FBcv:0000002	thermotaxis defective
FBcv:0000384	aging defective
FBcv:0000403	chemosensitive behavior defective
FBcv:0000424	cell death defective
FBcv:0000427	cell growth defective
FBcv:0000431	meiotic cell cycle defective
FBcv:0000439	chemical resistant
FBcv:0000440	chemical sensitive
FBcv:0000683	temperature response defective
FBcv:0001324	endocytosis defective
FBcv:0001325	exocytosis defective
FBcv:0006000	copulation defective
FBcv:0006004	oviposition defective
GO:0000003PHENOTYPE	reproduction phenotype
GO:0000070PHENOTYPE	mitotic sister chromatid segregation phenotype
GO:0000077PHENOTYPE	DNA damage checkpoint phenotype
GO:0000122PHENOTYPE	negative regulation of transcription from RNA polymerase II promoter phenotype
GO:0000132PHENOTYPE	establishment of mitotic spindle orientation phenotype
GO:0000226PHENOTYPE	microtubule cytoskeleton organization phenotype
GO:0000266PHENOTYPE	mitochondrial fission phenotype
GO:0000280PHENOTYPE	nuclear division phenotype
GO:0000281PHENOTYPE	mitotic cytokinesis phenotype
GO:0000380PHENOTYPE	alternative mRNA splicing, via spliceosome phenotype
GO:0000381PHENOTYPE	regulation of alternative mRNA splicing, via spliceosome phenotype
GO:0000478PHENOTYPE	endonucleolytic cleavage involved in rRNA processing 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:0000902PHENOTYPE	cell morphogenesis phenotype
GO:0000956PHENOTYPE	nuclear-transcribed mRNA catabolic process phenotype
GO:0001508PHENOTYPE	action potential phenotype
GO:0001556PHENOTYPE	oocyte maturation phenotype
GO:0001666PHENOTYPE	response to hypoxia phenotype
GO:0001708PHENOTYPE	cell fate specification phenotype
GO:0001709PHENOTYPE	cell fate determination phenotype
GO:0001712PHENOTYPE	ectodermal cell fate commitment phenotype
GO:0001714PHENOTYPE	endodermal cell fate specification phenotype
GO:0001764PHENOTYPE	neuron migration phenotype
GO:0001845PHENOTYPE	phagolysosome assembly phenotype
GO:0001881PHENOTYPE	receptor recycling phenotype
GO:0001932PHENOTYPE	regulation of protein phosphorylation phenotype
GO:0001966PHENOTYPE	thigmotaxis phenotype
GO:0002009PHENOTYPE	morphogenesis of an epithelium phenotype
GO:0002064PHENOTYPE	epithelial cell development phenotype
GO:0002119PHENOTYPE	nematode larval development phenotype
GO:0003990PHENOTYPE	acetylcholinesterase activity phenotype
GO:0004096PHENOTYPE	catalase activity phenotype
GO:0004674PHENOTYPE	protein serine/threonine kinase activity phenotype
GO:0005391PHENOTYPE	sodium:potassium-exchanging ATPase activity phenotype
GO:0005829PHENOTYPE	cytosol phenotype
GO:0005886PHENOTYPE	plasma membrane phenotype
GO:0005977PHENOTYPE	glycogen metabolic process phenotype
GO:0006112PHENOTYPE	energy reserve metabolic process phenotype
GO:0006120PHENOTYPE	mitochondrial electron transport, NADH to ubiquinone phenotype
GO:0006281PHENOTYPE	DNA repair phenotype
GO:0006298PHENOTYPE	mismatch repair phenotype
GO:0006302PHENOTYPE	double-strand break repair phenotype
GO:0006309PHENOTYPE	apoptotic DNA fragmentation 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:0006412PHENOTYPE	translation phenotype
GO:0006468PHENOTYPE	protein phosphorylation phenotype
GO:0006493PHENOTYPE	protein O-linked glycosylation phenotype
GO:0006585PHENOTYPE	dopamine biosynthetic process from tyrosine phenotype
GO:0006611PHENOTYPE	protein export from nucleus phenotype
GO:0006629PHENOTYPE	lipid metabolic process phenotype
GO:0006813PHENOTYPE	potassium ion transport phenotype
GO:0006814PHENOTYPE	sodium ion transport phenotype
GO:0006816PHENOTYPE	calcium ion transport phenotype
GO:0006874PHENOTYPE	cellular calcium ion homeostasis phenotype
GO:0006888PHENOTYPE	ER to Golgi vesicle-mediated transport phenotype
GO:0006897PHENOTYPE	endocytosis phenotype
GO:0006898PHENOTYPE	receptor-mediated endocytosis phenotype
GO:0006914PHENOTYPE	autophagy phenotype
GO:0006915PHENOTYPE	apoptotic process phenotype
GO:0006935PHENOTYPE	chemotaxis phenotype
GO:0006936PHENOTYPE	muscle contraction phenotype
GO:0006937PHENOTYPE	regulation of muscle contraction phenotype
GO:0006970PHENOTYPE	response to osmotic stress phenotype
GO:0006974PHENOTYPE	cellular response to DNA damage stimulus phenotype
GO:0006979PHENOTYPE	response to oxidative stress phenotype
GO: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:0007009PHENOTYPE	plasma membrane organization phenotype
GO:0007015PHENOTYPE	actin filament organization phenotype
GO:0007017PHENOTYPE	microtubule-based process phenotype
GO:0007040PHENOTYPE	lysosome organization phenotype
GO:0007052PHENOTYPE	mitotic spindle organization phenotype
GO:0007059PHENOTYPE	chromosome segregation phenotype
GO:0007064PHENOTYPE	mitotic sister chromatid cohesion phenotype
GO:0007076PHENOTYPE	mitotic chromosome condensation phenotype
GO:0007079PHENOTYPE	mitotic chromosome movement towards spindle pole phenotype
GO:0007080PHENOTYPE	mitotic metaphase plate congression phenotype
GO:0007097PHENOTYPE	nuclear migration phenotype
GO:0007098PHENOTYPE	centrosome cycle phenotype
GO:0007099PHENOTYPE	centriole replication phenotype
GO:0007100PHENOTYPE	mitotic centrosome separation phenotype
GO:0007131PHENOTYPE	reciprocal meiotic recombination phenotype
GO:0007140PHENOTYPE	male meiosis phenotype
GO:0007155PHENOTYPE	cell adhesion phenotype
GO:0007163PHENOTYPE	establishment or maintenance of cell polarity phenotype
GO:0007219PHENOTYPE	Notch signaling pathway phenotype
GO:0007267PHENOTYPE	cell-cell signaling phenotype
GO:0007268PHENOTYPE	synaptic transmission phenotype
GO:0007269PHENOTYPE	neurotransmitter secretion 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:0007286PHENOTYPE	spermatid development phenotype
GO:0007338PHENOTYPE	single fertilization phenotype
GO:0007346PHENOTYPE	regulation of mitotic cell cycle phenotype
GO:0007368PHENOTYPE	determination of left/right symmetry phenotype
GO:0007369PHENOTYPE	gastrulation phenotype
GO:0007389PHENOTYPE	pattern specification process phenotype
GO:0007399PHENOTYPE	nervous system development phenotype
GO:0007409PHENOTYPE	axonogenesis phenotype
GO:0007411PHENOTYPE	axon guidance phenotype
GO:0007413PHENOTYPE	axonal fasciculation phenotype
GO:0007501PHENOTYPE	mesodermal cell fate specification phenotype
GO:0007517PHENOTYPE	muscle organ development phenotype
GO:0007538PHENOTYPE	primary sex determination phenotype
GO:0007548PHENOTYPE	sex differentiation phenotype
GO:0007588PHENOTYPE	excretion phenotype
GO:0007606PHENOTYPE	sensory perception of chemical stimulus phenotype
GO:0007611PHENOTYPE	learning or memory phenotype
GO:0007617PHENOTYPE	mating behavior phenotype
GO:0007618PHENOTYPE	mating phenotype
GO:0007622PHENOTYPE	rhythmic behavior phenotype
GO:0007626PHENOTYPE	locomotory behavior phenotype
GO:0007631PHENOTYPE	feeding behavior phenotype
GO:0007635PHENOTYPE	chemosensory behavior phenotype
GO:0007638PHENOTYPE	mechanosensory behavior phenotype
GO:0008045PHENOTYPE	motor neuron axon guidance phenotype
GO:0008078PHENOTYPE	mesodermal cell migration phenotype
GO:0008088PHENOTYPE	axon cargo transport phenotype
GO:0008089PHENOTYPE	anterograde axon cargo transport phenotype
GO:0008104PHENOTYPE	protein localization phenotype
GO:0008285PHENOTYPE	negative regulation of cell proliferation phenotype
GO:0008306PHENOTYPE	associative learning phenotype
GO:0008340PHENOTYPE	determination of adult lifespan phenotype
GO:0008355PHENOTYPE	olfactory learning phenotype
GO:0008356PHENOTYPE	asymmetric cell division phenotype
GO:0008361PHENOTYPE	regulation of cell size phenotype
GO:0008406PHENOTYPE	gonad development 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:0008610PHENOTYPE	lipid biosynthetic process phenotype
GO:0008630PHENOTYPE	intrinsic apoptotic signaling pathway in response to DNA damage phenotype
GO:0008757PHENOTYPE	S-adenosylmethionine-dependent methyltransferase activity phenotype
GO:0009100PHENOTYPE	glycoprotein metabolic process phenotype
GO:0009306PHENOTYPE	protein secretion phenotype
GO:0009314PHENOTYPE	response to radiation phenotype
GO:0009408PHENOTYPE	response to heat phenotype
GO:0009411PHENOTYPE	response to UV phenotype
GO:0009593PHENOTYPE	detection of chemical stimulus phenotype
GO:0009612PHENOTYPE	response to mechanical stimulus phenotype
GO:0009636PHENOTYPE	response to toxic substance phenotype
GO:0009791PHENOTYPE	post-embryonic development phenotype
GO:0009792PHENOTYPE	embryo development ending in birth or egg hatching phenotype
GO:0009880PHENOTYPE	embryonic pattern specification phenotype
GO:0009887PHENOTYPE	organ morphogenesis phenotype
GO:0009948PHENOTYPE	anterior/posterior axis specification phenotype
GO:0009952PHENOTYPE	anterior/posterior pattern specification phenotype
GO:0009954PHENOTYPE	proximal/distal pattern formation phenotype
GO:0009957PHENOTYPE	epidermal cell fate specification phenotype
GO:0010035PHENOTYPE	response to inorganic substance phenotype
GO:0010038PHENOTYPE	response to metal ion phenotype
GO:0010070PHENOTYPE	zygote asymmetric cell division 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:0010248PHENOTYPE	establishment or maintenance of transmembrane electrochemical gradient phenotype
GO:0010452PHENOTYPE	histone H3-K36 methylation phenotype
GO:0010468PHENOTYPE	regulation of gene expression phenotype
GO:0010506PHENOTYPE	regulation of autophagy phenotype
GO:0010628PHENOTYPE	positive regulation of gene expression phenotype
GO:0010629PHENOTYPE	negative regulation of gene expression phenotype
GO:0014018PHENOTYPE	neuroblast fate specification phenotype
GO:0014055PHENOTYPE	acetylcholine secretion, neurotransmission phenotype
GO:0015012PHENOTYPE	heparan sulfate proteoglycan biosynthetic process phenotype
GO:0015464PHENOTYPE	acetylcholine receptor activity phenotype
GO:0015833PHENOTYPE	peptide transport phenotype
GO:0015837PHENOTYPE	amine transport phenotype
GO:0016050PHENOTYPE	vesicle organization phenotype
GO:0016051PHENOTYPE	carbohydrate biosynthetic process phenotype
GO:0016055PHENOTYPE	Wnt signaling pathway phenotype
GO:0016079PHENOTYPE	synaptic vesicle exocytosis phenotype
GO:0016125PHENOTYPE	sterol metabolic process phenotype
GO:0016126PHENOTYPE	sterol biosynthetic process phenotype
GO:0016197PHENOTYPE	endosomal transport phenotype
GO:0016203PHENOTYPE	muscle attachment phenotype
GO:0016236PHENOTYPE	macroautophagy phenotype
GO:0016246PHENOTYPE	RNA interference phenotype
GO:0016331PHENOTYPE	morphogenesis of embryonic epithelium phenotype
GO:0016441PHENOTYPE	posttranscriptional gene silencing phenotype
GO:0016477PHENOTYPE	cell migration phenotype
GO:0016485PHENOTYPE	protein processing phenotype
GO:0016567PHENOTYPE	protein ubiquitination phenotype
GO:0016783PHENOTYPE	sulfurtransferase activity phenotype
GO:0017148PHENOTYPE	negative regulation of translation phenotype
GO:0018991PHENOTYPE	oviposition phenotype
GO:0019217PHENOTYPE	regulation of fatty acid metabolic process phenotype
GO:0019538PHENOTYPE	protein metabolic process phenotype
GO:0019915PHENOTYPE	lipid storage phenotype
GO:0019953PHENOTYPE	sexual reproduction phenotype
GO:0022604PHENOTYPE	regulation of cell morphogenesis phenotype
GO:0030010PHENOTYPE	establishment of cell polarity phenotype
GO:0030031PHENOTYPE	cell projection assembly phenotype
GO:0030036PHENOTYPE	actin cytoskeleton organization phenotype
GO:0030104PHENOTYPE	water homeostasis phenotype
GO:0030155PHENOTYPE	regulation of cell adhesion phenotype
GO:0030182PHENOTYPE	neuron differentiation phenotype
GO:0030198PHENOTYPE	extracellular matrix organization phenotype
GO:0030199PHENOTYPE	collagen fibril organization phenotype
GO:0030206PHENOTYPE	chondroitin sulfate biosynthetic process phenotype
GO:0030238PHENOTYPE	male sex determination phenotype
GO:0030240PHENOTYPE	skeletal muscle thin filament assembly phenotype
GO:0030241PHENOTYPE	skeletal muscle myosin thick filament assembly phenotype
GO:0030301PHENOTYPE	cholesterol transport phenotype
GO:0030308PHENOTYPE	negative regulation of cell growth phenotype
GO:0030334PHENOTYPE	regulation of cell migration phenotype
GO:0030421PHENOTYPE	defecation phenotype
GO:0030431PHENOTYPE	sleep phenotype
GO:0030703PHENOTYPE	eggshell formation phenotype
GO:0030728PHENOTYPE	ovulation phenotype
GO:0030866PHENOTYPE	cortical actin cytoskeleton organization phenotype
GO:0030953PHENOTYPE	astral microtubule organization phenotype
GO:0030968PHENOTYPE	endoplasmic reticulum unfolded protein response phenotype
GO:0031032PHENOTYPE	actomyosin structure organization phenotype
GO:0031034PHENOTYPE	myosin filament assembly phenotype
GO:0031103PHENOTYPE	axon regeneration phenotype
GO:0031124PHENOTYPE	mRNA 3'-end processing phenotype
GO:0031175PHENOTYPE	neuron projection development phenotype
GO:0031268PHENOTYPE	pseudopodium organization phenotype
GO:0031344PHENOTYPE	regulation of cell projection organization phenotype
GO:0031647PHENOTYPE	regulation of protein stability phenotype
GO:0031929PHENOTYPE	TOR signaling phenotype
GO:0031987PHENOTYPE	locomotion involved in locomotory behavior phenotype
GO:0032094PHENOTYPE	response to food phenotype
GO:0032456PHENOTYPE	endocytic recycling phenotype
GO:0032504PHENOTYPE	multicellular organism reproduction phenotype
GO:0032880PHENOTYPE	regulation of protein localization phenotype
GO:0032956PHENOTYPE	regulation of actin cytoskeleton organization phenotype
GO:0033314PHENOTYPE	mitotic DNA replication checkpoint phenotype
GO:0033365PHENOTYPE	protein localization to organelle phenotype
GO:0033563PHENOTYPE	dorsal/ventral axon guidance phenotype
GO:0033564PHENOTYPE	anterior/posterior axon guidance phenotype
GO:0034220PHENOTYPE	ion transmembrane transport phenotype
GO:0034394PHENOTYPE	protein localization to cell surface phenotype
GO:0034599PHENOTYPE	cellular response to oxidative stress phenotype
GO:0034607PHENOTYPE	turning behavior involved in mating phenotype
GO:0034613PHENOTYPE	cellular protein localization phenotype
GO:0034976PHENOTYPE	response to endoplasmic reticulum stress phenotype
GO:0035046PHENOTYPE	pronuclear migration phenotype
GO:0035150PHENOTYPE	regulation of tube size phenotype
GO:0035176PHENOTYPE	social behavior phenotype
GO:0035177PHENOTYPE	larval foraging behavior phenotype
GO:0035195PHENOTYPE	gene silencing by miRNA phenotype
GO:0035264PHENOTYPE	multicellular organism growth phenotype
GO:0035295PHENOTYPE	tube development phenotype
GO:0035418PHENOTYPE	protein localization to synapse phenotype
GO:0035545PHENOTYPE	determination of left/right asymmetry in nervous system phenotype
GO:0035966PHENOTYPE	response to topologically incorrect protein phenotype
GO:0040001PHENOTYPE	establishment of mitotic spindle localization phenotype
GO:0040009PHENOTYPE	regulation of growth rate phenotype
GO:0040010PHENOTYPE	positive 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:0040022PHENOTYPE	feminization of hermaphroditic germ-line phenotype
GO:0040024PHENOTYPE	dauer larval development phenotype
GO:0040025PHENOTYPE	vulval development phenotype
GO:0040034PHENOTYPE	regulation of development, heterochronic phenotype
GO:0040036PHENOTYPE	regulation of fibroblast growth factor receptor signaling pathway phenotype
GO:0040038PHENOTYPE	polar body extrusion after meiotic divisions phenotype
GO:0040040PHENOTYPE	thermosensory behavior phenotype
GO:0042048PHENOTYPE	olfactory behavior phenotype
GO:0042073PHENOTYPE	intraciliary transport phenotype
GO:0042074PHENOTYPE	cell migration involved in gastrulation phenotype
GO:0042127PHENOTYPE	regulation of cell proliferation phenotype
GO:0042176PHENOTYPE	regulation of protein catabolic process phenotype
GO:0042391PHENOTYPE	regulation of membrane potential phenotype
GO:0042407PHENOTYPE	cristae formation phenotype
GO:0042417PHENOTYPE	dopamine metabolic process phenotype
GO:0042438PHENOTYPE	melanin biosynthetic process phenotype
GO:0042490PHENOTYPE	mechanoreceptor differentiation phenotype
GO:0042493PHENOTYPE	response to drug phenotype
GO:0042594PHENOTYPE	response to starvation phenotype
GO:0042659PHENOTYPE	regulation of cell fate specification phenotype
GO:0042692PHENOTYPE	muscle cell differentiation phenotype
GO:0042693PHENOTYPE	muscle cell fate commitment phenotype
GO:0042694PHENOTYPE	muscle cell fate specification phenotype
