic steatosis
HP:0001399	Hepatic failure
HP:0001402	Hepatocellular carcinoma
HP:0001406	Intrahepatic cholestasis
HP:0001407	Hepatic cysts
HP:0001408	Bile duct proliferation
HP:0001409	Portal hypertension
HP:0001410	Decreased liver function
HP:0001440	Metatarsal synostosis
HP:0001507	Growth abnormality
HP:0001508	Failure to thrive
HP:0001511	Intrauterine growth retardation
HP:0001513	Obesity
HP:0001537	Umbilical hernia
HP:0001539	Omphalocele
HP:0001541	Ascites
HP:0001543	Gastroschisis
HP:0001547	Abnormality of the rib cage
HP:0001552	Barrel-shaped chest
HP:0001561	Polyhydramnios
HP:0001562	Oligohydramnios
HP:0001586	Vesicovaginal fistula
HP:0001595	Abnormality of the hair
HP:0001602	Laryngeal stenosis
HP:0001607	Subglottic stenosis
HP:0001627	Abnormal heart morphology
HP:0001629	Ventricular septal defect
HP:0001631	Atrial septal defect
HP:0001634	Mitral valve prolapse
HP:0001635	Congestive heart failure
HP:0001638	Cardiomyopathy
HP:0001640	Cardiomegaly
HP:0001642	Pulmonic stenosis
HP:0001643	Patent ductus arteriosus
HP:0001644	Dilated cardiomyopathy
HP:0001647	Bicuspid aortic valve
HP:0001649	Tachycardia
HP:0001650	Aortic valve stenosis
HP:0001651	Dextrocardia
HP:0001653	Mitral regurgitation
HP:0001655	Patent foramen ovale
HP:0001657	Prolonged QT interval
HP:0001659	Aortic regurgitation
HP:0001660	Truncus arteriosus
HP:0001662	Bradycardia
HP:0001663	Ventricular fibrillation
HP:0001667	Right ventricular hypertrophy
HP:0001669	Transposition of the great arteries
HP:0001674	Complete atrioventricular canal defect
HP:0001678	Atrioventricular block
HP:0001679	Abnormality of the aorta
HP:0001680	Coarctation of aorta
HP:0001683	Ectopia cordis
HP:0001684	Secundum atrial septal defect
HP:0001688	Sinus bradycardia
HP:0001696	Situs inversus totalis
HP:0001698	Pericardial effusion
HP:0001700	Myocardial necrosis
HP:0001701	Pericarditis
HP:0001712	Left ventricular hypertrophy
HP:0001718	Mitral stenosis
HP:0001719	Double outlet right ventricle
HP:0001724	Aortic dilatation
HP:0001733	Pancreatitis
HP:0001734	Annular pancreas
HP:0001737	Pancreatic cysts
HP:0001738	Exocrine pancreatic insufficiency
HP:0001741	Phimosis
HP:0001743	Abnormality of the spleen
HP:0001744	Splenomegaly
HP:0001746	Asplenia
HP:0001747	Accessory spleen
HP:0001750	Single ventricle
HP:0001762	Talipes equinovarus
HP:0001789	Hydrops fetalis
HP:0001799	Short nail
HP:0001824	Weight loss
HP:0001871	Abnormality of blood and blood-forming tissues
HP:0001873	Thrombocytopenia
HP:0001875	Neutropenia
HP:0001876	Pancytopenia
HP:0001877	Abnormality of erythrocytes
HP:0001878	Hemolytic anemia
HP:0001879	Abnormality of eosinophils
HP:0001880	Eosinophilia
HP:0001881	Abnormality of leukocytes
HP:0001882	Leukopenia
HP:0001888	Lymphopenia
HP:0001892	Abnormal bleeding
HP:0001894	Thrombocytosis
HP:0001896	Reticulocytopenia
HP:0001899	Increased hematocrit
HP:0001901	Polycythemia
HP:0001902	Giant platelets
HP:0001903	Anemia
HP:0001909	Leukemia
HP:0001911	Abnormality of granulocytes
HP:0001923	Reticulocytosis
HP:0001927	Acanthocytosis
HP:0001931	Hypochromic anemia
HP:0001935	Microcytic anemia
HP:0001939	Abnormality of metabolism/homeostasis
HP:0001941	Acidosis
HP:0001942	Metabolic acidosis
HP:0001943	Hypoglycemia
HP:0001944	Dehydration
HP:0001947	Renal tubular acidosis
HP:0001948	Alkalosis
HP:0001959	Polydipsia
HP:0001961	Hypoplastic heart
HP:0001967	Diffuse mesangial sclerosis
HP:0001970	Tubulointerstitial nephritis
HP:0001972	Macrocytic anemia
HP:0001974	Leukocytosis
HP:0001978	Extramedullary hematopoiesis
HP:0001981	Schistocytosis
HP:0001987	Hyperammonemia
HP:0001999	Abnormal facial shape
HP:0002006	Facial cleft
HP:0002014	Diarrhea
HP:0002015	Dysphagia
HP:0002019	Constipation
HP:0002021	Pyloric stenosis
HP:0002023	Anal atresia
HP:0002025	Anal stenosis
HP:0002028	Chronic diarrhea
HP:0002031	Abnormality of esophagus morphology
HP:0002032	Esophageal atresia
HP:0002033	Poor suck
HP:0002034	Abnormality of the rectum
HP:0002035	Rectal prolapse
HP:0002037	Inflammation of the large intestine
HP:0002043	Esophageal stricture
HP:0002045	Hypothermia
HP:0002048	Renal cortical atrophy
HP:0002062	Morphological abnormality of the pyramidal tract
HP:0002067	Bradykinesia
HP:0002069	Generalized tonic-clonic seizures
HP:0002072	Chorea
HP:0002084	Encephalocele
HP:0002088	Abnormality of lung morphology
HP:0002089	Pulmonary hypoplasia
HP:0002090	Pneumonia
HP:0002092	Pulmonary arterial hypertension
HP:0002093	Respiratory insufficiency
HP:0002097	Emphysema
HP:0002098	Respiratory distress
HP:0002104	Apnea
HP:0002107	Pneumothorax
HP:0002110	Bronchiectasis
HP:0002119	Ventriculomegaly
HP:0002121	Absence seizures
HP:0002143	Abnormality of the spinal cord
HP:0002148	Hypophosphatemia
HP:0002149	Hyperuricemia
HP:0002150	Hypercalciuria
HP:0002152	Hyperproteinemia
HP:0002153	Hyperkalemia
HP:0002155	Hypertriglyceridemia
HP:0002157	Azotemia
HP:0002170	Intracranial hemorrhage
HP:0002171	Gliosis
HP:0002179	Opisthotonus
HP:0002180	Neurodegeneration
HP:0002181	Cerebral edema
HP:0002185	Neurofibrillary tangles
HP:0002198	Dilated fourth ventricle
HP:0002202	Pleural effusion
HP:0002206	Pulmonary fibrosis
HP:0002208	Coarse hair
HP:0002212	Curly hair
HP:0002239	Gastrointestinal hemorrhage
HP:0002240	Hepatomegaly
HP:0002242	Abnormality of the intestine
HP:0002244	Abnormality of the small intestine
HP:0002247	Duodenal atresia
HP:0002249	Melena
HP:0002250	Abnormality of the large intestine
HP:0002251	Aganglionic megacolon
HP:0002267	Exaggerated startle response
HP:0002269	Abnormality of neuronal migration
HP:0002298	Absent hair
HP:0002299	Brittle hair
HP:0002304	Akinesia
HP:0002305	Athetosis
HP:0002323	Anencephaly
HP:0002335	Agenesis of cerebellar vermis
HP:0002363	Abnormality of brainstem morphology
HP:0002380	Fasciculations
HP:0002383	Encephalitis
HP:0002385	Paraparesis
HP:0002398	Degeneration of anterior horn cells
HP:0002408	Cerebral arteriovenous malformation
HP:0002410	Aqueductal stenosis
HP:0002414	Spina bifida
HP:0002418	Abnormality of midbrain morphology
HP:0002446	Astrocytosis
HP:0002450	Abnormal motor neuron morphology
HP:0002457	Abnormal head movements
HP:0002486	Myotonia
HP:0002487	Hyperkinesis
HP:0002533	Abnormal posturing
HP:0002557	Hypoplastic nipples
HP:0002558	Supernumerary nipple
HP:0002561	Absent nipple
HP:0002570	Steatorrhea
HP:0002573	Hematochezia
HP:0002575	Tracheoesophageal fistula
HP:0002577	Abnormality of the stomach
HP:0002578	Gastroparesis
HP:0002586	Peritonitis
HP:0002588	Duodenal ulcer
HP:0002591	Polyphagia
HP:0002592	Gastric ulcer
HP:0002594	Pancreatic hypoplasia
HP:0002597	Abnormality of the vasculature
HP:0002605	Hepatic necrosis
HP:0002607	Bowel incontinence
HP:0002613	Biliary cirrhosis
HP:0002615	Hypotension
HP:0002616	Aortic root dilatation
HP:0002617	Dilatation
HP:0002619	Varicose veins
HP:0002621	Atherosclerosis
HP:0002623	Overriding aorta
HP:0002624	Venous abnormality
HP:0002629	Gastrointestinal arteriovenous malformation
HP:0002633	Vasculitis
HP:0002634	Arteriosclerosis
HP:0002644	Abnormality of pelvic girdle bone morphology
HP:0002647	Aortic dissection
HP:0002650	Scoliosis
HP:0002659	Increased susceptibility to fractures
HP:0002664	Neoplasm
HP:0002665	Lymphoma
HP:0002666	Pheochromocytoma
HP:0002669	Osteosarcoma
HP:0002671	Basal cell carcinoma
HP:0002682	Broad skull
HP:0002715	Abnormality of the immune system
HP:0002716	Lymphadenopathy
HP:0002718	Recurrent bacterial infections
HP:0002719	Recurrent infections
HP:0002720	IgA deficiency
HP:0002732	Lymph node hypoplasia
HP:0002733	Abnormality of the lymph nodes
HP:0002745	Oral leukoplakia
HP:0002748	Rickets
HP:0002749	Osteomalacia
HP:0002751	Kyphoscoliosis
HP:0002753	Thin bony cortex
HP:0002754	Osteomyelitis
HP:0002758	Osteoarthritis
HP:0002763	Abnormal cartilage morphology
HP:0002766	Relatively short spine
HP:0002777	Tracheal stenosis
HP:0002779	Tracheomalacia
HP:0002789	Tachypnea
HP:0002791	Hypoventilation
HP:0002795	Functional respiratory abnormality
HP:0002797	Osteolysis
HP:0002808	Kyphosis
HP:0002813	Abnormality of limb bone morphology
HP:0002823	Abnormality of femur morphology
HP:0002835	Aspiration
HP:0002836	Bladder exstrophy
HP:0002840	Lymphadenitis
HP:0002846	Abnormality of B cells
HP:0002849	Absence of lymph node germinal center
HP:0002850	IgM deficiency
HP:0002858	Meningioma
HP:0002859	Rhabdomyosarcoma
HP:0002860	Squamous cell carcinoma
HP:0002861	Melanoma
HP:0002883	Hyperventilation
HP:0002884	Hepatoblastoma
HP:0002885	Medulloblastoma
HP:0002894	Neoplasm of the pancreas
HP:0002900	Hypokalemia
HP:0002901	Hypocalcemia
HP:0002902	Hyponatremia
HP:0002904	Hyperbilirubinemia
HP:0002905	Hyperphosphatemia
HP:0002910	Elevated hepatic transaminases
HP:0002913	Myoglobinuria
HP:0002914	Hyperchloriduria
HP:0002917	Hypomagnesemia
HP:0002918	Hypermagnesemia
HP:0002919	Ketonuria
HP:0002920	Decreased circulating ACTH level
HP:0002924	obsolete Decreased circulating aldosterone level
HP:0002926	Abnormality of thyroid physiology
HP:0002927	Histidinuria
HP:0002937	Hemivertebrae
HP:0002948	Vertebral fusion
HP:0002949	Fused cervical vertebrae
HP:0002953	Vertebral compression fractures
HP:0002960	Autoimmunity
HP:0002980	Femoral bowing
HP:0002982	Tibial bowing
HP:0002983	Micromelia
HP:0002984	Hypoplasia of the radius
HP:0002986	Radial bowing
HP:0002990	Fibular aplasia
HP:0002991	Abnormality of fibula morphology
HP:0002992	Abnormality of tibia morphology
HP:0003006	Neuroblastoma
HP:0003010	Prolonged bleeding time
HP:0003022	Hypoplasia of the ulna
HP:0003026	Short long bone
HP:0003031	Ulnar bowing
HP:0003038	Fibular hypoplasia
HP:0003072	Hypercalcemia
HP:0003073	Hypoalbuminemia
HP:0003074	Hyperglycemia
HP:0003075	Hypoproteinemia
HP:0003076	Glycosuria
HP:0003077	Hyperlipidemia
HP:0003081	Increased urinary potassium
HP:0003085	Long fibula
HP:0003097	Short femur
HP:0003100	Slender long bone
HP:0003103	Abnormal cortical bone morphology
HP:0003107	Abnormality of cholesterol metabolism
HP:0003109	Hyperphosphaturia
HP:0003110	Abnormality of urine homeostasis
HP:0003111	Abnormality of ion homeostasis
HP:0003112	Abnormality of serum amino acid levels
HP:0003113	Hypochloremia
HP:0003115	Abnormal EKG
HP:0003117	Abnormality of circulating hormone level
HP:0003118	Increased circulating cortisol level
HP:0003119	Abnormality of lipid metabolism
HP:0003124	Hypercholesterolemia
HP:0003127	Hypocalciuria
HP:0003131	Cystinuria
HP:0003134	Abnormality of peripheral nerve conduction
HP:0003138	Increased blood urea nitrogen
HP:0003141	Hyperbetalipoproteinemia
HP:0003146	Hypocholesterolemia
HP:0003149	Hyperuricosuria
HP:0003154	Increased circulating ACTH level
HP:0003159	Hyperoxaluria
HP:0003166	Increased urinary taurine
HP:0003173	Hypoplastic pubic bone
HP:0003175	Hypoplastic ischia
HP:0003187	Breast hypoplasia
HP:0003189	Long nose
HP:0003194	Short nasal bridge
HP:0003196	Short nose
HP:0003198	Myopathy
HP:0003202	Skeletal muscle atrophy
HP:0003207	Arterial calcification
HP:0003212	Increased IgE level
HP:0003218	Oroticaciduria
HP:0003228	Hypernatremia
HP:0003231	Hypertyrosinemia
HP:0003233	Hypoalphalipoproteinemia
HP:0003234	Decreased plasma carnitine
HP:0003236	Elevated serum creatine phosphokinase
HP:0003237	Increased IgG level
HP:0003250	Aplasia of the vagina
HP:0003251	Male infertility
HP:0003254	Abnormality of DNA repair
HP:0003259	Elevated serum creatinine
HP:0003261	Increased IgA level
HP:0003270	Abdominal distention
HP:0003271	Visceromegaly
HP:0003292	Decreased serum leptin
HP:0003296	Hyperthreoninuria
HP:0003297	Hyperlysinuria
HP:0003298	Spina bifida occulta
HP:0003307	Hyperlordosis
HP:0003310	Abnormality of the odontoid process
HP:0003323	Progressive muscle weakness
HP:0003330	Abnormal bone structure
HP:0003351	Decreased circulating renin level
HP:0003355	Aminoaciduria
HP:0003362	Increased circulating very-low-density lipoprotein cholesterol
HP:0003363	Abdominal situs inversus
HP:0003396	Syringomyelia
HP:0003429	CNS hypomyelination
HP:0003464	Abnormal cholesterol homeostasis
HP:0003468	Abnormality of the vertebrae
HP:0003470	Paralysis
HP:0003496	Increased IgM level
HP:0003527	Hyperprostaglandinuria
HP:0003532	Ornithinuria
HP:0003537	Hypouricemia
HP:0003540	Impaired platelet aggregation
HP:0003541	Urinary glycosaminoglycan excretion
HP:0003560	Muscular dystrophy
HP:0003641	Hemoglobinuria
HP:0003646	Bicarbonaturia
HP:0003687	Centrally nucleated skeletal muscle fibers
HP:0003712	Skeletal muscle hypertrophy
HP:0003750	Increased muscle fatiguability
HP:0003758	Reduced subcutaneous adipose tissue
HP:0003761	Calcinosis
HP:0003765	Psoriasiform dermatitis
HP:0003808	Abnormal muscle tone
HP:0003811	Neonatal death
HP:0003826	Stillbirth
HP:0003862	Absent humerus
HP:0003865	Bowed humerus
HP:0003974	Absent radius
HP:0003982	Aplasia of the ulna
HP:0003988	Long ulna
HP:0004099	Macrodactyly
HP:0004231	Carpal bone aplasia
HP:0004295	Abnormality of the gastric mucosa
HP:0004298	Abnormality of the abdominal wall
HP:0004303	Abnormality of muscle fibers
HP:0004311	Abnormality of macrophages
HP:0004312	Abnormality of reticulocytes
HP:0004313	Decreased antibody level in blood
HP:0004315	IgG deficiency
HP:0004322	Short stature
HP:0004323	Abnormality of body weight
HP:0004324	Increased body weight
HP:0004325	Decreased body weight
HP:0004326	Cachexia
HP:0004332	Abnormality of lymphocytes
HP:0004337	Abnormality of amino acid metabolism
HP:0004348	Abnormality of bone mineral density
HP:0004361	Abnormality of circulating leptin level
HP:0004362	Abnormality of enteric ganglion morphology
HP:0004370	Abnormality of temperature regulation
HP:0004378	Abnormality of the anus
HP:0004380	Aortic valve calcification
HP:0004382	Mitral valve calcification
HP:0004386	Gastrointestinal inflammation
HP:0004398	Peptic ulcer
HP:0004401	Meconium ileus
HP:0004408	Abnormality of the sense of smell
HP:0004414	Abnormality of the pulmonary artery
HP:0004415	Pulmonary artery stenosis
HP:0004422	Biparietal narrowing
HP:0004444	Spherocytosis
HP:0004445	Elliptocytosis
HP:0004446	Stomatocytosis
HP:0004447	Poikilocytosis
HP:0004484	Craniofacial asymmetry
HP:0004510	Pancreatic islet-cell hyperplasia
HP:0004646	Hypoplasia of the nasal bone
HP:0004727	Impaired renal concentrating ability
HP:0004756	Ventricular tachycardia
HP:0004762	Hypoplasia of right ventricle
HP:0004783	Duodenal polyposis
HP:0004791	Esophageal ulceration
HP:0004823	Anisopoikilocytosis
HP:0004836	Acute promyelocytic leukemia
HP:0004840	Hypochromic microcytic anemia
HP:0004857	Hyperchromic macrocytic anemia
HP:0004871	Perineal fistula
HP:0004890	Elevated pulmonary artery pressure
HP:0004927	Pulmonary artery dilatation
HP:0004942	Aortic aneurysm
HP:0004960	Absent pulmonary artery
HP:0004962	Thoracic aorta calcification
HP:0004963	Calcification of the aorta
HP:0004971	Pulmonary artery hypoplasia
HP:0005102	Cochlear degeneration
HP:0005105	Abnormal nasal morphology
HP:0005110	Atrial fibrillation
HP:0005111	Dilatation of the ascending aorta
HP:0005133	Right ventricular dilatation
HP:0005145	Coronary artery stenosis
HP:0005156	Hypoplastic left atrium
HP:0005160	Total anomalous pulmonary venous return
HP:0005164	Dysplastic pulmonary valve
HP:0005165	Shortened PR interval
HP:0005180	Tricuspid regurgitation
HP:0005182	Bicuspid pulmonary valve
HP:0005207	Gastric hypertrophy
HP:0005213	Pancreatic calcification
HP:0005214	Intestinal obstruction
HP:0005222	Bowel diverticulosis
HP:0005225	Intestinal edema
HP:0005237	Degenerative liver disease
HP:0005261	Joint hemorrhage
HP:0005263	Gastritis
HP:0005266	Intestinal polyp
HP:0005273	Absent nasal septal cartilage
HP:0005303	Aortic arch calcification
HP:0005317	Increased pulmonary vascular resistance
HP:0005326	Hypoplastic philtrum
HP:0005343	Hypoplasia of the bladder
HP:0005359	Aplasia of the thymus
HP:0005365	Severe B lymphocytopenia
HP:0005403	Decrease in T cell count
HP:0005404	Increase in B cell number
HP:0005415	Decreased number of CD8+ T cells
HP:0005466	Hypoplasia of the frontal bone
HP:0005473	Fusion of middle ear ossicles
HP:0005479	IgE deficiency
HP:0005506	Chronic myelogenous leukemia
HP:0005513	Increased megakaryocyte count
HP:0005518	Increased mean corpuscular volume
HP:0005528	Bone marrow hypocellularity
HP:0005537	Decreased mean platelet volume
HP:0005548	Megakaryocytopenia
HP:0005563	Decreased numbers of nephrons
HP:0005576	Tubulointerstitial fibrosis
HP:0005580	Duplication of renal pelvis
HP:0005645	Intervertebral disk calcification
HP:0005736	Short tibia
HP:0005792	Short humerus
HP:0005815	Supernumerary ribs
HP:0005922	Abnormal hand morphology
HP:0005938	Abnormal respiratory motile cilium morphology
HP:0005990	Thyroid hypoplasia
HP:0006000	Ureteral obstruction
HP:0006254	Elevated alpha-fetoprotein
HP:0006266	Small placenta
HP:0006267	Large placenta
HP:0006270	Hypoplastic spleen
HP:0006274	Reduced pancreatic beta cells
HP:0006277	Pancreatic hyperplasia
HP:0006280	Chronic pancreatitis
HP:0006288	Advanced eruption of teeth
HP:0006292	Abnormality of dental eruption
HP:0006297	Hypoplasia of dental enamel
HP:0006424	Elongated radius
HP:0006426	Rudimentary to absent tibiae
HP:0006443	Patellar aplasia
HP:0006482	Abnormality of dental morphology
HP:0006485	Agenesis of incisor
HP:0006487	Bowing of the long bones
HP:0006515	Interstitial pneumonitis
HP:0006517	Alveolar proteinosis
HP:0006548	Pulmonary arteriovenous malformation
HP:0006560	Biliary hyperplasia
HP:0006568	Increased hepatic glycogen content
HP:0006660	Aplastic clavicles
HP:0006682	Ventricular extrasystoles
HP:0006690	Myocardial calcification
HP:0006693	Myocardial steatosis
HP:0006698	Dilatation of the ventricular cavity
HP:0006739	Squamous cell carcinoma of the skin
HP:0006771	Duodenal adenocarcinoma
HP:0006827	Atrophy of the spinal cord
HP:0006872	Cerebral hypoplasia
HP:0006891	Thick cerebral cortex
HP:0006956	Dilation of lateral ventricles
HP:0006958	Abnormal auditory evoked potentials
HP:0006989	Dysplastic corpus callosum
HP:0007027	Poorly formed metencephalon
HP:0007033	Cerebellar dysplasia
HP:0007082	Dilated third ventricle
HP:0007265	Absent mesencephalon
HP:0007343	Abnormal morphology of the limbic system
HP:0007430	Generalized edema
HP:0007485	Absence of subcutaneous fat
HP:0007544	Piebaldism
HP:0007656	Lacrimal gland aplasia
HP:0007670	Abnormal vestibulo-ocular reflex
HP:0007676	Hypoplasia of the iris
HP:0007703	Abnormality of retinal pigmentation
HP:0007734	Enlarged lacrimal glands
HP:0007770	Hypoplasia of the retina
HP:0007772	Impaired smooth pursuit
HP:0007774	Hypoplasia of the ciliary body
HP:0007787	Posterior subcapsular cataract
HP:0007795	Anterior cortical cataract
HP:0007862	Retinal calcification
HP:0007957	Corneal opacity
HP:0007968	Remnants of the hyaloid vascular system
HP:0007971	Lamellar cataract
HP:0007973	Retinal dysplasia
HP:0007990	Hypoplastic iris stroma
HP:0008034	Abnormal iris pigmentation
HP:0008063	Aplasia/Hypoplasia of the lens
HP:0008070	Sparse hair
HP:0008151	Prolonged prothrombin time
HP:0008163	Decreased circulating cortisol level
HP:0008165	Reduced circulating T-helper cells
HP:0008188	Thyroid dysgenesis
HP:0008191	Thyroid agenesis
HP:0008208	Parathyroid hyperplasia
HP:0008216	Adrenal gland dysgenesis
HP:0008221	Adrenal hyperplasia
HP:0008222	Female infertility
HP:0008232	Elevated follicle stimulating hormone
HP:0008239	Adrenal medullary hypoplasia
HP:0008247	Euthyroid hyperthyroxinemia
HP:0008249	Thyroid hyperplasia
HP:0008277	Abnormality of zinc homeostasis
HP:0008322	Abnormal mitochondrial morphology
HP:0008364	Abnormality of the calcaneus
HP:0008368	Tarsal synostosis
HP:0008372	Abnormality of vitamin A metabolism
HP:0008404	Nail dystrophy
HP:0008417	Vertebral hypoplasia
HP:0008419	Intervertebral disc degeneration
HP:0008428	Vertebral clefting
HP:0008465	Absent vertebra
HP:0008516	Abnormality of the vertebral spinous processes
HP:0008551	Microtia
HP:0008609	Morphological abnormality of the middle ear
HP:0008628	Abnormality of the stapes
HP:0008665	Clitoral hypertrophy
HP:0008669	Abnormal spermatogenesis
HP:0008682	Acute tubular necrosis
HP:0008687	Hypoplasia of the prostate
HP:0008696	Renal hamartoma
HP:0008697	Hypoplasia of the fallopian tube
HP:0008707	Absent scrotum
HP:0008711	Benign prostatic hyperplasia
HP:0008724	Hypoplasia of the ovary
HP:0008726	Hypoplasia of the vagina
HP:0008734	Decreased testicular size
HP:0008753	Aplasia of the epiglottis
HP:0008817	Aplastic pubic bones
HP:0008873	Disproportionate short-limb short stature
HP:0008887	Adipose tissue loss
HP:0008986	Agenesis of the diaphragm
HP:0009004	Hypoplasia of the musculature
HP:0009121	Abnormal axial skeleton morphology
HP:0009124	Abnormality of adipose tissue
HP:0009125	Lipodystrophy
HP:0009380	Aplasia of the fingers
HP:0009555	Hypoplasia of the pharynx
HP:0009591	Abnormality of the vestibulocochlear nerve
HP:0009701	Metacarpal synostosis
HP:0009702	Carpal synostosis
HP:0009720	Adenoma sebaceum
HP:0009730	Rhabdomyoma
HP:0009733	Glioma
HP:0009741	Nephrosclerosis
HP:0009792	Teratoma
HP:0009794	Branchial anomaly
HP:0009803	Short phalanx of finger
HP:0009887	Abnormality of hair pigmentation
HP:0009892	Anotia
HP:0009893	Telangiectasia of the ear
HP:0009894	Thickened ears
HP:0009900	Unilateral deafness
HP:0009910	Aplasia of the middle ear ossicles
HP:0009914	Cyclopia
HP:0009916	Anisocoria
HP:0009918	Ectopia pupillae
HP:0009919	Retinoblastoma
HP:0009922	Vascular remnant arising from the disc
HP:0009927	Aplasia of the nose
HP:0009932	Single naris
HP:0009933	Narrow naris
HP:0010048	Aplasia of metacarpal bones
HP:0010049	Short metacarpal
HP:0010286	Abnormality of the salivary glands
HP:0010290	Short hard palate
HP:0010296	Ankyloglossia
HP:0010297	Bifid tongue
HP:0010299	Abnormality of dentin
HP:0010307	Stridor
HP:0010309	Bifid sternum
HP:0010310	Chylothorax
HP:0010316	Ebstein's anomaly of the tricuspid valve
HP:0010317	Scapular aplasia
HP:0010442	Polydactyly
HP:0010444	Pulmonary insufficiency
HP:0010445	Primum atrial septal defect
HP:0010446	Tricuspid stenosis
HP:0010459	True hermaphroditism
HP:0010463	Aplasia of the ovary
HP:0010493	Long metacarpals
HP:0010497	Sirenomelia
HP:0010504	Increased length of the tibia
HP:0010516	Thymus hyperplasia
HP:0010537	Wide cranial sutures
HP:0010605	Chalazion
HP:0010614	Fibroma
HP:0010626	Anterior pituitary agenesis
HP:0010627	Anterior pituitary hypoplasia
HP:0010648	Dermal translucency
HP:0010650	Hypoplasia of the premaxilla
HP:0010651	Abnormality of the meninges
HP:0010663	Abnormality of thalamus morphology
HP:0010679	Elevated tissue non-specific alkaline phosphatase
HP:0010683	Low tissue non-specific alkaline phosphatase
HP:0010695	Sutural cataract
HP:0010696	Polar cataract
HP:0010700	Total cataract
HP:0010701	Abnormal immunoglobulin level
HP:0010702	Increased antibody level in blood
HP:0010719	Abnormality of hair texture
HP:0010728	Aplasia of the retina
HP:0010743	Short metatarsal
HP:0010757	Aplasia of the premaxilla
HP:0010758	Abnormality of the premaxilla
HP:0010764	Short eyelashes
HP:0010772	Anomalous pulmonary venous return
HP:0010775	Vascular ring
HP:0010783	Erythema
HP:0010784	Uterine neoplasm
HP:0010789	Abnormality of the Leydig cells
HP:0010790	Hyoplasia of the Leydig cells
HP:0010791	Hyperplasia of the Leydig cells
HP:0010799	Pinealoma
HP:0010808	Protruding tongue
HP:0010824	Abnormality of the fifth cranial nerve
HP:0010826	Abnormality of the twelfth cranial nerve
HP:0010827	Abnormality of the seventh cranial nerve
HP:0010831	Impaired proprioception
HP:0010836	Abnormality of copper homeostasis
HP:0010876	Abnormality of circulating protein level
HP:0010882	Pulmonary valve atresia
HP:0010883	Aortic valve atresia
HP:0010906	Hyperhistidinemia
HP:0010923	Anterior subcapsular cataract
HP:0010975	Abnormality of B cell number
HP:0010976	B lymphocytopenia
HP:0010978	Abnormality of immune system physiology
HP:0010987	Abnormality of cellular immune system
HP:0010999	Aplasia of the optic tract
HP:0011001	Increased bone mineral density
HP:0011002	Osteopetrosis
HP:0011014	Abnormal glucose homeostasis
HP:0011015	Abnormality of blood glucose concentration
HP:0011017	Abnormality of cell physiology
HP:0011018	Abnormality of the cell cycle
HP:0011021	Abnormality of circulating enzyme level
HP:0011025	Abnormality of cardiovascular system physiology
HP:0011028	Abnormality of blood circulation
HP:0011029	Internal hemorrhage
HP:0011031	Abnormality of iron homeostasis
HP:0011032	Abnormality of fluid regulation
HP:0011034	Amyloidosis
HP:0011037	Decreased urine output
HP:0011054	Agenesis of molar
HP:0011063	Abnormality of incisor morphology
HP:0011068	Odontoma
HP:0011069	Increased number of teeth
HP:0011070	Abnormality of molar morphology
HP:0011073	Abnormality of dental color
HP:0011096	Peripheral demyelination
HP:0011102	Ileal atresia
HP:0011105	Hypervolemia
HP:0011106	Hypovolemia
HP:0011111	Abnormality of immune serum protein physiology
HP:0011113	Abnormality of cytokine secretion
HP:0011115	Abnormality of chemokine secretion
HP:0011116	Abnormality of interferon secretion
HP:0011117	Abnormality of interleukin secretion
HP:0011118	Abnormality of tumor necrosis factor secretion
HP:0011121	Abnormality of skin morphology
HP:0011122	Abnormality of skin physiology
HP:0011123	Inflammatory abnormality of the skin
HP:0011124	Abnormality of epidermal morphology
HP:0011130	Abnormality of renal calyx morphology
HP:0011136	Aplasia of the sweat glands
HP:0011138	Abnormality of skin adnexa morphology
HP:0011224	Ablepharon
HP:0011273	Anisocytosis
HP:0011280	Abnormality of urine calcium concentration
HP:0011281	Abnormality of urine catecholamine concentration
HP:0011282	Abnormality of hindbrain morphology
HP:0011297	Abnormality of digit
HP:0011314	Abnormality of long bone morphology
HP:0011323	Cleft of chin
HP:0011329	Abnormality of cranial sutures
HP:0011359	Dry hair
HP:0011372	Aplasia of the inner ear
HP:0011373	Incomplete partition of the cochlea
HP:0011375	Cochlear aplasia
HP:0011376	Morphological abnormality of the vestibule of the inner ear
HP:0011377	Aplasia of the vestibule
HP:0011380	Morphological abnormality of the semicircular canal
HP:0011381	Aplasia of the semicircular canal
HP:0011390	Morphological abnormality of the inner ear
HP:0011393	Aplasia of the vestibular nerve.
HP:0011423	Hyperchloremia
HP:0011441	Abnormality of the medulla oblongata
HP:0011455	Absent malleus
HP:0011456	Absent stapes
HP:0011457	Loss of eyelashes
HP:0011467	Absent gallbladder
HP:0011472	Abnormality of small intestinal villus morphology
HP:0011473	Villous atrophy
HP:0011483	Anterior synechiae of the anterior chamber
HP:0011484	Posterior synechiae of the anterior chamber
HP:0011486	Abnormality of corneal thickness
HP:0011487	Increased corneal thickness
HP:0011490	Abnormality of Descemet's membrane
HP:0011496	Corneal neovascularization
HP:0011499	Mydriasis
HP:0011536	Right atrial isomerism
HP:0011537	Left atrial isomerism
HP:0011538	Atrial situs inversus
HP:0011555	Double inlet left ventricle
HP:0011560	Mitral atresia
HP:0011565	Common atrium
HP:0011573	Hypoplastic tricuspid valve
HP:0011581	Double outlet left ventricle
HP:0011588	Cervical aortic arch
HP:0011590	Double aortic arch
HP:0011599	Mesocardia
HP:0011604	Aortopulmonary window
HP:0011611	Interrupted aortic arch
HP:0011613	Interrupted aortic arch type B
HP:0011616	Pulmonary situs inversus
HP:0011622	Inlet ventricular septal defect
HP:0011623	Muscular ventricular septal defect
HP:0011641	Coronary artery fistula
HP:0011645	Dilatation of the sinus of Valsalva
HP:0011675	Arrhythmia
HP:0011681	Subarterial ventricular septal defect
HP:0011682	Perimembranous ventricular septal defect
HP:0011710	Bundle branch block
HP:0011718	Abnormality of the pulmonary veins
HP:0011729	Abnormality of joint mobility
HP:0011733	Abnormality of adrenal physiology
HP:0011742	Ectopic adrenal gland
HP:0011756	Posterior pituitary agenesis
HP:0011788	Increased serum free triiodothyronine
HP:0011800	Midface retrusion
HP:0011801	Enlargement of parotid gland
HP:0011804	Abnormality of muscle physiology
HP:0011805	Abnormality of muscle morphology
HP:0011839	Abnormality of T cell count
HP:0011840	Abnormality of T cell physiology
HP:0011842	Abnormality of skeletal morphology
HP:0011844	Abnormal appendicular skeleton morphology
HP:0011849	Abnormal bone ossification
HP:0011850	Parotitis
HP:0011851	Hemopericardium
HP:0011854	Hemoperitoneum
HP:0011862	Abnormal bone collagen fibril morphology
HP:0011869	Abnormal platelet function
HP:0011875	Abnormal platelet morphology
HP:0011877	Increased mean platelet volume
HP:0011885	Hemorrhage of the eye
HP:0011893	Abnormal leukocyte count
HP:0011902	Abnormal hemoglobin
HP:0011935	Decreased urinary urate
HP:0011969	Elevated luteinizing hormone
HP:0011970	Cerebral amyloid angiopathy
HP:0011974	Myelofibrosis
HP:0011990	Abnormality of neutrophil physiology
HP:0011992	Abnormality of neutrophil morphology
HP:0011995	Atrial septal dilatation
HP:0012020	Right aortic arch
HP:0012050	Anasarca
HP:0012068	Aspartylglucosaminuria
HP:0012072	Aciduria
HP:0012081	Enlarged cerebellum
HP:0012085	Pyuria
HP:0012086	Abnormal urinary color
HP:0012087	Abnormal mitochondrial shape
HP:0012089	Arteritis
HP:0012090	Abnormality of pancreas morphology
HP:0012091	Abnormality of pancreas physiology
HP:0012092	Abnormality of exocrine pancreas physiology
HP:0012093	Abnormality of endocrine pancreas physiology
HP:0012094	Abnormal pancreas size
HP:0012099	Abnormality of circulating catecholamine level
HP:0012100	Abnormal circulating creatinine level
HP:0012101	Decreased serum creatinine
HP:0012107	Increased fibular diameter
HP:0012112	Abnormality of circulating corticosterone level
HP:0012114	Endometrial carcinoma
HP:0012115	Hepatitis
HP:0012116	Abnormal albumin level
HP:0012117	Hyperalbuminemia
HP:0012132	Erythroid hyperplasia
HP:0012133	Erythroid hypoplasia
HP:0012151	Hemothorax
HP:0012153	Hypotriglyceridemia
HP:0012154	Anhedonia
HP:0012165	Oligodactyly
HP:0012167	Hair-pulling
HP:0012176	Abnormality of natural killer cells
HP:0012177	Abnormal natural killer cell physiology
HP:0012184	Hyperalphalipoproteinemia
HP:0012197	Insulinoma
HP:0012205	Globozoospermia
HP:0012206	Abnormal sperm motility
HP:0012211	Abnormal renal physiology
HP:0012213	Decreased glomerular filtration rate
HP:0012226	Ovarian teratoma
HP:0012232	Shortened QT interval
HP:0012238	Hyperchylomicronemia
HP:0012243	Abnormal genital system morphology
HP:0012244	Abnormal sex determination
HP:0012245	Sex reversal
HP:0012248	Prolonged PR interval
HP:0012249	Abnormal ST segment
HP:0012252	Abnormal respiratory system morphology
HP:0012253	Abnormal respiratory epithelium morphology
HP:0012261	Abnormal respiratory motile cilium physiology
HP:0012269	Abnormal muscle glycogen content
HP:0012281	Chylous ascites
HP:0012285	Abnormal hypothalamus physiology
HP:0012286	Abnormal hypothalamus morphology
HP:0012303	Abnormality of the aortic arch
HP:0012304	Hypoplastic aortic arch
HP:0012310	Abnormal monocyte count
HP:0012311	Monocytosis
HP:0012312	Monocytopenia
HP:0012330	Pyelonephritis
HP:0012331	Abnormal autonomic nervous system morphology
HP:0012332	Abnormal autonomic nervous system physiology
HP:0012337	Abnormal homeostasis
HP:0012338	Abnormal energy expenditure
HP:0012364	Decreased urinary potassium
HP:0012368	Flat face
HP:0012372	Abnormal eye morphology
HP:0012373	Abnormal eye physiology
HP:0012378	Fatigue
HP:0012379	Abnormal enzyme/coenzyme activity
HP:0012384	Rhinitis
HP:0012385	Camptodactyly
HP:0012386	Absent hallux
HP:0012415	Abnormal blood gas level
HP:0012416	Hypercapnia
HP:0012417	Hypocapnia
HP:0012418	Hypoxemia
HP:0012437	Abnormal gallbladder morphology
HP:0012438	Abnormal gallbladder physiology
HP:0012440	Abnormal biliary tract morphology
HP:0012443	Abnormality of brain morphology
HP:0012444	Brain atrophy
HP:0012447	Abnormal myelination
HP:0012450	Chronic constipation
HP:0012465	Elevated hepatic iron concentration
HP:0012471	Thick vermilion border
HP:0012472	Eclabion
HP:0012490	Panniculitis
HP:0012503	Abnormality of the pituitary gland
HP:0012505	Enlarged pituitary gland
HP:0012506	Small pituitary gland
HP:0012517	Reduced catalase activity
HP:0012521	Optic nerve aplasia
HP:0012524	Abnormal platelet shape
HP:0012533	Allodynia
HP:0012535	Abnormal synaptic transmission
HP:0012543	Hemosiderinuria
HP:0012569	Delayed menarche
HP:0012585	Renal atrophy
HP:0012590	Abnormal urine output
HP:0012592	Albuminuria
HP:0012594	Microalbuminuria
HP:0012598	Abnormal urine potassium concentration
HP:0012599	Abnormal urine phosphate concentration
HP:0012601	Hypochloriduria
HP:0012603	Abnormal urine sodium concentration
HP:0012608	Hypermagnesiuria
HP:0012609	Hypomagnesiuria
HP:0012611	Increased urinary urate
HP:0012613	Increased urinary sulfate
HP:0012621	Persistent cloaca
HP:0012632	Abnormal intraocular pressure
HP:0012638	Abnormality of nervous system physiology
HP:0012639	Abnormality of nervous system morphology
HP:0012647	Abnormal inflammatory response
HP:0012648	Decreased inflammatory response
HP:0012649	Increased inflammatory response
HP:0012673	Aplasia of the upper vagina
HP:0012675	Iron accumulation in brain
HP:0012676	Copper accumulation in brain
HP:0012680	Abnormality of the pineal gland
HP:0012688	Abnormality of pineal physiology
HP:0012722	Heart block
HP:0012723	Sinoatrial block
HP:0012731	Ectopic anterior pituitary gland
HP:0012744	Femoral aplasia
HP:0012757	Abnormal neuron morphology
HP:0012767	Abnormal placental size
HP:0012776	Abnormality of the ciliary body
HP:0012790	Abnormal intramembranous ossification
HP:0012795	Abnormality of the optic disc
HP:0012804	Corneal ulceration
HP:0012806	Proboscis
HP:0012819	Myocarditis
HP:0012861	Ovotestis
HP:0012862	Abnormal germ cell morphology
HP:0012863	Abnormal male germ cell morphology
HP:0012864	Abnormal sperm morphology
HP:0012872	Abnormal vas deferens morphology
HP:0012873	Absent vas deferens
HP:0012874	Abnormal male reproductive system physiology
HP:0012875	Abnormal ejaculation
HP:0020006	Ciliary body coloboma
HP:0025016	Abnormal capillary morphology
HP:0025028	Abnormality of enteric nervous system morphology
HP:0025057	Abnormality of olfactory lobe morphology
HP:0025100	Abnormal morphology of the hippocampus
HP:0025321	Copper accumulation in liver
HP:0030010	Hydrometrocolpos
HP:0030011	Imperforate hymen
HP:0030012	Abnormal female reproductive system physiology
HP:0030037	Bifid ureter
HP:0030039	Fused thoracic vertebrae
HP:0030040	Fused lumbar vertebrae
HP:0030047	Abnormality of lateral ventricle
HP:0030050	Narcolepsy
HP:0030075	Ductal carcinoma in situ
HP:0030078	Lung adenocarcinoma
HP:0030082	Abnormal drinking behavior
HP:0030084	Clinodactyly
HP:0030087	Abnormal serum testosterone level
HP:0030088	Increased serum testosterone level
HP:0030146	Abnormal liver parenchyma morphology
HP:0030151	Cholangitis
HP:0030160	Cervicitis
HP:0030187	Titubation
HP:0030191	Abnormal peripheral nervous system synaptic transmission
HP:0030276	Small scrotum
HP:0030277	Abnormal vertebral pedicle morphology
HP:0030301	Abnormality of the anterior commissure
HP:0030304	Abnormal number of vertebrae
HP:0030305	Decreased number of vertebrae
HP:0030313	Abnormal periosteum morphology
HP:0030332	Abnormal T cell morphology
HP:0030333	Abnormal alpha-beta T cell morphology
HP:0030334	Abnormal CD4-positive, CD25-positive, alpha-beta regulatory T cell morphology
HP:0030338	Abnormal circulating gonadotropin level
HP:0030339	Decreased circulating gonadotropin level
HP:0030341	Decreased circulating follicle stimulating hormone level
HP:0030344	Decreased circulating luteinizing hormone level
HP:0030345	Abnormal circulating luteinizing hormone level
HP:0030358	Non-small cell lung carcinoma
HP:0030359	Squamous cell lung carcinoma
HP:0030424	Epididymal cyst
HP:0030431	Osteochondroma
HP:0030434	Pilomatrixoma
HP:0030439	Anal canal adenocarcinoma
HP:0030666	Retinal neovascularization
HP:0030680	Abnormality of cardiovascular system morphology
HP:0030681	Abnormal morphology of myocardial trabeculae
HP:0030683	Vaginitis
HP:0030684	Abnormal adiponectin level
HP:0030685	Decreased adiponectin level
HP:0030686	Increased adiponectin level
HP:0030687	Abnormal glucagon level
HP:0030692	Brain neoplasm
HP:0030716	Acrania
HP:0030718	Right atrial enlargement
HP:0030731	Carcinoma
HP:0030732	Dysplastic tricuspid valve
HP:0030735	Ureterovesical junction obstruction
HP:0030746	Intraventricular hemorrhage
HP:0030759	Adipocyte hypertrophy
HP:0030760	Renal fibrosis
HP:0030761	obsolete Renal glomerular fibrosis
HP:0030762	Mesangiolysis
HP:0030769	Exencephaly
HP:0030770	Craniorachischisis
HP:0030781	Increased circulating free fatty acid level
HP:0030791	Abnormal jaw morphology
HP:0030809	Abnormal tongue morphology
HP:0030853	Heterotaxy
HP:0030875	Abnormality of pulmonary circulation
HP:0030971	Abnormal vena cava morphology
HP:0031066	Abnormal ovarian physiology
HP:0040006	Mortality/Aging
HP:0040012	Chromosome breakage
HP:0040013	Decreased mitochondrial number
HP:0040014	Increased mitochondrial number
HP:0040071	Abnormal morphology of ulna
HP:0040075	Hypopituitarism
HP:0040077	Abnormal concentration of calcium in blood
HP:0040084	Abnormal circulating renin
HP:0040085	Abnormal circulating aldosterone
HP:0040086	Abnormal prolactin level
HP:0040088	Abnormal lymphocyte count
HP:0040100	Abnormality of the vestibular window
HP:0040106	Morphological abnormality of the lateral semicircular canal
HP:0040107	Morphological abnormality of the posterior semicircular canal
HP:0040109	Morphological abnormality of the utricle
HP:0040110	Morphological abnormality of the saccule
HP:0040115	Abnormality of the Eustachian tube
HP:0040116	Aplasia of the Eustachian tube
HP:0040134	Abnormal hepatic iron concentration
HP:0040162	Orthokeratosis
HP:0040170	Abnormality of hair growth
HP:0040171	Decreased serum testosterone level
HP:0040176	Abnormal level of phospholipids
HP:0040181	Chapped lip
HP:0040189	Scaling skin
HP:0040194	Increased head circumference
HP:0040206	Abnormal level of neopterin
HP:0040210	Abnormal level of biopterin
HP:0040213	Hypopnea
HP:0040215	Abnormal circulating insulin level
HP:0040216	Hypoinsulinemia
HP:0040217	Elevated hemoglobin A1c
HP:0040218	Reduced natural killer cell number
HP:0040219	Absent natural killer cells
HP:0040238	Impaired neutrophil chemotaxis
HP:0040273	Adenocarcinoma of the intestines
HP:0040274	Adenocarcinoma of the small intestine
HP:0040275	Adenocarcinoma of the large intestine
HP:0040276	Adenocarcinoma of the colon
HP:0040298	Hyperplasia of the endometrium
HP:0040302	Hyperglycerolemia
HP:0040318	Red urine
HP:0040326	Hypoplasia of the olfactory bulb
HP:0045005	Neural tube defect
HP:0045006	Aplasia of lymphatic vessels
HP:0045009	Abnormal morphology of the radius
HP:0045013	Decreased urinary glucose concentration
HP:0045058	Abnormality of the testis size
HP:0100018	Nuclear cataract
HP:0100019	Cortical cataract
HP:0100022	Abnormality of movement
HP:0100026	Arteriovenous malformation
HP:0100240	Synostosis of joints
HP:0100242	Sarcoma
HP:0100243	Leiomyosarcoma
HP:0100244	Fibrosarcoma
HP:0100245	Desmoid tumors
HP:0100246	Osteoma
HP:0100249	Calcification of muscles
HP:0100257	Ectrodactyly
HP:0100258	Preaxial polydactyly
HP:0100259	Postaxial polydactyly
HP:0100261	Abnormal tendon morphology
HP:0100318	Lafora bodies
HP:0100494	Abnormality of mast cells
HP:0100495	Mastocytosis
HP:0100512	Vitamin D deficiency
HP:0100515	Pollakisuria
HP:0100519	Anuria
HP:0100522	Thymoma
HP:0100523	Liver abscess
HP:0100539	Periorbital edema
HP:0100540	Palpebral edema
HP:0100543	Cognitive impairment
HP:0100545	Arterial stenosis
HP:0100547	Abnormality of forebrain morphology
HP:0100577	Urinary bladder inflammation
HP:0100596	Absent nares
HP:0100598	Pulmonary edema
HP:0100604	Neoplasm of the lip
HP:0100614	Myositis
HP:0100615	Ovarian neoplasm
HP:0100616	Testicular teratoma
HP:0100625	Enlarged thorax
HP:0100629	Midline facial cleft
HP:0100633	Esophagitis
HP:0100643	Abnormality of nail color
HP:0100671	Abnormal trabecular bone morphology
HP:0100678	Premature skin wrinkling
HP:0100679	Lack of skin elasticity
HP:0100686	Enthesitis
HP:0100689	Decreased corneal thickness
HP:0100697	Neurofibrosarcoma
HP:0100706	Abnormality of the oligodendroglia
HP:0100710	Impulsivity
HP:0100723	Gastrointestinal stroma tumor
HP:0100731	Transverse facial cleft
HP:0100732	Pancreatic fibrosis
HP:0100736	Abnormality of the soft palate
HP:0100737	Abnormality of the hard palate
HP:0100738	Abnormal eating behavior
HP:0100750	Atelectasis
HP:0100763	Abnormality of the lymphatic system
HP:0100769	Synovitis
HP:0100771	Hypoperistalsis
HP:0100774	Hyperostosis
HP:0100783	Breast aplasia
HP:0100788	Fused lips
HP:0100792	Acantholysis
HP:0100796	Orchitis
HP:0100801	Pancreatic aplasia
HP:0100806	Sepsis
HP:0100827	Lymphocytosis
HP:0100828	Increase in T cell count
HP:0100851	Abnormal emotion/affect behavior
HP:0100852	Abnormal fear/anxiety-related behavior
HP:0100878	Enlarged uterus
HP:0100879	Enlarged ovaries
HP:0100889	Abnormality of the ductus choledochus
HP:0100890	Cyst of the ductus choledochus
HP:0100891	Bifid xiphoid process
HP:0100957	Abnormality of the renal medulla
HP:0100961	Enlarged hippocampus
HP:0200007	Abnormal size of the palpebral fissures
HP:0200023	Priapism
HP:0200037	Skin vesicle
HP:0200042	Skin ulcer
HP:0200057	Marcus Gunn pupil
HP:0200058	Angiosarcoma
HP:0200098	Absent skin pigmentation
HP:0400005	Short ear
HP:0410003	Cleft primary palate
HP:0410005	Cleft hard palate
HP:0410009	Abnormality of the somatic nervous system
HP:0430007	Symblepharon
HP:0430009	Hypoplasia of eyelid
HP:3000002	Abnormal inner ear epithelium morphology
HP:3000047	Abnormality of glossopharyngeal nerve
HP:3000052	Abnormality of hyoid bone
MP:0000005	increased brown adipose tissue amount
MP:0000008	increased white adipose tissue amount
MP:0000010	abnormal abdominal fat pad morphology
MP:0000013	abnormal adipose tissue distribution
MP:0000015	abnormal ear pigmentation
MP:0000020	scaly ears
MP:0000023	abnormal ear position
MP:0000025	otic hypertelorism
MP:0000029	abnormal malleus morphology
MP:0000030	abnormal tympanic ring morphology
MP:0000031	abnormal cochlea morphology
MP:0000033	absent scala media
MP:0000035	abnormal membranous labyrinth morphology
MP:0000039	abnormal otic capsule morphology
MP:0000041	absent endolymphatic duct
MP:0000042	abnormal organ of Corti morphology
MP:0000043	organ of Corti degeneration
MP:0000044	absent organ of Corti
MP:0000045	abnormal hair cell morphology
MP:0000046	abnormal sulcus ampullaris morphology
MP:0000048	abnormal stria vascularis morphology
MP:0000054	delayed ear emergence
MP:0000060	delayed bone ossification
MP:0000064	failure of secondary bone resorption
MP:0000065	abnormal bone marrow cavity morphology
MP:0000071	axial skeleton hypoplasia
MP:0000073	absent craniofacial bones
MP:0000074	abnormal neurocranium morphology
MP:0000075	absent neurocranium
MP:0000077	abnormal interparietal bone morphology
MP:0000078	abnormal supraoccipital bone morphology
MP:0000079	abnormal basioccipital bone morphology
MP:0000080	abnormal exoccipital bone morphology
MP:0000082	overlapping parietal bones
MP:0000084	abnormal fontanelle morphology
MP:0000087	absent mandible
MP:0000088	short mandible
MP:0000091	short premaxilla
MP:0000094	absent alveolar process
MP:0000097	short maxilla
MP:0000098	abnormal vomer bone morphology
MP:0000099	absent vomer bone
MP:0000100	abnormal ethmoidal bone morphology
MP:0000101	absent ethmoidal bone
MP:0000104	abnormal sphenoid bone morphology
MP:0000105	impaired ossification of basisphenoid bone
MP:0000106	abnormal basisphenoid bone morphology
MP:0000107	abnormal frontal bone morphology
MP:0000109	abnormal parietal bone morphology
MP:0000116	abnormal tooth development
MP:0000117	absent tooth primordium
MP:0000118	arrest of tooth development
MP:0000124	absent teeth
MP:0000126	brittle teeth
MP:0000127	degenerate molars
MP:0000128	growth retardation of molars
MP:0000129	ameloblast degeneration
MP:0000131	abnormal long bone epiphysis morphology
MP:0000132	thickened long bone epiphysis
MP:0000133	abnormal long bone metaphysis morphology
MP:0000134	abnormal compact bone thickness
MP:0000136	abnormal microglial cell morphology
MP:0000139	absent vertebral transverse processes
MP:0000140	absent vertebral pedicles
MP:0000141	abnormal vertebral body morphology
MP:0000151	absent ribs
MP:0000152	absent proximal rib
MP:0000155	asymmetric rib joints
MP:0000157	abnormal sternum morphology
MP:0000158	absent sternum
MP:0000159	abnormal xiphoid process morphology
MP:0000164	abnormal cartilage development
MP:0000165	abnormal long bone hypertrophic chondrocyte zone
MP:0000166	abnormal chondrocyte morphology
MP:0000167	decreased chondrocyte number
MP:0000168	abnormal bone marrow development
MP:0000172	abnormal bone marrow cell number
MP:0000175	absent bone marrow cell
MP:0000180	abnormal circulating cholesterol level
MP:0000181	abnormal circulating LDL cholesterol level
MP:0000183	decreased circulating LDL cholesterol level
MP:0000184	abnormal circulating HDL cholesterol level
MP:0000187	abnormal triglyceride level
MP:0000192	abnormal mineral level
MP:0000202	abnormal circulating alkaline phosphatase level
MP:0000203	abnormal circulating aspartate transaminase level
MP:0000208	decreased hematocrit
MP:0000215	absent erythrocytes
MP:0000216	absent erythroid progenitor cell
MP:0000219	increased neutrophil cell number
MP:0000226	abnormal mean corpuscular volume
MP:0000228	abnormal thrombopoiesis
MP:0000229	abnormal megakaryocyte differentiation
MP:0000230	abnormal systemic arterial blood pressure
MP:0000233	abnormal blood flow velocity
MP:0000238	absent pre-B cells
MP:0000239	absent common myeloid progenitor cells
MP:0000242	impaired fertilization
MP:0000245	abnormal erythropoiesis
MP:0000248	macrocytosis
MP:0000249	abnormal blood vessel physiology
MP:0000250	abnormal vasoconstriction
MP:0000255	vasculature congestion
MP:0000256	echinocytosis
MP:0000259	abnormal vascular development
MP:0000260	abnormal angiogenesis
MP:0000262	poor arterial differentiation
MP:0000263	absent organized vascular network
MP:0000264	failure of vascular branching
MP:0000265	atretic vasculature
MP:0000267	abnormal heart development
MP:0000269	abnormal heart looping
MP:0000270	abnormal heart tube morphology
MP:0000275	heart hyperplasia
MP:0000277	abnormal heart shape
MP:0000278	abnormal myocardial fiber morphology
MP:0000279	ventricular hypoplasia
MP:0000280	thin ventricular wall
MP:0000281	abnormal interventricular septum morphology
MP:0000282	abnormal interatrial septum morphology
MP:0000285	abnormal heart valve morphology
MP:0000286	abnormal mitral valve morphology
MP:0000288	abnormal pericardium morphology
MP:0000291	enlarged pericardium
MP:0000292	distended pericardium
MP:0000293	absent myocardial trabeculae
MP:0000295	trabecula carnea hypoplasia
MP:0000296	absent trabeculae carneae
MP:0000297	abnormal atrioventricular cushion morphology
MP:0000298	absent atrioventricular cushions
MP:0000299	failure of atrioventricular cushion closure
MP:0000300	thin atrioventricular cushion
MP:0000301	decreased atrioventricular cushion size
MP:0000313	abnormal cell death
MP:0000316	cellular necrosis
MP:0000321	increased bone marrow cell number
MP:0000322	increased granulocyte number
MP:0000328	increased enterocyte cell number
MP:0000332	hemoglobinemia
MP:0000333	decreased bone marrow cell number
MP:0000334	decreased granulocyte number
MP:0000336	decreased mast cell number
MP:0000339	decreased enterocyte cell number
MP:0000341	abnormal bile color
MP:0000343	altered response to myocardial infarction
MP:0000344	absent Cajal-Retzius cell
MP:0000346	broad head
MP:0000348	abnormal aerobic fitness
MP:0000350	abnormal cell proliferation
MP:0000351	increased cell proliferation
MP:0000352	decreased cell proliferation
MP:0000358	abnormal cell morphology
MP:0000359	abnormal mast cell morphology
MP:0000361	decreased mast cell protease storage
