HP:0000504 Abnormality of vision HP:0000505 Visual impairment HP:0000618 Blindness HP:0001508 Failure to thrive HP:0001510 Growth delay HP:0001511 Intrauterine growth retardation HP:0001635 Congestive heart failure HP:0002067 Bradykinesia HP:0002269 Abnormality of neuronal migration HP:0003130 Abnormal peripheral myelination HP:0004359 Abnormal circulating fatty-acid concentration HP:0004363 Abnormal circulating calcium concentration HP:0010831 Impaired proprioception HP:0010901 Abnormal circulating methionine concentration HP:0011014 Abnormal glucose homeostasis HP:0011018 Abnormality of the cell cycle HP:0011028 Abnormality of blood circulation HP:0011036 Abnormality of renal excretion HP:0011400 Abnormal CNS myelination HP:0011675 Arrhythmia HP:0012347 Abnormal protein N-linked glycosylation HP:0012358 Abnormal protein O-linked glycosylation HP:0012447 Abnormal myelination HP:0012535 Abnormal synaptic transmission HP:0030895 Abnormal gastrointestinal motility HP:0031377 Abnormal cell proliferation HP:0100529 Abnormal blood phosphate concentration MP:0000060 delayed bone ossification MP:0000118 arrest of tooth development MP:0001155 arrest of spermatogenesis MP:0001633 poor circulation MP:0002113 abnormal skeleton development MP:0003416 premature bone ossification MP:0003417 premature endochondral bone ossification MP:0003786 premature aging MP:0004022 abnormal cone electrophysiology MP:0004251 failure of heart looping MP:0005528 decreased renal glomerular filtration rate MP:0005573 increased pulmonary respiratory rate MP:0008261 arrest of male meiosis MP:0012177 delayed head development ZP:0000002 somitogenesis disrupted, abnormal ZP:0000003 somite specification disrupted, abnormal ZP:0000004 determination of left/right asymmetry in lateral mesoderm disrupted, abnormal ZP:0000005 ectoderm development disrupted, abnormal ZP:0000006 lateral mesoderm development disrupted, abnormal ZP:0000007 blood vessel morphogenesis disrupted, abnormal ZP:0000008 hematopoietic stem cell differentiation disrupted, abnormal ZP:0000009 blood decreased amount, abnormal ZP:0000010 somite border somite 5 amorphous, abnormal ZP:0000011 somite quality, abnormal ZP:0000012 somite morphology, abnormal ZP:0000013 somite shape, abnormal ZP:0000014 somite border somite 7 amorphous, abnormal ZP:0000015 somite border somite 8 amorphous, abnormal ZP:0000016 somite border somite 6 amorphous, abnormal ZP:0000017 somite border somite 9 amorphous, abnormal ZP:0000018 post-vent region quality, abnormal ZP:0000019 intersegmental vessel malformed, abnormal ZP:0000020 somite border irregular spatial pattern, abnormal ZP:0000021 somite border deformed, abnormal ZP:0000022 hematopoietic stem cell decreased amount, abnormal ZP:0000023 hindbrain morphology, abnormal ZP:0000024 motor neuron spinal cord decreased amount, abnormal ZP:0000025 spinal cord interneuron decreased amount, abnormal ZP:0000026 trunk decreased length, abnormal ZP:0000027 post-vent region decreased length, abnormal ZP:0000028 endoderm development disrupted, abnormal ZP:0000029 retinal ganglion cell axon guidance disrupted, abnormal ZP:0000030 skeletal muscle fiber development disrupted, abnormal ZP:0000031 swim bladder inflation arrested, abnormal ZP:0000032 brain quality, abnormal ZP:0000033 endoderm morphology, abnormal ZP:0000034 hindbrain quality, abnormal ZP:0000035 midbrain hindbrain boundary malformed, abnormal ZP:0000036 neural crest quality, abnormal ZP:0000038 pericardium edematous, abnormal ZP:0000039 swim bladder physical object quality, abnormal ZP:0000040 yolk quality, abnormal ZP:0000041 pharyngeal arch 3-7 skeleton quality, abnormal ZP:0000042 cerebellum malformed, abnormal ZP:0000043 eye decreased size, abnormal ZP:0000044 heart quality, abnormal ZP:0000045 liver mislocalised anteriorly, abnormal ZP:0000046 pectoral fin bud aplastic, abnormal ZP:0000047 retinal photoreceptor layer disorganized, abnormal ZP:0000048 retina morphology, abnormal ZP:0000049 surface structure quality, abnormal ZP:0000050 optic tectum decreased size, abnormal ZP:0000051 optic tectum disorganized, abnormal ZP:0000053 RoL2 rhombomere 4 mislocalised, abnormal ZP:0000054 head decreased size, abnormal ZP:0000055 pectoral fin quality, abnormal ZP:0000056 pectoral fin aplastic, abnormal ZP:0000057 Meckel's cartilage decreased size, abnormal ZP:0000058 Meckel's cartilage fused with ceratohyal cartilage, abnormal ZP:0000059 exocrine pancreas mislocalised anteriorly, abnormal ZP:0000060 endocrine pancreas mislocalised anteriorly, abnormal ZP:0000061 fin bud aplastic, abnormal ZP:0000062 palatoquadrate cartilage decreased size, abnormal ZP:0000063 palatoquadrate cartilage fused with hyosymplectic cartilage, abnormal ZP:0000064 ceratohyal cartilage decreased size, abnormal ZP:0000065 hyosymplectic cartilage decreased size, abnormal ZP:0000066 ceratobranchial cartilage absent, abnormal ZP:0000067 RoL2 increased amount, abnormal ZP:0000068 Mauthner neuron absent, abnormal ZP:0000069 axon guidance disrupted, abnormal ZP:0000070 olfactory bulb development disrupted, abnormal ZP:0000071 neuromast primordium migration delayed, abnormal ZP:0000072 posterior lateral line nerve development disrupted, abnormal ZP:0000073 innervation disrupted, abnormal ZP:0000074 fasciculation of sensory neuron axon disrupted, abnormal ZP:0000075 olfactory placode disorganized, abnormal ZP:0000076 posterior lateral line nerve decreased length, abnormal ZP:0000077 glomerular layer aplastic, abnormal ZP:0000078 olfactory bulb disorganized, abnormal ZP:0000079 GABAergic neuron olfactory bulb decreased amount, abnormal ZP:0000080 dopaminergic neuron olfactory bulb decreased amount, abnormal ZP:0000081 olfactory epithelium disorganized, abnormal ZP:0000082 olfactory epithelium split, abnormal ZP:0000083 posterior lateral line neuromast malformed, abnormal ZP:0000084 posterior lateral line neuromast decreased amount, abnormal ZP:0000085 posterior lateral line primordium circular, abnormal ZP:0000086 posterior lateral line primordium crescent-shaped, abnormal ZP:0000087 anterior lateral line neuromast decreased amount, abnormal ZP:0000088 olfactory receptor cell spatial pattern, abnormal ZP:0000089 axon olfactory receptor cell decreased length, abnormal ZP:0000090 axon olfactory receptor cell disorganized, abnormal ZP:0000091 neuromast hair cell decreased amount, abnormal ZP:0000092 uroporphyrinogen decarboxylase activity decreased rate, abnormal ZP:0000093 porphyrin-containing compound metabolic process disrupted, abnormal ZP:0000094 blood quality, abnormal ZP:0000095 whole organism lethal (sensu genetics), abnormal ZP:0000096 nucleate erythrocyte fluorescence, abnormal ZP:0000097 endoderm formation process quality, abnormal ZP:0000098 endodermal cell fate specification disrupted, abnormal ZP:0000100 brain morphology, abnormal ZP:0000101 endodermal cell endoderm decreased amount, abnormal ZP:0000102 yolk increased size, abnormal ZP:0000103 extension decreased length, abnormal ZP:0000104 extension increased thickness, abnormal ZP:0000105 fourth ventricle collapsed, abnormal ZP:0000106 gut aplastic, abnormal ZP:0000107 heart morphology, abnormal ZP:0000108 heart cleft, abnormal ZP:0000109 heart duplicated, abnormal ZP:0000110 notochord aplastic, abnormal ZP:0000111 somite fused with somite, abnormal ZP:0000112 tectal ventricle collapsed, abnormal ZP:0000113 heart tube duplicated, abnormal ZP:0000114 heart tube bifurcated, abnormal ZP:0000115 nervous system quality, abnormal ZP:0000116 anterior-posterior axis whole organism curved ventral, abnormal ZP:0000117 head hypoplastic, abnormal ZP:0000118 forebrain ventricle collapsed, abnormal ZP:0000119 endochondral ossification disrupted, abnormal ZP:0000120 chondrocyte differentiation delayed, abnormal ZP:0000121 eye mislocalised, abnormal ZP:0000122 notochord undulate, abnormal ZP:0000123 mouth absent, abnormal ZP:0000124 head malformed, abnormal ZP:0000125 Meckel's cartilage mislocalised, abnormal ZP:0000126 Meckel's cartilage malformed, abnormal ZP:0000127 ceratobranchial 5 bone composition, abnormal ZP:0000128 pharyngeal arch aplastic, abnormal ZP:0000129 neurocranial trabecula decreased size, abnormal ZP:0000130 neurocranial trabecula malformed, abnormal ZP:0000131 ceratohyal cartilage mislocalised, abnormal ZP:0000132 ceratohyal cartilage malformed, abnormal ZP:0000133 ethmoid cartilage decreased size, abnormal ZP:0000134 cranial cartilage disorganized, abnormal ZP:0000135 pharyngeal arch cartilage disorganized, abnormal ZP:0000136 ceratobranchial cartilage decreased size, abnormal ZP:0000137 perichordal connective tissue morphology, abnormal ZP:0000138 chondrocyte disorganized, abnormal ZP:0000139 gastrulation with mouth forming second quality, abnormal ZP:0000140 gastrulation with mouth forming second disrupted, abnormal ZP:0000141 dorsal/ventral pattern formation disrupted, abnormal ZP:0000142 epidermal cell fate specification disrupted, abnormal ZP:0000143 post-anal tail morphogenesis disrupted, abnormal ZP:0000144 post-anal tail morphogenesis having extra processual parts post-anal tail morphogenesis, abnormal ZP:0000145 tail bud mislocalised posteriorly, abnormal ZP:0000146 heart rudiment unfused from heart rudiment, abnormal ZP:0000147 notochord quality, abnormal ZP:0000148 notochord increased width, abnormal ZP:0000149 otic placode disorganized, abnormal ZP:0000150 otic placode aplastic, abnormal ZP:0000151 pronephric duct hypoplastic, abnormal ZP:0000152 somite circular, abnormal ZP:0000153 somite increased width, abnormal ZP:0000154 paraxial mesoderm morphology, abnormal ZP:0000155 paraxial mesoderm has extra parts of type adaxial cell, abnormal ZP:0000156 anterior-posterior axis paraxial mesoderm decreased length, abnormal ZP:0000157 rhombomere 5 fused with left side right side rhombomere 5, abnormal ZP:0000158 rhombomere 3 increased length, abnormal ZP:0000159 whole organism shape, abnormal ZP:0000160 whole organism wholly dorsalized, abnormal ZP:0000161 whole organism ovate, abnormal ZP:0000162 whole organism has extra parts of type post-vent region, abnormal ZP:0000163 trunk condensed, abnormal ZP:0000164 trunk rotational curvature, abnormal ZP:0000165 post-vent region aplastic, abnormal ZP:0000166 post-vent region has extra parts of type tail bud, abnormal ZP:0000167 post-vent region has extra parts of type notochord, abnormal ZP:0000168 neural tube morphology, abnormal ZP:0000169 pectoral fin mislocalised, abnormal ZP:0000170 neuron spinal cord neural rod increased amount, abnormal ZP:0000171 neuron spinal cord neural rod mislocalised laterally, abnormal ZP:0000172 blood cell decreased amount, abnormal ZP:0000173 erythroid lineage cell absent, abnormal ZP:0000174 cell proliferation in hindbrain decreased occurrence, abnormal ZP:0000175 fourth ventricle development disrupted, abnormal ZP:0000176 hypothalamus development process quality, abnormal ZP:0000177 hindbrain development disrupted, abnormal ZP:0000178 retinoic acid catabolic process decreased rate, abnormal ZP:0000179 forebrain morphogenesis process quality, abnormal ZP:0000180 embryonic retina morphogenesis in camera-type eye process quality, abnormal ZP:0000181 optic vesicle wholly ventralized, abnormal ZP:0000182 diencephalon physical object quality, abnormal ZP:0000183 forebrain physical object quality, abnormal ZP:0000184 fourth ventricle structure, abnormal ZP:0000185 optic stalk malformed, abnormal ZP:0000186 retinal pigmented epithelium mislocalised, abnormal ZP:0000187 retina malformed, abnormal ZP:0000188 retina physical object quality, abnormal ZP:0000189 optic cup physical object quality, abnormal ZP:0000190 optic fissure closure incomplete, abnormal ZP:0000191 embryonic heart tube morphogenesis decreased process quality, abnormal ZP:0000192 endocardium morphogenesis decreased process quality, abnormal ZP:0000194 cardiac muscle tissue morphogenesis decreased process quality, abnormal ZP:0000195 cardioblast migration to the midline involved in heart field formation decreased process quality, abnormal ZP:0000196 postoptic commissure increased width, abnormal ZP:0000197 myocardium mislocalised, abnormal ZP:0000198 endocardium mislocalised, abnormal ZP:0000199 abnormal(ly) malformed endocardium cell ZP:0000200 startle response disrupted, abnormal ZP:0000201 optokinetic behavior disrupted, abnormal ZP:0000202 larval locomotory behavior rhythm quality, abnormal ZP:0000203 response to absence of light disrupted, abnormal ZP:0000204 response to auditory stimulus disrupted, abnormal ZP:0000205 axon midline choice point recognition disrupted, abnormal ZP:0000206 musculoskeletal movement quality, abnormal ZP:0000208 neuromuscular process controlling balance disrupted, abnormal ZP:0000209 equilibrioception disrupted, abnormal ZP:0000210 commissural neuron axon guidance disrupted, abnormal ZP:0000211 postoptic commissure decreased width, abnormal ZP:0000212 whole organism viability, abnormal ZP:0000213 whole organism movement behavioral quality, abnormal ZP:0000214 post-vent region movement quality, abnormal ZP:0000215 hindbrain commissure disorganized, abnormal ZP:0000216 axon Mauthner neuron mislocalised, abnormal ZP:0000217 liver development disrupted, abnormal ZP:0000218 yolk low brightness, abnormal ZP:0000219 liver primordium duplicated, abnormal ZP:0000220 post-vent region morphology, abnormal ZP:0000221 fin regeneration disrupted, abnormal ZP:0000222 heart looping disrupted, abnormal ZP:0000223 heart development disrupted, abnormal ZP:0000224 whole organism curvature, abnormal ZP:0000225 head increased variability of size, abnormal ZP:0000226 ossification involved in bone maturation delayed, abnormal ZP:0000227 calcium ion import decreased process quality, abnormal ZP:0000228 cAMP biosynthetic process decreased rate, abnormal ZP:0000229 GTP biosynthetic process decreased rate, abnormal ZP:0000231 heart composition, abnormal ZP:0000232 heart decreased contractility, abnormal ZP:0000233 heart decreased functionality, abnormal ZP:0000234 splanchnocranium hypoplastic, abnormal ZP:0000235 mandibular arch skeleton hypoplastic, abnormal ZP:0000236 sarcomere organization disrupted, abnormal ZP:0000237 striated muscle cell development disrupted, abnormal ZP:0000238 actin filament bundle distribution disrupted, abnormal ZP:0000239 whole organism immobile, abnormal ZP:0000240 whole organism bent, abnormal ZP:0000241 muscle trunk refractivity, abnormal ZP:0000242 sarcomere skeletal muscle disorganized, abnormal ZP:0000243 Z disc skeletal muscle disorganized, abnormal ZP:0000246 actin filament fast muscle cell disorganized, abnormal ZP:0000247 actin filament fast muscle cell distributed, abnormal ZP:0000249 myofibril fast muscle cell degenerate, abnormal ZP:0000250 myofibril fast muscle cell disorganized, abnormal ZP:0000254 spinal cord motor neuron cell fate specification disrupted, abnormal ZP:0000255 spinal cord oligodendrocyte cell fate specification disrupted, abnormal ZP:0000256 glioblast (sensu Vertebrata) spinal cord absent, abnormal ZP:0000257 glioblast (sensu Vertebrata) spinal cord decreased amount, abnormal ZP:0000258 secondary motor neuron spinal cord decreased amount, abnormal ZP:0000259 radial glial cell spinal cord disorganized, abnormal ZP:0000260 radial glial cell spinal cord decreased amount, abnormal ZP:0000261 dopaminergic neuron diencephalon increased amount, abnormal ZP:0000262 lymphangiogenesis arrested, abnormal ZP:0000263 thoracic duct hypoplastic, abnormal ZP:0000264 vascular lymphangioblast hypoplastic, abnormal ZP:0000265 lymphangiogenesis disrupted, abnormal ZP:0000266 opercle curved, abnormal ZP:0000267 opercle decreased width, abnormal ZP:0000268 symplectic decreased size, abnormal ZP:0000269 Meckel's cartilage morphology, abnormal ZP:0000270 palatoquadrate cartilage truncated, abnormal ZP:0000271 hyosymplectic cartilage elongated, abnormal ZP:0000272 hyosymplectic cartilage deformed, abnormal ZP:0000273 thoracic duct absent, abnormal ZP:0000274 thoracic duct wholeness, abnormal ZP:0000276 oligodendrocyte development arrested, abnormal ZP:0000277 rhombomere boundary formation disrupted, abnormal ZP:0000279 radial glial cell division in pallium increased occurrence, abnormal ZP:0000280 cell differentiation involved in pronephros development disrupted, abnormal ZP:0000282 central nervous system cellular quality, abnormal ZP:0000283 hindbrain increased rate cell death, abnormal ZP:0000284 epithelium hindbrain disorganized, abnormal ZP:0000286 neuroepithelial cell hindbrain aggregated, abnormal ZP:0000287 blood vessel telencephalon prominent, abnormal ZP:0000288 blood vessel telencephalon dilated, abnormal ZP:0000289 blood vessel telencephalon increased diameter, abnormal ZP:0000290 neural plate morphology, abnormal ZP:0000291 pronephros cellular quality, abnormal ZP:0000292 capillary optic tectum decreased variability of size, abnormal ZP:0000293 blood vessel optic tectum decreased variability of size, abnormal ZP:0000294 dorsal telencephalon has extra parts of type ventricular zone radial glial cell, abnormal ZP:0000295 radial glial cell dorsal telencephalon proliferative, abnormal ZP:0000296 neuron posterior lateral line ganglion increased amount, abnormal ZP:0000297 caudal fin blood vessel broken, abnormal ZP:0000298 caudal fin blood vessel increased diameter, abnormal ZP:0000299 caudal fin blood vessel hemorrhagic, abnormal ZP:0000300 caudal fin blood vessel displaced, abnormal ZP:0000301 peripheral neuron decreased length, abnormal ZP:0000302 somitogenesis decreased functionality, abnormal ZP:0000303 cell cycle arrested, abnormal ZP:0000304 cell population proliferation decreased occurrence, abnormal ZP:0000305 embryo development arrested, abnormal ZP:0000306 whole organism dead, abnormal ZP:0000307 post-vent region arrested segmentation, abnormal ZP:0000308 portion of tissue necrotic, abnormal ZP:0000309 pigment cell decreased amount, abnormal ZP:0000310 spliceosomal snRNP assembly decreased process quality, abnormal ZP:0000311 apoptotic process increased occurrence, abnormal ZP:0000312 Cajal body organization decreased process quality, abnormal ZP:0000313 mRNA cis splicing, via spliceosome decreased occurrence, abnormal ZP:0000314 cell whole organism apoptotic, abnormal ZP:0000315 cell whole organism dead, abnormal ZP:0000316 Cajal body cell decreased amount, abnormal ZP:0000317 small nuclear ribonucleoprotein complex cell dispersed, abnormal ZP:0000318 neural crest cell development disrupted, abnormal ZP:0000319 brain hydrocephalic, abnormal ZP:0000320 hindbrain hydrocephalic, abnormal ZP:0000321 fourth ventricle increased size, abnormal ZP:0000322 midbrain hydrocephalic, abnormal ZP:0000323 tectal ventricle increased size, abnormal ZP:0000324 whole organism decreased size, abnormal ZP:0000325 melanocyte trunk decreased amount, abnormal ZP:0000326 melanocyte post-vent region decreased amount, abnormal ZP:0000327 DoLA increased amount, abnormal ZP:0000328 melanocyte spatial pattern, abnormal ZP:0000329 melanocyte decreased amount, abnormal ZP:0000330 neural crest cell decreased amount, abnormal ZP:0000331 neuron increased amount, abnormal ZP:0000332 heart morphogenesis disrupted, abnormal ZP:0000333 determination of left/right symmetry disrupted, abnormal ZP:0000334 heart development delayed, abnormal ZP:0000335 blood circulation disrupted, abnormal ZP:0000336 thalamus development process quality, abnormal ZP:0000337 thalamus development decreased process quality, abnormal ZP:0000338 Wnt-activated signaling pathway involved in forebrain neuron fate commitment disrupted, abnormal ZP:0000339 forebrain development disrupted, abnormal ZP:0000340 embryonic eye morphogenesis disrupted, abnormal ZP:0000341 epithelial cell proliferation increased occurrence, abnormal ZP:0000342 canonical Wnt signaling pathway increased occurrence, abnormal ZP:0000343 cell migration in diencephalon delayed, abnormal ZP:0000344 epiphysis increased size, abnormal ZP:0000345 photoreceptor cell epiphysis increased amount, abnormal ZP:0000346 neuron epiphysis increased amount, abnormal ZP:0000347 floor plate quality, abnormal ZP:0000348 peripheral olfactory organ absent, abnormal ZP:0000349 olfactory placode aplastic, abnormal ZP:0000350 optic vesicle absent, abnormal ZP:0000351 postoptic commissure aplastic, abnormal ZP:0000352 antero-lateral region prechordal plate decreased size, abnormal ZP:0000353 telencephalon decreased size, abnormal