GO:0042713PHENOTYPE	sperm ejaculation phenotype
GO:0042755PHENOTYPE	eating behavior phenotype
GO:0042771PHENOTYPE	intrinsic apoptotic signaling pathway in response to DNA damage by p53 class mediator phenotype
GO:0042776PHENOTYPE	mitochondrial ATP synthesis coupled proton transport phenotype
GO:0042789PHENOTYPE	mRNA transcription from RNA polymerase II promoter phenotype
GO:0043025PHENOTYPE	neuronal cell body phenotype
GO:0043050PHENOTYPE	pharyngeal pumping phenotype
GO:0043052PHENOTYPE	thermotaxis phenotype
GO:0043053PHENOTYPE	dauer entry phenotype
GO:0043054PHENOTYPE	dauer exit phenotype
GO:0043057PHENOTYPE	backward locomotion phenotype
GO:0043065PHENOTYPE	positive regulation of apoptotic process phenotype
GO:0043066PHENOTYPE	negative regulation of apoptotic process phenotype
GO:0043067PHENOTYPE	regulation of programmed cell death phenotype
GO:0043068PHENOTYPE	positive regulation of programmed cell death phenotype
GO:0043069PHENOTYPE	negative regulation of programmed cell death phenotype
GO:0043087PHENOTYPE	regulation of GTPase activity phenotype
GO:0043161PHENOTYPE	proteasome-mediated ubiquitin-dependent protein catabolic process phenotype
GO:0043277PHENOTYPE	apoptotic cell clearance phenotype
GO:0043279PHENOTYPE	response to alkaloid phenotype
GO:0043282PHENOTYPE	pharyngeal muscle development phenotype
GO:0043414PHENOTYPE	macromolecule methylation phenotype
GO:0043476PHENOTYPE	pigment accumulation phenotype
GO:0043570PHENOTYPE	maintenance of DNA repeat elements phenotype
GO:0043652PHENOTYPE	engulfment of apoptotic cell phenotype
GO:0043970PHENOTYPE	histone H3-K9 acetylation phenotype
GO:0045087PHENOTYPE	innate immune response phenotype
GO:0045089PHENOTYPE	positive regulation of innate immune response phenotype
GO:0045132PHENOTYPE	meiotic chromosome segregation phenotype
GO:0045143PHENOTYPE	homologous chromosome segregation phenotype
GO:0045165PHENOTYPE	cell fate commitment phenotype
GO:0045167PHENOTYPE	asymmetric protein localization involved in cell fate determination phenotype
GO:0045168PHENOTYPE	cell-cell signaling involved in cell fate commitment phenotype
GO:0045176PHENOTYPE	apical protein localization phenotype
GO:0045184PHENOTYPE	establishment of protein localization phenotype
GO:0045185PHENOTYPE	maintenance of protein location phenotype
GO:0045214PHENOTYPE	sarcomere organization phenotype
GO:0045217PHENOTYPE	cell-cell junction maintenance phenotype
GO:0045595PHENOTYPE	regulation of cell differentiation phenotype
GO:0045604PHENOTYPE	regulation of epidermal cell differentiation phenotype
GO:0045664PHENOTYPE	regulation of neuron differentiation phenotype
GO:0045793PHENOTYPE	positive regulation of cell size phenotype
GO:0045892PHENOTYPE	negative regulation of transcription, DNA-templated phenotype
GO:0045893PHENOTYPE	positive regulation of transcription, DNA-templated phenotype
GO:0045930PHENOTYPE	negative regulation of mitotic cell cycle phenotype
GO:0045944PHENOTYPE	positive regulation of transcription from RNA polymerase II promoter phenotype
GO:0045995PHENOTYPE	regulation of embryonic development phenotype
GO:0046488PHENOTYPE	phosphatidylinositol metabolic process phenotype
GO:0046676PHENOTYPE	negative regulation of insulin secretion phenotype
GO:0046686PHENOTYPE	response to cadmium ion phenotype
GO:0046959PHENOTYPE	habituation phenotype
GO:0048149PHENOTYPE	behavioral response to ethanol phenotype
GO:0048308PHENOTYPE	organelle inheritance phenotype
GO:0048333PHENOTYPE	mesodermal cell differentiation phenotype
GO:0048477PHENOTYPE	oogenesis phenotype
GO:0048488PHENOTYPE	synaptic vesicle endocytosis phenotype
GO:0048489PHENOTYPE	synaptic vesicle transport phenotype
GO:0048546PHENOTYPE	digestive tract morphogenesis phenotype
GO:0048557PHENOTYPE	embryonic digestive tract morphogenesis phenotype
GO:0048560PHENOTYPE	establishment of anatomical structure orientation phenotype
GO:0048566PHENOTYPE	embryonic digestive tract development phenotype
GO:0048598PHENOTYPE	embryonic morphogenesis phenotype
GO:0048599PHENOTYPE	oocyte development phenotype
GO:0048609PHENOTYPE	multicellular organismal reproductive process phenotype
GO:0048644PHENOTYPE	muscle organ morphogenesis phenotype
GO:0048665PHENOTYPE	neuron fate specification phenotype
GO:0048666PHENOTYPE	neuron development phenotype
GO:0048675PHENOTYPE	axon extension phenotype
GO:0048729PHENOTYPE	tissue morphogenesis phenotype
GO:0048730PHENOTYPE	epidermis morphogenesis phenotype
GO:0048747PHENOTYPE	muscle fiber development phenotype
GO:0048755PHENOTYPE	branching morphogenesis of a nerve phenotype
GO:0048812PHENOTYPE	neuron projection morphogenesis phenotype
GO:0048846PHENOTYPE	axon extension involved in axon guidance phenotype
GO:0048858PHENOTYPE	cell projection morphogenesis phenotype
GO:0050708PHENOTYPE	regulation of protein secretion phenotype
GO:0050803PHENOTYPE	regulation of synapse structure or activity phenotype
GO:0050807PHENOTYPE	regulation of synapse organization phenotype
GO:0050808PHENOTYPE	synapse organization phenotype
GO:0050829PHENOTYPE	defense response to Gram-negative bacterium phenotype
GO:0050832PHENOTYPE	defense response to fungus phenotype
GO:0050892PHENOTYPE	intestinal absorption phenotype
GO:0050905PHENOTYPE	neuromuscular process phenotype
GO:0050913PHENOTYPE	sensory perception of bitter taste phenotype
GO:0050918PHENOTYPE	positive chemotaxis phenotype
GO:0050920PHENOTYPE	regulation of chemotaxis phenotype
GO:0050954PHENOTYPE	sensory perception of mechanical stimulus phenotype
GO:0051026PHENOTYPE	chiasma assembly phenotype
GO:0051046PHENOTYPE	regulation of secretion phenotype
GO:0051094PHENOTYPE	positive regulation of developmental process phenotype
GO:0051146PHENOTYPE	striated muscle cell differentiation phenotype
GO:0051177PHENOTYPE	meiotic sister chromatid cohesion phenotype
GO:0051179PHENOTYPE	localization phenotype
GO:0051225PHENOTYPE	spindle assembly phenotype
GO:0051270PHENOTYPE	regulation of cellular component movement phenotype
GO:0051276PHENOTYPE	chromosome organization phenotype
GO:0051296PHENOTYPE	establishment of meiotic spindle orientation phenotype
GO:0051301PHENOTYPE	cell division phenotype
GO:0051302PHENOTYPE	regulation of cell division phenotype
GO:0051304PHENOTYPE	chromosome separation phenotype
GO:0051306PHENOTYPE	mitotic sister chromatid separation phenotype
GO:0051307PHENOTYPE	meiotic chromosome separation phenotype
GO:0051321PHENOTYPE	meiotic cell cycle phenotype
GO:0051403PHENOTYPE	stress-activated MAPK cascade phenotype
GO:0051493PHENOTYPE	regulation of cytoskeleton organization phenotype
GO:0051567PHENOTYPE	histone H3-K9 methylation phenotype
GO:0051664PHENOTYPE	nuclear pore localization phenotype
GO:0051759PHENOTYPE	sister chromosome movement towards spindle pole involved in meiotic sister chromatid segregation phenotype
GO:0051932PHENOTYPE	synaptic transmission, GABAergic phenotype
GO:0051983PHENOTYPE	regulation of chromosome segregation phenotype
GO:0055001PHENOTYPE	muscle cell development phenotype
GO:0055002PHENOTYPE	striated muscle cell development phenotype
GO:0055069PHENOTYPE	zinc ion homeostasis phenotype
GO:0055072PHENOTYPE	iron ion homeostasis phenotype
GO:0055088PHENOTYPE	lipid homeostasis phenotype
GO:0060065PHENOTYPE	uterus development phenotype
GO:0060179PHENOTYPE	male mating behavior phenotype
GO:0060259PHENOTYPE	regulation of feeding behavior phenotype
GO:0060271PHENOTYPE	cilium morphogenesis phenotype
GO:0060323PHENOTYPE	head morphogenesis phenotype
GO:0060429PHENOTYPE	epithelium development phenotype
GO:0060465PHENOTYPE	pharynx development phenotype
GO:0060471PHENOTYPE	cortical granule exocytosis phenotype
GO:0060573PHENOTYPE	cell fate specification involved in pattern specification phenotype
GO:0060581PHENOTYPE	cell fate commitment involved in pattern specification phenotype
GO:0060582PHENOTYPE	cell fate determination involved in pattern specification phenotype
GO:0060756PHENOTYPE	foraging behavior phenotype
GO:0060828PHENOTYPE	regulation of canonical Wnt signaling pathway phenotype
GO:0061025PHENOTYPE	membrane fusion phenotype
GO:0061061PHENOTYPE	muscle structure development phenotype
GO:0061062PHENOTYPE	regulation of nematode larval development phenotype
GO:0065003PHENOTYPE	macromolecular complex assembly phenotype
GO:0070482PHENOTYPE	response to oxygen levels phenotype
GO:0071158PHENOTYPE	positive regulation of cell cycle arrest phenotype
GO:0071542PHENOTYPE	dopaminergic neuron differentiation phenotype
GO:0071688PHENOTYPE	striated muscle myosin thick filament assembly phenotype
GO:0071689PHENOTYPE	muscle thin filament assembly phenotype
GO:0071711PHENOTYPE	basement membrane organization phenotype
GO:0071850PHENOTYPE	mitotic cell cycle arrest phenotype
GO:0080135PHENOTYPE	regulation of cellular response to stress phenotype
GO:0090307PHENOTYPE	mitotic spindle assembly phenotype
GO:0090329PHENOTYPE	regulation of DNA-dependent DNA replication phenotype
GO:0090386PHENOTYPE	phagosome maturation involved in apoptotic cell clearance phenotype
GO:0090387PHENOTYPE	phagolysosome assembly involved in apoptotic cell clearance phenotype
GO:0098609PHENOTYPE	cell-cell adhesion phenotype
GO:0098662PHENOTYPE	inorganic cation transmembrane transport phenotype
GO:0098773PHENOTYPE	skin epidermis development phenotype
GO:1901031PHENOTYPE	regulation of response to reactive oxygen species phenotype
GO:1903827PHENOTYPE	regulation of cellular protein localization phenotype
GO:1904081PHENOTYPE	positive regulation of transcription from RNA polymerase II promoter involved in neuron differentiation phenotype
GO:2000249PHENOTYPE	regulation of actin cytoskeleton reorganization phenotype
GO:2000377PHENOTYPE	regulation of reactive oxygen species metabolic process phenotype
HP:0001507	Growth abnormality
HP:0001508	Failure to thrive
HP:0001511	Intrauterine growth retardation
HP:0002269	Abnormality of neuronal migration
HP:0008322	Abnormal mitochondrial morphology
HP:0008669	Abnormal spermatogenesis
HP:0011018	Abnormality of the cell cycle
HP:0011019	Abnormality of chromosome condensation
HP:0012535	Abnormal synaptic transmission
HP:0031377	Abnormal cell proliferation
MP:0001547	abnormal lipid level
MP:0003111	abnormal cell nucleus morphology
MP:0003702	abnormal chromosome morphology
MP:0003950	abnormal plasma membrane morphology
MP:0004272	abnormal basement membrane morphology
MP:0004792	abnormal synaptic vesicle number
MP:0005058	abnormal lysosome morphology
MP:0005404	abnormal axon morphology
MP:0005437	abnormal glycogen level
MP:0008415	abnormal neurite morphology
MP:0008830	abnormal nucleolus morphology
MP:0009378	abnormal endoplasmic reticulum morphology
MP:0009538	abnormal synapse morphology
MP:0010207	abnormal telomere morphology
MP:0011743	abnormal Golgi apparatus morphology
MP:0012603	abnormal glutathione level
MP:0013202	abnormal cilium morphology
MP:0013258	abnormal extracellular matrix morphology
MP:0014010	abnormal peroxisome morphology
MP:0030675	abnormal acetylcholine level
MP:0030731	abnormal gamma-aminobutyric acid level
WBPhenotype:0000000	chromosome instability
WBPhenotype:0000001	body posture variant
WBPhenotype:0000002	kinker
WBPhenotype:0000004	constitutive egg laying
WBPhenotype:0000005	hyperactive egg laying
WBPhenotype:0000006	egg laying defective
WBPhenotype:0000007	bag of worms
WBPhenotype:0000010	drug hypersensitive
WBPhenotype:0000011	drug resistant
WBPhenotype:0000012	dauer constitutive
WBPhenotype:0000013	dauer defective
WBPhenotype:0000014	cord commissures variant
WBPhenotype:0000015	positive chemotaxis defective
WBPhenotype:0000016	aldicarb hypersensitive
WBPhenotype:0000017	aldicarb resistant
WBPhenotype:0000018	pharyngeal pumping increased
WBPhenotype:0000019	pharyngeal pumping reduced
WBPhenotype:0000020	pharyngeal pumping irregular
WBPhenotype:0000021	squat
WBPhenotype:0000022	long
WBPhenotype:0000023	serotonin hypersensitive
WBPhenotype:0000024	serotonin resistant
WBPhenotype:0000025	blistered
WBPhenotype:0000026	lipid depleted
WBPhenotype:0000027	organism metabolism processing variant
WBPhenotype:0000028	RNA processing variant
WBPhenotype:0000029	systemic RNAi variant
WBPhenotype:0000032	sick
WBPhenotype:0000033	developmental timing variant
WBPhenotype:0000034	embryonic polarity variant
WBPhenotype:0000035	larval body morphology variant
WBPhenotype:0000036	adult body morphology variant
WBPhenotype:0000037	egg morphology variant
WBPhenotype:0000038	exploded through vulva
WBPhenotype:0000039	life span phenotype
WBPhenotype:0000040	one cell arrest early emb
WBPhenotype:0000041	osmotic integrity variant
WBPhenotype:0000043	general pace of development variant
WBPhenotype:0000044	egg size defective early emb
WBPhenotype:0000045	developmental delay postembryonic
WBPhenotype:0000046	pace of P lineage defective early emb
WBPhenotype:0000049	postembryonic development variant
WBPhenotype:0000050	embryonic lethal
WBPhenotype:0000051	embryonic terminal arrest variable emb
WBPhenotype:0000052	maternal effect lethal emb
WBPhenotype:0000053	paralyzed arrested elongation two fold
WBPhenotype:0000054	larval lethal
WBPhenotype:0000055	early larval arrest
WBPhenotype:0000056	late larval arrest
WBPhenotype:0000057	early larval lethal
WBPhenotype:0000058	late larval lethal
WBPhenotype:0000059	larval arrest
WBPhenotype:0000060	adult lethal
WBPhenotype:0000061	extended life span
WBPhenotype:0000062	lethal
WBPhenotype:0000063	terminal arrest variable
WBPhenotype:0000064	sexually dimorphic lethality
WBPhenotype:0000065	X0 lethal
WBPhenotype:0000066	XX lethal
WBPhenotype:0000068	cellular oxidative stress response variant
WBPhenotype:0000069	progeny variant
WBPhenotype:0000070	male tail morphology variant
WBPhenotype:0000071	head morphology variant
WBPhenotype:0000072	body morphology variant
WBPhenotype:0000073	tail morphology variant
WBPhenotype:0000075	cuticle attachment variant
WBPhenotype:0000076	epithelial attachment variant
WBPhenotype:0000077	cuticle shedding defect
WBPhenotype:0000078	seam cells stacked
WBPhenotype:0000079	branched adult alae
WBPhenotype:0000080	no anterior pharynx
WBPhenotype:0000081	L1 arrest
WBPhenotype:0000082	L2 arrest
WBPhenotype:0000083	L3 arrest
WBPhenotype:0000084	L4 arrest
WBPhenotype:0000085	swollen intestine
WBPhenotype:0000087	body wall cell development variant
WBPhenotype:0000088	body muscle displaced
WBPhenotype:0000089	alpha amanitin resistant
WBPhenotype:0000090	epidermis cuticle detached
WBPhenotype:0000091	epidermis muscle detached
WBPhenotype:0000092	intestinal cell proliferation variant
WBPhenotype:0000093	lineage variant
WBPhenotype:0000094	anus development variant
WBPhenotype:0000095	M lineage variant
WBPhenotype:0000097	AB lineage variant
WBPhenotype:0000099	P lineages variant
WBPhenotype:0000100	cell UV response variant
WBPhenotype:0000101	UV induced apoptosis increased
WBPhenotype:0000102	presynaptic vesicle cluster variant
WBPhenotype:0000103	gut granule development variant
WBPhenotype:0000105	oocyte meiotic maturation variant
WBPhenotype:0000106	inhibition of oocyte maturation variant
WBPhenotype:0000107	inhibition of ovulation variant
WBPhenotype:0000111	pattern of gene expression variant
WBPhenotype:0000112	protein expression variant
WBPhenotype:0000113	RNA expression variant
WBPhenotype:0000114	mRNA expression variant
WBPhenotype:0000115	anterior pharynx variant
WBPhenotype:0000116	mid larval lethal
WBPhenotype:0000117	L1 lethal
WBPhenotype:0000118	L2 lethal
WBPhenotype:0000119	protein expression increased
WBPhenotype:0000120	protein expression reduced
WBPhenotype:0000121	translation variant
WBPhenotype:0000122	post translational processing variant
WBPhenotype:0000123	enzyme expression level reduced
WBPhenotype:0000124	enzyme activity reduced
WBPhenotype:0000125	enzyme activity increased
WBPhenotype:0000126	general pace of development defective early emb
WBPhenotype:0000127	dauer recovery variant
WBPhenotype:0000128	temperature induced dauer formation increased
WBPhenotype:0000129	temperature induced dauer formation defective