MP:0000362	decreased mast cell histamine storage
MP:0000364	abnormal vascular regression
MP:0000370	head blaze
MP:0000371	diluted coat color
MP:0000372	irregular coat pigmentation
MP:0000373	belly spot
MP:0000376	folliculitis
MP:0000377	abnormal hair follicle morphology
MP:0000378	absent hair follicles
MP:0000379	decreased hair follicle number
MP:0000380	small hair follicles
MP:0000381	enlarged hair follicles
MP:0000382	underdeveloped hair follicles
MP:0000383	abnormal hair follicle orientation
MP:0000384	distorted hair follicle pattern
MP:0000385	distended hair follicles
MP:0000387	disorganized inner root sheath cells
MP:0000388	absent hair follicle inner root sheath
MP:0000389	disorganized outer root sheath cells
MP:0000390	disorganized matrix sheath cells
MP:0000391	premature hair follicle generation
MP:0000392	accelerated hair follicle regression
MP:0000394	absent hair follicle melanin granules
MP:0000396	increased curvature of hairs
MP:0000397	abnormal guard hair morphology
MP:0000398	splitting of guard hairs
MP:0000399	increased curvature of guard hairs
MP:0000400	abnormal awl hair morphology
MP:0000401	increased curvature of awl hairs
MP:0000402	abnormal zigzag hair morphology
MP:0000403	increased curvature of zigzag hairs
MP:0000404	decreased curvature of zigzag hairs
MP:0000405	abnormal auchene hair morphology
MP:0000406	increased curvature of auchene hairs
MP:0000407	abnormal duvet hair morphology
MP:0000408	absent duvet hair
MP:0000411	shiny fur
MP:0000413	polyphalangy
MP:0000417	short hair
MP:0000418	focal hair loss
MP:0000420	ruffled hair
MP:0000421	mottled coat
MP:0000422	delayed hair appearance
MP:0000423	delayed hair regrowth
MP:0000424	retarded hair growth
MP:0000426	ectopic hair growth
MP:0000427	abnormal hair cycle
MP:0000428	abnormal craniofacial morphology
MP:0000430	absent maxillary shelf
MP:0000431	absent palatine bone horizontal plate
MP:0000438	abnormal cranium morphology
MP:0000439	enlarged cranium
MP:0000440	domed cranium
MP:0000443	abnormal snout morphology
MP:0000447	flattened snout
MP:0000448	pointed snout
MP:0000451	scaly muzzle
MP:0000453	absent mouth
MP:0000455	abnormal maxilla morphology
MP:0000458	abnormal mandible morphology
MP:0000459	abnormal presacral vertebrae morphology
MP:0000460	mandible hypoplasia
MP:0000461	decreased presacral vertebrae number
MP:0000462	abnormal digestive system morphology
MP:0000464	increased presacral vertebrae number
MP:0000466	esophageal epithelium hyperplasia
MP:0000468	abnormal esophageal epithelium morphology
MP:0000469	abnormal esophageal squamous epithelium morphology
MP:0000471	abnormal stomach epithelium morphology
MP:0000472	abnormal stomach non-glandular epithelium morphology
MP:0000473	abnormal stomach glandular epithelium morphology
MP:0000474	abnormal foregut morphology
MP:0000478	delayed intestine development
MP:0000479	abnormal enterocyte morphology
MP:0000481	abnormal enterocyte cell number
MP:0000486	abnormal pulmonary trunk morphology
MP:0000487	absent enterocytes
MP:0000488	abnormal intestinal epithelium morphology
MP:0000490	abnormal crypts of Lieberkuhn morphology
MP:0000491	crypts of Lieberkuhn abscesses
MP:0000494	abnormal cecum morphology
MP:0000495	abnormal colon morphology
MP:0000497	abnormal small intestine placement
MP:0000498	absent jejunum
MP:0000500	small intestinal prolapse
MP:0000501	abnormal digestive secretion
MP:0000503	excessive digestive secretion
MP:0000505	decreased digestive secretion
MP:0000507	absent digestive secretion
MP:0000508	right-sided isomerism
MP:0000510	remittent intestinal hemorrhage
MP:0000511	abnormal intestinal mucosa morphology
MP:0000512	intestinal ulcer
MP:0000516	abnormal renal/urinary system morphology
MP:0000521	abnormal kidney cortex morphology
MP:0000523	cortical renal glomerulopathies
MP:0000524	decreased renal tubule number
MP:0000526	small inner medullary pyramid
MP:0000527	abnormal kidney development
MP:0000528	delayed kidney development
MP:0000530	abnormal kidney blood vessel morphology
MP:0000531	right pulmonary isomerism
MP:0000532	kidney vascular congestion
MP:0000533	kidney hemorrhage
MP:0000535	ureter urothelium hyperplasia
MP:0000538	abnormal urinary bladder morphology
MP:0000540	abnormal urinary bladder urothelium morphology
MP:0000542	left-sided isomerism
MP:0000543	absent urinary bladder urothelium
MP:0000544	thin urinary bladder urothelium
MP:0000548	long limbs
MP:0000549	absent limbs
MP:0000550	abnormal forelimb morphology
MP:0000551	absent forelimb
MP:0000556	abnormal hindlimb morphology
MP:0000557	absent hindlimb
MP:0000566	synostosis
MP:0000567	truncation of digits
MP:0000568	ectopic digits
MP:0000569	abnormal digit pigmentation
MP:0000571	interdigital webbing
MP:0000573	enlarged hind paws
MP:0000574	abnormal foot pad morphology
MP:0000575	increased foot pad pigmentation
MP:0000577	absent eccrine glands
MP:0000578	ulcerated paws
MP:0000579	abnormal nail morphology
MP:0000580	deformed nails
MP:0000582	toenail hyperkeratosis
MP:0000583	long toenails
MP:0000585	kinked tail
MP:0000588	thick tail
MP:0000589	thin tail
MP:0000592	short tail
MP:0000596	abnormal liver development
MP:0000597	delayed hepatic development
MP:0000600	liver hypoplasia
MP:0000601	small liver
MP:0000602	enlarged liver sinusoidal spaces
MP:0000603	pale liver
MP:0000606	decreased hepatocyte number
MP:0000607	abnormal hepatocyte morphology
MP:0000608	dissociated hepatocytes
MP:0000614	absent salivary gland
MP:0000615	abnormal palatine gland morphology
MP:0000616	decreased ductal branching in the palatine gland
MP:0000617	increased salivary gland mucosal cell number
MP:0000618	small salivary gland
MP:0000619	salivary gland epithelial hyperplasia
MP:0000620	narrow salivary ducts
MP:0000621	increased salivary adenocarcinoma incidence
MP:0000622	increased salivation
MP:0000623	decreased salivation
MP:0000627	abnormal mammary gland morphology
MP:0000628	abnormal mammary gland development
MP:0000630	mammary gland hyperplasia
MP:0000631	abnormal neuroendocrine gland morphology
MP:0000635	pituitary gland hyperplasia
MP:0000643	absent adrenal medulla
MP:0000645	absent adrenergic chromaffin cells
MP:0000646	enlarged adrenocortical cells
MP:0000647	abnormal sebaceous gland morphology
MP:0000648	absent sebaceous gland
MP:0000649	sebaceous gland atrophy
MP:0000652	enlarged sebaceous gland
MP:0000653	abnormal sex gland morphology
MP:0000660	lateral prostate gland hypoplasia
MP:0000661	small prostate gland ventral lobe
MP:0000662	abnormal branching of the mammary ductal tree
MP:0000664	small prostate gland anterior lobe
MP:0000665	decreased ductal branching in the coagulating gland
MP:0000666	decreased prostate gland duct number
MP:0000671	bulbourethral gland hypoplasia
MP:0000675	abnormal eccrine sweat gland morphology
MP:0000676	abnormal body water content
MP:0000679	increased percent water in carcass
MP:0000680	absent parathyroid glands
MP:0000683	decreased percent water in carcass
MP:0000687	small lymphoid organs
MP:0000688	lymphoid hyperplasia
MP:0000692	small spleen
MP:0000693	spleen hyperplasia
MP:0000696	abnormal Peyer's patch morphology
MP:0000701	abnormal lymph node size
MP:0000702	enlarged lymph nodes
MP:0000703	abnormal thymus morphology
MP:0000704	abnormal thymus development
MP:0000706	small thymus
MP:0000709	enlarged thymus
MP:0000711	thymus cortex hypoplasia
MP:0000714	increased thymocyte number
MP:0000715	decreased thymocyte number
MP:0000726	absent lymphocyte
MP:0000727	absent CD8-positive, alpha-beta T cells
MP:0000729	abnormal myogenesis
MP:0000730	increased satellite cell number
MP:0000731	increased collagen deposition in the muscles
MP:0000733	abnormal muscle development
MP:0000736	delayed muscle development
MP:0000737	abnormal myotome development
MP:0000738	impaired muscle contractility
MP:0000740	impaired smooth muscle contractility
MP:0000741	impaired contractility of urinary bladder detrusor smooth muscle
MP:0000742	impaired contractility of ileal smooth muscle
MP:0000746	weakness
MP:0000749	muscle degeneration
MP:0000750	abnormal muscle regeneration
MP:0000754	paresis
MP:0000755	hindlimb paralysis
MP:0000756	forelimb paralysis
MP:0000759	abnormal skeletal muscle morphology
MP:0000761	thin diaphragm muscle
MP:0000763	abnormal filiform papillae morphology
MP:0000764	abnormal tongue epithelium morphology
MP:0000765	abnormal tongue squamous epithelium morphology
MP:0000766	absent tongue squamous epithelium
MP:0000767	abnormal smooth muscle morphology
MP:0000771	abnormal brain size
MP:0000776	abnormal inferior colliculus morphology
MP:0000777	increased inferior colliculus size
MP:0000778	abnormal nervous system tract morphology
MP:0000781	decreased corpus callosum size
MP:0000784	forebrain hypoplasia
MP:0000786	abnormal embryonic neuroepithelial layer differentiation
MP:0000787	abnormal telencephalon morphology
MP:0000788	abnormal cerebral cortex morphology
MP:0000790	abnormal stratification in cerebral cortex
MP:0000791	delaminated cerebral cortex
MP:0000792	abnormal cortical marginal zone morphology
MP:0000794	abnormal parietal lobe morphology
MP:0000798	abnormal frontal lobe morphology
MP:0000801	abnormal temporal lobe morphology
MP:0000804	abnormal occipital lobe morphology
MP:0000805	abnormal visual cortex morphology
MP:0000808	abnormal hippocampus development
MP:0000809	absent hippocampus
MP:0000811	hippocampal neuron degeneration
MP:0000812	abnormal dentate gyrus morphology
MP:0000813	abnormal hippocampus layer morphology
MP:0000814	absent dentate gyrus
MP:0000815	abnormal Ammon gyrus morphology
MP:0000818	abnormal amygdala morphology
MP:0000819	abnormal olfactory bulb morphology
MP:0000820	abnormal choroid plexus morphology
MP:0000821	choroid plexus hyperplasia
MP:0000822	abnormal brain ventricle morphology
MP:0000826	abnormal third ventricle morphology
MP:0000828	abnormal fourth ventricle morphology
MP:0000830	abnormal diencephalon morphology
MP:0000831	diencephalon hyperplasia
MP:0000833	thalamus hyperplasia
MP:0000835	abnormal subthalamic nucleus morphology
MP:0000836	abnormal substantia nigra morphology
MP:0000839	hypothalamus hyperplasia
MP:0000840	abnormal epithalamus morphology
MP:0000842	absent superior olivary complex
MP:0000843	absent facial nuclei
MP:0000844	abnormal pontine flexure morphology
MP:0000848	abnormal pons morphology
MP:0000850	absent cerebellum
MP:0000852	small cerebellum
MP:0000853	absent cerebellar foliation
MP:0000854	abnormal cerebellum development
MP:0000855	accelerated formation of intralobular fissures
MP:0000856	abnormal cerebellar plate morphology
MP:0000857	abnormal cerebellar foliation
MP:0000858	altered metastatic potential
MP:0000859	abnormal somatosensory cortex morphology
MP:0000860	abnormal primary somatosensory cortex morphology
MP:0000861	disorganized barrel cortex
MP:0000862	absent barrels in primary somatosensory cortex
MP:0000863	abnormal secondary somatosensory cortex morphology
MP:0000864	abnormal cerebellum vermis morphology
MP:0000867	abnormal cerebellum anterior vermis morphology
MP:0000868	decreased anterior vermis size
MP:0000869	abnormal cerebellum posterior vermis morphology
MP:0000870	absent cerebellum vermis lobule VIII
MP:0000871	absent cerebellum vermis lobule IX
MP:0000872	abnormal cerebellum external granule cell layer morphology
MP:0000873	thin external granule cell layer
MP:0000874	irregular external granule cell layer
MP:0000875	abnormal cerebellar Purkinje cell layer
MP:0000876	Purkinje cell degeneration
MP:0000877	abnormal Purkinje cell morphology
MP:0000879	increased Purkinje cell number
MP:0000880	decreased Purkinje cell number
MP:0000884	delaminated Purkinje cell layer
MP:0000885	ectopic Purkinje cell
MP:0000886	abnormal cerebellar granule layer morphology
MP:0000887	delaminated cerebellar granule layer
MP:0000888	absent cerebellar granule layer
MP:0000889	abnormal cerebellar molecular layer
MP:0000890	thin cerebellar molecular layer
MP:0000898	midbrain hyperplasia
MP:0000899	abnormal corpora quadrigemina morphology
MP:0000900	decreased colliculi size
MP:0000904	abnormal superior colliculus morphology
MP:0000905	increased superior colliculus size
MP:0000906	abnormal trigeminal V mesencephalic nucleus morphology
MP:0000907	small mesencephalic trigeminal nucleus
MP:0000908	absent mesencephalic trigeminal nucleus
MP:0000909	abnormal facial motor nucleus morphology
MP:0000910	small facial motor nucleus
MP:0000911	abnormal trigeminal motor nucleus morphology
MP:0000912	small trigeminal motor nucleus
MP:0000913	abnormal brain development
MP:0000917	obstructive hydrocephaly
MP:0000919	cranioschisis
MP:0000923	abnormal roof plate morphology
MP:0000924	absent roof plate
MP:0000925	abnormal floor plate morphology
MP:0000926	absent floor plate
MP:0000927	small floor plate
MP:0000928	incomplete rostral neuropore closure
MP:0000929	open neural tube
MP:0000930	wavy neural tube
MP:0000932	absent notochord
MP:0000933	abnormal rhombomere morphology
MP:0000934	abnormal telencephalon development
MP:0000935	abnormal folding of telencephalic vesicles
MP:0000936	small embryonic telencephalon
MP:0000939	decreased motor neuron number
MP:0000940	abnormal motor neuron innervation pattern
MP:0000947	convulsive seizures
MP:0000948	nonconvulsive seizures
MP:0000950	abnormal seizure response to pharmacological agent
MP:0000951	sporadic seizures
MP:0000952	abnormal CNS glial cell morphology
MP:0000954	decreased oligodendrocyte progenitor number
MP:0000956	decreased spinal cord size
MP:0000958	peripheral nervous system degeneration
MP:0000959	abnormal somatic sensory system morphology
MP:0000960	abnormal sensory ganglion morphology
MP:0000961	abnormal dorsal root ganglion morphology
MP:0000962	disorganized dorsal root ganglion
MP:0000963	fused dorsal root ganglion
MP:0000964	small dorsal root ganglion
MP:0000965	abnormal sensory neuron morphology
MP:0000966	decreased sensory neuron number
MP:0000968	abnormal sensory neuron innervation pattern
MP:0000969	abnormal nociceptor morphology
MP:0000972	abnormal mechanoreceptor morphology
MP:0000973	abnormal cutaneous/subcutaneous mechanoreceptor morphology
MP:0000976	hyperinnervation of hair guard cells
MP:0000978	hyperinnervation of hair-tylotrich cells
MP:0000980	absent hair-down neurons
MP:0000981	hyperinnervation of hair-down cells
MP:0000982	abnormal Meissner's corpuscle morphology
MP:0000983	enlarged Meissner's corpuscles
MP:0000984	hyperinnervation of Meissner's corpuscle
MP:0000985	abnormal Merkel's receptor morphology
MP:0000986	increased Merkel's receptor number
MP:0000987	hyperinnervation of Merkel's receptor
MP:0000988	abnormal pacinian corpuscle morphology
MP:0000992	absent primary muscle spindle
MP:0000995	absent secondary muscle spindle
MP:0000996	partial loss of secondary muscle spindle
MP:0000997	abnormal joint capsule morphology
MP:0000999	abnormal golgi tendon organ morphology
MP:0001000	absent golgi tendon organ
MP:0001002	abnormal taste bud morphology
MP:0001003	abnormal olfactory receptor morphology
MP:0001004	abnormal retinal photoreceptor morphology
MP:0001005	abnormal retinal rod cell morphology
MP:0001006	abnormal retinal cone cell morphology
MP:0001007	abnormal sympathetic system morphology
MP:0001008	abnormal sympathetic ganglion morphology
MP:0001009	paravertebral ganglia hyperplasia
MP:0001010	prevertebral ganglia hyperplasia
MP:0001011	abnormal superior cervical ganglion morphology
MP:0001012	superior cervical ganglion hypertrophy
MP:0001013	enlarged superior cervical ganglion
MP:0001014	absent superior cervical ganglion
MP:0001015	small superior cervical ganglion
MP:0001017	abnormal stellate ganglion morphology
MP:0001019	abnormal L4 dorsal root ganglion morphology
MP:0001020	L4 dorsal root ganglion hypertrophy
MP:0001021	small L4 dorsal root ganglion
MP:0001022	abnormal L5 dorsal root ganglion morphology
MP:0001023	L5 dorsal root ganglion hypertrophy
MP:0001024	small L5 dorsal root ganglion
MP:0001025	abnormal sympathetic neuron morphology
MP:0001026	abnormal adrenergic neuron morphology
MP:0001033	abnormal parasympathetic system morphology
MP:0001034	abnormal parasympathetic ganglion morphology
MP:0001035	abnormal submandibular ganglion morphology
MP:0001036	small submandibular ganglion
MP:0001037	abnormal parasympathetic neuron morphology
MP:0001038	abnormal cholinergic neuron morphology
MP:0001046	abnormal enteric neuron morphology
MP:0001047	abnormal enteric cholinergic neuron morphology
MP:0001048	absent enteric neurons
MP:0001051	abnormal somatic motor system morphology
MP:0001052	abnormal innervation pattern to muscle
MP:0001053	abnormal neuromuscular synapse morphology
MP:0001054	failure of neuromuscular synapse presynaptic differentiation
MP:0001055	failure of neuromuscular synapse postsynaptic differentiation
MP:0001061	abnormal oculomotor nerve morphology
MP:0001062	absent oculomotor nerve
MP:0001063	abnormal trochlear nerve morphology
MP:0001064	absent trochlear nerve
MP:0001066	absent trigeminal nerve
MP:0001067	absent mandibular nerve
MP:0001068	abnormal mandibular nerve branching
MP:0001070	abnormal abducens nerve morphology
MP:0001074	abnormal vagus nerve morphology
MP:0001075	abnormal accessory nerve morphology
MP:0001077	abnormal spinal nerve morphology
MP:0001078	abnormal phrenic nerve morphology
MP:0001079	absent phrenic nerve
MP:0001080	defasiculated phrenic nerve
MP:0001081	abnormal cranial ganglia morphology
MP:0001082	abnormal geniculate ganglion morphology
MP:0001083	small geniculate ganglion
MP:0001084	abnormal petrosal ganglion morphology
MP:0001085	small petrosal ganglion
MP:0001086	absent petrosal ganglion
MP:0001087	abnormal nodose ganglion morphology
MP:0001088	small nodose ganglion
MP:0001089	absent nodose ganglion
MP:0001092	abnormal trigeminal ganglion morphology
MP:0001093	small trigeminal ganglion
MP:0001094	trigeminal ganglion hypertrophy
MP:0001095	enlarged trigeminal ganglion
MP:0001096	abnormal glossopharyngeal ganglion morphology
MP:0001097	abnormal superior glossopharyngeal ganglion morphology
MP:0001098	small superior glossopharyngeal ganglion
MP:0001100	abnormal vagus ganglion morphology
MP:0001101	abnormal superior vagus ganglion morphology
MP:0001102	small superior vagus ganglion
MP:0001105	abnormal PNS glial cell morphology
MP:0001106	abnormal Schwann cell morphology
MP:0001107	decreased Schwann cell number
MP:0001108	absent Schwann cells
MP:0001109	absent Schwann cell precursors
MP:0001117	absent gametes
MP:0001119	abnormal female reproductive system morphology
MP:0001120	abnormal uterus morphology
MP:0001123	dilated uterus
MP:0001124	abnormal gametes
MP:0001125	abnormal oocyte morphology
MP:0001128	ovary hyperplasia
MP:0001129	impaired ovarian folliculogenesis
MP:0001130	abnormal ovarian folliculogenesis
MP:0001131	abnormal ovarian follicle morphology
MP:0001132	absent mature ovarian follicles
MP:0001133	impaired luteal cell differentiation
MP:0001134	absent corpus luteum
MP:0001135	abnormal uterine cervix morphology
MP:0001136	dilated uterine cervix
MP:0001137	abnormal uterine cervix epithelium morphology
MP:0001138	abnormal uterine cervix squamous epithelium morphology
MP:0001139	abnormal vagina morphology
MP:0001140	abnormal vagina epithelium morphology
MP:0001142	abnormal vagina orifice morphology
MP:0001143	constricted vagina orifice
MP:0001149	testicular hyperplasia
MP:0001150	enlarged scrotum
MP:0001153	small seminiferous tubules
MP:0001154	seminiferous tubule degeneration
MP:0001155	arrest of spermatogenesis
MP:0001157	small seminal vesicle
MP:0001158	abnormal prostate gland morphology
MP:0001159	absent prostate gland
MP:0001163	abnormal prostate gland anterior lobe morphology
MP:0001167	prostate gland epithelial hyperplasia
MP:0001168	abnormal prostate gland epithelium morphology
MP:0001169	abnormal bulbourethral gland morphology
MP:0001170	bulbourethral gland hyperplasia
MP:0001176	abnormal lung development
MP:0001179	thick pulmonary interalveolar septum
MP:0001181	absent lungs
MP:0001182	lung hemorrhage
MP:0001183	overexpanded pulmonary alveoli
MP:0001184	absent pulmonary alveoli
MP:0001186	pigmentation phenotype
MP:0001188	hyperpigmentation
MP:0001191	abnormal skin condition
MP:0001194	dermatitis
MP:0001195	flaky skin
MP:0001196	shiny skin
MP:0001197	oily skin
MP:0001200	thick skin
MP:0001202	skin photosensitivity
MP:0001203	increased sensitivity to skin irradiation
MP:0001204	decreased sensitivity to skin irradiation
MP:0001210	skin ridges
MP:0001212	skin lesions
MP:0001213	abnormal skin cell number
MP:0001214	skin hyperplasia
MP:0001217	absent epidermis
MP:0001218	thin epidermis
MP:0001220	epidermal necrosis
MP:0001221	epidermal atrophy
MP:0001222	epidermal hyperplasia
MP:0001224	abnormal keratinocyte apoptosis
MP:0001230	epidermal desquamation
MP:0001231	abnormal epidermis stratum basale morphology
MP:0001232	absent epidermis stratum basale
MP:0001233	abnormal epidermis suprabasal layer morphology
MP:0001234	absent suprabasal layer
MP:0001235	disorganized suprabasal layer
MP:0001236	abnormal epidermis stratum spinosum morphology
MP:0001237	enlarged spinous cells
MP:0001238	thin epidermis stratum spinosum
MP:0001239	abnormal epidermis stratum granulosum morphology
MP:0001240	abnormal epidermis stratum corneum morphology
MP:0001241	absent epidermis stratum corneum
MP:0001243	abnormal dermal layer morphology
MP:0001244	thin dermal layer
MP:0001245	thick dermal layer
MP:0001246	mixed cellular infiltration to dermis
MP:0001247	dermal cysts
MP:0001251	dermis papillary layer hypercellularity
MP:0001256	abnormal body length
MP:0001257	increased body length
MP:0001258	decreased body length
MP:0001264	increased body size
MP:0001265	decreased body size
MP:0001272	increased metastatic potential
MP:0001273	decreased metastatic potential
MP:0001274	curly vibrissae
MP:0001278	kinked vibrissae
MP:0001279	wavy vibrissae
MP:0001280	loss of vibrissae
MP:0001281	increased vibrissae length
MP:0001282	short vibrissae
MP:0001283	sparse vibrissae
MP:0001284	absent vibrissae
MP:0001286	abnormal eye development
MP:0001288	abnormal lens induction
MP:0001289	persistence of hyaloid vascular system
MP:0001290	delayed eyelid opening
MP:0001292	abnormal lens vesicle development
MP:0001299	abnormal eye distance/ position
MP:0001302	eyelids open at birth
MP:0001305	enlarged lens
MP:0001307	fused cornea and lens
MP:0001308	abnormal lens polarity
MP:0001309	hydropic eye lens fibers
MP:0001313	increased incidence of corneal inflammation
MP:0001318	pupil opacity
MP:0001319	irregularly shaped pupil
MP:0001320	small pupils
MP:0001324	abnormal eye pigmentation
MP:0001327	decreased retinal photoreceptor cell number
MP:0001328	disorganized retinal layers
MP:0001329	retina hyperplasia
MP:0001332	abnormal optic nerve innervation
MP:0001337	dry eyes
MP:0001345	Meibomian gland atrophy
MP:0001346	abnormal lacrimal gland morphology
MP:0001348	abnormal lacrimal gland physiology
MP:0001349	excessive tearing
MP:0001353	increased aggression towards mice
MP:0001354	increased aggression towards males
MP:0001355	submission towards male mice
MP:0001356	increased aggression towards females
MP:0001357	increased aggression towards humans
MP:0001358	aggression towards inanimate objects
MP:0001360	abnormal social investigation
MP:0001361	social withdrawal
MP:0001363	increased anxiety-related response
MP:0001364	decreased anxiety-related response
MP:0001375	abnormal mating preference
MP:0001376	abnormal mating receptivity
MP:0001377	abnormal mating frequency
MP:0001379	abnormal penile erection
MP:0001380	reduced male mating frequency
MP:0001382	abnormal nursing
MP:0001384	abnormal pup retrieval
MP:0001385	pup cannibalization
MP:0001386	abnormal maternal nurturing
MP:0001391	abnormal tail movements
MP:0001392	abnormal locomotor behavior
MP:0001394	circling
MP:0001395	bidirectional circling
MP:0001396	unidirectional circling
MP:0001400	hyperresponsive
MP:0001401	jumpy
MP:0001402	hypoactivity
MP:0001404	no spontaneous movement
MP:0001405	impaired coordination
MP:0001407	short stride length
MP:0001409	increased stereotypic behavior
MP:0001410	head bobbing
MP:0001411	spinning
MP:0001412	excessive scratching
MP:0001413	abnormal response to new environment
MP:0001415	increased exploration in new environment
MP:0001417	decreased exploration in new environment
MP:0001423	abnormal liquid preference
MP:0001425	abnormal alcohol consumption
MP:0001428	adipsia
MP:0001432	abnormal food preference
MP:0001435	no suckling reflex
MP:0001437	no swallowing reflex
MP:0001438	aphagia
MP:0001440	abnormal grooming behavior
MP:0001441	increased grooming behavior
MP:0001442	decreased grooming behavior
MP:0001443	poor grooming
MP:0001446	abnormal whisker trimming behavior
MP:0001447	abnormal nest building behavior
MP:0001448	abnormal huddling behavior
MP:0001454	abnormal cued conditioning behavior
MP:0001458	abnormal object recognition memory
MP:0001460	abnormal olfactory -discrimination memory
MP:0001462	abnormal avoidance learning behavior
MP:0001463	abnormal spatial learning
MP:0001468	abnormal temporal memory
MP:0001469	abnormal contextual conditioning behavior
MP:0001473	reduced long term potentiation
MP:0001475	reduced long term depression
MP:0001485	abnormal pinna reflex
MP:0001486	abnormal startle reflex
MP:0001488	increased startle reflex
MP:0001489	decreased startle reflex
MP:0001490	abnormal vibrissae reflex
MP:0001491	unresponsive to tactile stimuli
MP:0001492	abnormal pilomotor reflex
MP:0001496	audiogenic seizures
MP:0001499	abnormal kindling response
MP:0001500	reduced kindling response
MP:0001501	abnormal sleep pattern
MP:0001502	abnormal circadian rhythm
MP:0001505	hunched posture
MP:0001506	limp posture
MP:0001510	abnormal coat appearance
MP:0001511	disheveled coat
MP:0001512	trunk curl
MP:0001513	limb grasping
MP:0001515	abnormal grip strength
MP:0001522	impaired swimming
MP:0001523	impaired righting response
MP:0001524	impaired limb coordination
MP:0001525	impaired balance
MP:0001526	abnormal placing response
MP:0001529	abnormal vocalization
MP:0001533	abnormal skeleton physiology
MP:0001539	decreased caudal vertebrae number
MP:0001541	abnormal osteoclast physiology
MP:0001542	abnormal bone strength
MP:0001545	abnormal hematopoietic system physiology
MP:0001547	abnormal lipid level
MP:0001553	abnormal circulating free fatty acids level
MP:0001565	abnormal circulating phosphate level
MP:0001569	abnormal circulating bilirubin level
MP:0001573	abnormal circulating alanine transaminase level
MP:0001574	abnormal oxygen level
MP:0001586	abnormal erythrocyte cell number
MP:0001589	abnormal mean corpuscular hemoglobin
MP:0001598	abnormal blood viscosity
MP:0001599	abnormal blood volume
MP:0001601	abnormal myelopoiesis
MP:0001602	impaired myelopoiesis
MP:0001603	failure of myelopoiesis
MP:0001606	impaired hematopoiesis
MP:0001613	abnormal vasodilation
MP:0001619	abnormal vascular permeability
MP:0001622	abnormal vasculogenesis
MP:0001625	cardiac hypertrophy
MP:0001627	abnormal cardiac output
MP:0001629	abnormal heart rate
MP:0001633	poor circulation
MP:0001648	abnormal apoptosis
MP:0001649	abnormal symphysis menti morphology
MP:0001650	abnormal seizure response to electrical stimulation
MP:0001652	colonic necrosis
MP:0001653	gastric necrosis
MP:0001655	multifocal hepatic necrosis
MP:0001656	focal hepatic necrosis
MP:0001657	abnormal induced morbidity/mortality
MP:0001658	increased mortality induced by gamma-irradiation
MP:0001661	extended life span
MP:0001663	abnormal digestive system physiology
MP:0001664	abnormal digestion
MP:0001666	abnormal intestinal absorption
MP:0001668	abnormal intestinal fructose absorption
MP:0001669	abnormal intestinal glucose absorption
MP:0001670	abnormal intestinal mineral absorption
MP:0001671	abnormal vitamin absorption
MP:0001672	abnormal embryo development
MP:0001674	abnormal germ layer development
MP:0001675	abnormal ectoderm development
MP:0001676	abnormal apical ectodermal ridge morphology
MP:0001677	absent apical ectodermal ridge
MP:0001678	thick apical ectodermal ridge
MP:0001679	thin apical ectodermal ridge
MP:0001680	abnormal mesoderm development
MP:0001683	absent mesoderm
MP:0001684	abnormal axial mesoderm
MP:0001685	abnormal endoderm development
MP:0001687	thin endoderm
MP:0001688	abnormal somite development
MP:0001689	incomplete somite formation
MP:0001690	failure of somite differentiation
MP:0001691	abnormal somite shape
MP:0001693	failure of primitive streak formation
MP:0001694	absent egg cylinders
MP:0001695	abnormal gastrulation
MP:0001696	failure to gastrulate
MP:0001697	abnormal embryo size
MP:0001698	decreased embryo size
MP:0001699	increased embryo size
MP:0001700	abnormal embryo turning
MP:0001701	incomplete embryo turning
MP:0001704	abnormal dorsal-ventral axis patterning
MP:0001705	abnormal proximal-distal axis patterning
MP:0001706	abnormal left-right axis patterning
MP:0001710	absent amniotic folds
MP:0001711	abnormal placenta morphology
MP:0001712	abnormal placenta development
MP:0001713	decreased trophoblast giant cell number
MP:0001714	absent trophoblast giant cells
MP:0001715	placental labyrinth hypoplasia
MP:0001716	abnormal placenta labyrinth morphology
MP:0001717	absent ectoplacental cone
MP:0001718	abnormal visceral yolk sac morphology
MP:0001719	absent vitelline blood vessels
MP:0001721	absent visceral yolk sac blood islands
MP:0001722	pale yolk sac
MP:0001723	disorganized yolk sac vascular plexus
MP:0001724	abnormal extraembryonic endoderm formation
MP:0001725	abnormal umbilical cord morphology
MP:0001726	abnormal allantois morphology
MP:0001727	abnormal embryo implantation
MP:0001728	failure of embryo implantation
MP:0001729	impaired embryo implantation
MP:0001730	embryonic growth arrest
MP:0001739	abnormal adrenal gland secretion
MP:0001740	failure of adrenal epinephrine secretion
MP:0001742	absent circulating adrenaline
MP:0001743	absent circulating noradrenaline
MP:0001744	hypersecretion of corticosterone
MP:0001745	increased circulating corticosterone level
MP:0001746	abnormal pituitary secretion
MP:0001747	hypersecretion of adrenocorticotropin
MP:0001749	suppressed circulating follicle stimulating hormone level
MP:0001752	abnormal hypothalamus secretion
MP:0001753	hypersecretion of corticotropin-releasing hormone
MP:0001754	increased circulating corticotropin-releasing hormone level
MP:0001760	abnormal urine enzyme level
MP:0001761	abnormal urination pattern
MP:0001770	abnormal iron level
MP:0001771	abnormal circulating magnesium level
MP:0001775	abnormal selenium level
MP:0001776	abnormal circulating sodium level
MP:0001780	decreased brown adipose tissue amount
MP:0001781	abnormal white adipose tissue amount
MP:0001783	decreased white adipose tissue amount
MP:0001786	skin edema
MP:0001787	pericardial edema
MP:0001792	impaired wound healing
MP:0001793	altered susceptibility to infection
MP:0001798	impaired macrophage phagocytosis
MP:0001800	abnormal humoral immune response
MP:0001802	arrested B cell differentiation
MP:0001819	abnormal immune cell physiology
MP:0001824	abnormal thymus involution
MP:0001825	arrested T cell differentiation
MP:0001828	abnormal T cell activation
MP:0001829	increased activated T cell number
MP:0001830	decreased activated T cell number
MP:0001835	abnormal antigen presentation
MP:0001836	abnormal antigen presentation via MHC class I
MP:0001837	defective assembly of class I molecules
MP:0001838	defective intracellular transport of class I molecules
MP:0001839	abnormal level of surface class I molecules
MP:0001840	increased level of surface class I molecules
MP:0001841	decreased level of surface class I molecules
MP:0001844	autoimmune response
MP:0001849	ear inflammation
MP:0001850	increased susceptibility to otitis media
MP:0001851	eye inflammation
MP:0001853	heart inflammation
MP:0001854	atrial endocarditis
MP:0001855	abnormal atrial thrombosis
MP:0001863	vascular inflammation
MP:0001866	nasal inflammation
MP:0001868	ovary inflammation
MP:0001870	salivary gland inflammation
MP:0001874	acanthosis
MP:0001881	abnormal mammary gland physiology
MP:0001882	abnormal lactation
MP:0001883	increased mammary adenocarcinoma incidence
MP:0001884	mammary gland alveolar hyperplasia
MP:0001885	mammary gland duct hyperplasia
MP:0001889	delayed brain development
MP:0001898	abnormal long term depression
MP:0001899	absent long term depression
MP:0001900	impaired synaptic plasticity
MP:0001901	absence of NMDA-mediated synaptic currents
MP:0001902	reduced NMDA-mediated synaptic currents
MP:0001905	abnormal dopamine level
MP:0001906	increased dopamine level
MP:0001908	abnormal somatosensory cortex physiology
MP:0001909	reduced NMDA receptor mediated synaptic activity in barrel cortex
MP:0001911	abnormal cerebrospinal fluid production
MP:0001921	reduced fertility
MP:0001922	reduced male fertility
MP:0001923	reduced female fertility
MP:0001927	abnormal estrous cycle
MP:0001928	abnormal ovulation
MP:0001929	abnormal gametogenesis
MP:0001930	abnormal meiosis
MP:0001931	abnormal oogenesis
MP:0001932	abnormal spermiogenesis
MP:0001933	abnormal litter size
MP:0001934	increased litter size
MP:0001935	decreased litter size
MP:0001937	abnormal sexual maturation
MP:0001939	secondary sex reversal
MP:0001940	testis hypoplasia
MP:0001942	abnormal lung volume
MP:0001945	bronchoconstriction
MP:0001947	abnormal mucociliary clearance
MP:0001950	abnormal respiratory sounds
MP:0001951	abnormal breathing pattern
MP:0001952	increased airway responsiveness
MP:0001961	abnormal reflex
MP:0001963	abnormal hearing physiology
MP:0001968	abnormal touch/ nociception
MP:0001970	abnormal pain threshold
MP:0001973	increased thermal nociceptive threshold
MP:0001980	abnormal chemically-elicited antinociception
MP:0001981	increased chemically-elicited antinociception
MP:0001982	decreased chemically-elicited antinociception
MP:0001983	abnormal olfactory system physiology
MP:0001985	abnormal gustatory system physiology
MP:0001986	abnormal taste sensitivity
MP:0001987	alcohol preference
MP:0001988	cocaine preference
MP:0001993	abnormal blinking
MP:0001994	increased blinking frequency
MP:0001999	photosensitivity
MP:0002003	miotic pupils
MP:0002007	increased cellular sensitivity to gamma-irradiation
MP:0002009	preneoplasia
MP:0002014	increased papilloma incidence
MP:0002015	epithelioid cysts
MP:0002018	increased malignant tumor incidence
MP:0002019	abnormal tumor incidence
MP:0002020	increased tumor incidence
MP:0002021	increased incidence of induced tumors
MP:0002023	increased B cell derived lymphoma incidence
MP:0002024	increased T cell derived lymphoma incidence
MP:0002031	increased adrenal gland tumor incidence
MP:0002037	increased fibrohistocytoma incidence
MP:0002041	increased pituitary adenoma incidence
MP:0002043	increased colon hamartoma incidence
MP:0002044	increased colonic adenoma incidence
MP:0002045	increased renal cystadenoma incidence
MP:0002047	increased hepatic hemangioma incidence
MP:0002048	increased lung adenoma incidence
MP:0002049	increased extremity angiosarcoma incidence
MP:0002051	increased skin papilloma incidence
MP:0002052	decreased tumor incidence
MP:0002053	decreased incidence of induced tumors
MP:0002059	abnormal seminal vesicle morphology
MP:0002062	abnormal associative learning
MP:0002063	abnormal learning/memory/conditioning
MP:0002066	abnormal motor capabilities/coordination/movement
MP:0002067	abnormal sensory capabilities/reflexes/nociception
MP:0002068	abnormal parental behavior
MP:0002080	prenatal lethality
MP:0002082	postnatal lethality
MP:0002083	premature death
MP:0002084	abnormal developmental patterning
MP:0002085	abnormal embryonic tissue morphology
MP:0002086	abnormal extraembryonic tissue morphology
MP:0002088	abnormal embryonic growth/weight/body size
MP:0002089	abnormal postnatal growth/weight/body size
MP:0002098	abnormal vibrissa morphology
MP:0002102	abnormal ear morphology
MP:0002109	abnormal limb morphology
MP:0002111	abnormal tail morphology
MP:0002113	abnormal skeleton development
MP:0002116	abnormal craniofacial bone morphology
MP:0002118	abnormal lipid homeostasis
MP:0002119	dipsosis
MP:0002123	abnormal definitive hematopoiesis
MP:0002135	abnormal kidney morphology
MP:0002138	abnormal hepatobiliary system morphology
MP:0002139	abnormal hepatobiliary system physiology
MP:0002145	abnormal T cell differentiation
MP:0002148	abnormal hypersensitivity reaction
MP:0002151	abnormal neural tube morphology
MP:0002161	abnormal fertility/fecundity
MP:0002163	abnormal gland morphology
MP:0002164	abnormal gland physiology
MP:0002166	altered tumor susceptibility
MP:0002169	no abnormal phenotype detected
MP:0002174	abnormal gastrulation movements
MP:0002175	decreased brain weight
MP:0002176	increased brain weight
MP:0002177	abnormal outer ear morphology
MP:0002182	abnormal astrocyte morphology
MP:0002184	abnormal innervation
MP:0002188	small heart
MP:0002190	disorganized myocardium
MP:0002191	abnormal artery morphology
MP:0002193	minimal clonic seizures
MP:0002194	maximal tonic hindlimb extension seizures
MP:0002199	abnormal brain commissure morphology
MP:0002200	abnormal brain ventricular system morphology
MP:0002204	abnormal neurotransmitter level
MP:0002206	abnormal CNS synaptic transmission
MP:0002207	abnormal long term potentiation
MP:0002209	decreased germ cell number
MP:0002211	abnormal primary sex determination
MP:0002212	abnormal secondary sex determination
MP:0002214	streak gonad
MP:0002216	abnormal seminiferous tubule morphology
MP:0002217	small lymph nodes
MP:0002218	increased lymph node number
MP:0002219	decreased lymph node number
MP:0002220	large lymphoid organs
MP:0002221	abnormal lymph organ size
MP:0002223	lymphoid hypoplasia
MP:0002224	abnormal spleen size
MP:0002227	abnormal spleen capsule morphology
MP:0002230	abnormal primitive streak formation
MP:0002231	abnormal primitive streak morphology
MP:0002234	abnormal pharynx morphology
MP:0002235	abnormal external nares morphology
MP:0002236	abnormal internal nares morphology
MP:0002237	abnormal nasal cavity morphology
MP:0002239	abnormal nasal septum morphology
MP:0002240	abnormal paranasal sinus morphology
MP:0002241	abnormal laryngeal mucosa goblet cell morphology
MP:0002243	abnormal vomeronasal organ morphology
MP:0002244	abnormal turbinate morphology
MP:0002247	abnormal maxillary sinus morphology
MP:0002249	abnormal larynx morphology
MP:0002251	abnormal nasopharynx morphology
MP:0002252	abnormal oropharynx morphology
MP:0002253	abnormal pharyngeal muscle morphology
MP:0002254	reproductive system inflammation
MP:0002256	abnormal laryngeal cartilage morphology
MP:0002257	abnormal arytenoid cartilage morphology
MP:0002258	abnormal cricoid cartilage morphology
MP:0002260	abnormal thyroid cartilage morphology
MP:0002263	abnormal laryngeal muscle morphology
MP:0002264	abnormal bronchus morphology
MP:0002267	abnormal bronchiole morphology
MP:0002268	abnormal terminal bronchiole morphology
MP:0002269	muscular atrophy
MP:0002270	abnormal pulmonary alveolus morphology
MP:0002271	abnormal pulmonary alveolar duct morphology
MP:0002273	abnormal pulmonary alveolus epithelial cell morphology
MP:0002274	abnormal type I pneumocyte morphology
MP:0002275	abnormal type II pneumocyte morphology
MP:0002276	abnormal lung interstitium morphology
MP:0002277	abnormal respiratory mucosa morphology
MP:0002279	abnormal diaphragm morphology
MP:0002280	abnormal intercostal muscle morphology
MP:0002281	abnormal respiratory mucosa goblet cell morphology
MP:0002282	abnormal trachea morphology
MP:0002284	abnormal tracheal smooth muscle morphology
MP:0002285	abnormal tracheal ciliated epithelium morphology
MP:0002292	abnormal gestational length
MP:0002293	long gestation period
MP:0002294	short gestation period
MP:0002297	abnormal forced expiratory flow rates
MP:0002304	abnormal total lung capacity
MP:0002306	abnormal functional residual capacity
MP:0002309	abnormal vital capacity
MP:0002310	decreased susceptibility to hepatic steatosis
MP:0002311	abnormal inspiratory capacity
MP:0002313	abnormal tidal volume
MP:0002314	abnormal respiratory mechanics
MP:0002316	anoxia
MP:0002319	hyperoxia
MP:0002323	decreased susceptibility to hyperlipidemia
MP:0002324	abnormal alveolocapillary membrane morphology
MP:0002328	abnormal airway resistance
MP:0002330	abnormal bronchial provocation
MP:0002332	abnormal exercise endurance
MP:0002333	abnormal lung compliance
MP:0002334	abnormal airway responsiveness
MP:0002335	decreased airway responsiveness
MP:0002336	abnormal pulmonary gas exchange
MP:0002337	abnormal whole-body plethysmography
MP:0002338	abnormal pulmonary ventilation
MP:0002340	abnormal axillary lymph node morphology
MP:0002343	abnormal lymph node cortex morphology
MP:0002344	abnormal lymph node B cell domain morphology
MP:0002345	abnormal lymph node primary follicle morphology
MP:0002346	abnormal lymph node secondary follicle morphology
MP:0002347	abnormal lymph node T cell domain morphology
MP:0002348	abnormal lymph node medulla morphology
MP:0002349	abnormal afferent lymphatic vessel morphology
MP:0002351	abnormal cervical lymph node morphology
MP:0002352	abnormal popliteal lymph node morphology
MP:0002353	abnormal inguinal lymph node morphology
MP:0002356	abnormal spleen red pulp morphology
MP:0002357	abnormal spleen white pulp morphology
MP:0002358	abnormal spleen periarteriolar lymphoid sheath morphology
MP:0002359	abnormal spleen germinal center morphology
MP:0002360	abnormal spleen B cell corona morphology
MP:0002362	abnormal spleen marginal zone morphology
MP:0002363	abnormal spleen marginal sinus morphology
MP:0002364	abnormal thymus size
MP:0002367	abnormal thymus lobule morphology
MP:0002368	abnormal thymus capsule morphology
MP:0002369	abnormal thymus subcapsular epithelium morphology
MP:0002371	abnormal thymus cortex morphology
MP:0002375	abnormal thymus medulla morphology
MP:0002376	abnormal dendritic cell physiology
MP:0002377	abnormal mucosa-associated lymphoid tissue morphology
MP:0002378	abnormal gut-associated lymphoid tissue morphology
MP:0002379	abnormal oropharyngeal lymphoid tissue morphology
MP:0002388	abnormal Peyer's patch epithelium morphology
MP:0002389	abnormal Peyer's patch follicle morphology
MP:0002391	abnormal Peyer's patch germinal center morphology
MP:0002392	abnormal Peyer's patch T cell area morphology
MP:0002393	abnormal bronchus-associated lymphoid tissue morphology
MP:0002397	abnormal bone marrow morphology
MP:0002398	abnormal bone marrow cell morphology/development
MP:0002399	abnormal pluripotent precursor cell morphology
MP:0002400	abnormal multipotent stem cell morphology
MP:0002401	abnormal lymphopoiesis
MP:0002403	abnormal pre-B cell morphology
MP:0002404	increased intestinal adenoma incidence
MP:0002405	respiratory system inflammation
MP:0002407	abnormal double-negative T cell morphology
MP:0002408	abnormal double-positive T cell morphology
MP:0002409	decreased susceptibility to infection
MP:0002410	decreased susceptibility to viral infection
MP:0002411	decreased susceptibility to bacterial infection
MP:0002413	abnormal megakaryocyte progenitor cell morphology
MP:0002414	abnormal myeloblast morphology/development
MP:0002415	abnormal neutrophil differentiation
MP:0002416	abnormal proerythroblast morphology
MP:0002417	abnormal megakaryocyte morphology
MP:0002418	increased susceptibility to viral infection
MP:0002419	abnormal innate immunity
MP:0002420	abnormal adaptive immunity
MP:0002421	abnormal cell-mediated immunity
MP:0002427	disproportionate dwarf
MP:0002429	abnormal blood cell morphology/development
MP:0002432	abnormal CD4-positive, alpha beta T cell morphology
MP:0002433	abnormal T-helper 1 cell morphology
MP:0002434	abnormal T-helper 2 cell morphology
MP:0002435	abnormal effector T cell morphology
MP:0002436	abnormal CD8-positive, alpha-beta cytotoxic T cell morphology
MP:0002439	abnormal plasma cell morphology
MP:0002440	abnormal memory B cell morphology
MP:0002442	abnormal leukocyte physiology
MP:0002445	abnormal mononuclear cell differentiation
MP:0002450	abnormal lymph organ development
MP:0002451	abnormal macrophage physiology
MP:0002452	abnormal professional antigen presenting cell physiology
MP:0002453	abnormal B lymphocyte antigen presentation
MP:0002454	abnormal macrophage antigen presentation
MP:0002455	abnormal dendritic cell antigen presentation
MP:0002462	abnormal granulocyte physiology
MP:0002464	abnormal basophil physiology
MP:0002465	abnormal eosinophil physiology
MP:0002467	impaired neutrophil phagocytosis
MP:0002471	abnormal complement pathway
MP:0002472	impaired complement alternative pathway
MP:0002473	impaired complement classical pathway
MP:0002491	decreased IgD level
MP:0002496	increased IgD level
MP:0002498	abnormal acute inflammation
MP:0002499	chronic inflammation
MP:0002500	granulomatous inflammation
MP:0002503	abnormal histamine physiology
MP:0002531	abnormal type I hypersensitivity reaction
MP:0002533	abnormal type III hypersensitivity reaction
MP:0002534	abnormal type IV hypersensitivity reaction
MP:0002551	abnormal blood coagulation
MP:0002556	abnormal cocaine consumption
MP:0002558	abnormal circadian period
MP:0002559	abnormal circadian persistence
MP:0002560	arrhythmic circadian persistence
MP:0002561	abnormal circadian phase
MP:0002562	prolonged circadian period
MP:0002563	shortened circadian period
MP:0002564	advanced circadian phase
MP:0002565	delayed circadian phase
MP:0002566	abnormal sexual interaction
MP:0002570	alcohol aversion
MP:0002573	behavioral despair
MP:0002574	increased vertical activity
MP:0002575	increased circulating ketone body level
MP:0002577	reduced enamel thickness
MP:0002578	impaired ability to fire action potentials
MP:0002579	disorganized secondary lens fibers
MP:0002580	duodenal lesions
MP:0002581	abnormal ileum morphology
MP:0002582	disorganized extraembryonic tissue
MP:0002583	absent extraembryonic ectoderm
MP:0002584	small ectoplacental cone
MP:0002591	decreased mean corpuscular volume
MP:0002593	high mean erythrocyte cell number
MP:0002594	low mean erythrocyte cell number
MP:0002596	abnormal hematocrit
MP:0002602	abnormal eosinophil cell number
MP:0002606	increased basophil cell number
MP:0002607	decreased basophil cell number
MP:0002620	abnormal monocyte morphology
MP:0002621	delayed neural tube closure
MP:0002622	abnormal cochlear hair cell morphology
MP:0002623	abnormal vestibular hair cell morphology
MP:0002629	hyperactivity elicited by ethanol administration
MP:0002630	abnormal endocochlear potential
MP:0002631	abnormal epididymis morphology
MP:0002632	vestigial tail
MP:0002634	abnormal sensorimotor gating
MP:0002635	reduced sensorimotor gating
MP:0002636	delayed vaginal opening
MP:0002637	small uterus
MP:0002638	abnormal pupillary reflex
MP:0002645	abnormal intestinal cholesterol absorption
MP:0002646	increased intestinal cholesterol absorption
MP:0002647	decreased intestinal cholesterol absorption
MP:0002648	delaminated enamel
MP:0002649	abnormal enamel rod pattern
MP:0002650	abnormal ameloblast morphology
MP:0002651	abnormal sciatic nerve morphology
MP:0002652	thin myocardium
MP:0002653	abnormal ependyma morphology
MP:0002654	spongiform encephalopathy
MP:0002655	abnormal keratinocyte morphology
MP:0002656	abnormal keratinocyte differentiation
MP:0002657	chondrodystrophy
MP:0002658	abnormal liver regeneration
MP:0002660	abnormal caput epididymis morphology
MP:0002661	abnormal corpus epididymis morphology
MP:0002662	abnormal cauda epididymis morphology
MP:0002663	absent blastocoele
MP:0002665	decreased circulating corticosterone level
MP:0002668	abnormal circulating potassium level
MP:0002671	belted
MP:0002672	abnormal pharyngeal arch artery morphology
MP:0002673	abnormal sperm number
MP:0002675	asthenozoospermia
MP:0002676	uterus hyperplasia