ZP:0000354 telencephalon aplastic, abnormal ZP:0000355 eye quality, abnormal ZP:0000356 eye absent, abnormal ZP:0000357 eye aplastic, abnormal ZP:0000358 forebrain quality, abnormal ZP:0000359 forebrain decreased size, abnormal ZP:0000360 heart linear, abnormal ZP:0000362 cardiac muscle cell heart decreased amount, abnormal ZP:0000364 trigeminal placode increased size, abnormal ZP:0000365 sensory neuron trigeminal placode mislocalised anteriorly, abnormal ZP:0000366 presumptive telencephalon aplastic, abnormal ZP:0000367 presumptive diencephalon increased size, abnormal ZP:0000368 dorsal thalamus cellular quality, abnormal ZP:0000369 epithelial cell posterior intestine increased amount, abnormal ZP:0000370 epithelial cell intestinal bulb increased amount, abnormal ZP:0000372 anterior-posterior axis whole organism deformed, abnormal ZP:0000373 anterior commissure aplastic, abnormal ZP:0000374 head apoptotic, abnormal ZP:0000375 head degenerate, abnormal ZP:0000376 adenohypophysis decreased size, abnormal ZP:0000377 endocardial cushion hyperplastic, abnormal ZP:0000378 cardiac jelly increased volume, abnormal ZP:0000379 intestine morphology, abnormal ZP:0000380 intestine increased thickness, abnormal ZP:0000381 parapineal organ position, abnormal ZP:0000382 primary neuron tract of the postoptic commissure morphology, abnormal ZP:0000383 intestinal bulb epithelium increased thickness, abnormal ZP:0000384 intestinal bulb epithelium disorganized, abnormal ZP:0000385 intestinal bulb epithelium cellular quality, abnormal ZP:0000386 mid diencephalic organizer increased thickness, abnormal ZP:0000387 mid diencephalic organizer cellular quality, abnormal ZP:0000388 dorso-rostral cluster absent, abnormal ZP:0000389 intestinal epithelial cell proliferative, abnormal ZP:0000390 vasculature development disrupted, abnormal ZP:0000391 swim bladder morphogenesis process quality, abnormal ZP:0000392 swim bladder morphology, abnormal ZP:0000393 neutrophil blood island decreased amount, abnormal ZP:0000394 pancreas primordium physical object quality, abnormal ZP:0000395 pharyngeal arch physical object quality, abnormal ZP:0000396 nucleate erythrocyte decreased amount, abnormal ZP:0000397 central nervous system necrotic, abnormal ZP:0000398 whole organism necrotic, abnormal ZP:0000399 head flat, abnormal ZP:0000400 lens quality, abnormal ZP:0000401 eye degenerate, abnormal ZP:0000402 eye decreased pigmentation, abnormal ZP:0000403 gut hypoplastic, abnormal ZP:0000404 liver hypoplastic, abnormal ZP:0000405 retinal pigmented epithelium degenerate, abnormal ZP:0000406 sensory system quality, abnormal ZP:0000407 head decreased width, abnormal ZP:0000408 activation of cysteine-type endopeptidase activity involved in apoptotic process increased occurrence, abnormal ZP:0000409 locomotion decreased process quality, abnormal ZP:0000410 pericardium swollen, abnormal ZP:0000411 swim bladder aplastic, abnormal ZP:0000412 cranial nerve II aplastic, abnormal ZP:0000413 ventricular system increased size, abnormal ZP:0000414 ventral mandibular arch malformed, abnormal ZP:0000415 lens development in camera-type eye disrupted, abnormal ZP:0000416 endocardium development disrupted, abnormal ZP:0000417 retina layer formation disrupted, abnormal ZP:0000418 lens fiber cell development disrupted, abnormal ZP:0000419 lens fiber cell morphogenesis disrupted, abnormal ZP:0000420 lens morphology, abnormal ZP:0000421 lens structure, abnormal ZP:0000422 lens separated from retina, abnormal ZP:0000423 nucleus lens increased amount, abnormal ZP:0000424 cell lens loose, abnormal ZP:0000425 fourth ventricle decreased size, abnormal ZP:0000426 heart increased amount, abnormal ZP:0000427 heart bifurcated, abnormal ZP:0000428 midbrain quality, abnormal ZP:0000429 midbrain morphology, abnormal ZP:0000430 somite degenerate, abnormal ZP:0000431 myotome increased size, abnormal ZP:0000433 actin filament myotome increased length, abnormal ZP:0000435 muscle tendon junction myotome morphology, abnormal ZP:0000436 myosin filament myotome disorganized, abnormal ZP:0000437 ventricular system collapsed, abnormal ZP:0000438 somite border shape, abnormal ZP:0000439 somite border aplastic, abnormal ZP:0000440 corneal epithelium morphology, abnormal ZP:0000441 corneal epithelium undulate, abnormal ZP:0000442 cell death increased occurrence, abnormal ZP:0000443 trigeminal ganglion malformed, abnormal ZP:0000444 pharyngeal arch malformed, abnormal ZP:0000445 ceratobranchial cartilage hypotrophic, abnormal ZP:0000446 epibranchial ganglion malformed, abnormal ZP:0000447 pharyngeal arch 2 morphology, abnormal ZP:0000448 pharyngeal arch 1 morphology, abnormal ZP:0000449 blood vessel development disrupted, abnormal ZP:0000450 blood circulation arrested, abnormal ZP:0000451 hemopoiesis disrupted, abnormal ZP:0000452 heart contraction rhythm quality, abnormal ZP:0000454 heart tube morphology, abnormal ZP:0000455 intersegmental vessel aplastic, abnormal ZP:0000456 trunk vasculature morphology, abnormal ZP:0000457 vascular cord morphology, abnormal ZP:0000458 heart jogging disrupted, abnormal ZP:0000459 mRNA catabolic process disrupted, abnormal ZP:0000460 embryonic heart tube left/right pattern formation disrupted, abnormal ZP:0000461 somite asymmetrical, abnormal ZP:0000462 heart looping delayed, abnormal ZP:0000463 heart contraction arrested, abnormal ZP:0000464 determination of digestive tract left/right asymmetry disrupted, abnormal ZP:0000465 blood island decreased size, abnormal ZP:0000466 heart orientation left-right axis whole organism, abnormal ZP:0000467 heart aligned with central region whole organism, abnormal ZP:0000468 heart tube aligned with central region whole organism, abnormal ZP:0000469 ventral fin fold decreased size, abnormal ZP:0000470 post-vent region decreased size, abnormal ZP:0000471 intestine orientation left-right axis whole organism, abnormal ZP:0000472 intersegmental vessel shortened, abnormal ZP:0000473 whole organism decreased length, abnormal ZP:0000474 neuron degenerate, abnormal ZP:0000475 neural crest cell migration disrupted, abnormal ZP:0000476 mesodermal cell migration disrupted, abnormal ZP:0000477 thyroid gland development disrupted, abnormal ZP:0000478 pectoral fin morphogenesis disrupted, abnormal ZP:0000479 enteric nervous system development disrupted, abnormal ZP:0000480 digestive tract development disrupted, abnormal ZP:0000481 smooth muscle cell differentiation disrupted, abnormal ZP:0000482 heart contraction disrupted, abnormal ZP:0000483 heart contraction decreased intensity, abnormal ZP:0000484 heart formation disrupted, abnormal ZP:0000485 determination of intestine left/right asymmetry disrupted, abnormal ZP:0000486 cardiac ventricle structure, abnormal ZP:0000487 heart primordium unfused from heart primordium, abnormal ZP:0000488 myocardial precursor heart primordium decreased amount, abnormal ZP:0000489 fin quality, abnormal ZP:0000490 heart malformed, abnormal ZP:0000491 heart rudiment bifurcated, abnormal ZP:0000492 lateral plate mesoderm decreased width, abnormal ZP:0000493 liver duplicated, abnormal ZP:0000494 pancreas duplicated, abnormal ZP:0000495 pectoral fin bud decreased size, abnormal ZP:0000496 dentary shape, abnormal ZP:0000497 thyroid follicle decreased amount, abnormal ZP:0000498 thyroid primordium decreased size, abnormal ZP:0000499 neuron enteric nervous system decreased amount, abnormal ZP:0000500 Meckel's cartilage decreased length, abnormal ZP:0000501 smooth muscle cell intestine morphology, abnormal ZP:0000502 neuron intestine decreased amount, abnormal ZP:0000503 epicardium aplastic, abnormal ZP:0000504 cardiac muscle cell organization quality, abnormal ZP:0000505 retinal cone cell decreased amount, abnormal ZP:0000506 embryonic hemopoiesis disrupted, abnormal ZP:0000507 hemoglobin biosynthetic process disrupted, abnormal ZP:0000508 pigmentation disrupted, abnormal ZP:0000509 ventral fin fold kinked, abnormal ZP:0000510 trunk decreased pigmentation, abnormal ZP:0000511 intersegmental vessel decreased size, abnormal ZP:0000512 dorsal longitudinal anastomotic vessel structure, abnormal ZP:0000513 nucleate erythrocyte shape, abnormal ZP:0000514 nucleate erythrocyte low saturation, abnormal ZP:0000515 nucleate erythrocyte increased size, abnormal ZP:0000516 nucleate erythrocyte immature, abnormal ZP:0000517 nucleus nucleate erythrocyte morphology, abnormal ZP:0000518 cranial ganglion neoplastic, abnormal ZP:0000519 neuronal stem cell cranial ganglion increased amount, abnormal ZP:0000520 neuron cranial ganglion proliferative, abnormal ZP:0000521 esophagus inflamed, abnormal ZP:0000522 cranial nerve neoplastic, abnormal ZP:0000523 intestinal bulb inflamed, abnormal ZP:0000524 whole organism neoplastic, invasive, abnormal ZP:0000525 pigment cell irregular spatial pattern, abnormal ZP:0000526 mitotic cell cycle duration, abnormal ZP:0000527 brain hemorrhagic, abnormal ZP:0000528 cardiac ventricle decreased size, abnormal ZP:0000529 dorsal aorta closed, abnormal ZP:0000530 dorsal aorta collapsed, abnormal ZP:0000531 dorsal aorta aplastic, abnormal ZP:0000532 heart increased size, abnormal ZP:0000533 sarcomere heart increased size, abnormal ZP:0000534 cardiac muscle cell heart increased size, abnormal ZP:0000535 atrium increased size, abnormal ZP:0000536 cranial vasculature broken, abnormal ZP:0000537 intersegmental vessel collapsed, abnormal ZP:0000538 cardiac muscle cell atrial myocardium increased amount, abnormal ZP:0000539 cardiac muscle cell atrial myocardium decreased mass density, abnormal ZP:0000540 subintestinal vein collapsed, abnormal ZP:0000541 cardiac muscle cell ventricular myocardium increased amount, abnormal ZP:0000542 cardiac muscle cell ventricular myocardium increased mass density, abnormal ZP:0000543 myeloid cell differentiation process quality, abnormal ZP:0000544 granulocyte differentiation decreased rate, abnormal ZP:0000545 granulocyte differentiation decreased occurrence, abnormal ZP:0000546 definitive hemopoiesis process quality, abnormal ZP:0000547 definitive hemopoiesis disrupted, abnormal ZP:0000548 myeloid cell blood island absent, abnormal ZP:0000549 myeloid cell blood island decreased amount, abnormal ZP:0000550 hematopoietic multipotent progenitor cell blood island absent, abnormal ZP:0000551 cranium shape, abnormal ZP:0000552 hematopoietic stem cell ventral wall of dorsal aorta decreased amount, abnormal ZP:0000553 myeloid cell ventral wall of dorsal aorta absent, abnormal ZP:0000554 myeloid cell ventral wall of dorsal aorta decreased amount, abnormal ZP:0000555 neutrophil ventral wall of dorsal aorta decreased amount, abnormal ZP:0000556 hematopoietic multipotent progenitor cell ventral wall of dorsal aorta absent, abnormal ZP:0000557 hematopoietic stem cell aplastic, abnormal ZP:0000558 erythroid progenitor cell absent, abnormal ZP:0000559 macrophage increased amount, abnormal ZP:0000560 lymphocyte decreased amount, abnormal ZP:0000561 monocyte decreased amount, abnormal ZP:0000562 thrombocyte decreased amount, abnormal ZP:0000563 neutrophil decreased amount, abnormal ZP:0000564 cranium decreased size, abnormal ZP:0000565 somitogenesis delayed, abnormal ZP:0000566 calcium-dependent cell-cell adhesion via plasma membrane cell adhesion molecules disrupted, abnormal ZP:0000567 epiboly involved in gastrulation with mouth forming second delayed, abnormal ZP:0000568 axis decreased length, abnormal ZP:0000569 yolk circular, abnormal ZP:0000570 gut quality, abnormal ZP:0000571 liver quality, abnormal ZP:0000572 palate decreased size, abnormal ZP:0000573 palate fused with palate, abnormal ZP:0000574 central nervous system development disrupted, abnormal ZP:0000575 notochord development disrupted, abnormal ZP:0000576 ball increased size, abnormal ZP:0000577 central nervous system morphology, abnormal ZP:0000578 central nervous system malformed, abnormal ZP:0000581 cranium edematous, abnormal ZP:0000582 myotome increased width, abnormal ZP:0000583 caudal fin curled, abnormal ZP:0000584 caudal fin decreased length, abnormal ZP:0000585 whole organism shortened, abnormal ZP:0000586 anterior-posterior axis whole organism decreased length, abnormal ZP:0000588 central artery decreased length, abnormal ZP:0000589 central artery decreased branchiness, abnormal ZP:0000592 neural retina development disrupted, abnormal ZP:0000593 cell population proliferation increased occurrence, abnormal ZP:0000594 embryo development delayed, abnormal ZP:0000595 head development disrupted, abnormal ZP:0000596 retinal pigmented epithelium quality, abnormal ZP:0000597 retinal pigmented epithelium decreased pigmentation, abnormal ZP:0000598 head quality, abnormal ZP:0000599 pigment granule melanocyte decreased amount, abnormal ZP:0000600 pigment granule xanthophore decreased amount, abnormal ZP:0000601 pigment granule iridophore decreased amount, abnormal ZP:0000602 heart jogging arrested, abnormal ZP:0000603 floor plate formation arrested, abnormal ZP:0000604 floor plate formation disrupted, abnormal ZP:0000605 neural plate anterior/posterior regionalization disrupted, abnormal ZP:0000606 developmental process delayed, abnormal ZP:0000607 cell migration involved in gastrulation disrupted, abnormal ZP:0000608 axial mesodermal cell fate specification disrupted, abnormal ZP:0000609 convergent extension disrupted, abnormal ZP:0000610 ventral region central nervous system decreased size, abnormal ZP:0000611 floor plate absent, abnormal ZP:0000612 floor plate decreased size, abnormal ZP:0000613 floor plate aplastic, abnormal ZP:0000614 ventral region floor plate hypoplastic, abnormal ZP:0000615 hypothalamus decreased size, abnormal ZP:0000616 prechordal plate morphology, abnormal ZP:0000617 spinal cord morphology, abnormal ZP:0000618 axial chorda mesoderm morphology, abnormal ZP:0000619 axial chorda mesoderm aplastic, abnormal ZP:0000620 eye mislocalised medially, abnormal ZP:0000621 eye decreased distance eye, abnormal ZP:0000622 eye fused with eye, abnormal ZP:0000623 anterior region fourth ventricle absent, abnormal ZP:0000624 notochord morphology, abnormal ZP:0000625 notochord structure, abnormal ZP:0000626 notochord decreased size, abnormal ZP:0000627 notochord bent, abnormal ZP:0000628 notochord curved ventral, abnormal ZP:0000629 nucleus notochord decreased amount, abnormal ZP:0000630 cell notochord morphology, abnormal ZP:0000631 heart tube centered, abnormal ZP:0000632 medial longitudinal fasciculus fused with medial longitudinal fasciculus, abnormal ZP:0000633 axon medial longitudinal fasciculus disorganized, abnormal ZP:0000634 cranial nerve IV fused with cranial nerve IV, abnormal ZP:0000635 central canal absent, abnormal ZP:0000636 trunk curved ventral, abnormal ZP:0000637 post-vent region curved, abnormal ZP:0000638 post-vent region curved ventral, abnormal ZP:0000639 neuroectoderm morphology, abnormal ZP:0000640 neural tube quality, abnormal ZP:0000641 cell presumptive floor plate decreased amount, abnormal ZP:0000642 cell presumptive floor plate undifferentiated, abnormal ZP:0000643 floor plate rhombomere region aplastic, abnormal ZP:0000644 parachordal cartilage fused with parachordal cartilage, abnormal ZP:0000645 chondrocranium morphology, abnormal ZP:0000646 trabecula cranii fused with trabecula cranii, abnormal ZP:0000647 anterior neural plate morphology, abnormal ZP:0000648 cranial neural crest cell mislocalised ventrally, abnormal ZP:0000649 axon secondary motor neuron decreased amount, abnormal ZP:0000650 lens decreased size, abnormal ZP:0000651 lens immature, abnormal ZP:0000652 eye decreased diameter, abnormal ZP:0000653 retina structure, abnormal ZP:0000654 retina decreased size, abnormal ZP:0000655 retina disorganized, abnormal ZP:0000656 pupil decreased diameter, abnormal ZP:0000657 retinal ganglion cell decreased amount, abnormal ZP:0000658 skeletal muscle tissue development delayed, abnormal ZP:0000659 skeletal muscle tissue development disrupted, abnormal ZP:0000660 myofibril assembly disrupted, abnormal ZP:0000661 embryonic cranial skeleton morphogenesis disrupted, abnormal ZP:0000663 cephalic musculature decreased amount, abnormal ZP:0000664 whole organism movement quality, abnormal ZP:0000665 ceratohyal cartilage decreased length, abnormal ZP:0000666 chondrocyte ceratohyal cartilage morphology, abnormal ZP:0000667 chondrocyte ceratohyal cartilage decreased size, abnormal ZP:0000669 muscle disorganized, abnormal ZP:0000671 sarcomere muscle disorganized, abnormal ZP:0000672 chondrocyte stacked, abnormal ZP:0000674 fast muscle cell decreased process quality muscle fiber development, abnormal ZP:0000675 heart morphogenesis decreased process quality, abnormal ZP:0000676 cell population proliferation increased rate, abnormal ZP:0000677 myeloid cell differentiation disrupted, abnormal ZP:0000678 embryonic heart tube development disrupted, abnormal ZP:0000679 cardioblast migration to the midline involved in heart field formation disrupted, abnormal ZP:0000680 heart primordium unfused from left side right side heart primordium, abnormal ZP:0000681 swim bladder non-functional, abnormal ZP:0000682 gut immature, abnormal ZP:0000683 gut deformed, abnormal ZP:0000684 heart hypoplastic, abnormal ZP:0000685 heart physical object quality, abnormal ZP:0000686 heart tube malformed, abnormal ZP:0000688 cardiac muscle cell decreased amount, abnormal ZP:0000689 sprouting angiogenesis process quality, abnormal ZP:0000691 nitric oxide biosynthetic process disrupted, abnormal ZP:0000692 blood circulation absent, abnormal ZP:0000693 regulation of cardiac muscle contraction by calcium ion signaling disrupted, abnormal ZP:0000694 calcium-mediated signaling disrupted, abnormal ZP:0000695 erythrocyte differentiation process quality, abnormal ZP:0000697 embryonic hemopoiesis decreased process quality, abnormal ZP:0000698 nucleate erythrocyte development disrupted, abnormal ZP:0000699 artery morphogenesis delayed, abnormal ZP:0000700 venous blood vessel morphogenesis disrupted, abnormal ZP:0000701 regulation of cardiac muscle contraction disrupted, abnormal ZP:0000702 heart contraction absent, abnormal ZP:0000703 primitive hemopoiesis process quality, abnormal ZP:0000704 distal tubule development arrested, abnormal ZP:0000705 proximal convoluted tubule development arrested, abnormal ZP:0000706 blood vessel lumenization disrupted, abnormal ZP:0000707 blood flow rate, abnormal ZP:0000708 blood increased accumulation caudal vein, abnormal ZP:0000709 blood accumulation blood vasculature, abnormal ZP:0000710 blood accumulation trunk, abnormal ZP:0000711 brain decreased size, abnormal ZP:0000712 cardiac ventricle conductivity, abnormal ZP:0000713 cardiac ventricle decreased functionality, abnormal ZP:0000714 cardiac ventricle decreased diameter, abnormal ZP:0000715 dorsal aorta structure, abnormal ZP:0000716 dorsal aorta unlumenized, abnormal ZP:0000717 brain vasculature hemorrhagic, abnormal ZP:0000718 fourth ventricle decreased diameter, abnormal ZP:0000719 heart non-contractile, abnormal ZP:0000720 liver decreased size, abnormal ZP:0000721 basibranchial condensed, abnormal ZP:0000722 blood vessel endothelial cell common cardinal vein decreased amount, abnormal ZP:0000723 anterior cardinal vein unlumenized, abnormal ZP:0000724 atrium dilated, abnormal ZP:0000725 posterior cardinal vein unlumenized, abnormal ZP:0000726 thymus decreased size, abnormal ZP:0000727 hematopoietic multipotent progenitor cell thymus decreased amount, abnormal ZP:0000728 trunk increased accumulation anterior side nucleate erythrocyte, abnormal ZP:0000729 hematopoietic multipotent progenitor cell trunk decreased amount, abnormal ZP:0000730 ventricular system decreased size, abnormal ZP:0000731 cranial vasculature unlumenized, abnormal ZP:0000732 palatoquadrate arch decreased length, abnormal ZP:0000733 intersegmental vessel structure, abnormal ZP:0000734 intersegmental vessel structure, cavities, abnormal ZP:0000735 caudal vein plexus decreased size, abnormal ZP:0000737 ceratohyal cartilage orientation ceratohyal cartilage, abnormal ZP:0000738 simple columnar epithelium displaced, abnormal ZP:0000739 simple cuboidal epithelium displaced, abnormal ZP:0000740 ceratobranchial cartilage orientation ceratobranchial cartilage, abnormal ZP:0000741 pronephric glomerulus unfused from pronephric glomerulus, abnormal ZP:0000742 basilar artery decreased diameter, abnormal ZP:0000743 