WBPhenotype:0000130	pheromone induced dauer formation enhanced
WBPhenotype:0000131	pheromone induced dauer formation defective
WBPhenotype:0000132	pheromone induced dauer formation variant
WBPhenotype:0000133	expression lipogenic enzyme reduced
WBPhenotype:0000134	gene expression level reduced
WBPhenotype:0000135	gene expression level high
WBPhenotype:0000136	mRNA levels increased
WBPhenotype:0000137	mRNA levels reduced
WBPhenotype:0000138	lipid composition variant
WBPhenotype:0000139	stress induced lethality variant
WBPhenotype:0000140	stress induced arrest variant
WBPhenotype:0000141	stress induced lethality increased
WBPhenotype:0000142	cell stress response variant
WBPhenotype:0000143	organism UV response variant
WBPhenotype:0000144	pathogen induced cell death increased
WBPhenotype:0000145	fertility phenotype
WBPhenotype:0000148	starvation induced dauer formation variant
WBPhenotype:0000150	starvation induced dauer formation defective
WBPhenotype:0000151	anterior pharynx extra cells
WBPhenotype:0000152	no cleavage furrow first division early emb
WBPhenotype:0000153	body wall muscle contraction abnormal
WBPhenotype:0000154	reduced brood size
WBPhenotype:0000155	cell polarity reversed
WBPhenotype:0000157	posterior body wall contraction defecation cycle variant
WBPhenotype:0000161	nuclear rotation variant
WBPhenotype:0000162	pale larva
WBPhenotype:0000163	clear larva
WBPhenotype:0000164	thin
WBPhenotype:0000165	cell fusion variant
WBPhenotype:0000166	seam cell fusion variant
WBPhenotype:0000167	precocious seam cell fusion
WBPhenotype:0000168	alae secretion variant
WBPhenotype:0000169	early exit cell cycle
WBPhenotype:0000170	precocious alae
WBPhenotype:0000174	basal lamina development variant
WBPhenotype:0000175	hypercontracted
WBPhenotype:0000177	acetylcholinesterase reduced
WBPhenotype:0000178	cell degeneration
WBPhenotype:0000179	neuron degeneration
WBPhenotype:0000181	axon trajectory variant
WBPhenotype:0000184	apoptosis fails to occur
WBPhenotype:0000187	egg round
WBPhenotype:0000188	gonad arm morphology variant
WBPhenotype:0000189	hypodermis disorganized
WBPhenotype:0000190	no dauer recovery
WBPhenotype:0000194	first polar body position variant
WBPhenotype:0000195	distal tip cell migration variant
WBPhenotype:0000196	distal tip cell morphology variant
WBPhenotype:0000197	cell induction variant
WBPhenotype:0000199	male tail sensory ray development variant
WBPhenotype:0000200	pericellular component development variant
WBPhenotype:0000201	cuticle development variant
WBPhenotype:0000202	alae variant
WBPhenotype:0000203	odorant adaptation variant
WBPhenotype:0000204	anterior body contraction defecation cycle variant
WBPhenotype:0000205	expulsion variant
WBPhenotype:0000206	autosomal nondisjunction meiosis
WBPhenotype:0000207	defecation cycle variant
WBPhenotype:0000208	long defecation cycle
WBPhenotype:0000209	short defecation cycle
WBPhenotype:0000210	defecation contraction variant
WBPhenotype:0000212	body constriction
WBPhenotype:0000215	no germ line
WBPhenotype:0000218	vulval cell induction increased
WBPhenotype:0000219	vulval cell induction reduced
WBPhenotype:0000220	vulva cell fate specification variant
WBPhenotype:0000221	neurotransmitter metabolism variant
WBPhenotype:0000224	serotonin deficient
WBPhenotype:0000227	male turning defective
WBPhenotype:0000228	spontaneous mutation rate increased
WBPhenotype:0000229	small
WBPhenotype:0000230	tail withered
WBPhenotype:0000231	body size variant
WBPhenotype:0000232	CAN cell migration variant
WBPhenotype:0000233	dopamine metabolism variant
WBPhenotype:0000234	dopamine deficient
WBPhenotype:0000237	foraging hyperactive
WBPhenotype:0000238	foraging reduced
WBPhenotype:0000239	vulval cell lineage variant
WBPhenotype:0000240	blast cell proliferation reduced
WBPhenotype:0000241	accumulated cell corpses
WBPhenotype:0000242	body elongation defective
WBPhenotype:0000243	engulfment failure by killer cell
WBPhenotype:0000245	SM migration variant
WBPhenotype:0000246	defecation cycle variable length
WBPhenotype:0000247	sodium chemotaxis defective
WBPhenotype:0000249	osmotic avoidance defective
WBPhenotype:0000251	octopamine deficient
WBPhenotype:0000252	caffeine resistant
WBPhenotype:0000253	movement erratic
WBPhenotype:0000254	chloride chemotaxis defective
WBPhenotype:0000255	amphid phasmid neuron morphology variant
WBPhenotype:0000256	amphid neuron morphology variant
WBPhenotype:0000257	phasmid neuron morphology variant
WBPhenotype:0000258	cell secretion variant
WBPhenotype:0000260	sheath cell secretion failure
WBPhenotype:0000262	axoneme morphology variant
WBPhenotype:0000263	axoneme short
WBPhenotype:0000264	cAMP chemotaxis defective
WBPhenotype:0000266	cell cleavage variant
WBPhenotype:0000267	cell cleavage delayed
WBPhenotype:0000270	pleiotropic defects severe early emb
WBPhenotype:0000272	egg laying irregular
WBPhenotype:0000273	thrashing reduced
WBPhenotype:0000274	dead eggs laid
WBPhenotype:0000275	organism UV hypersensitive
WBPhenotype:0000276	organism X ray response variant
WBPhenotype:0000277	rhythm slow
WBPhenotype:0000279	spicule insertion defective
WBPhenotype:0000280	breaks in alae
WBPhenotype:0000281	male sex muscle development variant
WBPhenotype:0000282	hermaphrodite sex muscle development variant
WBPhenotype:0000283	vulva uterus connection defective
WBPhenotype:0000284	sperm transfer defective
WBPhenotype:0000285	ray tips swollen
WBPhenotype:0000286	embryo disorganized
WBPhenotype:0000288	distal germline variant
WBPhenotype:0000289	uterus morphology variant
WBPhenotype:0000290	sperm absent
WBPhenotype:0000291	no oocytes
WBPhenotype:0000293	alimentary system pigmentation variant
WBPhenotype:0000294	intestine dark
WBPhenotype:0000295	thermotolerance increased
WBPhenotype:0000296	spicules crumpled
WBPhenotype:0000297	rays fused
WBPhenotype:0000298	rays displaced
WBPhenotype:0000299	sensillum morphology variant
WBPhenotype:0000300	amphid sheath cell morphology variant
WBPhenotype:0000301	distal tip cell reflex failure
WBPhenotype:0000302	benzaldehyde chemotaxis defective
WBPhenotype:0000303	diacetyl chemotaxis defective
WBPhenotype:0000304	isoamyl alcohol chemotaxis defective
WBPhenotype:0000305	pheromone sensation variant
WBPhenotype:0000306	transgene expression variant
WBPhenotype:0000308	dauer development phenotype
WBPhenotype:0000309	SDS sensitive dauer
WBPhenotype:0000310	cilia absent
WBPhenotype:0000312	dauer pheromone production defective
WBPhenotype:0000313	meiotic progression during oogenesis variant
WBPhenotype:0000314	scrawny
WBPhenotype:0000315	mechanosensation variant
WBPhenotype:0000316	touch resistant tail
WBPhenotype:0000318	cell cycle delayed
WBPhenotype:0000319	large
WBPhenotype:0000320	reduced viability after freezing
WBPhenotype:0000322	nose rounded
WBPhenotype:0000323	head swollen
WBPhenotype:0000324	short
WBPhenotype:0000325	arecoline hypersensitive
WBPhenotype:0000327	corpus contraction defect
WBPhenotype:0000328	terminal bulb contraction variant
WBPhenotype:0000329	pumping asynchronous
WBPhenotype:0000330	pharyngeal relaxation defective
WBPhenotype:0000332	inhibitors of sodium potassium ATPase hypersensitive
WBPhenotype:0000333	pharyngeal pumps brief
WBPhenotype:0000334	isthmus corpus slippery
WBPhenotype:0000335	pharynx slippery
WBPhenotype:0000336	terminal bulb relaxation variant
WBPhenotype:0000337	grinder relaxation defective
WBPhenotype:0000338	tail swelling
WBPhenotype:0000339	transient bloating
WBPhenotype:0000340	imipramine resistant
WBPhenotype:0000341	imipramine hypersensitive
WBPhenotype:0000342	bursa morphology variant
WBPhenotype:0000344	cloacal structures protrude
WBPhenotype:0000345	VPC cell division variant
WBPhenotype:0000346	adult pigmentation variant
WBPhenotype:0000347	rectal development variant
WBPhenotype:0000349	flaccid
WBPhenotype:0000350	hermaphrodite tail spike variant
WBPhenotype:0000351	failure to hatch
WBPhenotype:0000352	backing uncoordinated
WBPhenotype:0000353	backing increased
WBPhenotype:0000354	cell differentiation variant
WBPhenotype:0000355	HSN differentiation precocious
WBPhenotype:0000357	unfertilized oocytes laid
WBPhenotype:0000358	extra cell division postembryonic
WBPhenotype:0000359	tunicamycin response variant
WBPhenotype:0000360	cytoplasmic streaming defective
WBPhenotype:0000361	lima bean arrest
WBPhenotype:0000362	blastocoel variant
WBPhenotype:0000364	gut granule birefringence misplaced
WBPhenotype:0000365	embryo osmotic integrity defective early emb
WBPhenotype:0000366	three fold arrest
WBPhenotype:0000367	comma arrest emb
WBPhenotype:0000368	one point five fold arrest emb
WBPhenotype:0000369	pretzel arrest
WBPhenotype:0000370	egg long
WBPhenotype:0000372	no polar body formation
WBPhenotype:0000373	egg shape variable
WBPhenotype:0000376	no uterine cavity
WBPhenotype:0000378	pharyngeal pumping shallow
WBPhenotype:0000379	head notched
WBPhenotype:0000380	expulsion infrequent
WBPhenotype:0000381	serotonin reuptake inhibitor resistant
WBPhenotype:0000383	lipid synthesis defective
WBPhenotype:0000385	sperm excess
WBPhenotype:0000386	genotoxic chemical induced apoptosis variant
WBPhenotype:0000387	sperm nonmotile
WBPhenotype:0000388	sperm morphology variant
WBPhenotype:0000389	hermaphrodite sperm fertilization defective
WBPhenotype:0000390	spermatid activation defective
WBPhenotype:0000391	defecation missing motor steps
WBPhenotype:0000392	intestinal fluorescence increased
WBPhenotype:0000393	cell migration failure
WBPhenotype:0000394	electrophoretic variant protein
WBPhenotype:0000395	no differentiated gametes
WBPhenotype:0000396	non reflexed gonad arms
WBPhenotype:0000397	harsh body touch resistant
WBPhenotype:0000398	light body touch resistant
WBPhenotype:0000399	somatic gonad development variant
WBPhenotype:0000400	somatic gonad primordium development defective
WBPhenotype:0000401	no uterus
WBPhenotype:0000402	avoids bacterial lawn
WBPhenotype:0000403	sperm transfer initiation defective
WBPhenotype:0000405	giant oocytes
WBPhenotype:0000406	lumpy
WBPhenotype:0000408	dauer recovery inhibited
WBPhenotype:0000409	organism morphology variable
WBPhenotype:0000410	no defecation cycle
WBPhenotype:0000411	rod like larval lethal
WBPhenotype:0000412	octanol chemotaxis defective
WBPhenotype:0000413	pharyngeal muscle paralyzed
WBPhenotype:0000414	cell fate transformation
WBPhenotype:0000415	necrotic cell death variant
WBPhenotype:0000416	yolk synthesis variant
WBPhenotype:0000419	L3 lethal
WBPhenotype:0000420	levamisole hypersensitive
WBPhenotype:0000421	levamisole resistant
WBPhenotype:0000422	twitcher
WBPhenotype:0000423	head muscle contraction variant
WBPhenotype:0000424	antibody staining variant
WBPhenotype:0000425	antibody staining reduced
WBPhenotype:0000426	antibody staining increased
WBPhenotype:0000428	no adult cuticle
WBPhenotype:0000430	male copulatory structure development variant
WBPhenotype:0000432	male copulatory structure absent
WBPhenotype:0000433	DNA synthesis variant
WBPhenotype:0000434	sexual maturation defective
WBPhenotype:0000436	protein subcellular localization variant
WBPhenotype:0000438	retarded heterochronic variations
WBPhenotype:0000439	precocious heterochronic variations
WBPhenotype:0000440	excretory canals long
WBPhenotype:0000441	tail rounded
WBPhenotype:0000442	larval development retarded
WBPhenotype:0000443	spicule morphology variant
WBPhenotype:0000444	bursa elongated
WBPhenotype:0000445	yolk synthesis in males
WBPhenotype:0000446	supernumerary molt
WBPhenotype:0000447	adult development variant
WBPhenotype:0000448	adult cuticle development variant
WBPhenotype:0000451	head protrusion
WBPhenotype:0000452	tail protrusions
WBPhenotype:0000453	body protrusions
WBPhenotype:0000454	head twisted
WBPhenotype:0000455	jerky movement
WBPhenotype:0000456	touch resistant
WBPhenotype:0000457	organism starvation hypersensitive
WBPhenotype:0000458	starvation resistant
WBPhenotype:0000459	pesticide response variant
WBPhenotype:0000460	paraquat response variant
WBPhenotype:0000461	paraquat resistant
WBPhenotype:0000462	paraquat hypersensitive
WBPhenotype:0000463	metabolic pathway variant
WBPhenotype:0000464	oxygen response variant
WBPhenotype:0000466	high oxygen hypersensitive
WBPhenotype:0000467	age associated fluorescence increased
WBPhenotype:0000468	age associated fluorescence reduced
WBPhenotype:0000469	Q neuroblast lineage migration variant
WBPhenotype:0000470	HSN migration variant
WBPhenotype:0000471	ALM migration variant
WBPhenotype:0000472	endoderm absent
WBPhenotype:0000473	progressive paralysis
WBPhenotype:0000475	muscle detached
WBPhenotype:0000476	progressive muscle detachment
WBPhenotype:0000477	nucleolus refraction variant
WBPhenotype:0000478	isothermal tracking behavior variant
WBPhenotype:0000480	pyrazine chemotaxis defective
WBPhenotype:0000481	negative chemotaxis variant
WBPhenotype:0000483	no gut granules
WBPhenotype:0000484	embryo small
WBPhenotype:0000485	dauer death increased
WBPhenotype:0000486	colchicine hypersensitive
WBPhenotype:0000487	colchicine resistant
WBPhenotype:0000488	chloroquine hypersensitive
WBPhenotype:0000490	pharynx disorganized
WBPhenotype:0000491	isthmus morphology defective
WBPhenotype:0000492	corpus morphology defective
WBPhenotype:0000493	metacorpus morphology defective
WBPhenotype:0000494	two fold arrest
WBPhenotype:0000495	ray ectopic
WBPhenotype:0000496	male postdeirid sensilla absent
WBPhenotype:0000500	acetylcholinesterase inhibitor hypersensitive
WBPhenotype:0000501	left handed roller
WBPhenotype:0000502	right handed roller
WBPhenotype:0000503	endoreduplication variant
WBPhenotype:0000504	nuclear division variant
WBPhenotype:0000505	male ray morphology variant
WBPhenotype:0000506	bursa swollen
WBPhenotype:0000508	nonsense mRNA accumulation
WBPhenotype:0000509	sperm pseudopod variant
WBPhenotype:0000510	vulval invagination variant L4
WBPhenotype:0000511	nuclear positioning variant
WBPhenotype:0000512	VNC nuclear positioning variant
WBPhenotype:0000514	rubber band
WBPhenotype:0000515	ventral nerve cord development variant
WBPhenotype:0000516	ventral cord disorganized
WBPhenotype:0000518	development phenotype
WBPhenotype:0000519	physiology phenotype
WBPhenotype:0000520	morphology phenotype
WBPhenotype:0000521	pigmentation phenotype
WBPhenotype:0000525	organism behavior variant
WBPhenotype:0000527	organism pigmentation phenotype
WBPhenotype:0000529	cell development variant
WBPhenotype:0000531	organism development variant
WBPhenotype:0000532	body region morphology variant
WBPhenotype:0000533	cell morphology variant
WBPhenotype:0000535	organism morphology variant
WBPhenotype:0000536	cell physiology phenotype
WBPhenotype:0000539	dorsal nerve cord development variant
WBPhenotype:0000540	muscle arm development variant
WBPhenotype:0000541	cord commissures fail to reach target
WBPhenotype:0000542	fat
WBPhenotype:0000543	forward kinker
WBPhenotype:0000544	backward kinker
WBPhenotype:0000545	egg retention
WBPhenotype:0000546	early eggs laid
WBPhenotype:0000547	starved
WBPhenotype:0000548	muscle dystrophy
WBPhenotype:0000549	head muscle dystrophy
WBPhenotype:0000550	body muscle dystrophy
WBPhenotype:0000551	omega turns variant
WBPhenotype:0000553	muscle birefringence variant
WBPhenotype:0000554	hypoosmotic shock hypersensitive
WBPhenotype:0000555	drug adaptation variant
WBPhenotype:0000556	dopamine adaptation variant
WBPhenotype:0000557	dopamine adaptation defective
WBPhenotype:0000559	calcium channel modulator hypersensitive
WBPhenotype:0000561	head levamisole resistant
WBPhenotype:0000562	body levamisole resistant
WBPhenotype:0000563	shrinker
WBPhenotype:0000564	echo defecation cycle
WBPhenotype:0000565	coiler
WBPhenotype:0000566	ventral coiler
WBPhenotype:0000569	axon varicosities
WBPhenotype:0000571	axon vesicle variant
WBPhenotype:0000572	neuronal outgrowth variant
WBPhenotype:0000574	excretory canal short
WBPhenotype:0000576	organism physiology phenotype
WBPhenotype:0000577	organism homeostasis metabolism variant
WBPhenotype:0000578	body axis development variant
WBPhenotype:0000583	dumpy