MP:0002678	increased follicle recruitment
MP:0002679	abnormal corpus luteum morphology
MP:0002680	decreased corpora lutea number
MP:0002681	increased corpora lutea number
MP:0002682	decreased mature ovarian follicle number
MP:0002683	delayed fertility
MP:0002685	abnormal spermatogonia proliferation
MP:0002691	small stomach
MP:0002694	abnormal pancreas secretion
MP:0002696	decreased circulating glucagon level
MP:0002697	abnormal eye size
MP:0002698	abnormal sclera morphology
MP:0002699	abnormal vitreous body morphology
MP:0002700	opacity of vitreous body
MP:0002702	decreased circulating free fatty acid level
MP:0002703	abnormal renal tubule morphology
MP:0002704	tubular nephritis
MP:0002705	dilated renal tubules
MP:0002706	abnormal kidney size
MP:0002707	abnormal kidney weight
MP:0002710	increased glucagon secretion
MP:0002711	decreased glucagon secretion
MP:0002712	increased circulating glucagon level
MP:0002714	increased glycogen catabolism rate
MP:0002715	decreased glycogen catabolism rate
MP:0002716	small male preputial glands
MP:0002717	abnormal male preputial gland morphology
MP:0002718	abnormal inner cell mass morphology
MP:0002722	abnormal immune system organ morphology
MP:0002724	enhanced wound healing
MP:0002729	abnormal inner ear canal morphology
MP:0002730	head shaking
MP:0002731	megacolon
MP:0002732	increased trichoepithelioma incidence
MP:0002733	abnormal thermal nociception
MP:0002734	abnormal mechanical nociception
MP:0002735	abnormal chemical nociception
MP:0002736	abnormal nociception after inflammation
MP:0002738	hyperresponsive to tactile stimuli
MP:0002739	abnormal olfactory bulb development
MP:0002741	small olfactory bulb
MP:0002742	enlarged submandibular lymph nodes
MP:0002745	abnormal atrioventricular valve morphology
MP:0002746	abnormal semilunar valve morphology
MP:0002747	abnormal aortic valve morphology
MP:0002753	dilated heart left ventricle
MP:0002757	decreased vertical activity
MP:0002758	long tail
MP:0002759	abnormal caudal vertebrae morphology
MP:0002761	abnormal hippocampal mossy fiber morphology
MP:0002762	ectopic cerebellar granule cells
MP:0002763	ectopic Bergmann glia cells
MP:0002766	situs inversus
MP:0002767	situs ambiguus
MP:0002768	small adrenal glands
MP:0002770	absent bulbourethral gland
MP:0002771	absent prostate gland anterior lobe
MP:0002772	brachypodia
MP:0002774	small prostate gland
MP:0002776	Sertoli cell hyperplasia
MP:0002777	absent ovarian follicles
MP:0002778	meroanencephaly
MP:0002779	abnormal sex gland secretion
MP:0002782	abnormal testes secretion
MP:0002783	abnormal ovarian secretion
MP:0002784	abnormal Sertoli cell morphology
MP:0002785	absent Leydig cells
MP:0002787	pseudohermaphroditism
MP:0002792	abnormal retinal vasculature morphology
MP:0002796	impaired skin barrier function
MP:0002797	increased thigmotaxis
MP:0002798	abnormal active avoidance behavior
MP:0002799	abnormal passive avoidance behavior
MP:0002800	abnormal short term object recognition memory
MP:0002801	abnormal long term object recognition memory
MP:0002802	abnormal discrimination learning
MP:0002803	abnormal operant conditioning behavior
MP:0002804	abnormal motor learning
MP:0002805	abnormal conditioned taste aversion behavior
MP:0002806	abnormal conditioned emotional response
MP:0002807	abnormal eye blink conditioning behavior
MP:0002809	increased spinal cord size
MP:0002813	microcytosis
MP:0002814	hyperchromasia
MP:0002817	abnormal tooth mineralization
MP:0002819	abnormal pulp cavity morphology
MP:0002822	catalepsy
MP:0002823	abnormal rib development
MP:0002824	abnormal chorioallantoic fusion
MP:0002825	abnormal notochord morphology
MP:0002826	tonic seizures
MP:0002827	abnormal renal corpuscle morphology
MP:0002828	abnormal renal glomerular capsule morphology
MP:0002829	abnormal juxtaglomerular apparatus morphology
MP:0002831	absent Peyer's patches
MP:0002833	increased heart weight
MP:0002834	decreased heart weight
MP:0002836	abnormal chorion morphology
MP:0002837	dystrophic cardiac calcinosis
MP:0002838	decreased susceptibility to dystrophic cardiac calcinosis
MP:0002839	increased susceptibility to dystrophic cardiac calcinosis
MP:0002840	abnormal lens fiber morphology
MP:0002841	impaired skeletal muscle contractility
MP:0002842	increased systemic arterial blood pressure
MP:0002843	decreased systemic arterial blood pressure
MP:0002844	aortic hypertrophy
MP:0002845	abnormal aortic weight
MP:0002847	abnormal renal glomerular filtration rate
MP:0002849	abnormal saccharin consumption
MP:0002850	saccharin preference
MP:0002853	hyposulfatemia
MP:0002855	abnormal cochlear ganglion morphology
MP:0002856	abnormal vestibular ganglion morphology
MP:0002857	cochlear ganglion degeneration
MP:0002859	abnormal inner ear canal fusion
MP:0002861	abnormal tail bud morphology
MP:0002862	altered righting response
MP:0002863	improved righting response
MP:0002864	abnormal ocular fundus morphology
MP:0002865	increased growth rate
MP:0002869	increased anti-insulin autoantibody level
MP:0002870	decreased anti-insulin autoantibody level
MP:0002873	normal phenotype
MP:0002874	decreased hemoglobin content
MP:0002875	decreased erythrocyte cell number
MP:0002877	abnormal melanocyte morphology
MP:0002879	increased cellular sensitivity to X-ray irradiation
MP:0002881	long hair
MP:0002883	chromatolysis
MP:0002885	abnormal AMPA-mediated synaptic currents
MP:0002886	abnormal glutamate-mediated receptor currents
MP:0002887	decreased susceptibility to pharmacologically induced seizures
MP:0002888	abnormal NMDA-mediated synaptic currents
MP:0002891	increased insulin sensitivity
MP:0002892	decreased superior colliculus size
MP:0002894	abnormal otolith morphology
MP:0002895	abnormal otolithic membrane morphology
MP:0002896	abnormal bone mineralization
MP:0002897	blotchy skin
MP:0002898	absent cartilage
MP:0002904	increased circulating parathyroid hormone level
MP:0002905	decreased circulating parathyroid hormone level
MP:0002906	increased susceptibility to pharmacologically induced seizures
MP:0002907	abnormal parturition
MP:0002908	delayed wound healing
MP:0002910	abnormal excitatory postsynaptic currents
MP:0002911	abnormal inhibitory postsynaptic potential
MP:0002912	abnormal excitatory postsynaptic potential
MP:0002914	abnormal endplate potential
MP:0002915	abnormal synaptic depression
MP:0002916	increased synaptic depression
MP:0002917	decreased synaptic depression
MP:0002918	abnormal paired-pulse facilitation
MP:0002919	enhanced paired-pulse facilitation
MP:0002920	decreased paired-pulse facilitation
MP:0002921	abnormal post-tetanic potentiation
MP:0002922	decreased post-tetanic potentiation
MP:0002923	increased post-tetanic potentiation
MP:0002924	delayed CNS synapse formation
MP:0002925	abnormal cardiovascular development
MP:0002928	abnormal bile duct morphology
MP:0002929	abnormal bile duct development
MP:0002931	glutaricadicuria
MP:0002935	chronic joint inflammation
MP:0002938	white spotting
MP:0002939	head spot
MP:0002941	increased circulating alanine transaminase level
MP:0002942	decreased circulating alanine transaminase level
MP:0002944	increased lactate dehydrogenase level
MP:0002945	abnormal inhibitory postsynaptic currents
MP:0002946	delayed axon extension
MP:0002948	abnormal neuron specification
MP:0002950	abnormal neural crest cell migration
MP:0002951	small thyroid gland
MP:0002952	ventricular cardiomyopathy
MP:0002953	thick ventricular wall
MP:0002955	increased compensatory renal growth
MP:0002956	decreased compensatory renal growth
MP:0002961	abnormal axon guidance
MP:0002963	decreased urine protein level
MP:0002964	aortic elastic tissue lesions
MP:0002969	impaired social transmission of food preference
MP:0002970	abnormal white adipose tissue morphology
MP:0002971	abnormal brown adipose tissue morphology
MP:0002972	abnormal cardiac muscle contractility
MP:0002975	vascular smooth muscle hypertrophy
MP:0002976	vascular smooth muscle hypotrophy
MP:0002978	absent otoliths
MP:0002980	abnormal postural reflex
MP:0002981	increased liver weight
MP:0002982	abnormal primordial germ cell migration
MP:0002983	increased retinal ganglion cell number
MP:0002987	abnormal urine osmolality
MP:0002988	decreased urine osmolality
MP:0002989	small kidney
MP:0002990	short ureter
MP:0002991	abnormal sebaceous gland physiology
MP:0002992	abnormal sebaceous lipid secretion
MP:0002995	primary sex reversal
MP:0002997	enlarged seminal vesicle
MP:0002998	abnormal bone remodeling
MP:0002999	abnormal bone healing
MP:0003005	abnormal hippocampal fimbria morphology
MP:0003006	abnormal hippocampal fornix morphology
MP:0003007	ectopic thymus
MP:0003008	enhanced long term potentiation
MP:0003010	decreased mortality induced by ionizing radiation
MP:0003011	delayed dark adaptation
MP:0003012	no phenotypic analysis
MP:0003016	increased circulating bicarbonate level
MP:0003017	decreased circulating bicarbonate level
MP:0003021	abnormal coronary flow rate
MP:0003022	increased coronary flow rate
MP:0003023	decreased coronary flow rate
MP:0003025	increased vasoconstriction
MP:0003026	decreased vasoconstriction
MP:0003027	abnormal blood pH regulation
MP:0003029	alkalemia
MP:0003030	acidemia
MP:0003033	abnormal pulmonary vascular resistance
MP:0003035	decreased pulmonary vascular resistance
MP:0003036	vertebral transformation
MP:0003037	increased myocardial infarction size
MP:0003038	decreased myocardial infarction size
MP:0003039	increased time of peak ischemic contracture
MP:0003043	hypoalgesia
MP:0003044	impaired basement membrane formation
MP:0003047	abnormal thoracic vertebrae morphology
MP:0003048	abnormal cervical vertebrae morphology
MP:0003049	abnormal lumbar vertebrae morphology
MP:0003050	abnormal sacral vertebrae morphology
MP:0003051	curly tail
MP:0003055	abnormal long bone epiphyseal plate morphology
MP:0003057	abnormal epicardium morphology
MP:0003058	increased insulin secretion
MP:0003059	decreased insulin secretion
MP:0003060	increased aerobic running capacity
MP:0003061	decreased aerobic running capacity
MP:0003062	abnormal coping response
MP:0003063	increased coping response
MP:0003064	decreased coping response
MP:0003065	abnormal liver copper level
MP:0003067	decreased liver copper level
MP:0003069	abnormal superior semicircular canal morphology
MP:0003070	increased vascular permeability
MP:0003071	decreased vascular permeability
MP:0003072	abnormal metatarsal bone morphology
MP:0003073	abnormal metacarpal bone morphology
MP:0003075	altered response to CNS ischemic injury
MP:0003076	increased susceptibility to ischemic brain injury
MP:0003078	aphakia
MP:0003080	increased natural killer cell mediated cytotoxicity
MP:0003081	abnormal soleus morphology
MP:0003082	abnormal gastrocnemius morphology
MP:0003083	abnormal tibialis anterior morphology
MP:0003085	abnormal egg cylinder morphology
MP:0003087	absent allantois
MP:0003088	abnormal prepulse inhibition
MP:0003089	decreased skin tensile strength
MP:0003090	abnormal muscle precursor cell migration
MP:0003091	abnormal cell migration
MP:0003092	decreased corneal stroma thickness
MP:0003093	abnormal cornea anterior stroma morphology
MP:0003094	abnormal cornea posterior stroma morphology
MP:0003095	abnormal corneal stroma development
MP:0003096	increased corneal light-scattering
MP:0003097	abnormal tendon stiffness
MP:0003098	decreased tendon stiffness
MP:0003105	abnormal heart atrium morphology
MP:0003106	abnormal fear-related response
MP:0003107	abnormal response to novelty
MP:0003108	short zygomatic bone
MP:0003110	absent malleus processus brevis
MP:0003111	abnormal cell nucleus morphology
MP:0003114	pigmented parathyroid gland
MP:0003115	abnormal respiratory system development
MP:0003119	abnormal digestive system development
MP:0003120	abnormal tracheal cartilage morphology
MP:0003121	genetic imprinting
MP:0003122	maternal imprinting
MP:0003123	paternal imprinting
MP:0003125	abnormal septation of the cloaca
MP:0003126	abnormal external female genitalia morphology
MP:0003127	abnormal clitoris morphology
MP:0003128	splayed clitoris
MP:0003131	increased erythrocyte cell number
MP:0003132	increased pre-B cell number
MP:0003133	increased early pro-B cell number
MP:0003134	increased late pro-B cell number
MP:0003136	yellow coat color
MP:0003137	abnormal impulse conducting system conduction
MP:0003138	absent tympanic ring
MP:0003140	dilated heart atrium
MP:0003141	cardiac fibrosis
MP:0003143	enlarged otoliths
MP:0003144	decreased otolith number
MP:0003145	detached otolithic membrane
MP:0003146	absent cochlear ganglion
MP:0003149	abnormal tectorial membrane morphology
MP:0003150	detached tectorial membrane
MP:0003151	absent tunnel of Corti
MP:0003152	abnormal pillar cell differentiation
MP:0003153	early eyelid opening
MP:0003155	abnormal telomere length
MP:0003156	abnormal leukocyte migration
MP:0003159	abnormal esophageal smooth muscle morphology
MP:0003160	abnormal esophagus development
MP:0003161	absent lateral semicircular canal
MP:0003162	decreased lateral semicircular canal size
MP:0003163	absent posterior semicircular canal
MP:0003164	decreased posterior semicircular canal size
MP:0003165	absent superior semicircular canal
MP:0003166	decreased superior semicircular canal size
MP:0003167	abnormal scala tympani morphology
MP:0003168	abnormal scala vestibuli morphology
MP:0003169	abnormal scala media morphology
MP:0003171	phenotypic reversion
MP:0003172	abnormal lysosome physiology
MP:0003173	decreased lysosomal enzyme secretion
MP:0003174	increased lysosomal enzyme secretion
MP:0003175	reversion by mitotic recombination
MP:0003176	reversion by viral sequence excision
MP:0003178	left pulmonary isomerism
MP:0003180	abnormal pulmonary endothelial cell surface
MP:0003182	decreased pulmonary endothelial cell surface
MP:0003184	increased angiotensin I-converting enzyme activity
MP:0003185	decreased angiotensin I-converting enzyme activity
MP:0003186	abnormal redox activity
MP:0003190	fused synovial joints
MP:0003192	increased cholesterol efflux
MP:0003193	decreased cholesterol efflux
MP:0003194	abnormal frequency of paradoxical sleep
MP:0003196	calcified skin
MP:0003198	calcified tendon
MP:0003200	calcified joint
MP:0003201	extremity edema
MP:0003202	abnormal neuron apoptosis
MP:0003203	increased neuron apoptosis
MP:0003204	decreased neuron apoptosis
MP:0003207	decreased cellular sensitivity to gamma-irradiation
MP:0003208	abnormal neuromere morphology
MP:0003209	abnormal pulmonary elastic fiber morphology
MP:0003211	abnormal aorta elastic fiber morphology
MP:0003212	increased susceptibility to age related obesity
MP:0003213	decreased susceptibility to age related obesity
MP:0003221	abnormal cardiomyocyte apoptosis
MP:0003222	increased cardiomyocyte apoptosis
MP:0003223	decreased cardiomyocyte apoptosis
MP:0003224	neuron degeneration
MP:0003225	axonal dystrophy
MP:0003226	absent modiolus
MP:0003227	abnormal vascular branching morphogenesis
MP:0003228	abnormal sinus venosus morphology
MP:0003229	abnormal vitelline vasculature morphology
MP:0003230	abnormal umbilical artery morphology
MP:0003231	abnormal placenta vasculature
MP:0003232	abnormal forebrain development
MP:0003234	enhanced NMDA-mediated synaptic currents
MP:0003235	abnormal alisphenoid bone morphology
MP:0003236	abnormal lens capsule morphology
MP:0003237	abnormal lens epithelium morphology
MP:0003240	loss of hippocampal neurons
MP:0003241	loss of cortex neurons
MP:0003242	loss of basal ganglia neurons
MP:0003243	abnormal dopaminergic neuron morphology
MP:0003244	loss of dopaminergic neurons
MP:0003245	abnormal GABAergic neuron morphology
MP:0003246	loss of GABAergic neurons
MP:0003247	abnormal glutaminergic neuron morphology
MP:0003248	loss of glutamate neurons
MP:0003252	abnormal bile duct physiology
MP:0003253	dilated bile duct
MP:0003269	colon polyps
MP:0003271	abnormal duodenum morphology
MP:0003277	increased esophageal papilloma incidence
MP:0003283	abnormal digestive organ placement
MP:0003284	abnormal large intestine placement
MP:0003289	abnormal intestinal peristalsis
MP:0003299	gastric polyps
MP:0003305	proctitis
MP:0003306	small intestinal inflammation
MP:0003310	reduced modiolus
MP:0003312	abnormal locomotor coordination
MP:0003313	abnormal locomotor activation
MP:0003315	abnormal perineum morphology
MP:0003324	increased liver adenoma incidence
MP:0003329	amyloid beta deposits
MP:0003337	exocrine pancreas hyperplasia
MP:0003338	pancreas lipomatosis
MP:0003340	acute pancreas inflammation
MP:0003346	abnormal pectoral muscle morphology
MP:0003350	increased circulating levels of thyroid hormone
MP:0003351	decreased circulating levels of thyroid hormone
MP:0003355	decreased ovulation rate
MP:0003356	impaired luteinization
MP:0003357	impaired granulosa cell differentiation
MP:0003358	abnormal hypaxial muscle morphology
MP:0003359	hypaxial muscle hypoplasia
MP:0003360	abnormal depression-related behavior
MP:0003365	increased glucagonoma incidence
MP:0003367	increased circulating glucocorticoid level
MP:0003368	decreased circulating glucocorticoid level
MP:0003369	abnormal circulating estrogen level
MP:0003370	increased circulating estrogen level
MP:0003371	decreased circulating estrogen level
MP:0003379	absent sexual maturation
MP:0003380	abnormal intestine regeneration
MP:0003381	vitreal fibroplasia
MP:0003382	straub tail
MP:0003383	abnormal gluconeogenesis
MP:0003384	abnormal ventral body wall morphology
MP:0003385	abnormal body wall morphology
MP:0003388	absent pericardium
MP:0003393	decreased cardiac output
MP:0003394	increased cardiac output
MP:0003395	abnormal subclavian artery morphology
MP:0003396	abnormal embryonic hematopoiesis
MP:0003397	increased muscle weight
MP:0003398	increased skeletal muscle size
MP:0003400	kinked neural tube
MP:0003401	enlarged tail bud
MP:0003402	decreased liver weight
MP:0003403	absent placental labyrinth
MP:0003404	absent enamel
MP:0003406	failure of zygotic cell division
MP:0003407	abnormal central nervous system regeneration
MP:0003408	increased width of hypertrophic chondrocyte zone
MP:0003409	decreased width of hypertrophic chondrocyte zone
MP:0003410	abnormal artery development
MP:0003411	abnormal vein development
MP:0003412	abnormal afterhyperpolarization
MP:0003413	hair follicle degeneration
MP:0003414	epidermal cyst
MP:0003416	premature bone ossification
MP:0003417	premature endochondral bone ossification
MP:0003418	premature intramembranous bone ossification
MP:0003419	delayed endochondral bone ossification
MP:0003420	delayed intramembranous bone ossification
MP:0003421	abnormal thyroid gland development
MP:0003422	abnormal thrombolysis
MP:0003423	reduced thrombolysis
MP:0003424	premature neuronal precursor differentiation
MP:0003425	abnormal optic vesicle formation
MP:0003426	pulmonary interstitial fibrosis
MP:0003429	insensitivity to growth hormone
MP:0003430	increased pancreatic islet cell adenoma incidence
MP:0003434	decreased susceptibility to induced choroidal neovascularization
MP:0003435	herniated seminal vesicle
MP:0003436	decreased susceptibility to induced arthritis
MP:0003437	abnormal carotid body morphology
MP:0003438	abnormal carotid body physiology
MP:0003439	abnormal glycerol level
MP:0003440	decreased glycerol level
MP:0003441	increased glycerol level
MP:0003442	decreased circulating glycerol level
MP:0003444	abnormal neurotransmitter uptake
MP:0003447	decreased tumor growth/size
MP:0003448	abnormal tumor morphology
MP:0003449	abnormal intestinal goblet cell morphology
MP:0003450	enlarged pancreas
MP:0003451	absent olfactory bulb
MP:0003452	abnormal parotid gland morphology
MP:0003453	abnormal keratinocyte physiology
MP:0003455	decreased susceptibility to induced retinal damage
MP:0003456	absent tail
MP:0003457	abnormal circulating ketone body level
MP:0003458	decreased circulating ketone body level
MP:0003459	increased fear-related response
MP:0003460	decreased fear-related response
MP:0003461	abnormal response to novel object
MP:0003462	abnormal response to novel odor
MP:0003463	abnormal single cell response
MP:0003465	increased single cell response threshold
MP:0003466	decreased single cell response threshold
MP:0003469	decreased single cell response intensity
MP:0003470	abnormal summary potential
MP:0003477	abnormal nerve fiber response
MP:0003479	abnormal nerve fiber response intensity
MP:0003481	decreased nerve fiber response intensity
MP:0003483	decreased nerve fiber response threshold
MP:0003484	abnormal channel response
MP:0003486	abnormal channel response intensity
MP:0003488	decreased channel response intensity
MP:0003489	increased channel response threshold
MP:0003492	abnormal involuntary movement
MP:0003495	increased parathyroid adenoma incidence
MP:0003496	increased thyroid adenoma incidence
MP:0003497	insensitivity to parathyroid hormone
MP:0003501	iodide oxidation defect
MP:0003505	increased prolactinoma incidence
MP:0003509	increased circulating dihydrotestosterone level
MP:0003510	decreased circulating dihydrotestosterone level
MP:0003511	abnormal labium morphology
MP:0003527	small vulva
MP:0003531	abnormal vagina development
MP:0003534	blind vagina
MP:0003542	abnormal vascular endothelial cell development
MP:0003543	abnormal vascular endothelial cell differentiation
MP:0003544	abnormal vascular endothelial cell migration
MP:0003545	increased alcohol consumption
MP:0003546	decreased alcohol consumption
MP:0003547	abnormal pulmonary pressure
MP:0003550	short perineum
MP:0003553	abnormal foreskin morphology
MP:0003562	abnormal pancreatic beta cell physiology
MP:0003563	abnormal pancreatic alpha cell physiology
MP:0003564	abnormal insulin secretion
MP:0003565	abnormal glucagon secretion
MP:0003566	abnormal cell adhesion
MP:0003567	abnormal fetal cardiomyocyte proliferation
MP:0003568	uterus atresia
MP:0003570	increased uterus leiomyoma incidence
MP:0003572	abnormal uterus development
MP:0003574	abnormal oviduct morphology
MP:0003575	absent oviduct
MP:0003579	increased ovarian carcinoma incidence
MP:0003582	abnormal ovary development
MP:0003585	large ureter
MP:0003586	dilated ureter
MP:0003588	ureter stenosis
MP:0003589	abnormal ureter physiology
MP:0003590	ureteral reflux
MP:0003596	epididymal inflammation
MP:0003599	large penis
MP:0003607	abnormal prostate gland physiology
MP:0003613	abnormal kidney medulla development
MP:0003626	kidney medulla hypoplasia
MP:0003627	abnormal leukocyte tethering or rolling
MP:0003628	abnormal leukocyte adhesion
MP:0003630	abnormal urothelium morphology
MP:0003631	nervous system phenotype
MP:0003634	abnormal glial cell morphology
MP:0003637	cochlear ganglion hypoplasia
MP:0003638	abnormal response/metabolism to endogenous compounds
MP:0003639	abnormal response to vitamins
MP:0003641	small lung
MP:0003642	absent seminal vesicle
MP:0003643	spleen atrophy
MP:0003644	thymus atrophy
MP:0003645	increased pancreatic beta cell number
MP:0003647	absent oligodendrocytes
MP:0003648	abnormal radial glial cell morphology
MP:0003649	decreased heart right ventricle size
MP:0003651	abnormal axon extension
MP:0003652	abnormal skin turgor
MP:0003653	decreased skin turgor
MP:0003656	abnormal erythrocyte physiology
MP:0003657	abnormal erythrocyte osmotic lysis
MP:0003659	abnormal lymph circulation
MP:0003661	abnormal locus ceruleus morphology
MP:0003662	abnormal long bone epiphyseal plate proliferative zone
MP:0003663	abnormal thermosensation
MP:0003665	endophthalmitis
MP:0003666	impaired sperm capacitation
MP:0003668	abnormal periodontal ligament morphology
MP:0003669	periodontal ligament hypercellularity
MP:0003670	dilated renal glomerular capsule
MP:0003672	abnormal ureter development
MP:0003673	abnormal inguinal canal morphology
MP:0003674	oxidative stress
MP:0003677	abnormal ear lobe morphology
MP:0003684	abnormal inferior olivary complex morphology
MP:0003685	abnormal cardiac ganglion morphology
MP:0003686	abnormal eye muscle morphology
MP:0003687	abnormal intraocular muscle morphology
MP:0003690	abnormal glial cell physiology
MP:0003691	abnormal microglial cell physiology
MP:0003693	abnormal blastocyst hatching
MP:0003694	failure of blastocyst to hatch from the zona pellucida
MP:0003695	delayed blastocyst hatching from the zona pellucida
MP:0003696	abnormal zona pellucida morphology
MP:0003697	absent zona pellucida
MP:0003700	abnormal oviduct transport
MP:0003701	elevated level of mitotic sister chromatid exchange
MP:0003702	abnormal chromosome morphology
MP:0003703	abnormal vestibulocochlear ganglion morphology
MP:0003704	abnormal hair follicle development
MP:0003705	abnormal hypodermis morphology
MP:0003706	abnormal cell nucleus count
MP:0003707	increased cell nucleus count
MP:0003708	binucleate
MP:0003710	abnormal physiological neovascularization
MP:0003711	pathological neovascularization
MP:0003713	abnormal ear rotation
MP:0003714	absent platelets
MP:0003718	maternal effect
MP:0003719	abnormal pericyte morphology
MP:0003721	increased tumor growth/size
MP:0003722	absent ureter
MP:0003724	increased susceptibility to induced arthritis
MP:0003725	increased autoantibody level
MP:0003726	decreased autoantibody level
MP:0003727	abnormal retinal layer morphology
MP:0003728	abnormal retinal photoreceptor layer morphology
MP:0003729	abnormal photoreceptor outer segment morphology
MP:0003730	abnormal photoreceptor inner segment morphology
MP:0003731	abnormal retinal outer nuclear layer morphology
MP:0003732	abnormal retinal outer plexiform layer morphology
MP:0003733	abnormal retinal inner nuclear layer morphology
MP:0003734	abnormal retinal inner plexiform layer morphology
MP:0003742	narrow head
MP:0003745	abnormal mucosal lining of the mouth
MP:0003747	mouth mucosal ulcer
MP:0003750	increased mouth tumor incidence
MP:0003752	increased oral papilloma incidence
MP:0003755	abnormal palate morphology
MP:0003761	arched palate
MP:0003763	abnormal thymus physiology
MP:0003769	abnormal lip morphology
MP:0003786	premature aging
MP:0003787	abnormal imprinting
MP:0003790	absent CD4-positive, alpha beta T cells
MP:0003791	abnormal minor salivary gland morphology
MP:0003792	abnormal major salivary gland morphology
MP:0003793	abnormal submandibular gland morphology
MP:0003794	delayed somite formation
MP:0003798	abnormal Harderian gland pigmentation
MP:0003799	impaired macrophage chemotaxis
MP:0003800	monodactyly
MP:0003806	abnormal nucleotide metabolism
MP:0003808	increased atrioventricular cushion size
MP:0003810	abnormal hair cuticle
MP:0003811	abnormal hair cortex morphology
MP:0003812	abnormal hair medulla
MP:0003813	abnormal hair follicle dermal papilla morphology
MP:0003814	vascular smooth muscle hypoplasia
MP:0003816	abnormal pituitary gland development
MP:0003817	abnormal pituitary diverticulum morphology
MP:0003818	abnormal eye muscle development
MP:0003819	increased left ventricle diastolic pressure
MP:0003820	increased left ventricle systolic pressure
MP:0003821	decreased left ventricle diastolic pressure
MP:0003822	decreased left ventricle systolic pressure
MP:0003823	increased left ventricle developed pressure
MP:0003824	decreased left ventricle developed pressure
MP:0003825	abnormal pillar cell morphology
MP:0003826	abnormal Mullerian duct morphology
MP:0003827	abnormal Wolffian duct morphology
MP:0003829	impaired febrile response
MP:0003830	abnormal testis development
MP:0003833	decreased satellite cell number
MP:0003834	abnormal adrenergic chromaffin cell morphology
MP:0003838	abnormal milk ejection
MP:0003839	abnormal insulin clearance
MP:0003840	abnormal coronal suture morphology
MP:0003841	abnormal lambdoidal suture morphology
MP:0003842	abnormal metopic suture morphology
MP:0003843	abnormal sagittal suture morphology
MP:0003845	abnormal decidualization
MP:0003846	matted coat
MP:0003847	disorganized lens bow
MP:0003849	greasy coat
MP:0003850	abnormal thymocyte activation
MP:0003851	skeletal muscle interstitial fibrosis
MP:0003852	skeletal muscle necrosis
MP:0003854	abnormal forelimb stylopod morphology
MP:0003855	abnormal forelimb zeugopod morphology
MP:0003856	abnormal hindlimb stylopod morphology
MP:0003857	abnormal hindlimb zeugopod morphology
MP:0003858	enhanced coordination
MP:0003860	abnormal carbon dioxide level
MP:0003861	abnormal nervous system development
MP:0003862	decreased aggression towards males
MP:0003863	decreased aggression towards mice
MP:0003864	abnormal midbrain development
MP:0003866	abnormal defecation
MP:0003867	increased defecation amount
MP:0003868	abnormal feces composition
MP:0003869	ectopic cartilage
MP:0003871	abnormal myelin sheath morphology
MP:0003872	absent heart right ventricle
MP:0003873	pharyngeal arch hypoplasia
MP:0003874	absent pharyngeal arches
MP:0003875	abnormal hair follicle regression
MP:0003877	abnormal serotonergic neuron morphology
MP:0003878	abnormal ear physiology
MP:0003879	abnormal hair cell physiology
MP:0003880	abnormal central pattern generator function
MP:0003881	abnormal nephron morphology
MP:0003883	enlarged stomach
MP:0003884	decreased macrophage cell number
MP:0003885	abnormal rostral-caudal body axis extension
MP:0003886	abnormal embryonic epiblast morphology
MP:0003887	increased hepatocyte apoptosis
MP:0003888	liver hemorrhage
MP:0003889	enhanced sensorimotor gating
MP:0003890	abnormal embryonic-extraembryonic boundary morphology
MP:0003891	increased allantois apoptosis
MP:0003892	abnormal gastric gland morphology
MP:0003893	increased hepatocyte proliferation
MP:0003894	abnormal Purkinje cell innervation
MP:0003895	increased ectoderm apoptosis
MP:0003898	abnormal QRS complex
MP:0003901	abnormal PR interval
MP:0003902	abnormal cell mass
MP:0003903	increased cell mass
MP:0003904	decreased cell mass
MP:0003905	abnormal aorta elastin content
MP:0003907	decreased aorta elastin content
MP:0003908	decreased stereotypic behavior
MP:0003913	increased heart right ventricle weight
MP:0003915	increased left ventricle weight
MP:0003916	decreased heart left ventricle weight
MP:0003917	increased kidney weight
MP:0003918	decreased kidney weight
MP:0003920	abnormal heart right ventricle morphology
MP:0003921	abnormal heart left ventricle morphology
MP:0003922	abnormal heart right atrium morphology
MP:0003923	abnormal heart left atrium morphology
MP:0003925	abnormal cellular glucose import
MP:0003926	impaired cellular glucose import
MP:0003927	enhanced cellular glucose import
MP:0003928	increased heart rate variability
MP:0003929	decreased heart rate variability
MP:0003930	abnormal tooth hard tissue morphology
MP:0003932	abnormal molar crown morphology
MP:0003933	abnormal cementum morphology
MP:0003934	abnormal pancreas development
MP:0003935	abnormal craniofacial development
MP:0003936	abnormal reproductive system development
MP:0003938	abnormal ear development
MP:0003939	abnormal myotome morphology
MP:0003941	abnormal skin development
MP:0003942	abnormal urinary system development
MP:0003943	abnormal hepatobiliary system development
MP:0003944	abnormal T cell subpopulation ratio
MP:0003945	abnormal lymphocyte physiology
MP:0003946	renal necrosis
MP:0003947	abnormal cholesterol level
MP:0003948	abnormal gas homeostasis
MP:0003949	abnormal circulating lipid level
MP:0003950	abnormal plasma membrane morphology
MP:0003953	abnormal hormone level
MP:0003954	abnormal Reichert's membrane morphology
MP:0003955	abnormal ultimobranchial body morphology
MP:0003956	abnormal body size
MP:0003957	abnormal nitric oxide homeostasis
MP:0003958	heart valve hyperplasia
MP:0003959	abnormal lean body mass
MP:0003960	increased lean body mass
MP:0003961	decreased lean body mass
MP:0003962	abnormal adrenaline level
MP:0003963	abnormal corticosterone level
MP:0003964	abnormal noradrenaline level
MP:0003965	abnormal pituitary hormone level
MP:0003966	abnormal adrenocorticotropin level
MP:0003967	abnormal follicle stimulating hormone level
MP:0003968	abnormal growth hormone level
MP:0003971	abnormal thyroid-stimulating hormone level
MP:0003972	decreased pituitary hormone level
MP:0003973	increased pituitary hormone level
MP:0003974	abnormal endocardium morphology
MP:0003975	increased circulating VLDL triglyceride level
MP:0003976	decreased circulating VLDL triglyceride level
MP:0003979	increased circulating carnitine level
MP:0003980	increased circulating phospholipid level
MP:0003981	decreased circulating phospholipid level
MP:0003982	increased cholesterol level
MP:0003983	decreased cholesterol level
MP:0003984	embryonic growth retardation
MP:0003986	small cochlear ganglion
MP:0003987	small vestibular ganglion
MP:0003988	disorganized embryonic tissue
MP:0003989	abnormal barrel cortex morphology
MP:0003990	decreased neurotransmitter release
MP:0003992	increased mortality induced by ionizing radiation
MP:0003993	abnormal ventral spinal root morphology
MP:0003994	abnormal dorsal spinal root morphology
MP:0003995	abnormal uterine artery morphology
MP:0003996	clonic seizures
MP:0003998	decreased thermal nociceptive threshold
MP:0003999	enhanced passive avoidance behavior
MP:0004000	impaired passive avoidance behavior
MP:0004001	decreased hepatocyte proliferation
MP:0004002	abnormal jejunum morphology
MP:0004003	abnormal vascular endothelial cell physiology
MP:0004004	patent ductus venosus
MP:0004005	impaired contractility of intestinal smooth muscle
MP:0004006	impaired contractility of jejunal smooth muscle
MP:0004007	abnormal lung vasculature morphology
MP:0004008	abnormal GABA-mediated receptor currents
MP:0004009	abnormal diastolic filling velocity
MP:0004011	decreased diastolic filling velocity
MP:0004014	abnormal uterine environment
MP:0004015	abnormal oviduct environment
MP:0004016	decreased bone mass
MP:0004017	duplex kidney
MP:0004018	abnormal galactose homeostasis
MP:0004019	abnormal vitamin homeostasis
MP:0004021	abnormal rod electrophysiology
MP:0004022	abnormal cone electrophysiology
MP:0004023	abnormal chromosome number
MP:0004024	aneuploidy
MP:0004025	polyploidy
MP:0004027	trisomy
MP:0004029	spontaneous chromosome breakage
MP:0004030	induced chromosome breakage
MP:0004031	insulitis
MP:0004032	abnormal interventricular groove morphology
MP:0004034	belly blaze
MP:0004035	abnormal sublingual gland morphology
MP:0004036	abnormal muscle relaxation
MP:0004037	increased muscle relaxation
MP:0004038	lymphangiectasis
MP:0004039	abnormal cardiac cell glucose uptake
MP:0004041	increased susceptibility to kidney reperfusion injury
MP:0004042	decreased susceptibility to kidney reperfusion injury
MP:0004043	abnormal pH regulation
MP:0004045	abnormal cell cycle checkpoint function
MP:0004046	abnormal mitosis
MP:0004047	abnormal milk composition
MP:0004053	abnormal synchondrosis
MP:0004054	abnormal periocular mesenchyme morphology
MP:0004055	atrium hypoplasia
MP:0004056	abnormal myocardium compact layer morphology
MP:0004057	thin myocardium compact layer
MP:0004058	abnormal ventricle papillary muscle morphology
MP:0004061	papillary muscle hypoplasia
MP:0004063	dilated heart left atrium
MP:0004064	decreased susceptibility to induced muscular atrophy
MP:0004065	increased susceptibility to induced muscular atrophy
MP:0004066	abnormal primitive node morphology
MP:0004067	abnormal trabecula carnea morphology
MP:0004068	dilated dorsal aorta
MP:0004069	abnormal muscle spindle morphology
MP:0004070	abnormal P wave
MP:0004071	prolonged P wave
MP:0004072	abnormal frontal plane axis
MP:0004073	caudal body truncation
MP:0004074	abnormal Schwann cell precursor morphology
MP:0004075	decreased Schwann cell precursor number
MP:0004076	abnormal vitelline vascular remodeling
MP:0004077	abnormal striatum morphology
MP:0004079	abnormal putamen morphology
MP:0004080	abnormal nucleus accumbens morphology
MP:0004081	abnormal globus pallidus morphology
MP:0004082	abnormal habenula morphology
MP:0004083	polysyndactyly
MP:0004084	abnormal cardiac muscle relaxation
MP:0004085	abnormal heartbeat
MP:0004086	absent heartbeat
MP:0004087	abnormal muscle fiber morphology
MP:0004088	abnormal sarcoplasmic reticulum morphology
MP:0004089	dilated sarcoplasmic reticulum
MP:0004090	abnormal sarcomere morphology
MP:0004091	abnormal Z lines
MP:0004092	absent Z lines
MP:0004093	diffuse Z lines
MP:0004094	abnormal M lines
MP:0004095	ocular distichiasis
MP:0004096	abnormal midbrain-hindbrain boundary development
MP:0004097	abnormal cerebellar cortex morphology
MP:0004098	abnormal cerebellar granule cell morphology
MP:0004100	abnormal spinal cord interneuron morphology
MP:0004101	abnormal brain interneuron morphology
MP:0004102	abnormal dorsal striatum morphology
MP:0004103	abnormal ventral striatum morphology
MP:0004105	corneal abrasion
MP:0004106	lymphatic vessel hyperplasia
MP:0004107	abnormal thoracic duct morphology
MP:0004109	abnormal Sertoli cell development
MP:0004111	abnormal coronary artery morphology
MP:0004112	abnormal arteriole morphology
MP:0004114	abnormal atrioventricular node morphology
MP:0004115	abnormal sinoatrial node morphology
MP:0004116	abnormal atrioventricular bundle conduction
MP:0004117	abnormal atrioventricular bundle morphology
MP:0004120	cardiac ischemia
MP:0004121	abnormal sarcolemma morphology
MP:0004122	abnormal sinus arrhythmia
MP:0004123	abnormal impulse conducting system morphology
MP:0004124	abnormal Purkinje fiber morphology
MP:0004125	abnormal venule morphology
MP:0004126	thin hypodermis
MP:0004127	thick hypodermis
MP:0004129	abnormal respiratory quotient
MP:0004130	abnormal muscle cell glucose uptake
MP:0004131	abnormal motile primary cilium morphology
MP:0004132	absent embryonic cilia
MP:0004134	abnormal chest morphology
MP:0004135	abnormal mammary gland embryonic development
MP:0004136	abnormal tongue muscle morphology
MP:0004137	abnormal gastric surface mucous cell morphology
MP:0004138	abnormal mucous neck cell morphology
MP:0004139	abnormal gastric parietal cell morphology
MP:0004140	abnormal gastric chief cell morphology
MP:0004141	abnormal enteroendocrine cell morphology
MP:0004143	muscle hypertonia
MP:0004145	abnormal muscle electrophysiology
MP:0004146	absent M lines
MP:0004147	increased porphyrin level
MP:0004148	increased compact bone thickness
MP:0004149	increased bone strength
MP:0004150	absent caveolae
MP:0004151	decreased circulating iron level
MP:0004152	abnormal circulating iron level
MP:0004153	increased renal tubule apoptosis
MP:0004155	decreased susceptibility to induced pancreatitis
MP:0004156	abnormal QT variability
MP:0004160	retroesophageal right subclavian artery
MP:0004162	abnormal mammillary body morphology
MP:0004163	abnormal adenohypophysis morphology
MP:0004164	abnormal neurohypophysis morphology
MP:0004165	abnormal lateral geniculate nucleus morphology
MP:0004167	abnormal cingulate gyrus morphology
MP:0004170	abnormal orbitofrontal cortex morphology
MP:0004171	abnormal pallium development
MP:0004173	abnormal intervertebral disk morphology
MP:0004174	abnormal spine curvature
MP:0004177	tail telangiectases
MP:0004178	neck telangiectases
MP:0004179	transmission ratio distortion
MP:0004180	failure of initiation of embryo turning
MP:0004181	abnormal carotid artery morphology
MP:0004182	abnormal spermiation
MP:0004183	abnormal sympathetic nervous system physiology
MP:0004184	abnormal baroreceptor physiology
MP:0004185	abnormal adipocyte glucose uptake
MP:0004186	abnormal area postrema morphology
MP:0004187	cardia bifida
MP:0004188	delayed embryo turning
MP:0004189	abnormal alveolar process morphology
MP:0004190	abnormal direction of embryo turning
MP:0004191	neuronal intranuclear inclusions
MP:0004192	abnormal kidney pyramid morphology
MP:0004193	abnormal kidney papilla morphology
MP:0004194	abnormal kidney pelvis morphology
MP:0004196	abnormal prenatal growth/weight/body size
MP:0004197	abnormal fetal growth/weight/body size
MP:0004198	abnormal fetal size
MP:0004199	increased fetal size
MP:0004200	decreased fetal size
MP:0004201	fetal growth retardation
MP:0004202	pulmonary hyperplasia
MP:0004203	abnormal cranial flexure morphology
MP:0004205	absent hyoid bone
MP:0004206	abnormal dermomyotome development
MP:0004209	abnormal sweet taste sensitivity
MP:0004210	abnormal bitter taste sensitivity
MP:0004211	abnormal sour taste sensitivity
MP:0004212	abnormal salty taste sensitivity
MP:0004213	abnormal umami taste sensitivity
MP:0004214	abnormal long bone diaphysis morphology
MP:0004215	abnormal myocardial fiber physiology
MP:0004216	salt-resistant hypertension
MP:0004217	salt-sensitive hypertension
MP:0004218	meiotic nondisjunction during M1 phase
MP:0004220	abnormal peripheral nervous system regeneration
MP:0004221	abnormal iridocorneal angle
MP:0004222	iris synechia
MP:0004223	hypoplastic trabecular meshwork
MP:0004224	absent trabecular meshwork
MP:0004226	absent Schlemm's canal
MP:0004227	increased cellular sensitivity to ionizing radiation
MP:0004228	decreased cellular sensitivity to ionizing radiation
MP:0004229	abnormal embryonic erythropoiesis
MP:0004230	abnormal embryonic erythrocyte morphology
MP:0004231	abnormal calcium ion homeostasis
MP:0004232	decreased muscle weight
MP:0004234	abnormal masticatory muscle morphology
MP:0004235	abnormal masseter muscle morphology
MP:0004236	absent masseter muscle
MP:0004237	abnormal pterygoid muscle morphology
MP:0004238	absent pterygoid muscle
MP:0004239	abnormal temporalis muscle morphology
MP:0004243	abnormal motor nerve collateral sprouting
MP:0004244	abnormal miscarriage rate
MP:0004245	genital hemorrhage
MP:0004246	abnormal extensor digitorum longus morphology
MP:0004247	small pancreas
MP:0004248	abnormal epaxial muscle morphology
MP:0004249	abnormal crista ampullaris morphology
MP:0004250	tau protein deposits
MP:0004251	failure of heart looping
MP:0004252	abnormal direction of heart looping
MP:0004253	bifid atrial appendage
MP:0004255	abnormal spongiotrophoblast layer morphology
MP:0004256	abnormal maternal decidual layer morphology
MP:0004257	abnormal placenta weight
MP:0004261	abnormal embryonic neuroepithelium morphology
MP:0004262	abnormal physical strength
MP:0004263	abnormal limb posture
MP:0004264	abnormal extraembryonic tissue physiology
MP:0004265	abnormal placental transport
MP:0004266	pale placenta
MP:0004267	abnormal optic tract morphology
MP:0004268	abnormal optic stalk morphology
MP:0004269	abnormal optic cup morphology
MP:0004270	analgesia
MP:0004272	abnormal basement membrane morphology
MP:0004273	abnormal basal lamina morphology
MP:0004274	abnormal embryonic/fetal subventricular zone morphology
MP:0004275	abnormal postnatal subventricular zone morphology
MP:0004276	abnormal medial ganglionic eminence morphology
MP:0004277	abnormal lateral ganglionic eminence morphology
MP:0004279	abnormal rostral migratory stream morphology
MP:0004280	abnormal oculomotor nucleus morphology
MP:0004281	abnormal hypoglossal nucleus morphology
MP:0004283	absent corneal endothelium
MP:0004285	absent Descemet membrane
MP:0004286	abnormal internal auditory canal morphology
MP:0004287	abnormal spiral limbus morphology
MP:0004288	abnormal spiral ligament morphology
MP:0004289	abnormal bony labyrinth
MP:0004290	abnormal stapes footplate morphology
MP:0004292	abnormal spiral ligament fibrocyte morphology
MP:0004293	abnormal type I spiral ligament fibrocytes
MP:0004294	abnormal type II spiral ligament fibrocytes
MP:0004296	abnormal type IV spiral ligament fibrocytes
MP:0004297	abnormal proprioceptive neuron morphology
MP:0004298	vestibular ganglion degeneration
MP:0004299	absent vestibular ganglion
MP:0004300	abnormal organ of Corti supporting cell morphology
MP:0004301	absent organ of Corti supporting cells
MP:0004302	abnormal Deiters cell morphology
MP:0004303	abnormal Hensen cell morphology
MP:0004304	absent spiral limbus
MP:0004305	abnormal Rosenthal canal morphology
MP:0004306	small Rosenthal canal
MP:0004307	absent Rosenthal canal
MP:0004308	abnormal basilar membrane morphology
MP:0004309	absent otic vesicle
MP:0004310	small otic vesicle
MP:0004311	otic vesicle hypoplasia
MP:0004312	absent pillar cells
MP:0004313	absent vestibulocochlear ganglion
MP:0004315	absent vestibular saccule
MP:0004316	enlarged vestibular saccule
MP:0004317	small vestibular saccule
MP:0004318	absent incus
MP:0004322	abnormal sternebra morphology
MP:0004323	sternum hypoplasia
MP:0004324	vestibular hair cell degeneration
MP:0004325	absent vestibular hair cells
MP:0004327	increased vestibular hair cell number
MP:0004328	decreased vestibular hair cell number
MP:0004329	vestibular saccular degeneration
MP:0004330	abnormal vestibular saccular macula morphology
MP:0004331	vestibular saccular macula degeneration
MP:0004332	utricular degeneration
MP:0004333	abnormal utricular macula morphology
MP:0004334	utricular macular degeneration
MP:0004335	enlarged utricle
MP:0004336	small utricle
MP:0004338	small clavicle
MP:0004340	short scapula
MP:0004342	scapular bone foramen
MP:0004345	abnormal acromion morphology
MP:0004346	absent acromion
MP:0004347	abnormal scapular spine morphology
MP:0004348	long femur
MP:0004350	long humerus
MP:0004353	abnormal deltoid tuberosity morphology
MP:0004354	absent deltoid tuberosity
MP:0004355	short radius
MP:0004362	cochlear hair cell degeneration
MP:0004363	stria vascularis degeneration
MP:0004364	thin stria vascularis
MP:0004365	abnormal strial basal cell morphology
MP:0004366	abnormal strial marginal cell morphology
MP:0004367	abnormal strial intermediate cell morphology
MP:0004368	abnormal stria vascularis vasculature morphology
MP:0004369	absent utricle
MP:0004372	bowed fibula
MP:0004375	enlarged frontal bone
MP:0004376	absent frontal bone
MP:0004377	small frontal bone
MP:0004378	frontal bone foramen
MP:0004379	wide frontal bone
MP:0004380	short frontal bone
MP:0004381	abnormal hair follicle melanocyte morphology
MP:0004382	abnormal hair follicle melanogenesis
MP:0004383	absent interparietal bone
MP:0004384	small interparietal bone
MP:0004385	interparietal bone hypoplasia
MP:0004386	enlarged interparietal bone
MP:0004387	abnormal prechordal plate morphology
MP:0004388	absent prechordal plate
MP:0004389	abnormal respiratory bronchiole morphology
MP:0004391	abnormal respiratory conducting tube morphology
MP:0004392	abnormal CD8-positive, alpha-beta T cell physiology
MP:0004393	abnormal cochlear inner hair cell morphology
MP:0004395	increased cochlear inner hair cell number
MP:0004396	decreased cochlear inner hair cell number
MP:0004397	absent cochlear inner hair cells
MP:0004398	cochlear inner hair cell degeneration
MP:0004399	abnormal cochlear outer hair cell morphology
MP:0004401	increased cochlear outer hair cell number
MP:0004402	decreased cochlear outer hair cell number
MP:0004403	absent cochlear outer hair cells
MP:0004404	cochlear outer hair cell degeneration
MP:0004405	absent cochlear hair cells
MP:0004406	abnormal cochlear hair cell number
MP:0004407	increased cochlear hair cell number
MP:0004408	decreased cochlear hair cell number
MP:0004409	abnormal crista ampullaris neuroepithelium morphology
MP:0004410	absent endocochlear potential
MP:0004411	decreased endocochlear potential
MP:0004412	abnormal cochlear microphonics
MP:0004413	absent cochlear microphonics
MP:0004414	decreased cochlear microphonics
MP:0004415	abnormal cochlear nerve compound action potential
MP:0004416	absent cochlear nerve compound action potential
MP:0004417	decreased cochlear nerve compound action potential
MP:0004418	small parietal bone
MP:0004419	absent parietal bone
MP:0004420	parietal bone hypoplasia
MP:0004421	enlarged parietal bone
MP:0004422	small temporal bone
MP:0004423	abnormal squamosal bone morphology
MP:0004424	temporal bone hypoplasia
MP:0004425	abnormal otolith organ morphology
MP:0004426	abnormal cochlear labyrinth morphology
MP:0004427	abnormal vestibular labyrinth morphology