central artery physical object quality, abnormal ZP:0000744 central artery decreased diameter, abnormal ZP:0000745 hematopoietic system decreased functionality, abnormal ZP:0000746 trabecular layer aplastic, abnormal ZP:0000747 sarcomere ventricular myocardium disorganized, abnormal ZP:0000748 hepatic sinusoid aplastic, abnormal ZP:0000749 blood vessel collapsed, abnormal ZP:0000751 nucleate erythrocyte absent, abnormal ZP:0000752 cardiac muscle cell increased amount, abnormal ZP:0000753 cardiac muscle cell electric potential, abnormal ZP:0000754 cardiac muscle cell decreased area, abnormal ZP:0000755 abnormal(ly) disrupted diencephalon development ZP:0000756 Z disc cardiac muscle cell shape, abnormal ZP:0000758 hematopoietic multipotent progenitor cell decreased amount, abnormal ZP:0000759 midbrain hindbrain boundary aplastic, abnormal ZP:0000760 cerebellum decreased thickness, abnormal ZP:0000761 extension decreased thickness, abnormal ZP:0000762 fin aplastic, abnormal ZP:0000763 fourth ventricle opaque, abnormal ZP:0000764 otic placode decreased size, abnormal ZP:0000765 optic tectum increased size, abnormal ZP:0000766 post-vent region bent, abnormal ZP:0000767 RNA processing premature, abnormal ZP:0000768 translational initiation premature, abnormal ZP:0000769 gastrulation arrested, abnormal ZP:0000770 nodal signaling pathway premature, abnormal ZP:0000772 epiboly arrested, abnormal ZP:0000774 nucleus yolk syncytial layer increased amount, abnormal ZP:0000775 blastomere delayed RNA localization, abnormal ZP:0000776 whole organism decreased life span, abnormal ZP:0000777 neural crest cell migration decreased process quality, abnormal ZP:0000778 regulation of smoothened signaling pathway disrupted, abnormal ZP:0000779 regulation of mitotic cell cycle, embryonic process quality, abnormal ZP:0000781 neural crest cell differentiation decreased process quality, abnormal ZP:0000782 diencephalon development disrupted, abnormal ZP:0000783 neurogenesis disrupted, abnormal ZP:0000784 melanocyte differentiation decreased process quality, abnormal ZP:0000785 forebrain development decreased process quality, abnormal ZP:0000788 cell proliferation in midbrain disrupted, abnormal ZP:0000789 negative regulation of transcription, DNA-templated disrupted, abnormal ZP:0000790 embryonic neurocranium morphogenesis decreased process quality, abnormal ZP:0000791 embryonic viscerocranium morphogenesis decreased process quality, abnormal ZP:0000792 xanthophore differentiation decreased process quality, abnormal ZP:0000793 melanocyte migration decreased process quality, abnormal ZP:0000794 hindbrain malformed, abnormal ZP:0000795 hypothalamus cellular quality, abnormal ZP:0000796 retinal neural layer decreased size, abnormal ZP:0000797 fourth ventricle malformed, abnormal ZP:0000798 midbrain malformed, abnormal ZP:0000799 tectal ventricle decreased size, abnormal ZP:0000800 tectal ventricle malformed, abnormal ZP:0000801 ventral thalamus decreased size, abnormal ZP:0000802 ventral thalamus cellular quality, abnormal ZP:0000803 head has fewer parts of type xanthoblast, abnormal ZP:0000805 trunk has fewer parts of type xanthoblast, abnormal ZP:0000806 trunk has fewer parts of type melanoblast, abnormal ZP:0000807 neural tube malformed, abnormal ZP:0000808 cranial neural crest mislocalised dorsally, abnormal ZP:0000809 optic fissure malformed, abnormal ZP:0000810 stomodeum decreased size, abnormal ZP:0000811 pharyngeal arch cellular quality, abnormal ZP:0000812 neurocranial trabecula shortened, abnormal ZP:0000815 medial region ethmoid cartilage absent, abnormal ZP:0000816 pharyngeal arch cartilage hypoplastic, abnormal ZP:0000819 pharyngeal arch 2 decreased size, abnormal ZP:0000820 pharyngeal arch 2 malformed, abnormal ZP:0000821 pharyngeal arch 1 decreased size, abnormal ZP:0000822 neural crest cell cellular quality, abnormal ZP:0000823 melanoblast mislocalised, abnormal ZP:0000824 melanoblast aggregated, abnormal ZP:0000825 circadian regulation of gene expression process quality, abnormal ZP:0000826 cardiac muscle cell atrium increased amount, abnormal ZP:0000827 cardiac muscle myoblast presumptive atrium primitive heart tube increased amount, abnormal ZP:0000829 thigmotaxis decreased occurrence, abnormal ZP:0000830 voltage-gated sodium channel activity amplitude, abnormal ZP:0000831 voltage-gated sodium channel activity decreased occurrence, abnormal ZP:0000832 mechanosensory behavior disrupted, abnormal ZP:0000833 larval locomotory behavior decreased occurrence, abnormal ZP:0000834 neuron differentiation process quality, abnormal ZP:0000836 axon collateral dorsal root ganglion mislocalised laterally, abnormal ZP:0000837 neuron neural crest derived dorsal root ganglion mislocalised ventrally, abnormal ZP:0000838 neuron dorsal root ganglion mobile, abnormal ZP:0000839 neuron dorsal root ganglion mislocalised ventrally, abnormal ZP:0000840 voltage-gated sodium channel complex mechanoreceptor cell decreased functionality, abnormal ZP:0000841 Rohon-Beard neuron present, abnormal ZP:0000842 Rohon-Beard neuron membrane potential, abnormal ZP:0000843 Rohon-Beard neuron increased life span, abnormal ZP:0000844 Rohon-Beard neuron decreased functionality, abnormal ZP:0000845 primary motor neuron decreased functionality, abnormal ZP:0000846 axon secondary motor neuron misrouted, abnormal ZP:0000850 nucleus yolk syncytial layer aggregated, abnormal ZP:0000853 macula utricle has fewer parts of type hair cell, abnormal ZP:0000854 semicircular canal malformed, abnormal ZP:0000856 whole organism curved ventral, abnormal ZP:0000857 pillar of the semicircular canal unfused from pillar of the semicircular canal, abnormal ZP:0000858 macula saccule has fewer parts of type hair cell, abnormal ZP:0000859 neuromast hair cell morphology, abnormal ZP:0000860 cardiac ventricle dilated, abnormal ZP:0000861 kidney increased size, abnormal ZP:0000862 kidney hyperplastic, abnormal ZP:0000863 kidney has extra parts of type erythroid progenitor cell, abnormal ZP:0000864 nucleate erythrocyte binucleate, abnormal ZP:0000865 nucleate erythrocyte spherical, abnormal ZP:0000866 nucleate erythrocyte teardrop-shaped, abnormal ZP:0000867 nucleus nucleate erythrocyte structure, abnormal ZP:0000868 convergent extension involved in gastrulation disrupted, abnormal ZP:0000869 anterior-posterior axis whole organism shortened, abnormal ZP:0000870 ossification disrupted, abnormal ZP:0000871 embryonic viscerocranium morphogenesis disrupted, abnormal ZP:0000872 cartilage morphogenesis disrupted, abnormal ZP:0000873 otic lateral line neuromast decreased amount, abnormal ZP:0000874 cleithrum decreased length, abnormal ZP:0000875 cleithrum malformed, abnormal ZP:0000876 dentary malformed, abnormal ZP:0000877 dentary curved caudal, abnormal ZP:0000878 dentary fused with maxilla, abnormal ZP:0000879 mandibular muscle wholly dorsalized, abnormal ZP:0000880 opercle shape, abnormal ZP:0000881 opercle size, abnormal ZP:0000882 opercle increased size, abnormal ZP:0000883 opercle decreased size, abnormal ZP:0000884 opercle increased width, abnormal ZP:0000885 opercle aplastic, abnormal ZP:0000886 opercle increased variability of size, abnormal ZP:0000887 cartilaginous joint opercle increased thickness, abnormal ZP:0000888 cartilaginous joint opercle distended, abnormal ZP:0000889 maxilla malformed, abnormal ZP:0000890 maxilla curved caudal, abnormal ZP:0000891 branchiostegal ray position, abnormal ZP:0000892 branchiostegal ray decreased size, abnormal ZP:0000893 branchiostegal ray malformed, abnormal ZP:0000894 branchiostegal ray falciform, abnormal ZP:0000895 mouth quality, abnormal ZP:0000896 mouth concave 3-D shape, abnormal ZP:0000897 symplectic absent, abnormal ZP:0000898 infraorbital lateral line neuromast decreased amount, abnormal ZP:0000899 opercular lateral line neuromast absent, abnormal ZP:0000901 opercular lateral line neuromast mislocalised dorsally, abnormal ZP:0000902 opercular lateral line neuromast decreased amount, abnormal ZP:0000903 middle lateral line neuromast decreased amount, abnormal ZP:0000904 Meckel's cartilage absent, abnormal ZP:0000905 Meckel's cartilage bent, abnormal ZP:0000906 Meckel's cartilage aplastic, abnormal ZP:0000907 Meckel's cartilage protruding, abnormal ZP:0000908 Meckel's cartilage mislocalised posteriorly, abnormal ZP:0000909 Meckel's cartilage fused with palatoquadrate cartilage, abnormal ZP:0000910 splanchnocranium quality, abnormal ZP:0000911 joint mandibular arch skeleton absent, abnormal ZP:0000912 pharyngeal arch 3 skeleton decreased length, abnormal ZP:0000913 pharyngeal arch 4 skeleton decreased length, abnormal ZP:0000914 ceratobranchial 5 bone decreased length, abnormal ZP:0000915 ceratobranchial 5 bone malformed, abnormal ZP:0000916 ventral mandibular arch decreased size, abnormal ZP:0000917 ventral mandibular arch aplastic, abnormal ZP:0000918 ventral mandibular arch orientation eye, abnormal ZP:0000919 pharyngeal arch 2 skeleton decreased size, abnormal ZP:0000920 palatoquadrate cartilage increased length, abnormal ZP:0000921 ceratohyal cartilage morphology, abnormal ZP:0000922 ceratohyal cartilage structure, abnormal ZP:0000923 ceratohyal cartilage absent, abnormal ZP:0000924 ceratohyal cartilage inverted, abnormal ZP:0000925 ceratohyal cartilage aplastic, abnormal ZP:0000926 ventral hyoid arch morphology, abnormal ZP:0000927 hyosymplectic cartilage increased width, abnormal ZP:0000928 anterior lateral line neuromast increased amount, abnormal ZP:0000929 anterior lateral line neuromast mislocalised, abnormal ZP:0000930 pharyngeal arch 2 position, abnormal ZP:0000931 pharyngeal arch 1 position, abnormal ZP:0000932 pharyngeal arch 1 malformed, abnormal ZP:0000934 joint pharyngeal arch 1 physical object quality, abnormal ZP:0000935 ceratohyal-branchiostegal ray joint morphology, abnormal ZP:0000936 interhyal-epihyal joint absent, abnormal ZP:0000937 melanosome localization disrupted, abnormal ZP:0000938 swimming behavior decreased duration, abnormal ZP:0000939 swimming behavior disrupted, abnormal ZP:0000940 cellular pigment accumulation arrested, abnormal ZP:0000941 retina development in camera-type eye disrupted, abnormal ZP:0000942 optomotor response decreased process quality, abnormal ZP:0000943 eye morphology, abnormal ZP:0000944 photoreceptor cell retinal photoreceptor layer absent, abnormal ZP:0000945 pigment cell quality, abnormal ZP:0000946 melanocyte area, abnormal ZP:0000947 melanosome melanocyte spatial pattern, abnormal ZP:0000948 melanosome melanocyte dispersed, abnormal ZP:0000949 retinal bipolar neuron increased amount, abnormal ZP:0000950 heme biosynthetic process disrupted, abnormal ZP:0000951 liver has extra parts of type erythroid lineage cell, abnormal ZP:0000952 kidney has extra parts of type erythroid lineage cell, abnormal ZP:0000953 hemoglobin complex nucleate erythrocyte composition, abnormal ZP:0000954 determination of pancreatic left/right asymmetry disrupted, abnormal ZP:0000955 determination of heart left/right asymmetry disrupted, abnormal ZP:0000956 determination of liver left/right asymmetry disrupted, abnormal ZP:0000958 heart mislocalised, abnormal ZP:0000959 liver mislocalised, abnormal ZP:0000960 pancreas mislocalised, abnormal ZP:0000961 trunk bent, abnormal ZP:0000962 axonal fasciculation disrupted, abnormal ZP:0000963 synapse assembly increased occurrence, abnormal ZP:0000965 retinal ganglion cell axon guidance quality, abnormal ZP:0000966 retinal ganglion cell axon guidance process quality, abnormal ZP:0000967 anterior/posterior axon guidance process quality, abnormal ZP:0000968 anterior/posterior axon guidance disrupted, abnormal ZP:0000969 collateral sprouting in absence of injury increased occurrence, abnormal ZP:0000970 axon trigeminal ganglion increased branchiness, abnormal ZP:0000971 axon collateral trigeminal ganglion increased length, abnormal ZP:0000972 trigeminal ganglion has extra parts of type sensory neuron presynaptic active zone sensory neuron, abnormal ZP:0000973 cranial nerve III mislocalised, abnormal ZP:0000974 axon optic chiasm morphology, abnormal ZP:0000975 supraoptic tract misrouted, abnormal ZP:0000977 neuron projection dorso-rostral cluster mislocalised, abnormal ZP:0000978 neuron projection dorso-rostral cluster misrouted, abnormal ZP:0000980 axon dopaminergic neuron mislocalised medially, abnormal ZP:0000981 dopaminergic neuron adjacent to axon anterior-posterior axis hindbrain, abnormal ZP:0000982 dopaminergic neuron adjacent to axon anterior-posterior axis spinal cord, abnormal ZP:0000983 dopaminergic neuron adjacent to axon axis spinal cord, abnormal ZP:0000984 axon retinal ganglion cell mislocalised, abnormal ZP:0000985 axon retinal ganglion cell misrouted, abnormal ZP:0000986 retinal ganglion cell displaced to axon hindbrain, abnormal ZP:0000987 retinal ganglion cell displaced to axon telencephalon, abnormal ZP:0000988 retinal ganglion cell displaced to axon ventral region diencephalon, abnormal ZP:0000989 retinal ganglion cell displaced to axon contralateral side eye, abnormal ZP:0000990 vestibular reflex disrupted, abnormal ZP:0000992 anterior macula fused with posterior macula, abnormal ZP:0000993 inner ear decreased size, abnormal ZP:0000995 semicircular canal decreased size, abnormal ZP:0000996 lapillus mislocalised, abnormal ZP:0000997 lapillus fused with sagitta, abnormal ZP:0000998 hair cell anterior macula decreased amount, abnormal ZP:0000999 posterior lateral line neuromast absent, abnormal ZP:0001000 whole organism balance, abnormal ZP:0001001 whole organism decreased coordination, abnormal ZP:0001003 otolith fused with otolith, abnormal ZP:0001004 vestibular reflex delayed, abnormal ZP:0001005 hair cell macula utricle irregular spatial pattern, abnormal ZP:0001006 utricle lacks parts or has fewer parts of type hair cell, abnormal ZP:0001007 hair cell utricle morphology, abnormal ZP:0001008 hair cell mislocalised, abnormal ZP:0001009 hair cell apoptotic, abnormal ZP:0001010 otic vesicle decreased size, abnormal ZP:0001015 epibranchial ganglion decreased amount, abnormal ZP:0001016 eye development disrupted, abnormal ZP:0001017 lens morphogenesis in camera-type eye arrested, abnormal ZP:0001018 lens morphogenesis in camera-type eye disrupted, abnormal ZP:0001019 type B pancreatic cell differentiation disrupted, abnormal ZP:0001020 embryo development paedomorphic growth, abnormal ZP:0001021 anterior/posterior pattern specification disrupted, abnormal ZP:0001022 lens elliptic, abnormal ZP:0001023 lens aplastic, abnormal ZP:0001024 lens protruding, abnormal ZP:0001025 cornea mislocalised, abnormal ZP:0001026 rhombomere condensed, abnormal ZP:0001027 peptide hormone secreting cell endocrine pancreas increased amount, abnormal ZP:0001028 pancreatic B cell absent, abnormal ZP:0001029 pancreatic B cell decreased amount, abnormal ZP:0001030 pancreatic A cell increased amount, abnormal ZP:0001031 pancreatic A cell decreased amount, abnormal ZP:0001032 D cell decreased amount, abnormal ZP:0001033 larval locomotory behavior amplitude, abnormal ZP:0001034 larval locomotory behavior increased frequency, abnormal ZP:0001035 collateral sprouting increased occurrence, abnormal ZP:0001036 whole organism increased speed, abnormal ZP:0001037 motor neuron decreased amount, abnormal ZP:0001038 axon collateral motor neuron increased amount, abnormal ZP:0001039 cartilage development disrupted, abnormal ZP:0001040 dentary decreased size, abnormal ZP:0001041 maxilla decreased size, abnormal ZP:0001042 coracoid absent, abnormal ZP:0001043 retroarticular aplastic, abnormal ZP:0001044 ceratobranchial bone decreased size, abnormal ZP:0001045 ceratobranchial bone aplastic, abnormal ZP:0001046 ceratohyal bone aplastic, abnormal ZP:0001047 entopterygoid aplastic, abnormal ZP:0001048 hyomandibula aplastic, abnormal ZP:0001049 head circular, abnormal ZP:0001050 pectoral fin decreased length, abnormal ZP:0001051 pectoral fin decreased size, abnormal ZP:0001052 mandibular arch skeleton morphology, abnormal ZP:0001053 ceratobranchial 5 bone decreased size, abnormal ZP:0001054 palatoquadrate arch quality, abnormal ZP:0001055 neurocranial trabecula aplastic, abnormal ZP:0001056 palatoquadrate cartilage aplastic, abnormal ZP:0001057 ethmoid cartilage aplastic, abnormal ZP:0001058 hyosymplectic cartilage aplastic, abnormal ZP:0001059 parachordal cartilage aplastic, abnormal ZP:0001060 basal plate cartilage aplastic, abnormal ZP:0001061 scapulocoracoid decreased size, abnormal ZP:0001062 scapulocoracoid aplastic, abnormal ZP:0001063 cranial cartilage aplastic, abnormal ZP:0001064 cranial cartilage decreased amount, abnormal ZP:0001065 pharyngeal arch cartilage absent, abnormal ZP:0001066 basihyal cartilage aplastic, abnormal ZP:0001067 ceratobranchial cartilage aplastic, abnormal ZP:0001068 neurocranium absent, abnormal ZP:0001069 pharyngeal arch 3-7 decreased size, abnormal ZP:0001070 type B pancreatic cell differentiation decreased process quality, abnormal ZP:0001071 Notch signaling pathway disrupted, abnormal ZP:0001072 exocrine pancreas development decreased process quality, abnormal ZP:0001073 intrahepatic bile duct development disrupted, abnormal ZP:0001074 intrahepatic bile duct development decreased process quality, abnormal ZP:0001075 hepaticobiliary system development disrupted, abnormal ZP:0001076 gall bladder development disrupted, abnormal ZP:0001077 otic vesicle aplastic, abnormal ZP:0001078 fin fold actinotrichium decreased amount, abnormal ZP:0001079 liver green, abnormal ZP:0001080 pancreas green, abnormal ZP:0001081 acinar cell pancreas decreased amount, abnormal ZP:0001082 cleithrum decreased size, abnormal ZP:0001083 dentary aplastic, abnormal ZP:0001084 dorsal root ganglion irregular spatial pattern, abnormal ZP:0001085 dorsal root ganglion decreased amount, abnormal ZP:0001086 gall bladder decreased size, abnormal ZP:0001087 maxilla aplastic, abnormal ZP:0001088 branchiostegal ray aplastic, abnormal ZP:0001089 parasphenoid decreased size, abnormal ZP:0001090 whole organism decreased thickness, abnormal ZP:0001091 post-vent region increased curvature, abnormal ZP:0001092 ceratobranchial 5 bone aplastic, abnormal ZP:0001093 endocrine pancreas mislocalised, abnormal ZP:0001094 endocrine pancreas lacks all parts of type secondary islet, abnormal ZP:0001095 pancreatic duct morphology, abnormal ZP:0001096 pancreatic duct malformed, abnormal ZP:0001097 pancreatic duct dilated, abnormal ZP:0001098 pancreatic duct decreased branchiness, abnormal ZP:0001099 pancreatic duct has fewer parts of type cell, abnormal ZP:0001100 basal plate cartilage decreased size, abnormal ZP:0001101 pectoral fin endoskeletal disc decreased size, abnormal ZP:0001102 occipital arch cartilage decreased size, abnormal ZP:0001103 digestive system duct amorphous, abnormal ZP:0001104 bile canaliculus decreased length, abnormal ZP:0001105 bile canaliculus increased width, abnormal ZP:0001106 intrahepatic bile duct morphology, abnormal ZP:0001107 intrahepatic bile duct malformed, abnormal ZP:0001108 primary islet decreased size, abnormal ZP:0001109 melanocyte increased size, abnormal ZP:0001110 hepatocyte organization quality, abnormal ZP:0001111 iridophore decreased amount, abnormal ZP:0001112 hypothalamus physical object quality, abnormal ZP:0001113 hypothalamus has fewer parts of type neurosecretory neuron, abnormal ZP:0001114 hypothalamus has fewer parts of type dopaminergic neuron, abnormal ZP:0001115 dopaminergic neuron diencephalon decreased amount, abnormal ZP:0001116 dopaminergic neuron forebrain decreased amount, abnormal ZP:0001117 serotonergic neuron forebrain decreased amount, abnormal ZP:0001119 preoptic area physical object quality, abnormal ZP:0001120 caudal tuberculum physical object quality, abnormal ZP:0001121 embryonic pattern specification disrupted, abnormal ZP:0001122 pharyngeal system development disrupted, abnormal ZP:0001123 canonical Wnt signaling pathway decreased occurrence, abnormal ZP:0001124 cilium Kupffer's vesicle decreased length, abnormal ZP:0001125 brain apoptotic, abnormal ZP:0001126 brain malformed, abnormal ZP:0001127 hindbrain disorganized, abnormal ZP:0001129 tail bud morphology, abnormal ZP:0001130 tail bud decreased length, abnormal ZP:0001132 pharyngeal arch 3-7 skeleton decreased size, abnormal ZP:0001133 cerebellum apoptotic, abnormal ZP:0001135 midbrain apoptotic, abnormal ZP:0001136 