WBPhenotype:0000585	cell homeostasis metabolism variant
WBPhenotype:0000586	bleach hypersensitive
WBPhenotype:0000590	cell corpse number variant
WBPhenotype:0000591	metal response variant
WBPhenotype:0000592	copper response variant
WBPhenotype:0000593	copper hypersensitive
WBPhenotype:0000595	head behavior variant
WBPhenotype:0000600	epithelial system morphology variant
WBPhenotype:0000601	excretory secretory system morphology variant
WBPhenotype:0000603	muscle system morphology variant
WBPhenotype:0000604	nervous system morphology variant
WBPhenotype:0000605	reproductive system morphology variant
WBPhenotype:0000610	excretory system physiology variant
WBPhenotype:0000611	muscle system physiology variant
WBPhenotype:0000612	nervous system physiology variant
WBPhenotype:0000613	reproductive system physiology variant
WBPhenotype:0000617	alimentary system development variant
WBPhenotype:0000619	epithelial system development variant
WBPhenotype:0000621	excretory system development variant
WBPhenotype:0000622	muscle system development variant
WBPhenotype:0000624	reproductive system development variant
WBPhenotype:0000628	spindle assembly defective early emb
WBPhenotype:0000630	quinine chemotaxis defective
WBPhenotype:0000632	axon fasciculation variant
WBPhenotype:0000633	axon branching variant
WBPhenotype:0000634	pharyngeal pumping variant
WBPhenotype:0000636	neuron degeneration variant
WBPhenotype:0000637	dauer formation variant
WBPhenotype:0000638	molt defect
WBPhenotype:0000639	temperature induced dauer formation variant
WBPhenotype:0000641	activity level variant
WBPhenotype:0000642	hyperactive
WBPhenotype:0000643	locomotion variant
WBPhenotype:0000644	paralyzed
WBPhenotype:0000645	roller
WBPhenotype:0000646	sluggish
WBPhenotype:0000648	male mating variant
WBPhenotype:0000649	vulva location variant
WBPhenotype:0000651	constipated
WBPhenotype:0000652	sensory system variant
WBPhenotype:0000653	mechanosensory system variant
WBPhenotype:0000654	synaptic vesicle exocytosis variant
WBPhenotype:0000655	GABA synaptic transmission variant
WBPhenotype:0000656	acetylcholine synaptic transmission variant
WBPhenotype:0000657	neuronal synaptic transmission variant
WBPhenotype:0000660	social feeding increased
WBPhenotype:0000661	solitary feeding increased
WBPhenotype:0000662	foraging behavior variant
WBPhenotype:0000663	osmotic avoidance variant
WBPhenotype:0000664	exaggerated body bends
WBPhenotype:0000665	connection of gonad variant
WBPhenotype:0000667	gonad displaced
WBPhenotype:0000668	endomitotic oocytes
WBPhenotype:0000669	sex muscle development variant
WBPhenotype:0000671	resistant to copper
WBPhenotype:0000672	presynaptic vesicle cluster localization variant
WBPhenotype:0000673	brood size variant
WBPhenotype:0000675	zygotic lethal
WBPhenotype:0000676	growth rate variant
WBPhenotype:0000677	chemosensation defective
WBPhenotype:0000679	transgene subcellular localization variant
WBPhenotype:0000680	aldicarb response variant
WBPhenotype:0000681	DMPP response variant
WBPhenotype:0000682	feminization of germline
WBPhenotype:0000683	masculinization of germline
WBPhenotype:0000684	fewer germ cells
WBPhenotype:0000685	larval growth slow
WBPhenotype:0000686	organism ionizing radiation response variant
WBPhenotype:0000687	feminization of XX and XO animals
WBPhenotype:0000688	sterile
WBPhenotype:0000689	maternal sterile
WBPhenotype:0000690	gonad migration variant
WBPhenotype:0000692	male sterile
WBPhenotype:0000693	male sperm fertilization defect
WBPhenotype:0000694	hermaphrodite sterile
WBPhenotype:0000695	vulva morphology variant
WBPhenotype:0000696	everted vulva
WBPhenotype:0000697	protruding vulva
WBPhenotype:0000698	vulvaless
WBPhenotype:0000699	vulva development variant
WBPhenotype:0000700	multivulva
WBPhenotype:0000701	epithelial development variant
WBPhenotype:0000702	epithelial cell fusion failure
WBPhenotype:0000703	epithelial morphology variant
WBPhenotype:0000704	excretory canal morphology variant
WBPhenotype:0000705	intestinal cell development variant
WBPhenotype:0000706	gut granule biogenesis reduced
WBPhenotype:0000709	pharyngeal morphology variant
WBPhenotype:0000710	intestinal morphology variant
WBPhenotype:0000711	organism hypersensitive ionizing radiation
WBPhenotype:0000712	germ cell ionizing radiation response variant
WBPhenotype:0000715	muscle excess
WBPhenotype:0000716	muscle cell attachment variant
WBPhenotype:0000717	gene expression variant
WBPhenotype:0000718	dosage compensation variant
WBPhenotype:0000724	protein secretion variant
WBPhenotype:0000727	enzyme activity variant
WBPhenotype:0000731	germ cell hypersensitive ionizing radiation
WBPhenotype:0000732	DNA metabolism variant
WBPhenotype:0000734	hypodermal cell physiology variant
WBPhenotype:0000735	endoreduplication of hypodermal nuclei variant
WBPhenotype:0000737	germ cell resistant ionizing radiation
WBPhenotype:0000739	DNA damage response variant
WBPhenotype:0000741	DNA damage checkpoint variant
WBPhenotype:0000742	DNA recombination variant
WBPhenotype:0000743	RNAi response variant
WBPhenotype:0000744	transgene induced cosuppression variant
WBPhenotype:0000745	transposon silencing variant
WBPhenotype:0000747	pharyngeal contraction defective
WBPhenotype:0000748	asymmetric cell division defective early emb
WBPhenotype:0000752	L2 larval development variant
WBPhenotype:0000755	L1 L2 molt defect
WBPhenotype:0000758	L4 adult molt defect
WBPhenotype:0000759	spindle defective early emb
WBPhenotype:0000760	spindle orientation defective early emb
WBPhenotype:0000761	spindle position orientation defective early emb
WBPhenotype:0000762	spindle position defective early emb
WBPhenotype:0000764	embryonic cell organization biogenesis variant
WBPhenotype:0000765	spindle elongation integrity defective early emb
WBPhenotype:0000766	centrosome pair and associated pronuclear rotation variant
WBPhenotype:0000767	integrity of membranous organelles defective early emb
WBPhenotype:0000768	cytoplasmic structure defective early emb
WBPhenotype:0000769	cytoplasmic appearance defective early emb
WBPhenotype:0000770	embryonic cell morphology variant
WBPhenotype:0000771	centrosome attachment defective early emb
WBPhenotype:0000772	sister chromatid segregation defective early emb
WBPhenotype:0000774	gametogenesis variant
WBPhenotype:0000776	passage through meiosis defective early emb
WBPhenotype:0000777	polar body extrusion defective early emb
WBPhenotype:0000778	feeding inefficient
WBPhenotype:0000779	late embryonic arrest
WBPhenotype:0000780	shaker
WBPhenotype:0000781	body wall muscle thin filament variant
WBPhenotype:0000782	body wall muscle thick filament variant
WBPhenotype:0000783	M line absent
WBPhenotype:0000784	male fertility variant
WBPhenotype:0000787	posterior pale
WBPhenotype:0000792	anterior body morphology variant
WBPhenotype:0000793	posterior body morphology variant
WBPhenotype:0000794	posterior body thin
WBPhenotype:0000795	body axis behavior variant
WBPhenotype:0000796	posterior body uncoordinated
WBPhenotype:0000800	posterior region development variant
WBPhenotype:0000802	dorsal region development variant
WBPhenotype:0000803	head development variant
WBPhenotype:0000805	tail development variant
WBPhenotype:0000806	hermaphrodite fertility variant
WBPhenotype:0000811	epithelial cell development variant
WBPhenotype:0000813	gland cell development variant
WBPhenotype:0000815	muscle cell development variant
WBPhenotype:0000817	uterine vulval cell development variant
WBPhenotype:0000820	embryonic behavior variant
WBPhenotype:0000823	germline proliferation variant
WBPhenotype:0000824	embryonic cell lineage variant
WBPhenotype:0000825	postembryonic cell lineage variant
WBPhenotype:0000827	V lineages variant
WBPhenotype:0000828	T lineages variant
WBPhenotype:0000829	Q lineage variant
WBPhenotype:0000830	B lineage variant
WBPhenotype:0000832	C lineage variant
WBPhenotype:0000833	U lineage variant
WBPhenotype:0000834	E lineage variant
WBPhenotype:0000835	F lineage variant
WBPhenotype:0000836	gonadal lineage variant
WBPhenotype:0000837	hermaphrodite gonadal lineage variant
WBPhenotype:0000839	Z1 hermaphrodite lineage variant
WBPhenotype:0000840	Z4 hermaphrodite lineage variant
WBPhenotype:0000843	male mating efficiency reduced
WBPhenotype:0000844	serotonin induced pumping variant
WBPhenotype:0000845	levamisole response variant
WBPhenotype:0000846	presynaptic region physiology variant
WBPhenotype:0000847	presynaptic component localization variant
WBPhenotype:0000850	touch resistant anterior body
WBPhenotype:0000851	ciliated neuron physiology variant
WBPhenotype:0000852	coelomocyte development variant
WBPhenotype:0000853	intraflagellar transport variant
WBPhenotype:0000854	intraflagellar transport defective
WBPhenotype:0000857	excretory cell development variant
WBPhenotype:0000858	excretory duct cell development variant
WBPhenotype:0000861	body wall muscle development variant
WBPhenotype:0000862	bloated
WBPhenotype:0000863	male fertility reduced
WBPhenotype:0000864	early elongation arrest
WBPhenotype:0000866	germ cell arrest
WBPhenotype:0000868	paralyzed body
WBPhenotype:0000878	chemosensory neuron development variant
WBPhenotype:0000879	telomere length regulation variant
WBPhenotype:0000881	cilia mislocalized
WBPhenotype:0000882	dendrite development variant
WBPhenotype:0000883	nerve ring development variant
WBPhenotype:0000884	AWB morphology variant
WBPhenotype:0000885	engulfment variant
WBPhenotype:0000886	worm phenotype
WBPhenotype:0000888	male behavior variant
WBPhenotype:0000889	sexually dimorphic physiology variant
WBPhenotype:0000892	hermaphrodite germline proliferation variant
WBPhenotype:0000893	male germline proliferation variant
WBPhenotype:0000894	germ cell differentiation variant
WBPhenotype:0000898	blast cell morphology variant
WBPhenotype:0000899	epithelial cell morphology variant
WBPhenotype:0000900	germ cell morphology variant
WBPhenotype:0000901	gland cell morphology variant
WBPhenotype:0000902	intestinal cell morphology variant
WBPhenotype:0000904	muscle cell morphology variant
WBPhenotype:0000905	neuron morphology variant
WBPhenotype:0000907	anus morphology variant
WBPhenotype:0000910	rectal morphology variant
WBPhenotype:0000911	coelomocyte morphology variant
WBPhenotype:0000915	pale adult
WBPhenotype:0000916	excretory cell morphology variant
WBPhenotype:0000917	excretory duct cell morphology variant
WBPhenotype:0000923	nonstriated muscle morphology variant
WBPhenotype:0000924	striated muscle morphology variant
WBPhenotype:0000925	sex muscle morphology variant
WBPhenotype:0000926	body wall muscle morphology variant
WBPhenotype:0000928	male physiology variant
WBPhenotype:0000930	sexually dimorphic development variant
WBPhenotype:0000932	bisphenol A hypersensitive
WBPhenotype:0000933	MS lineage variant
WBPhenotype:0000934	developmental morphology variant
WBPhenotype:0000935	D lineage variant
WBPhenotype:0000938	male V lineages variant
WBPhenotype:0000939	male T lineages variant
WBPhenotype:0000942	accessory cell development variant
WBPhenotype:0000948	cuticle morphology variant
WBPhenotype:0000949	pseudocoelom morphology variant
WBPhenotype:0000952	anterior ganglion development variant
WBPhenotype:0000961	pattern of transgene expression variant
WBPhenotype:0000962	level of transgene expression variant
WBPhenotype:0000963	male pigmentation variant
WBPhenotype:0000964	DMPP resistant
WBPhenotype:0000965	somatic cell death variant
WBPhenotype:0000966	germline mortal
WBPhenotype:0000968	tail spike variant
WBPhenotype:0000970	embryonic pigmentation variant
WBPhenotype:0000972	neuronal sheath cell morphology variant
WBPhenotype:0000976	ventral cord patterning variant
WBPhenotype:0000977	somatic gonad morphology variant
WBPhenotype:0000978	spermatheca physiology variant
WBPhenotype:0000979	spermatheca dilation defective
WBPhenotype:0000980	pharyngeal contraction variant
WBPhenotype:0000981	spermatocyte meiosis variant
WBPhenotype:0000982	spermatid maturation variant
WBPhenotype:0000983	fertilization defective
WBPhenotype:0000987	germ cell physiology variant
WBPhenotype:0000988	gland cell physiology variant
WBPhenotype:0000994	intestinal contractions variant
WBPhenotype:0000996	expulsion defective
WBPhenotype:0000997	cryophilic
WBPhenotype:0000998	thermophilic
WBPhenotype:0000999	athermotactic
WBPhenotype:0001003	L4 lethal
WBPhenotype:0001004	pharyngeal relaxation variant
WBPhenotype:0001005	backward locomotion variant
WBPhenotype:0001006	pharyngeal pumping rate variant
WBPhenotype:0001010	clear
WBPhenotype:0001011	complex phenotype early emb
WBPhenotype:0001012	organism pathogen response variant
WBPhenotype:0001013	pathogen susceptibility increased
WBPhenotype:0001014	pathogen resistance increased
WBPhenotype:0001016	larval growth variant
WBPhenotype:0001017	adult growth variant
WBPhenotype:0001018	cytokinesis variant emb
WBPhenotype:0001019	mid larval arrest
WBPhenotype:0001020	embryonic lethal late emb
WBPhenotype:0001021	male sexual development variant
WBPhenotype:0001022	hermaphrodite sexual development variant
WBPhenotype:0001024	male morphology variant
WBPhenotype:0001025	hermaphrodite morphology variant
WBPhenotype:0001026	nuclear morphology variation early emb
WBPhenotype:0001027	nuclear position defective early emb
WBPhenotype:0001029	patchy coloration
WBPhenotype:0001030	pronuclear envelope defective early emb
WBPhenotype:0001031	pronuclear migration reduced early emb
WBPhenotype:0001033	proximal germ cell proliferation variant
WBPhenotype:0001034	pronuclear nuclear appearance defective early emb
WBPhenotype:0001035	nuclear appearance number defective early emb
WBPhenotype:0001036	sterile F1
WBPhenotype:0001037	sterile progeny
WBPhenotype:0001038	tumorous germline
WBPhenotype:0001040	chemosensory response variant
WBPhenotype:0001041	meiosis defective early emb
WBPhenotype:0001042	neuron function reduced
WBPhenotype:0001043	interphase entry defective early emb
WBPhenotype:0001044	cortical dynamics defective early emb
WBPhenotype:0001045	sporadic pumping
WBPhenotype:0001046	pharyngeal muscle morphology variant
WBPhenotype:0001048	odorant chemosensory response variant
WBPhenotype:0001055	bromide chemotaxis defective
WBPhenotype:0001056	iodide chemotaxis defective
WBPhenotype:0001057	lithium chemotaxis defective
WBPhenotype:0001058	potassium chemotaxis defective
WBPhenotype:0001059	magnesium chemotaxis defective
WBPhenotype:0001060	AWC odorant chemotaxis defective
WBPhenotype:0001061	AWA odorant chemotaxis defective
WBPhenotype:0001062	late paralysis arrested elongation two fold
WBPhenotype:0001063	egg laying phases variant
WBPhenotype:0001065	fewer egg laying events during active
WBPhenotype:0001066	inactive phase variant
WBPhenotype:0001068	egg laying serotonin resistant
WBPhenotype:0001072	response to food variant
WBPhenotype:0001073	egg laying response to food variant
WBPhenotype:0001075	vulval muscle physiology variant
WBPhenotype:0001077	chromosome segregation variant karyomeres early emb
WBPhenotype:0001078	cytokinesis defective early emb
WBPhenotype:0001079	cytoplasmic dynamics defective early emb
WBPhenotype:0001080	excessive blebbing early emb
WBPhenotype:0001082	large cytoplasmic granules early emb
WBPhenotype:0001083	multiple cytoplasmic cavities early emb
WBPhenotype:0001084	sodium chloride chemotaxis defective
WBPhenotype:0001085	butanone chemotaxis defective
WBPhenotype:0001086	trimethylthiazole chemotaxis defective
WBPhenotype:0001090	thermotolerance reduced
WBPhenotype:0001092	larval defecation defect
WBPhenotype:0001093	intestinal physiology variant
WBPhenotype:0001095	organism high sodium chloride hypersensitive
WBPhenotype:0001096	protrusion at vulval region
WBPhenotype:0001097	premature spermatocyte germ cell differentiation
WBPhenotype:0001098	no rectum
WBPhenotype:0001099	nose twisted
WBPhenotype:0001100	early embryonic lethal
WBPhenotype:0001101	egg laying response to drug variant
WBPhenotype:0001102	mitotic spindle defective early emb
WBPhenotype:0001103	spindle absent early emb