MP:0004428	abnormal type I vestibular cell
MP:0004430	abnormal Claudius cell morphology
MP:0004431	abnormal hair cell mechanoelectric transduction
MP:0004432	abnormal cochlear hair cell physiology
MP:0004433	abnormal cochlear inner hair cell physiology
MP:0004434	abnormal cochlear outer hair cell physiology
MP:0004435	abnormal cochlear outer hair cell electromotility
MP:0004436	absent cochlear outer hair cell electromotility
MP:0004437	decreased cochlear outer hair cell electromotility
MP:0004438	abnormal vestibular hair cell physiology
MP:0004439	absent Meckel's cartilage
MP:0004440	absent occipital bone
MP:0004441	small occipital bone
MP:0004442	occipital bone foramen
MP:0004443	absent supraoccipital bone
MP:0004444	small supraoccipital bone
MP:0004445	small exoccipital bone
MP:0004447	small basioccipital bone
MP:0004448	abnormal presphenoid bone morphology
MP:0004449	absent presphenoid bone
MP:0004450	presphenoid bone hypoplasia
MP:0004451	short presphenoid bone
MP:0004452	abnormal pterygoid process morphology
MP:0004453	abnormal pterygoid bone morphology
MP:0004454	absent pterygoid process
MP:0004455	pterygoid bone hypoplasia
MP:0004456	small pterygoid bone
MP:0004457	abnormal orbitosphenoid bone morphology
MP:0004458	absent alisphenoid bone
MP:0004459	small alisphenoid bone
MP:0004460	alisphenoid bone hypoplasia
MP:0004461	basisphenoid bone hypoplasia
MP:0004462	small basisphenoid bone
MP:0004463	basisphenoid bone foramen
MP:0004464	absent strial basal cell tight junctions
MP:0004465	degeneration of organ of Corti supporting cells
MP:0004466	short cochlear outer hair cells
MP:0004467	absent zygomatic bone
MP:0004469	abnormal zygomatic arch morphology
MP:0004470	small nasal bone
MP:0004472	broad nasal bone
MP:0004473	absent nasal bone
MP:0004474	enlarged nasal bone
MP:0004475	palatine bone hypoplasia
MP:0004476	absent palatine bone
MP:0004477	turbinate hypoplasia
MP:0004480	abnormal round window morphology
MP:0004481	abnormal conjunctival epithelium morphology
MP:0004482	abnormal interdental cell morphology
MP:0004483	absent interdental cells
MP:0004484	altered response of heart to induced stress
MP:0004485	increased response of heart to induced stress
MP:0004486	decreased response of heart to induced stress
MP:0004487	type I spiral ligament fibrocyte degeneration
MP:0004488	type II spiral ligament fibrocyte degeneration
MP:0004489	type III spiral ligament fibrocyte degeneration
MP:0004490	type IV spiral ligament fibrocyte degeneration
MP:0004491	abnormal orientation of outer hair cell stereociliary bundles
MP:0004492	abnormal orientation of inner hair cell stereociliary bundles
MP:0004493	dilated cochlea
MP:0004494	abnormal synaptic glutamate release
MP:0004495	decreased synaptic glutamate release
MP:0004497	decreased organ of Corti supporting cell number
MP:0004498	increased organ of Corti supporting cell number
MP:0004499	increased incidence of tumors by chemical induction
MP:0004500	increased incidence of tumors by ionizing radiation induction
MP:0004501	increased incidence of tumors by UV-induction
MP:0004502	decreased incidence of tumors by chemical induction
MP:0004503	decreased incidence of tumors by ionizing radiation induction
MP:0004504	decreased incidence of tumors by UV induction
MP:0004505	decreased renal glomerulus number
MP:0004506	abnormal pubis morphology
MP:0004507	abnormal ischium morphology
MP:0004508	abnormal pectoral girdle bone morphology
MP:0004513	avnosmia
MP:0004514	dystocia
MP:0004515	abnormal vestibular hair cell stereociliary bundle morphology
MP:0004516	fused vestibular hair cell stereocilia
MP:0004517	decreased vestibular hair cell stereocilia number
MP:0004518	absent vestibular hair cell stereocilia
MP:0004519	thin vestibular hair cell stereocilia
MP:0004520	short vestibular hair cell stereocilia
MP:0004521	abnormal cochlear hair cell stereociliary bundle morphology
MP:0004522	abnormal orientation of cochlear hair cell stereociliary bundles
MP:0004523	decreased cochlear hair cell stereocilia number
MP:0004524	short cochlear hair cell stereocilia
MP:0004525	thin cochlear hair cell stereocilia
MP:0004526	absent cochlear hair cell stereocilia
MP:0004527	abnormal outer hair cell stereociliary bundle morphology
MP:0004528	fused outer hair cell stereocilia
MP:0004529	decreased outer hair cell stereocilia number
MP:0004530	absent outer hair cell stereocilia
MP:0004531	short outer hair cell stereocilia
MP:0004532	abnormal inner hair cell stereociliary bundle morphology
MP:0004533	fused inner hair cell stereocilia
MP:0004534	decreased inner hair cell stereocilia number
MP:0004535	absent inner hair cell stereocilia
MP:0004536	short inner hair cell stereocilia
MP:0004537	abnormal palatine bone horizontal plate morphology
MP:0004538	abnormal maxillary shelf morphology
MP:0004539	absent maxilla
MP:0004540	small maxilla
MP:0004542	impaired acrosome reaction
MP:0004543	abnormal sperm physiology
MP:0004544	absent esophagus
MP:0004545	enlarged esophagus
MP:0004546	esophagus hyperplasia
MP:0004548	dilated esophagus
MP:0004549	small trachea
MP:0004550	short trachea
MP:0004551	decreased tracheal cartilage ring number
MP:0004552	fused tracheal cartilage rings
MP:0004553	absent tracheal cartilage rings
MP:0004554	small pharynx
MP:0004556	enlarged allantois
MP:0004557	dilated allantois
MP:0004558	delayed allantois development
MP:0004559	small allantois
MP:0004560	abnormal chorionic plate morphology
MP:0004561	absent facial nerve
MP:0004562	abnormal inner hair cell synaptic ribbon morphology
MP:0004563	absent active-zone-anchored inner hair cell synaptic ribbon
MP:0004564	enlarged myocardial fiber
MP:0004565	small myocardial fiber
MP:0004566	myocardial fiber degeneration
MP:0004567	decreased myocardial fiber number
MP:0004568	fusion of glossopharyngeal and vagus nerve
MP:0004569	glossopharyngeal nerve hypoplasia
MP:0004570	absent glossopharyngeal nerve
MP:0004572	fusion of basioccipital and basisphenoid bone
MP:0004573	absent limb buds
MP:0004574	broad limb buds
MP:0004575	small limb buds
MP:0004576	abnormal foot plate morphology
MP:0004577	abnormal cochlear hair cell inter-stereocilial links morphology
MP:0004578	abnormal cochlear hair bundle tip links morphology
MP:0004580	abnormal cochlear hair bundle transient lateral links morphology
MP:0004582	absent cochlear hair bundle ankle links
MP:0004585	absent vestibular hair bundle shaft connectors
MP:0004586	pillar cell degeneration
MP:0004587	decreased cellular sensitivity to X-ray irradiation
MP:0004588	abnormal vestibular hair cell development
MP:0004589	abnormal cochlear hair cell development
MP:0004590	absent Deiters cells
MP:0004591	enlarged tectorial membrane
MP:0004592	small mandible
MP:0004593	long mandible
MP:0004594	abnormal mandibular coronoid process morphology
MP:0004595	abnormal mandibular condyloid process morphology
MP:0004596	abnormal mandibular angle morphology
MP:0004597	increased susceptibility to noise-induced hearing loss
MP:0004598	abnormal cochlear basement membrane morphology
MP:0004599	abnormal vertebral arch morphology
MP:0004600	abnormal vertebral transverse process morphology
MP:0004602	abnormal vertebral articular process morphology
MP:0004603	absent vertebral arch
MP:0004605	abnormal vertebral lamina morphology
MP:0004606	absent vertebral spinous process
MP:0004607	abnormal cervical atlas morphology
MP:0004608	abnormal cervical axis morphology
MP:0004611	increased susceptibility to ototoxicity-induced hearing loss
MP:0004612	fusion of vertebral bodies
MP:0004613	fusion of vertebral arches
MP:0004614	caudal vertebral transformation
MP:0004615	cervical vertebral transformation
MP:0004616	lumbar vertebral transformation
MP:0004617	sacral vertebral transformation
MP:0004618	thoracic vertebral transformation
MP:0004619	caudal vertebral fusion
MP:0004622	sacral vertebral fusion
MP:0004625	abnormal rib joint
MP:0004627	abnormal trochanter morphology
MP:0004628	Deiters cell degeneration
MP:0004629	abnormal spiral modiolar artery morphology
MP:0004630	spiral modiolar artery stenosis
MP:0004631	abnormal auditory cortex morphology
MP:0004632	abnormal cochlear OHC efferent innervation pattern
MP:0004633	abnormal cochlear IHC efferent innervation pattern
MP:0004636	decreased metacarpal bone number
MP:0004637	metacarpal bone hypoplasia
MP:0004640	decreased metatarsal bone number
MP:0004641	elongated metatarsal bones
MP:0004646	decreased cervical vertebrae number
MP:0004647	decreased lumbar vertebrae number
MP:0004648	decreased thoracic vertebrae number
MP:0004650	increased lumbar vertebrae number
MP:0004651	increased thoracic vertebrae number
MP:0004652	small caudal vertebrae
MP:0004653	absent caudal vertebrae
MP:0004656	absent sacral vertebrae
MP:0004657	small sacral vertebrae
MP:0004658	abnormal ventral tubercle of atlas morphology
MP:0004660	absent thyroid follicular cells
MP:0004662	abnormal thyroid diverticulum morphology
MP:0004664	delayed inner ear development
MP:0004665	abnormal stapedial artery morphology
MP:0004666	absent stapedial artery
MP:0004668	absent vertebral body
MP:0004669	enlarged vertebral body
MP:0004670	small vertebral body
MP:0004671	long ribs
MP:0004673	splayed ribs
MP:0004675	rib fractures
MP:0004677	truncated ribs
MP:0004679	xiphoid process foramen
MP:0004680	small xiphoid process
MP:0004681	intervertebral disk hypoplasia
MP:0004682	small intervertebral disk
MP:0004683	absent intervertebral disk
MP:0004688	absent ilium
MP:0004689	small ischium
MP:0004692	small pubis
MP:0004695	increased length of long bones
MP:0004696	abnormal thyroid follicle morphology
MP:0004697	abnormal thyroid follicular cell morphology
MP:0004698	abnormal thyroid parafollicular C-cell morphology
MP:0004700	abnormal circulating insulin-like growth factor I level
MP:0004701	decreased circulating insulin-like growth factor I level
MP:0004702	increased circulating insulin-like growth factor I level
MP:0004703	abnormal vertebral column morphology
MP:0004705	elongated vertebral body
MP:0004706	short vertebral body
MP:0004707	enlarged lumbar vertebrae
MP:0004708	short lumbar vertebrae
MP:0004709	cervical vertebrae degeneration
MP:0004710	small notochord
MP:0004711	persistence of notochord tissue
MP:0004712	notochord degeneration
MP:0004713	split notochord
MP:0004714	truncated notochord
MP:0004715	absent vestibulocochlear nerve
MP:0004716	abnormal cochlear nerve morphology
MP:0004717	absent cochlear nerve
MP:0004718	abnormal vestibular nerve morphology
MP:0004721	abnormal platelet dense granule morphology
MP:0004722	abnormal platelet dense granule number
MP:0004725	decreased platelet serotonin level
MP:0004726	abnormal nasal capsule morphology
MP:0004727	absent epididymis
MP:0004728	abnormal efferent ductules of testis morphology
MP:0004729	absent efferent ductules of testis
MP:0004731	increased circulating gastrin level
MP:0004732	decreased circulating gastrin level
MP:0004733	abnormal thoracic cavity morphology
MP:0004734	small thoracic cavity
MP:0004735	enlarged thoracic cavity
MP:0004736	abnormal distortion product otoacoustic emission
MP:0004737	absent distortion product otoacoustic emissions
MP:0004739	conductive hearing loss
MP:0004740	sensorineural hearing loss
MP:0004741	mixed hearing loss
MP:0004742	abnormal vestibular system physiology
MP:0004746	abnormal cochlear IHC afferent innervation pattern
MP:0004747	abnormal cochlear OHC afferent innervation pattern
MP:0004748	increased susceptibility to age-related hearing loss
MP:0004749	nonsyndromic hearing loss
MP:0004750	syndromic hearing loss
MP:0004751	increased length of allograft survival
MP:0004752	decreased length of allograft survival
MP:0004753	abnormal miniature excitatory postsynaptic currents
MP:0004754	abnormal kidney collecting duct morphology
MP:0004755	abnormal loop of Henle morphology
MP:0004756	abnormal proximal convoluted tubule morphology
MP:0004757	abnormal distal convoluted tubule morphology
MP:0004758	absent strial marginal cells
MP:0004759	decreased mitotic index
MP:0004760	increased mitotic index
MP:0004761	increased susceptibility to induced pancreatitis
MP:0004762	increased anti-double stranded DNA antibody level
MP:0004767	increased cochlear nerve compound action potential
MP:0004768	abnormal axonal transport
MP:0004769	abnormal synaptic vesicle morphology
MP:0004770	abnormal synaptic vesicle recycling
MP:0004771	increased anti-single stranded DNA antibody level
MP:0004772	abnormal bile secretion
MP:0004773	abnormal bile composition
MP:0004774	abnormal bile salt level
MP:0004775	abnormal vestibular dark cell morphology
MP:0004776	vestibular dark cell degeneration
MP:0004778	increased macrophage derived foam cell number
MP:0004780	abnormal surfactant secretion
MP:0004781	abnormal surfactant composition
MP:0004782	abnormal surfactant physiology
MP:0004783	abnormal cardinal vein morphology
MP:0004784	abnormal anterior cardinal vein morphology
MP:0004785	abnormal posterior cardinal vein morphology
MP:0004786	abnormal common cardinal vein morphology
MP:0004787	abnormal dorsal aorta morphology
MP:0004788	abnormal auditory cortex tonotopy
MP:0004789	increased bile salt level
MP:0004790	absent upper incisors
MP:0004791	absent lower incisors
MP:0004792	abnormal synaptic vesicle number
MP:0004793	abnormal synaptic vesicle clustering
MP:0004794	increased anti-nuclear antigen antibody level
MP:0004795	decreased anti-nuclear antigen antibody level
MP:0004796	increased anti-histone antibody level
MP:0004797	increased anti-erythrocyte antigen antibody level
MP:0004798	decreased anti-double stranded DNA antibody level
MP:0004799	increased susceptibility to experimental autoimmune encephalomyelitis
MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis
MP:0004801	increased susceptibility to systemic lupus erythematosus
MP:0004802	decreased susceptibility to systemic lupus erythematosus
MP:0004803	increased susceptibility to autoimmune diabetes
MP:0004804	decreased susceptibility to autoimmune diabetes
MP:0004805	absent oocytes
MP:0004806	absent germ cells
MP:0004807	abnormal paired-pulse inhibition
MP:0004808	abnormal hematopoietic stem cell morphology
MP:0004809	increased hematopoietic stem cell number
MP:0004810	decreased hematopoietic stem cell number
MP:0004811	abnormal neuron physiology
MP:0004812	abnormal linear vestibular evoked potential
MP:0004813	absent linear vestibular evoked potential
MP:0004814	reduced linear vestibular evoked potential
MP:0004815	abnormal somatic hypermutation frequency
MP:0004816	abnormal class switch recombination
MP:0004817	abnormal skeletal muscle mass
MP:0004818	increased skeletal muscle mass
MP:0004819	decreased skeletal muscle mass
MP:0004821	increased susceptibility to experimental autoimmune uveoretinitis
MP:0004822	decreased susceptibility to experimental autoimmune uveoretinitis
MP:0004823	increased susceptibility to experimental autoimmune myasthenia gravis
MP:0004824	decreased susceptibility to experimental autoimmune myasthenia gravis
MP:0004827	increased susceptibility to autoimmune hemolytic anemia
MP:0004828	decreased susceptibility to autoimmune hemolytic anemia
MP:0004829	increased anti-chromatin antibody level
MP:0004830	short incisors
MP:0004831	long incisors
MP:0004833	ovary atrophy
MP:0004834	ovary hemorrhage
MP:0004835	abnormal miniature endplate potential
MP:0004836	abnormal synaptic acetylcholine release
MP:0004837	abnormal neural fold formation
MP:0004838	abnormal neural fold elevation formation
MP:0004840	increased Deiters cell number
MP:0004841	abnormal small intestine crypts of Lieberkuhn morphology
MP:0004842	abnormal large intestine crypts of Lieberkuhn morphology
MP:0004843	abnormal Paneth cell morphology
MP:0004845	absent vestibuloocular reflex
MP:0004846	absent skeletal muscle
MP:0004847	abnormal liver weight
MP:0004848	abnormal liver size
MP:0004850	abnormal testis weight
MP:0004851	increased testis weight
MP:0004852	decreased testis weight
MP:0004853	abnormal ovary size
MP:0004855	increased ovary weight
MP:0004856	decreased ovary weight
MP:0004857	abnormal heart weight
MP:0004858	abnormal nervous system regeneration
MP:0004859	abnormal synaptic plasticity
MP:0004860	dilated kidney collecting duct
MP:0004861	abnormal Raphe nucleus morphology
MP:0004862	small scala tympani
MP:0004863	thin spiral ligament
MP:0004864	spiral ligament degeneration
MP:0004867	decreased platelet calcium level
MP:0004870	small premaxilla
MP:0004873	absent turbinates
MP:0004874	abnormal timing of postnatal eyelid opening
MP:0004875	increased mean systemic arterial blood pressure
MP:0004876	decreased mean systemic arterial blood pressure
MP:0004877	abnormal systemic vascular resistance
MP:0004878	increased systemic vascular resistance
MP:0004879	decreased systemic vascular resistance
MP:0004880	lung cysts
MP:0004882	enlarged lung
MP:0004883	abnormal vascular wound healing
MP:0004884	abnormal testis physiology
MP:0004885	abnormal endolymph
MP:0004887	decreased endolymph production
MP:0004888	abnormal perilymph
MP:0004889	increased energy expenditure
MP:0004890	decreased energy expenditure
MP:0004894	uterus atrophy
MP:0004895	vagina atrophy
MP:0004896	abnormal endometrium morphology
MP:0004898	uterine hemorrhage
MP:0004899	absent squamosal bone
MP:0004900	absent zygomatic arch
MP:0004901	decreased male germ cell number
MP:0004902	abnormal uterus size
MP:0004903	abnormal uterus weight
MP:0004904	increased uterus weight
MP:0004905	decreased uterus weight
MP:0004908	abnormal seminal vesicle weight
MP:0004909	increased seminal vesicle weight
MP:0004910	decreased seminal vesicle weight
MP:0004911	absent mandibular condyloid process
MP:0004912	absent mandibular coronoid process
MP:0004913	absent mandibular angle
MP:0004914	absent ultimobranchial body
MP:0004915	abnormal Reichert's cartilage morphology
MP:0004916	absent Reichert cartilage
MP:0004917	abnormal T cell selection
MP:0004918	abnormal negative T cell selection
MP:0004919	abnormal positive T cell selection
MP:0004920	increased placenta weight
MP:0004921	decreased placenta weight
MP:0004922	abnormal common crus morphology
MP:0004923	absent common crus
MP:0004925	decreased susceptibility to noise-induced hearing loss
MP:0004927	abnormal epididymis weight
MP:0004928	increased epididymis weight
MP:0004929	decreased epididymis weight
MP:0004930	small epididymis
MP:0004931	enlarged epididymis
MP:0004932	epididymis hypoplasia
MP:0004933	abnormal epididymis epithelium morphology
MP:0004934	epididymis epithelium degeneration
MP:0004936	impaired branching involved in ureteric bud morphogenesis
MP:0004937	dilated heart
MP:0004938	dilated vasculature
MP:0004940	abnormal B-1 B cell morphology
MP:0004941	abnormal regulatory T cell morphology
MP:0004942	abnormal B cell selection
MP:0004944	abnormal B cell negative selection
MP:0004945	abnormal bone resorption
MP:0004946	abnormal regulatory T cell physiology
MP:0004948	abnormal neuronal precursor proliferation
MP:0004949	absent neuronal precursor cells
MP:0004950	abnormal brain vasculature morphology
MP:0004951	abnormal spleen weight
MP:0004952	increased spleen weight
MP:0004953	decreased spleen weight
MP:0004955	increased thymus weight
MP:0004956	decreased thymus weight
MP:0004957	abnormal blastocyst morphology
MP:0004958	enlarged prostate gland
MP:0004961	increased prostate gland weight
MP:0004962	decreased prostate gland weight
MP:0004963	abnormal blastocoele morphology
MP:0004964	absent inner cell mass
MP:0004965	inner cell mass degeneration
MP:0004966	abnormal inner cell mass proliferation
MP:0004967	abnormal kidney epithelium morphology
MP:0004968	kidney epithelium hyperplasia
MP:0004969	pale kidney
MP:0004971	dermal hyperplasia
MP:0004972	abnormal regulatory T cell number
MP:0004973	increased regulatory T cell number
MP:0004974	decreased regulatory T cell number
MP:0004975	absent regulatory T cells
MP:0004976	abnormal B-1 B cell number
MP:0004977	increased B-1 B cell number
MP:0004978	decreased B-1 B cell number
MP:0004979	abnormal neuronal precursor cell number
MP:0004980	increased neuronal precursor cell number
MP:0004981	decreased neuronal precursor cell number
MP:0004982	abnormal osteoclast morphology
MP:0004983	abnormal osteoclast cell number
MP:0004984	increased osteoclast cell number
MP:0004985	decreased osteoclast cell number
MP:0004986	abnormal osteoblast morphology
MP:0004987	abnormal osteoblast cell number
MP:0004988	increased osteoblast cell number
MP:0004989	decreased osteoblast cell number
MP:0004990	abnormal ciliary ganglion morphology
MP:0004991	decreased bone strength
MP:0004993	decreased bone resorption
MP:0004994	abnormal brain wave pattern
MP:0004996	abnormal CNS synapse formation
MP:0004997	increased CNS synapse formation
MP:0004998	decreased CNS synapse formation
MP:0004999	abnormal blood-inner ear barrier function
MP:0005000	abnormal immune tolerance
MP:0005002	abnormal T cell clonal deletion
MP:0005004	abnormal lymphocyte anergy
MP:0005005	abnormal self tolerance
MP:0005006	abnormal osteoblast physiology
MP:0005010	abnormal CD8-positive, alpha beta T cell morphology
MP:0005012	decreased eosinophil cell number
MP:0005019	abnormal early pro-B cell
MP:0005020	abnormal late pro-B cell
MP:0005022	abnormal immature B cell morphology
MP:0005023	abnormal wound healing
MP:0005025	abnormal response to infection
MP:0005026	decreased susceptibility to parasitic infection
MP:0005027	increased susceptibility to parasitic infection
MP:0005028	abnormal trophectoderm morphology
MP:0005029	abnormal amnion morphology
MP:0005030	absent amnion
MP:0005031	abnormal trophoblast layer morphology
MP:0005032	abnormal ectoplacental cone morphology
MP:0005033	abnormal trophoblast giant cell morphology
MP:0005035	perianal ulcer
MP:0005037	mucous diarrhea
MP:0005039	hypoxia
MP:0005040	abnormal MHC II cell surface expression on macrophages
MP:0005041	abnormal antigen presentation via MHC class II
MP:0005042	abnormal level of surface class II molecules
MP:0005043	defective assembly of class II molecules
MP:0005046	absent spleen white pulp
MP:0005048	abnormal thrombosis
MP:0005058	abnormal lysosome morphology
MP:0005059	lysosomal protein accumulation
MP:0005060	accumulation of giant lysosomes in kidney/renal tubule cells
MP:0005070	impaired natural killer cell mediated cytotoxicity
MP:0005071	enlarged hair follicle melanin granules
MP:0005072	abnormal hair follicle melanin granule morphology
MP:0005074	impaired granulocyte bactericidal activity
MP:0005075	abnormal melanosome morphology
MP:0005076	abnormal cell differentiation
MP:0005077	abnormal melanogenesis
MP:0005078	abnormal cytotoxic T cell physiology
MP:0005079	decreased cytotoxic T cell cytolysis
MP:0005081	abnormal dermis reticular layer morphology
MP:0005087	decreased acute inflammation
MP:0005088	increased acute inflammation
MP:0005089	decreased double-negative T cell number
MP:0005090	increased double-negative T cell number
MP:0005091	increased double-positive T cell number
MP:0005092	decreased double-positive T cell number
MP:0005093	decreased B cell proliferation
MP:0005094	abnormal T cell proliferation
MP:0005095	decreased T cell proliferation
MP:0005096	erythroblastosis
MP:0005097	polychromatophilia
MP:0005098	abnormal optic choroid morphology
MP:0005100	abnormal choroid pigmentation
MP:0005101	abnormal ciliary body pigmentation
MP:0005104	abnormal tarsal bone morphology
MP:0005105	abnormal middle ear ossicle morphology
MP:0005106	abnormal incus morphology
MP:0005109	abnormal talus morphology
MP:0005111	hyperdipsia
MP:0005112	abnormal spinal cord ventral horn morphology
MP:0005113	decreased spinal cord ventral horn cell number
MP:0005114	premature hair loss
MP:0005116	abnormal circulating pituitary hormone level
MP:0005117	increased circulating pituitary hormone level
MP:0005118	decreased circulating pituitary hormone level
MP:0005119	decreased circulating thyroid-stimulating hormone level
MP:0005120	decreased circulating growth hormone level
MP:0005121	decreased circulating prolactin level
MP:0005122	increased circulating thyroid-stimulating hormone level
MP:0005123	increased circulating growth hormone level
MP:0005124	increased circulating prolactin level
MP:0005128	decreased adrenocorticotropin level
MP:0005129	increased adrenocorticotropin level
MP:0005130	decreased follicle stimulating hormone level
MP:0005131	increased follicle stimulating hormone level
MP:0005132	decreased luteinizing hormone level
MP:0005133	increased luteinizing hormone level
MP:0005134	decreased thyroid-stimulating hormone level
MP:0005135	increased thyroid-stimulating hormone level
MP:0005136	decreased growth hormone level
MP:0005137	increased growth hormone level
MP:0005138	decreased prolactin level
MP:0005140	decreased cardiac muscle contractility
MP:0005141	liver hyperplasia
MP:0005146	decreased circulating VLDL cholesterol level
MP:0005148	seminal vesicle hypoplasia
MP:0005149	abnormal gubernaculum morphology
MP:0005151	diffuse hepatic necrosis
MP:0005153	abnormal B cell proliferation
MP:0005154	increased B cell proliferation
MP:0005155	herniated intestine
MP:0005162	carpoptosis
MP:0005164	abnormal response to injury
MP:0005165	increased susceptibility to injury
MP:0005166	decreased susceptibility to injury
MP:0005167	abnormal blood-brain barrier function
MP:0005168	abnormal female meiosis
MP:0005169	abnormal male meiosis
MP:0005171	absent coat pigmentation
MP:0005172	decreased eye pigmentation
MP:0005174	abnormal tail pigmentation
MP:0005175	non-pigmented tail tip
MP:0005176	eyelids fail to open
MP:0005181	decreased circulating estradiol level
MP:0005182	increased circulating estradiol level
MP:0005183	abnormal circulating estradiol level
MP:0005184	abnormal circulating progesterone level
MP:0005185	decreased circulating progesterone level
MP:0005186	increased circulating progesterone level
MP:0005188	small penis
MP:0005189	abnormal anogenital distance
MP:0005191	head tilt
MP:0005192	increased motor neuron number
MP:0005193	abnormal anterior eye segment morphology
MP:0005194	abnormal anterior uvea morphology
MP:0005195	abnormal posterior eye segment morphology
MP:0005198	abnormal aqueous drainage system morphology
MP:0005199	abnormal iris pigment epithelium
MP:0005201	abnormal retinal pigment epithelium morphology
MP:0005203	abnormal trabecular meshwork morphology
MP:0005204	abnormal canal of Schlemm morphology
MP:0005205	abnormal eye anterior chamber morphology
MP:0005206	abnormal aqueous humor
MP:0005208	abnormal iris stroma morphology
MP:0005210	disorganized stomach mucosa
MP:0005211	increased stomach mucosa thickness
MP:0005213	gastric metaplasia
MP:0005214	regional gastric metaplasia
MP:0005215	abnormal pancreatic islet morphology
MP:0005216	abnormal pancreatic alpha cell morphology
MP:0005217	abnormal pancreatic beta cell morphology
MP:0005218	abnormal pancreatic delta cell morphology
MP:0005220	abnormal exocrine pancreas morphology
MP:0005221	abnormal rostral-caudal axis patterning
MP:0005222	abnormal somite size
MP:0005223	abnormal dorsal-ventral polarity of the somites
MP:0005224	abnormal left-right axis symmetry of the somites
MP:0005225	abnormal vertebrae development
MP:0005226	abnormal vertebral arch development
MP:0005227	abnormal vertebral body development
MP:0005229	abnormal intervertebral disk development
MP:0005231	abnormal brachial lymph node morphology
MP:0005232	abnormal mesenteric lymph node morphology
MP:0005236	abnormal olfactory nerve morphology
MP:0005237	abnormal olfactory tract morphology
MP:0005238	increased brain size
MP:0005239	abnormal Bruch membrane morphology
MP:0005240	abnormal amacrine cell morphology
MP:0005241	abnormal retinal ganglion layer morphology
MP:0005247	abnormal extraocular muscle morphology
MP:0005248	abnormal Harderian gland morphology
MP:0005249	abnormal palatine bone morphology
MP:0005250	Sertoli cell hypoplasia
MP:0005252	abnormal Meibomian gland morphology
MP:0005258	ocular hypertension
MP:0005260	ocular hypotension
MP:0005265	abnormal blood urea nitrogen level
MP:0005267	abnormal olfactory cortex morphology
MP:0005269	abnormal occipital bone morphology
MP:0005270	abnormal zygomatic bone morphology
MP:0005271	abnormal lacrimal bone morphology
MP:0005272	abnormal temporal bone morphology
MP:0005274	abnormal viscerocranium morphology
MP:0005275	abnormal skin tensile strength
MP:0005280	abnormal fatty acid level
MP:0005281	increased fatty acid level
MP:0005282	decreased fatty acid level
MP:0005283	increased unsaturated fatty acid level
MP:0005284	increased saturated fatty acid level
MP:0005285	decreased unsaturated fatty acid level
MP:0005286	decreased saturated fatty acid level
MP:0005288	abnormal oxygen consumption
MP:0005289	increased oxygen consumption
MP:0005290	decreased oxygen consumption
MP:0005292	improved glucose tolerance
MP:0005294	abnormal heart ventricle morphology
MP:0005296	abnormal humerus morphology
MP:0005298	abnormal clavicle morphology
MP:0005299	abnormal eye posterior chamber morphology
MP:0005300	abnormal corneal stroma morphology
MP:0005301	abnormal corneal endothelium morphology
MP:0005304	cystic bulbourethral gland
MP:0005305	prostate gland anterior lobe hyperplasia
MP:0005306	abnormal phalanx morphology
MP:0005307	head tossing
MP:0005308	abnormal circulating ammonia level
MP:0005310	abnormal salivary gland physiology
MP:0005313	absent adrenal gland
MP:0005316	abnormal response to tactile stimuli
MP:0005317	increased triglyceride level
MP:0005318	decreased triglyceride level
MP:0005319	abnormal enzyme/coenzyme level
MP:0005322	abnormal serotonin level
MP:0005325	abnormal renal glomerulus morphology
MP:0005326	abnormal podocyte morphology
MP:0005327	abnormal mesangial cell morphology
MP:0005329	abnormal myocardium layer morphology
MP:0005332	abnormal amino acid level
MP:0005334	abnormal fat pad morphology
MP:0005335	abnormal gonadal fat pad morphology
MP:0005336	abnormal inguinal fat pad morphology
MP:0005337	abnormal retroperitoneal fat pad morphology
MP:0005339	increased susceptibility to atherosclerosis
MP:0005340	altered susceptibility to atherosclerosis
MP:0005341	decreased susceptibility to atherosclerosis
MP:0005342	abnormal intestinal lipid absorption
MP:0005343	increased circulating aspartate transaminase level
MP:0005348	increased T cell proliferation
MP:0005350	increased susceptibility to autoimmune disorder
MP:0005351	decreased susceptibility to autoimmune disorder
MP:0005352	small cranium
MP:0005353	abnormal patella morphology
MP:0005354	abnormal ilium morphology
MP:0005356	positive geotaxis
MP:0005357	novel environmental response-related retropulsion
MP:0005359	growth retardation of incisors
MP:0005360	urolithiasis
MP:0005362	abnormal Langerhans cell physiology
MP:0005363	decreased susceptibility to prion infection
MP:0005364	increased susceptibility to prion infection
MP:0005365	abnormal bile salt homeostasis
MP:0005366	variegated coat color
MP:0005367	renal/urinary system phenotype
MP:0005369	muscle phenotype
MP:0005370	liver/biliary system phenotype
MP:0005371	limbs/digits/tail phenotype
MP:0005375	adipose tissue phenotype
MP:0005376	homeostasis/metabolism phenotype
MP:0005377	hearing/vestibular/ear phenotype
MP:0005378	growth/size/body region phenotype
MP:0005379	endocrine/exocrine gland phenotype
MP:0005380	embryo phenotype
MP:0005381	digestive/alimentary phenotype
MP:0005382	craniofacial phenotype
MP:0005384	cellular phenotype
MP:0005385	cardiovascular system phenotype
MP:0005386	behavior/neurological phenotype
MP:0005387	immune system phenotype
MP:0005388	respiratory system phenotype
MP:0005389	reproductive system phenotype
MP:0005390	skeleton phenotype
MP:0005391	vision/eye phenotype
MP:0005394	taste/olfaction phenotype
MP:0005397	hematopoietic system phenotype
MP:0005398	decreased susceptibility to fungal infection
MP:0005399	increased susceptibility to fungal infection
MP:0005400	abnormal vitamin level
MP:0005401	abnormal fat-soluble vitamin level
MP:0005402	abnormal action potential
MP:0005404	abnormal axon morphology
MP:0005406	abnormal heart size
MP:0005407	hyperalgesia
MP:0005409	darkened coat color
MP:0005411	delayed fertilization
MP:0005412	vascular stenosis
MP:0005413	vascular restenosis
MP:0005422	osteosclerosis
MP:0005423	abnormal somatic nervous system physiology
MP:0005425	increased macrophage cell number
MP:0005431	decreased oocyte number
MP:0005432	abnormal pro-B cell morphology
MP:0005433	absent early pro-B cells
MP:0005434	absent late pro-B cells
MP:0005437	abnormal glycogen level
MP:0005438	abnormal glycogen homeostasis
MP:0005439	decreased glycogen level
MP:0005440	increased glycogen level
MP:0005443	abnormal ethanol metabolism
MP:0005444	abnormal retinol metabolism
MP:0005445	abnormal neurotransmitter secretion
MP:0005447	abnormal synaptic norepinephrine release
MP:0005448	abnormal energy homeostasis
MP:0005449	abnormal food intake
MP:0005451	abnormal body composition
MP:0005452	abnormal adipose tissue amount
MP:0005455	increased susceptibility to weight gain
MP:0005457	abnormal percent body fat/body weight
MP:0005458	increased percent body fat/body weight
MP:0005459	decreased percent body fat/body weight
MP:0005460	abnormal leukopoiesis
MP:0005461	abnormal dendritic cell morphology
MP:0005462	abnormal mast cell differentiation
MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology
MP:0005465	abnormal T-helper 1 physiology
MP:0005466	abnormal T-helper 2 physiology
MP:0005468	abnormal thyroid hormone level
MP:0005469	abnormal thyroxine level
MP:0005471	decreased thyroxine level
MP:0005472	abnormal triiodothyronine level
MP:0005473	decreased triiodothyronine level
MP:0005474	increased triiodothyronine level
MP:0005476	abnormal circulating triiodothyronine level
MP:0005477	increased circulating thyroxine level
MP:0005478	decreased circulating thyroxine level
MP:0005479	decreased circulating triiodothyronine level
MP:0005488	bronchial epithelial hyperplasia
MP:0005489	vascular smooth muscle hyperplasia
MP:0005490	increased Clara cell number
MP:0005491	pancreatic islet hyperplasia
MP:0005492	exocrine pancreas hypoplasia
MP:0005493	stomach epithelial hyperplasia
MP:0005494	esophagogastric junction metaplasia
MP:0005497	optic nerve cupping
MP:0005498	hyporesponsive to tactile stimuli
MP:0005499	abnormal olfactory system morphology
MP:0005500	abnormal gustatory system morphology
MP:0005502	abnormal renal/urinary system physiology
MP:0005504	abnormal ligament morphology
MP:0005507	tail dragging
MP:0005516	increased liver regeneration
MP:0005517	decreased liver regeneration
MP:0005518	abnormal pancreas regeneration
MP:0005520	decreased pancreas regeneration
MP:0005522	increased circulating atrial natriuretic factor
MP:0005523	decreased circulating atrial natriuretic factor
MP:0005524	abnormal renal plasma flow rate
MP:0005525	increased renal plasma flow rate
MP:0005526	decreased renal plasma flow rate
MP:0005527	increased renal glomerular filtration rate
MP:0005528	decreased renal glomerular filtration rate
MP:0005529	abnormal renal vascular resistance
MP:0005530	decreased renal vascular resistance
MP:0005531	increased renal vascular resistance
MP:0005532	abnormal vascular resistance
MP:0005533	increased body temperature
MP:0005535	abnormal body temperature
MP:0005537	abnormal cerebral aqueduct morphology
MP:0005540	decreased urine albumin level
MP:0005541	abnormal iris stromal pigmentation
MP:0005545	abnormal lens development
MP:0005546	choroidal neovascularization
MP:0005547	abnormal Muller cell morphology
MP:0005548	retinal pigment epithelium atrophy
MP:0005549	retinal pigment epithelium hyperplasia
MP:0005551	abnormal eye electrophysiology
MP:0005556	abnormal renal filtration rate
MP:0005557	increased creatinine clearance
MP:0005559	increased circulating glucose level
MP:0005560	decreased circulating glucose level
MP:0005561	increased mean corpuscular hemoglobin
MP:0005562	decreased mean corpuscular hemoglobin
MP:0005563	abnormal hemoglobin content
MP:0005564	increased hemoglobin content
MP:0005566	decreased blood urea nitrogen level
MP:0005571	decreased lactate dehydrogenase level
MP:0005572	abnormal pulmonary respiratory rate
MP:0005573	increased pulmonary respiratory rate
MP:0005574	decreased pulmonary respiratory rate
MP:0005575	increased pulmonary ventilation
MP:0005576	decreased pulmonary ventilation
MP:0005580	periinsulitis
MP:0005581	abnormal renin activity
MP:0005582	increased renin activity
MP:0005583	decreased renin activity
MP:0005585	increased tidal volume
MP:0005586	decreased tidal volume
MP:0005587	abnormal Meckel's cartilage morphology
MP:0005590	increased vasodilation
MP:0005591	decreased vasodilation
MP:0005592	abnormal vascular smooth muscle morphology
MP:0005595	abnormal vascular smooth muscle physiology
MP:0005596	increased susceptibility to type I hypersensitivity reaction
MP:0005597	decreased susceptibility to type I hypersensitivity reaction
MP:0005598	decreased ventricle muscle contractility
MP:0005599	increased cardiac muscle contractility
MP:0005600	increased ventricle muscle contractility
MP:0005601	increased angiogenesis
MP:0005602	decreased angiogenesis
MP:0005603	neuron hypertrophy
MP:0005605	increased bone mass
MP:0005607	decreased bleeding time
MP:0005608	cardiac interstitial fibrosis
MP:0005609	abnormal circulating antidiuretic hormone level
MP:0005610	increased circulating antidiuretic hormone level
MP:0005611	decreased circulating antidiuretic hormone level
MP:0005612	decreased susceptibility to type II hypersensitivity reaction
MP:0005614	decreased susceptibility to type III hypersensitivity reaction
MP:0005615	increased susceptibility to type III hypersensitivity reaction
MP:0005616	decreased susceptibility to type IV hypersensitivity reaction
MP:0005617	increased susceptibility to type IV hypersensitivity reaction
MP:0005620	abnormal muscle contractility
MP:0005626	decreased plasma anion gap
MP:0005629	abnormal lung weight
MP:0005630	increased lung weight
MP:0005631	decreased lung weight
MP:0005632	decreased circulating aspartate transaminase level
MP:0005635	decreased circulating bilirubin level
MP:0005636	abnormal mineral homeostasis
MP:0005638	hemochromatosis
MP:0005639	hemosiderosis
MP:0005641	increased mean corpuscular hemoglobin concentration
MP:0005642	decreased mean corpuscular hemoglobin concentration
MP:0005643	decreased dopamine level
MP:0005644	agonadal
MP:0005646	abnormal pituitary gland physiology
MP:0005647	abnormal sex gland physiology
MP:0005648	heart right ventricle degeneration
MP:0005649	increased spleen neoplasm incidence
MP:0005650	abnormal limb bud morphology
MP:0005651	abnormal gonad rudiment morphology
MP:0005653	phototoxicity
MP:0005654	porphyria
MP:0005655	increased aggression
MP:0005656	decreased aggression
MP:0005657	abnormal neural plate morphology
MP:0005658	increased susceptibility to diet-induced obesity
MP:0005659	decreased susceptibility to diet-induced obesity
MP:0005660	abnormal circulating adrenaline level
MP:0005661	decreased circulating adrenaline level
MP:0005662	increased circulating adrenaline level
MP:0005663	abnormal circulating noradrenaline level
MP:0005664	decreased circulating noradrenaline level
MP:0005665	increased circulating noradrenaline level
MP:0005666	abnormal adipose tissue physiology
MP:0005669	increased circulating leptin level
MP:0005670	abnormal white adipose tissue physiology
MP:0005671	abnormal response to transplant
MP:0005672	increased susceptibility to graft versus host disease
MP:0005673	decreased susceptibility to graft versus host disease
MP:0005675	small gallbladder
MP:0006000	abnormal corneal epithelium morphology
MP:0006001	abnormal intestinal transit time
MP:0006002	abnormal small intestinal transit time
MP:0006003	abnormal large intestinal transit time
MP:0006006	increased sensory neuron number
MP:0006007	abnormal basal ganglion morphology
MP:0006010	absent strial intermediate cells
MP:0006011	abnormal endolymphatic duct morphology
MP:0006012	dilated endolymphatic duct
MP:0006013	absent endolymphatic sac
MP:0006014	dilated endolymphatic sac
MP:0006015	dilated lateral semicircular canal
MP:0006016	dilated posterior semicircular canal
MP:0006018	abnormal tympanic membrane morphology
MP:0006019	absent tympanic membrane
MP:0006020	decreased tympanic ring size
MP:0006021	abnormal Reissner membrane morphology
MP:0006023	detached Reissner membrane
MP:0006024	collapsed Reissner membrane
MP:0006025	distended Reissner membrane
MP:0006026	dilated terminal bronchiole tubes
MP:0006027	impaired lung alveolus development
MP:0006029	abnormal sclerotome morphology
MP:0006030	abnormal otic vesicle development
MP:0006031	abnormal pharyngeal pouch morphology
MP:0006032	abnormal ureteric bud morphology
MP:0006033	abnormal external auditory canal morphology
MP:0006036	abnormal mitochondrial physiology
MP:0006037	abnormal mitochondrial fission
MP:0006038	increased mitochondrial fission
MP:0006039	decreased mitochondrial fission
MP:0006042	increased apoptosis
MP:0006043	decreased apoptosis
MP:0006046	atrioventricular valve regurgitation
MP:0006049	semilunar valve regurgitation
MP:0006051	brainstem hemorrhage
MP:0006052	cerebellum hemorrhage
MP:0006054	spinal hemorrhage
MP:0006055	abnormal vascular endothelial cell morphology
MP:0006056	increased vascular endothelial cell number
MP:0006057	decreased vascular endothelial cell number
MP:0006058	decreased cerebral infarction size
MP:0006059	decreased susceptibility to ischemic brain injury
MP:0006060	increased cerebral infarction size
MP:0006063	abnormal inferior vena cava morphology
MP:0006064	abnormal superior vena cava morphology
MP:0006065	abnormal heart position or orientation
MP:0006066	decreased clearance of atrial thrombosis
MP:0006068	abnormal horizontal cell morphology
MP:0006069	abnormal retinal neuronal layer morphology
MP:0006070	increased retinal photoreceptor cell number
MP:0006071	abnormal retinal progenitor cell morphology
MP:0006072	abnormal retinal apoptosis
MP:0006073	abnormal retinal bipolar cell morphology
MP:0006074	abnormal retinal rod bipolar cell morphology
MP:0006075	abnormal retinal cone bipolar cell morphology
MP:0006076	abnormal circulating homocysteine level
MP:0006078	abnormal nipple morphology
MP:0006080	CNS ischemia
MP:0006082	CNS inflammation
MP:0006083	abnormal blood vessel elastic tissue morphology
MP:0006084	abnormal circulating phospholipid level
MP:0006086	decreased body mass index
MP:0006087	increased body mass index
MP:0006088	abnormal blood-cerebrospinal fluid barrier function
MP:0006092	abnormal olfactory sensory neuron morphology
MP:0006095	absent amacrine cells
MP:0006096	absent retinal bipolar cells
MP:0006097	abnormal cerebellar lobule formation
MP:0006098	absent cerebellar lobules
MP:0006099	thin cerebellar granule layer
MP:0006100	abnormal tegmentum morphology
MP:0006101	absent tegmentum
MP:0006102	decreased tegmentum size
MP:0006103	abnormal midbrain roof plate morphology
MP:0006104	abnormal tectum morphology
MP:0006105	small tectum
MP:0006106	absent tectum
MP:0006107	abnormal fetal atrioventricular canal morphology
MP:0006108	abnormal hindbrain development
MP:0006111	abnormal coronary circulation
MP:0006113	abnormal heart septum morphology
MP:0006123	tricuspid valve atresia
MP:0006126	abnormal cardiac outflow tract development
MP:0006134	artery occlusion
MP:0006137	venoocclusion
MP:0006141	abnormal atrioventricular node conduction
MP:0006142	abnormal sinoatrial node conduction
MP:0006143	increased systemic arterial diastolic blood pressure
MP:0006144	increased systemic arterial systolic blood pressure
MP:0006148	binocular blindness
MP:0006149	decreased visual acuity
MP:0006162	thick eyelids
MP:0006173	abnormal myeloid dendritic cell morphology
MP:0006182	increased retinal hemangioma incidence
MP:0006186	retinal fibrosis
MP:0006187	retinal deposits
MP:0006190	retinal ischemia
MP:0006200	vitreous body deposition
MP:0006201	vitreous body inflammation
MP:0006202	vitreous body hemorrhage
MP:0006204	embryonic lethality before implantation
MP:0006205	embryonic lethality between implantation and somite formation
MP:0006206	embryonic lethality between somite formation and embryo turning
MP:0006207	embryonic lethality during organogenesis
MP:0006208	lethality throughout fetal growth and development
MP:0006210	abnormal orbit size
MP:0006211	small orbits
MP:0006219	optic nerve degeneration
MP:0006223	optic nerve swelling
MP:0006225	ocular rupture
MP:0006236	absent Meibomian glands
MP:0006237	abnormal choroid vasculature morphology
MP:0006238	abnormal choriocapillaris morphology
MP:0006245	dislocated lens
MP:0006250	abnormal line of Schwalbe morphology
MP:0006254	thin cerebral cortex
MP:0006257	abnormal fungiform papillae morphology
MP:0006258	abnormal circumvallate papillae morphology
MP:0006260	abnormal gustatory papillae taste bud morphology
MP:0006262	increased testis tumor incidence
MP:0006263	decreased systemic arterial diastolic blood pressure
MP:0006264	decreased systemic arterial systolic blood pressure
MP:0006265	increased pulse pressure
MP:0006266	decreased pulse pressure
MP:0006267	abnormal intercalated disc morphology
MP:0006268	absent cardiac desmosomes
MP:0006269	abnormal mammary gland growth during pregnancy
MP:0006270	abnormal mammary gland growth during lactation
MP:0006271	abnormal involution of the mammary gland
MP:0006272	abnormal urine organic anion level
MP:0006273	abnormal urine organic cation level
MP:0006277	abnormal parasympathetic nervous system physiology
MP:0006279	abnormal limb development
MP:0006280	abnormal digit development
MP:0006281	abnormal tail development
MP:0006282	abnormal spinal cord dorsal horn morphology
MP:0006284	absent hypaxial muscle
MP:0006286	inner ear hypoplasia
MP:0006287	inner ear cysts
MP:0006288	small otic capsule
MP:0006289	otic capsule hypoplasia
MP:0006292	abnormal nasal placode morphology
MP:0006293	absent nasal placodes
MP:0006294	absent optic vesicle
MP:0006295	absent sclerotome
MP:0006298	abnormal platelet activation
MP:0006299	abnormal latent inhibition of conditioning behavior
MP:0006300	abnormal entorhinal cortex morphology
MP:0006301	abnormal mesenchyme morphology
MP:0006302	abnormal ectomesenchyme morphology
MP:0006303	abnormal retinal nerve fiber layer morphology
MP:0006305	abnormal optic eminence morphology
MP:0006306	abnormal nasal pit morphology
MP:0006307	abnormal seminiferous tubule size
MP:0006308	enlarged seminiferous tubules
MP:0006309	decreased retinal ganglion cell number
MP:0006315	abnormal urine protein level
MP:0006316	increased urine sodium level
MP:0006317	decreased urine sodium level
MP:0006319	abnormal epididymal fat pad morphology
MP:0006320	abnormal interscapular fat pad morphology
MP:0006321	increased myocardial fiber number
MP:0006322	abnormal perichondrium morphology
MP:0006323	abnormal extraembryonic mesoderm development
MP:0006324	abnormal cochlear nerve fiber response
MP:0006328	nonsyndromic hearing impairment
MP:0006330	syndromic hearing impairment
MP:0006331	abnormal patterning of the organ of Corti
MP:0006332	abnormal cochlear potential
MP:0006334	abnormal susceptibility to hearing loss
MP:0006335	abnormal hearing electrophysiology
MP:0006336	abnormal otoacoustic response
MP:0006337	abnormal first pharyngeal arch morphology
MP:0006338	abnormal second pharyngeal arch morphology
MP:0006339	abnormal third pharyngeal arch morphology
MP:0006340	abnormal fourth pharyngeal arch morphology
MP:0006341	small first pharyngeal arch
MP:0006342	absent first pharyngeal arch
MP:0006343	enlarged first pharyngeal arch
MP:0006344	small second pharyngeal arch
MP:0006345	absent second pharyngeal arch
MP:0006346	small pharyngeal arch
MP:0006347	abnormal sixth pharyngeal arch morphology