notochord truncated, abnormal ZP:0001137 somite decreased amount, abnormal ZP:0001140 central canal dilated, abnormal ZP:0001141 primary neuron rhombomere crowded, abnormal ZP:0001142 primary neuron rhombomere disorganized, abnormal ZP:0001143 head increased size, abnormal ZP:0001144 post-vent region truncated, abnormal ZP:0001145 post-vent region kinked, abnormal ZP:0001146 post-vent region has fewer parts of type somite, abnormal ZP:0001147 mandibular arch skeleton aplastic, abnormal ZP:0001149 pharyngeal arch 3-7 morphology, abnormal ZP:0001150 neuron hindbrain commissure absent, abnormal ZP:0001151 aortic arch morphology, abnormal ZP:0001155 cell projection radial glial cell irregular spatial pattern, abnormal ZP:0001157 neural retina development delayed, abnormal ZP:0001158 neural retina development decreased process quality, abnormal ZP:0001159 bone resorption decreased process quality, abnormal ZP:0001160 macrophage chemotaxis decreased process quality, abnormal ZP:0001161 brain lacks all parts of type microglial cell, abnormal ZP:0001162 spinal cord protruding into central canal, abnormal ZP:0001163 retina undifferentiated, abnormal ZP:0001164 retina proliferative, abnormal ZP:0001165 retina lacks all parts of type microglial cell, abnormal ZP:0001166 retina decreased process quality neurogenesis, abnormal ZP:0001167 retina delayed neuron differentiation, abnormal ZP:0001168 retina decreased process quality neuron differentiation, abnormal ZP:0001169 caudal vein mislocalised, abnormal ZP:0001170 osteoclast hemal arch decreased amount, abnormal ZP:0001171 central canal decreased diameter, abnormal ZP:0001172 osteoclast neural arch decreased amount, abnormal ZP:0001173 whole organism decreased pigmentation, abnormal ZP:0001174 melanophore stripe trunk disorganized, abnormal ZP:0001175 melanocyte hypodermis decreased amount, abnormal ZP:0001176 xanthophore hypodermis absent, abnormal ZP:0001177 vertebra decreased size, abnormal ZP:0001178 microglial cell decreased amount, abnormal ZP:0001179 melanocyte quality, abnormal ZP:0001180 melanocyte irregular spatial pattern, abnormal ZP:0001181 xanthophore quality, abnormal ZP:0001182 retinal ganglion cell undifferentiated, abnormal ZP:0001183 adaxial cell morphology, abnormal ZP:0001184 myofibril muscle pioneer decreased length, abnormal ZP:0001185 myofibril muscle pioneer decreased thickness, abnormal ZP:0001186 slow muscle cell malformed, abnormal ZP:0001187 myofibril slow muscle cell decreased length, abnormal ZP:0001188 myofibril slow muscle cell decreased thickness, abnormal ZP:0001189 fast muscle cell malformed, abnormal ZP:0001190 fast muscle cell unfused from fast muscle cell, abnormal ZP:0001191 myofibril fast muscle cell decreased length, abnormal ZP:0001192 heart edematous, abnormal ZP:0001193 inner ear quality, abnormal ZP:0001194 heart tube poorly differentiated, abnormal ZP:0001195 optic cup morphology, abnormal ZP:0001196 motor neuron quality, abnormal ZP:0001197 neuron apoptotic, abnormal ZP:0001199 ventricular system development disrupted, abnormal ZP:0001200 hypothalamus cell differentiation process quality, abnormal ZP:0001201 dopamine metabolic process quality, abnormal ZP:0001202 swim bladder inflation disrupted, abnormal ZP:0001203 musculoskeletal movement disrupted, abnormal ZP:0001204 sensory perception of touch disrupted, abnormal ZP:0001205 cell-cell adhesion involved in gastrulation disrupted, abnormal ZP:0001206 dopaminergic neuron differentiation process quality, abnormal ZP:0001207 cardiac ventricle increased size, abnormal ZP:0001208 cardiac ventricle decreased thickness, abnormal ZP:0001209 neurosecretory neuron hypothalamus decreased amount, abnormal ZP:0001210 dopaminergic neuron hypothalamus decreased amount, abnormal ZP:0001211 swim bladder uninflated, abnormal ZP:0001212 neurosecretory neuron preoptic area decreased amount, abnormal ZP:0001213 neurosecretory neuron caudal tuberculum decreased amount, abnormal ZP:0001214 dopaminergic neuron caudal tuberculum decreased amount, abnormal ZP:0001215 neuron projection ventricular zone decreased amount, abnormal ZP:0001216 head cuboid, abnormal ZP:0001217 blastoderm cell blastoderm circular, abnormal ZP:0001218 ventricular system increased volume, abnormal ZP:0001219 hepatic sinusoid morphology, abnormal ZP:0001220 hepatic sinusoid increased size, abnormal ZP:0001221 blood hepatic sinusoid increased volume, abnormal ZP:0001222 neuron projection anterior neural keel decreased amount, abnormal ZP:0001223 dopaminergic neuron decreased amount, abnormal ZP:0001224 embryonic heart tube formation disrupted, abnormal ZP:0001226 midbrain-hindbrain boundary morphogenesis disrupted, abnormal ZP:0001227 extracellular matrix organization disrupted, abnormal ZP:0001228 embryonic heart tube elongation delayed, abnormal ZP:0001229 embryonic heart tube elongation disrupted, abnormal ZP:0001230 cell migration involved in heart formation disrupted, abnormal ZP:0001231 brain flat, abnormal ZP:0001232 brain degenerate, abnormal ZP:0001233 brain unstructured, abnormal ZP:0001234 brain decreased diameter, abnormal ZP:0001235 brain surface feature shape, abnormal ZP:0001236 midbrain hindbrain boundary morphology, abnormal ZP:0001237 otic vesicle increased size, abnormal ZP:0001238 otic vesicle decreased width, abnormal ZP:0001239 otic vesicle elongated, abnormal ZP:0001240 epithelium otic vesicle morphology, abnormal ZP:0001241 pericardium increased size, abnormal ZP:0001242 yolk swollen, abnormal ZP:0001243 heart rudiment lacks parts or has fewer parts of type extracellular matrix heart rudiment, abnormal ZP:0001244 heart rudiment has fewer parts of type extracellular matrix heart rudiment, abnormal ZP:0001245 extracellular matrix heart rudiment composition, abnormal ZP:0001246 inner ear morphology, abnormal ZP:0001247 inner ear lacks all parts of type otolith, abnormal ZP:0001248 heart tube decreased length, abnormal ZP:0001249 semicircular canal aplastic, abnormal ZP:0001250 central canal decreased thickness, abnormal ZP:0001251 whole organism degenerate, abnormal ZP:0001252 embryonic structure inverted, abnormal ZP:0001253 head surface feature shape, abnormal ZP:0001254 trunk curved dorsal, abnormal ZP:0001255 post-vent region curved dorsal, abnormal ZP:0001256 forebrain ventricle decreased size, abnormal ZP:0001257 ventricular system structure, cavities, abnormal ZP:0001258 otolith decreased size, abnormal ZP:0001259 otolith decreased distance otolith, abnormal ZP:0001260 melanocyte morphology, abnormal ZP:0001261 apical part of cell neuroepithelial cell decreased width, abnormal ZP:0001262 thigmotaxis disrupted, abnormal ZP:0001263 mechanosensory behavior process quality, abnormal ZP:0001264 fluid transport disrupted, abnormal ZP:0001265 membrane depolarization process quality, abnormal ZP:0001266 regulation of resting membrane potential disrupted, abnormal ZP:0001267 cilium Kupffer's vesicle movement quality, abnormal ZP:0001268 gut mislocalised, abnormal ZP:0001269 thigmotaxis process quality, abnormal ZP:0001270 ventricular system dilated, abnormal ZP:0001272 retinal photoreceptor layer quality, abnormal ZP:0001273 retinal photoreceptor layer decreased thickness, abnormal ZP:0001274 retinal photoreceptor layer lacks parts or has fewer parts of type photoreceptor cell, abnormal ZP:0001275 retina increased occurrence cell death, abnormal ZP:0001276 cell retina disorganized, abnormal ZP:0001277 photoreceptor cell circular, abnormal ZP:0001278 photoreceptor cell apoptotic, abnormal ZP:0001279 photoreceptor outer segment photoreceptor cell deformed, abnormal ZP:0001280 Muller cell decreased amount, abnormal ZP:0001281 retinal bipolar neuron decreased amount, abnormal ZP:0001282 microtubule cytoskeleton organization decreased process quality, abnormal ZP:0001283 endodermal cell fate specification process quality, abnormal ZP:0001284 invagination involved in gastrulation with mouth forming second delayed, abnormal ZP:0001285 forerunner cell group split, abnormal ZP:0001286 yolk elongated, abnormal ZP:0001287 yolk flattened, abnormal ZP:0001288 microtubule yolk spatial pattern, abnormal ZP:0001289 nucleus yolk syncytial layer morphology, abnormal ZP:0001290 extension distended, abnormal ZP:0001291 dorsal fin absent, abnormal ZP:0001292 deep blastomere blastodisc shape, abnormal ZP:0001293 deep blastomere blastodisc crowded, abnormal ZP:0001294 mesodermal cell migration decreased rate, abnormal ZP:0001295 endothelial cell dorsal aorta decreased amount, abnormal ZP:0001296 prechordal plate decreased length, abnormal ZP:0001297 mesodermal cell hypoblast decreased speed, abnormal ZP:0001298 neural keel decreased length, abnormal ZP:0001299 filopodium retina increased amount, abnormal ZP:0001300 endothelial cell posterior cardinal vein decreased amount, abnormal ZP:0001301 intersegmental vessel morphology, abnormal ZP:0001302 endothelial cell intersegmental vessel decreased amount, abnormal ZP:0001303 caudal vein plexus decreased length, abnormal ZP:0001304 caudal vein plexus decreased width, abnormal ZP:0001305 caudal vein plexus decreased area, abnormal ZP:0001306 dorsal longitudinal anastomotic vessel disorganized, abnormal ZP:0001307 endothelial cell dorsal longitudinal anastomotic vessel decreased amount, abnormal ZP:0001308 subintestinal vein deformed, abnormal ZP:0001309 nucleate erythrocyte increased accumulation blood island, abnormal ZP:0001310 basophilic erythroblast increased size, abnormal ZP:0001311 erythroblast increased amount, abnormal ZP:0001312 nucleate erythrocyte desaturated blue, abnormal ZP:0001313 nucleate erythrocyte lacks all parts of type hemoglobin complex nucleate erythrocyte, abnormal ZP:0001314 convergent extension involved in axis elongation disrupted, abnormal ZP:0001315 palatoquadrate cartilage decreased length, abnormal ZP:0001316 pharyngeal arch cartilage bent, abnormal ZP:0001317 pharyngeal arch cartilage condensed, abnormal ZP:0001318 ceratobranchial cartilage decreased amount, abnormal ZP:0001319 dorsal/ventral pattern formation process quality, abnormal ZP:0001321 neural plate development disrupted, abnormal ZP:0001322 gastrulation decreased occurrence, abnormal ZP:0001323 brain development disrupted, abnormal ZP:0001324 anterior neural plate formation disrupted, abnormal ZP:0001325 epiboly delayed, abnormal ZP:0001326 epiboly decreased occurrence, abnormal ZP:0001330 tail bud aplastic, abnormal ZP:0001331 axis shortened, abnormal ZP:0001332 neural plate increased width, abnormal ZP:0001333 notochord broad, abnormal ZP:0001334 somite malformed, abnormal ZP:0001335 caudal fin deformed, abnormal ZP:0001337 whole organism increased occurrence apoptotic process, abnormal ZP:0001338 whole organism arrested embryo development, abnormal ZP:0001339 whole organism occurrence gene expression, abnormal ZP:0001340 whole organism decreased occurrence cell cycle phase transition, abnormal ZP:0001341 whole organism increased occurrence activation of cysteine-type endopeptidase activity involved in apoptotic signaling pathway, abnormal ZP:0001342 head aplastic, abnormal ZP:0001343 post-vent region absent, abnormal ZP:0001346 midbrain hindbrain boundary neural keel physical object quality, abnormal ZP:0001348 anterior-most region hindbrain apoptotic, abnormal ZP:0001349 eye apoptotic, abnormal ZP:0001350 forebrain apoptotic, abnormal ZP:0001353 hatching gland aplastic, abnormal ZP:0001354 polster aplastic, abnormal ZP:0001355 EVL physical object quality, abnormal ZP:0001356 EVL poorly differentiated, abnormal ZP:0001357 nucleus nucleate erythrocyte immature, abnormal ZP:0001358 hemoglobin complex nucleate erythrocyte absent, abnormal ZP:0001359 retinoic acid receptor signaling pathway disrupted, abnormal ZP:0001360 response to auditory stimulus decreased process quality, abnormal ZP:0001361 axonogenesis involved in innervation decreased process quality, abnormal ZP:0001362 clustering of voltage-gated calcium channels decreased process quality, abnormal ZP:0001363 presynaptic membrane assembly decreased process quality, abnormal ZP:0001365 eye movement quality, abnormal ZP:0001366 retina apoptotic, abnormal ZP:0001368 dendrite posterior lateral line nerve unbranched, abnormal ZP:0001370 melanocyte head increased amount, abnormal ZP:0001371 melanocyte increased amount, abnormal ZP:0001372 cytoskeleton of presynaptic active zone eye photoreceptor cell decreased length, abnormal ZP:0001373 cytoskeleton of presynaptic active zone retinal bipolar neuron morphology, abnormal ZP:0001374 rod bipolar cell decreased amount, abnormal ZP:0001375 voltage-gated calcium channel complex neuromast hair cell decreased distribution, abnormal ZP:0001376 cytoskeleton of presynaptic active zone neuromast hair cell decreased amount, abnormal ZP:0001377 cyclin-dependent protein serine/threonine kinase activity decreased occurrence, abnormal ZP:0001378 retina morphogenesis in camera-type eye disrupted, abnormal ZP:0001379 motor neuron brain increased amount, abnormal ZP:0001380 retinal ganglion cell layer morphology, abnormal ZP:0001381 motor neuron spinal cord increased amount, abnormal ZP:0001382 retinal inner nuclear layer morphology, abnormal ZP:0001383 retinal outer plexiform layer morphology, abnormal ZP:0001384 retinal outer nuclear layer morphology, abnormal ZP:0001385 Rohon-Beard neuron displaced to axis spinal cord, abnormal ZP:0001387 proneural cluster decreased size, abnormal ZP:0001388 sensory neuron decreased amount, abnormal ZP:0001389 Rohon-Beard neuron decreased amount, abnormal ZP:0001390 integument increased pigmentation, abnormal ZP:0001391 whole organism wholly ventralized, abnormal ZP:0001392 somite border U-shaped, abnormal ZP:0001393 posterior lateral line neuromast increased amount, abnormal ZP:0001394 afferent neuron truncated, abnormal ZP:0001395 vasculogenesis disrupted, abnormal ZP:0001396 lens development in camera-type eye delayed, abnormal ZP:0001397 retina layer formation delayed, abnormal ZP:0001398 closure of optic fissure arrested, abnormal ZP:0001399 central nervous system hemorrhagic, abnormal ZP:0001400 dorsal aorta morphology, abnormal ZP:0001402 eye hemorrhagic, abnormal ZP:0001405 somite decreased height, abnormal ZP:0001406 somite decreased size, abnormal ZP:0001408 ventricular system distended, abnormal ZP:0001409 intersegmental vessel decreased amount, abnormal ZP:0001410 intersegmental vessel increased branchiness, abnormal ZP:0001411 endocardium morphology, abnormal ZP:0001412 endocardium decreased size, abnormal ZP:0001414 interrenal primordium increased size, abnormal ZP:0001415 pronephric tubule morphology, abnormal ZP:0001416 pronephric tubule absent, abnormal ZP:0001417 pronephric podocyte decreased amount, abnormal ZP:0001420 hyaloid vessel morphology, abnormal ZP:0001422 hyaloid vessel decreased amount, abnormal ZP:0001423 hyaloid vessel branchiness, abnormal ZP:0001425 vasculature broken, abnormal ZP:0001428 epiboly involved in gastrulation with mouth forming second disrupted, abnormal ZP:0001429 microtubule yolk decreased thickness, abnormal ZP:0001430 endocardial progenitor cell migration to the midline involved in heart field formation decreased process quality, abnormal ZP:0001431 endocardium formation decreased process quality, abnormal ZP:0001432 whole organism morphology, abnormal ZP:0001433 establishment of spindle orientation process quality, abnormal ZP:0001434 post-vent region deformed, abnormal ZP:0001435 neural tube formation disrupted, abnormal ZP:0001436 cloaca development disrupted, abnormal ZP:0001437 epithelial cell migration involved in distal tubule morphogenesis disrupted, abnormal ZP:0001438 proctodeum unfused from anatomical region cloacal chamber, abnormal ZP:0001439 gut malformed, abnormal ZP:0001440 lateral plate mesoderm malformed, abnormal ZP:0001441 retinal pigmented epithelium morphology, abnormal ZP:0001442 pronephric duct decreased length, abnormal ZP:0001443 pronephric duct dilated, abnormal ZP:0001444 cilium pronephric duct disoriented, abnormal ZP:0001445 pronephros cystic, abnormal ZP:0001446 cloacal chamber distended, abnormal ZP:0001447 central canal malformed, abnormal ZP:0001448 whole organism curved, abnormal ZP:0001449 whole organism curved dorsal, abnormal ZP:0001450 myocardium malformed, abnormal ZP:0001451 head edematous, abnormal ZP:0001452 trunk edematous, abnormal ZP:0001453 extension decreased size, abnormal ZP:0001454 extension aplastic, abnormal ZP:0001455 trunk decreased width, abnormal ZP:0001456 visual behavior disrupted, abnormal ZP:0001457 melanosome transport delayed, abnormal ZP:0001458 detection of light stimulus involved in sensory perception decreased occurrence, abnormal ZP:0001459 intermediate cell mass of mesoderm aplastic, abnormal ZP:0001460 notochord deformed, abnormal ZP:0001461 somite U-shaped, abnormal ZP:0001462 heart looping arrested, abnormal ZP:0001463 epiboly involved in gastrulation with mouth forming second arrested, abnormal ZP:0001464 heart position, abnormal ZP:0001465 atrium structure, abnormal ZP:0001466 ventral region whole organism edematous, abnormal ZP:0001469 central nervous system neuron differentiation disrupted, abnormal ZP:0001470 synaptic transmission, glycinergic arrested, abnormal ZP:0001471 cellular response to mechanical stimulus disrupted, abnormal ZP:0001472 motor neuron spinal cord decreased functionality, abnormal ZP:0001473 motor neuron decreased functionality, abnormal ZP:0001474 polarity specification of dorsal/ventral axis disrupted, abnormal ZP:0001475 pronephros development disrupted, abnormal ZP:0001476 intermediate cell mass of mesoderm increased width, abnormal ZP:0001477 whole organism spindle-shaped, abnormal ZP:0001478 pronephric glomerulus morphology, abnormal ZP:0001479 platelet aggregation disrupted, abnormal ZP:0001480 thrombocyte activation disrupted, abnormal ZP:0001481 caudal artery decreased accumulation thrombocyte, abnormal ZP:0001482 thrombocyte distributed, abnormal ZP:0001483 thigmotaxis decreased rate, abnormal ZP:0001484 muscle contraction process quality, abnormal ZP:0001485 larval locomotory behavior decreased rate, abnormal ZP:0001486 skeletal muscle satellite cell proliferation increased occurrence, abnormal ZP:0001487 skeletal muscle fiber development process quality, abnormal ZP:0001488 somite disorganized, abnormal ZP:0001489 somite saccular, abnormal ZP:0001490 myofibril somite structure, abnormal ZP:0001491 myofibril somite necrotic, abnormal ZP:0001492 myofibril somite disorganized, abnormal ZP:0001493 myofibril somite mononucleate, abnormal ZP:0001494 somite detached from myofibril somite, abnormal ZP:0001495 trunk musculature quality, abnormal ZP:0001496 trunk musculature dystrophic, abnormal ZP:0001497 vertical myoseptum physical object quality, abnormal ZP:0001498 myotome degenerate, abnormal ZP:0001499 myotome refractivity, abnormal ZP:0001500 sarcolemma myotome disorganized, abnormal ZP:0001501 skeletal muscle myotome degenerate, abnormal ZP:0001502 muscle cell myotome degenerate, abnormal ZP:0001503 muscle cell myotome broken, abnormal ZP:0001504 skeletal muscle cell myotome decreased amount, abnormal ZP:0001505 skeletal muscle cell myotome degeneration, abnormal ZP:0001506 whole organism refractivity, abnormal ZP:0001507 muscle structure, abnormal ZP:0001508 muscle damaged, abnormal ZP:0001509 muscle refractivity, abnormal ZP:0001510 muscle decreased functionality, abnormal ZP:0001511 muscle decreased strength, abnormal ZP:0001512 muscle dystrophic, abnormal ZP:0001513 muscle organization quality, abnormal ZP:0001514 skeletal muscle atrophied, abnormal ZP:0001515 skeletal muscle increased accumulation fibrillar collagen trimer skeletal muscle cell, abnormal ZP:0001516 neutrophil skeletal muscle present, abnormal ZP:0001517 neutrophil skeletal muscle aggregated, abnormal ZP:0001518 skeletal muscle cell degenerate, abnormal ZP:0001519 skeletal muscle cell broken, abnormal ZP:0001520 skeletal muscle cell increased variability of size, abnormal ZP:0001521 skeletal muscle cell detached from myoseptum, abnormal ZP:0001522 nucleus skeletal muscle cell mislocalised, abnormal ZP:0001523 mitochondrion skeletal muscle cell irregular spatial pattern, abnormal ZP:0001524 mitochondrion skeletal muscle cell broken, abnormal ZP:0001525 myofibril skeletal muscle cell increased contractility, abnormal ZP:0001526 slow muscle cell detached from myoseptum, abnormal