WBPhenotype:0001104	P0 spindle absent early emb
WBPhenotype:0001105	P0 spindle position defective early emb
WBPhenotype:0001106	spindle orientation variant AB or P1 early emb
WBPhenotype:0001107	spindle rotation defective early emb
WBPhenotype:0001108	P0 spindle rotation failure early emb
WBPhenotype:0001109	P0 spindle rotation delayed early emb
WBPhenotype:0001110	aster defective early emb
WBPhenotype:0001112	aster AB resembles P1 aster early emb
WBPhenotype:0001113	P1 aster defective early emb
WBPhenotype:0001114	cell cycle defective early emb
WBPhenotype:0001115	cell cycle timing defective early emb
WBPhenotype:0001117	cell cell contacts abnormal early emb
WBPhenotype:0001118	cell position defective early emb
WBPhenotype:0001119	cell cycle slow early emb
WBPhenotype:0001120	relative cell cycle timing defective early emb
WBPhenotype:0001121	exaggerated asynchrony early emb
WBPhenotype:0001122	reversed asynchrony early emb
WBPhenotype:0001123	synchronous second division early emb
WBPhenotype:0001124	ABa ABp EMS synchronous division early emb
WBPhenotype:0001125	P2 EMS synchronous division early emb
WBPhenotype:0001126	cell cell contacts abnormal in four cell embryo
WBPhenotype:0001127	EMS anterior extension fails early emb
WBPhenotype:0001128	EMS anterior extension extreme early emb
WBPhenotype:0001129	cleavage furrow defective early emb
WBPhenotype:0001130	cytokinesis fails early emb
WBPhenotype:0001131	loose mitotic furrow early emb
WBPhenotype:0001133	division axis defective
WBPhenotype:0001134	Aba ABp division axis defective early emb
WBPhenotype:0001135	embryonic morphology defective early emb
WBPhenotype:0001136	embryonic morphology variant
WBPhenotype:0001137	embryos small early emb
WBPhenotype:0001138	nucleus defective early emb
WBPhenotype:0001139	nuclear envelope assembly variant early emb
WBPhenotype:0001141	nucleus reforms cell division remnant early emb
WBPhenotype:0001142	nuclear number defective early emb
WBPhenotype:0001143	multiple nuclei early emb
WBPhenotype:0001144	polar body number size early emb
WBPhenotype:0001145	polar body number defective early emb
WBPhenotype:0001146	polar body size defective early emb
WBPhenotype:0001147	polar body defective early emb
WBPhenotype:0001148	polar body reabsorbed early emb
WBPhenotype:0001150	polar body reabsorbed one two early emb
WBPhenotype:0001151	pronucleus centrosomes defective early emb
WBPhenotype:0001152	pronuclear migration defective early emb
WBPhenotype:0001153	pronuclear migration failure early emb
WBPhenotype:0001154	paternal pronucleus migrates early emb
WBPhenotype:0001155	pronuclei meet centrally early emb
WBPhenotype:0001156	pronuclear size defective early emb
WBPhenotype:0001157	pronuclear breakdown defective early emb
WBPhenotype:0001158	pronuclear breakdown asynchronous early emb
WBPhenotype:0001159	pronuclear morphology defective early emb
WBPhenotype:0001161	maternal pronucleus indistinct early emb
WBPhenotype:0001162	pronuclear number defective early emb
WBPhenotype:0001163	pronucleus formation failure early emb
WBPhenotype:0001164	excess pronucleus early emb
WBPhenotype:0001165	excess maternal pronucleus early emb
WBPhenotype:0001166	excess paternal pronucleus variant centrosome early emb
WBPhenotype:0001167	pseudocleavage defective early emb
WBPhenotype:0001168	pseudocleavage absent early emb
WBPhenotype:0001169	pseudocleavage exaggerated early emb
WBPhenotype:0001170	sterile F0 48 hours post injection
WBPhenotype:0001171	shortened life span
WBPhenotype:0001172	programmed cell death variant
WBPhenotype:0001173	non apoptotic cell death variant
WBPhenotype:0001174	chromosome disjunction defective
WBPhenotype:0001175	high incidence male progeny
WBPhenotype:0001176	one cell shape defective early emb
WBPhenotype:0001177	embryo osmotic pressure sensitive early emb
WBPhenotype:0001178	egg integrity defective early emb
WBPhenotype:0001180	accumulated germline cell corpses
WBPhenotype:0001181	accumulated somatic cell corpses
WBPhenotype:0001183	fat content reduced
WBPhenotype:0001184	fat content increased
WBPhenotype:0001185	embryonic developmental delay early emb
WBPhenotype:0001186	embryo delayed at pronuclear contact early emb
WBPhenotype:0001190	pharyngeal physiology variant
WBPhenotype:0001191	pharyngeal muscle physiology variant
WBPhenotype:0001193	disorganized pharyngeal EPG
WBPhenotype:0001194	extra and ectopic neuron
WBPhenotype:0001196	synchronization calcium signal defective pharynx
WBPhenotype:0001198	somatic sheath physiology variant
WBPhenotype:0001199	gonad sheath contractions variant
WBPhenotype:0001200	gonad sheath contraction rate reduced
WBPhenotype:0001201	no expulsion defecation
WBPhenotype:0001202	nicotine hypersensitive
WBPhenotype:0001203	nicotine resistant
WBPhenotype:0001204	muscimol resistant
WBPhenotype:0001206	movement variant
WBPhenotype:0001207	protein signaling variant
WBPhenotype:0001208	RNAi resistant
WBPhenotype:0001209	skiddy
WBPhenotype:0001211	cuticle integrity variant
WBPhenotype:0001212	cuticle fragile
WBPhenotype:0001213	locomotion reduced
WBPhenotype:0001215	germ cell mitosis variant
WBPhenotype:0001216	meiosis metaphase to anaphase transition block
WBPhenotype:0001217	germ cell mitosis metaphase to anaphase transition block
WBPhenotype:0001218	cell death sexually dimorphic variant
WBPhenotype:0001219	cell survival sexually dimorphic increased
WBPhenotype:0001220	cell death sexually dimorphic increased
WBPhenotype:0001221	nose touch defective
WBPhenotype:0001222	transposon mutator
WBPhenotype:0001223	germline RNAi resistant
WBPhenotype:0001224	axon outgrowth variant
WBPhenotype:0001225	phasmid socket absent
WBPhenotype:0001226	commissure variant
WBPhenotype:0001227	commissure absent
WBPhenotype:0001228	alae absent
WBPhenotype:0001230	anterior cell migration defective
WBPhenotype:0001231	intraflagellar transport accelerated
WBPhenotype:0001232	serotonin response variant
WBPhenotype:0001233	DAPI staining variant
WBPhenotype:0001234	nonanone chemotaxis defective
WBPhenotype:0001235	cell division polarity variant
WBPhenotype:0001236	transgene expression increased
WBPhenotype:0001239	mating latency increased
WBPhenotype:0001240	male tail sensory ray differentiation variant
WBPhenotype:0001242	intraflagellar transport slow
WBPhenotype:0001246	no transport distal segment cilia
WBPhenotype:0001247	anterograde transport defective
WBPhenotype:0001248	wing cilia morphology variant
WBPhenotype:0001249	amphid channel cilia morphology variant
WBPhenotype:0001251	amphid channel axoneme short
WBPhenotype:0001254	amphid channel cilia bulbous
WBPhenotype:0001255	wing cilia bulbous
WBPhenotype:0001256	DNA damage induced focus formation variant
WBPhenotype:0001257	cross link induced focus formation variant
WBPhenotype:0001258	RNAi enhanced
WBPhenotype:0001259	hermaphrodite fertility reduced
WBPhenotype:0001260	oocyte morphology variant
WBPhenotype:0001261	pale
WBPhenotype:0001262	vulval development incomplete
WBPhenotype:0001264	peroxisome physiology variant
WBPhenotype:0001265	head movement variant
WBPhenotype:0001266	genetic pathway activation variant
WBPhenotype:0001267	induced contraction rate variant
WBPhenotype:0001268	induced cell death variant
WBPhenotype:0001270	pathogen induced cell death reduced
WBPhenotype:0001271	pathogen induced death increased
WBPhenotype:0001272	vulval cell induction variant
WBPhenotype:0001274	organism heat hypersensitive
WBPhenotype:0001275	increased genetic pathway signal
WBPhenotype:0001276	ectopic expression transgene
WBPhenotype:0001277	transformer
WBPhenotype:0001278	transgene expression reduced
WBPhenotype:0001279	transgene expression reduced male
WBPhenotype:0001280	transgene expression reduced hermaphrodite
WBPhenotype:0001281	stuffed pharynx
WBPhenotype:0001282	mitochondrial metabolism variant
WBPhenotype:0001283	organelle metabolism variant
WBPhenotype:0001284	coenzyme Q depleted
WBPhenotype:0001285	induced pharyngeal pumping variant
WBPhenotype:0001286	food suppressed pumping variant
WBPhenotype:0001289	acetylcholinesterase inhibitor resistant
WBPhenotype:0001292	body wall muscle physiology variant
WBPhenotype:0001294	head bent
WBPhenotype:0001295	body twisted
WBPhenotype:0001296	lannate resistant
WBPhenotype:0001297	male tail development variant
WBPhenotype:0001298	hindgut morphology variant
WBPhenotype:0001299	cell division variant male
WBPhenotype:0001300	germ cell cytoplasmic morphology variant
WBPhenotype:0001301	P granule abnormal
WBPhenotype:0001302	P granule localization defective
WBPhenotype:0001303	extra and ectopic cell
WBPhenotype:0001304	hindgut damaged
WBPhenotype:0001305	hook morphology variant
WBPhenotype:0001306	male reproductive system morphology variant
WBPhenotype:0001308	weak pumping
WBPhenotype:0001309	amplitude of sinusoidal movement decreased
WBPhenotype:0001310	neuron positioning variant
WBPhenotype:0001312	neuron number variant
WBPhenotype:0001314	vulval muscle variant
WBPhenotype:0001315	electrophysiology phenotype
WBPhenotype:0001316	evoked postsynaptic current variant
WBPhenotype:0001317	evoked postsynaptic amplitude reduced
WBPhenotype:0001318	endogenous synaptic events variant
WBPhenotype:0001319	endogenous synaptic event frequency reduced
WBPhenotype:0001320	endogenous synaptic amplitude variant
WBPhenotype:0001321	presynaptic region morphology variant
WBPhenotype:0001323	vesicle morphology variant
WBPhenotype:0001324	cell ionizing radiation response variant
WBPhenotype:0001325	backing not sustained
WBPhenotype:0001327	cell gamma ray hypersensitive
WBPhenotype:0001328	posterior body dumpy
WBPhenotype:0001329	curly
WBPhenotype:0001330	egg laying event infrequent
WBPhenotype:0001331	motor neuron morphology variant
WBPhenotype:0001332	vesicle number variant
WBPhenotype:0001333	neuron cell body absent misplaced
WBPhenotype:0001334	hermaphrodite sex muscle morphology variant
WBPhenotype:0001336	male mating efficiency eliminated
WBPhenotype:0001339	egg laying levamisole resistant
WBPhenotype:0001340	egg laying imipramine resistant
WBPhenotype:0001341	egg laying phentolamine resistant
WBPhenotype:0001342	egg laying imipramine hypersensitive
WBPhenotype:0001343	meiotic spindle defective early emb
WBPhenotype:0001344	organelle organization biogenesis variant
WBPhenotype:0001345	cytoskeleton organization biogenesis variant
WBPhenotype:0001346	actin cytoskeleton dynamics phenotype
WBPhenotype:0001347	intestinal calcium signaling variant
WBPhenotype:0001349	protein phosphorylation variant
WBPhenotype:0001350	protein phosphorylation increased
WBPhenotype:0001351	protein phosphorylation reduced
WBPhenotype:0001352	endoplasmic reticulum metabolism variant
WBPhenotype:0001353	centration defective early emb
WBPhenotype:0001354	actin cytoskeleton filament morphology phenotype
WBPhenotype:0001355	gonad morphology variant
WBPhenotype:0001357	male gonad morphology variant
WBPhenotype:0001360	hermaphrodite self sterile
WBPhenotype:0001362	chromosome condensation failure
WBPhenotype:0001363	head cavity
WBPhenotype:0001364	male fan morphology variant
WBPhenotype:0001365	male bursa development variant
WBPhenotype:0001366	male fan development variant
WBPhenotype:0001368	spermatheca absent
WBPhenotype:0001369	protein interaction variant
WBPhenotype:0001370	protein protein interaction variant
WBPhenotype:0001371	protein RNA interaction variant
WBPhenotype:0001372	protein DNA interaction variant
WBPhenotype:0001373	protein RNA interaction abolished
WBPhenotype:0001374	pronuclear nuclear appearance variant emb
WBPhenotype:0001375	transgene expression undetectable
WBPhenotype:0001376	transgene expression undetectable cell specific
WBPhenotype:0001377	break induced focus formation variant
WBPhenotype:0001378	mitotic chromosome segregation variant
WBPhenotype:0001379	organism toxic chemical response variant
WBPhenotype:0001380	anoxia hypersensitive
WBPhenotype:0001381	anoxia resistant
WBPhenotype:0001382	protein modification variant
WBPhenotype:0001383	protein methylation variant
WBPhenotype:0001384	fertility reduced
WBPhenotype:0001385	precocious oogenesis
WBPhenotype:0001386	fertilization defective hermaphrodite
WBPhenotype:0001387	fertilization defect male
WBPhenotype:0001388	organism hypersensitive gamma irradiation
WBPhenotype:0001390	cell UV hypersensitive
WBPhenotype:0001391	gamma ray induced apoptosis increased
WBPhenotype:0001393	cell acidification variant
WBPhenotype:0001394	cell acidification defective
WBPhenotype:0001395	body vacuole
WBPhenotype:0001396	pumping absent
WBPhenotype:0001397	necrotic cell death increased
WBPhenotype:0001400	level of protein expression variant
WBPhenotype:0001402	connected mitochondria
WBPhenotype:0001403	antibody subcellular localization variant
WBPhenotype:0001404	ectopic expression antibody
WBPhenotype:0001405	protein aggregation variant
WBPhenotype:0001407	protein expression reduced cell specific
WBPhenotype:0001408	pattern protein expression variant
WBPhenotype:0001409	protein expression ectopic
WBPhenotype:0001410	protein expression absent
WBPhenotype:0001411	cuticle carbohydrate surface variant
WBPhenotype:0001412	alae morphology variant
WBPhenotype:0001413	bacterially unswollen
WBPhenotype:0001414	male mating defective
WBPhenotype:0001415	pathogen adherence variant
WBPhenotype:0001416	pathogen adherence defect
WBPhenotype:0001417	organism desiccation response variant
WBPhenotype:0001418	organism hypersensitive desiccation
WBPhenotype:0001419	emetine hypersensitive
WBPhenotype:0001420	biofilm absent head
WBPhenotype:0001422	endocytic transport defect
WBPhenotype:0001423	coelomocyte physiology variant
WBPhenotype:0001424	oocyte physiology variant
WBPhenotype:0001425	receptor mediated endocytosis defective
WBPhenotype:0001426	coelomocyte endocytosis defective
WBPhenotype:0001427	cytoplasmic appearance variant
WBPhenotype:0001428	intestinal vacuole
WBPhenotype:0001429	granules cytoplasm
WBPhenotype:0001430	lysosome organization biogenesis variant
WBPhenotype:0001431	pointed tail tip male
WBPhenotype:0001432	over retracted male tail
WBPhenotype:0001433	precocious cell fusion
WBPhenotype:0001434	chemotaxis variant
WBPhenotype:0001435	ammonium chloride chemotaxis defective
WBPhenotype:0001436	nose touch hypersensitive
WBPhenotype:0001437	octanol chemotaxis hypersensitive
WBPhenotype:0001438	odorant positive chemotaxis defective
WBPhenotype:0001441	aqueous positive chemotaxis defective
WBPhenotype:0001442	sodium acetate chemotaxis defective
WBPhenotype:0001443	aqueous chemosensory response variant
WBPhenotype:0001444	aqueous adaptation defective
WBPhenotype:0001445	sodium acetate adaptation defective
WBPhenotype:0001446	sodium chloride adaptation defective
WBPhenotype:0001447	ammonium chloride adaptation defective
WBPhenotype:0001448	odorant negative chemotaxis defective
WBPhenotype:0001450	aqueous negative chemotaxis variant
WBPhenotype:0001452	octanol chemotaxis variant
WBPhenotype:0001453	high sodium chloride concentration osmotic avoidance variant
WBPhenotype:0001454	quinine chemotaxis variant
WBPhenotype:0001461	sodium acetate chemotaxis variant
WBPhenotype:0001462	sodium chloride chemotaxis variant
WBPhenotype:0001468	benzaldehyde chemotaxis variant
WBPhenotype:0001469	butanone chemotaxis variant
WBPhenotype:0001470	diacetyl chemotaxis variant
WBPhenotype:0001474	pyrazine chemotaxis variant
WBPhenotype:0001476	anterior body contraction variant
WBPhenotype:0001477	anterograde transport variant
WBPhenotype:0001478	body elongation variant
WBPhenotype:0001479	dauer pheromone sensation variant
WBPhenotype:0001481	thrashing increased
WBPhenotype:0001482	frequency body bend reduced
WBPhenotype:0001483	late stage egg laid
WBPhenotype:0001484	ammonium acetate chemotaxis defective
WBPhenotype:0001485	ER stress response variant
WBPhenotype:0001486	unfolded protein accumulation
WBPhenotype:0001487	male spicule development variant
WBPhenotype:0001492	no back end
WBPhenotype:0001493	VPC cell division precocious