MP:0006349	decreased circulating copper level
MP:0006350	increased circulating copper level
MP:0006352	decreased glycosylated hemoglobin level
MP:0006354	abnormal fourth pharyngeal arch artery morphology
MP:0006355	abnormal sixth pharyngeal arch artery morphology
MP:0006356	abnormal third pharyngeal arch artery morphology
MP:0006357	abnormal circulating mineral level
MP:0006358	absent pinna reflex
MP:0006359	absent startle reflex
MP:0006361	abnormal female germ cell morphology
MP:0006363	absent auchene hairs
MP:0006364	absent awl hair
MP:0006365	absent guard hair
MP:0006366	absent zigzag hairs
MP:0006369	supernumerary incisors
MP:0006370	abnormal hair follicle pheomelanosome pheomelanin content
MP:0006371	absent hair follicle pheomelanosome pheomelanin
MP:0006372	impaired placental function
MP:0006373	abnormal circulating angiotensinogen level
MP:0006375	increased circulating angiotensinogen level
MP:0006376	decreased circulating angiotensinogen level
MP:0006377	abnormal vestibulocollic reflex
MP:0006378	abnormal spermatogonia morphology
MP:0006379	abnormal spermatocyte morphology
MP:0006380	abnormal spermatid morphology
MP:0006382	abnormal lung epithelium morphology
MP:0006383	abnormal cochlear frequency tuning
MP:0006384	enhanced cochlear frequency tuning
MP:0006386	absent somites
MP:0006388	abnormal auditory summating potential
MP:0006389	abnormal vestibular endolymph
MP:0006391	abnormal vestibular endolymph ionic homeostasis
MP:0006392	abnormal nucleus pulposus morphology
MP:0006393	absent nucleus pulposus
MP:0006394	abnormal vertebral epiphyseal plate morphology
MP:0006396	decreased long bone epiphyseal plate size
MP:0006397	disorganized long bone epiphyseal plate
MP:0006398	increased long bone epiphyseal plate size
MP:0006399	abnormal long bone epiphyseal ossification zone morphology
MP:0006400	decreased molar number
MP:0006401	absent male preputial gland
MP:0006402	small molars
MP:0006403	abnormal cochlear endolymph ionic homeostasis
MP:0006404	abnormal lumbar dorsal root ganglion morphology
MP:0006405	abnormal L3 dorsal root ganglion morphology
MP:0006408	dorsal root ganglion hypoplasia
MP:0006409	vestibular ganglion hypoplasia
MP:0006410	abnormal common myeloid progenitor cell morphology
MP:0006411	upturned snout
MP:0006412	abnormal T cell apoptosis
MP:0006413	increased T cell apoptosis
MP:0006414	decreased T cell apoptosis
MP:0006415	absent testes
MP:0006416	abnormal rete testis morphology
MP:0006417	rete testis obstruction
MP:0006418	abnormal testis cord formation
MP:0006419	disorganized testis cords
MP:0006420	abnormal peritubular myoid cell morphology
MP:0006421	decreased number of peritubular myoid cells
MP:0006422	increased mammary adenoacanthoma incidence
MP:0006423	dilated rete testis
MP:0006424	absent testis cords
MP:0006425	absent Mullerian ducts
MP:0006426	Mullerian duct degeneration
MP:0006427	ectopic Leydig cells
MP:0006428	ectopic Sertoli cells
MP:0006429	abnormal hyaline cartilage morphology
MP:0006431	abnormal fibrocartilage morphology
MP:0006432	abnormal costal cartilage morphology
MP:0006433	abnormal articular cartilage morphology
MP:0008001	hypochlorhydria
MP:0008002	hyperchlorhydria
MP:0008003	achlorhydria
MP:0008004	abnormal stomach pH
MP:0008006	increased stomach pH
MP:0008007	abnormal cellular replicative senescence
MP:0008008	early cellular replicative senescence
MP:0008009	delayed cellular replicative senescence
MP:0008010	increased gastric adenocarcinoma incidence
MP:0008013	cecum polyps
MP:0008014	increased lung tumor incidence
MP:0008018	increased facial tumor incidence
MP:0008019	increased liver tumor incidence
MP:0008020	abnormal dermal mast cell morphology
MP:0008021	increased blastoma incidence
MP:0008022	dilated heart ventricle
MP:0008023	abnormal styloid process morphology
MP:0008024	absent lymph nodes
MP:0008025	brain vacuoles
MP:0008026	abnormal brain white matter morphology
MP:0008027	abnormal spinal cord white matter morphology
MP:0008028	pregnancy-related premature death
MP:0008029	abnormal paraxial mesoderm morphology
MP:0008030	abnormal Cajal-Retzius cell morphology
MP:0008031	decreased Cajal-Retzius cell number
MP:0008032	abnormal lipolysis
MP:0008033	impaired lipolysis
MP:0008034	enhanced lipolysis
MP:0008035	behavioral arrest
MP:0008036	abnormal NK T cell morphology
MP:0008038	abnormal NK T cell number
MP:0008039	increased NK T cell number
MP:0008040	decreased NK T cell number
MP:0008041	absent NK T cells
MP:0008042	abnormal NK T cell physiology
MP:0008044	increased NK cell number
MP:0008047	absent uterine NK cells
MP:0008048	abnormal memory T cell number
MP:0008049	increased memory T cell number
MP:0008050	decreased memory T cell number
MP:0008051	abnormal memory T cell physiology
MP:0008052	abnormal serous gland morphology
MP:0008053	abnormal NK cell differentiation
MP:0008054	abnormal uterine NK cell morphology
MP:0008055	increased urine osmolality
MP:0008056	abnormal retinal ganglion cell morphology
MP:0008057	abnormal DNA replication
MP:0008059	abnormal podocyte foot process morphology
MP:0008060	abnormal podocyte slit diaphragm morphology
MP:0008061	absent podocyte slit diaphragm
MP:0008062	abnormal podocyte slit junction morphology
MP:0008063	increased otic epithelial cell apoptosis
MP:0008064	decreased otic epithelial cell proliferation
MP:0008065	short endolymphatic duct
MP:0008066	small endolymphatic duct
MP:0008067	retinal ganglion cell degeneration
MP:0008068	absent retinal ganglion cell
MP:0008070	absent T cells
MP:0008073	abnormal CD4-positive, alpha beta T cell number
MP:0008074	increased CD4-positive, alpha beta T cell number
MP:0008075	decreased CD4-positive, alpha beta T cell number
MP:0008076	abnormal CD4-positive T cell differentiation
MP:0008077	abnormal CD8-positive, alpha-beta T cell number
MP:0008078	increased CD8-positive, alpha-beta T cell number
MP:0008080	abnormal CD8-positive, alpha-beta T cell differentiation
MP:0008081	abnormal single-positive T cell number
MP:0008082	increased single-positive T cell number
MP:0008083	decreased single-positive T cell number
MP:0008086	increased T-helper 1 cell number
MP:0008087	decreased T helper 1 cell number
MP:0008088	abnormal T-helper 1 cell differentiation
MP:0008090	increased T-helper 2 cell number
MP:0008091	decreased T-helper 2 cell number
MP:0008092	abnormal T-helper 2 cell differentiation
MP:0008093	abnormal memory B cell number
MP:0008094	absent memory B cells
MP:0008095	abnormal memory B cell differentiation
MP:0008096	abnormal plasma cell number
MP:0008097	increased plasma cell number
MP:0008098	decreased plasma cell number
MP:0008099	abnormal plasma cell differentiation
MP:0008100	absent plasma cells
MP:0008103	amacrine cell degeneration
MP:0008105	increased amacrine cell number
MP:0008106	decreased amacrine cell number
MP:0008107	absent horizontal cells
MP:0008109	abnormal small intestinal microvillus morphology
MP:0008111	abnormal granulocyte differentiation
MP:0008112	abnormal monocyte differentiation
MP:0008113	abnormal macrophage differentiation
MP:0008114	abnormal Kupffer cell morphology
MP:0008115	abnormal dendritic cell differentiation
MP:0008117	abnormal Langerhans cell morphology
MP:0008118	absent Langerhans cell
MP:0008119	decreased Langerhans cell number
MP:0008121	increased myeloid dendritic cell number
MP:0008122	decreased myeloid dendritic cell number
MP:0008124	decreased plasmacytoid dendritic cell number
MP:0008125	abnormal dendritic cell number
MP:0008126	increased dendritic cell number
MP:0008127	decreased dendritic cell number
MP:0008128	abnormal brain internal capsule morphology
MP:0008129	absent brain internal capsule
MP:0008130	abnormal pituitary intermediate lobe morphology
MP:0008132	increased Peyer's patch number
MP:0008133	decreased Peyer's patch number
MP:0008135	small Peyer's patches
MP:0008136	enlarged Peyer's patches
MP:0008137	absent podocytes
MP:0008138	absent podocyte foot process
MP:0008139	fused podocyte foot processes
MP:0008140	podocyte foot process effacement
MP:0008141	decreased small intestinal microvillus size
MP:0008142	decreased small intestinal villus size
MP:0008143	abnormal dendrite morphology
MP:0008146	asymmetric sternocostal joints
MP:0008147	asymmetric costovertebral joints
MP:0008148	abnormal sternocostal joint morphology
MP:0008149	abnormal costovertebral joint morphology
MP:0008151	increased diameter of long bones
MP:0008152	decreased diameter of femur
MP:0008154	decreased diameter of humerus
MP:0008155	decreased diameter of radius
MP:0008156	decreased diameter of tibia
MP:0008157	decreased diameter of ulna
MP:0008158	increased diameter of femur
MP:0008160	increased diameter of humerus
MP:0008161	increased diameter of radius
MP:0008162	increased diameter of tibia
MP:0008163	increased diameter of ulna
MP:0008164	abnormal B-1a B cell morphology
MP:0008166	abnormal B-2 B cell morphology
MP:0008167	increased B-1a cell number
MP:0008168	decreased B-1a cell number
MP:0008169	increased B-1b cell number
MP:0008170	decreased B-1b cell number
MP:0008171	abnormal mature B cell morphology
MP:0008172	abnormal follicular B cell morphology
MP:0008173	increased follicular B cell number
MP:0008174	decreased follicular B cell number
MP:0008175	absent follicular B cells
MP:0008176	abnormal germinal center B cell morphology
MP:0008177	increased germinal center B cell number
MP:0008178	decreased germinal center B cell number
MP:0008179	absent germinal center B cells
MP:0008180	abnormal marginal zone B cell morphology
MP:0008181	increased marginal zone B cell number
MP:0008182	decreased marginal zone B cell number
MP:0008183	absent marginal zone B cells
MP:0008185	decreased naive B cell number
MP:0008186	increased pro-B cell number
MP:0008187	absent pro-B cells
MP:0008188	abnormal transitional stage B cell morphology
MP:0008189	increased transitional stage B cell number
MP:0008190	decreased transitional stage B cell number
MP:0008191	abnormal follicular B cell physiology
MP:0008192	abnormal germinal center B cell physiology
MP:0008193	abnormal marginal zone B cell physiology
MP:0008194	abnormal memory B cell physiology
MP:0008195	abnormal professional antigen presenting cell morphology
MP:0008196	abnormal follicular dendritic cell morphology
MP:0008197	abnormal follicular dendritic cell physiology
MP:0008198	abnormal follicular dendritic cell antigen presentation
MP:0008200	decreased follicular dendritic cell number
MP:0008201	absent follicular dendritic cells
MP:0008202	absent B-1 B cells
MP:0008203	absent B-1a cells
MP:0008204	absent B-1b cells
MP:0008205	absent B-2 B cells
MP:0008206	increased B-2 B cell number
MP:0008207	decreased B-2 B cell number
MP:0008208	decreased pro-B cell number
MP:0008209	decreased pre-B cell number
MP:0008210	increased mature B cell number
MP:0008211	decreased mature B cell number
MP:0008212	absent mature B cells
MP:0008213	absent immature B cells
MP:0008214	increased immature B cell number
MP:0008215	decreased immature B cell number
MP:0008216	absent transitional stage B cells
MP:0008218	delayed emergence of vibrissae
MP:0008219	abnormal dorsal telencephalic commissure morphology
MP:0008221	abnormal hippocampal commissure morphology
MP:0008222	decreased hippocampal commissure size
MP:0008223	absent hippocampal commissure
MP:0008226	decreased anterior commissure size
MP:0008227	absent anterior commissure
MP:0008228	increased anterior commissure size
MP:0008232	abnormal cingulum morphology
MP:0008233	abnormal pro-B cell differentiation
MP:0008234	absent spleen marginal zone
MP:0008235	increased susceptibility to neuronal excitotoxicity
MP:0008236	decreased susceptibility to neuronal excitotoxicity
MP:0008237	abnormal ventral coat pigmentation
MP:0008238	abnormal dorsoventral coat patterning
MP:0008240	abnormal spleen marginal zone macrophage morphology
MP:0008241	abnormal metallophilic macrophage morphology
MP:0008242	abnormal perivascular macrophage morphology
MP:0008243	abnormal macrophage derived foam cell morphology
MP:0008244	abnormal peritoneal macrophage morphology
MP:0008245	abnormal alveolar macrophage morphology
MP:0008247	abnormal mononuclear cell morphology
MP:0008249	abnormal common lymphocyte progenitor cell morphology
MP:0008250	abnormal myeloid leukocyte morphology
MP:0008251	abnormal phagocyte morphology
MP:0008253	absent megakaryocytes
MP:0008256	abnormal myometrium morphology
MP:0008257	thin myometrium
MP:0008258	thin endometrium
MP:0008260	abnormal autophagy
MP:0008261	arrest of male meiosis
MP:0008262	abnormal hippocampus region morphology
MP:0008263	abnormal hippocampus CA1 region morphology
MP:0008264	absent hippocampus CA1 region
MP:0008265	abnormal hippocampus CA2 region morphology
MP:0008266	absent hippocampus CA2 region
MP:0008267	abnormal hippocampus CA3 region morphology
MP:0008268	absent hippocampus CA3 region
MP:0008269	abnormal hippocampus CA4 region morphology
MP:0008272	abnormal endochondral bone ossification
MP:0008274	failure of bone ossification
MP:0008275	failure of endochondral bone ossification
MP:0008276	failure of intramembranous bone ossification
MP:0008277	abnormal sternum ossification
MP:0008278	failure of sternum ossification
MP:0008279	arrest of spermiogenesis
MP:0008280	abnormal male germ cell apoptosis
MP:0008283	small hippocampus
MP:0008284	abnormal hippocampus pyramidal cell layer
MP:0008285	abnormal hippocampus granule cell layer
MP:0008286	abnormal hippocampus molecular cell layer
MP:0008287	abnormal subiculum morphology
MP:0008288	abnormal adrenal cortex morphology
MP:0008289	abnormal adrenal medulla morphology
MP:0008291	abnormal adrenocortical cell morphology
MP:0008292	enlarged adrenocortical cell nuclei
MP:0008293	abnormal adrenal gland zona glomerulosa morphology
MP:0008294	abnormal adrenal gland zona fasciculata morphology
MP:0008295	abnormal adrenal gland zona reticularis morphology
MP:0008296	abnormal adrenal gland x-zone morphology
MP:0008297	retention of the adrenal gland x-zone
MP:0008298	adrenergic chromaffin cell hyperplasia
MP:0008299	adrenal cortical hyperplasia
MP:0008300	enlarged adrenal medulla
MP:0008302	thin adrenal cortex
MP:0008303	early degeneration of the adrenal gland x-zone
MP:0008304	abnormal organ of Corti supporting cell differentiation
MP:0008306	abnormal organ of Corti supporting cell proliferation
MP:0008307	short scala media
MP:0008308	small scala media
MP:0008309	dilated scala media
MP:0008312	abnormal sympathetic postganglionic fiber morphology
MP:0008313	abnormal parasympathetic postganglionic fiber morphology
MP:0008314	abnormal pterygopalatine ganglion morphology
MP:0008315	abnormal otic ganglion morphology
MP:0008316	abnormal prevertebral ganglion morphology
MP:0008317	abnormal paravertebral ganglion morphology
MP:0008319	abnormal sympathetic afferent fiber morphology
MP:0008320	absent adenohypophysis
MP:0008321	small adenohypophysis
MP:0008322	abnormal somatotroph morphology
MP:0008323	abnormal lactotroph morphology
MP:0008324	abnormal melanotroph morphology
MP:0008325	abnormal gonadotroph morphology
MP:0008327	abnormal corticotroph morphology
MP:0008329	decreased somatotroph cell number
MP:0008330	absent somatotrophs
MP:0008331	increased lactotroph cell number
MP:0008332	decreased lactotroph cell number
MP:0008333	absent lactotrophs
MP:0008334	increased gonadotroph cell number
MP:0008335	decreased gonadotroph cell number
MP:0008336	absent gonadotrophs
MP:0008337	increased thyrotroph cell number
MP:0008338	decreased thyrotroph cell number
MP:0008339	absent thyrotrophs
MP:0008340	increased corticotroph cell number
MP:0008341	decreased corticotroph cell number
MP:0008343	abnormal gamma-delta T cell morphology
MP:0008344	abnormal mature gamma-delta T cell morphology
MP:0008345	abnormal gamma-delta T cell number
MP:0008346	increased gamma-delta T cell number
MP:0008347	decreased gamma-delta T cell number
MP:0008348	absent gamma-delta T cells
MP:0008349	abnormal gamma-delta intraepithelial T cell morphology
MP:0008350	increased gamma-delta intraepithelial T cell number
MP:0008351	decreased gamma-delta intraepithelial T cell number
MP:0008352	absent gamma-delta intraepithelial T cell
MP:0008353	increased mature gamma-delta T cell number
MP:0008354	decreased mature gamma-delta T cell number
MP:0008355	absent mature gamma-delta T cells
MP:0008356	abnormal gamma-delta T cell differentiation
MP:0008363	decreased CD8-positive, gamma-delta intraepithelial T cell number
MP:0008366	enlarged adenohypophysis
MP:0008367	absent pituitary intermediate lobe
MP:0008368	small pituitary intermediate lobe
MP:0008369	pituitary intermediate lobe hypoplasia
MP:0008370	enlarged pituitary intermediate lobe
MP:0008371	pituitary intermediate lobe hyperplasia
MP:0008372	small malleus
MP:0008373	short malleus
MP:0008374	abnormal malleus manubrium morphology
MP:0008375	short malleus manubrium
MP:0008376	small malleus manubrium
MP:0008377	absent malleus manubrium
MP:0008378	small malleus processus brevis
MP:0008380	abnormal gonial bone morphology
MP:0008381	absent gonial bone
MP:0008382	gonial bone hypoplasia
MP:0008383	enlarged gonial bone
MP:0008384	absent nasal capsule
MP:0008385	absent basisphenoid bone
MP:0008386	absent styloid process
MP:0008389	hypochromic macrocytic anemia
MP:0008390	abnormal primordial germ cell proliferation
MP:0008391	abnormal primordial germ cell morphology
MP:0008392	decreased primordial germ cell number
MP:0008393	absent primordial germ cells
MP:0008395	abnormal osteoblast differentiation
MP:0008396	abnormal osteoclast differentiation
MP:0008399	abnormal alpha-beta intraepithelial T cell morphology
MP:0008400	abnormal CD4-positive, alpha-beta intraepithelial T cell morphology
MP:0008401	abnormal CD8 positive, alpha-beta intraepithelial T cell morphology
MP:0008402	increased cellular sensitivity to alkylating agents
MP:0008403	decreased cellular sensitivity to alkylating agents
MP:0008404	increased cellular sensitivity to methylmethanesulfonate
MP:0008405	decreased cellular sensitivity to methylmethanesulfonate
MP:0008406	increased cellular sensitivity to hydrogen peroxide
MP:0008407	decreased cellular sensitivity to hydrogen peroxide
MP:0008409	increased cellular sensitivity to hydroxyurea
MP:0008410	increased cellular sensitivity to ultraviolet irradiation
MP:0008411	decreased cellular sensitivity to ultraviolet irradiation
MP:0008412	increased cellular sensitivity to oxidative stress
MP:0008413	decreased cellular sensitivity to oxidative stress
MP:0008414	abnormal spatial reference memory
MP:0008415	abnormal neurite morphology
MP:0008416	increased somatotroph cell size
MP:0008417	decreased somatotroph cell size
MP:0008418	abnormal cutaneous elastic fiber morphology
MP:0008419	abnormal cutaneous microfibril morphology
MP:0008423	decreased lactotroph cell size
MP:0008427	decreased corticotroph cell size
MP:0008428	abnormal spatial working memory
MP:0008429	absent parotid gland
MP:0008430	short squamosal bone
MP:0008431	abnormal short term spatial reference memory
MP:0008432	abnormal long term spatial reference memory
MP:0008436	decreased somatotroph secretory granule number
MP:0008437	absent somatotroph secretory granules
MP:0008438	abnormal cutaneous collagen fibril morphology
MP:0008439	abnormal cortical plate morphology
MP:0008440	abnormal subplate morphology
MP:0008441	thin cortical plate
MP:0008442	disorganized cortical plate
MP:0008443	absent subplate
MP:0008444	retinal cone cell degeneration
MP:0008445	increased retinal cone cell number
MP:0008446	decreased retinal cone cell number
MP:0008447	absent retinal cone cells
MP:0008448	abnormal retinal cone cell inner segment morphology
MP:0008449	abnormal retinal cone cell outer segment morphology
MP:0008450	retinal photoreceptor degeneration
MP:0008451	retinal rod cell degeneration
MP:0008453	decreased retinal rod cell number
MP:0008454	absent retinal rod cells
MP:0008455	abnormal retinal rod cell inner segment morphology
MP:0008456	abnormal retinal rod cell outer segment morphology
MP:0008457	abnormal cortical intermediate zone morphology
MP:0008458	abnormal cortical ventricular zone morphology
MP:0008459	abnormal circulating pancreatic peptide level
MP:0008460	absent dorsal root ganglion
MP:0008462	abnormal medium spiny neuron morphology
MP:0008463	abnormal peripheral lymph node morphology
MP:0008464	absent peripheral lymph nodes
MP:0008465	absent mesenteric lymph nodes
MP:0008466	enlarged mesenteric lymph nodes
MP:0008467	absent proprioceptive neurons
MP:0008468	absent muscle spindles
MP:0008469	abnormal protein level
MP:0008470	abnormal spleen B cell follicle morphology
MP:0008471	abnormal spleen primary B follicle morphology
MP:0008472	abnormal spleen secondary B follicle morphology
MP:0008473	abnormal spleen follicular dendritic cell network
MP:0008474	absent spleen germinal center
MP:0008475	intermingled spleen red and white pulp
MP:0008476	increased spleen red pulp amount
MP:0008477	decreased spleen red pulp amount
MP:0008478	increased spleen white pulp amount
MP:0008479	decreased spleen white pulp amount
MP:0008480	absent eye pigmentation
MP:0008481	increased spleen germinal center number
MP:0008482	decreased spleen germinal center number
MP:0008483	increased spleen germinal center size
MP:0008484	decreased spleen germinal center size
MP:0008485	increased muscle spindle number
MP:0008486	decreased muscle spindle number
MP:0008487	abnormal mesonephros morphology
MP:0008488	abnormal semicircular canal ampulla morphology
MP:0008489	slow postnatal weight gain
MP:0008490	enlarged dorsal root ganglion
MP:0008491	dorsal root ganglion hyperplasia
MP:0008492	dorsal root ganglion degeneration
MP:0008493	alpha-synuclein inclusion body
MP:0008494	absence of all nails
MP:0008495	decreased IgG1 level
MP:0008496	decreased IgG2a level
MP:0008497	decreased IgG2b level
MP:0008498	decreased IgG3 level
MP:0008499	increased IgG1 level
MP:0008500	increased IgG2a level
MP:0008501	increased IgG2b level
MP:0008502	increased IgG3 level
MP:0008503	abnormal spinal cord grey matter morphology
MP:0008504	abnormal adrenal chromaffin cell morphology
MP:0008505	absent adrenal chromaffin cells
MP:0008506	abnormal noradrenergic chromaffin cell morphology
MP:0008507	thin retinal ganglion layer
MP:0008508	thick retinal ganglion layer
MP:0008509	disorganized retinal ganglion layer
MP:0008510	absent retinal ganglion layer
MP:0008511	thin retinal inner nuclear layer
MP:0008512	disorganized retinal inner nuclear layer
MP:0008513	thin retinal inner plexiform layer
MP:0008514	absent retinal inner plexiform layer
MP:0008515	thin retinal outer nuclear layer
MP:0008516	disorganized retinal outer nuclear layer
MP:0008518	retinal outer nuclear layer degeneration
MP:0008519	thin retinal outer plexiform layer
MP:0008520	disorganized retinal outer plexiform layer
MP:0008521	abnormal Bowman membrane
MP:0008522	abnormal lymph node germinal center morphology
MP:0008524	increased plasmacytoid dendritic cell number
MP:0008525	decreased cranium height
MP:0008527	embryonic lethality at implantation
MP:0008529	enlarged optic nerve
MP:0008530	abnormal rostral-caudal patterning of the somites
MP:0008531	increased chemical nociceptive threshold
MP:0008532	decreased chemical nociceptive threshold
MP:0008533	abnormal anterior visceral endoderm morphology
MP:0008534	enlarged fourth ventricle
MP:0008535	enlarged lateral ventricles
MP:0008536	enlarged third ventricle
MP:0008537	increased susceptibility to induced colitis
MP:0008538	decreased zigzag hair amount
MP:0008539	decreased susceptibility to induced colitis
MP:0008540	abnormal cerebral hemisphere morphology
MP:0008541	leukostasis
MP:0008542	enlarged cervical lymph nodes
MP:0008544	impaired olfaction
MP:0008545	absent sperm flagellum
MP:0008546	abnormal vesicle-mediated transport
MP:0008547	abnormal neocortex morphology
MP:0008548	abnormal circulating interferon level
MP:0008550	abnormal circulating interferon-beta level
MP:0008551	abnormal circulating interferon-gamma level
MP:0008552	abnormal circulating tumor necrosis factor level
MP:0008553	increased circulating tumor necrosis factor level
MP:0008554	decreased circulating tumor necrosis factor level
MP:0008559	abnormal interferon-gamma secretion
MP:0008560	increased tumor necrosis factor secretion
MP:0008561	decreased tumor necrosis factor secretion
MP:0008562	increased interferon-alpha secretion
MP:0008563	decreased interferon-alpha secretion
MP:0008564	increased interferon-beta secretion
MP:0008565	decreased interferon-beta secretion
MP:0008566	increased interferon-gamma secretion
MP:0008567	decreased interferon-gamma secretion
MP:0008569	lethality at weaning
MP:0008570	lipidosis
MP:0008571	abnormal synaptic bouton morphology
MP:0008572	abnormal Purkinje cell dendrite morphology
MP:0008573	increased circulating interferon-alpha level
MP:0008574	decreased circulating interferon-alpha level
MP:0008575	increased circulating interferon-beta level
MP:0008576	decreased circulating interferon-beta level
MP:0008577	increased circulating interferon-gamma level
MP:0008578	decreased circulating interferon-gamma level
MP:0008579	abnormal Purkinje cell differentiation
MP:0008580	photoreceptor inner segment degeneration
MP:0008581	disorganized photoreceptor inner segment
MP:0008582	short photoreceptor inner segment
MP:0008583	absent photoreceptor inner segment
MP:0008584	photoreceptor outer segment degeneration
MP:0008585	absent photoreceptor outer segment
MP:0008586	disorganized photoreceptor outer segment
MP:0008587	short photoreceptor outer segment
MP:0008588	abnormal circulating interleukin level
MP:0008590	abnormal circulating interleukin-10 level
MP:0008591	increased circulating interleukin-1 level
MP:0008592	decreased circulating interleukin-1 level
MP:0008593	increased circulating interleukin-10 level
MP:0008594	decreased circulating interleukin-10 level
MP:0008595	abnormal circulating interleukin-6 level
MP:0008596	increased circulating interleukin-6 level
MP:0008597	decreased circulating interleukin-6 level
MP:0008599	increased circulating interleukin-2 level
MP:0008600	decreased circulating interleukin-2 level
MP:0008601	abnormal circulating interleukin-4 level
MP:0008602	increased circulating interleukin-4 level
MP:0008603	decreased circulating interleukin-4 level
MP:0008608	increased circulating interleukin-13 level
MP:0008609	decreased circulating interleukin-13 level
MP:0008611	increased circulating interleukin-15 level
MP:0008614	increased circulating interleukin-17 level
MP:0008615	decreased circulating interleukin-17 level
MP:0008617	increased circulating interleukin-12 level
MP:0008618	decreased circulating interleukin-12 level
MP:0008620	increased circulating interleukin-23 level
MP:0008623	increased circulating interleukin-3 level
MP:0008625	abnormal circulating interleukin-5 level
MP:0008626	increased circulating interleukin-5 level
MP:0008627	decreased circulating interleukin-5 level
MP:0008629	increased circulating interleukin-9 level
MP:0008632	increased circulating interleukin-16 level
MP:0008635	increased circulating interleukin-18 level
MP:0008636	decreased circulating interleukin-18 level
MP:0008638	increased circulating interleukin-1 alpha level
MP:0008639	decreased circulating interleukin-1 alpha level
MP:0008640	abnormal circulating interleukin-1 beta level
MP:0008641	increased circulating interleukin-1 beta level
MP:0008642	decreased circulating interleukin-1 beta level
MP:0008646	abnormal circulating interleukin-12b level
MP:0008647	increased circulating interleukin-12b level
MP:0008648	decreased circulating interleukin-12b level
MP:0008650	abnormal interleukin-1 secretion
MP:0008651	increased interleukin-1 secretion
MP:0008652	decreased interleukin-1 secretion
MP:0008654	increased interleukin-1 alpha secretion
MP:0008655	decreased interleukin-1 alpha secretion
MP:0008656	abnormal interleukin-1 beta secretion
MP:0008657	increased interleukin-1 beta secretion
MP:0008658	decreased interleukin-1 beta secretion
MP:0008660	increased interleukin-10 secretion
MP:0008661	decreased interleukin-10 secretion
MP:0008662	abnormal interleukin-12 secretion
MP:0008663	increased interleukin-12 secretion
MP:0008664	decreased interleukin-12 secretion
MP:0008669	increased interleukin-12b secretion
MP:0008670	decreased interleukin-12b secretion
MP:0008671	abnormal interleukin-13 secretion
MP:0008672	increased interleukin-13 secretion
MP:0008673	decreased interleukin-13 secretion
MP:0008676	decreased interleukin-15 secretion
MP:0008680	abnormal interleukin-17 secretion
MP:0008681	increased interleukin-17 secretion
MP:0008682	decreased interleukin-17 secretion
MP:0008684	increased interleukin-18 secretion
MP:0008685	decreased interleukin-18 secretion
MP:0008686	abnormal interleukin-2 secretion
MP:0008687	increased interleukin-2 secretion
MP:0008688	decreased interleukin-2 secretion
MP:0008690	increased interleukin-23 secretion
MP:0008691	decreased interleukin-23 secretion
MP:0008696	increased interleukin-3 secretion
MP:0008697	decreased interleukin-3 secretion
MP:0008698	abnormal interleukin-4 secretion
MP:0008699	increased interleukin-4 secretion
MP:0008700	decreased interleukin-4 secretion
MP:0008701	abnormal interleukin-5 secretion
MP:0008702	increased interleukin-5 secretion
MP:0008703	decreased interleukin-5 secretion
MP:0008704	abnormal interleukin-6 secretion
MP:0008705	increased interleukin-6 secretion
MP:0008706	decreased interleukin-6 secretion
MP:0008711	increased interleukin-9 secretion
MP:0008712	decreased interleukin-9 secretion
MP:0008713	abnormal cytokine level
MP:0008714	increased lung carcinoma incidence
MP:0008719	impaired neutrophil recruitment
MP:0008721	abnormal chemokine level
MP:0008723	impaired eosinophil recruitment
MP:0008724	impaired eosinophil chemotaxis
MP:0008725	enlarged heart atrium
MP:0008726	enlarged heart left atrium
MP:0008727	enlarged heart right atrium
MP:0008728	increased memory B cell number
MP:0008729	decreased memory B cell number
MP:0008730	fused phalanges
MP:0008731	abnormal hair shaft melanin granule morphology
MP:0008732	reduced hair shaft melanin granule number
MP:0008733	abnormal hair shaft melanin granule distribution
MP:0008734	decreased susceptibility to endotoxin shock
MP:0008735	increased susceptibility to endotoxin shock
MP:0008737	abnormal spleen physiology
MP:0008740	abnormal intestinal iron level
MP:0008741	abnormal heart iron level
MP:0008742	abnormal kidney iron level
MP:0008743	decreased liver iron level
MP:0008746	abnormal peripheral B cell anergy
MP:0008747	abnormal T cell anergy
MP:0008749	abnormal peripheral T cell anergy
MP:0008750	abnormal interferon level
MP:0008751	abnormal interleukin level
MP:0008752	abnormal tumor necrosis factor level
MP:0008753	abnormal osteocyte morphology
MP:0008754	abnormal T cell receptor V(D)J recombination
MP:0008755	abnormal immunoglobulin V(D)J recombination
MP:0008756	abnormal T cell receptor alpha chain V-J recombination
MP:0008757	abnormal T cell receptor gamma chain V-J recombination
MP:0008758	abnormal T cell receptor beta chain V(D)J recombination
MP:0008759	abnormal T cell receptor delta chain V(D)J recombination
MP:0008760	abnormal immunoglobulin heavy chain V(D)J recombination
MP:0008761	abnormal immunoglobulin light chain V-J recombination
MP:0008762	embryonic lethality
MP:0008763	abnormal mast cell degranulation
MP:0008764	increased mast cell degranulation
MP:0008765	decreased mast cell degranulation
MP:0008766	abnormal B cell receptor editing
MP:0008767	abnormal hair medullary septa cells
MP:0008768	abnormal hair medulla air spaces
MP:0008769	abnormal plasmacytoid dendritic cell physiology
MP:0008770	decreased survivor rate
MP:0008771	elongated vertebral column
MP:0008772	increased heart ventricle size
MP:0008775	abnormal heart ventricle pressure
MP:0008776	increased right ventricle peak pressure
MP:0008777	increased right ventricle diastolic pressure
MP:0008778	abnormal lymphangiogenesis
MP:0008779	abnormal maternal behavior
MP:0008780	increased pancreatic acinar cell carcinoma incidence
MP:0008781	abnormal B cell apoptosis
MP:0008782	increased B cell apoptosis
MP:0008783	decreased B cell apoptosis
MP:0008785	abnormal sternum manubrium morphology
MP:0008786	abnormal hindgut morphology
MP:0008787	abnormal tailgut morphology
MP:0008788	abnormal fetal cardiomyocyte morphology
MP:0008789	abnormal olfactory epithelium morphology
MP:0008790	abnormal NK cell degranulation
MP:0008791	decreased NK cell degranulation
MP:0008794	increased lens epithelium apoptosis
MP:0008796	increased lens fiber apoptosis
MP:0008799	oblique facial cleft
MP:0008800	increased small intestinal crypt cell apoptosis
MP:0008801	abnormal erythroid progenitor cell morphology
MP:0008802	abnormal intestinal smooth muscle morphology
MP:0008803	abnormal placental labyrinth vasculature morphology
MP:0008804	abnormal circulating amylase level
MP:0008805	decreased circulating amylase level
MP:0008806	increased circulating amylase level
MP:0008808	decreased spleen iron level
MP:0008809	increased spleen iron level
MP:0008810	increased circulating iron level
MP:0008811	abnormal brain iron level
MP:0008812	abnormal rostrocaudal coat patterning
MP:0008813	decreased common myeloid progenitor cell number
MP:0008817	hematoma
MP:0008818	abnormal interfrontal bone morphology
MP:0008823	abnormal interventricular septum membranous part morphology
MP:0008824	absent interventricular septum membranous part
MP:0008825	abnormal cardiac epithelial to mesenchymal transition
MP:0008826	abnormal splenic cell ratio
MP:0008827	abnormal thymus cell ratio
MP:0008828	abnormal lymph node cell ratio
MP:0008829	triphalangia
MP:0008830	abnormal nucleolus morphology
MP:0008831	abnormal insulin-like growth factor I level
MP:0008833	caudal hemivertebra
MP:0008834	abnormal melanosome transport
MP:0008837	increased transforming growth factor level
MP:0008838	decreased transforming growth factor level
MP:0008839	absent acrosome
MP:0008840	abnormal spike wave discharge
MP:0008841	ruptured lens capsule
MP:0008842	lipofuscinosis
MP:0008845	abnormal paraventricular hypothalamic nucleus morphology
MP:0008846	abnormal supraoptic nucleus morphology
MP:0008847	abnormal suprachiasmatic nucleus morphology
MP:0008850	increased hemoglobin concentration distribution width
MP:0008851	decreased hemoglobin concentration distribution width
MP:0008853	decreased abdominal adipose tissue amount
MP:0008854	bleb
MP:0008855	eye bleb
MP:0008856	fetal bleb
MP:0008857	myelencephalic blebs
MP:0008858	abnormal hair cycle anagen phase
MP:0008859	abnormal hair cycle catagen phase
MP:0008860	abnormal hair cycle telogen phase
MP:0008861	abnormal hair shedding
MP:0008862	asymmetric snout
MP:0008864	abnormal intestinal secretion
MP:0008866	chromosomal instability
MP:0008868	abnormal granulosa cell morphology
MP:0008869	anovulation
MP:0008870	increased mature ovarian follicle number
MP:0008871	abnormal ovarian follicle number
MP:0008872	abnormal physiological response to xenobiotic
MP:0008873	increased physiological sensitivity to xenobiotic
MP:0008874	decreased physiological sensitivity to xenobiotic
MP:0008875	abnormal xenobiotic pharmacokinetics
MP:0008876	decreased uterine NK cell number
MP:0008877	abnormal DNA methylation
MP:0008878	abnormal DNA methylation during gametogenesis
MP:0008879	submandibular gland inflammation
MP:0008880	lacrimal gland inflammation
MP:0008881	absent Harderian gland
MP:0008882	abnormal enterocyte physiology
MP:0008883	abnormal enterocyte proliferation
MP:0008884	abnormal enterocyte apoptosis
MP:0008885	increased enterocyte apoptosis
MP:0008886	abnormal PML bodies
MP:0008888	abnormal Cajal body morphology
MP:0008890	abnormal nuclear lamina morphology
MP:0008891	decreased hepatocyte apoptosis
MP:0008892	abnormal sperm flagellum morphology
MP:0008893	detached sperm flagellum
MP:0008894	abnormal intraepithelial T cell morphology
MP:0008895	abnormal intraepithelial T cell number
MP:0008896	increased IgG2c level
MP:0008897	decreased IgG2c level
MP:0008898	abnormal acrosome morphology
MP:0008899	plush coat
MP:0008901	absent epididymal fat pad
MP:0008902	abnormal renal fat pad morphology
MP:0008903	abnormal mesenteric fat pad morphology
MP:0008904	abnormal mammary fat pad morphology
MP:0008906	abnormal parametrial fat pad morphology
MP:0008907	decreased total fat pad weight
MP:0008908	increased total fat pad weight
MP:0008911	induced hyperactivity
MP:0008912	nervous
MP:0008913	weaving
MP:0008916	abnormal astrocyte physiology
MP:0008917	abnormal oligodendrocyte physiology
MP:0008918	microgliosis
MP:0008920	absent cervical axis
MP:0008921	increased neurotransmitter release
MP:0008922	abnormal cervical rib
MP:0008923	thoracoschisis
MP:0008924	decreased cerebellar granule cell number
MP:0008925	increased cerebellar granule cell number
MP:0008926	abnormal anterior definitive endoderm morphology
MP:0008929	abnormal central medial nucleus morphology
MP:0008932	abnormal embryonic tissue physiology
MP:0008933	abnormal motile primary cilium physiology
MP:0008934	absent choroid plexus
MP:0008938	decreased pituitary gland weight
MP:0008939	increased pituitary gland weight
MP:0008940	delayed balanopreputial separation
MP:0008943	increased sensitivity to induced cell death
MP:0008944	decreased sensitivity to induced cell death
MP:0008946	abnormal neuron number
MP:0008947	increased neuron number
MP:0008948	decreased neuron number
MP:0008953	abnormal pancreatic somatostatin secretion
MP:0008954	abnormal cellular hemoglobin content
MP:0008955	increased cellular hemoglobin content
MP:0008956	decreased cellular hemoglobin content
MP:0008957	abnormal placenta junctional zone morphology
MP:0008958	abnormal trophoblast glycogen cell morphology
MP:0008959	abnormal spongiotrophoblast cell morphology
MP:0008960	abnormal axon pruning
MP:0008961	abnormal basal metabolism
MP:0008962	abnormal carbon dioxide production
MP:0008963	increased carbon dioxide production
MP:0008964	decreased carbon dioxide production
MP:0008965	increased basal metabolism
MP:0008966	abnormal chiasmata formation
MP:0008967	absent chiasmata formation
MP:0008969	abnormal nasolacrimal duct morphology
MP:0008971	abnormal ethmoturbinate morphology
MP:0008972	ethmoturbinate hypoplasia
MP:0008974	proportional dwarf
MP:0008975	delayed male fertility
MP:0008976	delayed female fertility
MP:0008978	abnormal vagina weight
MP:0008980	decreased vagina weight
MP:0008983	small vagina
MP:0008985	hemimelia
MP:0008987	abnormal liver lobule morphology
MP:0008988	abnormal liver perisinusoidal space morphology
MP:0008989	abnormal liver sinusoid morphology
MP:0008990	abnormal Ito cell morphology
MP:0008991	abnormal bile canaliculus morphology
MP:0008992	abnormal portal lobule morphology
MP:0008993	abnormal portal triad morphology
MP:0008994	early vaginal opening
MP:0008995	early reproductive senescence
MP:0008996	abnormal blood osmolality
MP:0008997	increased blood osmolality
MP:0008998	decreased blood osmolality
MP:0008999	absent anus
MP:0009000	absent cecum
MP:0009003	abnormal vibrissa number
MP:0009004	progressive hair loss
MP:0009005	abnormal sesamoid bone of gastrocnemius morphology
MP:0009006	prolonged estrous cycle
MP:0009007	short estrous cycle
MP:0009008	delayed estrous cycle
MP:0009009	absent estrous cycle
MP:0009010	abnormal diestrus
MP:0009011	prolonged diestrus
MP:0009012	short diestrus
MP:0009013	abnormal proestrus
MP:0009014	prolonged proestrus
MP:0009015	short proestrus
MP:0009016	abnormal estrus
MP:0009017	prolonged estrus
MP:0009018	short estrus
MP:0009019	abnormal metestrus
MP:0009020	prolonged metestrus
MP:0009021	absent estrus
MP:0009022	abnormal brain meninges morphology
MP:0009025	abnormal brain dura mater morphology
MP:0009026	abnormal brain pia mater morphology
MP:0009027	abnormal subarachnoid space morphology
MP:0009038	decreased inferior colliculus size
MP:0009039	absent inferior colliculus
MP:0009043	increased pancreas adenoma incidence
MP:0009044	increased adrenal gland adenoma incidence
MP:0009045	muscle tetany
MP:0009047	short metestrus
MP:0009048	enlarged tectum
MP:0009049	abnormal hallux morphology
MP:0009050	dilated proximal convoluted tubules
MP:0009051	dilated distal convoluted tubules
MP:0009053	abnormal anal canal morphology
MP:0009055	abnormal internal anal sphincter morphology
MP:0009057	increased interleukin-21 secretion
MP:0009058	decreased interleukin-21 secretion
MP:0009062	impaired lectin complement pathway
MP:0009064	oviduct atrophy
MP:0009066	decreased oviduct weight
MP:0009069	dilated oviduct
MP:0009070	small oviduct
MP:0009071	short oviduct
MP:0009073	absent Wolffian ducts
MP:0009074	Wolffian duct degeneration
MP:0009075	rudimentary Wolffian ducts
MP:0009076	rudimentary Mullerian ducts
MP:0009078	adrenal gland hyperplasia
MP:0009079	prolapsed intervertebral disk
MP:0009080	uterus inflammation
MP:0009081	thin uterus
MP:0009082	uterus cysts
MP:0009083	uterus hypertrophy
MP:0009084	blind uterus
MP:0009085	abnormal uterine horn morphology
MP:0009086	blind uterine horn
MP:0009087	dilated uterine horn
MP:0009088	thin uterine horn
MP:0009089	short uterine horn
MP:0009090	myometrium hypoplasia
MP:0009091	endometrium hypoplasia
MP:0009093	oocyte degeneration
MP:0009094	abnormal endometrial gland morphology
MP:0009096	decreased endometrial gland number
MP:0009097	absent endometrial glands
MP:0009098	anovaginal fistula
MP:0009099	abnormal uterine NK cell physiology
MP:0009103	abnormal penile bone morphology
MP:0009104	small penile bone
MP:0009105	penis prolapse
MP:0009108	increased pancreas weight
MP:0009109	decreased pancreas weight
MP:0009113	increased pancreatic beta cell mass
MP:0009114	decreased pancreatic beta cell mass
MP:0009115	abnormal fat cell morphology
MP:0009116	abnormal brown fat cell morphology
MP:0009117	abnormal white fat cell morphology
MP:0009118	increased white fat cell size
MP:0009119	increased brown fat cell size
MP:0009121	increased white fat cell lipid droplet size
MP:0009122	decreased white fat cell lipid droplet size
MP:0009124	increased brown fat cell lipid droplet size
MP:0009125	decreased brown fat cell lipid droplet size
MP:0009127	increased brown fat cell number
MP:0009128	decreased brown fat cell number
MP:0009130	increased white fat cell number
MP:0009131	decreased white fat cell number
MP:0009132	abnormal white fat cell size
MP:0009133	decreased white fat cell size
MP:0009135	abnormal brown fat cell size
MP:0009136	decreased brown fat cell size
MP:0009137	decreased brown fat lipid droplet number
MP:0009139	failure of Mullerian duct regression
MP:0009140	dilated efferent ductules of testis
MP:0009141	increased prepulse inhibition
MP:0009142	decreased prepulse inhibition
MP:0009143	abnormal pancreatic duct morphology
MP:0009144	dilated pancreatic duct
MP:0009145	abnormal pancreatic acinus morphology
MP:0009146	abnormal pancreatic acinar cell morphology
MP:0009147	abnormal pancreatic acinar cell physiology
MP:0009148	pancreas necrosis
MP:0009149	decreased pancreatic acinar cell number
MP:0009150	pancreatic acinar cell atrophy
MP:0009151	increased pancreatic ductal adenocarcinoma incidence
MP:0009152	increased pancreatic intraepithelial neoplasia incidence
MP:0009154	pancreatic acinar hypoplasia
MP:0009155	pancreatic acinar hyperplasia
MP:0009157	ectopic pancreatic acinar cells
MP:0009158	absent pancreatic acinar cells
MP:0009159	increased pancreatic acinar cell number
MP:0009160	abnormal pancreatic acinar cell zymogen granule morphology
MP:0009161	pancreatic acinar cell zymogen granule accumulation
MP:0009162	absent pancreatic acinar cell zymogen granule
MP:0009163	absent pancreatic duct
MP:0009164	exocrine pancreas atrophy
MP:0009165	abnormal endocrine pancreas morphology
MP:0009167	increased pancreatic islet number
MP:0009168	decreased pancreatic islet number
MP:0009169	pancreatic islet hypoplasia
MP:0009170	abnormal pancreatic islet size
MP:0009172	small pancreatic islets
MP:0009173	absent pancreatic islets
MP:0009174	absent pancreatic beta cells
MP:0009175	abnormal pancreatic beta cell differentiation
MP:0009176	increased pancreatic alpha cell number
MP:0009177	decreased pancreatic alpha cell number
MP:0009178	absent pancreatic alpha cells
MP:0009179	abnormal pancreatic alpha cell differentiation
MP:0009180	increased pancreatic delta cell number
MP:0009181	decreased pancreatic delta cell number
MP:0009182	absent pancreatic delta cells
MP:0009183	abnormal pancreatic delta cell differentiation
MP:0009184	abnormal PP cell morphology
MP:0009185	increased PP cell number
MP:0009186	decreased PP cell number
MP:0009187	absent PP cells
MP:0009188	abnormal PP cell differentiation
MP:0009189	abnormal pancreatic epsilon cell morphology
MP:0009190	increased pancreatic epsilon cell number
MP:0009191	decreased pancreatic epsilon cell number
MP:0009193	abnormal pancreatic epsilon cell differentiation
MP:0009195	abnormal PP cell physiology
MP:0009199	abnormal external male genitalia morphology
MP:0009200	enlarged external male genitalia
MP:0009201	external male genitalia atrophy
MP:0009202	small external male genitalia
MP:0009203	external male genitalia hypoplasia
MP:0009204	absent external male genitalia
MP:0009206	absent internal male genitalia
MP:0009207	internal male genitalia hypoplasia
MP:0009208	abnormal female genitalia morphology
MP:0009210	absent internal female genitalia
MP:0009211	absent external female genitalia
MP:0009212	vulva atrophy
MP:0009213	absent male inguinal canal
MP:0009214	vas deferens hypoplasia
MP:0009215	absent uterine horn
MP:0009216	abnormal peritoneum morphology
MP:0009218	absent peritoneal vaginal process
MP:0009219	increased prostate intraepithelial neoplasia incidence
MP:0009220	increased prostate gland adenocarcinoma incidence
MP:0009221	uterus adenomyosis
MP:0009223	increased uterus carcinoma incidence
MP:0009224	absent endometrium
MP:0009226	small uterine cervix
MP:0009227	uterine cervix hypoplasia
MP:0009229	abnormal neurohypophysis median eminence morphology
MP:0009230	abnormal sperm head morphology
MP:0009231	detached acrosome
MP:0009232	abnormal sperm nucleus morphology
MP:0009233	enlarged sperm head
MP:0009234	absent sperm head
MP:0009235	small sperm head
MP:0009236	pinhead sperm
MP:0009237	kinked sperm flagellum
MP:0009238	coiled sperm flagellum
MP:0009239	short sperm flagellum
MP:0009241	thick sperm flagellum
MP:0009242	thin sperm flagellum
MP:0009243	hairpin sperm flagellum
MP:0009244	abnormal acid-activated cation-mediated receptor currents
MP:0009245	caudal rachischisis
MP:0009246	pale spleen
MP:0009247	meteorism
MP:0009248	small caput epididymis
MP:0009249	enlarged caput epididymis
MP:0009251	enlarged endometrial glands
MP:0009252	absent urinary bladder
MP:0009253	abnormal sympathetic neuron physiology
MP:0009254	disorganized pancreatic islets
MP:0009255	degranulated pancreatic beta cells
MP:0009256	enlarged corpus epididymis
MP:0009257	dilated seminiferous tubules
MP:0009258	abnormal thymocyte apoptosis
MP:0009262	absent semicircular canal ampulla
MP:0009263	abnormal eyelid fusion
MP:0009264	failure of eyelid fusion
MP:0009265	delayed eyelid fusion
MP:0009266	abnormal mesendoderm development
MP:0009267	abnormal cerebellum fissure morphology
MP:0009268	absent cerebellum fissure
MP:0009269	decreased fat cell size
MP:0009271	increased guard hair length
MP:0009272	decreased guard hair length
MP:0009273	abnormal hair shaft melanin granule shape
MP:0009278	abnormal bone marrow cell physiology
MP:0009280	reduced activated sperm motility
MP:0009282	reduced hyperactivated sperm motility
MP:0009283	decreased gonadal fat pad weight
MP:0009284	abnormal sympathetic neuron innervation pattern
MP:0009285	increased gonadal fat pad weight