ZP:0001527 fast muscle cell detached from myoseptum, abnormal ZP:0001528 histone H3-K9 methylation decreased occurrence, abnormal ZP:0001529 endocrine pancreas development process quality, abnormal ZP:0001530 endocrine pancreas malformed, abnormal ZP:0001531 blood circulation decreased rate, abnormal ZP:0001532 blood circulation increased rate, abnormal ZP:0001533 cardiac muscle cell proliferation increased occurrence, abnormal ZP:0001534 heart contraction increased rate, abnormal ZP:0001535 oncosis increased occurrence, abnormal ZP:0001536 cardiac muscle cell cardiac ventricle increased amount, abnormal ZP:0001537 cardiac muscle cell cardiac ventricle decreased amount, abnormal ZP:0001538 bulbus arteriosus increased size, abnormal ZP:0001539 nucleate erythrocyte basophilic, abnormal ZP:0001540 hemoglobin complex nucleate erythrocyte decreased amount, abnormal ZP:0001541 cardiac muscle cell hypertrophic, abnormal ZP:0001542 cardiac muscle cell increased size, abnormal ZP:0001543 cardiac muscle cell decreased size, abnormal ZP:0001544 cardiac muscle cell hyperplastic, abnormal ZP:0001545 myofibril cardiac muscle cell disorganized, abnormal ZP:0001546 yolk grey, abnormal ZP:0001547 cell-cell adhesion involved in mesendodermal cell migration disrupted, abnormal ZP:0001548 homotypic cell-cell adhesion arrested, abnormal ZP:0001549 embryonic cleavage arrested, abnormal ZP:0001550 cell migration involved in gastrulation decreased rate, abnormal ZP:0001551 chordate embryonic development arrested, abnormal ZP:0001552 hatching gland increased size, abnormal ZP:0001553 polster morphology, abnormal ZP:0001554 polster decreased length, abnormal ZP:0001555 tail bud decreased size, abnormal ZP:0001556 notochord kinked, abnormal ZP:0001557 mesodermal cell lateral mesoderm decreased speed, abnormal ZP:0001558 mesodermal cell lateral mesoderm misrouted, abnormal ZP:0001560 whole organism broken, abnormal ZP:0001561 cell neural tube mislocalised, abnormal ZP:0001562 neuron migration disrupted, abnormal ZP:0001563 axon guidance process quality, abnormal ZP:0001564 germ cell migration process quality, abnormal ZP:0001565 axon extension involved in axon guidance disrupted, abnormal ZP:0001566 posterior lateral line neuromast primordium migration process quality, abnormal ZP:0001567 posterior lateral line neuromast primordium migration disrupted, abnormal ZP:0001568 somite cellular quality, abnormal ZP:0001569 axon trigeminal ganglion position, abnormal ZP:0001570 posterior lateral line primordium physical object quality, abnormal ZP:0001571 olfactory receptor cell mislocalised, abnormal ZP:0001572 olfactory receptor cell mislocalised ventrally, abnormal ZP:0001573 olfactory receptor cell mislocalised medially, abnormal ZP:0001574 axon olfactory receptor cell misrouted, abnormal ZP:0001575 primordial germ cell quality, abnormal ZP:0001576 primordial germ cell mislocalised, abnormal ZP:0001579 sensory perception of light stimulus process quality, abnormal ZP:0001580 regulation of synaptic transmission, glutamatergic process quality, abnormal ZP:0001582 optomotor response decreased occurrence, abnormal ZP:0001583 gap junction horizontal cell increased amount, abnormal ZP:0001584 gap junction horizontal cell decreased size, abnormal ZP:0001585 connexin complex horizontal cell functionality, abnormal ZP:0001586 gastrulation delayed, abnormal ZP:0001587 gastrulation process quality, abnormal ZP:0001589 embryo development disrupted, abnormal ZP:0001590 dorsal convergence process quality, abnormal ZP:0001591 epiboly process quality, abnormal ZP:0001596 cell migration disrupted, abnormal ZP:0001597 definitive erythrocyte differentiation disrupted, abnormal ZP:0001598 hypothalamus increased size, abnormal ZP:0001599 optic vesicle increased size, abnormal ZP:0001600 optic vesicle has extra parts of type neurectodermal cell, abnormal ZP:0001601 otic vesicle morphology, abnormal ZP:0001602 telencephalon increased length, abnormal ZP:0001603 diencephalon increased length, abnormal ZP:0001604 diencephalon increased size, abnormal ZP:0001605 eye increased size, abnormal ZP:0001606 neural plate increased size, abnormal ZP:0001607 optic stalk increased size, abnormal ZP:0001608 retina increased size, abnormal ZP:0001609 head morphology, abnormal ZP:0001610 pectoral fin morphology, abnormal ZP:0001611 thalamus development disrupted, abnormal ZP:0001614 zona limitans intrathalamica morphology, abnormal ZP:0001615 embryonic camera-type eye morphogenesis disrupted, abnormal ZP:0001616 eye malformed, abnormal ZP:0001617 retinal pigmented epithelium split, abnormal ZP:0001618 rhombomere 5 aplastic, abnormal ZP:0001619 ocular blood vessel malformed, abnormal ZP:0001620 inner ear morphogenesis disrupted, abnormal ZP:0001621 otic vesicle shape, abnormal ZP:0001622 neuromast hair cell posterior lateral line neuromast decreased amount, abnormal ZP:0001623 otolith protruding, abnormal ZP:0001624 otolith decreased amount, abnormal ZP:0001625 pillar of the anterior semicircular canal malformed, abnormal ZP:0001626 pillar of the lateral semicircular canal malformed, abnormal ZP:0001627 pillar of the posterior semicircular canal malformed, abnormal ZP:0001628 semicircular canal development disrupted, abnormal ZP:0001629 notochord development quality, abnormal ZP:0001630 developmental pigmentation disrupted, abnormal ZP:0001631 notochord decreased length, abnormal ZP:0001632 notochord apoptotic, abnormal ZP:0001633 notochord undifferentiated, abnormal ZP:0001634 notochord poorly differentiated, abnormal ZP:0001635 basement membrane notochord decreased thickness, abnormal ZP:0001636 basement membrane notochord disorganized, abnormal ZP:0001638 endoplasmic reticulum notochord swollen, abnormal ZP:0001639 Golgi apparatus notochord structure, abnormal ZP:0001640 cell notochord structure, abnormal ZP:0001641 somite size, abnormal ZP:0001642 somite condensed, abnormal ZP:0001643 melanosome trunk absent, abnormal ZP:0001644 melanosome melanocyte absent, abnormal ZP:0001645 endoplasmic reticulum muscle cell swollen, abnormal ZP:0001646 Golgi apparatus muscle cell structure, abnormal ZP:0001647 central nervous system hypoplastic, abnormal ZP:0001648 thyroid follicle hypoplastic, abnormal ZP:0001649 whole organism lacks all parts of type extension, abnormal ZP:0001650 blood vessel remodeling disrupted, abnormal ZP:0001651 rhombomere formation decreased process quality, abnormal ZP:0001652 neural plate decreased length, abnormal ZP:0001653 common cardinal vein morphology, abnormal ZP:0001654 rhombomere 5 physical object quality, abnormal ZP:0001655 rhombomere 5 increased area, abnormal ZP:0001656 rhombomere 3 increased area, abnormal ZP:0001657 rhombomere 3 fused with rhombomere 5, abnormal ZP:0001658 rhombomere 4 decreased area, abnormal ZP:0001659 heart morphogenesis process quality, abnormal ZP:0001660 axon extension process quality, abnormal ZP:0001661 axon extension disrupted, abnormal ZP:0001662 axon caudal commissure decreased length, abnormal ZP:0001663 axon motor neuron increased branchiness, abnormal ZP:0001664 skeletal muscle contraction disrupted, abnormal ZP:0001665 acetylcholinesterase activity arrested, abnormal ZP:0001666 acetylcholinesterase activity disrupted, abnormal ZP:0001667 synaptic transmission, cholinergic increased duration, abnormal ZP:0001668 neuromuscular junction development process quality, abnormal ZP:0001669 behavior quality, abnormal ZP:0001670 locomotory behavior arrested, abnormal ZP:0001671 locomotory behavior disrupted, abnormal ZP:0001672 associative learning increased rate, abnormal ZP:0001673 locomotion behavioral quality of a process, abnormal ZP:0001674 Rohon-Beard neuron spinal cord apoptotic, abnormal ZP:0001675 notochord damaged, abnormal ZP:0001676 trunk musculature contractility, abnormal ZP:0001677 nuclear envelope trunk musculature shape, abnormal ZP:0001678 nuclear envelope trunk musculature vacuolated, abnormal ZP:0001679 acetylcholine-gated channel complex trunk musculature position, abnormal ZP:0001680 sarcoplasm trunk musculature vacuolated, abnormal ZP:0001681 myofibril trunk musculature decreased length, abnormal ZP:0001682 myofibril trunk musculature disorganized, abnormal ZP:0001683 whole organism paralysed, abnormal ZP:0001684 Rohon-Beard neuron neural tube apoptotic, abnormal ZP:0001685 axon motor neuron decreased size, abnormal ZP:0001686 axon motor neuron decreased thickness, abnormal ZP:0001687 acetylcholine-gated channel complex muscle cell decreased size, abnormal ZP:0001688 acetylcholine-gated channel complex muscle cell decreased amount, abnormal ZP:0001689 myosin filament slow muscle cell decreased amount, abnormal ZP:0001690 dendrite Rohon-Beard neuron decreased length, abnormal ZP:0001691 dendrite Rohon-Beard neuron decreased amount, abnormal ZP:0001692 pectoral fin development disrupted, abnormal ZP:0001693 pronephric duct development delayed, abnormal ZP:0001694 retinoic acid receptor signaling pathway process quality, abnormal ZP:0001695 otic vesicle decreased distance somite 1, abnormal ZP:0001696 swim bladder quality, abnormal ZP:0001697 yolk deformed, abnormal ZP:0001698 pharyngeal arch 3-7 skeleton absent, abnormal ZP:0001699 proximal region pronephric duct decreased length, abnormal ZP:0001700 distal region pronephric duct increased length, abnormal ZP:0001702 mandibular muscle morphology, abnormal ZP:0001703 myofibril medial rectus disorganized, abnormal ZP:0001704 cornea increased thickness, abnormal ZP:0001705 head misaligned with trunk, abnormal ZP:0001706 anterior-posterior axis head decreased length, abnormal ZP:0001707 pectoral fin absent, abnormal ZP:0001708 mandibular arch skeleton malformed, abnormal ZP:0001709 retinal outer plexiform layer disorganized, abnormal ZP:0001710 photoreceptor outer segment layer absent, abnormal ZP:0001711 anterior region vertebral column decreased length, abnormal ZP:0001712 pharyngeal arch 3-7 physical object quality, abnormal ZP:0001713 pronephric proximal convoluted tubule decreased length, abnormal ZP:0001714 pronephric distal late tubule increased length, abnormal ZP:0001715 corneal epithelium scalloped, abnormal ZP:0001716 corneal endothelium absent, abnormal ZP:0001717 heart valve formation disrupted, abnormal ZP:0001718 hyaluronan biosynthetic process disrupted, abnormal ZP:0001719 head decreased length, abnormal ZP:0001720 pectoral fin kinked, abnormal ZP:0001721 pharyngeal arch cartilage decreased size, abnormal ZP:0001722 atrioventricular valve morphology, abnormal ZP:0001723 atrioventricular valve aplastic, abnormal ZP:0001724 endocardial cushion morphology, abnormal ZP:0001725 lymph vessel development process quality, abnormal ZP:0001727 dendrite development disrupted, abnormal ZP:0001728 branching involved in lymph vessel morphogenesis process quality, abnormal ZP:0001729 olfactory bulb axon guidance disrupted, abnormal ZP:0001730 horizontal myoseptum lacks parts or has fewer parts of type axon RoP motor neuron, abnormal ZP:0001731 horizontal myoseptum lacks parts or has fewer parts of type axon motor neuron, abnormal ZP:0001732 parachordal vessel immature, abnormal ZP:0001733 parachordal vessel arrested venous endothelial cell migration involved in lymph vessel development, abnormal ZP:0001734 thoracic duct aplastic, abnormal ZP:0001735 VaP motor neuron protruding into axon muscle pioneer, abnormal ZP:0001737 neuron projection dorso-rostral cluster mislocalised dorsally, abnormal ZP:0001738 neuron projection dorso-rostral cluster multiple, abnormal ZP:0001739 axon olfactory receptor cell position, abnormal ZP:0001741 olfactory receptor cell attached to axon anterior commissure, abnormal ZP:0001746 olfactory receptor cell attached to axon lateral protoglomerulus 1, abnormal ZP:0001747 olfactory receptor cell attached to axon lateral protoglomerulus 2, abnormal ZP:0001748 dendrite efferent neuron mislocalised, abnormal ZP:0001749 dendrite efferent neuron decreased amount, abnormal ZP:0001750 hyaloid vessel irregular spatial pattern, abnormal ZP:0001751 hyaloid vessel increased thickness, abnormal ZP:0001753 nuclear migration disrupted, abnormal ZP:0001754 retina layer formation arrested, abnormal ZP:0001755 neuroblast development disrupted, abnormal ZP:0001757 dorsal motor nucleus of vagus nerve development disrupted, abnormal ZP:0001758 melanocyte differentiation delayed, abnormal ZP:0001759 tube formation disrupted, abnormal ZP:0001760 maintenance of epithelial cell apical/basal polarity disrupted, abnormal ZP:0001761 eye pigmentation disrupted, abnormal ZP:0001762 brain shape, abnormal ZP:0001763 retinal ganglion cell layer disorganized, abnormal ZP:0001764 heart decreased size, abnormal ZP:0001765 heart disorganized, abnormal ZP:0001766 heart dense, abnormal ZP:0001767 liver morphology, abnormal ZP:0001768 retinal pigmented epithelium structure, abnormal ZP:0001769 retinal pigmented epithelium patchy, abnormal ZP:0001770 retinal pigmented epithelium poorly differentiated, abnormal ZP:0001771 pronephros quality, abnormal ZP:0001772 retina quality, abnormal ZP:0001773 retina degenerate, abnormal ZP:0001774 retina cellular quality, abnormal ZP:0001775 retina unstratified, abnormal ZP:0001776 neuroepithelial cell retina positional polarity, abnormal ZP:0001777 atrium aplastic, abnormal ZP:0001778 cornea structure, abnormal ZP:0001779 anatomical surface cornea structure, abnormal ZP:0001780 ceratobranchial 5 bone has fewer parts of type ceratobranchial 5 tooth, abnormal ZP:0001781 corneal epithelium saccular, abnormal ZP:0001782 desmosome corneal epithelium decreased amount, abnormal ZP:0001783 corneal stroma disorganized, abnormal ZP:0001784 dorsolateral motor nucleus of vagal nerve malformed, abnormal ZP:0001785 nucleus neuroblast position, abnormal ZP:0001786 pigmented epithelial cell shape, abnormal ZP:0001787 pigment granule pigmented epithelial cell mislocalised, abnormal ZP:0001788 amacrine cell spatial pattern, abnormal ZP:0001789 corneal epithelial cell cellular adhesivity corneal epithelial cell, abnormal ZP:0001790 cell-cell junction neuroepithelial cell broken, abnormal ZP:0001791 endoderm decreased size, abnormal ZP:0001792 liver disorganized, abnormal ZP:0001793 pancreas decreased size, abnormal ZP:0001794 intestine decreased size, abnormal ZP:0001795 hepatoblast decreased size, abnormal ZP:0001796 atrioventricular valve formation disrupted, abnormal ZP:0001797 mesodermal cell fate specification increased process quality, abnormal ZP:0001798 atrioventricular canal development disrupted, abnormal ZP:0001799 presumptive mesoderm margin differentiated, abnormal ZP:0001800 atrioventricular canal morphology, abnormal ZP:0001801 cell endocardial cushion decreased amount, abnormal ZP:0001802 aortic arch 5 absent, abnormal ZP:0001803 heart contraction arrhythmic, abnormal ZP:0001804 cardiac ventricle increased diameter, abnormal ZP:0001805 heart tube increased size, abnormal ZP:0001806 cell morphogenesis disrupted, abnormal ZP:0001807 mesodermal cell migration delayed, abnormal ZP:0001808 notochord formation disrupted, abnormal ZP:0001809 muscle cell migration disrupted, abnormal ZP:0001810 glycosaminoglycan metabolic process disrupted, abnormal ZP:0001811 cell migration involved in gastrulation delayed, abnormal ZP:0001812 notochord morphogenesis disrupted, abnormal ZP:0001813 dorsal convergence delayed, abnormal ZP:0001814 Kupffer's vesicle oriented towards ciliated cell anterior region Kupffer's vesicle, abnormal ZP:0001815 adaxial cell shape, abnormal ZP:0001816 floor plate oriented towards ciliated cell anterior region floor plate, abnormal ZP:0001817 prechordal plate elongated, abnormal ZP:0001818 axis increased width, abnormal ZP:0001819 forebrain increased width, abnormal ZP:0001820 cell notochord disorganized, abnormal ZP:0001821 pronephric duct oriented towards ciliated cell anterior region pronephric duct, abnormal ZP:0001822 somite decreased length, abnormal ZP:0001823 myotome decreased length, abnormal ZP:0001824 rhombomere increased width, abnormal ZP:0001825 ventral fin fold dislocated cell proctodeum, abnormal ZP:0001826 anterior-posterior axis whole organism dwarf-like, abnormal ZP:0001827 medial-lateral axis whole organism increased length, abnormal ZP:0001828 post-vent region malformed, abnormal ZP:0001829 notochord post-vent region folded, abnormal ZP:0001830 Meckel's cartilage structure, abnormal ZP:0001831 chondrocyte Meckel's cartilage disorganized, abnormal ZP:0001832 chondrocyte ceratohyal cartilage disorganized, abnormal ZP:0001833 cranial cartilage deformed, abnormal ZP:0001834 extracellular matrix cranial cartilage composition, abnormal ZP:0001835 notochord posterior region folded, abnormal ZP:0001836 notochord posterior region separated from cell cell notochord posterior region, abnormal ZP:0001837 anterior neural plate increased width, abnormal ZP:0001838 slow muscle cell decreased length, abnormal ZP:0001839 slow muscle cell disorganized, abnormal ZP:0001841 visual behavior quality, abnormal ZP:0001842 thyroid gland development decreased process quality, abnormal ZP:0001843 endocrine system has fewer parts of type thyroid follicle, abnormal ZP:0001845 motor neuron spinal cord mislocalised, abnormal ZP:0001846 GABAergic neuron spinal cord increased amount, abnormal ZP:0001847 GABAergic neuron spinal cord mislocalised, abnormal ZP:0001848 cilium pronephros increased amount, abnormal ZP:0001849 multi-ciliated epithelial cell pronephros increased amount, abnormal ZP:0001850 contractile fiber pectoral fin musculature malformed, abnormal ZP:0001851 actin filament pectoral fin mislocalised, abnormal ZP:0001852 pectoral fin endoskeletal disc disorganized, abnormal ZP:0001853 inner ear development paedomorphic growth, abnormal ZP:0001854 anterior-posterior axis otic vesicle decreased length, abnormal ZP:0001855 inner ear decreased length, abnormal ZP:0001856 lateral semicircular canal decreased size, abnormal ZP:0001857 hair cell posterior crista absent, abnormal ZP:0001858 hair cell anterior crista absent, abnormal ZP:0001859 thyroid primordium malformed, abnormal ZP:0001860 hyosymplectic cartilage malformed, abnormal ZP:0001861 otic vesicle protrusion shape, abnormal ZP:0001862 otic vesicle protrusion malformed, abnormal ZP:0001863 pillar of the anterior semicircular canal increased thickness, abnormal ZP:0001864 pillar of the lateral semicircular canal increased thickness, abnormal ZP:0001866 retina dystrophic, abnormal ZP:0001867 photoreceptor outer segment layer shortened, abnormal ZP:0001868 optokinetic behavior arrested, abnormal ZP:0001869 optomotor response arrested, abnormal ZP:0001870 glial cell migration disrupted, abnormal ZP:0001871 Schwann cell differentiation arrested, abnormal ZP:0001872 Schwann cell development arrested, abnormal ZP:0001873 Schwann cell development disrupted, abnormal ZP:0001874 myelin assembly disrupted, abnormal ZP:0001875 oligodendrocyte differentiation arrested, abnormal ZP:0001876 semicircular canal morphogenesis disrupted, abnormal ZP:0001877 semicircular canal fusion arrested, abnormal ZP:0001878 melanocyte migration disrupted, abnormal ZP:0001879 otic vesicle distended, abnormal ZP:0001880 epithelial cell otic vesicle apoptotic, abnormal ZP:0001881 hair cell otic vesicle increased amount, abnormal ZP:0001882 anterior macula mislocalised, abnormal ZP:0001883 posterior lateral line nerve mislocalised, abnormal ZP:0001884 posterior lateral line nerve defasciculated, abnormal ZP:0001885 axon posterior lateral line nerve decreased amount, abnormal ZP:0001886 sodium channel complex posterior lateral line nerve asymmetrical, abnormal ZP:0001887 sodium channel complex posterior lateral line nerve elongated, abnormal ZP:0001888 sodium channel complex posterior lateral line nerve undistributed, abnormal ZP:0001889 sodium channel complex posterior lateral line nerve decreased amount, abnormal ZP:0001890 myelin sheath posterior lateral line nerve absent, abnormal ZP:0001891 myelinating Schwann cell posterior lateral line nerve absent, abnormal ZP:0001892 dorsal root ganglion absent, abnormal ZP:0001893 dorsal root ganglion increased amount, abnormal ZP:0001894 dorsal root ganglion mislocalised, abnormal ZP:0001895 inner ear malformed, abnormal ZP:0001896 lateral crista primordium aplastic, abnormal ZP:0001897 neuromast quality, abnormal ZP:0001898 posterior semicircular canal aplastic, abnormal ZP:0001899 