WBPhenotype:0001494	distal tip cell migration precocious
WBPhenotype:0001495	cell division precocious
WBPhenotype:0001496	metaphase to anaphase transition defect
WBPhenotype:0001497	mitotic metaphase to anaphase transition defect
WBPhenotype:0001498	sperm pseudopod physiology variant
WBPhenotype:0001499	meiotic chromosome segregation variant
WBPhenotype:0001500	pentanedione chemotaxis variant
WBPhenotype:0001503	ventral nerve cord maintenance variant
WBPhenotype:0001504	maternal effect sterile
WBPhenotype:0001505	spontaneous reversal variant
WBPhenotype:0001506	spontaneous reversal rate variant
WBPhenotype:0001507	Bacillus thuringiensis toxin resistant
WBPhenotype:0001508	anchor cell fusion defective
WBPhenotype:0001509	rays missing
WBPhenotype:0001510	neuronal cell fate specification variant
WBPhenotype:0001511	linker cell migration variant
WBPhenotype:0001512	loss of left right asymmetry
WBPhenotype:0001513	dense core vesicle exocytosis variant
WBPhenotype:0001514	synaptic vesicle endocytosis variant
WBPhenotype:0001515	struts variant
WBPhenotype:0001516	helical cuticle
WBPhenotype:0001517	annulae morphology variant
WBPhenotype:0001518	biogenic amine physiology variant
WBPhenotype:0001519	posterior cell migration variant
WBPhenotype:0001520	posterior neuron migration variant
WBPhenotype:0001521	body elongation retracted
WBPhenotype:0001522	spicules protrude
WBPhenotype:0001524	quiescence variant
WBPhenotype:0001525	terminal bulb morphology variant
WBPhenotype:0001526	ciliated neuron morphology variant
WBPhenotype:0001528	sensillum accessory cell morphology variant
WBPhenotype:0001530	cephalic sensillum morphology variant
WBPhenotype:0001531	labial sensillum morphology variant
WBPhenotype:0001532	inner labial morphology variant
WBPhenotype:0001533	outer labial morphology variant
WBPhenotype:0001534	neuronal ECM variant
WBPhenotype:0001535	deirid sensillum morphology variant
WBPhenotype:0001536	embryonic cell patterning variant
WBPhenotype:0001538	mRNA surveillance defective
WBPhenotype:0001539	dauer induction variant
WBPhenotype:0001540	dauer lifespan variant
WBPhenotype:0001541	dauer gonad arrest variant
WBPhenotype:0001545	dauer body morphology variant
WBPhenotype:0001547	dauer metabolism phenotype
WBPhenotype:0001551	dauer cuticle variant
WBPhenotype:0001552	dauer pharynx morphology variant
WBPhenotype:0001561	dauer inner labial sensillum variant
WBPhenotype:0001565	lysine chemotaxis defective
WBPhenotype:0001566	ventral enclosure variant
WBPhenotype:0001567	nuclei enlarged
WBPhenotype:0001568	mRNA export variant
WBPhenotype:0001569	body wall muscle myosin organization defective
WBPhenotype:0001570	body wall muscle actin organization defective
WBPhenotype:0001571	body wall muscle cell polarization variant
WBPhenotype:0001572	masculinized
WBPhenotype:0001573	nicotine response variant
WBPhenotype:0001574	ATP levels variant
WBPhenotype:0001575	ATP levels reduced
WBPhenotype:0001576	mitochondria spacing variant
WBPhenotype:0001577	mitochondria alignment variant
WBPhenotype:0001578	cholinergic agonist resistant
WBPhenotype:0001580	nuclear envelope breakdown variant
WBPhenotype:0001581	X linked gene expression enhanced
WBPhenotype:0001582	X linked gene expression reduced
WBPhenotype:0001583	XXX progeny
WBPhenotype:0001584	chromosome alignment variant
WBPhenotype:0001585	asymmetric cell division variant
WBPhenotype:0001586	multiple anchor cells
WBPhenotype:0001589	microtubule nucleation variant
WBPhenotype:0001592	fainter
WBPhenotype:0001593	transgene silencing variant
WBPhenotype:0001594	germline transgene silencing variant
WBPhenotype:0001595	somatic transgene silencing variant
WBPhenotype:0001596	tail bobbed
WBPhenotype:0001597	muscle missing
WBPhenotype:0001599	ouabain resistant
WBPhenotype:0001602	methiothepin resistant
WBPhenotype:0001603	cyproheptadine resistant
WBPhenotype:0001604	mianserin resistant
WBPhenotype:0001606	ethanol hypersensitive
WBPhenotype:0001608	enflurane hypersensitive
WBPhenotype:0001609	isoflurane hypersensitive
WBPhenotype:0001610	diethyl ether hypersensitive
WBPhenotype:0001611	halothane hypersensitive
WBPhenotype:0001612	ethanol resistant
WBPhenotype:0001613	paralysis response to ethanol resistant
WBPhenotype:0001617	ethosuximide resistant
WBPhenotype:0001618	halothane resistant
WBPhenotype:0001619	isoflurane resistant
WBPhenotype:0001621	organism oxidative stress response hypersensitive
WBPhenotype:0001622	egg laying serotonin hypersensitive
WBPhenotype:0001624	male tail curling serotonin resistant
WBPhenotype:0001625	male tail curling serotonin hypersensitive
WBPhenotype:0001627	locomotion rate serotonin hypersensitive
WBPhenotype:0001628	locomotion rate serotonin resistant
WBPhenotype:0001629	egg laying serotonin variant
WBPhenotype:0001630	gut obstructed
WBPhenotype:0001631	nullo X gamete
WBPhenotype:0001634	organism electrophilic stress hypersensitive
WBPhenotype:0001635	excess pharyngeal cells
WBPhenotype:0001636	excess intestinal cells
WBPhenotype:0001637	no Intestine
WBPhenotype:0001639	roaming reduced
WBPhenotype:0001640	acidification level defective
WBPhenotype:0001641	posterior body wall contraction defective
WBPhenotype:0001642	cell cleavage variant emb
WBPhenotype:0001643	excess hypodermal cells
WBPhenotype:0001644	protein metabolism variant
WBPhenotype:0001645	protein degradation variant
WBPhenotype:0001646	no pharynx
WBPhenotype:0001648	no posterior pharynx
WBPhenotype:0001649	Fluorouracil resistant
WBPhenotype:0001650	germ cell death response to 5 FU resistant
WBPhenotype:0001651	growth arrest response to 5 FU resistant
WBPhenotype:0001652	anchor cell invasion variant
WBPhenotype:0001653	cadmium response variant
WBPhenotype:0001654	cadmium resistant
WBPhenotype:0001655	cadmium hypersensitive
WBPhenotype:0001656	distal tip cell development variant
WBPhenotype:0001657	cell junction variant
WBPhenotype:0001658	intercellular junction variant
WBPhenotype:0001659	spermatheca morphology variant
WBPhenotype:0001660	loss of asymmetry ASE
WBPhenotype:0001661	loss of asymmetry AWC
WBPhenotype:0001662	spermatheca development variant
WBPhenotype:0001663	organism oxidative stress resistant
WBPhenotype:0001664	X chromosome nondisjunction
WBPhenotype:0001665	low incidence male progeny
WBPhenotype:0001666	organism hypersensitive X ray irradiation
WBPhenotype:0001667	methyl methanesulfonate hypersensitive
WBPhenotype:0001668	oocyte accumulation
WBPhenotype:0001670	presynaptic vesicle number reduced
WBPhenotype:0001671	vesicle organization variant
WBPhenotype:0001672	commisure growth variant
WBPhenotype:0001673	telomere homeostasis variant
WBPhenotype:0001675	male gonad development variant
WBPhenotype:0001676	touch receptor cell morphology variant
WBPhenotype:0001677	stage specific cuticle antigenicity variant
WBPhenotype:0001678	cuticle physiology variant
WBPhenotype:0001680	adoption of fused vulval cell fate
WBPhenotype:0001681	spindle orientation variant
WBPhenotype:0001682	organism UV resistant
WBPhenotype:0001683	spermatogenesis defective hermaphrodite
WBPhenotype:0001684	synaptic vesicle homeostasis variant
WBPhenotype:0001685	postsynaptic region morphology variant
WBPhenotype:0001687	surface antigenicity variant
WBPhenotype:0001688	surface coat variant
WBPhenotype:0001689	surface antigen negative
WBPhenotype:0001690	constitutive larval display
WBPhenotype:0001691	germ nuclei rachis
WBPhenotype:0001692	pheromone induced larval display defective
WBPhenotype:0001693	male posterior alae
WBPhenotype:0001694	spermatogenesis to oogenesis switch defective
WBPhenotype:0001696	biosynthesis variant
WBPhenotype:0001697	chondroitin biosynthesis variant
WBPhenotype:0001698	heparan sulfate biosynthesis variant
WBPhenotype:0001699	localized movement variant
WBPhenotype:0001700	swimming variant
WBPhenotype:0001701	spastic locomotion
WBPhenotype:0001702	directionality variant
WBPhenotype:0001703	body bend variant
WBPhenotype:0001704	multiple alae
WBPhenotype:0001707	nuclear import defective
WBPhenotype:0001708	protein export from nucleus defective
WBPhenotype:0001710	rhythmic tolerance to osmotic stress variant
WBPhenotype:0001711	rhythmic behavior variant
WBPhenotype:0001713	locomotory rhythm variant
WBPhenotype:0001715	pirouette frequency variant
WBPhenotype:0001716	forward point velocity variant
WBPhenotype:0001717	centroid velocity variant
WBPhenotype:0001719	unfolded protein response variant
WBPhenotype:0001720	spermatozoa retro location defective
WBPhenotype:0001722	pathogen infected pharynx increase
WBPhenotype:0001723	pathogen infected pharynx decrease
WBPhenotype:0001724	tunicamycin hypersensitive
WBPhenotype:0001725	cellular osmotic stress response variant
WBPhenotype:0001726	body length variant
WBPhenotype:0001727	body width variant
WBPhenotype:0001729	mating plug produced
WBPhenotype:0001731	thermal bias in tracking variant
WBPhenotype:0001733	pheromone suppressed pumping defective
WBPhenotype:0001734	starvation suppressed pumping defective
WBPhenotype:0001735	muscle cell activity variant
WBPhenotype:0001736	acetate chemotaxis defective
WBPhenotype:0001737	aqueous compound discrimination defective
WBPhenotype:0001738	ammonium chemotaxis defective
WBPhenotype:0001740	organ senescence variant
WBPhenotype:0001741	spontaneous spicule protraction
WBPhenotype:0001742	lipid synthesis increased
WBPhenotype:0001743	mitosis variant
WBPhenotype:0001745	adherens junction variant
WBPhenotype:0001746	tight junction defective
WBPhenotype:0001747	zinc response variant
WBPhenotype:0001748	pharynx unattached
WBPhenotype:0001749	zinc toxicity hypersensitive
WBPhenotype:0001750	zinc toxicity resistant
WBPhenotype:0001751	organism hypertonic lethality increased
WBPhenotype:0001753	coelomocyte uptake increased
WBPhenotype:0001754	endosome to lysosome trafficking defective
WBPhenotype:0001755	UV induced mitotic germ cell arrest defective
WBPhenotype:0001756	UV induced apoptosis decreased
WBPhenotype:0001757	neuropeptide metabolism variant
WBPhenotype:0001758	neuropeptide processing variant
WBPhenotype:0001759	21U RNA expression variant
WBPhenotype:0001760	G tract instability
WBPhenotype:0001761	axon midline crossing variant
WBPhenotype:0001762	uptake of yolk defective
WBPhenotype:0001763	uptake by intestinal cell defective
WBPhenotype:0001764	carbon dioxide response variant
WBPhenotype:0001765	carbon dioxide avoidance variant
WBPhenotype:0001766	cholesterol depletion hypersensitive
WBPhenotype:0001767	commissure handedness defective
WBPhenotype:0001769	cytoplasmic RNAi defective
WBPhenotype:0001770	endo siRNA binding variant
WBPhenotype:0001772	endogenous transposase levels increased
WBPhenotype:0001773	enhanced locomotion defective
WBPhenotype:0001774	gut on the exterior
WBPhenotype:0001775	hormetic temperature induced life span extension defective
WBPhenotype:0001776	siRNA expression variant
WBPhenotype:0001777	pre mRNA levels increased
WBPhenotype:0001778	nuclear RNAi defective
WBPhenotype:0001779	miRNA expression variant
WBPhenotype:0001780	associative learning variant
WBPhenotype:0001781	hypersensitivity to mutagen
WBPhenotype:0001782	anoxia response attenuated
WBPhenotype:0001783	ligand gated channel activity variant
WBPhenotype:0001785	associative memory defective
WBPhenotype:0001786	neuronal ion channel clustering defective
WBPhenotype:0001787	phototaxis defective
WBPhenotype:0001788	resistant to mutagens
WBPhenotype:0001789	temperature influenced life span variant
WBPhenotype:0001790	thermoreceptor currents absent
WBPhenotype:0001791	defecation cycle temperature compensation variant
WBPhenotype:0001792	nuclei small
WBPhenotype:0001793	aboc expulsion missing
WBPhenotype:0001794	cytoplasmic processing body variant
WBPhenotype:0001796	organism hypersensitive interstrand cross link agents
WBPhenotype:0001797	pachytene arrested germline nuclei
WBPhenotype:0001798	inhibition of synaptogenesis defective
WBPhenotype:0001800	pathogen induced antimicrobial gene expression variant
WBPhenotype:0001801	axodendritic polarity variant
WBPhenotype:0001802	body wall muscle relaxation defective
WBPhenotype:0001803	endosome biogenesis variant
WBPhenotype:0001804	fat associated bodies reduced
WBPhenotype:0001805	mitochondria vesiculated
WBPhenotype:0001806	protein stabilization variant
WBPhenotype:0001807	alternative splicing variant
WBPhenotype:0001808	cell corpse digestion variant
WBPhenotype:0001809	organelle fusion defective
WBPhenotype:0001810	oocyte septum formation variant
WBPhenotype:0001811	serotonin induced fat reduction variant
WBPhenotype:0001812	embryonic rupture
WBPhenotype:0001813	synapsis defective
WBPhenotype:0001814	crossover defective
WBPhenotype:0001815	desynapsis defective
WBPhenotype:0001817	enhanced taste aversion defective
WBPhenotype:0001818	neuron activation variant
WBPhenotype:0001819	pathogen load variant
WBPhenotype:0001820	bordering
WBPhenotype:0001823	sperm recruitment variant
WBPhenotype:0001824	meiotic progression prophase variant
WBPhenotype:0001825	rudimentary gonad
WBPhenotype:0001828	RNAi persistence variant
WBPhenotype:0001829	premature spermatid activation
WBPhenotype:0001830	response to multiple stressors variant
WBPhenotype:0001831	intestinal microvilli variant
WBPhenotype:0001832	nuclear pore variant
WBPhenotype:0001833	membrane trafficking variant
WBPhenotype:0001835	energy expenditure variant
WBPhenotype:0001836	eggshell morphology variant
WBPhenotype:0001837	diet induced life span variant
WBPhenotype:0001838	drug induced gene expression variant
WBPhenotype:0001839	phorbol ester resistant
WBPhenotype:0001841	second messenger mediated signaling variant
WBPhenotype:0001842	drug withdrawal response variant
WBPhenotype:0001843	hormone metabolism variant
WBPhenotype:0001844	lipid hydrolysis regulation variant
WBPhenotype:0001845	lipid modification variant
WBPhenotype:0001846	phagosome maturation defective
WBPhenotype:0001847	sterol induced dauer formation variant
WBPhenotype:0001848	tube morphogenesis variant
WBPhenotype:0001849	zinc homeostasis variant
WBPhenotype:0001850	radiation induced germ cell apoptosis variant
WBPhenotype:0001851	radiation induced reproductive cell death variant
WBPhenotype:0001852	antihelmintic response variant
WBPhenotype:0001853	AAD response variant
WBPhenotype:0001854	benomyl response variant
WBPhenotype:0001855	fluoride resistant
WBPhenotype:0001856	ivermectin response variant
WBPhenotype:0001857	pathogen induced gene expression variant
WBPhenotype:0001858	suppression of head oscillations defective
WBPhenotype:0001859	Dosage compensation complex assembly variant
WBPhenotype:0001860	endocytic recycling defective
WBPhenotype:0001861	environmental stimuli induced gene expression variant
WBPhenotype:0001862	manganese homeostasis variant
WBPhenotype:0001863	manganese response variant
WBPhenotype:0001864	protein transport variant
WBPhenotype:0001865	protein ubiquitination variant
WBPhenotype:0001866	reduced pathogen accumulation
WBPhenotype:0001867	mitotic spindle asters defective early emb
WBPhenotype:0001868	meiotic spindle defective
WBPhenotype:0001869	meiotic spindle positioning defective
WBPhenotype:0001870	meiotic spindle rotation defective
WBPhenotype:0001871	drug induced life span variant
WBPhenotype:0001872	drug induced locomotion variant
WBPhenotype:0001873	meiotic spindle assembly defective
WBPhenotype:0001874	protein neddylation variant
WBPhenotype:0001875	anaphase bridging
WBPhenotype:0001876	centriole biogenesis variant
WBPhenotype:0001877	nuclear membrane morphology variant
WBPhenotype:0001878	hydroxyurea response variant
WBPhenotype:0001879	hydroxyurea hypersensitive
WBPhenotype:0001881	endoplasmic reticulum symmetry variant early emb
WBPhenotype:0001882	aneuploidy
WBPhenotype:0001885	cleavage furrow initiation defective early emb
WBPhenotype:0001886	cleavage furrow termination defective early emb
WBPhenotype:0001887	excess seam cells
WBPhenotype:0001888	fat associated bodies increased
WBPhenotype:0001889	body wall muscle sarcomere morphology variant
WBPhenotype:0001890	body wall muscle dense body variant