MP:0009286	increased abdominal fat pad weight
MP:0009287	decreased abdominal fat pad weight
MP:0009288	increased epididymal fat pad weight
MP:0009289	decreased epididymal fat pad weight
MP:0009291	decreased femoral fat pad weight
MP:0009292	increased inguinal fat pad weight
MP:0009293	decreased inguinal fat pad weight
MP:0009294	increased interscapular fat pad weight
MP:0009295	decreased interscapular fat pad weight
MP:0009296	increased mammary fat pad weight
MP:0009297	decreased mammary fat pad weight
MP:0009298	increased mesenteric fat pad weight
MP:0009299	decreased mesenteric fat pad weight
MP:0009300	increased parametrial fat pad weight
MP:0009301	decreased parametrial fat pad weight
MP:0009302	increased renal fat pad weight
MP:0009303	decreased renal fat pad weight
MP:0009304	increased retroperitoneal fat pad weight
MP:0009305	decreased retroperitoneal fat pad weight
MP:0009307	decreased uterine fat pad weight
MP:0009308	increased adenocarcinoma incidence
MP:0009312	increased jejunum adenocarcinoma incidence
MP:0009315	increased rectum adenocarcinoma incidence
MP:0009317	increased follicular lymphoma incidence
MP:0009318	increased splenic marginal zone lymphoma incidence
MP:0009319	increased small lymphocytic lymphoma incidence
MP:0009320	increased lymphoblastic lymphoma incidence
MP:0009321	increased histiocytic sarcoma incidence
MP:0009322	increased splenocyte apoptosis
MP:0009323	abnormal spleen development
MP:0009324	absent hippocampal fimbria
MP:0009325	necrospermia
MP:0009326	absent maternal crouching
MP:0009327	abnormal maternal grooming
MP:0009328	delayed heart looping
MP:0009331	absent primitive node
MP:0009332	abnormal splenocyte morphology
MP:0009333	abnormal splenocyte physiology
MP:0009334	abnormal splenocyte proliferation
MP:0009335	decreased splenocyte proliferation
MP:0009336	increased splenocyte proliferation
MP:0009338	increased splenocyte number
MP:0009339	decreased splenocyte number
MP:0009340	abnormal splenocyte apoptosis
MP:0009341	decreased splenocyte apoptosis
MP:0009342	enlarged gallbladder
MP:0009343	dilated gallbladder
MP:0009345	abnormal trabecular bone thickness
MP:0009346	decreased trabecular bone thickness
MP:0009347	increased trabecular bone thickness
MP:0009349	increased urine pH
MP:0009350	decreased urine pH
MP:0009351	thin hair shaft
MP:0009352	impaired spacing of implantation sites
MP:0009353	twin decidual capsule
MP:0009354	emprosthotonos
MP:0009355	increased liver triglyceride level
MP:0009356	decreased liver triglyceride level
MP:0009357	abnormal seizure response to inducing agent
MP:0009358	environmentally induced seizures
MP:0009359	endometrium atrophy
MP:0009360	endometrium inflammation
MP:0009361	abnormal primordial ovarian follicle morphology
MP:0009362	abnormal primary ovarian follicle morphology
MP:0009363	abnormal secondary ovarian follicle morphology
MP:0009364	abnormal mature ovarian follicle morphology
MP:0009365	abnormal theca folliculi
MP:0009368	absent theca folliculi
MP:0009370	decreased theca cell number
MP:0009371	increased theca cell number
MP:0009372	abnormal cumulus oophorus
MP:0009373	abnormal cumulus expansion
MP:0009374	absent cumulus expansion
MP:0009375	thin zona pellucida
MP:0009376	abnormal manchette morphology
MP:0009377	ectopic manchette
MP:0009378	abnormal endoplasmic reticulum morphology
MP:0009379	abnormal foot pigmentation
MP:0009380	abnormal prostate gland ventral lobe morphology
MP:0009381	abnormal prostate gland dorsolateral lobe morphology
MP:0009382	abnormal cardiac jelly morphology
MP:0009384	cardiac valve regurgitation
MP:0009385	abnormal dermal pigmentation
MP:0009386	abnormal dermal melanocyte morphology
MP:0009387	abnormal epidermal pigmentation
MP:0009388	abnormal epidermal melanocyte morphology
MP:0009389	abnormal extracutaneous pigmentation
MP:0009391	abnormal leptomeninges pigmentation
MP:0009392	retinal gliosis
MP:0009393	abnormal resting posture
MP:0009394	increased uterine NK cell number
MP:0009395	increased nucleated erythrocyte cell number
MP:0009396	small endometrial glands
MP:0009397	increased trophoblast giant cell number
MP:0009399	increased skeletal muscle fiber size
MP:0009400	decreased skeletal muscle fiber size
MP:0009401	increased skeletal muscle fiber diameter
MP:0009402	decreased skeletal muscle fiber diameter
MP:0009403	increased variability of skeletal muscle fiber size
MP:0009405	increased skeletal muscle fiber number
MP:0009406	decreased skeletal muscle fiber number
MP:0009407	increased skeletal muscle fiber density
MP:0009408	decreased skeletal muscle fiber density
MP:0009409	abnormal skeletal muscle fiber type ratio
MP:0009410	abnormal skeletal muscle satellite cell proliferation
MP:0009411	abnormal skeletal muscle fiber triad morphology
MP:0009412	skeletal muscle fiber degeneration
MP:0009413	skeletal muscle fiber atrophy
MP:0009414	skeletal muscle fiber necrosis
MP:0009415	skeletal muscle degeneration
MP:0009416	cardiac muscle degeneration
MP:0009418	cardiac muscle atrophy
MP:0009419	skeletal muscle fibrosis
MP:0009420	skeletal muscle endomysial fibrosis
MP:0009421	increased gastrocnemius weight
MP:0009422	decreased gastrocnemius weight
MP:0009423	increased extensor digitorum longus weight
MP:0009424	decreased extensor digitorum longus weight
MP:0009425	increased soleus weight
MP:0009426	decreased soleus weight
MP:0009427	increased tibialis anterior weight
MP:0009428	decreased tibialis anterior weight
MP:0009429	decreased embryo weight
MP:0009430	increased embryo weight
MP:0009431	decreased fetal weight
MP:0009432	increased fetal weight
MP:0009433	polyovular ovarian follicle
MP:0009435	abnormal miniature inhibitory postsynaptic currents
MP:0009436	fragmentation of sleep/wake states
MP:0009438	cricoid and tracheal cartilage fusion
MP:0009439	increased myeloid sarcoma incidence
MP:0009441	delayed skin barrier formation
MP:0009443	parthenogenesis
MP:0009444	ovarian follicular cyst
MP:0009446	abnormal platelet dense granule physiology
MP:0009448	decreased platelet ATP level
MP:0009450	abnormal axon fasciculation
MP:0009451	abnormal chromosomal synapsis
MP:0009452	abnormal synaptonemal complex
MP:0009453	enhanced contextual conditioning behavior
MP:0009454	impaired contextual conditioning behavior
MP:0009455	enhanced cued conditioning behavior
MP:0009456	impaired cued conditioning behavior
MP:0009457	whorled hair
MP:0009458	abnormal skeletal muscle size
MP:0009459	skeletal muscle hyperplasia
MP:0009460	skeletal muscle hypoplasia
MP:0009462	skeletal muscle hypotrophy
MP:0009463	abnormal pituitary infundibular stalk morphology
MP:0009468	absent magnocellular neurosecretory cells
MP:0009469	increased skin hamartoma incidence
MP:0009470	mirror image duplication
MP:0009473	abnormal skin exfoliation
MP:0009474	thick epidermis stratum spinosum
MP:0009475	abnormal nicotine-mediated receptor currents
MP:0009476	enlarged cecum
MP:0009477	small cecum
MP:0009478	coiled cecum
MP:0009479	abnormal cecum development
MP:0009480	distended cecum
MP:0009481	cecum inflammation
MP:0009482	ileum inflammation
MP:0009483	enlarged ileum
MP:0009484	ileum hypertrophy
MP:0009485	distended ileum
MP:0009488	abnormal pancreatic islet cell apoptosis
MP:0009489	abnormal blood vessel endothelium morphology
MP:0009490	abnormal heart left atrium auricular region morphology
MP:0009492	abnormal gallbladder epithelium morphology
MP:0009493	abnormal cystic duct morphology
MP:0009497	abnormal intrahepatic bile duct morphology
MP:0009498	abnormal extrahepatic bile duct morphology
MP:0009500	abnormal interlobular bile duct morphology
MP:0009501	abnormal hepatic duct morphology
MP:0009503	abnormal mammary gland duct morphology
MP:0009504	abnormal mammary gland epithelium morphology
MP:0009505	abnormal mammary gland lobule morphology
MP:0009506	abnormal mammary gland alveolus morphology
MP:0009507	abnormal mammary gland connective tissue morphology
MP:0009509	absent rectum
MP:0009510	cecal atresia
MP:0009511	distended stomach
MP:0009512	abnormal cerebellar Golgi cell morphology
MP:0009516	enlarged salivary gland
MP:0009517	abnormal salivary gland duct morphology
MP:0009520	decreased submandibular gland size
MP:0009521	increased submandibular gland size
MP:0009522	submandibular gland hypoplasia
MP:0009523	submandibular gland hyperplasia
MP:0009524	absent submandibular gland
MP:0009525	abnormal submandibular duct morphology
MP:0009526	absent sublingual gland
MP:0009527	abnormal sublingual duct morphology
MP:0009532	decreased parotid gland size
MP:0009533	absent palatine gland
MP:0009534	absent anterior lingual gland
MP:0009535	abnormal skin sebaceous gland morphology
MP:0009536	abnormal interstitial cell of Cajal morphology
MP:0009537	interstitial cells of Cajal hyperplasia
MP:0009538	abnormal synapse morphology
MP:0009539	abnormal Hassall's corpuscle morphology
MP:0009540	absent Hassall's corpuscle
MP:0009541	increased thymocyte apoptosis
MP:0009542	decreased thymocyte apoptosis
MP:0009543	abnormal thymus corticomedullary boundary morphology
MP:0009544	abnormal thymus epithelium morphology
MP:0009545	abnormal dermis papillary layer morphology
MP:0009546	absent gastric milk in neonates
MP:0009550	increased urinary bladder carcinoma incidence
MP:0009551	increased urinary bladder transitional cell carcinoma incidence
MP:0009552	urinary bladder obstruction
MP:0009555	abnormal hair follicle melanin granule distribution
MP:0009557	decreased platelet ADP level
MP:0009559	thymus cortex hyperplasia
MP:0009560	absent epidermis stratum granulosum
MP:0009561	superior cervical ganglion degeneration
MP:0009562	abnormal odor adaptation
MP:0009563	dyskeratosis
MP:0009564	abnormal meiotic configurations
MP:0009567	mitotic nondisjunction
MP:0009568	abnormal red blood cell deformability
MP:0009569	abnormal left lung morphology
MP:0009570	abnormal right lung morphology
MP:0009571	abnormal right lung accessory lobe morphology
MP:0009573	abnormal right lung middle lobe morphology
MP:0009574	abnormal right lung caudal lobe morphology
MP:0009575	abnormal pubic symphysis morphology
MP:0009576	oral atresia
MP:0009577	abnormal developmental vascular remodeling
MP:0009578	otocephaly
MP:0009579	acephaly
MP:0009580	increased keratinocyte apoptosis
MP:0009581	decreased keratinocyte apoptosis
MP:0009582	abnormal keratinocyte proliferation
MP:0009583	increased keratinocyte proliferation
MP:0009584	decreased keratinocyte proliferation
MP:0009586	increased platelet aggregation
MP:0009587	abnormal plasma membrane sphingolipid content
MP:0009588	increased plasma membrane sphingolipid content
MP:0009589	sphingomyelinosis
MP:0009590	increased gonad tumor incidence
MP:0009591	increased liver adenocarcinoma incidence
MP:0009592	increased Leydig cell tumor incidence
MP:0009593	absent chorion
MP:0009594	abnormal corneocyte envelope morphology
MP:0009595	enlarged corneocyte envelope
MP:0009596	abnormal stratum corneum lipid matrix formation
MP:0009597	impaired stratum corneum desquamation
MP:0009598	thin epidermis stratum granulosum
MP:0009599	thick epidermis stratum granulosum
MP:0009600	hypergranulosis
MP:0009601	epidermis stratum granulosum hyperplasia
MP:0009602	abnormal keratohyalin granule morphology
MP:0009603	absent keratohyalin granules
MP:0009604	increased keratohyalin granule number
MP:0009605	decreased keratohyalin granule number
MP:0009606	increased keratohyalin granule size
MP:0009607	decreased keratohyalin granule size
MP:0009608	abnormal epidermal lamellar body morphology
MP:0009611	epidermis stratum spinosum hyperplasia
MP:0009612	thick epidermis suprabasal layer
MP:0009613	thin epidermis suprabasal layer
MP:0009614	absent epidermis stratum spinosum
MP:0009617	decreased brain zinc level
MP:0009619	abnormal optokinetic reflex
MP:0009621	primary vitreous hyperplasia
MP:0009622	absent inguinal lymph nodes
MP:0009623	enlarged inguinal lymph nodes
MP:0009624	small inguinal lymph nodes
MP:0009625	abnormal abdominal lymph node morphology
MP:0009626	abnormal celiac lymph node morphology
MP:0009628	absent brachial lymph nodes
MP:0009629	small brachial lymph nodes
MP:0009630	absent axillary lymph nodes
MP:0009631	enlarged axillary lymph nodes
MP:0009632	small axillary lymph nodes
MP:0009633	absent cervical lymph nodes
MP:0009634	absent popliteal lymph nodes
MP:0009635	enlarged popliteal lymph nodes
MP:0009636	small popliteal lymph nodes
MP:0009637	abnormal pretectal region morphology
MP:0009639	abnormal olivary pretectal nucleus morphology
MP:0009640	abnormal renal tubule epithelium morphology
MP:0009641	kidney degeneration
MP:0009642	abnormal blood homeostasis
MP:0009645	crystalluria
MP:0009647	decreased fertilization frequency
MP:0009648	abnormal superovulation
MP:0009649	delayed embryo implantation
MP:0009651	abnormal eyelid development
MP:0009652	abnormal palatal rugae morphology
MP:0009653	abnormal palate development
MP:0009654	abnormal primary palate development
MP:0009655	abnormal secondary palate development
MP:0009656	delayed chorioallantoic fusion
MP:0009657	failure of chorioallantoic fusion
MP:0009658	increased placenta apoptosis
MP:0009659	striated fur
MP:0009660	abnormal induced retinal neovascularization
MP:0009661	abnormal pregnancy
MP:0009662	abnormal uterine receptivity
MP:0009663	abnormal uterine-embryonic axis
MP:0009664	abnormal luminal closure
MP:0009665	abnormal embryo apposition
MP:0009666	abnormal embryo attachment
MP:0009669	abnormal postimplantation uterine environment
MP:0009671	abnormal uterus physiology
MP:0009673	increased birth weight
MP:0009674	decreased birth weight
MP:0009676	abnormal hemostasis
MP:0009677	abnormal spinal cord dorsal column morphology
MP:0009678	abnormal spinal cord lateral column morphology
MP:0009681	abnormal pyramidal decussation morphology
MP:0009682	abnormal anterior corticospinal tract morphology
MP:0009683	abnormal lateral corticospinal tract morphology
MP:0009684	abnormal spinal cord lateral motor column morphology
MP:0009685	abnormal spinal cord motor column morphology
MP:0009686	abnormal spinal cord medial motor column morphology
MP:0009687	empty decidua capsularis
MP:0009688	abnormal spinal cord central canal morphology
MP:0009689	abnormal neural tube ventricular layer morphology
MP:0009690	abnormal neural tube mantle layer morphology
MP:0009691	abnormal neural tube marginal layer morphology
MP:0009694	abnormal spinal cord commissure morphology
MP:0009695	abnormal spinal cord ventral commissure morphology
MP:0009697	abnormal copulation
MP:0009698	heart hemorrhage
MP:0009702	increased birth body size
MP:0009703	decreased birth body size
MP:0009705	abnormal midgut morphology
MP:0009706	absent midgut
MP:0009708	vaginal septum
MP:0009709	hydrometra
MP:0009711	abnormal conditioned place preference behavior
MP:0009712	impaired conditioned place preference behavior
MP:0009713	enhanced conditioned place preference behavior
MP:0009714	thin epidermis stratum basale
MP:0009715	thick epidermis stratum basale
MP:0009716	abnormal subcommissural organ morphology
MP:0009717	absent subcommissural organ
MP:0009718	absent Purkinje cell layer
MP:0009719	reduced cerebellar foliation
MP:0009720	abnormal mammary gland pattern
MP:0009721	increased mammary gland number
MP:0009722	abnormal nipple development
MP:0009724	ectopic nipples
MP:0009725	absent lens vesicle
MP:0009727	abnormal navicular morphology
MP:0009729	absent tarsus bones
MP:0009734	abnormal prostate gland duct morphology
MP:0009735	abnormal prostate gland development
MP:0009736	abnormal prostate gland branching morphogenesis
MP:0009737	prostate gland cysts
MP:0009738	enlarged prostate gland anterior lobe
MP:0009740	small prostate gland dorsolateral lobe
MP:0009741	ectopic mammary gland
MP:0009742	increased corneal stroma thickness
MP:0009745	abnormal behavioral response to xenobiotic
MP:0009746	enhanced behavioral response to xenobiotic
MP:0009747	impaired behavioral response to xenobiotic
MP:0009748	abnormal behavioral response to addictive substance
MP:0009749	enhanced behavioral response to addictive substance
MP:0009750	impaired behavioral response to addictive substance
MP:0009751	enhanced behavioral response to alcohol
MP:0009752	enhanced behavioral response to nicotine
MP:0009753	enhanced behavioral response to morphine
MP:0009754	enhanced behavioral response to cocaine
MP:0009755	impaired behavioral response to alcohol
MP:0009756	impaired behavioral response to nicotine
MP:0009757	impaired behavioral response to morphine
MP:0009758	impaired behavioral response to cocaine
MP:0009759	abnormal hair follicle bulge morphology
MP:0009760	abnormal mitotic spindle morphology
MP:0009761	abnormal meiotic spindle morphology
MP:0009762	abnormal mitotic spindle assembly checkpoint
MP:0009763	increased sensitivity to induced morbidity/mortality
MP:0009764	decreased sensitivity to induced morbidity/mortality
MP:0009765	abnormal xenobiotic induced morbidity/mortality
MP:0009766	increased sensitivity to xenobiotic induced morbidity/mortality
MP:0009767	decreased sensitivity to xenobiotic induced morbidity/mortality
MP:0009768	impaired somite development
MP:0009769	abnormal meiotic spindle assembly checkpoint
MP:0009770	abnormal optic chiasm morphology
MP:0009771	absent optic chiasm
MP:0009772	abnormal retinal development
MP:0009775	increased behavioral withdrawal response
MP:0009776	decreased behavioral withdrawal response
MP:0009777	abnormal behavioral response to anesthetic
MP:0009778	impaired behavioral response to anesthetic
MP:0009779	enhanced behavioral response to anesthetic
MP:0009780	abnormal chondrocyte physiology
MP:0009781	abnormal preimplantation embryo development
MP:0009782	abnormal basicranium angle
MP:0009783	abnormal melanoblast morphology
MP:0009784	abnormal melanoblast migration
MP:0009786	decreased susceptibility to infection induced morbidity/mortality
MP:0009787	increased susceptibility to infection induced morbidity/mortality
MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality
MP:0009789	decreased susceptibility to bacterial infection induced morbidity/mortality
MP:0009790	decreased susceptibility to viral infection induced morbidity/mortality
MP:0009791	increased susceptibility to viral infection induced morbidity/mortality
MP:0009793	sebaceous gland hypertrophy
MP:0009794	sebaceous gland hyperplasia
MP:0009795	epidermal spongiosis
MP:0009796	abnormal base-excision repair
MP:0009797	abnormal mismatch repair
MP:0009798	abnormal ophthalmic nerve morphology
MP:0009799	abnormal maxillary nerve morphology
MP:0009800	abnormal mandibular nerve morphology
MP:0009801	abnormal hair cortex keratinization
MP:0009804	abnormal interventricular foramen morphology
MP:0009806	abnormal otic vesicle morphology
MP:0009808	decreased oligodendrocyte number
MP:0009811	abnormal prostaglandin level
MP:0009812	abnormal bradykinin level
MP:0009813	abnormal leukotriene level
MP:0009814	increased prostaglandin level
MP:0009815	decreased prostaglandin level
MP:0009816	increased leukotriene level
MP:0009817	decreased leukotriene level
MP:0009818	abnormal thromboxane level
MP:0009820	abnormal liver vasculature morphology
MP:0009821	abnormal vestibular aqueduct morphology
MP:0009822	abnormal subarcuate fossa morphology
MP:0009823	abnormal sphingomyelin level
MP:0009824	spermatic granuloma
MP:0009826	abnormal dermis reticular layer collagen network
MP:0009827	skin detachment
MP:0009828	increased tumor latency
MP:0009829	enlarged eye anterior chamber
MP:0009830	abnormal sperm connecting piece morphology
MP:0009831	abnormal sperm midpiece morphology
MP:0009832	abnormal sperm mitochondrial sheath morphology
MP:0009833	absent sperm mitochondrial sheath
MP:0009834	abnormal sperm annulus morphology
MP:0009835	absent sperm annulus
MP:0009836	abnormal sperm principal piece morphology
MP:0009837	abnormal sperm end piece morphology
MP:0009838	abnormal sperm axoneme morphology
MP:0009839	multiflagellated sperm
MP:0009840	abnormal foam cell morphology
MP:0009841	foam cell reticulosis
MP:0009843	decreased neural crest cell number
MP:0009844	abnormal neural crest cell apoptosis
MP:0009845	abnormal neural crest cell morphology
MP:0009846	abnormal neural crest morphology
MP:0009848	increased horizontal stereotypic behavior
MP:0009849	increased vertical stereotypic behavior
MP:0009850	embryonic lethality between implantation and placentation
MP:0009851	abnormal Sertoli cell phagocytosis
MP:0009852	increased Sertoli cell phagocytosis
MP:0009853	decreased Sertoli cell phagocytosis
MP:0009856	failure of ejaculation
MP:0009857	absent kidney cortex
MP:0009858	abnormal cellular extravasation
MP:0009859	eye opacity
MP:0009861	abnormal pyloric sphincter morphology
MP:0009862	abnormal aorta elastic tissue morphology
MP:0009864	abnormal aorta endothelium morphology
MP:0009865	abnormal aorta smooth muscle morphology
MP:0009866	abnormal aorta wall morphology
MP:0009867	abnormal ascending aorta morphology
MP:0009868	abnormal descending thoracic aorta morphology
MP:0009869	abnormal descending aorta morphology
MP:0009870	abnormal abdominal aorta morphology
MP:0009871	abnormal aorta tunica adventitia morphology
MP:0009873	abnormal aorta tunica media morphology
MP:0009874	abnormal interdigital cell death
MP:0009875	absent interdigital cell death
MP:0009878	decreased susceptibility to bone fracture
MP:0009879	abnormal arcus anterior morphology
MP:0009882	absent palatal shelf
MP:0009883	palatal shelf hypoplasia
MP:0009884	palatal shelf fusion with tongue or mandible
MP:0009885	abnormal palatal shelf elevation
MP:0009886	failure of palatal shelf elevation
MP:0009887	abnormal palatal shelf fusion at midline
MP:0009888	palatal shelves fail to meet at midline
MP:0009889	persistence of medial edge epithelium during palatal shelf fusion
MP:0009891	abnormal palate bone morphology
MP:0009892	palate bone hypoplasia
MP:0009894	absent hard palate
MP:0009895	decreased palatine bone horizontal plate size
MP:0009896	palatine bone horizontal plate hypoplasia
MP:0009897	decreased maxillary shelf size
MP:0009898	maxillary shelf hypoplasia
MP:0009899	hyoid bone hypoplasia
MP:0009900	vomer bone hypoplasia
MP:0009901	abnormal frontonasal prominence morphology
MP:0009902	abnormal lateral nasal prominence morphology
MP:0009903	abnormal medial nasal prominence morphology
MP:0009904	tongue hypoplasia
MP:0009905	absent tongue
MP:0009910	bifurcated tongue
MP:0009911	increased hyoid bone size
MP:0009912	decreased hyoid bone size
MP:0009913	abnormal hyoid bone greater horn morphology
MP:0009914	abnormal hyoid bone lesser horn morphology
MP:0009915	absent hyoid bone lesser horns
MP:0009916	absent hyoid bone greater horns
MP:0009917	abnormal hyoid bone body morphology
MP:0009918	abnormal stylohyoid ligament morphology
MP:0009921	abnormal transitional stage T3 B cell morphology
MP:0009922	increased transitional stage T1 B cell number
MP:0009923	decreased transitional stage T1 B cell number
MP:0009925	increased transitional stage T2 B cell number
MP:0009926	decreased transitional stage T2 B cell number
MP:0009928	abnormal pinna hair pigmentation
MP:0009929	meningomyelocele
MP:0009930	fuzzy hair
MP:0009931	abnormal skin appearance
MP:0009932	skin fibrosis
MP:0009933	abnormal tail hair pigmentation
MP:0009934	abnormal hind foot hair pigmentation
MP:0009935	abnormal Meibomian gland acinus morphology
MP:0009936	abnormal dendritic spine morphology
MP:0009937	abnormal neuron differentiation
MP:0009938	abnormal hippocampus granule cell morphology
MP:0009939	abnormal hippocampus neuron morphology
MP:0009940	abnormal hippocampus pyramidal cell morphology
MP:0009941	abnormal olfactory bulb interneuron morphology
MP:0009942	abnormal olfactory bulb granule cell morphology
MP:0009943	abnormal olfactory bulb periglomerular cell morphology
MP:0009945	abnormal accessory olfactory bulb morphology
MP:0009946	abnormal olfactory bulb layer morphology
MP:0009947	abnormal olfactory bulb external plexiform layer morphology
MP:0009948	abnormal olfactory bulb glomerular layer morphology
MP:0009949	abnormal olfactory bulb granule cell layer morphology
MP:0009950	abnormal olfactory bulb internal plexiform layer morphology
MP:0009951	abnormal olfactory bulb mitral cell layer morphology
MP:0009952	abnormal olfactory bulb subventricular zone morphology
MP:0009954	abnormal mitral cell morphology
MP:0009955	abnormal olfactory bulb tufted cell morphology
MP:0009956	abnormal cerebellar layer morphology
MP:0009957	abnormal cerebellum vermis lobule morphology
MP:0009958	absent cerebellar granule cells
MP:0009959	abnormal cerebellar hemisphere morphology
MP:0009960	abnormal cerebellum anterior lobe morphology
MP:0009963	abnormal cerebellum hemisphere lobule morphology
MP:0009964	abnormal cerebellum lobule morphology
MP:0009965	abnormal cerebellum lateral hemisphere morphology
MP:0009967	abnormal neuron proliferation
MP:0009968	abnormal cerebellar granule cell precursor proliferation
MP:0009969	abnormal cerebral cortex pyramidal cell morphology
MP:0009970	increased hippocampus pyramidal cell number
MP:0009971	decreased hippocampus pyramidal cell number
MP:0009972	absent hippocampus pyramidal cells
MP:0009974	decreased cerebral cortex pyramidal cell number
MP:0009975	absent cerebral cortex pyramidal cells
MP:0009976	abnormal cerebellar peduncle morphology
MP:0009977	abnormal cerebellar granule cell migration
MP:0009978	abnormal cerebellum white matter morphology
MP:0009979	abnormal cerebellum deep nucleus morphology
MP:0009980	abnormal cerebellum dentate nucleus morphology
MP:0009983	abnormal cerebellum fastigial nucleus morphology
MP:0009988	abnormal cerebellum vermis lobule I morphology
MP:0009989	abnormal cerebellum vermis lobule II morphology
MP:0009990	abnormal cerebellum vermis lobule III morphology
MP:0009991	abnormal cerebellum vermis lobule IV morphology
MP:0009992	abnormal cerebellum vermis lobule IX morphology
MP:0009993	abnormal cerebellum vermis lobule V morphology
MP:0009994	abnormal cerebellum vermis lobule VI morphology
MP:0009995	abnormal cerebellum vermis lobule VII morphology
MP:0009997	abnormal cerebellum vermis lobule X morphology
MP:0010008	abnormal Purkinje cell migration
MP:0010009	abnormal piriform cortex morphology
MP:0010011	ectopic hippocampus pyramidal cells
MP:0010012	ectopic cerebral cortex pyramidal cells
MP:0010013	cerebral cortex pyramidal cell degeneration
MP:0010014	hippocampus pyramidal cell degeneration
MP:0010015	abnormal cuticular plate morphology
MP:0010017	visceral vascular congestion
MP:0010018	pulmonary vascular congestion
MP:0010019	liver vascular congestion
MP:0010020	spleen vascular congestion
MP:0010021	heart vascular congestion
MP:0010022	brain vascular congestion
MP:0010024	increased total body fat amount
MP:0010026	decreased liver cholesterol level
MP:0010027	increased liver cholesterol level
MP:0010029	abnormal basicranium morphology
MP:0010035	increased erythrocyte clearance
MP:0010037	ectopic melanocytes
MP:0010038	abnormal placenta physiology
MP:0010039	abnormal trophoblast giant cell proliferation
MP:0010040	abnormal oval cell morphology
MP:0010041	absent oval cells
MP:0010042	abnormal oval cell physiology
MP:0010043	abnormal frontonasal suture morphology
MP:0010045	increased omental fat pad weight
MP:0010046	decreased omental fat pad weight
MP:0010047	axonal spheroids
MP:0010048	abnormal primitive streak regression
MP:0010050	hypermyelination
MP:0010052	increased grip strength
MP:0010053	decreased grip strength
MP:0010055	abnormal sensory neuron physiology
MP:0010056	ectopic skeletal muscle
MP:0010057	abnormal olfactory bulb outer nerve layer morphology
MP:0010060	abnormal creatine level
MP:0010061	increased creatine level
MP:0010062	decreased creatine level
MP:0010064	increased circulating creatine level
MP:0010065	decreased circulating creatine level
MP:0010067	increased red blood cell distribution width
MP:0010068	decreased red blood cell distribution width
MP:0010069	increased serotonin level
MP:0010070	decreased serotonin level
MP:0010072	increased pruritus
MP:0010073	decreased pruritus
MP:0010075	abnormal circulating phytosterol level
MP:0010078	increased circulating phytosterol level
MP:0010080	abnormal hepatocyte physiology
MP:0010081	posterior microphthalmia
MP:0010082	sternebra fusion
MP:0010084	abnormal long lived plasma cell morphology
MP:0010087	increased circulating fructosamine level
MP:0010088	decreased circulating fructosamine level
MP:0010091	decreased circulating creatine kinase level
MP:0010095	increased chromosomal stability
MP:0010096	abnormal incisor color
MP:0010097	abnormal retinal blood vessel morphology
MP:0010098	abnormal retinal blood vessel pattern
MP:0010099	abnormal thoracic cage shape
MP:0010100	increased cervical vertebrae number
MP:0010101	increased sacral vertebrae number
MP:0010102	increased caudal vertebrae number
MP:0010103	small thoracic cage
MP:0010105	abnormal sublingual ganglion morphology
MP:0010106	abnormal circulating pyruvate kinase level
MP:0010107	abnormal renal reabsorbtion
MP:0010108	abnormal renal water reabsorbtion
MP:0010109	abnormal renal sodium reabsorbtion
MP:0010110	abnormal renal phosphate reabsorbtion
MP:0010111	abnormal renal calcium reabsorbtion
MP:0010113	abnormal sacrum morphology
MP:0010114	abnormal coccyx morphology
MP:0010115	abnormal embryonic cloaca morphology
MP:0010116	abnormal primitive urogenital sinus morphology
MP:0010117	abnormal lateral plate mesoderm morphology
MP:0010118	abnormal intermediate mesoderm
MP:0010122	abnormal bone mineral content
MP:0010123	increased bone mineral content
MP:0010124	decreased bone mineral content
MP:0010126	abnormal distal visceral endoderm morphology
MP:0010129	increased DN1 thymic pro-T cell number
MP:0010130	decreased DN1 thymic pro-T cell number
MP:0010131	increased DN2 thymocyte number
MP:0010132	decreased DN2 thymocyte number
MP:0010133	increased DN3 thymocyte number
MP:0010134	decreased DN3 thymocyte number
MP:0010135	increased DN4 thymocyte number
MP:0010136	decreased DN4 thymocyte number
MP:0010137	delayed exit from anagen phase
MP:0010139	aortitis
MP:0010140	phlebitis
MP:0010143	enhanced fertility
MP:0010144	abnormal tumor vascularization
MP:0010149	abnormal synaptic dopamine release
MP:0010150	abnormal mandibule ramus morphology
MP:0010151	abnormal spinal cord ependymal layer morphology
MP:0010152	abnormal brain ependyma morphology
MP:0010154	abnormal gastroesophageal sphincter physiology
MP:0010155	abnormal intestine physiology
MP:0010156	abnormal small intestinal crypt cell physiology
MP:0010157	abnormal small intestinal crypt cell proliferation
MP:0010158	abnormal intestine development
MP:0010159	abnormal enterocyte differentiation
MP:0010160	increased oligodendrocyte number
MP:0010161	decreased brain cholesterol level
MP:0010162	increased brain cholesterol level
MP:0010163	hemolysis
MP:0010166	increased response to stress-induced hyperthermia
MP:0010167	decreased response to stress-induced hyperthermia
MP:0010168	increased CD4-positive, CD25-positive, alpha-beta regulatory T cell number
MP:0010169	decreased CD4-positive, CD25-positive, alpha-beta regulatory T cell number
MP:0010170	abnormal glial cell apoptosis
MP:0010171	abnormal centroacinar cell of Langerhans morphology
MP:0010172	abnormal mammary gland epithelium physiology
MP:0010173	increased mammary gland epithelial cell proliferation
MP:0010174	decreased mammary gland epithelial cell proliferation
MP:0010175	leptocytosis
MP:0010176	dacryocytosis
MP:0010178	increased number of Howell-Jolly bodies
MP:0010179	rough coat
MP:0010180	increased susceptibility to weight loss
MP:0010181	decreased susceptibility to weight loss
MP:0010182	decreased susceptibility to weight gain
MP:0010183	abnormal CD4-positive helper T cell morphology
MP:0010186	increased T follicular helper cell number
MP:0010187	decreased T follicular helper cell number
MP:0010188	abnormal T follicular helper cell differentiation
MP:0010189	abnormal T follicular helper cell physiology
MP:0010191	abnormal choroid melanocyte morphology
MP:0010192	abnormal retinal melanin granule morphology
MP:0010193	abnormal choroid melanin granule morphology
MP:0010195	abnormal lymphatic vessel endothelium morphology
MP:0010196	abnormal lymphatic vessel smooth muscle morphology
MP:0010197	abnormal lymphatic vessel endothelial cell morphology
MP:0010198	decreased lymphatic vessel endothelial cell number
MP:0010200	enlarged lymphatic vessel
MP:0010202	focal dorsal hair loss
MP:0010203	focal ventral hair loss
MP:0010205	abnormal oligodendrocyte apoptosis
MP:0010207	abnormal telomere morphology
MP:0010209	abnormal circulating chemokine level
MP:0010210	abnormal circulating cytokine level
MP:0010211	abnormal acute phase protein level
MP:0010212	abnormal circulating C-reactive protein level
MP:0010213	abnormal circulating fibrinogen level
MP:0010214	abnormal circulating serum amyloid protein level
MP:0010215	abnormal circulating complement protein level
MP:0010219	increased T-helper 17 cell number
MP:0010220	decreased T-helper 17 cell number
MP:0010221	abnormal T-helper 17 cell differentiation
MP:0010222	abnormal T-helper 17 cell physiology
MP:0010223	abnormal immunoglobulin transcytosis
MP:0010224	abnormal heart ventricle outflow tract morphology
MP:0010225	abnormal quadriceps morphology
MP:0010226	increased quadriceps weight
MP:0010227	decreased quadriceps weight
MP:0010228	decreased transitional stage T3 B cell number
MP:0010229	increased transitional stage T3 B cell number
MP:0010231	transverse fur striping
MP:0010232	delayed skin pigmentation appearance
MP:0010233	hairless tail
MP:0010234	abnormal vibrissa follicle morphology
MP:0010235	abnormal retina inner limiting membrane morphology
MP:0010236	abnormal retina outer limiting membrane morphology
MP:0010238	increased skeletal muscle weight
MP:0010239	decreased skeletal muscle weight
MP:0010240	decreased skeletal muscle size
MP:0010241	abnormal aortic arch development
MP:0010243	increased kidney copper level
MP:0010244	decreased kidney copper level
MP:0010247	increased intestine copper level
MP:0010248	decreased intestine copper level
MP:0010249	lactation failure
MP:0010250	absent thymus cortex
MP:0010264	increased hepatoma incidence
MP:0010265	decreased hepatoma incidence
MP:0010266	decreased liver tumor incidence
MP:0010267	decreased lung tumor incidence
MP:0010268	decreased lymphoma incidence
MP:0010269	decreased mammary gland tumor incidence
MP:0010274	increased organ/body region tumor incidence
MP:0010276	increased intraocular melanoma incidence
MP:0010277	increased astrocytoma incidence
MP:0010279	increased gastrointestinal tumor incidence
MP:0010280	increased skeletal tumor incidence
MP:0010282	decreased organ/body region tumor incidence
MP:0010286	increased plasmacytoma incidence
MP:0010287	increased reproductive system tumor incidence
MP:0010288	increased gland tumor incidence
MP:0010289	increased urinary system tumor incidence
MP:0010291	increased cardiovascular system tumor incidence
MP:0010292	increased alimentary system tumor incidence
MP:0010294	increased kidney tumor incidence
MP:0010296	increased hemolymphoid system tumor incidence
MP:0010297	increased hepatobiliary system tumor incidence
MP:0010299	increased mammary gland tumor incidence
MP:0010300	increased skin tumor incidence
MP:0010301	increased stomach tumor incidence
MP:0010303	increased retina tumor incidence
MP:0010304	increased choroid tumor incidence
MP:0010305	increased iris tumor incidence
MP:0010306	increased hamartoma incidence
MP:0010307	abnormal tumor latency
MP:0010308	decreased tumor latency
MP:0010309	increased mesothelioma incidence
MP:0010310	increased Schwannoma incidence
MP:0010315	increased cholangiocarcinoma incidence
MP:0010316	increased thyroid tumor incidence
MP:0010318	increased salivary gland tumor incidence
MP:0010319	increased submandibular gland tumor incidence
MP:0010320	increased pituitary gland tumor incidence
MP:0010321	increased parathyroid gland tumor incidence
MP:0010322	increased cutaneous melanoma incidence
MP:0010323	retropulsion
MP:0010324	abnormal malleus processus brevis morphology
MP:0010325	abnormal malleus head morphology
MP:0010326	malleus hypoplasia
MP:0010328	thin malleus neck
MP:0010329	abnormal lipoprotein level
MP:0010330	abnormal circulating lipoprotein level
MP:0010331	abnormal apolipoprotein level
MP:0010332	abnormal circulating apolipoprotein level
MP:0010333	abnormal circulating apolipoprotein E level
MP:0010335	fused first pharyngeal arch
MP:0010336	increased acute lymphoblastic leukemia incidence
MP:0010337	increased chronic lymphocytic leukemia incidence
MP:0010344	increased hibernoma incidence
MP:0010345	increased thyroid C-cell carcinoma incidence
MP:0010346	increased thyroid carcinoma incidence
MP:0010347	osseous metaplasia
MP:0010348	increased pancreatic islet cell carcinoma incidence
MP:0010350	increased pituitary adenohypophysis tumor incidence
MP:0010351	increased pituitary melanotroph tumor incidence
MP:0010352	gastrointestinal tract polyps
MP:0010354	increased odontosarcoma incidence
MP:0010355	abnormal first pharyngeal arch artery morphology
MP:0010356	abnormal second pharyngeal arch artery morphology
MP:0010357	increased prostate gland tumor incidence
MP:0010358	abnormal free fatty acids level
MP:0010359	increased liver free fatty acids level
MP:0010360	decreased liver free fatty acids level
MP:0010361	increased gangliosarcoma incidence
MP:0010362	increased ganglioneuroma incidence
MP:0010364	increased fibroadenoma incidence
MP:0010365	increased thymus tumor incidence
MP:0010366	increased adrenal cortical tumor incidence
MP:0010367	increased spindle cell carcinoma incidence
MP:0010368	abnormal lymphatic system physiology
MP:0010369	abnormal thalamus neuron morphology
MP:0010371	abnormal epiglottis morphology
MP:0010373	myeloid hyperplasia
MP:0010375	increased kidney iron level
MP:0010376	decreased kidney iron level
MP:0010377	abnormal gut flora balance
MP:0010378	increased respiratory quotient
MP:0010379	decreased respiratory quotient
MP:0010380	abnormal inner cell mass apoptosis
MP:0010382	abnormal dosage compensation, by inactivation of X chromosome
MP:0010383	increased adenoma incidence
MP:0010384	increased renal carcinoma incidence
MP:0010387	abnormal Bergmann glial cell morphology
MP:0010388	abnormal Bergmann glial cell differentiation
MP:0010389	mosaic coat color
MP:0010390	increased adrenocortical adenoma incidence
MP:0010392	prolonged QRS complex duration
MP:0010393	shortened QRS complex duration
MP:0010394	decreased QRS amplitude
MP:0010395	abnormal pharyngeal arch development
MP:0010396	ectopic pharyngeal arch
MP:0010397	abnormal otic capsule development
MP:0010398	decreased liver glycogen level
MP:0010399	decreased skeletal muscle glycogen level
MP:0010401	increased skeletal muscle glycogen level
MP:0010412	atrioventricular septal defect
MP:0010414	partial atrioventricular septal defect
MP:0010416	interventricular septum membranous part aneurysm
MP:0010423	heart right ventricle aneurysm
MP:0010425	abnormal heart and great vessel attachment
MP:0010426	abnormal heart and great artery attachment
MP:0010428	abnormal heart right ventricle outflow tract morphology
MP:0010429	abnormal heart left ventricle outflow tract morphology
MP:0010435	abnormal heart atrium and ventricle connection
MP:0010436	abnormal coronary sinus morphology
MP:0010437	absent coronary sinus
MP:0010439	abnormal hepatic vein morphology
MP:0010443	total anomalous pulmonary venous connection, intracardiac
MP:0010446	heart left ventricle hypoplasia
MP:0010449	heart right ventricle outflow tract stenosis
MP:0010451	kidney microaneurysm
MP:0010452	retina microaneurysm
MP:0010453	abnormal coronary vein morphology
MP:0010454	abnormal truncus arteriosus septation
MP:0010458	pulmonary trunk hypoplasia
MP:0010459	supravalvar pulmonary trunk stenosis
MP:0010464	abnormal aortic arch and aortic arch branch attachment
MP:0010465	aberrant origin of the right subclavian artery
MP:0010468	abnormal thoracic aorta morphology
MP:0010469	ascending aorta hypoplasia
MP:0010471	supravalvar aortic stenosis
MP:0010472	abnormal ascending aorta and coronary artery attachment
MP:0010473	descending aorta dilation
MP:0010477	coronary artery aneurysm
MP:0010478	intracranial aneurysm
MP:0010479	brain aneurysm
MP:0010482	abnormal aortic sinus morphology
MP:0010486	absent right subclavian artery
MP:0010487	abnormal right subclavian artery morphology
MP:0010488	abnormal left subclavian artery morphology
MP:0010489	abnormal heart atrium auricular region morphology
MP:0010490	abnormal inferior vena cava valve morphology
MP:0010492	abnormal atrium endocardium morphology
MP:0010493	abnormal atrium myocardium morphology
MP:0010496	abnormal pectinate muscle morphology
MP:0010498	abnormal interventricular septum muscular part morphology
MP:0010499	abnormal ventricle myocardium morphology
MP:0010500	myocardium hypoplasia
MP:0010501	atrium myocardium hypoplasia
MP:0010502	ventricle myocardium hypoplasia
MP:0010503	myocardial trabeculae hypoplasia
MP:0010504	abnormal RR interval
MP:0010505	abnormal T wave
MP:0010506	prolonged RR interval
MP:0010507	shortened RR interval
MP:0010509	decreased P wave amplitude
MP:0010510	absent P wave
MP:0010512	absent PR interval
MP:0010514	fragmented QRS complex
MP:0010515	abnormal Q wave
MP:0010526	aortic arch coarctation
MP:0010533	atrioventricular node hypoplasia
MP:0010537	tumor regression
MP:0010539	decreased level of surface class II molecules
MP:0010540	long stride length
MP:0010541	aorta hypoplasia
MP:0010543	aorta tubular hypoplasia
MP:0010544	interrupted aorta
MP:0010545	abnormal heart layer morphology
MP:0010546	abnormal subendocardium layer morphology
MP:0010547	abnormal mesocardium morphology
MP:0010551	abnormal coronary vessel morphology
MP:0010553	prolonged HV interval
MP:0010554	shortened HV interval
MP:0010556	thin ventricle myocardium compact layer
MP:0010558	sinus venosus hypoplasia
MP:0010560	intraventricular block
MP:0010561	absent coronary vessels
MP:0010563	increased heart right ventricle size
MP:0010564	abnormal fetal ductus arteriosus morphology
MP:0010565	absent fetal ductus arteriosus
MP:0010566	abnormal left posterior bundle morphology
MP:0010567	abnormal right bundle morphology
MP:0010568	abnormal bulbus cordis morphology
MP:0010570	prolonged ST segment
MP:0010571	shortened ST segment
MP:0010572	persistent right dorsal aorta
MP:0010576	premature closure of the ductus arteriosus
MP:0010578	abnormal heart left ventricle size
MP:0010579	increased heart left ventricle size
MP:0010580	decreased heart left ventricle size
MP:0010581	abnormal atrium myocardial trabeculae morphology
MP:0010583	abnormal conotruncus morphology
MP:0010584	abnormal conotruncus septation
MP:0010585	abnormal conotruncal ridge morphology
MP:0010586	absent conotruncal ridges
MP:0010587	conotruncal ridge hypoplasia
MP:0010588	conotruncal ridge hyperplasia
MP:0010589	common truncal valve
MP:0010591	enlarged aortic valve
MP:0010592	abnormal atrioventricular septum morphology
MP:0010593	thick aortic valve cusps
MP:0010594	thick aortic valve
MP:0010595	abnormal aortic valve cusp morphology
MP:0010597	absent aortic valve cusps
MP:0010598	abnormal aortic valve anulus morphology
MP:0010600	enlarged pulmonary valve
MP:0010601	thick pulmonary valve
MP:0010602	abnormal pulmonary valve cusp morphology
MP:0010604	absent pulmonary valve cusps
MP:0010605	thick pulmonary valve cusps
MP:0010607	common atrioventricular valve
MP:0010610	patent aortic valve
MP:0010611	patent pulmonary valve
MP:0010613	abnormal mitral valve anulus morphology
MP:0010614	abnormal mitral valve cusp morphology
MP:0010617	thick mitral valve cusps
MP:0010618	enlarged mitral valve
MP:0010620	thick mitral valve
MP:0010621	abnormal tricuspid valve anulus morphology
MP:0010622	abnormal tricuspid valve cusp morphology
MP:0010625	absent tricuspid valve cusps
MP:0010626	thick tricuspid valve cusps
MP:0010627	enlarged tricuspid valve
MP:0010629	thick tricuspid valve
MP:0010630	abnormal cardiac muscle tissue morphology
MP:0010632	cardiac muscle necrosis
MP:0010633	myocardial hypertrophy
MP:0010634	increased QRS amplitude
MP:0010635	aorta pulmonary collateral arteries
MP:0010639	altered tumor pathology
MP:0010640	ventricular myocardium compact layer hypoplasia
MP:0010641	descending aorta stenosis
MP:0010642	absent third pharyngeal arch
MP:0010643	absent fourth pharyngeal arch
MP:0010644	absent sixth pharyngeal arch
MP:0010645	failure of conotruncal ridge closure
MP:0010646	absent pulmonary vein
MP:0010650	abnormal aorticopulmonary septum morphology
MP:0010651	aorticopulmonary septal defect
MP:0010652	absent aorticopulmonary septum
MP:0010653	abnormal Wallerian degeneration
MP:0010654	slow Wallerian degeneration
MP:0010655	absent cardiac jelly
MP:0010656	thick myocardium
MP:0010657	absent pulmonary trunk
MP:0010658	thoracic aorta aneurysm
MP:0010659	abdominal aorta aneurysm
MP:0010661	ascending aorta aneurysm
MP:0010662	abnormal intersomitic artery morphology
MP:0010663	abnormal brachiocephalic trunk morphology
MP:0010664	abnormal vitelline artery morphology
MP:0010666	abnormal vitelline vein morphology
MP:0010667	abnormal umbilical vein morphology
MP:0010668	abnormal hepatic portal vein morphology
MP:0010674	increased activation-induced B cell apoptosis
MP:0010675	decreased activation-induced B cell apoptosis
MP:0010677	decreased activation-induced cell death of T cells
MP:0010680	abnormal skin adnexa physiology
MP:0010681	abnormal hair follicle bulb morphology
MP:0010682	abnormal hair follicle infundibulum morphology
MP:0010683	dilated hair follicle infundibulum
MP:0010684	abnormal hair follicle outer root sheath morphology
MP:0010685	abnormal hair follicle inner root sheath morphology
MP:0010686	abnormal hair follicle matrix region morphology
MP:0010687	absent hair follicle dermal papilla
MP:0010688	hair follicle outer rooth sheath hyperplasia
MP:0010689	thin hair follicle outer rooth sheath
MP:0010690	thick hair follicle outer rooth sheath
MP:0010693	thin hair follicle inner root sheath
MP:0010695	abnormal blood pressure regulation
MP:0010696	increased siderocyte number
MP:0010697	abnormal systemic arterial blood pressure regulation
MP:0010699	dilated hair follicles
MP:0010700	hair follicle comedo
MP:0010701	fusion of atlas and odontoid process
MP:0010702	split cervical atlas
MP:0010703	split cervical axis
MP:0010704	abnormal optic canal morphology
MP:0010705	absent metoptic pillar
MP:0010706	ventral rotation of lens
MP:0010707	decreased ventral retina size
MP:0010709	absent eye anterior chamber
MP:0010710	absent sclera
MP:0010712	absent nasolacrimal duct
MP:0010713	corneal-lenticular stalk
MP:0010716	optic disc coloboma
MP:0010718	choroid coloboma
MP:0010720	absent sublingual duct
MP:0010722	persistent cervical thymus
MP:0010724	thick interventricular septum
MP:0010725	thin interventricular septum
MP:0010728	fusion of atlas and occipital bones
MP:0010729	absent arcus anterior
MP:0010730	absent odontoid process
MP:0010731	absent ventral tubercle of atlas
MP:0010732	abnormal node of Ranvier morphology
MP:0010733	abnormal axon initial segment morphology
MP:0010734	abnormal paranode morphology
MP:0010735	abnormal paranodal axoglial junction morphology
MP:0010736	abnormal extraembryonic ectoderm morphology
MP:0010738	abnormal internode morphology
MP:0010739	abnormal axolemma morphology
MP:0010740	abnormal dendritic cell chemotaxis
MP:0010741	abnormal melanocyte proliferation
MP:0010742	increased Schwann cell number
MP:0010743	delayed suture closure
MP:0010744	abnormal cervical flexure morphology
MP:0010745	abnormal pre-Botzinger complex morphology
MP:0010746	abnormal pre-Botzinger complex physiology