anterior semicircular canal aplastic, abnormal ZP:0001900 integument lacks all parts of type pigment cell, abnormal ZP:0001901 hair cell macula mislocalised, abnormal ZP:0001902 semicircular canal morphology, abnormal ZP:0001903 semicircular canal decreased thickness, abnormal ZP:0001904 semicircular canal disorganized, abnormal ZP:0001905 posterior macula mislocalised, abnormal ZP:0001906 otolith organ decreased size, abnormal ZP:0001907 hair cell posterior crista increased amount, abnormal ZP:0001908 neuron statoacoustic (VIII) ganglion apoptotic, abnormal ZP:0001909 hair cell anterior crista increased amount, abnormal ZP:0001910 posterior lateral line neuromast quality, abnormal ZP:0001911 glial cell posterior lateral line absent, abnormal ZP:0001912 whole organism lacks all parts of type melanoblast, abnormal ZP:0001913 pigment cell head absent, abnormal ZP:0001914 pigment cell trunk absent, abnormal ZP:0001915 melanoblast post-vent region decreased amount, abnormal ZP:0001916 glial cell enteric nervous system decreased amount, abnormal ZP:0001917 neuron enteric nervous system absent, abnormal ZP:0001918 presumptive enteric nervous system aplastic, abnormal ZP:0001919 lateral line quality, abnormal ZP:0001920 otolith quality, abnormal ZP:0001921 vagal ganglion malformed, abnormal ZP:0001922 axon motor neuron structure, abnormal ZP:0001923 axon motor neuron defasciculated, abnormal ZP:0001924 glial cell mislocalised, abnormal ZP:0001925 filopodium glial cell increased speed, abnormal ZP:0001926 filopodium glial cell increased length, abnormal ZP:0001927 pigment cell spatial pattern, abnormal ZP:0001928 melanocyte absent, abnormal ZP:0001929 myelinating Schwann cell morphology, abnormal ZP:0001930 myelinating Schwann cell absent, abnormal ZP:0001931 xanthophore morphology, abnormal ZP:0001932 melanoblast absent, abnormal ZP:0001933 melanoblast decreased amount, abnormal ZP:0001934 hatching arrested, abnormal ZP:0001935 hatching gland development arrested, abnormal ZP:0001936 secretory granule hatching gland cell decreased size, abnormal ZP:0001937 secretory granule hatching gland cell decreased amount, abnormal ZP:0001938 peripheral nervous system development disrupted, abnormal ZP:0001939 melanocyte differentiation disrupted, abnormal ZP:0001941 autonomic nervous system development disrupted, abnormal ZP:0001944 otic vesicle hypoplastic, abnormal ZP:0001945 postoptic commissure decreased size, abnormal ZP:0001946 pharyngeal arch 3-7 skeleton morphology, abnormal ZP:0001947 pharyngeal arch 3-7 skeleton has fewer parts of type ceratobranchial cartilage, abnormal ZP:0001951 neuron peripheral nervous system distributed, abnormal ZP:0001952 retinal pigmented epithelium protruding, abnormal ZP:0001954 neuron dorsal root ganglion decreased amount, abnormal ZP:0001955 gill decreased size, abnormal ZP:0001956 adrenergic neuron locus coeruleus absent, abnormal ZP:0001957 adrenergic neuron medulla oblongata absent, abnormal ZP:0001958 quadrate decreased length, abnormal ZP:0001959 quadrate decreased size, abnormal ZP:0001960 whole organism lacks all parts of type neuron sympathetic nervous system, abnormal ZP:0001963 Meckel's cartilage sloped downward, abnormal ZP:0001964 Meckel's cartilage fused with Meckel's cartilage, abnormal ZP:0001965 mandibular arch skeleton decreased size, abnormal ZP:0001966 mandibular arch skeleton disorganized, abnormal ZP:0001967 mandibular arch skeleton protruding, abnormal ZP:0001968 mandibular arch skeleton mislocalised ventrally, abnormal ZP:0001969 pharyngeal arch 3 skeleton decreased size, abnormal ZP:0001970 pharyngeal arch 7 skeleton decreased size, abnormal ZP:0001971 pharyngeal arch 6 skeleton absent, abnormal ZP:0001972 pharyngeal arch 4 skeleton absent, abnormal ZP:0001973 pharyngeal arch 5 skeleton absent, abnormal ZP:0001974 pharyngeal arch 2 skeleton morphology, abnormal ZP:0001975 palatoquadrate cartilage mislocalised, abnormal ZP:0001976 palatoquadrate cartilage disorganized, abnormal ZP:0001977 ceratohyal cartilage hypoplastic, abnormal ZP:0001978 ceratohyal cartilage medially rotated, abnormal ZP:0001979 ethmoid cartilage split, abnormal ZP:0001981 trabecula cranii decreased length, abnormal ZP:0001982 trabecula cranii decreased thickness, abnormal ZP:0001983 trabecula communis absent, abnormal ZP:0001984 basihyal cartilage decreased length, abnormal ZP:0001985 basihyal cartilage decreased size, abnormal ZP:0001986 basihyal cartilage mislocalised laterally, abnormal ZP:0001988 neurocranium decreased size, abnormal ZP:0001989 pharyngeal arch 2 disorganized, abnormal ZP:0001992 anterior catecholaminergic tract decreased size, abnormal ZP:0001995 response to light stimulus disrupted, abnormal ZP:0001996 circadian regulation of gene expression disrupted, abnormal ZP:0001997 intersegmental vessel increased length, abnormal ZP:0001998 female germ-line stem cell population maintenance disrupted, abnormal ZP:0001999 oocyte absent, abnormal ZP:0002000 primordial germ cell decreased amount, abnormal ZP:0002001 vasculogenesis process quality, abnormal ZP:0002002 cell migration involved in sprouting angiogenesis disrupted, abnormal ZP:0002003 cell migration involved in gastrulation process quality, abnormal ZP:0002004 blood vessel endothelial cell migration process quality, abnormal ZP:0002005 muscle cell development disrupted, abnormal ZP:0002006 dorsal convergence disrupted, abnormal ZP:0002007 endoderm mislocalised anteriorly, abnormal ZP:0002008 gut morphology, abnormal ZP:0002009 gut bifurcated, abnormal ZP:0002010 pancreas morphology, abnormal ZP:0002011 pancreatic B cell pancreas dispersed, abnormal ZP:0002012 angiogenic sprout primordial hindbrain channel mislocalised, abnormal ZP:0002013 angiogenic sprout primordial hindbrain channel decreased amount, abnormal ZP:0002014 lateral dorsal aorta malformed, abnormal ZP:0002015 intestine duplicated, abnormal ZP:0002016 basilar artery absent, abnormal ZP:0002017 basilar artery unlumenized, abnormal ZP:0002018 basilar artery agenesis, abnormal ZP:0002019 blood vessel endothelial cell mislocalised, abnormal ZP:0002020 endodermal cell circular, abnormal ZP:0002021 endodermal cell mislocalised anteriorly, abnormal ZP:0002022 endodermal cell displaced to margin, abnormal ZP:0002023 filopodium endodermal cell decreased amount, abnormal ZP:0002024 endodermal cell orientation filopodium dorsal-ventral axis whole organism, abnormal ZP:0002025 regionalization disrupted, abnormal ZP:0002026 cardiac conduction system development disrupted, abnormal ZP:0002027 type B pancreatic cell development disrupted, abnormal ZP:0002028 hindbrain morphogenesis disrupted, abnormal ZP:0002029 pancreas development disrupted, abnormal ZP:0002030 digestive tract morphogenesis disrupted, abnormal ZP:0002031 cardiac ventricle non-contractile, abnormal ZP:0002032 hindbrain irregular spatial pattern, abnormal ZP:0002033 otic vesicle circular, abnormal ZP:0002034 otic vesicle wholly anterioralized, abnormal ZP:0002035 rhombomere 6 morphology, abnormal ZP:0002036 swim bladder agenesis, abnormal ZP:0002037 liver aplastic, abnormal ZP:0002038 liver agenesis, abnormal ZP:0002039 pancreas hypoplastic, abnormal ZP:0002040 pancreas aplastic, abnormal ZP:0002041 pancreas variability of size, abnormal ZP:0002042 pancreas agenesis, abnormal ZP:0002043 semicircular canal shape, abnormal ZP:0002044 kidney cystic, abnormal ZP:0002045 rhombomere 5 morphology, abnormal ZP:0002046 intestinal bulb structure, abnormal ZP:0002047 endocrine pancreas quality, abnormal ZP:0002048 pancreatic bud aplastic, abnormal ZP:0002049 otolith shape, abnormal ZP:0002050 atrioventricular node closed, abnormal ZP:0002051 atrioventricular node decreased functionality, abnormal ZP:0002052 intrahepatic bile duct decreased length, abnormal ZP:0002053 intrahepatic bile duct hypoplastic, abnormal ZP:0002054 intrahepatic bile duct dilated, abnormal ZP:0002055 islet disorganized, abnormal ZP:0002056 pancreatic B cell disorganized, abnormal ZP:0002057 dorsal convergence decreased rate, abnormal ZP:0002058 mediolateral intercalation disrupted, abnormal ZP:0002059 retinal neural layer hypoplastic, abnormal ZP:0002060 yolk edematous, abnormal ZP:0002062 cranial nerve II defasciculated, abnormal ZP:0002063 sensory neuron axon guidance disrupted, abnormal ZP:0002064 axon Rohon-Beard neuron mislocalized adaxially, abnormal ZP:0002065 axon Rohon-Beard neuron subdermal, abnormal ZP:0002066 slow muscle cell decreased amount, abnormal ZP:0002068 lens separated from cell lens epithelium, abnormal ZP:0002070 cell population proliferation disrupted, abnormal ZP:0002071 lens fiber cell differentiation disrupted, abnormal ZP:0002072 retina decreased thickness, abnormal ZP:0002074 optic tectum morphology, abnormal ZP:0002075 amacrine cell decreased amount, abnormal ZP:0002076 anterior-posterior axis hindbrain decreased length, abnormal ZP:0002077 anterior region hindbrain decreased size, abnormal ZP:0002078 spinal cord decreased length, abnormal ZP:0002079 neural keel wholly anterioralized, abnormal ZP:0002080 neural plate wholly anterioralized, abnormal ZP:0002081 spinal cord neural keel decreased length, abnormal ZP:0002082 midbrain hindbrain boundary neural plate mislocalised posteriorly, abnormal ZP:0002083 midbrain hindbrain boundary neural keel morphology, abnormal ZP:0002084 angiogenesis disrupted, abnormal ZP:0002085 hemopoiesis decreased process quality, abnormal ZP:0002086 erythrocyte differentiation disrupted, abnormal ZP:0002087 selective angioblast sprouting disrupted, abnormal ZP:0002088 regulation of fibroblast growth factor receptor signaling pathway disrupted, abnormal ZP:0002089 artery morphogenesis disrupted, abnormal ZP:0002090 embryonic retina morphogenesis in camera-type eye disrupted, abnormal ZP:0002091 dorsal aorta fused with posterior cardinal vein, abnormal ZP:0002092 macrophage blood island decreased amount, abnormal ZP:0002093 heart inverted, abnormal ZP:0002094 grey matter optic tectum decreased mass, abnormal ZP:0002095 optic cup wholly ventralized, abnormal ZP:0002096 Meckel's cartilage fused with hyosymplectic cartilage, abnormal ZP:0002097 palatoquadrate cartilage rotated, abnormal ZP:0002098 palatoquadrate cartilage flattened, abnormal ZP:0002099 ceratohyal cartilage fused with ceratobranchial cartilage, abnormal ZP:0002100 cranial cartilage morphology, abnormal ZP:0002101 cranial cartilage mislocalised, abnormal ZP:0002102 ceratobranchial cartilage fused with ceratobranchial cartilage, abnormal ZP:0002103 thrombocyte absent, abnormal ZP:0002104 cranial cartilage fused with cranial cartilage, abnormal ZP:0002105 brain segmentation disrupted, abnormal ZP:0002106 facial nerve motor nucleus mislocalised, abnormal ZP:0002107 neuron rhombomere organization quality, abnormal ZP:0002108 whole organism lacks all parts of type mandibular arch skeleton, abnormal ZP:0002109 pectoral fin atrophied, abnormal ZP:0002110 ethmoid cartilage deformed, abnormal ZP:0002111 trabecula cranii decreased size, abnormal ZP:0002112 trabecula cranii deformed, abnormal ZP:0002113 CNS interneuron decreased amount, abnormal ZP:0002114 endoderm development process quality, abnormal ZP:0002115 neural crest cell differentiation process quality, abnormal ZP:0002116 embryonic viscerocranium morphogenesis process quality, abnormal ZP:0002117 pharyngeal system development process quality, abnormal ZP:0002118 pectoral fin bud physical object quality, abnormal ZP:0002119 pharyngeal pouch 3 aplastic, abnormal ZP:0002120 pharyngeal pouch 6 aplastic, abnormal ZP:0002121 pharyngeal pouch 5 aplastic, abnormal ZP:0002122 pharyngeal pouch 4 aplastic, abnormal ZP:0002123 pharyngeal arch 7 skeleton aplastic, abnormal ZP:0002124 pharyngeal arch 6 skeleton aplastic, abnormal ZP:0002125 pharyngeal arch 4 skeleton aplastic, abnormal ZP:0002126 pharyngeal arch 5 skeleton aplastic, abnormal ZP:0002127 mesodermal cell migration persistence, abnormal ZP:0002128 mesodermal cell migration increased rate, abnormal ZP:0002130 anterior lateral line neuromast hair cell development disrupted, abnormal ZP:0002131 posterior lateral line neuromast hair cell development disrupted, abnormal ZP:0002132 involution involved in gastrulation with mouth forming second disrupted, abnormal ZP:0002133 otic vesicle morphogenesis disrupted, abnormal ZP:0002134 prechordal plate flat, abnormal ZP:0002135 prechordal plate increased length, abnormal ZP:0002136 prechordal plate increased width, abnormal ZP:0002137 heart rudiment malformed, abnormal ZP:0002138 mesodermal cell hypoblast spatial pattern, abnormal ZP:0002140 mesodermal cell hypoblast cellular motility, abnormal ZP:0002141 liver bilateral, abnormal ZP:0002142 neural keel increased length, abnormal ZP:0002143 notochord increased thickness, abnormal ZP:0002144 saccule decreased size, abnormal ZP:0002145 semicircular canal broken into two pieces, abnormal ZP:0002146 utricle increased size, abnormal ZP:0002147 posterior lateral line neuromast decreased size, abnormal ZP:0002148 posterior lateral line has fewer parts of type posterior lateral line neuromast, abnormal ZP:0002149 caudal fin blistered, abnormal ZP:0002150 endoderm caudal fin blistered, abnormal ZP:0002151 pharyngeal endoderm disorganized, abnormal ZP:0002152 pharyngeal endoderm mislocalised posteriorly, abnormal ZP:0002153 Meckel's cartilage hypoplastic, abnormal ZP:0002154 Meckel's cartilage disorganized, abnormal ZP:0002155 mandibular arch skeleton shape, abnormal ZP:0002156 mandibular arch skeleton size, abnormal ZP:0002157 mandibular arch skeleton mislocalised, abnormal ZP:0002158 neurocranial trabecula hypoplastic, abnormal ZP:0002159 pharyngeal ectoderm disorganized, abnormal ZP:0002160 pharyngeal ectoderm increased area, abnormal ZP:0002161 ethmoid cartilage hypoplastic, abnormal ZP:0002162 neuromast hair cell anterior lateral line decreased amount, abnormal ZP:0002163 otolith increased size, abnormal ZP:0002164 otolith malformed, abnormal ZP:0002165 oral ectoderm hypoplastic, abnormal ZP:0002166 oral ectoderm disorganized, abnormal ZP:0002167 oral ectoderm mislocalised anteriorly, abnormal ZP:0002169 neuromast hair cell apoptotic, abnormal ZP:0002170 heart contraction process quality, abnormal ZP:0002172 cardiac muscle contraction irregular rhythm, abnormal ZP:0002173 cardiac conduction rhythm quality, abnormal ZP:0002174 cardiac ventricle non-functional, abnormal ZP:0002175 cardiac muscle cell cardiac ventricle non-contractile, abnormal ZP:0002176 heart contractility, abnormal ZP:0002177 chondrocyte Meckel's cartilage decreased size, abnormal ZP:0002178 atrial myocardium contractility, abnormal ZP:0002179 pronephric podocyte unfused from pronephric podocyte, abnormal ZP:0002180 ventricular myocardium decreased thickness, abnormal ZP:0002181 ventricular myocardium non-functional, abnormal ZP:0002182 sprouting angiogenesis decreased process quality, abnormal ZP:0002183 axonogenesis disrupted, abnormal ZP:0002184 midbrain development disrupted, abnormal ZP:0002185 neuron projection development disrupted, abnormal ZP:0002186 yolk decreased size, abnormal ZP:0002187 brain vasculature has fewer parts of type central artery, abnormal ZP:0002188 somite deformed, abnormal ZP:0002189 axon facial nerve motor nucleus decreased length, abnormal ZP:0002190 trunk deformed, abnormal ZP:0002191 axon trigeminal motor nucleus decreased length, abnormal ZP:0002192 cytoskeleton motor neuron disorganized, abnormal ZP:0002193 axon motor neuron decreased branchiness, abnormal ZP:0002194 microtubule Mauthner neuron decreased amount, abnormal ZP:0002195 microtubule cytoskeleton Mauthner neuron decreased mass density, abnormal ZP:0002196 cell aging increased magnitude, abnormal ZP:0002197 yolk necrotic, abnormal ZP:0002198 yolk opaque, abnormal ZP:0002199 yolk dark grey, abnormal ZP:0002200 extension absent, abnormal ZP:0002201 liver composition, abnormal ZP:0002202 whole organism edematous, abnormal ZP:0002203 trunk decreased thickness, abnormal ZP:0002204 muscle composition, abnormal ZP:0002205 cardiac atrium development disrupted, abnormal ZP:0002207 retinoic acid receptor signaling pathway decreased process quality, abnormal ZP:0002210 posterior lateral line neuromast primordium migration arrested, abnormal ZP:0002211 protoneuromast posterior lateral line primordium morphology, abnormal ZP:0002212 thigmotaxis decreased process quality, abnormal ZP:0002213 central nervous system projection neuron axonogenesis disrupted, abnormal ZP:0002214 sclerotome development disrupted, abnormal ZP:0002215 centrum length, abnormal ZP:0002216 adaxial cell somite decreased amount, abnormal ZP:0002217 hemal arch irregular spatial pattern, abnormal ZP:0002218 horizontal myoseptum absent, abnormal ZP:0002219 myotome shape, abnormal ZP:0002220 neural arch irregular spatial pattern, abnormal ZP:0002221 sclerotome spatial pattern, abnormal ZP:0002222 post-vent region shape, abnormal ZP:0002223 vertebra structure, abnormal ZP:0002224 somite border absent, abnormal ZP:0002225 somite border inconspicuous, abnormal ZP:0002226 axon MiP motor neuron irregular spatial pattern, abnormal ZP:0002227 axon MiP motor neuron decreased length, abnormal ZP:0002228 axon CaP motoneuron irregular spatial pattern, abnormal ZP:0002229 axon CaP motoneuron increased amount, abnormal ZP:0002230 axon CaP motoneuron decreased length, abnormal ZP:0002231 head pointed, abnormal ZP:0002232 habenula development disrupted, abnormal ZP:0002233 neurogenesis increased occurrence, abnormal ZP:0002234 cell division increased occurrence, abnormal ZP:0002235 cerebellum has extra parts of type neuron, abnormal ZP:0002236 epithelium third ventricle morphology, abnormal ZP:0002237 columnar/cuboidal epithelial cell third ventricle circular, abnormal ZP:0002238 third ventricle cellular adhesivity columnar/cuboidal epithelial cell columnar/cuboidal epithelial cell third ventricle, abnormal ZP:0002239 dorsal habenular nucleus morphology, abnormal ZP:0002240 dorsal habenular nucleus has extra parts of type right side neuron, abnormal ZP:0002241 dorsal habenular nucleus has extra parts of type lateral region neuron, abnormal ZP:0002242 dorsal habenular nucleus has fewer parts of type medial region neuron, abnormal ZP:0002243 neuron dorsal habenular nucleus spatial pattern, abnormal ZP:0002244 habenula has extra parts of type left side neuron, abnormal ZP:0002245 habenula has extra parts of type right side neuron, abnormal ZP:0002246 hyomandibula decreased size, abnormal ZP:0002247 anterior-posterior axis whole organism curved dorsal, abnormal ZP:0002248 head decreased volume, abnormal ZP:0002249 extracellular matrix mandibular arch skeleton sparse, abnormal ZP:0002250 chondrocyte mandibular arch skeleton cellular quality, abnormal ZP:0002251 cartilage element morphology, abnormal ZP:0002252 cell-cell junction columnar/cuboidal epithelial cell decreased amount, abnormal ZP:0002253 endoplasmic reticulum chondrocyte decreased volume, abnormal ZP:0002254 filamentous actin neuroepithelial cell decreased amount, abnormal ZP:0002255 midbrain hindbrain boundary condensed, abnormal ZP:0002256 fourth ventricle distended, abnormal ZP:0002257 cranium hypoplastic, abnormal ZP:0002258 cranium malformed, abnormal ZP:0002259 notochord morphogenesis decreased process quality, abnormal ZP:0002260 notochord cell vacuolation decreased process quality, abnormal ZP:0002261 retina morphogenesis in camera-type eye process quality, abnormal ZP:0002262 vacuole notochord broken, abnormal ZP:0002263 retinal pigmented epithelium physical object quality, abnormal ZP:0002264 retinal pigmented epithelium translucent, abnormal ZP:0002265 post-vent region decreased pigmentation, abnormal ZP:0002266 pharyngeal arch 3-7 shape, abnormal ZP:0002267 melanocyte larval melanophore stripe translucent, abnormal ZP:0002268 pigment cell patchy, abnormal ZP:0002269 melanocyte malformed, abnormal ZP:0002270 melanocyte translucent, abnormal ZP:0002271 photoreceptor outer segment eye photoreceptor cell decreased size, abnormal ZP:0002272 brain necrotic, abnormal ZP:0002273 yolk non-functional, abnormal ZP:0002274 chromosome peripheral nervous system amount, abnormal ZP:0002275 trunk necrotic, abnormal ZP:0002276 mandibular arch skeleton increased thickness, abnormal ZP:0002277 cell aging decreased magnitude, abnormal ZP:0002278 heart necrotic, abnormal ZP:0002279 pectoral fin shape, abnormal ZP:0002280 