WBPhenotype:0001891	M line variant
WBPhenotype:0001893	mitochondrial membrane potential reduced
WBPhenotype:0001894	nuclear number variant
WBPhenotype:0001895	parental chromosome mixing defective
WBPhenotype:0001896	gamma ray induced apoptosis decreased
WBPhenotype:0001898	meiotic sister chromatid segregation variant
WBPhenotype:0001900	reduced levels of reduced glutathione
WBPhenotype:0001901	fat associated bodies variant
WBPhenotype:0001902	fat associated body size increased
WBPhenotype:0001903	centrosome biogenesis variant
WBPhenotype:0001904	manganese toxicity resistant
WBPhenotype:0001905	fewer eggs laid
WBPhenotype:0001906	hypodermal cell elongation defective
WBPhenotype:0001907	dorsal intercalation defective
WBPhenotype:0001908	ventral closure defective
WBPhenotype:0001910	kinetochore organization variant
WBPhenotype:0001911	axon regeneration defective
WBPhenotype:0001912	fewer coelomocytes
WBPhenotype:0001913	excess coelomocytes
WBPhenotype:0001914	fewer pharyngeal cells
WBPhenotype:0001915	mRNA expression ectopic
WBPhenotype:0001916	increased pathogen survival
WBPhenotype:0001917	protein acetylation variant
WBPhenotype:0001919	gut granules enlarged
WBPhenotype:0001920	twisted pharynx
WBPhenotype:0001921	meiotic DNA double strand break formation variant
WBPhenotype:0001922	axonal transport variant
WBPhenotype:0001923	fewer seam cells
WBPhenotype:0001924	oocytes stacked
WBPhenotype:0001925	oocytes disorganized
WBPhenotype:0001926	gonad sheath contraction rate increased
WBPhenotype:0001927	extra distal tip cells
WBPhenotype:0001928	extra gonad arms
WBPhenotype:0001929	linker cell absent
WBPhenotype:0001930	muscle arm development defective
WBPhenotype:0001931	muscle arm axon connection variant
WBPhenotype:0001932	myopodia present
WBPhenotype:0001933	synaptic vesicle tag abnormal in mechanosensory neurons
WBPhenotype:0001934	vulval muscle extension variant
WBPhenotype:0001936	resistant to protein aggregation induced paralysis
WBPhenotype:0001937	hypersensitive to protein aggregation induced paralysis
WBPhenotype:0001938	DNA repair variant
WBPhenotype:0001939	bitter tastant response variant
WBPhenotype:0001940	rachis morphology variant
WBPhenotype:0001941	rachis narrow
WBPhenotype:0001942	rachis absent
WBPhenotype:0001943	rachis wide
WBPhenotype:0001944	oocyte number decreased
WBPhenotype:0001945	oocytes small
WBPhenotype:0001946	pachytene progression during oogenesis variant
WBPhenotype:0001947	diplotene progression during oogenesis variant
WBPhenotype:0001948	diakinesis progression during oogenesis variant
WBPhenotype:0001949	diakinesis region organization variant
WBPhenotype:0001950	diplotene region organization variant
WBPhenotype:0001951	pachytene region organization variant
WBPhenotype:0001952	germline nuclear positioning variant
WBPhenotype:0001953	nuclear fallout
WBPhenotype:0001954	diplotene absent during oogenesis
WBPhenotype:0001955	multiple nuclei oocyte
WBPhenotype:0001956	oocytes lack nucleus
WBPhenotype:0001957	gonad small
WBPhenotype:0001958	gonad degenerate
WBPhenotype:0001959	spindle pole pulling force variant
WBPhenotype:0001960	spindle oscillation variant
WBPhenotype:0001961	reproductive longevity extended
WBPhenotype:0001962	missing distal tip cells
WBPhenotype:0001964	dopaminergic fate atypical
WBPhenotype:0001966	cell endomembrane physiology variant
WBPhenotype:0001967	meiotic chromatin reorganization variant
WBPhenotype:0001968	somatic gonad precursor symmetrical sisters
WBPhenotype:0001969	germ cell compartment morphology variant
WBPhenotype:0001970	germ cell compartment nuclei number variant
WBPhenotype:0001971	germ cell compartment anucleate
WBPhenotype:0001972	germ cell compartment multinucleate
WBPhenotype:0001973	germ cell compartment size variant
WBPhenotype:0001974	germ cell compartment small
WBPhenotype:0001975	germ cell compartment large
WBPhenotype:0001977	germ cell partition morphology variant
WBPhenotype:0001978	germ cell partition absent
WBPhenotype:0001979	gonad vesiculated
WBPhenotype:0001980	germ cell compartment expansion variant
WBPhenotype:0001981	germ cell compartment expansion absent
WBPhenotype:0001982	cell membrane organization biogenesis variant
WBPhenotype:0001983	lawn leaving behavior variant
WBPhenotype:0001984	long range axon migration variant
WBPhenotype:0001985	short range axon migration variant
WBPhenotype:0001986	high temperature induced L1 arrest
WBPhenotype:0001987	acetylcholinesterase activity variant
WBPhenotype:0001988	detergent hypersensitive
WBPhenotype:0001989	hypoxia hypersensitive
WBPhenotype:0001990	hypoxia resistant
WBPhenotype:0001991	hypoxia response attenuated
WBPhenotype:0001992	extra gonadal sheath cells
WBPhenotype:0001993	fewer gonadal sheath cells
WBPhenotype:0001994	left right handedness variant
WBPhenotype:0001995	cell cycle progression variant
WBPhenotype:0001997	nuclear anchoring variant
WBPhenotype:0001998	hypersensitive to laser ablation
WBPhenotype:0001999	conflicting sensory integration variant
WBPhenotype:0002000	recovery from enhanced locomotion variant
WBPhenotype:0002001	synapse density variant
WBPhenotype:0002002	supernumerary centrosomes
WBPhenotype:0002004	actomyosin contractility defective
WBPhenotype:0002006	anaphase I progression variant early embryo
WBPhenotype:0002007	cortical blebs present
WBPhenotype:0002009	proteasome core activity variant
WBPhenotype:0002010	protein turnover variant
WBPhenotype:0002011	bivulva
WBPhenotype:0002012	meiotic chromosome organization variant
WBPhenotype:0002013	univalent meiotic chromosomes
WBPhenotype:0002014	current measurement variant
WBPhenotype:0002015	voltage measurement variant
WBPhenotype:0002016	biotin chemotaxis defective
WBPhenotype:0002018	retarded seam cell fusion
WBPhenotype:0002025	cell size decreased
WBPhenotype:0002028	mechanoreceptor current variant
WBPhenotype:0002029	metal homeostasis variant
WBPhenotype:0002030	magnesium homeostasis variant
WBPhenotype:0002031	lectin response variant
WBPhenotype:0002032	lectin binding variant
WBPhenotype:0002033	lectin binding occurs
WBPhenotype:0002035	resistant to lectin
WBPhenotype:0002036	susceptible to lectin
WBPhenotype:0002037	nuclear envelope organization variant
WBPhenotype:0002038	ciliary localization defective
WBPhenotype:0002039	retrograde transport variant
WBPhenotype:0002040	asymmetric chromosome segregation
WBPhenotype:0002041	molt variant
WBPhenotype:0002043	hermaphrodite mating efficiency reduced
WBPhenotype:0002045	cell corpse number decreased
WBPhenotype:0002046	iron homeostasis variant
WBPhenotype:0002047	muscimol response variant
WBPhenotype:0002048	abamectin resistant
WBPhenotype:0002051	ascaroside biosynthesis variant
WBPhenotype:0002052	ascaroside biosynthesis defective
WBPhenotype:0002053	ivermectin resistant
WBPhenotype:0002054	magnesium hypersensitivity
WBPhenotype:0002055	photocurrent defective
WBPhenotype:0002056	eating variant
WBPhenotype:0002057	Bacillus thuringiensis toxin hypersensitive
WBPhenotype:0002058	pore forming toxin response variant
WBPhenotype:0002059	pore forming toxin hypersensitive
WBPhenotype:0002060	pore forming toxin resistant
WBPhenotype:0002061	chromosome decondensation variant
WBPhenotype:0002062	chromosome decondensation failure
WBPhenotype:0002066	basement membrane gap expansion variant
WBPhenotype:0002067	apical constriction variant
WBPhenotype:0002068	astral microtubule asymmetry defective
WBPhenotype:0002069	axon termination defective
WBPhenotype:0002070	egg laying response to muscimol variant
WBPhenotype:0002071	body lengthening response to muscimol variant
WBPhenotype:0002072	carbohydrate metabolism variant
WBPhenotype:0002073	cation homeostasis variant
WBPhenotype:0002075	eggshell formation variant
WBPhenotype:0002076	cortical granule exocytosis variant
WBPhenotype:0002077	dopamine resistant
WBPhenotype:0002078	histone methylation variant
WBPhenotype:0002079	delayed reproductive maturity
WBPhenotype:0002081	peptide uptake by intestinal cell increased
WBPhenotype:0002082	peptide uptake by intestinal cell decreased
WBPhenotype:0002084	crossover interference variant
WBPhenotype:0002086	crossover distribution variant
WBPhenotype:0002087	hydrogen sulfide hypersensitive
WBPhenotype:0002088	hypersensitive to dauer pheromone
WBPhenotype:0002089	cell component morphology variant
WBPhenotype:0002090	endosome morphology variant
WBPhenotype:0002091	late endosome morphology variant
WBPhenotype:0002092	early endosome morphology variant
WBPhenotype:0002094	RAB-11 recycling endosome morphology variant
WBPhenotype:0002095	lysosome-related organelle morphology variant
WBPhenotype:0002098	cell component localization variant
WBPhenotype:0002099	lysosome-related organelle localization variant
WBPhenotype:0002100	endosome localization variant
WBPhenotype:0002101	endoplasmic reticulum localization variant
WBPhenotype:0002102	golgi apparatus localization variant
WBPhenotype:0002103	lysosome localization variant
WBPhenotype:0002104	recycling endosome localization variant
WBPhenotype:0002105	late endosome localization variant
WBPhenotype:0002106	early endosome localization variant
WBPhenotype:0002107	RAB-11 recycling endosome localization variant
WBPhenotype:0002110	RME-1 recycling endosome morphology variant
WBPhenotype:0002113	synapsis formation variant
WBPhenotype:0002114	swimming induced paralysis
WBPhenotype:0002115	suicidal
WBPhenotype:0002116	subviable
WBPhenotype:0002117	occurences of decapitation
WBPhenotype:0002118	population fitness phenotype
WBPhenotype:0002119	alternative splicing defective
WBPhenotype:0002120	mitochondrial DNA repair variant
WBPhenotype:0002122	persistence of paternal mitochondria
WBPhenotype:0002124	circumferential actin bundles disorganized
WBPhenotype:0002125	growth inhibition response to chemical
WBPhenotype:0002126	intestinal fluorescence decreased
WBPhenotype:0002127	intraflagellar transport velocity variant
WBPhenotype:0002128	leaving assay defective
WBPhenotype:0002129	mitochondrial DNA copy number variant
WBPhenotype:0002130	post mating variant
WBPhenotype:0002131	muscle cell ultrastructure variant
WBPhenotype:0002132	protein complex organization variant
WBPhenotype:0002133	ooplasmic streaming slow
WBPhenotype:0002134	predator escape defective
WBPhenotype:0002136	no anchor cell
WBPhenotype:0002137	reduced translation initiation
WBPhenotype:0002138	acquired thermotolerance variant
WBPhenotype:0002139	linker cell morphology variant
WBPhenotype:0002140	male attraction response variant
WBPhenotype:0002141	oxygen consumption variant
WBPhenotype:0002142	mitochondrial respiratory chain variant
WBPhenotype:0002143	mitochondrial respiratory complex II variant
WBPhenotype:0002145	siRNA processing defective
WBPhenotype:0002146	small RNA germline expression variant
WBPhenotype:0002147	small RNA somatic expression variant
WBPhenotype:0002149	X cluster small RNA expression variant
WBPhenotype:0002150	exo-RNAi response variant
WBPhenotype:0002151	mRNA deadenylation variant
WBPhenotype:0002153	dsRNA processing defective
WBPhenotype:0002154	polysome mRNA association variant
WBPhenotype:0002155	pre miRNA processing defective
WBPhenotype:0002156	temperature learning variant
WBPhenotype:0002157	translation repression variant
WBPhenotype:0002158	P granule degradation defective
WBPhenotype:0002159	increased pathogen accumulation
WBPhenotype:0002160	intraflagellar transport complex destabilized
WBPhenotype:0002161	mitotic chromatin remodeling variant
WBPhenotype:0002162	multipolar mitotic spindle
WBPhenotype:0002163	oxygen consumption decreased
WBPhenotype:0002166	muscle membrane potential variant
WBPhenotype:0002167	transgenerational accumulation of histone methylation
WBPhenotype:0002168	transgenerational loss of fertility
WBPhenotype:0002169	reproductive longevity shortened
WBPhenotype:0002170	calcium mediated signaling variant
WBPhenotype:0002171	alkaline pH chemotaxis variant
WBPhenotype:0002172	pathogen release variant
WBPhenotype:0002174	cell number decreased
WBPhenotype:0002175	cell number increased
WBPhenotype:0002176	seam cell morphology variant
WBPhenotype:0002178	plasma membrane leaflet composition variant
WBPhenotype:0002180	apoptotic cell shedding variant
WBPhenotype:0002181	extra excretory cells
WBPhenotype:0002182	reactive oxygen species homeostasis variant
WBPhenotype:0002183	oxidative DNA damage variant
WBPhenotype:0002184	starvation induced apoptosis variant
WBPhenotype:0002185	cell fate transformation to endoderm
WBPhenotype:0002186	cell fate transformation to pharyngeal muscle
WBPhenotype:0002187	cell fate transformation to body wall muscle
WBPhenotype:0002188	male somatic gonad development variant
WBPhenotype:0002189	extra linker cells
WBPhenotype:0002190	fewer hypodermal cells
WBPhenotype:0002191	fewer sex myoblasts
WBPhenotype:0002192	extra sex myoblasts
WBPhenotype:0002193	posterior reversed vulval lineage
WBPhenotype:0002195	food dependent growth variant
WBPhenotype:0002196	outward rectifying current variant
WBPhenotype:0002198	neuromuscular junction organization variant
WBPhenotype:0002199	neuron calcium transient levels variant
WBPhenotype:0002200	oviduct muscle defective
WBPhenotype:0002201	apoptotic DNA degradation defective
WBPhenotype:0002202	pharynx extension defective
WBPhenotype:0002204	procorpus contraction defective
WBPhenotype:0002205	hypersensitive to galactose
WBPhenotype:0002206	galactose metabolism variant
WBPhenotype:0002207	missing gonad arms
WBPhenotype:0002209	hook development variant
WBPhenotype:0002210	extra rays
WBPhenotype:0002211	phasmid neuron dye filling defect
WBPhenotype:0002212	amphid neuron dye filling defect
WBPhenotype:0002213	kinase activity reduced
WBPhenotype:0002214	extra pharyngeal muscle cells
WBPhenotype:0002215	fewer body wall muscles
WBPhenotype:0002216	pattern antibody staining variant
WBPhenotype:0002218	arsenite hypersensitive
WBPhenotype:0002219	fluoranthene hypersensitive
WBPhenotype:0002220	antimonite hypersensitivity
WBPhenotype:0002223	manganese hypersensitivity
WBPhenotype:0002224	mercury hypersensitive
WBPhenotype:0002226	cobalt hypersensitive
WBPhenotype:0002230	metal accumulation increased
WBPhenotype:0002231	manganese induced oxidative stress response
WBPhenotype:0002232	synaptic remodeling variant
WBPhenotype:0002233	osmolarity modulated swimming variant
WBPhenotype:0002234	increased acidified compartments
WBPhenotype:0002235	growth defective on low phosphate media
WBPhenotype:0002236	endo lysosomal degradation pathway defective
WBPhenotype:0002237	endocytic recycling compartment organization and biogenesis defective
WBPhenotype:0002238	increased levels of reactive oxygen species
WBPhenotype:0002239	reduced levels of reactive oxygen species
WBPhenotype:0002240	gut granule morphology variant
WBPhenotype:0002241	feeding reduced
WBPhenotype:0002242	hypersensitive to iron deficiency
WBPhenotype:0002243	phytochelatin synthesis deficient
WBPhenotype:0002244	arsenic hypersensitive
WBPhenotype:0002245	endogenous zinc levels reduced
WBPhenotype:0002248	hypersensitive to zinc deficiency
WBPhenotype:0002251	silver nanoparticle hypersensitive
WBPhenotype:0002252	increased susceptibility to viral infection
WBPhenotype:0002253	22G RNA expression reduced
WBPhenotype:0002255	amino acid metabolism variant
WBPhenotype:0002256	selenium response variant
WBPhenotype:0002257	iron hypersensitive
WBPhenotype:0002258	nickel toxicity resistant
WBPhenotype:0002259	dendritic termini number reduced
WBPhenotype:0002260	gamete necrotic death increased
WBPhenotype:0002261	neurite connectivity defective
WBPhenotype:0002262	postsynaptic component localization variant
WBPhenotype:0002263	mitochondrial membrane potential increased
WBPhenotype:0002264	ATP levels increased
WBPhenotype:0002265	lysosome-related organelle biogenesis variant
WBPhenotype:0002266	mitochondrial content variant
WBPhenotype:0002267	mitochondrial content increased
WBPhenotype:0002268	mitochondrial content decreased
WBPhenotype:0002269	oxygen consumption increased