MP:0010747	abnormal enamel organ morphology
MP:0010749	absent visual evoked potential
MP:0010750	increased susceptibility to parasitic infection induced morbidity/mortality
MP:0010751	decreased susceptibility to parasitic infection induced morbidity/mortality
MP:0010752	impaired mucociliary clearance
MP:0010754	abnormal heart left ventricle pressure
MP:0010755	abnormal heart right ventricle pressure
MP:0010758	increased right ventricle systolic pressure
MP:0010759	decreased right ventricle systolic pressure
MP:0010760	abnormal macrophage chemotaxis
MP:0010761	abnormal microglial cell chemotaxis
MP:0010762	abnormal microglial cell activation
MP:0010763	abnormal hematopoietic stem cell physiology
MP:0010767	abnormal female meiosis I arrest
MP:0010769	abnormal survival
MP:0010770	preweaning lethality
MP:0010771	integument phenotype
MP:0010772	abnormal pollex morphology
MP:0010773	supernumerary molars
MP:0010776	abnormal placenta metrial gland morphology
MP:0010778	abnormal stomach fundus morphology
MP:0010779	abnormal stomach muscularis externa morphology
MP:0010780	abnormal stomach smooth muscle circular layer morphology
MP:0010781	pyloric sphincter hypertrophy
MP:0010782	stomach smooth muscle circular layer hypertrophy
MP:0010783	abnormal stomach wall morphology
MP:0010784	abnormal forestomach morphology
MP:0010785	abnormal stomach pyloric region morphology
MP:0010786	stomach fundus hypertrophy
MP:0010787	gastric cysts
MP:0010788	stomach hypoplasia
MP:0010790	abnormal stomach pyloric antrum morphology
MP:0010794	abnormal stomach submucosa morphology
MP:0010797	abnormal pyloric gastric gland morphology
MP:0010798	abnormal stomach cardiac region morphology
MP:0010799	stomach mucosa hyperplasia
MP:0010800	abnormal submucous nerve plexus morphology
MP:0010801	abnormal myenteric nerve plexus morphology
MP:0010802	abnormal intestinal enteroendocrine cell morphology
MP:0010803	abnormal stomach enteroendocrine cell morphology
MP:0010805	abnormal stomach smooth muscle outer longitudinal layer morphology
MP:0010807	abnormal stomach position or orientation
MP:0010808	right-sided stomach
MP:0010809	abnormal Clara cell morphology
MP:0010810	increased type II pneumocyte number
MP:0010811	decreased type II pneumocyte number
MP:0010812	absent type II pneumocytes
MP:0010813	abnormal alveolar lamellar body morphology
MP:0010814	absent alveolar lamellar bodies
MP:0010815	enlarged alveolar lamellar bodies
MP:0010816	decreased type I pneumocyte number
MP:0010817	absent type I pneumocytes
MP:0010818	adhesive atelectasis
MP:0010819	primary atelectasis
MP:0010820	abnormal pleura morphology
MP:0010821	abnormal visceral pleura morphology
MP:0010824	absent right lung accessory lobe
MP:0010825	abnormal lung saccule morphology
MP:0010826	absent lung saccules
MP:0010827	small lung saccule
MP:0010829	increased bronchioalveolar stem cell number
MP:0010831	lethality, incomplete penetrance
MP:0010833	abnormal memory T cell morphology
MP:0010835	increased CD4-positive, alpha-beta memory T cell number
MP:0010836	decreased CD4-positive, alpha-beta memory T cell number
MP:0010838	increased CD8-positive, alpha-beta memory T cell number
MP:0010839	decreased CD8-positive, alpha-beta memory T cell number
MP:0010844	increased effector memory CD4-positive, alpha-beta T cell number
MP:0010845	decreased effector memory CD4-positive, alpha-beta T cell number
MP:0010847	increased central memory CD8 positive, alpha-beta T cell number
MP:0010850	increased effector memory CD8-positive, alpha-beta T cell number
MP:0010851	decreased effector memory CD8-positive, alpha-beta T cell number
MP:0010853	abnormal lung position or orientation
MP:0010855	pulmonary hyperemia
MP:0010856	dilated respiratory conducting tubes
MP:0010857	pulmonary necrosis
MP:0010858	pulmonary epithelial necrosis
MP:0010859	abnormal anterior commissure pars anterior morphology
MP:0010860	abnormal anterior commissure pars posterior morphology
MP:0010861	increased respiratory mucosa goblet cell number
MP:0010862	decreased respiratory mucosa goblet cell number
MP:0010863	absent respiratory mucosa goblet cells
MP:0010864	abnormal enamel knot morphology
MP:0010866	abnormal prenatal body size
MP:0010868	increased bone trabecula number
MP:0010869	decreased bone trabecula number
MP:0010870	absent bone trabeculae
MP:0010872	increased trabecular bone mass
MP:0010873	decreased trabecular bone mass
MP:0010874	abnormal bone volume
MP:0010875	increased bone volume
MP:0010876	decreased bone volume
MP:0010877	abnormal trabecular bone volume
MP:0010878	increased trabecular bone volume
MP:0010879	decreased trabecular bone volume
MP:0010880	small esophagus
MP:0010881	esophagus hypoplasia
MP:0010882	trachea hypoplasia
MP:0010885	absent trachea
MP:0010887	pale lung
MP:0010889	small alveolar lamellar bodies
MP:0010890	decreased alveolar lamellar body number
MP:0010891	increased alveolar lamellar body number
MP:0010892	increased oligodendrocyte progenitor number
MP:0010893	abnormal posterior commissure morphology
MP:0010894	pulmonary alveolar edema
MP:0010895	increased lung compliance
MP:0010896	decreased lung compliance
MP:0010897	abnormal bronchiole epithelium morphology
MP:0010898	abnormal pulmonary alveolus epithelium morphology
MP:0010899	abnormal pulmonary alveolar system morphology
MP:0010900	abnormal pulmonary interalveolar septum morphology
MP:0010901	abnormal pulmonary alveolar parenchyma morphology
MP:0010902	abnormal pulmonary alveolar sac morphology
MP:0010903	abnormal pulmonary alveolus wall morphology
MP:0010904	abnormal alveolar pore morphology
MP:0010905	absent alveolar pores
MP:0010906	abnormal lung bud morphology
MP:0010907	absent lung buds
MP:0010908	dilated pulmonary alveolar ducts
MP:0010909	pulmonary alveolar hemorrhage
MP:0010910	bronchiolar epithelial hyperplasia
MP:0010911	abnormal pulmonary acinus morphology
MP:0010912	herniated liver
MP:0010914	abnormal solitary pulmonary neuroendocrine cell morphology
MP:0010915	increased solitary pulmonary neuroendocrine cell number
MP:0010916	decreased solitary pulmonary neuroendocrine cell number
MP:0010917	absent solitary pulmonary neuroendocrine cells
MP:0010918	abnormal pulmonary neuroendocrine body morphology
MP:0010919	increased number of pulmonary neuroendocrine bodies
MP:0010920	decreased number of pulmonary neuroendocrine bodies
MP:0010921	absent pulmonary neuroendocrine bodies
MP:0010922	alveolitis
MP:0010923	calcified pulmonary alveolus
MP:0010924	abnormal osteoid morphology
MP:0010926	increased osteoid volume
MP:0010927	decreased osteoid volume
MP:0010929	increased osteoid thickness
MP:0010930	decreased osteoid thickness
MP:0010932	increased trabecular bone connectivity density
MP:0010933	decreased trabecular bone connectivity density
MP:0010934	increased subcutaneous adipose tissue amount
MP:0010935	increased airway resistance
MP:0010936	decreased airway resistance
MP:0010937	increased total lung capacity
MP:0010938	decreased total lung capacity
MP:0010939	abnormal mandibular prominence morphology
MP:0010940	abnormal maxillary prominence morphology
MP:0010941	abnormal foramen magnum morphology
MP:0010943	abnormal bronchus epithelium morphology
MP:0010944	respiratory epithelium hypertrophy
MP:0010945	lung epithelium hyperplasia
MP:0010946	hyperpnea
MP:0010947	abnormal single-strand DNA break repair
MP:0010948	abnormal double-strand DNA break repair
MP:0010949	decreased Clara cell number
MP:0010950	abnormal lung hysteresivity
MP:0010951	abnormal lipid oxidation
MP:0010952	abnormal fatty acid beta-oxidation
MP:0010953	abnormal fatty acid oxidation
MP:0010954	abnormal cellular respiration
MP:0010955	abnormal respiratory electron transport chain
MP:0010956	abnormal mitochondrial ATP synthesis coupled electron transport
MP:0010957	abnormal aerobic respiration
MP:0010959	abnormal oxidative phosphorylation
MP:0010961	increased compact bone mass
MP:0010962	decreased compact bone mass
MP:0010963	abnormal compact bone volume
MP:0010964	increased compact bone volume
MP:0010965	decreased compact bone volume
MP:0010967	increased compact bone area
MP:0010968	decreased compact bone area
MP:0010969	absent compact bone
MP:0010970	abnormal compact bone lamellar structure
MP:0010973	increased periosteum thickness
MP:0010975	abnormal lung lobe morphology
MP:0010976	small lung lobe
MP:0010977	fused right lung lobes
MP:0010978	absent ureteric bud
MP:0010979	small ureteric bud
MP:0010980	ectopic ureteric bud
MP:0010981	abnormal branching involved in ureteric bud morphogenesis
MP:0010982	abnormal ureteric bud elongation
MP:0010983	abnormal ureteric bud invasion
MP:0010984	abnormal metanephric mesenchyme morphology
MP:0010985	abnormal kidney mesenchyme morphology
MP:0010986	abnormal mesonephric mesenchyme morphology
MP:0010987	abnormal nephrogenic mesenchyme morphogenesis
MP:0010988	abnormal bronchial cartilage morphology
MP:0010992	increased surfactant secretion
MP:0010993	decreased surfactant secretion
MP:0010994	aerophagia
MP:0010995	abnormal lung alveolus development
MP:0010996	increased aorta wall thickness
MP:0010997	decreased aorta wall thickness
MP:0011000	abnormal allogrooming behavior
MP:0011001	absence of AMPA-mediated synaptic currents
MP:0011002	enhanced AMPA-mediated synaptic currents
MP:0011003	reduced AMPA-mediated synaptic currents
MP:0011004	abnormal epidermal stem cell morphology
MP:0011006	abnormal epidermal stem cell proliferation
MP:0011009	increased circulating glutamate dehydrogenase level
MP:0011011	impaired lung lobe morphogenesis
MP:0011013	bronchiolectasis
MP:0011014	decreased core body temperature
MP:0011015	decreased body surface temperature
MP:0011016	increased core body temperature
MP:0011018	pulmonary hyaline membrane formation
MP:0011019	abnormal adaptive thermogenesis
MP:0011020	abnormal circadian temperature homeostasis
MP:0011021	abnormal circadian regulation of heart rate
MP:0011022	abnormal circadian regulation of systemic arterial blood pressure
MP:0011024	abnormal branching involved in lung morphogenesis
MP:0011025	abnormal branching involved in trachea morphogenesis
MP:0011026	impaired branching involved in trachea morphogenesis
MP:0011028	impaired branching involved in bronchus morphogenesis
MP:0011030	impaired branching involved in preterminal bronchiole morphogenesis
MP:0011031	abnormal branching involved in terminal bronchiole morphogenesis
MP:0011032	impaired branching involved in terminal bronchiole morphogenesis
MP:0011034	impaired branching involved in respiratory bronchiole morphogenesis
MP:0011038	impaired branching involved in alveolar sac morphogenesis
MP:0011039	abnormal vestibuloocular dark reflex
MP:0011040	abnormal vestibuloocular light reflex
MP:0011041	abnormal vertical vestibuloocular reflex
MP:0011042	abnormal horizontal vestibuloocular reflex
MP:0011044	increased lung elastance
MP:0011045	decreased lung elastance
MP:0011047	increased lung tissue damping
MP:0011049	impaired adaptive thermogenesis
MP:0011053	decreased respiratory motile cilia number
MP:0011054	absent respiratory motile cilia
MP:0011056	abnormal brain ependyma motile cilium morphology
MP:0011057	absent brain ependyma motile cilia
MP:0011058	abnormal spinal cord motile cilium morphology
MP:0011059	abnormal ependyma motile cilium morphology
MP:0011060	abnormal kinocilium morphology
MP:0011061	abnormal inner hair cell kinocilium morphology
MP:0011062	abnormal outer hair cell kinocilium morphology
MP:0011063	absent inner hair cell kinocilia
MP:0011064	abnormal vestibular hair cell kinocilium morphology
MP:0011065	abnormal kidney epithelial cell primary cilium morphology
MP:0011066	abnormal renal tubule epithelial cell primary cilium morphology
MP:0011067	abnormal somatostatin level
MP:0011068	abnormal ependyma motile cilium physiology
MP:0011069	abnormal brain ependyma motile cilium physiology
MP:0011071	absent Clara cells
MP:0011072	abnormal macrophage cytokine production
MP:0011073	abnormal macrophage apoptosis
MP:0011075	abnormal macrophage activation involved in immune response
MP:0011076	increased macrophage nitric oxide production
MP:0011077	decreased macrophage nitric oxide production
MP:0011078	increased macrophage cytokine production
MP:0011079	decreased macrophage cytokine production
MP:0011080	increased macrophage apoptosis
MP:0011081	decreased macrophage apoptosis
MP:0011082	abnormal gastrointestinal motility
MP:0011083	lethality at weaning, complete penetrance
MP:0011084	lethality at weaning, incomplete penetrance
MP:0011085	postnatal lethality, complete penetrance
MP:0011086	postnatal lethality, incomplete penetrance
MP:0011087	neonatal lethality, complete penetrance
MP:0011088	neonatal lethality, incomplete penetrance
MP:0011089	perinatal lethality, complete penetrance
MP:0011090	perinatal lethality, incomplete penetrance
MP:0011091	prenatal lethality, complete penetrance
MP:0011092	embryonic lethality, complete penetrance
MP:0011093	embryonic lethality at implantation, complete penetrance
MP:0011094	embryonic lethality before implantation, complete penetrance
MP:0011095	embryonic lethality between implantation and placentation, complete penetrance
MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance
MP:0011097	embryonic lethality between somite formation and embryo turning, complete penetrance
MP:0011098	embryonic lethality during organogenesis, complete penetrance
MP:0011099	lethality throughout fetal growth and development, complete penetrance
MP:0011100	preweaning lethality, complete penetrance
MP:0011101	prenatal lethality, incomplete penetrance
MP:0011102	embryonic lethality, incomplete penetrance
MP:0011103	embryonic lethality at implantation, incomplete penetrance
MP:0011104	embryonic lethality before implantation, incomplete penetrance
MP:0011105	embryonic lethality between implantation and placentation, incomplete penetrance
MP:0011106	embryonic lethality between implantation and somite formation, incomplete penetrance
MP:0011107	embryonic lethality between somite formation and embryo turning, incomplete penetrance
MP:0011108	embryonic lethality during organogenesis, incomplete penetrance
MP:0011109	lethality throughout fetal growth and development, incomplete penetrance
MP:0011110	preweaning lethality, incomplete penetrance
MP:0011111	lethality during fetal growth through weaning, complete penetrance
MP:0011112	lethality during fetal growth through weaning, incomplete penetrance
MP:0011113	abnormal airway basal cell morphology
MP:0011114	abnormal airway basal cell differentiation
MP:0011115	airway basal cell hyperplasia
MP:0011116	absent Reichert's membrane
MP:0011117	abnormal susceptibility to weight gain
MP:0011120	increased primordial ovarian follicle number
MP:0011121	decreased primordial ovarian follicle number
MP:0011122	absent primordial ovarian follicles
MP:0011123	abnormal primary ovarian follicle number
MP:0011124	increased primary ovarian follicle number
MP:0011125	decreased primary ovarian follicle number
MP:0011128	increased secondary ovarian follicle number
MP:0011129	decreased secondary ovarian follicle number
MP:0011131	abnormal lung endothelial cell physiology
MP:0011134	decreased lung endothelial cell migration
MP:0011136	increased lung endothelial cell adhesion
MP:0011137	decreased lung endothelial cell adhesion
MP:0011139	increased lung endothelial cell proliferation
MP:0011140	decreased lung endothelial cell proliferation
MP:0011141	increased lung endothelial cell apoptosis
MP:0011142	abnormal lung-associated mesenchyme development
MP:0011143	thick lung-associated mesenchyme
MP:0011144	thin lung-associated mesenchyme
MP:0011145	abnormal mesenchymal cell differentiation involved in lung development
MP:0011146	abnormal mesenchymal cell proliferation involved in lung development
MP:0011147	increased mesenchymal cell proliferation involved in lung development
MP:0011148	decreased mesenchymal cell proliferation involved in lung development
MP:0011149	abnormal hippocampus stratum lacunosum morphology
MP:0011150	abnormal hippocampus stratum oriens morphology
MP:0011151	abnormal hippocampus stratum radiatum morphology
MP:0011155	absent hippocampus stratum oriens
MP:0011156	abnormal hypodermis fat layer morphology
MP:0011157	abnormal hypodermis muscle layer morphology
MP:0011158	absent hypodermis muscle layer
MP:0011159	abnormal epidermal-dermal junction morphology
MP:0011160	dermal-epidermal separation
MP:0011163	increased wet-to-dry lung weight ratio
MP:0011165	abnormal tooth root development
MP:0011166	absent molar root
MP:0011167	abnormal adipose tissue development
MP:0011168	abnormal fat cell differentiation
MP:0011169	abnormal white fat cell differentation
MP:0011170	abnormal brown fat cell differentiation
MP:0011171	increased number of Heinz bodies
MP:0011172	abnormal otic pit morphology
MP:0011176	abnormal erythroblast morphology
MP:0011177	abnormal erythroblast number
MP:0011178	increased erythroblast number
MP:0011179	decreased erythroblast number
MP:0011180	abnormal hematopoietic cell number
MP:0011181	increased hematopoietic cell number
MP:0011182	decreased hematopoietic cell number
MP:0011183	abnormal primitive endoderm morphology
MP:0011184	absent embryonic epiblast
MP:0011185	absent primitive endoderm
MP:0011186	abnormal visceral endoderm morphology
MP:0011187	abnormal parietal endoderm morphology
MP:0011188	increased erythrocyte protoporphyrin level
MP:0011189	small embryonic epiblast
MP:0011190	thick embryonic epiblast
MP:0011191	increased embryonic epiblast cell apoptosis
MP:0011192	decreased embryonic epiblast cell proliferation
MP:0011193	embryonic epiblast cell degeneration
MP:0011194	abnormal hair follicle physiology
MP:0011195	increased hair follicle apoptosis
MP:0011197	abnormal proamniotic cavity morphology
MP:0011198	absent proamniotic cavity
MP:0011199	abnormal amniotic cavity morphology
MP:0011200	abnormal extraembryonic coelom morphology
MP:0011201	abnormal visceral yolk sac cavity morphology
MP:0011202	abnormal ectoplacental cavity morphology
MP:0011203	abnormal parietal yolk sac morphology
MP:0011204	abnormal visceral yolk sac blood island morphology
MP:0011205	excessive folding of visceral yolk sac
MP:0011206	absent visceral yolk sac
MP:0011207	absent ectoplacental cavity
MP:0011208	small proamniotic cavity
MP:0011209	absent extraembryonic coelom
MP:0011210	abnormal temporomandibular joint morphology
MP:0011215	decreased brain copper level
MP:0011221	decreased intestinal calcium absorption
MP:0011223	dilated lymph node medullary sinus
MP:0011224	abnormal lymph node medullary cord morphology
MP:0011225	lymph node medullary cord hyperplasia
MP:0011226	abnormal thiamin level
MP:0011227	abnormal vitamin B12 level
MP:0011228	abnormal vitamin D level
MP:0011229	abnormal vitamin C level
MP:0011230	abnormal folic acid level
MP:0011231	abnormal vitamin E level
MP:0011232	abnormal vitamin A level
MP:0011234	abnormal retinol level
MP:0011235	abnormal blood oxygen capacity
MP:0011237	decreased blood oxygen capacity
MP:0011238	abnormal inner ear development
MP:0011239	abnormal skin coloration
MP:0011240	abnormal fetal derived definitive erythrocyte morphology
MP:0011241	abnormal fetal derived definitive erythrocyte cell number
MP:0011242	increased fetal derived definitive erythrocyte cell number
MP:0011243	decreased fetal derived definitive erythrocyte cell number
MP:0011246	abnormal fetal liver hematopoietic progenitor cell morphology
MP:0011250	abdominal situs ambiguus
MP:0011251	bronchial situs inversus
MP:0011253	situs inversus with levocardia
MP:0011254	superior-inferior ventricles
MP:0011255	abnormal anterior visceral endoderm cell migration
MP:0011256	abnormal neural fold morphology
MP:0011257	abnormal head fold morphology
MP:0011259	abnormal cephalic neural fold morphology
MP:0011260	abnormal head mesenchyme morphology
MP:0011261	abnormal limb mesenchyme morphology
MP:0011262	abnormal pharyngeal arch mesenchyme morphology
MP:0011263	abnormal spleen mesenchyme morphology
MP:0011264	abnormal cardiac mesenchyme morphology
MP:0011265	abnormal pancreas mesenchyme morphology
MP:0011266	abnormal frontonasal mesenchyme morphology
MP:0011267	abnormal excitatory postsynaptic current amplitude
MP:0011269	increased excitatory postsynaptic current amplitude
MP:0011270	decreased excitatory postsynaptic current amplitude
MP:0011273	prolonged excitatory postsynaptic current decay time
MP:0011274	short excitatory postsynaptic current decay time
MP:0011275	abnormal behavioral response to light
MP:0011276	increased tail pigmentation
MP:0011277	decreased tail pigmentation
MP:0011278	increased ear pigmentation
MP:0011279	decreased ear pigmentation
MP:0011281	abnormal olfactory epithelium cilium morphology
MP:0011282	increased podocyte apoptosis
MP:0011285	increased circulating erythropoietin level
MP:0011287	increased erythropoietin level
MP:0011289	abnormal nephron number
MP:0011291	nephron necrosis
MP:0011292	absent nephron
MP:0011293	dilated nephron
MP:0011294	renal glomerulus hypertrophy
MP:0011295	abnormal tubuloglomerular feedback response
MP:0011296	decreased tubuloglomerular feedback response
MP:0011297	absent tubuloglomerular feedback response
MP:0011298	ureter hypoplasia
MP:0011299	abnormal macula densa morphology
MP:0011300	abnormal juxtaglomerular cell morphology
MP:0011301	juxtaglomerular cell hyperplasia
MP:0011302	abnormal extraglomerular mesangial cell morphology
MP:0011303	absent kidney papilla
MP:0011304	kidney papillary atrophy
MP:0011305	dilated kidney calyx
MP:0011307	kidney medulla cysts
MP:0011309	abnormal kidney arterial blood vessel morphology
MP:0011310	abnormal kidney capillary morphology
MP:0011311	abnormal kidney venous blood vessel morphology
MP:0011312	abnormal kidney afferent arteriole morphology
MP:0011313	abnormal kidney efferent arteriole morphology
MP:0011314	abnormal kidney cortex artery morphology
MP:0011316	abnormal kidney interlobular artery morphology
MP:0011317	abnormal renal artery morphology
MP:0011318	abnormal right renal artery morphology
MP:0011320	abnormal glomerular capillary morphology
MP:0011321	abnormal peritubular capillary morphology
MP:0011323	abnormal renal vein morphology
MP:0011327	abnormal left renal vein morphology
MP:0011331	abnormal papillary duct morphology
MP:0011332	abnormal kidney outer medulla morphology
MP:0011333	abnormal kidney inner medulla morphology
MP:0011334	abnormal nephrogenic zone morphology
MP:0011336	abnormal kidney pelvis urothelium morphology
MP:0011337	abnormal perihilar interstitium morphology
MP:0011338	abnormal mesangial matrix morphology
MP:0011339	abnormal glomerular mesangium morphology
MP:0011341	abnormal loop of Henle descending limb morphology
MP:0011344	abnormal loop of Henle ascending limb thick segment morphology
MP:0011345	truncated loop of Henle
MP:0011347	abnormal kidney medullary ray morphology
MP:0011348	abnormal renal glomerulus basement membrane morphology
MP:0011349	abnormal renal glomerulus basement membrane thickness
MP:0011350	abnormal proximal convoluted tubule brush border morphology
MP:0011351	absent proximal convoluted tubule brush border
MP:0011352	proximal convoluted tubule brush border loss
MP:0011354	absent renal glomerulus
MP:0011359	decreased glomerular capillary number
MP:0011360	kidney cortex hypoplasia
MP:0011363	renal glomerulus atrophy
MP:0011364	abnormal metanephros morphology
MP:0011365	small metanephros
MP:0011366	absent metanephros
MP:0011368	increased kidney apoptosis
MP:0011369	increased renal glomerulus apoptosis
MP:0011371	decreased kidney apoptosis
MP:0011372	decreased renal tubule apoptosis
MP:0011376	abnormal kidney corticomedullary boundary morphology
MP:0011378	abnormal kidney outer medulla inner stripe morphology
MP:0011379	abnormal kidney outer medulla outer stripe morphology
MP:0011382	abnormal kidney lobule morphology
MP:0011383	abnormal kidney capsule morphology
MP:0011384	abnormal progesterone level
MP:0011386	increased metanephric mesenchyme apoptosis
MP:0011387	absent metanephric mesenchyme
MP:0011388	absent heart
MP:0011389	absent optic disc
MP:0011390	abnormal fetal cardiomyocyte physiology
MP:0011392	increased fetal cardiomyocyte apoptosis
MP:0011394	increased fetal cardiomyocyte proliferation
MP:0011395	decreased fetal cardiomyocyte proliferation
MP:0011396	abnormal sleep behavior
MP:0011400	lethality, complete penetrance
MP:0011401	abnormal vascular smooth muscle development
MP:0011402	renal cast
MP:0011404	pyelitis
MP:0011406	abnormal retrotrapezoid nucleus morphology
MP:0011407	absent nephrogenic zone
MP:0011408	renal tubule hypertrophy
MP:0011409	increased renal glomerulus basement membrane thickness
MP:0011411	abnormal gonadal ridge morphology
MP:0011412	gonadal ridge hypoplasia
MP:0011413	colorless urine
MP:0011415	abnormal aldosterone level
MP:0011416	abnormal testis interstitial tissue morphology
MP:0011417	abnormal renal transport
MP:0011418	leukocyturia
MP:0011419	erythrocyturia
MP:0011422	kidney medulla atrophy
MP:0011425	abnormal kidney interstitium morphology
MP:0011426	abnormal ureter smooth muscle morphology
MP:0011427	mesangial cell hyperplasia
MP:0011428	mesangial cell hypoplasia
MP:0011429	absent mesangial cell
MP:0011431	increased urine flow rate
MP:0011432	decreased urine flow rate
MP:0011433	glomerular capillary congestion
MP:0011437	glomerulus hemorrhage
MP:0011438	absent kidney medulla
MP:0011439	abnormal kidney cell proliferation
MP:0011440	increased kidney cell proliferation
MP:0011441	decreased kidney cell proliferation
MP:0011442	abnormal renal sodium ion transport
MP:0011443	abnormal renal water transport
MP:0011445	abnormal renal protein reabsorption
MP:0011447	abnormal renal glucose reabsorption
MP:0011448	decreased dopaminergic neuron number
MP:0011450	ectopic dopaminergic neuron
MP:0011451	increased susceptibility to dopaminergic neuron neurotoxicity
MP:0011452	decreased susceptibility to dopaminergic neuron neurotoxicity
MP:0011453	abnormal glomerular capillary endothelium morphology
MP:0011454	abnormal glomerular endothelium fenestra morphology
MP:0011455	absent glomerular endothelium fenestra
MP:0011457	abnormal metanephric ureteric bud development
MP:0011464	bilirubinuria
MP:0011465	abnormal urine urea nitrogen level
MP:0011466	increased urine urea nitrogen level
MP:0011467	decreased urine urea nitrogen level
MP:0011468	abnormal urine amino acid level
MP:0011470	increased urine creatinine level
MP:0011471	decreased urine creatinine level
MP:0011475	abnormal glycosaminoglycan level
MP:0011476	abnormal urine nucleotide level
MP:0011477	abnormal urine nucleoside level
MP:0011480	impaired ureteric peristalsis
MP:0011483	renal glomerular synechia
MP:0011484	abnormal ureter urothelium morphology
MP:0011485	abnormal urethra urothelium morphology
MP:0011486	ectopic ureter
MP:0011487	abnormal ureteropelvic junction morphology
MP:0011488	abnormal ureterovesical junction morphology
MP:0011489	ureteropelvic junction atresia
MP:0011490	ureteropelvic junction stenosis
MP:0011493	double ureter
MP:0011494	abnormal pigmentation pattern
MP:0011496	abnormal head size
MP:0011498	abnormal glomerular capsule parietal layer morphology
MP:0011499	abnormal glomerular capsule space morphology
MP:0011500	decreased glomerular capsule space
MP:0011501	increased glomerular capsule space
MP:0011502	parietal capsular epithelium metaplasia
MP:0011503	distended jejunum
MP:0011504	abnormal limb long bone morphology
MP:0011506	glomerular crescent
MP:0011507	abnormal kidney thrombosis
MP:0011508	glomerular capillary thrombosis
MP:0011509	dilated glomerular capillary
MP:0011510	biventricular, discordant atrioventricular connection
MP:0011511	biventricular, ambiguous atrioventricular connection
MP:0011512	mesangial cell interposition
MP:0011513	abnormal vertebral artery morphology
MP:0011514	skin hemorrhage
MP:0011518	abnormal cell chemotaxis
MP:0011520	increased placental labyrinth size
MP:0011521	decreased placental labyrinth size
MP:0011522	abnormal placental labyrinth villi morphology
MP:0011523	thin placenta labyrinth
MP:0011524	thick placenta labyrinth
MP:0011525	abnormal placenta intervillous maternal lacunae morphology
MP:0011526	abnormal placenta fetal blood space morphology
MP:0011527	disorganized placental labyrinth
MP:0011528	abnormal placental labyrinth villi branching morphogenesis
MP:0011529	increased placenta intervillous maternal lacunae size
MP:0011530	fused radius and ulna
MP:0011531	abnormal syncytiotrophoblast morphology
MP:0011532	decreased urine major urinary protein level
MP:0011533	increased urine major urinary protein level
MP:0011534	granular kidney
MP:0011540	increased urine aldosterone level
MP:0011541	decreased urine aldosterone level
MP:0011543	increased urine antidiuretic hormone level
MP:0011546	increased urine progesterone level
MP:0011549	increased urine corticosterone level
MP:0011550	decreased urine corticosterone level
MP:0011551	variegated eye pigmentation pattern
MP:0011553	increased urine deoxycorticosterone level
MP:0011555	increased urine microglobulin level
MP:0011556	increased urine beta2-microglobulin level
MP:0011557	increased susceptibility to induced choroid neovascularization
MP:0011559	increased urine insulin level
MP:0011561	renal glomerulus lipidosis
MP:0011564	decreased urine prostaglandin level
MP:0011565	kidney papillary hypoplasia
MP:0011566	abnormal complement protein level
MP:0011567	increased renal glomerulus lobularity
MP:0011568	decreased foot pigmentation
MP:0011569	abnormal azygos vein morphology
MP:0011570	esophageal achalasia
MP:0011572	abnormal aorta bulb morphology
MP:0011578	increased lipoprotein lipase activity
MP:0011579	decreased lipoprotein lipase activity
MP:0011581	increased triglyceride lipase activity
MP:0011582	decreased triglyceride lipase activity
MP:0011584	increased alkaline phosphatase activity
MP:0011585	decreased alkaline phosphatase activity
MP:0011588	decreased ornithine carbamoyltransferase activity
MP:0011590	increased hormone-sensitive lipase activity
MP:0011591	decreased hormone-sensitive lipase activity
MP:0011592	abnormal catalase activity
MP:0011593	increased catalase activity
MP:0011597	decreased purine-nucleoside phosphorylase activity
MP:0011602	increased glutathione peroxidase activity
MP:0011603	decreased glutathione peroxidase activity
MP:0011606	decreased glucokinase activity
MP:0011609	decreased glyceraldehyde-3-phosphate dehydrogenase (NAD+) (phosphorylating) activity
MP:0011610	abnormal primordial germ cell apoptosis
MP:0011611	abnormal circulating ghrelin level
MP:0011612	increased circulating ghrelin level
MP:0011613	decreased circulating ghrelin level
MP:0011614	slow aging
MP:0011615	submucous cleft palate
MP:0011617	abnormal habituation
MP:0011619	abnormal dishabituation
MP:0011620	abnormal habituation to a new environment
MP:0011621	abnormal habituation to a novel object
MP:0011622	abnormal habituation to a novel odor
MP:0011624	abnormal sensitization to xenobiotic
MP:0011625	cystolithiasis
MP:0011626	orotic acid urinary bladder stones
MP:0011627	decreased skin pigmentation
MP:0011630	increased mitochondria size
MP:0011631	decreased mitochondria size
MP:0011632	dilated mitochondria
MP:0011634	abnormal mitochondrial inner membrane morphology
MP:0011635	abnormal mitochondrial crista morphology
MP:0011636	disorganized mitochondrial cristae
MP:0011637	abnormal mitochondrial matrix morphology
MP:0011638	abnormal mitochondrial chromosome morphology
MP:0011639	decreased mitochondrial DNA content
MP:0011640	abnormal aorta collagen fibril morphology
MP:0011641	abnormal pulmonary collagen fibril morphology
MP:0011643	abnormal tendon collagen fibril morphology
MP:0011644	abnormal oviduct epithelium motile cilium morphology
MP:0011645	absent oviduct epithelium motile cilium
MP:0011648	thick heart valve cusps
MP:0011649	immotile respiratory cilia
MP:0011650	abnormal corneal stroma collagen fibril morphology
MP:0011655	abnormal systemic artery morphology
MP:0011661	persistent truncus arteriosus type i
MP:0011662	persistent truncus arteriosus type ii
MP:0011664	persistent truncus arteriosus type iv
MP:0011665	d-loop transposition of the great arteries
MP:0011666	double outlet right ventricle, ventricular defect committed to aorta
MP:0011667	double outlet right ventricle with atrioventricular septal defect
MP:0011668	double outlet right ventricle, Taussig bing type
MP:0011670	double outlet right ventricle, noncommitted ventricular septal defect
MP:0011673	unbalanced complete common atrioventricular canal
MP:0011674	multiple major aortopulmonary collateral arteries
MP:0011677	abnormal olfactory sensory neuron physiology
MP:0011678	abnormal vomeronasal sensory neuron physiology
MP:0011679	abnormal vomeronasal sensory neuron morphology
MP:0011681	atrium cysts
MP:0011682	renal glomerulus cysts
MP:0011683	dual inferior vena cava
MP:0011684	coronary-cameral fistula to right ventricle
MP:0011685	abnormal limb paddle morphology
MP:0011687	decreased epidermal stem cell number
MP:0011689	absent neutrophils
MP:0011692	increased chondrocyte number
MP:0011695	absent hematopoietic stem cells
MP:0011696	absent mast cells
MP:0011697	vacuolated lens
MP:0011698	abnormal brown adipose tissue physiology
MP:0011699	abnormal brown adipose tissue thermogenesis
MP:0011701	decreased cumulus expansion
MP:0011702	abnormal fibroblast proliferation
MP:0011703	increased fibroblast proliferation
MP:0011704	decreased fibroblast proliferation
MP:0011705	absent fibroblast proliferation
MP:0011706	abnormal fibroblast migration
MP:0011707	impaired fibroblast cell migration
MP:0011708	decreased fibroblast cell migration
MP:0011709	increased fibroblast cell migration
MP:0011710	enhanced osteoblast differentiation
MP:0011711	impaired osteoblast differentiation
MP:0011721	abnormal bone mineralization involved in bone maturation
MP:0011722	abnormal ossification involved in bone maturation
MP:0011723	ectopic neuron
MP:0011724	ectopic cortical neuron
MP:0011727	ectopic ovary
MP:0011729	abnormal pineal gland melatonin secretion
MP:0011730	increased myelin sheath thickness
MP:0011731	decreased myelin sheath thickness
MP:0011732	decreased somite size
MP:0011733	fused somites
MP:0011735	increased urine ammonia level
MP:0011736	decreased urine ammonia level
MP:0011737	hypodipsia
MP:0011739	abnormal Boettcher cell morphology
MP:0011741	increased urine nitrite level
MP:0011742	decreased urine nitrite level
MP:0011743	abnormal Golgi apparatus morphology
MP:0011744	abnormal kidney epithelial cell primary cilium physiology
MP:0011745	isolation of the left subclavian artery
MP:0011746	spleen fibrosis
MP:0011748	intestinal fibrosis
MP:0011749	perivascular fibrosis
MP:0011750	abnormal seminiferous tubule epithelium morphology
MP:0011751	abnormal X-Y chromosome synapsis during male meiosis
MP:0011753	decreased podocyte number
MP:0011754	abnormal kidney collecting duct intercalated cell morphology
MP:0011757	abnormal kidney collecting duct principal cell morphology
MP:0011758	renal ischemia
MP:0011759	absent Rathke's pouch
MP:0011760	abnormal ureteric bud tip morphology
MP:0011761	abnormal ureteric bud trunk morphology
MP:0011763	urethritis
MP:0011766	abnormal urinary bladder mucosa morphology
MP:0011769	urinary bladder fibrosis
MP:0011770	increased urine selenium level
MP:0011771	abnormal genital tubercle morphology
MP:0011772	genital tubercle hypoplasia
MP:0011773	abnormal urinary bladder blood vessel morphology
MP:0011774	abnormal urinary bladder detrusor smooth muscle morphology
MP:0011775	rectal atresia
MP:0011777	abnormal male prostatic urethra morphology
MP:0011780	abnormal female urethra morphology
MP:0011781	abnormal bulbourethral gland physiology
MP:0011783	abnormal ureteral orifice morphology
MP:0011784	abnormal urinary bladder neck morphology
MP:0011789	increased urethra carcinoma incidence
MP:0011797	blind ureter
MP:0011799	increased urinary bladder weight
MP:0011802	seminal vesiculitis
MP:0011805	decreased cell migration
MP:0011806	decreased dermal fibroblast proliferation
MP:0011807	decreased lung fibroblast proliferation
MP:0011808	abnormal myoblast differentiation
MP:0011815	increased pre-pro B cell number
MP:0011816	decreased pre-pro B cell number
MP:0011819	increased pancreatic beta cell proliferation
MP:0011820	decreased pancreatic beta cell proliferation
MP:0011822	increased CD8-positive, alpha-beta memory T cell proliferation
MP:0011825	decreased cell chemotaxis
MP:0011826	increased lymphocyte chemotaxis
MP:0011827	impaired neuron differentiation
MP:0011828	urinary bladder cysts
MP:0011831	abnormal visual contrast sensitivity
MP:0011833	abnormal cremaster muscle morphology
MP:0011835	abnormal urogenital fold morphology
MP:0011843	abnormal kidney collecting duct epithelium morphology
MP:0011844	kidney collecting duct atrophy
MP:0011846	decreased kidney collecting duct number
MP:0011850	absent clitoral bone
MP:0011851	abnormal embryonic cloaca development
MP:0011855	abnormal glomerular filtration barrier morphology
MP:0011856	abnormal glomerular filtration barrier function
MP:0011857	short kidney papilla
MP:0011858	elongated kidney papilla
MP:0011859	decreased renal glomerulus basement membrane thickness
MP:0011860	abnormal peritubular capillary endothelium morphology
MP:0011861	increased cranium height
MP:0011862	decreased cranium length
MP:0011864	abnormal podocyte adhesion
MP:0011865	abnormal podocyte motility
MP:0011868	podocyte microvillus transformation
MP:0011869	detached podocyte
MP:0011870	abnormal podocyte polarity
MP:0011871	podocyte hypertrophy
MP:0011873	enlarged uterine horn
MP:0011874	enlarged urinary bladder
MP:0011875	absent stomach
MP:0011877	absent liver
MP:0011881	distended duodenum
MP:0011882	enlarged duodenum
MP:0011884	absent colon
MP:0011885	abnormal circulating lipase level
MP:0011886	increased circulating lipase level
MP:0011887	decreased circulating lipase level
MP:0011890	increased circulating ferritin level
MP:0011891	decreased circulating ferritin level
MP:0011894	decreased circulating transferrin level
MP:0011895	abnormal circulating unsaturated transferrin level
MP:0011896	increased circulating unsaturated transferrin level
MP:0011897	decreased circulating unsaturated transferrin level
MP:0011898	abnormal platelet cell number
MP:0011902	increased hematopoietic stem cell proliferation
MP:0011903	decreased hematopoietic stem cell proliferation
MP:0011904	abnormal Schwann cell physiology
MP:0011906	increased Schwann cell proliferation
MP:0011910	decreased pancreatic endocrine progenitor cell proliferation
MP:0011911	abnormal pancreatic endocrine progenitor cell physiology
MP:0011913	abnormal reticulocyte cell number
MP:0011915	increased heart left atrium weight
MP:0011919	abnormal R wave
MP:0011922	abnormal circulating osteocalcin level
MP:0011923	abnormal bladder urine volume
MP:0011924	abnormal liver zinc level
MP:0011925	abnormal heart echocardiography feature
MP:0011926	abnormal cardiac valve physiology
MP:0011929	abnormal aortic valve flow
MP:0011932	abnormal endocrine pancreas development
MP:0011934	abnormal branching involved in pancreas development
MP:0011939	increased food intake
MP:0011940	decreased food intake
MP:0011941	increased fluid intake
MP:0011942	decreased fluid intake
MP:0011943	abnormal circadian feeding behavior
MP:0011945	increased eating frequency
MP:0011946	decreased eating frequency
MP:0011947	abnormal fluid intake
MP:0011951	increased cardiac stroke volume
MP:0011952	decreased cardiac stroke volume
MP:0011953	prolonged PQ interval
MP:0011954	shortened PQ interval
MP:0011957	decreased compensatory feeding amount
MP:0011958	increased compensatory feeding amount
MP:0011959	abnormal eye posterior chamber depth
MP:0011960	abnormal eye anterior chamber depth
MP:0011963	abnormal total retina thickness
MP:0011964	increased total retina thickness
MP:0011965	decreased total retina thickness
MP:0011966	abnormal auditory brainstem response waveform shape
MP:0011967	increased or absent threshold for auditory brainstem response
MP:0011968	decreased threshold for auditory brainstem response
MP:0011969	abnormal circulating triglyceride level
MP:0011971	increased circulating lactate dehydrogenase level
MP:0011972	decreased circulating lactate dehydrogenase level
MP:0011974	intestinal stenosis
MP:0011975	neuronal cytoplasmic inclusions
MP:0011976	sweet preference
MP:0011977	abnormal sodium ion homeostasis
MP:0011978	abnormal potassium ion homeostasis
MP:0011979	abnormal magnesium ion homeostasis
MP:0011982	decreased microglial cell number
MP:0011986	decreased macrophage proliferation
MP:0011987	abnormal GABAergic neuron physiology
MP:0011994	increased nerve conduction velocity
MP:0011995	decreased leukemia incidence
MP:0011996	abnormal retinal inner nuclear layer thickness
MP:0011997	abnormal retinal outer nuclear layer thickness
MP:0011998	decreased embryonic cilium length
MP:0011999	abnormal tail length
MP:0012000	abnormal limb position
MP:0012001	abnormal touch escape response
MP:0012002	impaired touch escape response
MP:0012003	abnormal septum of telencephalon morphology
MP:0012004	abnormal septum pellucidum morphology
MP:0012006	abnormal hippocampus physiology
MP:0012007	abnormal chloride level
MP:0012008	delayed parturition
MP:0012009	early parturition
MP:0012010	parturition failure
MP:0012013	abnormal innate avoidance response
MP:0012014	abnormal olfactory neuron innervation pattern
MP:0012017	grizzled coat color
MP:0012020	abnormal olfactory epithelium physiology
MP:0012022	increased melanocyte number
MP:0012023	decreased melanocyte number
MP:0012024	abnormal nephron morphogenesis
MP:0012026	abnormal S-shaped body morphology
MP:0012027	abnormal embryonic cilium location or orientation
MP:0012028	abnormal visceral endoderm physiology
MP:0012029	abnormal electroretinogram waveform feature
MP:0012034	abnormal a wave shape
MP:0012035	abnormal b-wave shape
MP:0012040	abnormal c wave shape
MP:0012043	increased myoepithelioma incidence
MP:0012045	increased susceptibility to hypertension
MP:0012046	decreased susceptibility to hypertension
MP:0012049	increased susceptilbility to retinal ischemic injury
MP:0012050	decreased susceptilbility to retinal ischemic injury
MP:0012055	abnormal phrenic nerve innervation pattern to diaphragm
MP:0012056	abnormal polar trophectoderm morphology
MP:0012057	abnormal mural trophectoderm morphology
MP:0012058	abnormal morula morphology
MP:0012059	thick diaphragm muscle
MP:0012060	diaphragm muscle hyperplasia
MP:0012061	abnormal central tendon morphology
MP:0012062	small tail bud
MP:0012063	absent tail bud
MP:0012065	increased astrocyte number
MP:0012066	decreased astrocyte number
MP:0012067	abnormal olfactory gland morphology
MP:0012069	abnormal horizontal basal cell of olfactory epithelium morphology
MP:0012072	decreased susceptibility to osteoporosis
MP:0012073	premature mammary gland growth during pregnancy
MP:0012075	impaired mammary gland growth during pregnancy
MP:0012076	abnormal agouti pigmentation
MP:0012078	abnormal tail ring morphology
MP:0012081	absent heart tube
MP:0012082	delayed heart development
MP:0012083	absent foregut
MP:0012084	truncated foregut
MP:0012085	midface hypoplasia
MP:0012086	absent hindgut
MP:0012089	decreased midbrain size
MP:0012090	midbrain hypoplasia
MP:0012091	increased midbrain size
MP:0012092	diencephalon hypoplasia
MP:0012093	absent nodal flow
MP:0012094	abnormal Reichert's membrane thickness
MP:0012095	increased Reichert's membrane thickness
MP:0012096	decreased Reichert's membrane thickness
MP:0012098	increased spongiotrophoblast size
MP:0012099	decreased spongiotrophoblast size
MP:0012100	absent spongiotrophoblast
MP:0012101	acoria
MP:0012102	absent trophectoderm
MP:0012104	small amniotic cavity
MP:0012105	delayed gastrulation
MP:0012106	impaired exercise endurance
MP:0012107	enhanced exercise endurance
MP:0012108	increased trophoblast glycogen cell number
MP:0012109	decreased trophoblast glycogen cell number
MP:0012111	failure of morula compaction
MP:0012113	decreased inner cell mass proliferation
MP:0012114	absent inner cell mass proliferation
MP:0012117	decreased trophectoderm cell proliferation
MP:0012118	absent trophectoderm cell proliferation
MP:0012119	increased trophectoderm apoptosis
MP:0012120	trophectoderm cell degeneration
MP:0012122	abnormal iris transillumination
MP:0012124	increased bronchoconstrictive response
MP:0012125	decreased bronchoconstrictive response
MP:0012126	abnormal placenta hemotrichorial membrane morphology
MP:0012127	absent placenta hemotrichorial membrane
MP:0012128	abnormal blastocyst formation
MP:0012129	failure of blastocyst formation
MP:0012131	small visceral yolk sac
MP:0012132	abnormal midbrain-hindbrain boundary morphology
MP:0012133	absent midbrain-hindbrain boundary
MP:0012134	absent umbilical cord
MP:0012135	embryonic-extraembryonic boundary constriction
MP:0012136	absent forebrain
MP:0012138	decreased forebrain size
MP:0012139	increased forebrain size
MP:0012142	absent amniotic cavity
MP:0012143	decreased a wave amplitude
MP:0012144	decreased b wave amplitude
MP:0012145	increased a wave amplitude
MP:0012146	increased b wave amplitude
MP:0012147	increased a wave implicit time
MP:0012148	decreased a wave implicit time
MP:0012149	decreased b wave implicit time
MP:0012150	increased b wave implicit time
MP:0012151	increased a wave latency
MP:0012153	increased b wave latency
MP:0012155	abnormal optic pit morphology
MP:0012156	rostral-caudal axis duplication
MP:0012157	rostral body truncation
MP:0012158	absent visceral endoderm
MP:0012159	absent anterior visceral endoderm
MP:0012161	absent distal visceral endoderm
MP:0012162	absent parietal endoderm
MP:0012163	abnormal dental mesenchyme morphology
MP:0012164	abnormal conjunctiva goblet cell morphology
MP:0012165	absent neural folds
MP:0012167	abnormal epigenetic regulation of gene expression
MP:0012168	abnormal optic placode morphology
MP:0012169	optic placode degeneration
MP:0012170	absent optic placodes
MP:0012172	abnormal amniotic fluid composition
MP:0012173	short rostral-caudal axis
MP:0012176	abnormal head development
MP:0012177	delayed head development
MP:0012178	absent frontonasal prominence
MP:0012179	abnormal splanchnic mesoderm morphology
MP:0012180	abnormal somatic mesoderm morphology
MP:0012181	increased somite number
MP:0012182	abnormal presomitic mesoderm morphology
MP:0012183	decreased paraxial mesoderm size
MP:0012184	absent paraxial mesoderm
MP:0012185	abnormal muscle precursor cell morphology
MP:0012186	abnormal muscle precursor cell physiology
MP:0012188	increased regulatory T cell apoptosis
MP:0012193	increased keratinocyte migration
MP:0012194	decreased keratinocyte migration
MP:0012197	impaired myofibroblast differentiation
MP:0012200	increased endothelial cell proliferation
MP:0012201	decreased endothelial cell proliferation
MP:0012203	abnormal neuronal stem cell morphology
MP:0012204	abnormal neuronal stem cell physiology
MP:0012206	increased neuronal stem cell self-renewal
MP:0012207	decreased neuronal stem cell self-renewal
MP:0012216	decreased plasmalogen level
MP:0012217	increased plasmalogen level
MP:0012218	decreased brain plasmalogen level
MP:0012222	decreased circulating prothrombin level
MP:0012226	increased sterol level
MP:0012230	abnormal sphingolipid level
MP:0012231	abnormal ganglioside level
MP:0012232	abnormal ceramide level
MP:0012234	abnormal hepatic diverticulum morphology
MP:0012235	abnormal liver bud morphology
MP:0012236	abnormal cholangiocyte morphology
MP:0012237	increased cholangiocyte apoptosis
MP:0012238	abnormal cholangiocyte primary cilium morphology
MP:0012240	abnormal hepatoblast morphology