pectoral fin stubby, abnormal ZP:0002281 cartilage element decreased length, abnormal ZP:0002282 cartilage element rough, abnormal ZP:0002283 cartilage element wrinkled, abnormal ZP:0002284 ball opaque, abnormal ZP:0002285 hindbrain undulate, abnormal ZP:0002286 midbrain hindbrain boundary decreased thickness, abnormal ZP:0002287 forebrain protruding, abnormal ZP:0002288 nerve peripheral nervous system neoplastic, abnormal ZP:0002289 optic tectum opaque, abnormal ZP:0002290 otolith organ deformed, abnormal ZP:0002291 pigmentation decreased occurrence, abnormal ZP:0002292 eye color, abnormal ZP:0002293 fin malformed, abnormal ZP:0002294 gut decreased size, abnormal ZP:0002295 retinal pigmented epithelium malformed, abnormal ZP:0002296 whole organism low saturation, abnormal ZP:0002297 whole organism unpigmented, abnormal ZP:0002298 pectoral fin ruffled, abnormal ZP:0002299 melanocyte punctate, abnormal ZP:0002300 thymus decreased occurrence cell population proliferation, abnormal ZP:0002301 epithelial cell thymus decreased amount, abnormal ZP:0002302 trunk undulate, abnormal ZP:0002303 pharyngeal arch 3-7 aplastic, abnormal ZP:0002304 telencephalon deformed, abnormal ZP:0002305 extension deformed, abnormal ZP:0002306 otic placode shape, abnormal ZP:0002307 alternative mRNA splicing, via spliceosome process quality, abnormal ZP:0002308 regulation of alternative mRNA splicing, via spliceosome disrupted, abnormal ZP:0002309 eye necrotic, abnormal ZP:0002310 whole organism circling, abnormal ZP:0002311 head necrotic, abnormal ZP:0002312 S phase increased duration, abnormal ZP:0002313 hindbrain surface feature shape, abnormal ZP:0002314 head shape, abnormal ZP:0002316 heparan sulfate proteoglycan biosynthetic process decreased occurrence, abnormal ZP:0002317 chondroitin sulfate biosynthetic process process quality, abnormal ZP:0002318 chondroitin sulfate proteoglycan biosynthetic process decreased occurrence, abnormal ZP:0002319 sulfation decreased occurrence, abnormal ZP:0002320 endochondral bone morphogenesis delayed, abnormal ZP:0002321 opercle malformed, abnormal ZP:0002322 mandibular arch skeleton decreased length, abnormal ZP:0002323 mandibular arch skeleton condensed, abnormal ZP:0002324 collagen trimer cranial cartilage morphology, abnormal ZP:0002325 collagen type I trimer cranial cartilage decreased amount, abnormal ZP:0002326 collagen type II trimer cranial cartilage decreased amount, abnormal ZP:0002327 collagen type VI trimer cranial cartilage absent, abnormal ZP:0002328 pharyngeal arch cartilage decreased length, abnormal ZP:0002329 pharyngeal arch cartilage increased thickness, abnormal ZP:0002330 pharyngeal arch cartilage oriented, abnormal ZP:0002331 chondrocyte pharyngeal arch cartilage circular, abnormal ZP:0002332 chondrocyte pharyngeal arch cartilage disorganized, abnormal ZP:0002333 liver development paedomorphic growth, abnormal ZP:0002334 exocrine pancreas development paedomorphic growth, abnormal ZP:0002335 regulation of cell cycle disrupted, abnormal ZP:0002336 yolk shape, abnormal ZP:0002337 melanophore stripe yolk absent, abnormal ZP:0002338 gut increased width, abnormal ZP:0002339 cell gut increased amount, abnormal ZP:0002340 anterior region notochord increased width, abnormal ZP:0002341 retina perforate, abnormal ZP:0002342 retina increased occurrence intrinsic apoptotic signaling pathway by p53 class mediator, abnormal ZP:0002343 cell retina apoptotic, abnormal ZP:0002344 facial nerve motor nucleus morphology, abnormal ZP:0002345 neuron statoacoustic (VIII) ganglion decreased amount, abnormal ZP:0002346 common lymphoid progenitor thymus primordium absent, abnormal ZP:0002347 trunk curved, abnormal ZP:0002348 trunk degenerate, abnormal ZP:0002349 neural crest cell post-vent region present, abnormal ZP:0002350 exocrine pancreas aplastic, abnormal ZP:0002351 optic fissure open, abnormal ZP:0002352 melanophore stripe decreased amount, abnormal ZP:0002353 melanocyte melanophore stripe decreased amount, abnormal ZP:0002354 hematopoietic stem cell ventral wall of dorsal aorta absent, abnormal ZP:0002355 motor neuron mislocalised, abnormal ZP:0002356 CNS neuron (sensu Vertebrata) decreased amount, abnormal ZP:0002357 melanocyte position, abnormal ZP:0002358 melanocyte mislocalised, abnormal ZP:0002359 melanocyte cellular motility, abnormal ZP:0002360 endocrine cell mislocalised, abnormal ZP:0002361 endodermal cell decreased amount, abnormal ZP:0002362 vacuole notochord disorganized, abnormal ZP:0002363 trunk has fewer parts of type melanocyte, abnormal ZP:0002364 trunk has fewer parts of type iridophore, abnormal ZP:0002365 iridophore quality, abnormal ZP:0002366 spindle pole proliferative region increased amount, abnormal ZP:0002367 chondrocyte intercalation involved in growth plate cartilage morphogenesis disrupted, abnormal ZP:0002368 cell junction organization disrupted, abnormal ZP:0002369 ceratohyal bone absent, abnormal ZP:0002370 hyomandibula absent, abnormal ZP:0002371 Meckel's cartilage decreased distance anterior side posterior side ceratohyal cartilage, abnormal ZP:0002372 fibrillar collagen trimer cranial cartilage absent, abnormal ZP:0002373 collagen type II trimer cranial cartilage absent, abnormal ZP:0002374 extracellular matrix cranial cartilage decreased size, abnormal ZP:0002376 pharyngeal arch cartilage aplastic, abnormal ZP:0002377 chondrocyte pharyngeal arch cartilage crowded, abnormal ZP:0002378 chondrocranium cartilage aplastic, abnormal ZP:0002379 perichondral bone aplastic, abnormal ZP:0002380 perichondrium aplastic, abnormal ZP:0002381 chondrocyte morphology, abnormal ZP:0002382 chondrocyte fused with chondrocyte, abnormal ZP:0002383 chondrocyte attached to chondrocyte, abnormal ZP:0002384 fibrillar collagen trimer chondrocyte decreased amount, abnormal ZP:0002385 plasma membrane chondrocyte smooth, abnormal ZP:0002386 extracellular matrix chondrocyte condensed, abnormal ZP:0002387 extracellular matrix chondrocyte decreased area, abnormal ZP:0002388 cell projection membrane chondrocyte absent, abnormal ZP:0002389 mitotic M phase temporally extended, abnormal ZP:0002390 spindle organization disrupted, abnormal ZP:0002391 mitotic chromosome movement towards spindle pole disrupted, abnormal ZP:0002392 mitotic metaphase plate congression disrupted, abnormal ZP:0002393 spindle assembly disrupted, abnormal ZP:0002394 lens protruding out of eye, abnormal ZP:0002395 retinal neural layer disorganized, abnormal ZP:0002397 retina has fewer parts of type cell retina, abnormal ZP:0002398 retina lacks parts or has fewer parts of type centrosome cell, abnormal ZP:0002399 retina increased duration mitotic M phase, abnormal ZP:0002400 retina arrested mitotic prometaphase, abnormal ZP:0002401 retina increased duration mitotic prometaphase, abnormal ZP:0002402 retina increased duration M phase, abnormal ZP:0002403 retina increased occurrence apoptotic process, abnormal ZP:0002407 retina increased duration cell division, abnormal ZP:0002408 caudal fin curved, abnormal ZP:0002409 neuron head apoptotic, abnormal ZP:0002410 trunk sigmoid, abnormal ZP:0002411 gamma-tubulin complex cell mislocalised, abnormal ZP:0002412 spindle cell disorganized, abnormal ZP:0002413 spindle pole centrosome cell absent, abnormal ZP:0002414 optic tectum necrotic, abnormal ZP:0002415 cytokinesis disrupted, abnormal ZP:0002416 chromosome segregation disrupted, abnormal ZP:0002417 swim bladder collapsed, abnormal ZP:0002418 germ plasm blastomere mislocalised, abnormal ZP:0002419 mouth protruding, abnormal ZP:0002420 blastoderm morphology, abnormal ZP:0002421 cleavage furrow blastoderm absent, abnormal ZP:0002422 cleavage furrow blastoderm decreased length, abnormal ZP:0002423 cleavage furrow blastoderm malformed, abnormal ZP:0002424 nucleus cell condensed, abnormal ZP:0002425 midbody cell decreased mass density, abnormal ZP:0002426 melanosome transport disrupted, abnormal ZP:0002427 Kupffer's vesicle decreased size, abnormal ZP:0002428 embryo development process quality, abnormal ZP:0002429 hindbrain opaque, abnormal ZP:0002430 lens increased size, abnormal ZP:0002431 yolk extension absent, abnormal ZP:0002432 fin deformed, abnormal ZP:0002433 retinal pigment epithelium development process quality, abnormal ZP:0002434 eye pigment granule organization process quality, abnormal ZP:0002436 melanosome organization process quality, abnormal ZP:0002437 retinal cell programmed cell death increased rate, abnormal ZP:0002438 developmental pigmentation process quality, abnormal ZP:0002439 eye pigmentation process quality, abnormal ZP:0002440 swim bladder formation process quality, abnormal ZP:0002441 neuron apoptotic process increased rate, abnormal ZP:0002442 retinal pigmented epithelium increased thickness, abnormal ZP:0002443 retinal pigmented epithelium vacuolated, abnormal ZP:0002444 retinal pigmented epithelium mottled, abnormal ZP:0002445 melanosome retinal pigmented epithelium decreased size, abnormal ZP:0002446 melanosome retinal pigmented epithelium malformed, abnormal ZP:0002447 melanosome retinal pigmented epithelium broken, abnormal ZP:0002448 retinal outer nuclear layer disorganized, abnormal ZP:0002449 intrahepatic bile duct distended, abnormal ZP:0002450 intrahepatic bile duct decreased amount, abnormal ZP:0002451 melanocyte degree of pigmentation, abnormal ZP:0002452 eye photoreceptor cell malformed, abnormal ZP:0002453 photoreceptor outer segment eye photoreceptor cell malformed, abnormal ZP:0002454 photoreceptor outer segment eye photoreceptor cell elongated, abnormal ZP:0002455 swim bladder formation delayed, abnormal ZP:0002456 whole organism decreased weight, abnormal ZP:0002457 muscle contraction decreased occurrence, abnormal ZP:0002458 locomotion decreased occurrence, abnormal ZP:0002459 swim bladder formation arrested, abnormal ZP:0002460 striated muscle myosin thick filament assembly disrupted, abnormal ZP:0002461 muscle thin filament assembly disrupted, abnormal ZP:0002462 myofibril slow muscle cell disorganized, abnormal ZP:0002463 sarcomere fast muscle cell decreased amount, abnormal ZP:0002464 mitotic S phase duration, abnormal ZP:0002465 mitotic M phase duration, abnormal ZP:0002466 regulation of heart rate disrupted, abnormal ZP:0002467 fat cell differentiation decreased occurrence, abnormal ZP:0002468 cellular senescence increased occurrence, abnormal ZP:0002469 sinus venosus increased accumulation blood, abnormal ZP:0002470 integument rough, abnormal ZP:0002471 slow muscle cell myotome undulate, abnormal ZP:0002472 slow muscle cell myotome decreased amount, abnormal ZP:0002473 trunk apoptotic, abnormal ZP:0002474 Meckel's cartilage alignment palatoquadrate cartilage, abnormal ZP:0002475 ceratohyal cartilage mislocalised posteriorly, abnormal ZP:0002476 pharyngeal arch cartilage physical object quality, abnormal ZP:0002477 fat cell decreased amount, abnormal ZP:0002478 axis increased curvature, abnormal ZP:0002479 dorsal longitudinal anastomotic vessel morphology, abnormal ZP:0002480 dorsal longitudinal anastomotic vessel absent, abnormal ZP:0002481 vasculature branchiness, abnormal ZP:0002482 heart morphogenesis delayed, abnormal ZP:0002484 ear development disrupted, abnormal ZP:0002485 cardiac ventricle hypoplastic, abnormal ZP:0002486 spinal cord apoptotic, abnormal ZP:0002487 hair cell inner ear absent, abnormal ZP:0002488 posterior crista primordium aplastic, abnormal ZP:0002489 anterior crista primordium aplastic, abnormal ZP:0002490 fast muscle cell decreased amount, abnormal ZP:0002491 CaP motoneuron decreased amount, abnormal ZP:0002492 axon CaP motoneuron decreased functionality, abnormal ZP:0002493 retinal ganglion cell absent, abnormal ZP:0002494 muscle contraction arrested, abnormal ZP:0002495 germ cell migration disrupted, abnormal ZP:0002496 primordial germ cell misrouted, abnormal ZP:0002497 retina layer formation process quality, abnormal ZP:0002498 growth disrupted, abnormal ZP:0002499 hindbrain decreased size, abnormal ZP:0002500 midbrain hindbrain boundary deformed, abnormal ZP:0002501 pericardium dilated, abnormal ZP:0002502 heart dilated, abnormal ZP:0002503 midbrain decreased size, abnormal ZP:0002506 heart looping process quality, abnormal ZP:0002507 opsin transport disrupted, abnormal ZP:0002508 left/right pattern formation disrupted, abnormal ZP:0002509 cloacal chamber deformed, abnormal ZP:0002512 kidney edematous, abnormal ZP:0002513 anterior-posterior axis whole organism curved, abnormal ZP:0002516 pronephric glomerulus cystic, abnormal ZP:0002517 pronephric tubule pronephric glomerulus increased diameter, abnormal ZP:0002518 pronephric proximal convoluted tubule increased diameter, abnormal ZP:0002520 establishment of mitotic spindle orientation disrupted, abnormal ZP:0002521 cilium movement decreased frequency, abnormal ZP:0002522 neural fold folding delayed, abnormal ZP:0002523 facial nerve development disrupted, abnormal ZP:0002524 establishment of cell polarity disrupted, abnormal ZP:0002525 convergent extension involved in gastrulation process quality, abnormal ZP:0002526 Kupffer's vesicle increased size, abnormal ZP:0002527 ventral region brain condensed, abnormal ZP:0002528 central nervous system degenerate, abnormal ZP:0002529 floor plate increased width, abnormal ZP:0002530 floor plate distended, abnormal ZP:0002532 ciliated cell floor plate increased amount, abnormal ZP:0002533 hindbrain process quality motor neuron migration, abnormal ZP:0002534 rhombomere 6 lacks all parts of type branchiomotor neuron, abnormal ZP:0002535 spinal cord duplicated, abnormal ZP:0002536 axial chorda mesoderm decreased length, abnormal ZP:0002537 axial chorda mesoderm increased width, abnormal ZP:0002538 extension increased width, abnormal ZP:0002539 eye decreased width, abnormal ZP:0002540 fourth ventricle duplicated, abnormal ZP:0002541 neural keel increased thickness, abnormal ZP:0002542 neural keel increased width, abnormal ZP:0002543 neural rod morphology, abnormal ZP:0002544 neural rod increased thickness, abnormal ZP:0002545 neural rod increased width, abnormal ZP:0002546 cilium pronephric duct disorganized, abnormal ZP:0002547 cilium pronephric duct decreased functionality, abnormal ZP:0002548 multi-ciliated epithelial cell pronephric duct disorganized, abnormal ZP:0002549 ciliated cell pronephros decreased amount, abnormal ZP:0002550 somite flat, abnormal ZP:0002551 motor neuron facial nerve motor nucleus mislocalised, abnormal ZP:0002552 gall bladder mislocalised laterally, abnormal ZP:0002553 gall bladder left side of whole organism, abnormal ZP:0002554 paraxial mesoderm decreased length, abnormal ZP:0002555 paraxial mesoderm increased width, abnormal ZP:0002556 cloacal chamber malformed, abnormal ZP:0002557 ciliated cell cloacal chamber decreased amount, abnormal ZP:0002558 rhombomere 5 lacks all parts of type branchiomotor neuron, abnormal ZP:0002559 rhombomere 7 lacks all parts of type branchiomotor neuron, abnormal ZP:0002560 branchiomotor neuron rhombomere 4 mislocalised, abnormal ZP:0002561 presumptive pronephric mesoderm mislocalised laterally, abnormal ZP:0002562 whole organism increased curvature, abnormal ZP:0002563 head hydrocephalic, abnormal ZP:0002564 trunk increased curvature, abnormal ZP:0002565 somite trunk morphology, abnormal ZP:0002566 post-vent region vacuolated, abnormal ZP:0002567 post-vent region clavate, abnormal ZP:0002568 somite post-vent region morphology, abnormal ZP:0002569 neural tube increased thickness, abnormal ZP:0002570 neural tube increased width, abnormal ZP:0002571 cell projection branchiomotor neuron lateral orientation, abnormal ZP:0002573 ciliated cell increased angle to mitotic spindle apical-basal axis relative to substrate pronephros, abnormal ZP:0002574 neuroepithelial cell mislocalised, abnormal ZP:0002575 heart centered, abnormal ZP:0002576 pronephric duct detached from cell pronephric glomerular basement membrane pronephros, abnormal ZP:0002577 cell proliferation in forebrain decreased occurrence, abnormal ZP:0002578 anterior region hindbrain truncated, abnormal ZP:0002579 neuronal cell body cranial nerve V position, abnormal ZP:0002580 motor neuron cranial nerve V disorganized, abnormal ZP:0002581 rhombomere 2 apoptotic, abnormal ZP:0002582 rhombomere 5 apoptotic, abnormal ZP:0002583 rhombomere 3 decreased width, abnormal ZP:0002584 rhombomere 3 apoptotic, abnormal ZP:0002585 rhombomere 4 apoptotic, abnormal ZP:0002586 caudal tuberculum has fewer parts of type dopaminergic neuron, abnormal ZP:0002587 trunk decreased size, abnormal ZP:0002588 larval locomotory behavior process quality, abnormal ZP:0002589 whole organism unbalanced, abnormal ZP:0002590 whole organism decreased behavioural activity, abnormal ZP:0002591 exit from mitosis disrupted, abnormal ZP:0002592 establishment or maintenance of apical/basal cell polarity disrupted, abnormal ZP:0002593 motor neuron precursor migration involved in dorsal motor nucleus of vagus nerve formation disrupted, abnormal ZP:0002594 apical junction assembly disrupted, abnormal ZP:0002595 lens perforate, abnormal ZP:0002596 retinal neural layer positional polarity, abnormal ZP:0002597 apical junction complex retinal neural layer mislocalised, abnormal ZP:0002598 proliferative region eye increased size, abnormal ZP:0002599 proliferative region eye mislocalised, abnormal ZP:0002600 fourth ventricle decreased volume, abnormal ZP:0002601 heart immature, abnormal ZP:0002602 retinal pigmented epithelium perforate, abnormal ZP:0002603 retina immature, abnormal ZP:0002604 cardiac muscle cell heart tube size, abnormal ZP:0002605 cardiac muscle cell heart tube structure, abnormal ZP:0002606 post-vent region curled, abnormal ZP:0002607 neuron optic cup decreased amount, abnormal ZP:0002608 retinal inner plexiform layer patchy, abnormal ZP:0002609 retinal outer plexiform layer patchy, abnormal ZP:0002610 pericardial cavity increased size, abnormal ZP:0002611 vagal ganglion fused with vagal ganglion, abnormal ZP:0002612 neuroepithelial cell positional polarity, abnormal ZP:0002613 apical junction complex cardiac muscle cell structure, abnormal ZP:0002614 axonal defasciculation process quality, abnormal ZP:0002615 learning or memory process quality, abnormal ZP:0002616 locomotory behavior increased rate, abnormal ZP:0002617 long-term synaptic potentiation decreased magnitude, abnormal ZP:0002618 innervation decreased occurrence, abnormal ZP:0002619 brain disorganized, abnormal ZP:0002620 ventral region diencephalon morphology, abnormal ZP:0002621 fourth ventricle morphology, abnormal ZP:0002622 trigeminal ganglion has fewer parts of type sensory neuron, abnormal ZP:0002623 axon terminus trigeminal ganglion increased amount, abnormal ZP:0002624 ventral telencephalon morphology, abnormal ZP:0002625 lateral longitudinal fasciculus decreased length, abnormal ZP:0002626 axon lateral longitudinal fasciculus defasciculated, abnormal ZP:0002627 cranial nerve position, abnormal ZP:0002628 whole organism increased behavioural activity, abnormal ZP:0002629 anterior-most region head truncated, abnormal ZP:0002630 anterior-most region head flattened, abnormal ZP:0002631 Meckel's cartilage increased width, abnormal ZP:0002632 Meckel's cartilage increased angle to anterior-posterior axis whole organism, abnormal ZP:0002633 forebrain ventricle morphology, abnormal ZP:0002634 ceratohyal cartilage increased angle to basihyal cartilage, abnormal ZP:0002635 axon Rohon-Beard neuron increased branchiness, abnormal ZP:0002636 axon terminus Rohon-Beard neuron increased amount, abnormal ZP:0002637 bone mineralization delayed, abnormal ZP:0002638 posterior lateral line neuromast primordium migration decreased rate, abnormal ZP:0002639 posterior lateral line primordium decreased speed, abnormal ZP:0002640 posterior lateral line primordium mislocalised, abnormal ZP:0002641 cardioblast migration decreased process quality, abnormal ZP:0002642 cell myocardium malformed, abnormal ZP:0002643 midbrain hindbrain boundary structure, abnormal ZP:0002644 forebrain structure, abnormal ZP:0002645 intersegmental vein malformed, abnormal ZP:0002646 posterior caudal vein malformed, abnormal ZP:0002647 dorsal longitudinal anastomotic vessel malformed, abnormal ZP:0002648 alkaline phosphatase activity decreased occurrence, abnormal ZP:0002649 post-vent region curvature, abnormal ZP:0002650 pronephric tubule increased distance plasma membrane plasma