WBPhenotype:0002270	metabolite content decreased
WBPhenotype:0002272	protein carbonylation variant
WBPhenotype:0002273	dietary sugar response variant
WBPhenotype:0002275	plugged excretory pore
WBPhenotype:0002276	dauer lifespan shortened
WBPhenotype:0002277	dauer lifespan extended
WBPhenotype:0002278	acute functional tolerance to alcohol defective
WBPhenotype:0002279	fat associated body size decreased
WBPhenotype:0002280	organism osmotic stress resistant
WBPhenotype:0002281	organism osmotic stress hypersensitive
WBPhenotype:0002282	autophagy increased
WBPhenotype:0002283	autophagy reduced
WBPhenotype:0002284	head bend angle variant
WBPhenotype:0002285	head bend angle decreased
WBPhenotype:0002286	head bend angle increased
WBPhenotype:0002287	tail movement variant
WBPhenotype:0002288	tail bend angle variant
WBPhenotype:0002289	tail bend angle increased
WBPhenotype:0002290	tail bend angle decreased
WBPhenotype:0002291	body posture amplitude variant
WBPhenotype:0002292	body posture amplitude decreased
WBPhenotype:0002293	body posture amplitude increased
WBPhenotype:0002294	body posture wavelength variant
WBPhenotype:0002295	body posture wavelength decreased
WBPhenotype:0002296	body posture wavelength increased
WBPhenotype:0002298	coiling frequency variant
WBPhenotype:0002299	coiling frequency decreased
WBPhenotype:0002300	coiling frequency increased
WBPhenotype:0002301	nose movement variant
WBPhenotype:0002302	nose movement decreased
WBPhenotype:0002303	nose movement increased
WBPhenotype:0002308	pausing variant
WBPhenotype:0002309	pausing decreased
WBPhenotype:0002310	pausing increased
WBPhenotype:0002312	turning frequency variant
WBPhenotype:0002313	turning frequency increased
WBPhenotype:0002314	turning frequency reduced
WBPhenotype:0002317	dwelling increased
WBPhenotype:0002318	dwelling reduced
WBPhenotype:0002319	roaming increased
WBPhenotype:0002320	reversal variant
WBPhenotype:0002321	forward point velocity decreased
WBPhenotype:0002322	forward point velocity increased
WBPhenotype:0002323	backward point velocity variant
WBPhenotype:0002324	backward point velocity decreased
WBPhenotype:0002325	backward point velocity increased
WBPhenotype:0002326	velocity of movement decreased
WBPhenotype:0002327	velocity of movement increased
WBPhenotype:0002328	amplitude of sinusoidal movement increased
WBPhenotype:0002332	track length variant
WBPhenotype:0002335	path curvature variant
WBPhenotype:0002336	path curvature increased
WBPhenotype:0002337	path curvature decreased
WBPhenotype:0002338	body proportion variant
WBPhenotype:0002341	bent posture variant
WBPhenotype:0002342	bent posture increased
WBPhenotype:0002343	bent posture decreased
WBPhenotype:0002344	backing decreased
WBPhenotype:0002345	forward locomotion variant
WBPhenotype:0002346	forward locomotion increased
WBPhenotype:0002347	forward locomotion decreased
WBPhenotype:0002348	frequency of body bends increased
WBPhenotype:0002349	phosphatidylinositol 3-phosphate levels reduced
WBPhenotype:0002350	hydrogen peroxide levels increased
WBPhenotype:0002351	hydrogen peroxide levels reduced
WBPhenotype:0002352	tRNA expression increased
WBPhenotype:0002353	tRNA expression decreased
WBPhenotype:0002354	increased susceptibility to fungal infection
WBPhenotype:0002355	increased susceptibility to bacterial pathogens
WBPhenotype:0002357	metabolite content increased
WBPhenotype:0002358	transdifferentiation defective
WBPhenotype:0002359	protein carbonylation increased
WBPhenotype:0002360	cold hypersensitive
WBPhenotype:0002361	membrane fluidity increased
WBPhenotype:0002362	protein sumoylation variant
WBPhenotype:0002363	cholesterol depletion resistant
WBPhenotype:0002364	axonal degeneration
WBPhenotype:0002365	regenerative axonal fusion defective
WBPhenotype:0002366	touch-induced suppression of head movement defective
WBPhenotype:0002367	non-living barrier escape defective
WBPhenotype:0002368	lysosomal refractile body accumulation
WBPhenotype:0002369	sister cell division timing asynchrony reduced
WBPhenotype:0002370	noxious heat avoidance defective
WBPhenotype:0002371	vesicle maturation defective
WBPhenotype:0002372	presynaptic vesicle morphology altered
WBPhenotype:0002373	conditional attraction to bacterial lawn
WBPhenotype:0002374	RNAi transport defective
WBPhenotype:0002375	reversion of swimming paralysis
WBPhenotype:0002376	mRNA poly-A tail length decreased
WBPhenotype:0002377	mRNA poly-A tail length increased
WBPhenotype:0002378	pathogen avoidance variant
WBPhenotype:0002379	mitochondria localization variant
WBPhenotype:0002380	neuron degeneration enhanced
WBPhenotype:0002381	pheromone production variant
WBPhenotype:0002382	resistant to bioactive compound
WBPhenotype:0002385	high pH avoidance defective
WBPhenotype:0002386	fibrous body-membranous organelle (FB-MO) assembly variant
WBPhenotype:0002387	supernumerary asters
WBPhenotype:0002388	metaphase variant
WBPhenotype:0002389	anaphase variant
WBPhenotype:0002390	variable cell division timing
WBPhenotype:0002391	cytokinesis failure
WBPhenotype:0002392	age dependent somatic depletion of fat
WBPhenotype:0002393	anterior posterior neurite growth variant
WBPhenotype:0002394	phagosome sealing defective
WBPhenotype:0002395	corpse engulfment initiation variant
WBPhenotype:0002396	tumor prolapse frequency decreased
WBPhenotype:0002397	tumor prolapse frequency increased
WBPhenotype:0002398	starved L1 larvae aggregation variant
WBPhenotype:0002399	neurotransmitter response variant
WBPhenotype:0002400	glucose intolerant
WBPhenotype:0002401	excess fatty acids
WBPhenotype:0002402	cell position defective
WBPhenotype:0002403	P cell misalignment at ventral midline
WBPhenotype:0002404	cell cell contacts abnormal
WBPhenotype:0002405	pheromone behavioral response variant
WBPhenotype:0002410	cleavage furrow defective
WBPhenotype:0002413	multiple nuclei
WBPhenotype:0002414	spindle variant
WBPhenotype:0002416	spindle position variant
WBPhenotype:0002420	chromatin modification variant
WBPhenotype:0002421	cold resistant
WBPhenotype:0002422	tunicamycin resistant
WBPhenotype:0002428	intestinal degeneration
WBPhenotype:0002429	protein glycosylation variant
WBPhenotype:0002430	mitochondrial DNA damage variant
WBPhenotype:0002431	alternative lengthening of telomeres
WBPhenotype:0002433	EGF-induced sleep resistant
WBPhenotype:0002434	mitochondrial stress response variant
WBPhenotype:0002436	high susceptibility to induced DNA damage
WBPhenotype:0002438	repetitive transgene expression reduced
WBPhenotype:0002440	sperm fertility defective
WBPhenotype:0002441	pharyngeal inter-pump interval increased
WBPhenotype:0002442	pharyngeal pump duration increased
WBPhenotype:0002443	spicule protraction variant
WBPhenotype:0002457	ectopic vulva in male
WBPhenotype:0002458	maternal effect morphology variant
WBPhenotype:0002459	hyperinduction of antimicrobial peptide expression after infection
WBPhenotype:0002460	no induction of antimicrobial peptide expression after infection
WBPhenotype:0002462	pathogen adherence increased
WBPhenotype:0002463	hookless
WBPhenotype:0002464	multiple hooks
WBPhenotype:0002465	histone ubiquitination variant
WBPhenotype:0002466	RNA methylation variant
WBPhenotype:0002467	male reproductive longevity extended
WBPhenotype:0002468	translation rate reduced
WBPhenotype:0002469	plate tap habituation variant
WBPhenotype:0002471	cilia length increased
WBPhenotype:0002472	cilia length decreased
WBPhenotype:0002473	autophagy block
WBPhenotype:0002474	viral resistance increased
WBPhenotype:0002476	pharynx length increased
WBPhenotype:0002477	ribosome localization variant
WBPhenotype:0002479	axon regeneration enhanced
WBPhenotype:0002481	heme levels decreased
WBPhenotype:0002482	heme levels increased
WBPhenotype:0002483	fungal resistance increased
WBPhenotype:0002486	persistent primordial germ cell lobes
WBPhenotype:0002488	intestinal integrity increased
WBPhenotype:0002489	intestinal integrity reduced
WBPhenotype:0002490	ectopic axon outgrowth
WBPhenotype:0002491	ectopic neurite outgrowth
WBPhenotype:0002492	ectopic body wall muscle
WBPhenotype:0002493	ectopic cell
WBPhenotype:0002494	ectopic endoderm
WBPhenotype:0002495	ectopic hypodermis
WBPhenotype:0002496	ectopic neuron
WBPhenotype:0002497	ectopic pharyngeal muscle
WBPhenotype:0002501	ectopic cleavage furrow early emb
WBPhenotype:0002502	protein acetylation increased
WBPhenotype:0002503	meiotic DNA double strand break formation increased
WBPhenotype:0002504	pathogen release reduced
WBPhenotype:0002506	pathogen infection clearance rate increased
WBPhenotype:0002507	pathogen infection clearance rate decreased
WBPhenotype:0002508	extra neuron
WBPhenotype:0002509	extra dopaminergic neuron
WBPhenotype:0002510	fewer neurons
WBPhenotype:0002511	fewer glutamatergic neurons
WBPhenotype:0002512	thermosensory behavior variant
WBPhenotype:0002514	backing absent
WBPhenotype:0002515	organism pathogen response defective
WBPhenotype:0002517	burrowing assay distance reduced
WBPhenotype:0002519	axon length reduced
WBPhenotype:0002521	gap junction plaque number increased
WBPhenotype:0002523	slow recovery from starvation-induced L1 arrest
WBPhenotype:0002524	molybdenum cofactor depletion hypersensitive
WBPhenotype:0002526	response to molybdenum cofactor depletion abnormal
WBPhenotype:0002528	miRNA biogenesis defective
WBPhenotype:0002532	allophagy defective
WBPhenotype:0002534	antimicrobial gene expression variant
WBPhenotype:0002535	dye filling defect
WBPhenotype:0002537	P granule number reduced
WBPhenotype:0002538	calcium signaling in spermatheca variant
WBPhenotype:0002539	antimicrobial gene expression increased
WBPhenotype:0002540	lawn leaving reduced
WBPhenotype:0002541	radiation induced germ cell apoptosis resistant
WBPhenotype:0002542	intranuclear chromatin localization variant
WBPhenotype:0002544	hypersensitive to Enterobacter commensals
WBPhenotype:0002547	gut Enterobacteriaceae bloom
WBPhenotype:0002548	kinker from conflicting forward and backward body bend propagation
WBPhenotype:0002549	increased frequency of spontaneous reversal initiation
WBPhenotype:0002550	conflicted kinker with gradual backward movement
WBPhenotype:0002560	burrowing in response to high population density increased
WBPhenotype:0002562	lysosome homeostasis abnormal
WBPhenotype:0002563	neuron physiology phenotype
WBPhenotype:0002567	long-term associative olfactory memory defective
WBPhenotype:0002572	mitophagy abnormal
WBPhenotype:0002573	mitophagy reduced
WBPhenotype:0002576	gene expression level variation reduced
WBPhenotype:0002581	cell position variability increased
WBPhenotype:0002583	miniature inhibitory post-synaptic current amplitude increased
WBPhenotype:0002584	bisphenol A resistant
WBPhenotype:0002587	Pluronic gel burrowing impaired
WBPhenotype:0002588	basement membrane phenotype
WBPhenotype:0004001	hermaphrodite mating variant
WBPhenotype:0004003	mate finding defective
WBPhenotype:0004004	male response to contact defective
WBPhenotype:0004006	post hermaphrodite contact variant
WBPhenotype:0004007	periodic spicule prodding defective
WBPhenotype:0004008	sustained spicule protraction defective
WBPhenotype:0004009	approximate vulval location variant
WBPhenotype:0004012	sperm transfer continuation defective
WBPhenotype:0004014	post male contact variant
WBPhenotype:0004016	dauer nictation behavior variant
WBPhenotype:0004017	locomotor coordination variant
WBPhenotype:0004018	sinusoidal movement variant
WBPhenotype:0004022	amplitude of sinusoidal movement variant
WBPhenotype:0004023	frequency of body bend variant
WBPhenotype:0004024	wavelength of movement variant
WBPhenotype:0004025	velocity of movement variant
WBPhenotype:0004026	nose touch variant
WBPhenotype:0004027	plate tap reflex variant
WBPhenotype:0004028	slowing response on food variant
WBPhenotype:0004030	male response to hermaphrodite variant
WBPhenotype:0004031	mate searching variant
WBPhenotype:0006001	squashed vulva
WBPhenotype:0008001	embryonic cell fate specification variant
WBPhenotype:0010003	cell corpse appearance delayed
WBPhenotype:0010004	cell corpse degradation variant
ZP:0000303	cell cycle arrested, abnormal
ZP:0000304	cell population proliferation decreased occurrence, abnormal
ZP:0000305	embryo development arrested, abnormal
ZP:0000606	developmental process delayed, abnormal
ZP:0000676	cell population proliferation increased rate, abnormal
ZP:0001563	axon guidance process quality, abnormal
ZP:0001587	gastrulation process quality, abnormal
ZP:0002428	embryo development process quality, abnormal
ZP:0003211	hatching delayed, abnormal
ZP:0003267	muscle attachment process quality, abnormal
ZP:0004316	mRNA splicing, via spliceosome process quality, abnormal
ZP:0004500	nervous system development process quality, abnormal
ZP:0004703	cell migration process quality, abnormal
ZP:0004741	neuron development process quality, abnormal
ZP:0004747	digestive tract development process quality, abnormal
ZP:0004939	apoptotic process decreased occurrence, abnormal
ZP:0004962	apoptotic process increased rate, abnormal
ZP:0005933	lipid metabolic process process quality, abnormal
ZP:0006859	developmental growth process quality, abnormal
ZP:0006865	chromosome segregation process quality, abnormal
ZP:0007567	vesicle-mediated transport process quality, abnormal
ZP:0008973	neuromuscular synaptic transmission process quality, abnormal
ZP:0009477	response to starvation process quality, abnormal
ZP:0010496	cell division decreased rate, abnormal
ZP:0011560	cytokinesis process quality, abnormal
ZP:0012599	behavior process quality, abnormal
ZP:0012632	spermatogenesis delayed, abnormal
ZP:0012634	sex determination process quality, abnormal
ZP:0012861	actin cytoskeleton organization process quality, abnormal
ZP:0012870	apoptotic process process quality, abnormal
ZP:0013137	cell division process quality, abnormal
ZP:0013172	cell fate specification process quality, abnormal
ZP:0013230	larval development process quality, abnormal
ZP:0013553	gonad development process quality, abnormal
ZP:0013585	serotonin metabolic process process quality, abnormal
ZP:0013737	establishment or maintenance of cell polarity process quality, abnormal
ZP:0013923	response to light stimulus process quality, abnormal
ZP:0014134	developmental process decreased rate, abnormal
ZP:0014483	innate immune response process quality, abnormal
ZP:0014592	response to wounding process quality, abnormal
ZP:0014639	hatching process quality, abnormal
ZP:0014781	adult behavior process quality, abnormal
ZP:0014893	response to gamma radiation process quality, abnormal
ZP:0015844	response to chemical process quality, abnormal
ZP:0016367	synapse assembly process quality, abnormal
ZP:0016446	response to oxidative stress process quality, abnormal
ZP:0016569	cell division absent, abnormal
ZP:0017152	germ cell development process quality, abnormal
ZP:0018279	axon development process quality, abnormal
ZP:0019342	cell adhesion process quality, abnormal
ZP:0019910	ovulation process quality, abnormal
ZP:0020346	social behavior process quality, abnormal
ZP:0021180	RNA catabolic process process quality, abnormal
ZP:0022720	feeding behavior process quality, abnormal
ZP:0022916	response to heat process quality, abnormal
ZP:0100495	response to stress process quality, abnormal
ZP:0100734	autophagy process quality, abnormal
ZP:0101282	defecation process quality, abnormal
ZP:0103242	response to osmotic stress process quality, abnormal
ZP:0103694	oocyte development process quality, abnormal
ZP:0104533	pharynx development process quality, abnormal
ZP:0105902	circadian behavior process quality, abnormal
ZP:0106498	response to external stimulus process quality, abnormal
ZP:0106949	response to drug process quality, abnormal
ZP:0106959	microtubule cytoskeleton organization process quality, abnormal
ZP:0107125	response to hypoxia process quality, abnormal
ZP:0137232	microtubule polymerization process quality, abnormal
ZP:0138283	neuron projection development process quality, abnormal