MP:0012242	abnormal hepatoblast differentiation
MP:0012243	decreased hepatoblast number
MP:0012244	increased hepatoblast apoptosis
MP:0012245	abnormal hepatoblast migration
MP:0012246	abnormal hepatic cord morphology
MP:0012247	absent cornea
MP:0012248	absent dermatome
MP:0012249	absent myotome
MP:0012250	absent heart valves
MP:0012251	abnormal diaphragm development
MP:0012252	abnormal septum transversum morphology
MP:0012253	abnormal intersomitic vessel morphology
MP:0012254	absent intersomitic vessels
MP:0012256	abnormal philtrum morphology
MP:0012261	increased hindbrain apoptosis
MP:0012263	decreased hindbrain size
MP:0012264	hindbrain hypoplasia
MP:0012265	increased hindbrain size
MP:0012267	abnormal red nucleus morphology
MP:0012268	absent red nucleus
MP:0012269	nuchal edema
MP:0012270	cardiac edema
MP:0012271	abnormal chordamesoderm morphology
MP:0012272	decreased axial mesoderm size
MP:0012273	axial mesoderm hypoplasia
MP:0012274	increased axial mesoderm size
MP:0012276	absent prechordal mesoderm
MP:0012277	increased tail bud apoptosis
MP:0012278	abnormal cardiogenic mesoderm morphology
MP:0012279	wide sternum
MP:0012280	abnormal sternebra size
MP:0012281	decreased sternebra size
MP:0012282	abnormal sternebra number
MP:0012283	decreased sternebra number
MP:0012284	increased sternebra number
MP:0012285	misaligned sternebrae
MP:0012286	decreased frequency of paradoxical sleep
MP:0012287	increased frequency of paradoxical sleep
MP:0012288	abnormal paradoxical sleep pattern
MP:0012289	abnormal non-rapid eye movement sleep pattern
MP:0012291	increased slow-wave sleep duration
MP:0012293	impaired active avoidance behavior
MP:0012294	enhanced active avoidance behavior
MP:0012297	hyperactivity elicited by feed restriction
MP:0012298	hypoactivity in response to feed restriction
MP:0012299	hydropic allantois
MP:0012300	abnormal umbilical cord blood vessel morphology
MP:0012302	umbilical artery stenosis
MP:0012303	umbilical vein stenosis
MP:0012305	umbilical cord hemorrhage
MP:0012306	enhanced spatial learning
MP:0012307	impaired spatial learning
MP:0012310	persistent ductus caroticus
MP:0012311	decreased defecation amount
MP:0012312	impaired avoidance learning behavior
MP:0012314	enhanced learning
MP:0012315	impaired learning
MP:0012317	impaired conditioning behavior
MP:0012318	slow extinction of fear memory
MP:0012319	fast extinction of fear memory
MP:0012320	abnormal body fat mass
MP:0012322	decreased total tissue mass
MP:0012323	increased total tissue mass
MP:0012325	decreased circulating antithrombin level
MP:0012328	decreased circulating factor VIII level
MP:0012329	increased circulating factor VIII level
MP:0012331	increased circulating fibrinogen level
MP:0012335	increased circulating homocysteine level
MP:0012337	increased vitamin D level
MP:0012338	decreased bile salt level
MP:0012341	low preference for an addictive substance
MP:0012347	low sweet preference
MP:0012349	increased susceptibility to induction of seizure by inducing agent
MP:0012355	decreased prothrombin time
MP:0012358	decreased partial thromboplastin time
MP:0012359	increased partial thromboplastin time
MP:0012361	decreased large unstained cell number
MP:0012362	increased large unstained cell number
MP:0012367	decreased erythrocyte magnesium level
MP:0012368	increased erythrocyte magnesium level
MP:0012370	decreased erythrocyte potassium level
MP:0012372	abnormal erythrocyte ion content
MP:0012384	abnormal erythrocyte ion transport
MP:0012397	abnormal nucleated erythrocyte cell number
MP:0012401	long nails
MP:0012403	abnormal nail plate morphology
MP:0012405	abnormal nail matrix morphology
MP:0012411	increased granulosa cell tumor incidence
MP:0012419	decreased cardiovascular system tumor incidence
MP:0012434	decreased intestinal adenoma incidence
MP:0012436	increased colon tumor incidence
MP:0012437	increased Harderian gland tumor incidence
MP:0012443	increased corpus callosum size
MP:0012444	thin hippocampus molecular cell layer
MP:0012446	thin hippocampus stratum oriens
MP:0012458	decreased hippocampus pyramidal cell length
MP:0012459	increased dentate gyrus size
MP:0012460	decreased dentate gyrus size
MP:0012462	decreased brain internal capsule size
MP:0012467	increased striatum area
MP:0012468	decreased striatum area
MP:0012480	decreased amygdala size
MP:0012484	decreased corticospinal tract size
MP:0012489	abnormal retrosplenial region morphology
MP:0012490	abnormal cochlear VIII nucleus morphology
MP:0012492	pharyngeal arch artery hypoplasia
MP:0012493	absent pharyngeal arch arteries
MP:0012494	dilated pharyngeal arch arteries
MP:0012495	pharyngeal arch artery stenosis
MP:0012496	abnormal pleuropericardial membrane morphology
MP:0012498	abnormal cardiogenic plate morphology
MP:0012499	absent cardiogenic plate
MP:0012501	abnormal pericardial cavity morphology
MP:0012503	increased midbrain apoptosis
MP:0012504	increased forebrain apoptosis
MP:0012505	increased neural tube apoptosis
MP:0012507	midbrain atrophy
MP:0012508	forebrain atrophy
MP:0012509	neural tube degeneration
MP:0012510	abnormal aortic sac morphology
MP:0012511	dilated aortic sac
MP:0012513	absent sternum body
MP:0012515	abnormal heart apex morphology
MP:0012516	absent metencephalon
MP:0012517	absent diencephalon
MP:0012518	abnormal Brunner's gland morphology
MP:0012519	dilated Brunner's glands
MP:0012520	absent Brunner's glands
MP:0012523	abnormal upper lip morphology
MP:0012524	abnormal lower lip morphology
MP:0012525	abnormal rhombic lip morphology
MP:0012528	abnormal zone of polarizing activity morphology
MP:0012529	abnormal decidua basalis morphology
MP:0012530	abnormal decidua capsularis morphology
MP:0012531	delayed limb development
MP:0012532	abnormal surface ectoderm morphology
MP:0012533	uveal coloboma
MP:0012534	abnormal optic fissure morphology
MP:0012535	abnormal optic fissure closure
MP:0012536	delayed optic fissure closure
MP:0012537	abnormal hyaloid artery morphology
MP:0012539	Bergmeister's papilla
MP:0012540	abnormal lamina terminalis morphology
MP:0012541	absent lamina terminalis
MP:0012544	abnormal caudal neuropore morphology
MP:0012547	spina bifida cystica
MP:0012548	myelocele
MP:0012555	decreased cell death
MP:0012556	increased cell death
MP:0012557	decreased calcium uptake by cardiac muscle
MP:0012558	increased calcium uptake by cardiac muscle
MP:0012559	decreased forebrain volume
MP:0012563	increased tumor incidence following infection
MP:0012570	increased mammary gland tumor incidence in breeding females
MP:0012571	increased mammary gland tumor incidence in virgin females
MP:0012572	increased susceptibility to chemically induced skin inflammation
MP:0012574	decreased noradrenaline level
MP:0012575	increased noradrenaline level
MP:0012592	decreased brain choline acetyltransferase activity
MP:0012593	increased brain choline acetyltransferase activity
MP:0012604	decreased glutathione level
MP:0012606	increased glutathione level
MP:0012615	decreased circulating factor IX level
MP:0012616	increased circulating factor IX level
MP:0012634	decreased phospholipase A2 level
MP:0012652	decreased catalase level
MP:0012661	decreased circulating ceruloplasmin level
MP:0012664	decreased circulating haptoglobin level
MP:0012666	increased circulating haptoglobin level
MP:0012667	split sternal manubrium
MP:0012669	abnormal somite segmentation clock
MP:0012670	prolonged somite segmentation clock period
MP:0012671	retinal spots
MP:0012674	tomacula
MP:0012675	enlarged floor plate
MP:0012677	absent brain ventricles
MP:0012678	absent fourth ventricle
MP:0012679	absent third ventricle
MP:0012680	absent lateral ventricles
MP:0012681	collapsed brain ventricles
MP:0012683	absent telencephalon
MP:0012684	abnormal pleural cavity morphology
MP:0012685	abnormal primitive streak elongation
MP:0012686	everted embryonic neuroepithelium
MP:0012688	abnormal heart ventricles weight
MP:0012691	abnormal acetaminophen metabolism
MP:0012700	abnormal endocardial heart tube morphology
MP:0012701	increased embryonic neuroepithelium apoptosis
MP:0012702	increased embryonic neuroepithelium thickness
MP:0012703	decreased embryonic neuroepithelium thickness
MP:0012704	abnormal embryonic neuroepithelial cell proliferation
MP:0012705	increased embryonic neuroepithelial cell proliferation
MP:0012706	decreased embryonic neuroepithelial cell proliferation
MP:0012707	incomplete caudal neuropore closure
MP:0012708	delayed rostral neuropore closure
MP:0012709	delayed caudal neuropore closure
MP:0012710	diastematomyelia
MP:0012714	decreased ventral ectodermal ridge size
MP:0012717	increased hemangioblast number
MP:0012719	abnormal neck morphology
MP:0012722	absent neck
MP:0012723	abnormal nuchal region morphology
MP:0012724	absent head fold
MP:0012725	small sebaceous gland
MP:0012726	abnormal uterine spiral artery morphology
MP:0012727	abnormal uterine spiral artery remodeling
MP:0012728	abnormal somite border morphology
MP:0012729	abnormal common carotid artery morphology
MP:0012730	abnormal internal carotid artery morphology
MP:0012731	abnormal external carotid artery morphology
MP:0012732	abnormal perineural vascular plexus morphology
MP:0012733	abnormal behavioral response to methamphetamine
MP:0012734	abnormal response to radiation
MP:0012735	abnormal response to exercise
MP:0012736	abnormal polar body morphology
MP:0012737	abnormal primary polar body morphology
MP:0012738	abnormal secondary polar body morphology
MP:0012739	abnormal anterior primitive streak morphology
MP:0012740	abnormal posterior primitive streak morphology
MP:0012743	increased inner cell mass apoptosis
MP:0012744	increased neural crest cell apoptosis
MP:0012745	abnormal neural crest cell physiology
MP:0012746	abnormal neural crest cell delamination
MP:0012747	abnormal cardiac neural crest cell morphology
MP:0012748	increased cardiac neural crest cell number
MP:0012749	decreased cardiac neural crest cell number
MP:0012750	absent cardiac neural crest cells
MP:0012751	impaired cardiac neural crest cell differentiation
MP:0012752	abnormal cardiac neural crest cell migration
MP:0012754	abnormal cranial neural crest cell morphology
MP:0012755	decreased cranial neural crest cell number
MP:0012756	impaired cranial neural crest cell differentiation
MP:0012757	abnormal cranial neural crest cell migration
MP:0012759	increased cranial neural crest cell proliferation
MP:0012760	decreased cranial neural crest cell proliferation
MP:0012761	increased cranial neural crest cell apoptosis
MP:0012764	increased alpha-beta T cell number
MP:0012765	decreased alpha-beta T cell number
MP:0012767	increased KLRG1-positive NK cell number
MP:0012768	decreased KLRG1-positive NK cell number
MP:0012779	abnormal brain cholesterol level
MP:0012785	decreased rhombomere 1 size
MP:0012786	increased rhombomere 1 size
MP:0012788	abnormal rhombomere 2 morphology
MP:0012792	abnormal rhombomere 3 morphology
MP:0012793	decreased rhombomere 3 size
MP:0012794	increased rhombomere 3 size
MP:0012795	absent rhombomere 3
MP:0012796	abnormal rhombomere 4 morphology
MP:0012798	increased rhombomere 4 size
MP:0012800	abnormal rhombomere 5 morphology
MP:0012801	decreased rhombomere 5 size
MP:0012803	absent rhombomere 5
MP:0012805	decreased rhombomere 6 size
MP:0012816	abnormal rhombomere boundary morphology
MP:0012817	rhombomere fusion
MP:0012818	rhombomere transformation
MP:0013000	absent cerebral aqueduct
MP:0013001	abnormal enteric neural crest cell morphology
MP:0013002	decreased enteric neural crest cell number
MP:0013003	absent enteric neural crest cell
MP:0013005	decreased enteric neural crest cell proliferation
MP:0013006	abnormal enteric neural crest cell migration
MP:0013007	abnormal vagal neural crest cell migration
MP:0013009	increased vagal neural crest cell apoptosis
MP:0013011	absent vagal neural crest cells
MP:0013012	abnormal trunk neural crest cell migration
MP:0013013	abnormal trunk neural crest cell morphology
MP:0013014	increased trunk neural crest cell apoptosis
MP:0013022	increased Ly6C high monocyte number
MP:0013023	decreased Ly6C high monocyte number
MP:0013025	increased Ly6C low monocyte number
MP:0013026	decreased Ly6C low monocyte number
MP:0013116	focal hair loss in head/neck region
MP:0013123	head/neck swellings
MP:0013138	thin body
MP:0013139	moribund
MP:0013140	excessive vocalization
MP:0013146	eye lesions
MP:0013148	mastitis
MP:0013154	increased KLRG1+ CD8 alpha beta T cell number
MP:0013155	decreased KLRG1+ CD8 alpha beta T cell number
MP:0013157	increased KLRG1+ CD4 alpha beta T cell number
MP:0013158	decreased KLRG1+ CD4 alpha beta T cell number
MP:0013159	Purkinje cell axonal dystrophy
MP:0013162	abnormal thyroid gland isthmus morphology
MP:0013163	absent thyroid gland isthmus
MP:0013164	abnormal forelimb bud morphology
MP:0013165	absent forelimb buds
MP:0013166	small forelimb buds
MP:0013167	abnormal hindlimb bud morphology
MP:0013168	absent hindlimb buds
MP:0013169	small hindlimb buds
MP:0013173	trigeminal ganglion degeneration
MP:0013174	pharynx stenosis
MP:0013175	bifurcated tail
MP:0013176	abnormal tail position or orientation
MP:0013177	abnormal tail tip morphology
MP:0013178	tail necrosis
MP:0013179	wavy tail
MP:0013180	truncated tail bud
MP:0013181	absent placenta
MP:0013182	increased spinal cord apoptosis
MP:0013183	absent trigeminal ganglion
MP:0013184	hemorrhagic ascites
MP:0013185	absent anterior definitive endoderm
MP:0013186	abnormal basilar artery morphology
MP:0013187	dilated basilar artery
MP:0013189	abnormal exploration in a new environment
MP:0013191	increased sebaceous gland number
MP:0013192	decreased sebaceous gland number
MP:0013193	sebaceous gland hypoplasia
MP:0013197	decreased embryonic cilium number
MP:0013199	increased head mesenchyme apoptosis
MP:0013200	head mesenchyme hypoplasia
MP:0013202	abnormal cilium morphology
MP:0013203	abnormal primary cilium morphology
MP:0013205	abnormal nonmotile primary cilium morphology
MP:0013206	abnormal motile cilium morphology
MP:0013207	absent endoderm
MP:0013209	abnormal motile cilium physiology
MP:0013213	abnormal embryonic neuroepithelium primary cilium morphology
MP:0013214	decreased embryonic neuroepithelium primary cilium number
MP:0013216	absent ectoderm
MP:0013217	abnormal posterior definitive endoderm morphology
MP:0013218	abnormal substantia nigra pars reticulata morphology
MP:0013219	abnormal substantia nigra pars compacta morphology
MP:0013220	increased pancreas apoptosis
MP:0013221	pancreatic acinar-to-ductal metaplasia
MP:0013222	abnormal first pharyngeal pouch morphology
MP:0013227	small brain ventricles
MP:0013228	brain ventricle stenosis
MP:0013236	ovary degeneration
MP:0013237	abnormal skeletal muscle regeneration
MP:0013239	impaired skeletal muscle regeneration
MP:0013241	embryo tissue necrosis
MP:0013243	abnormal carbohydrate metabolism
MP:0013248	placenta junctional zone necrosis
MP:0013249	adipose tissue necrosis
MP:0013250	abnormal dental pulp morphology
MP:0013251	dental pulp necrosis
MP:0013258	abnormal extracellular matrix morphology
MP:0013262	abnormal mouth floor morphology
MP:0013265	abnormal fourth pharyngeal pouch morphology
MP:0013267	first pharyngeal arch hypoplasia
MP:0013268	second pharyngeal arch hypoplasia
MP:0013272	abnormal translation
MP:0013273	abnormal translational elongation
MP:0013277	abnormal fasted circulating glucose level
MP:0013278	decreased fasted circulating glucose level
MP:0013279	increased fasted circulating glucose level
MP:0013281	increased cytotoxic T cell cytolysis
MP:0013283	failure of ventral body wall closure
MP:0013285	abnormal renal filtration
MP:0013288	premature acrosome reaction
MP:0013289	abnormal mitotic cytokinesis
MP:0013290	persistent ultimobranchial bodies
MP:0013291	ectopic pancreas
MP:0013292	embryonic lethality prior to organogenesis
MP:0013293	embryonic lethality prior to tooth bud stage
MP:0013294	prenatal lethality prior to heart atrial septation
MP:0013298	increased susceptibility to colitis induced morbidity/mortality
MP:0013299	decreased susceptibility to colitis induced morbidity/mortality
MP:0013300	abnormal submandibular gland physiology
MP:0013302	increased pancreas iron level
MP:0013303	decreased pancreas iron level
MP:0013304	osteophytes
MP:0013307	increased adrenal gland weight
MP:0013308	decreased adrenal gland weight
MP:0013309	adrenal gland cyst
MP:0013310	abnormal adrenal gland development
MP:0013312	absent ovary capsule
MP:0013313	female preputial gland hypoplasia
MP:0013317	abnormal seminal vesicle development
MP:0013318	abnormal branching involved in seminal vesicle morphogenesis
MP:0013319	seminal vesicle atrophy
MP:0013320	dilated seminal vesicles
MP:0013321	squamous metaplasia of seminal vesicles
MP:0013322	squamous metaplasia of prostate gland
MP:0013323	abnormal ampullary gland morphology
MP:0013329	abnormal preputial gland morphology
MP:0013330	abnormal male accessory sex gland morphology
MP:0013331	abnormal lacrimal gland development
MP:0013334	adenohypophysis peliosis
MP:0013336	pituitary gland hypertrophy
MP:0013337	abnormal adenohypophysis development
MP:0013338	abnormal neurohypophysis development
MP:0013340	abnormal pituicyte morphology
MP:0013341	abnormal folliculo-stellate cell morphology
MP:0013342	bifurcated Rathke's pouch
MP:0013344	increased pituitary gland apoptosis
MP:0013346	increased melanotroph apoptosis
MP:0013347	increased corticotroph apoptosis
MP:0013348	adenohypophysis hyperplasia
MP:0013349	small Rathke's pouch
MP:0013350	Rathke's pouch hypoplasia
MP:0013351	abnormal Rathke's pouch development
MP:0013352	abnormal Rathke's pouch apoptosis
MP:0013355	adenohypophysis hypertrophy
MP:0013356	ectopic pituitary gland
MP:0013361	absent pineal recess
MP:0013362	absent pineal gland
MP:0013364	enlarged pineal gland
MP:0013366	adrenal gland atrophy
MP:0013368	abnormal sweat gland physiology
MP:0013373	increased sebum secretion
MP:0013375	abnormal sebocyte morphology
MP:0013376	abnormal sebocyte differentiation
MP:0013377	abnormal sebocyte number
MP:0013378	increased sebocyte number
MP:0013379	decreased sebocyte cell number
MP:0013382	small perianal sebaceous gland
MP:0013385	abnormal Meibomian gland development
MP:0013387	Meibomian gland hypertrophy
MP:0013388	small Meibomian gland
MP:0013389	Meibomian gland hypoplasia
MP:0013391	abnormal Meibomian gland physiology
MP:0013392	Meibomian gland inflammation
MP:0013394	abnormal palpebral conjunctiva morphology
MP:0013396	eyelid hyperplasia
MP:0013398	uterus fibrosis
MP:0013399	endometrium fibrosis
MP:0013400	abnormal endometrial gland development
MP:0013401	increased endometrial gland number
MP:0013404	decreased circulating lactate level
MP:0013405	increased circulating lactate level
MP:0013407	abnormal dendritic epidermal T cell morphology
MP:0013414	decreased myeloid cell number in bone marrow
MP:0013415	increased myeloid cell number in bone marrow
MP:0013417	decreased memory-marker gamma-delta T cell number
MP:0013418	increased memory-marker gamma-delta T cell number
MP:0013420	decreased CD5-positive gamma-delta T cell number
MP:0013421	increased CD5-positive gamma-delta T cell number
MP:0013424	increased KLRG1-positive gamma-delta T cell number
MP:0013429	decreased memory CD4-positive, CD25-positive, alpha-beta regulatory T cell number
MP:0013430	increased memory CD4-positive, CD25-positive, alpha-beta regulatory T cell number
MP:0013433	increased KLRG1-positive CD4-positive, CD25-positive, alpha-beta regulatory T cell number
MP:0013435	decreased CD8-positive, naive alpha-beta T cell number
MP:0013436	increased CD8-positive, naive alpha-beta T cell number
MP:0013440	abnormal exorbital lacrimal gland morphology
MP:0013443	Harderian gland hyperplasia
MP:0013445	Harderian gland atrophy
MP:0013447	Harderian gland hypertrophy
MP:0013452	increased lacrimal gland apoptosis
MP:0013454	lacrimal gland hypertrophy
MP:0013455	lacrimal gland atrophy
MP:0013457	increased eccrine gland number
MP:0013458	decreased eccrine gland number
MP:0013460	periocular dermatitis
MP:0013462	abnormal conjunctiva goblet cell number
MP:0013464	decreased conjunctiva goblet cell number
MP:0013467	diaphragmitis
MP:0013468	chromodacryorrhea
MP:0013470	absent lacrimal gland bud
MP:0013474	abnormal lacrimal gland branching morphogenesis
MP:0013476	abnormal Harderian gland porphyrin secretion
MP:0013478	corneal limbitis
MP:0013481	abnormal ileum crypts of Lieberkuhn morphology
MP:0013482	abnormal duodenum crypts of Lieberkuhn morphology
MP:0013483	abnormal jejunum crypts of Lieberkuhn morphology
MP:0013485	increased Paneth cell number
MP:0013486	decreased Paneth cell number
MP:0013487	abnormal Paneth cell physiology
MP:0013488	increased keratoacanthoma incidence
MP:0013490	absent infundibular recess of third ventricle
MP:0013492	oral erythroplakia
MP:0013494	abnormal trachea gland morphology
MP:0013495	decreased trachea gland number
MP:0013496	abnormal trachea development
MP:0013497	trachea occlusion
MP:0013498	trachea inflammation
MP:0013499	trachea fibrosis
MP:0013500	abnormal fibroblast apoptosis
MP:0013501	increased fibroblast apoptosis
MP:0013502	decreased fibroblast apoptosis
MP:0013504	increased embryonic tissue cell apoptosis
MP:0013505	decreased embryonic tissue cell apoptosis
MP:0013507	increased ovary apoptosis
MP:0013508	increased granulosa cell apoptosis
MP:0013511	increased CD4-negative NK T cell number
MP:0013513	decreased memory-marker CD4-negative NK T cell number
MP:0013514	increased memory-marker CD4-negative NK T cell number
MP:0013517	increased KLRG1-positive CD4-negative NK T cell number
MP:0013519	decreased CD4-positive NK T cell number
MP:0013520	increased CD4-positive NK T cell number
MP:0013522	decreased memory-marker CD4-positive NK T cell number
MP:0013523	increased memory-marker CD4-positive NK T cell number
MP:0013525	decreased KLRG1-positive CD4-positive NK T cell number
MP:0013526	increased KLRG1-positive CD4-positive NK T cell number
MP:0013527	absent conjunctiva goblet cells
MP:0013528	thyroid cyst
MP:0013529	decreased nipple number
MP:0013531	abnormal periderm development
MP:0013532	abnormal parotid gland physiology
MP:0013533	sublingual gland inflammation
MP:0013538	increased Harderian gland adenoma incidence
MP:0013539	increased ovary adenoma incidence
MP:0013540	increased submandibular gland apoptosis
MP:0013541	abnormal submandibular gland development
MP:0013542	abnormal submandibular gland branching morphogenesis
MP:0013550	abnormal secondary palate morphology
MP:0013551	decreased cerebellar granule cell precursor proliferation
MP:0013558	abnormal exocrine gland morphology
MP:0013565	abnormal adrenal gland capsule morphology
MP:0013566	dilated gastric glands
MP:0013567	gastric gland atrophy
MP:0013568	gastric gland degeneration
MP:0013569	gastric gland hyperplasia
MP:0013572	abnormal parathyroid gland chief cell morphology
MP:0013573	abnormal parathyroid gland development
MP:0013574	ectopic parathyroid gland
MP:0013575	abnormal forestomach-glandular stomach junction morphology
MP:0013576	small forestomach
MP:0013577	forestomach hypoplasia
MP:0013578	abnormal stomach glandular region morphology
MP:0013579	increased adrenal gland apoptosis
MP:0013580	abnormal nasal gland morphology
MP:0013581	nasal gland degeneration
MP:0013582	abnormal lateral nasal gland morphology
MP:0013583	salivary gland degeneration
MP:0013584	pancreas degeneration
MP:0013585	thymus cortex atrophy
MP:0013586	thymus medulla atrophy
MP:0013587	absent thymus medulla
MP:0013588	small thymus medulla
MP:0013589	thymus medulla hypoplasia
MP:0013590	enlarged thymus medulla
MP:0013591	thymus medulla hyperplasia
MP:0013592	small thymus cortex
MP:0013593	enlarged thymus cortex
MP:0013594	abnormal parotid gland acinus morphology
MP:0013595	absent vomeronasal organ
MP:0013597	small vomeronasal organ
MP:0013598	Leydig cell hypertrophy
MP:0013599	Leydig cell atrophy
MP:0013600	testis degeneration
MP:0013601	increased testis apoptosis
MP:0013602	abnormal Leydig cell differentiation
MP:0013603	abnormal fetal Leydig cell differentiation
MP:0013604	abnormal adult Leydig cell differentiation
MP:0013605	abnormal ovarian bursa morphology
MP:0013607	ovary fibrosis
MP:0013608	abnormal ovarian cortex morphology
MP:0013609	abnormal ovarian medulla morphology
MP:0013611	abnormal bile duct epithelium morphology
MP:0013613	abnormal volumetric bone mineral density
MP:0013614	abnormal areal bone mineral density
MP:0013615	increased volumetric bone mineral density
MP:0013616	decreased volumetric bone mineral density
MP:0013617	increased areal bone mineral density
MP:0013618	decreased areal bone mineral density
MP:0013619	abnormal long bone internal diameter
MP:0013620	increased internal diameter of femur
MP:0013621	decreased internal diameter of femur
MP:0013623	increased femur compact bone thickness
MP:0013624	decreased femur compact bone thickness
MP:0013626	decreased femur yield load
MP:0013630	increased bone trabecular spacing
MP:0013631	decreased bone trabecular spacing
MP:0013633	decreased femur maximal load
MP:0013638	decreased femur stiffness
MP:0013639	decreased bone stiffness
MP:0013640	increased bone stiffness
MP:0013646	decreased energy dissipated prior to femur fracture
MP:0013648	increased CD11b-high dendritic cell number
MP:0013649	decreased CD11b-high dendritic cell number
MP:0013651	increased CD11b-low dendritic cell number
MP:0013652	decreased CD11b-low dendritic cell number
MP:0013655	decreased CD103-positive CD11b-low dendritic cell number
MP:0013657	abnormal blood cell morphology
MP:0013659	abnormal erythroid lineage cell morphology
MP:0013662	decreased myeloid cell number
MP:0013666	decreased immature NK cell number
MP:0013669	decreased Ly6C-positive immature NK cell number
MP:0013673	increased mature NK cell number
MP:0013675	decreased Ly6C-positive mature NK cell number
MP:0013678	decreased Ly6C-positive NK T cell number
MP:0013679	increased Ly6C-positive NK T cell number
MP:0013684	increased early germinal center B cell number
MP:0013685	decreased late germinal center B cell number
MP:0013691	decreased CD5-positive Ly6C-positive T cell number
MP:0013692	increased CD5-positive Ly6C-positive T cell number
MP:0013693	abnormal hemopoiesis
MP:0013696	increased granulocyte monocyte progenitor cell number
MP:0013697	decreased granulocyte monocyte progenitor cell number
MP:0013701	abnormal mature B cell number
MP:0013704	increased megakaryocyte-erythroid progenitor cell number
MP:0013705	decreased megakaryocyte-erythroid progenitor cell number
MP:0013708	abnormal hematopoietic precursor cell number
MP:0013711	abnormal inguinal mammary gland morphology
MP:0013712	abnormal thoracic mammary gland morphology
MP:0013716	hypolactation
MP:0013717	hyperlactation
MP:0013718	galactostasis
MP:0013719	pale mammary gland
MP:0013720	abnormal mammary line morphology
MP:0013721	abnormal mammary placode morphology
MP:0013724	decreased circulating tyrosine level
MP:0013730	glutathionuria
MP:0013731	immature cataract
MP:0013733	squamous metaplasia of bulbourethral gland
MP:0013734	squamous metaplasia of preputial gland
MP:0013735	squamous metaplasia of urethral gland
MP:0013736	abnormal bulbourethral gland development
MP:0013737	small bulbourethral gland
MP:0013738	abnormal testis tunica albuginea morphology
MP:0013740	Meibomian gland hyperplasia
MP:0013741	absent thymus corticomedullary boundary
MP:0013742	absent ciliary body
MP:0013744	abnormal conjunctival sac morphology
MP:0013745	abnormal eyelid margin morphology
MP:0013751	increased cystadenoma incidence
MP:0013754	abnormal ocular surface morphology
MP:0013762	abnormal effector T cell number
MP:0013763	increased T-helper cell number
MP:0013765	iris hyperplasia
MP:0013766	absent palatal rugae
MP:0013767	decreased palatal rugae number
MP:0013768	decreased marginal zone precursor B cell number
MP:0013771	decreased effector memory T-helper cell number
MP:0013772	increased effector memory T-helper cell number
MP:0013774	decreased KLRG1-positive T-helper cell number
MP:0013775	increased KLRG1-positive T-helper cell number
MP:0013778	abnormal mammary gland myoepithelium morphology
MP:0013779	abnormal mammary gland myoepithelium physiology
MP:0013781	abnormal mammary gland luminal epithelium morphology
MP:0013782	abnormal mammary duct terminal end bud morphology
MP:0013784	abnormal mammary gland bud elongation
MP:0013785	abnormal mammary gland bud morphology
MP:0013788	external nares atresia
MP:0013792	abnormal small intestine goblet cell morphology
MP:0013794	abnormal intestinal villus goblet cell morphology
MP:0013795	abnormal colon goblet cell morphology
MP:0013796	abnormal duodenal goblet cell morphology
MP:0013797	abnormal ileal goblet cell morphology
MP:0013798	abnormal jeujunal goblet cell morphology
MP:0013799	abnormal intestinal goblet cell physiology
MP:0013802	abnormal IgG2 level
MP:0013803	increased IgG2 level
MP:0013808	abnormal tunnel of Corti morphology
MP:0013809	absent pectinate muscle
MP:0013810	absent brachiocephalic trunk
MP:0013812	enlarged orbital veins
MP:0013813	dilated hepatic portal vein
MP:0013814	abnormal hepatic portal vein connection
MP:0013815	abnormal digastric muscle morphology
MP:0013818	abnormal oral cavity morphology
MP:0013820	absent optic cup
MP:0013823	absent segment of anterior cerebral artery
MP:0013824	abnormal hypoglossal canal morphology
MP:0013825	small hypoglossal canal
MP:0013826	absent hypoglossal canal
MP:0013827	thin oculomotor nerve
MP:0013828	thin facial nerve
MP:0013829	thin splanchnic nerve
MP:0013830	abnormal intrathoracic topology of vagus nerve
MP:0013831	vagus nerve compression
MP:0013832	thin vagus nerve
MP:0013833	absent olfactory nerve
MP:0013834	thin hypoglossal nerve
MP:0013835	absent hypoglossal nerve
MP:0013836	abnormal hypoglossal nerve topology
MP:0013840	absent segment of posterior cerebral artery
MP:0013841	abnormal lymphatic vessel topology
MP:0013842	ductus venosus stenosis
MP:0013843	hepatic portal vein stenosis
MP:0013844	abnormal perichondrial ossification
MP:0013845	abnormal eye muscle topology
MP:0013846	retropharyngeal edema
MP:0013847	retropleural edema
MP:0013848	subcutaneous edema
MP:0013849	absent abducens nerve
MP:0013850	absent posterior commissure
MP:0013851	abnormal Wolffian duct topology
MP:0013852	abnormal Mullerian duct topology
MP:0013853	abnormal hepatic portal vein formation
MP:0013855	absent celiac artery
MP:0013857	abnormal abdominal muscle morphology
MP:0013858	abnormal azygos vein topology
MP:0013859	abnormal vitelline vein connection
MP:0013860	anastomosis between common carotid and vertebral artery
MP:0013861	abnormal pancreas topology
MP:0013862	abnormal cecum position
MP:0013864	enlarged paraumbilical vein
MP:0013865	abnormal dorsal pancreas topology
MP:0013867	abnormal ventral pancreas morphology
MP:0013871	abnormal stapedial artery topology
MP:0013873	abnormal ductus venosus morphology
MP:0013874	abnormal ductus venosus topology
MP:0013875	trigeminal neuroma
MP:0013876	absent ductus venosus valve
MP:0013877	abnormal ductus venosus valve morphology
MP:0013878	abnormal ductus venosus valve topology
MP:0013879	duplication of ductus venosus
MP:0013883	increased CD4-positive, CD25-positive NK T cell number
MP:0013891	increased common myeloid progenitor cell number
MP:0013892	increased common lymphocyte progenitor cell number
MP:0013893	decreased common lymphocyte progenitor cell number
MP:0013894	abnormal behavioral response to amphetamine
MP:0013897	decreased eyelid cilium number
MP:0013899	abnormal seminal vesicle epithelium morphology
MP:0013900	seminal vesicle epithelium degeneration
MP:0013901	absent female preputial gland
MP:0013903	abnormal seminal vesicle fluid composition
MP:0013904	abnormal seminal vesicle muscle layer morphology
MP:0013905	preputial gland inflammation
MP:0013906	absent embryonic telencephalon
MP:0013907	abnormal cerebrospinal fluid flow
MP:0013908	small lateral ventricles
MP:0013912	abnormal circardian rhythm entrainment
MP:0013913	absent costovertebral joint
MP:0013914	absent intracranial segment of vertebral artery
MP:0013915	abnormal brachial plexus formation
MP:0013916	decreased intestine length
MP:0013917	persistent right 6th pharyngeal arch artery
MP:0013918	abnormal endolymphatic sac topology
MP:0013923	small prevertebral sympathetic ganglia
MP:0013924	abnormal dural venous sinus morphology
MP:0013925	abnormal vascular plexus formation
MP:0013927	abnormal facial nerve topology
MP:0013928	thin motoric part of trigeminal nerve
MP:0013929	absent eye muscles
MP:0013930	abnormal digastric muscle connection
MP:0013931	abnormal olfactory bulb position
MP:0013932	fragmented Meckel's cartilage
MP:0013933	short Meckel's cartilage
MP:0013935	basal brain tissue herniation
MP:0013936	abnormal thymus topology
MP:0013937	absent lobe of thyroid gland
MP:0013941	abnormal enthesis morphology
MP:0013943	abnormal ureter topology
MP:0013945	abnormal elbow joint morphology
MP:0013948	intraembryonal intestine elongation
MP:0013949	fusion of axis and occipital bones
MP:0013950	abnormal dorsal root ganglion topology
MP:0013952	retro-esophageal left subclavian artery
MP:0013953	left sided brachiocephalic trunk
MP:0013955	increased colon length
MP:0013956	decreased colon length
MP:0013957	increased small intestine length
MP:0013958	decreased small intestine length
MP:0013959	increased large intestine length
MP:0013961	abnormal Hensen stripe morphology
MP:0013962	absent Hensen stripe
MP:0013963	jugular vein stenosis
MP:0013965	abnormally deep median sulcus of tongue
MP:0013966	abnormal infrahyoid muscle morphology
MP:0013967	abnormal infrahyoid muscle connection
MP:0013968	multiple persisting craniopharyngeal ducts
MP:0013969	reduced sympathetic cervical ganglion size
MP:0013970	absent connection between subcutaneous lymph vessels and lymph sac
MP:0013971	blood in lymph vessels
MP:0013973	abnormal hepatic vein connection
MP:0013975	abnormal coronary sinus connection
MP:0013976	abnormal left vena cava superior connection
MP:0013977	symmetric azygos veins
MP:0013978	abnormal carotid artery origin
MP:0013979	abnormal subclavian artery origin
MP:0013980	abnormal pulmonary artery origin
MP:0013981	double lumen aortic arch
MP:0013982	inverse situs of great intrathoracic arteries
MP:0013985	abnormal umbilical vein topology
MP:0013986	abnormal vitelline vein topology
MP:0013987	absent intrahepatic inferior vena cava segment
MP:0013988	absent portal vein segment
MP:0013992	persistent dorsal ophthalmic artery
MP:0013994	abnormal parasellar internal carotid artery branch morphology
MP:0013995	abnormal external carotid artery origin
MP:0013996	abnormal vertebral artery origin
MP:0013997	abnormal internal carotid artery topology
MP:0013998	absent canalicular internal carotid artery segment
MP:0013999	absent parasellar internal carotid artery
MP:0014000	anastomosis between internal carotid artery and basilar artery
MP:0014001	abnormal vertebral artery topology
MP:0014002	absent extracranial vertebral artery segment
MP:0014003	additional anastomosis between intracranial vertebral arteries
MP:0014004	absent basilar artery segment
MP:0014006	absent posterior communicating artery
MP:0014009	anastomosis between middle cerebral arteries
MP:0014010	abnormal peroxisome morphology
MP:0014011	abnormal ovary tissue architecture
MP:0014012	abnormal cranial blood vasculature morphology
MP:0014017	abnormal Wolffian duct connection
MP:0014018	embryo tumor
MP:0014019	embryo cyst
MP:0014021	heterochrony
MP:0014022	abnormal duodenum topology
MP:0014023	abnormal intestine placement
MP:0014026	abnormal respiratory epithelial transmembrane transport
MP:0014028	decreased respiratory epithelial chloride transmembrane transport
MP:0014033	abnormal submucosal gland morphology
MP:0014038	increased hepatocyte number
MP:0014040	increased cellular sensitivity to DNA damaging agents
MP:0014044	absent cardiac outflow tract
MP:0014045	Mallory bodies
MP:0014046	abnormal mitophagy
MP:0014049	increased T cell acute lymphoblastic leukemia incidence
MP:0014051	abnormal maxillary-premaxillary suture morphology
MP:0014052	increased male germ cell apoptosis
MP:0014056	increased sebocyte proliferation
MP:0014057	abnormal mammary gland stroma morphology
MP:0014059	abnormal photoreceptor connecting cilium morphology
MP:0014060	abnormal platelet alpha-granule morphology
MP:0014062	nervous system inclusion bodies
MP:0014071	increased cardiac muscle glycogen level
MP:0014074	increased brain glycogen level
MP:0014075	decreased brain glycogen level
MP:0014076	absent Paneth cells
MP:0014077	ectopic Paneth cells
MP:0014079	decreased small intestinal villus number
MP:0014080	fused small intestinal villi
MP:0014081	branched small intestinal villi
MP:0014082	decreased small intestinal villus height
MP:0014083	blunted small intestinal villi
MP:0014085	stomach non-glandular epithelium hyperkeratosis
MP:0014088	abnormal Kimura membrane morphology
MP:0014089	abnormal tectorial membrane marginal band morphology
MP:0014090	abnormal tectorial membrane covernet morphology
MP:0014091	abnormal tectorial membrane striated-sheet matrix morphology
MP:0014098	decreased pancreatic amylase secretion
MP:0014100	increased chondrocyte proliferation
MP:0014101	decreased chondrocyte proliferation
MP:0014103	increased chondrocyte apoptosis
MP:0014105	abnormal chondrocyte differentiation
MP:0014106	delayed chondrocyte differentiation
MP:0014115	cognitive inflexibility
MP:0014117	increased pancreatic beta cell apoptosis
MP:0014118	decreased pancreatic beta cell apoptosis
MP:0014119	abnormal mandibular nerve innervation pattern
MP:0014121	increased pancreatic islet cell apoptosis
MP:0014122	decreased pancreatic islet cell apoptosis
MP:0014124	increased amylin secretion
MP:0014125	decreased amylin secretion
MP:0014126	increased mammary gland apoptosis
MP:0014128	increased Harderian gland adenocarcinoma incidence
MP:0014129	thymus fibrosis
MP:0014130	thymus cysts
MP:0014134	abnormal embryo morphology
MP:0014142	increased body fat mass
MP:0014143	decreased body fat mass
MP:0014144	abnormal white adipose tissue mass
MP:0014145	increased white adipose tissue mass
MP:0014146	decreased white adipose tissue mass
MP:0014147	lacrimal gland necrosis
MP:0014148	lacrimal gland degeneration
MP:0014149	abnormal lacrimal gland innervation pattern
MP:0014152	absent exorbital lacrimal gland
MP:0014153	absent intraorbital lacrimal gland
MP:0014154	Meibomian gland degeneration
MP:0014155	absent olfactory epithelium
MP:0014158	esophagus fibrosis
MP:0014159	stomach fibrosis
MP:0014163	abnormal ciliary muscle morphology
MP:0014164	abnormal ciliary process morphology
MP:0014165	absent ciliary process
MP:0014166	ectopic cranial bone
MP:0014167	ectopic bone
MP:0014168	abnormal brown adipose tissue mass
MP:0014169	decreased brown adipose tissue mass
MP:0014171	increased fatty acid oxidation
MP:0014172	decreased fatty acid oxidation
MP:0014173	increased fatty acid beta-oxidation
MP:0014174	decreased fatty acid beta-oxidation
MP:0014175	abnormal ciliary epithelium morphology
MP:0014176	abnormal cilary zonule morphology
MP:0014178	increased brain apoptosis
MP:0014179	abnormal blood-retinal barrier function
MP:0014180	abnormal thymus apoptosis
MP:0014181	abnormal respiratory epithelial sodium ion transmembrane transport
MP:0014182	decreased respiratory epithelial sodium ion transmembrane transport
MP:0014183	increased respiratory epithelial sodium ion transmembrane transport
MP:0014193	decreased epididymal cell proliferation
MP:0014194	increased epididymal epithelium cell proliferation
MP:0014198	absent pituitary infundibular stalk
MP:0014200	abnormal respiratory epithelium physiology
MP:0014201	abnormal intestinal epithelium physiology
MP:0014206	decreased intestinal epithelial sodium ion transmembrane transport
MP:0014208	decreased intestinal epithelial chloride transmembrane transport
MP:0014219	decreased intestinal mucosa thickness
MP:0014222	decreased colon goblet cell number
MP:0014224	increased ileal goblet cell number
MP:0014226	abnormal alveolar macrophage physiology
MP:0014228	increased alveolar macrophage number
MP:0014230	dilated crypts of Lieberkuhn
MP:0014231	intestinal mucus accumulation
MP:0014232	pancreatic acinus dilation
MP:0014233	bile duct epithelium hyperplasia
MP:0020001	decreased response to antigen
MP:0020002	increased response to antigen
MP:0020010	decreased bone mineral density of femur
MP:0020011	increased bone mineral density of femur
MP:0020016	decreased aldehyde dehydrogenase activity
MP:0020039	increased bone ossification
MP:0020040	decreased bone ossification
MP:0020066	abnormal neocortex size
MP:0020067	increased neocortex size
MP:0020069	decreased neocortex size
MP:0020070	decreased neocortex volume
MP:0020078	decreased brain tyrosine 3-monooxygenase activity
MP:0020080	increased bone mineralization
MP:0020082	increased hippocampus volume
MP:0020083	decreased hippocampus volume
MP:0020087	increased susceptibility to non-insulin-dependent diabetes
MP:0020088	decreased susceptibility to non-insulin-dependent diabetes
MP:0020089	increased susceptibility to diet-induced non-insulin dependent diabetes
MP:0020090	decreased susceptibility to diet-induced non-insulin dependent diabetes
MP:0020101	abnormal hepatic glucose production
MP:0020102	increased hepatic glucose production
MP:0020103	decreased hepatic glucose production
MP:0020117	decreased sphingosine level
MP:0020126	decreased circulating HDL phospholipid level
MP:0020129	decreased circulating non-HDL phospholipid level
MP:0020134	abnormal gallbladder size
MP:0020135	abnormal heart ventricle wall thickness
MP:0020137	decreased bone mineralization
MP:0020138	delayed bone mineralization
MP:0020140	increased brain external capsule size
MP:0020141	decreased brain external capsule size
MP:0020142	increased anti-sperm antibody level
MP:0020151	abnormal circulating non-HDL cholesterol level
MP:0020152	abnormal oocyte number
MP:0020153	abnormal urine albumin level
MP:0020154	impaired humoral immune response
MP:0020155	enhanced humoral immune response
MP:0020157	abnormal behavioral response to alcohol
MP:0020160	abnormal behavioral response to nicotine
MP:0020161	increased vascular endothelial cell proliferation
MP:0020168	decreased thyroid gland weight
MP:0020169	increased thyroid gland weight
MP:0020174	abnormal IgG level
MP:0020175	abnormal IgG1 level
MP:0020183	altered susceptibility to fungal infection
MP:0020184	altered susceptibility to parasitic infection
MP:0020185	altered susceptibility to viral infection
MP:0020186	altered susceptibility to bacterial infection
MP:0020187	altered susceptibility to prion infection
MP:0020194	abnormal glycosphingolipid level
MP:0020211	slow movement
MP:0020213	enhanced leukocyte migration
MP:0020214	susceptible to malignant hyperthermia
MP:0020215	impaired blood coagulation
MP:0020216	decreased circulating complement protein level
MP:0020234	decreased basal metabolism
MP:0020237	increased proline level
MP:0020240	increased skeletal muscle cell apoptosis
MP:0020244	increased pyruvate kinase activity
MP:0020252	abnormal collagen level
MP:0020253	increased collagen level
MP:0020254	decreased collagen level
MP:0020280	increased creatine kinase level
MP:0020288	ectopic limbs
MP:0020301	short tongue
MP:0020309	increased creatine kinase activity
MP:0020316	decreased vascular endothelial cell proliferation
MP:0020318	increased vascular endothelial cell adhesion
MP:0020321	increased vascular endothelial cell apoptosis
MP:0020322	decreased vascular endothelial cell apoptosis
MP:0020326	dilated capillary
MP:0020327	abnormal capillary branching pattern
MP:0020329	decreased capillary density
MP:0020330	increased capillary density
MP:0020331	increased capillary tortuosity
MP:0020332	impaired leukocyte tethering or rolling
MP:0020333	enhanced leukocyte tethering or rolling
MP:0020335	abnormal dentate gyrus neuron dendrite morphology
MP:0020338	abnormal hippocampal pyramidal neuron dendrite morphology
MP:0020340	abnormal inhibitory learning
MP:0020344	abnormal susceptibility to injury induced morbidity/mortality
MP:0020345	abnormal myocardial fiber currents
MP:0020346	abnormal mycardial fiber calcium currents
MP:0020347	abnormal mycoardial fiber sodium currents
MP:0020348	decreased olfactory sensory neuron number
MP:0020350	fused pharyngeal arches
MP:0020351	decreased vocalization
MP:0020352	abnormal endoplasmic reticulum physiology
MP:0020353	abnormal endoplasmic reticulum stress
MP:0020354	increased endoplasmic reticulum stress
MP:0020355	abnormal Sertoli cell barrier morphology
MP:0020356	abnormal Sertoli cell barrier function
MP:0020357	abnormal excitatory synapse morphology
MP:0020358	abnormal inhibitory synapse morphology
MP:0020359	abnormal ribbon synapse morphology
MP:0020361	abnormal symmetric synapse morphology
MP:0020362	abnormal male germ cell physiology
MP:0020366	decreased brain iron level
MP:0020367	increased heart iron level
MP:0020368	decreased heart iron level
MP:0020369	increased intestinal iron level
MP:0020373	abnormal blood vessel lumen formation
MP:0020378	abnormal cell cytoskeleton morphology
MP:0020382	increased kidney epithelial cell primary cilium length
MP:0020383	decreased kidney epithelial cell primary cilium length
MP:0020384	absent kidney epithelial cell primary cilium
MP:0020385	decreased intestinal iron level
MP:0020386	adipose tissue inflammation
MP:0020388	decreased radial glial cell number
MP:0020389	increased radial glial cell number
MP:0020390	abnormal radial glial cell endfoot morphology
MP:0020391	radial glial endfoot detachment
MP:0020392	abnormal radial glial cell apoptosis
MP:0020393	increased neuronal precursor proliferation
MP:0020394	decreased neuronal precursor proliferation
MP:0020395	abnormal response to social novelty
MP:0020396	abnormal social recognition
MP:0020399	enhanced megakaryocyte emperipolesis
MP:0020401	argininuria
MP:0020407	abnormal placental thrombosis
MP:0020408	altered susceptibility to induced thrombosis
MP:0020409	abnormal cardiac thrombosis
MP:0020411	increased abdominal adipose tissue amount
MP:0020413	increased amnion apoptosis
MP:0020414	abnormal fibroblast physiology
MP:0020415	abnormal fibroblast chemotaxis
MP:0020416	decreased fibroblast chemotaxis
MP:0020417	increased fibroblast chemotaxis
MP:0020419	decreased cardiac muscle relaxation
MP:0020421	increased freezing behavior
MP:0020426	abnormal beige fat cell physiology
MP:0020427	increased hepatocyte karyomegaly
MP:0020431	decreased platelet alpha-granule number
MP:0020432	decreased platelet dense granule number
MP:0020434	increased astrocyte size
MP:0030000	abnormal subglottis morphology
MP:0030002	increased lung apoptosis
MP:0030003	hippocampus atrophy
MP:0030004	hippocampus hypoplasia
MP:0030005	increased retinal apoptosis
MP:0030006	decreased retinal apoptosis
MP:0030007	abnormal bone marrow adipose tissue morphology
MP:0030009	increased bone marrow adipose tissue amount
MP:0030011	small cervical lymph nodes
MP:0030012	impaired central nervous system regeneration
MP:0030013	improved central nervous system regeneration
MP:0030014	calcified brain
MP:0030016	increased adipocyte glucose uptake
MP:0030017	decreased adipocyte glucose uptake
MP:0030018	increased cardiac cell glucose uptake
MP:0030020	decreased cardiac cell glucose uptake
MP:0030021	increased muscle cell glucose uptake
MP:0030022	decreased muscle cell glucose uptake
MP:0030024	abnormal meiotic attachment of telomere to nuclear envelope
MP:0030026	small Meckel's cartilage
MP:0030027	basioccipital bone hypoplasia
MP:0030028	absent exoccipital bone
MP:0030030	Wormian bones
MP:3000003	abnormal Ebner's gland morphology