membrane pronephric tubule, abnormal ZP:0002651 microvillus pronephric tubule decreased amount, abnormal ZP:0002652 epithelium pronephric tubule structure, abnormal ZP:0002653 brush border epithelial cell pronephric tubule disorganized, abnormal ZP:0002654 gut epithelium structure, abnormal ZP:0002655 gut epithelium increased distance plasma membrane plasma membrane gut epithelium, abnormal ZP:0002656 podocyte morphology, abnormal ZP:0002657 heart jogging decreased process quality, abnormal ZP:0002658 atrioventricular valve formation decreased process quality, abnormal ZP:0002659 cell migration in hindbrain disrupted, abnormal ZP:0002660 endocardial cell differentiation decreased process quality, abnormal ZP:0002661 heart rudiment mislocalised, abnormal ZP:0002662 heart rudiment bilateral symmetry, abnormal ZP:0002663 heart rudiment rotated, abnormal ZP:0002664 caudal fin decreased size, abnormal ZP:0002665 lateral mesoderm mislocalised, abnormal ZP:0002666 epithelium neural tube duplicated, abnormal ZP:0002667 endocardium atrioventricular canal decreased length, abnormal ZP:0002669 cardiac jelly decreased volume, abnormal ZP:0002670 endothelial cell atrioventricular canal endocardium scaly, abnormal ZP:0002671 neurosecretory neuron diencephalon mislocalised, abnormal ZP:0002672 preoptic area morphology, abnormal ZP:0002673 neuroendocrine cell decreased amount, abnormal ZP:0002674 notochord degenerate, abnormal ZP:0002675 notochord condensed, abnormal ZP:0002676 yolk morphology, abnormal ZP:0002677 melanosome post-vent region absent, abnormal ZP:0002678 regulation of cell population proliferation disrupted, abnormal ZP:0002679 maintenance of DNA repeat elements disrupted, abnormal ZP:0002680 whole organism neoplastic, abnormal ZP:0002682 pharyngeal arch cartilage malformed, abnormal ZP:0002683 chondrocranium cartilage malformed, abnormal ZP:0002684 ceratobranchial cartilage curved, abnormal ZP:0002685 ceratobranchial cartilage shortened, abnormal ZP:0002686 S phase delayed, abnormal ZP:0002687 retinal bipolar neuron differentiation disrupted, abnormal ZP:0002688 embryonic retina morphogenesis in camera-type eye delayed, abnormal ZP:0002689 camera-type eye photoreceptor cell differentiation disrupted, abnormal ZP:0002690 regulation of neural retina development disrupted, abnormal ZP:0002691 retinal inner nuclear layer unstructured, abnormal ZP:0002692 cell retinal inner nuclear layer undifferentiated, abnormal ZP:0002693 retinal outer nuclear layer unstructured, abnormal ZP:0002694 cell retinal outer nuclear layer undifferentiated, abnormal ZP:0002695 amacrine cell absent, abnormal ZP:0002696 retinal cone cell absent, abnormal ZP:0002697 retinal rod cell decreased amount, abnormal ZP:0002698 retinal bipolar neuron absent, abnormal ZP:0002699 digestive system development disrupted, abnormal ZP:0002700 liver absent, abnormal ZP:0002701 exocrine pancreas decreased size, abnormal ZP:0002702 endoplasmic reticulum chondrocyte morphology, abnormal ZP:0002703 larval locomotory behavior arrested, abnormal ZP:0002704 larval locomotory behavior disrupted, abnormal ZP:0002705 muscle attachment decreased occurrence, abnormal ZP:0002706 skeletal muscle organ development process quality, abnormal ZP:0002707 heart structure, abnormal ZP:0002708 basibranchial structure, abnormal ZP:0002709 basibranchial mislocalised ventrally, abnormal ZP:0002710 basihyal bone decreased length, abnormal ZP:0002711 basihyal bone mislocalised ventrally, abnormal ZP:0002712 trunk musculature structure, abnormal ZP:0002713 trunk musculature disorganized, abnormal ZP:0002714 ceratobranchial bone structure, abnormal ZP:0002715 ceratobranchial bone mislocalised ventrally, abnormal ZP:0002716 vertical myoseptum malformed, abnormal ZP:0002717 myotome malformed, abnormal ZP:0002718 Meckel's cartilage displaced, abnormal ZP:0002719 intercalated disc myocardium disorganized, abnormal ZP:0002720 ceratohyal cartilage mislocalised ventrally, abnormal ZP:0002721 myofibril skeletal muscle cell disorganized, abnormal ZP:0002722 sarcomere skeletal muscle cell structure, abnormal ZP:0002723 actin filament slow muscle cell disorganized, abnormal ZP:0002724 myosin filament slow muscle cell disorganized, abnormal ZP:0002725 myofibril cardiac muscle cell absent, abnormal ZP:0002726 caudal commissure defasciculated, abnormal ZP:0002727 diencephalic white matter split, abnormal ZP:0002728 diencephalic white matter decreased amount, abnormal ZP:0002729 blood vessel remodeling decreased occurrence, abnormal ZP:0002730 ball edematous, abnormal ZP:0002731 caudal division of the internal carotid artery increased size, abnormal ZP:0002732 primordial hindbrain channel increased size, abnormal ZP:0002733 blood vasculature quality, abnormal ZP:0002734 cranial vasculature malformed, abnormal ZP:0002735 basal communicating artery increased size, abnormal ZP:0002736 basal communicating artery attached to primordial midbrain channel, abnormal ZP:0002737 blood vessel endothelial cell basal communicating artery increased amount, abnormal ZP:0002739 endothelial cell basal communicating artery decreased amount, abnormal ZP:0002740 posterior communicating artery increased size, abnormal ZP:0002741 blood vessel endothelial cell posterior communicating artery increased amount, abnormal ZP:0002743 basilar artery increased size, abnormal ZP:0002744 basilar artery attached to primordial hindbrain channel, abnormal ZP:0002745 central artery atretic, abnormal ZP:0002746 cranial blood vessel dilated, abnormal ZP:0002747 endothelial cell increased amount, abnormal ZP:0002748 thymus development disrupted, abnormal ZP:0002749 brain vasculature fragile, abnormal ZP:0002750 cranial vasculature fragile, abnormal ZP:0002751 cranial vasculature hemorrhagic, abnormal ZP:0002752 basihyal bone aplastic, abnormal ZP:0002753 mandibular arch skeleton duplicated, abnormal ZP:0002754 pharyngeal arch 2 skeleton aplastic, abnormal ZP:0002755 ceratobranchial 1 cartilage malformed, abnormal ZP:0002756 pharyngeal arch 2 physical object quality, abnormal ZP:0002757 myeloid cell decreased amount, abnormal ZP:0002758 multicellular organism development disrupted, abnormal ZP:0002759 nervous system development disrupted, abnormal ZP:0002760 neural tube development disrupted, abnormal ZP:0002761 brain structure, abnormal ZP:0002762 anterior-posterior axis brain decreased size, abnormal ZP:0002763 neuron hindbrain decreased amount, abnormal ZP:0002764 cerebellum morphology, abnormal ZP:0002765 diencephalon morphology, abnormal ZP:0002766 diencephalon lacks all parts of type third ventricle, abnormal ZP:0002767 somite decreased thickness, abnormal ZP:0002768 somite elongated, abnormal ZP:0002769 somite flattened, abnormal ZP:0002770 tegmentum morphology, abnormal ZP:0002771 neuron trigeminal ganglion decreased amount, abnormal ZP:0002772 axon brainstem and spinal white matter decreased amount, abnormal ZP:0002773 medial longitudinal fasciculus decreased thickness, abnormal ZP:0002774 head flattened, abnormal ZP:0002775 neural tube unlumenized, abnormal ZP:0002776 hindbrain interneuron decreased amount, abnormal ZP:0002777 dorsal longitudinal fasciculus decreased thickness, abnormal ZP:0002778 neuron dorso-rostral cluster decreased amount, abnormal ZP:0002779 axon CaP motoneuron decreased amount, abnormal ZP:0002780 primary motor neuron decreased amount, abnormal ZP:0002781 neuroepithelial cell decreased amount, abnormal ZP:0002782 ribosomal small subunit assembly disrupted, abnormal ZP:0002783 ribosome biogenesis disrupted, abnormal ZP:0002784 intestinal bulb decreased size, abnormal ZP:0002785 epithelial cell intestine cuboid, abnormal ZP:0002786 intestinal epithelium shape, abnormal ZP:0002787 intestinal epithelium decreased size, abnormal ZP:0002788 intestinal epithelium decreased thickness, abnormal ZP:0002789 autolysosome intestinal epithelium increased amount, abnormal ZP:0002790 intestinal villus sparse, abnormal ZP:0002791 apical-basal axis relative to substrate intestinal bulb epithelium decreased length, abnormal ZP:0002792 neural crest cell migration process quality, abnormal ZP:0002793 motor neuron axon guidance process quality, abnormal ZP:0002794 spinal cord motor neuron differentiation process quality, abnormal ZP:0002795 axon MiP motor neuron absent, abnormal ZP:0002796 neural crest cell lacks parts or has fewer parts of type filopodium neural crest cell, abnormal ZP:0002797 bone mineralization disrupted, abnormal ZP:0002798 ceratobranchial 5 tooth absent, abnormal ZP:0002799 ceratobranchial 5 tooth decreased size, abnormal ZP:0002800 ceratohyal cartilage flattened, abnormal ZP:0002801 cranial cartilage absent, abnormal ZP:0002802 mitotic cell cycle disrupted, abnormal ZP:0002803 intramembranous ossification postdisplaced growth, abnormal ZP:0002804 endochondral ossification predisplaced growth, abnormal ZP:0002805 thigmotaxis arrested, abnormal ZP:0002806 renal system process decreased process quality, abnormal ZP:0002807 adult locomotory behavior behavioral quality of a process, abnormal ZP:0002808 magnesium ion homeostasis decreased process quality, abnormal ZP:0002809 swimming behavior duration, abnormal ZP:0002810 swimming behavior decreased process quality, abnormal ZP:0002811 growth decreased magnitude, abnormal ZP:0002812 melanin biosynthetic process delayed, abnormal ZP:0002813 melanin biosynthetic process disrupted, abnormal ZP:0002814 epithelial cell proliferation decreased occurrence, abnormal ZP:0002815 calcium ion homeostasis decreased process quality, abnormal ZP:0002816 centrum composition, abnormal ZP:0002817 pronephric duct obstructed, abnormal ZP:0002818 urostyle composition, abnormal ZP:0002819 metapterygoid ossified, abnormal ZP:0002820 maxilla composition, abnormal ZP:0002821 basihyal bone ossified, abnormal ZP:0002822 caudal vertebra condensed, abnormal ZP:0002823 hypural composition, abnormal ZP:0002824 integument decreased pigmentation, abnormal ZP:0002826 skeletal system quality, abnormal ZP:0002827 frontal bone composition, abnormal ZP:0002828 hemal arch composition, abnormal ZP:0002829 kidney calcified, abnormal ZP:0002830 kidney decreased functionality, abnormal ZP:0002831 parasphenoid composition, abnormal ZP:0002832 premaxilla composition, abnormal ZP:0002833 ceratohyal bone ossified, abnormal ZP:0002834 quadrate ossified, abnormal ZP:0002835 epihyal ossified, abnormal ZP:0002836 ectopterygoid composition, abnormal ZP:0002837 entopterygoid composition, abnormal ZP:0002838 epural composition, abnormal ZP:0002839 hyomandibula ossified, abnormal ZP:0002840 symplectic ossified, abnormal ZP:0002841 neural arch composition, abnormal ZP:0002842 trunk lacks all parts of type melanocyte, abnormal ZP:0002843 Weberian apparatus malformed, abnormal ZP:0002844 Weberian apparatus condensed, abnormal ZP:0002845 Weberian vertebra condensed, abnormal ZP:0002846 corpuscles of Stannius physical object quality, abnormal ZP:0002847 ceratobranchial 1 bone ossified, abnormal ZP:0002848 ceratobranchial 4 bone ossified, abnormal ZP:0002849 ceratobranchial 3 bone ossified, abnormal ZP:0002850 ceratobranchial 2 bone ossified, abnormal ZP:0002851 exocrine pancreas hypoplastic, abnormal ZP:0002852 renal tubule calcified, abnormal ZP:0002853 parapophysis/rib malformed, abnormal ZP:0002854 caudal fin lepidotrichium composition, abnormal ZP:0002855 vertebral column kinked, abnormal ZP:0002856 epithelial cell of pancreas decreased area, abnormal ZP:0002857 melanocyte intensity, abnormal ZP:0002858 melanocyte low saturation, abnormal ZP:0002859 melanocyte colorless, abnormal ZP:0002860 melanocyte decreased size, abnormal ZP:0002861 melanocyte necrotic, abnormal ZP:0002862 melanocyte decreased pigmentation, abnormal ZP:0002863 melanocyte disrupted regulation of membrane potential, abnormal ZP:0002864 melanosome melanocyte malformed, abnormal ZP:0002865 melanosome melanocyte aggregated, abnormal ZP:0002866 melanoblast decreased pigmentation, abnormal ZP:0002867 acinar cell decreased size, abnormal ZP:0002868 mitotic prometaphase arrested, abnormal ZP:0002869 mitotic centrosome separation disrupted, abnormal ZP:0002870 chromosome condensation increased occurrence, abnormal ZP:0002871 mitotic cell cycle, embryonic disrupted, abnormal ZP:0002872 mitotic sister chromatid separation disrupted, abnormal ZP:0002873 mitotic spindle assembly disrupted, abnormal ZP:0002874 median fin fold apoptotic, abnormal ZP:0002875 tail bud apoptotic, abnormal ZP:0002876 integument fragile, abnormal ZP:0002877 head deformed, abnormal ZP:0002878 centrosome cell position, abnormal ZP:0002879 centrosome cell variability of size, abnormal ZP:0002880 mitotic spindle cell disorganized, abnormal ZP:0002881 neuron decreased amount, abnormal ZP:0002882 intestinal villus absent, abnormal ZP:0002883 heart congested, abnormal ZP:0002884 detection of light stimulus involved in visual perception decreased process quality, abnormal ZP:0002885 retina decreased functionality, abnormal ZP:0002886 swim bladder development disrupted, abnormal ZP:0002887 liver shape, abnormal ZP:0002888 liver primordium decreased size, abnormal ZP:0002889 blastema quality, abnormal ZP:0002890 determination of left/right asymmetry in lateral mesoderm process quality, abnormal ZP:0002891 regulation of fibroblast growth factor receptor signaling pathway process quality, abnormal ZP:0002893 apical protein localization disrupted, abnormal ZP:0002894 epithelial cilium movement involved in determination of left/right asymmetry process quality, abnormal ZP:0002895 cell migration involved in heart development disrupted, abnormal ZP:0002896 Kupffer's vesicle development process quality, abnormal ZP:0002897 basement membrane organization disrupted, abnormal ZP:0002898 Kupffer's vesicle malformed, abnormal ZP:0002899 Kupffer's vesicle physical object quality, abnormal ZP:0002901 forerunner cell group decreased size, abnormal ZP:0002902 forerunner cell group physical object quality, abnormal ZP:0002903 extension morphology, abnormal ZP:0002904 heart symmetry, abnormal ZP:0002905 lateral plate mesoderm symmetry, abnormal ZP:0002906 post-vent region distended, abnormal ZP:0002907 regulation of mitotic cell cycle, embryonic disrupted, abnormal ZP:0002908 hypoblast apoptotic, abnormal ZP:0002909 whole organism dwarf-like, abnormal ZP:0002910 anatomical surface whole organism decreased area, abnormal ZP:0002911 adherens junction organization process quality, abnormal ZP:0002912 blood vessel lumenization process quality, abnormal ZP:0002913 intersegmental vessel unlumenized, abnormal ZP:0002914 adherens junction blood vessel endothelial cell physical object quality, abnormal ZP:0002915 whole organism atrophied, abnormal ZP:0002916 ceratohyal cartilage bent, abnormal ZP:0002917 musculature system quality, abnormal ZP:0002918 muscle degenerate, abnormal ZP:0002919 exocrine pancreas development disrupted, abnormal ZP:0002920 intestine hypoplastic, abnormal ZP:0002921 gut epithelium morphology, abnormal ZP:0002922 epithelial cilium movement involved in extracellular fluid movement decreased rate, abnormal ZP:0002923 determination of left/right symmetry process quality, abnormal ZP:0002925 heart bilateral symmetry, abnormal ZP:0002926 lateral plate mesoderm bilateral symmetry, abnormal ZP:0002927 pronephric duct increased diameter, abnormal ZP:0002928 cilium pronephric duct decreased length, abnormal ZP:0002929 cilium pronephric duct decreased amount, abnormal ZP:0002930 trunk increased width, abnormal ZP:0002931 pronephric tubule cystic, abnormal ZP:0002932 pharyngeal arch 3-7 decreased length, abnormal ZP:0002933 extension constricted, abnormal ZP:0002934 neurocranium shape, abnormal ZP:0002935 muscle attachment disrupted, abnormal ZP:0002936 muscle attachment decreased process quality, abnormal ZP:0002937 locomotion involved in locomotory behavior decreased rate, abnormal ZP:0002938 locomotion involved in locomotory behavior disrupted, abnormal ZP:0002939 T-tubule organization process quality, abnormal ZP:0002940 receptor clustering disrupted, abnormal ZP:0002941 camera-type eye morphogenesis process quality, abnormal ZP:0002942 dorsal aorta separated from intersegmental vessel dorsal longitudinal anastomotic vessel, abnormal ZP:0002943 lens malformed, abnormal ZP:0002944 swim bladder absent, abnormal ZP:0002945 myoseptum somite deformed, abnormal ZP:0002946 intersegmental vessel somite absent, abnormal ZP:0002947 intersegmental vessel somite disorganized, abnormal ZP:0002948 granular layer corpus cerebelli disorganized, abnormal ZP:0002949 skeletal muscle cell trunk musculature retracted, abnormal ZP:0002950 vertical myoseptum increased width, abnormal ZP:0002951 vertical myoseptum deformed, abnormal ZP:0002952 vertical myoseptum U-shaped, abnormal ZP:0002953 basement membrane vertical myoseptum irregular spatial pattern, abnormal ZP:0002954 cornea absent, abnormal ZP:0002955 basement membrane myotome malformed, abnormal ZP:0002956 muscle tendon junction myotome malformed, abnormal ZP:0002957 muscle tendon junction myotome disorganized, abnormal ZP:0002958 muscle tendon junction myotome U-shaped, abnormal ZP:0002959 myotome detached from muscle cell muscle tendon junction myotome, abnormal ZP:0002960 caudal fin kinked, abnormal ZP:0002961 myoseptum broken, abnormal ZP:0002962 whole organism decreased speed, abnormal ZP:0002963 whole organism dystrophic, abnormal ZP:0002964 muscle cell post-vent region morphology, abnormal ZP:0002965 skeletal muscle cell post-vent region retracted, abnormal ZP:0002966 muscle necrotic, abnormal ZP:0002967 sarcoplasmic reticulum muscle unstructured, abnormal ZP:0002968 sarcomere muscle morphology, abnormal ZP:0002969 sarcomere muscle decreased amount, abnormal ZP:0002970 skeletal muscle dystrophic, abnormal ZP:0002971 muscle cell detached from vertical myoseptum, abnormal ZP:0002972 muscle cell detached from muscle cell, abnormal ZP:0002973 skeletal muscle cell detached from vertical myoseptum, abnormal ZP:0002974 terminal cisterna skeletal muscle cell malformed, abnormal ZP:0002975 T-tubule skeletal muscle cell malformed, abnormal ZP:0002976 skeletal muscle cell separated from sarcolemma sarcolemma skeletal muscle cell, abnormal ZP:0002977 feeding behavior increased process quality, abnormal ZP:0002978 whole organism increased length, abnormal ZP:0002979 determination of left/right asymmetry in lateral mesoderm decreased process quality, abnormal ZP:0002980 optokinetic behavior decreased rate, abnormal ZP:0002981 protein localization disrupted, abnormal ZP:0002982 determination of pancreatic left/right asymmetry decreased process quality, abnormal ZP:0002984 lateral mesoderm morphogenesis decreased process quality, abnormal ZP:0002985 detection of light stimulus involved in visual perception arrested, abnormal ZP:0002986 notochord cell development decreased process quality, abnormal ZP:0002987 epithelial cilium movement involved in determination of left/right asymmetry decreased process quality, abnormal ZP:0002988 muscle tissue development disrupted, abnormal ZP:0002989 Kupffer's vesicle development decreased process quality, abnormal ZP:0002990 basement membrane assembly decreased process quality, abnormal ZP:0002991 determination of digestive tract left/right asymmetry decreased process quality, abnormal ZP:0002992 determination of liver left/right asymmetry decreased process quality, abnormal ZP:0002994 retinal ganglion cell layer dispersed, abnormal ZP:0002995 hypochord morphology, abnormal ZP:0002996 lens mislocalised, abnormal ZP:0002997 lens degenerate, abnormal ZP:0002998 lens hypoplastic, abnormal ZP:0002999 lens disorganized, abnormal ZP:0003000 lens displaced, abnormal ZP:0003001 midbrain hindbrain boundary shape, abnormal ZP:0003002 eye shape, abnormal ZP:0003003 eye mislocalised ventrally, abnormal ZP:0003004 lateral plate mesoderm mislocalised, abnormal ZP:0003005 lateral plate mesoderm disorganized, abnormal ZP:0003006 laminin complex lateral plate mesoderm decreased amount, abnormal ZP:0003007 liver bilateral symmetry, abnormal ZP:0003008 liver primordium bilateral symmetry, abnormal ZP:0003009 notochord hypotrophic, abnormal ZP:0003010 notochord decreased thickness, abnormal ZP:0003011 notochord cellular quality, abnormal ZP:0003012 notochord moderately well differentiated, abnormal ZP:0003013 vacuole notochord decreased size, abnormal ZP:0003014 vacuole notochord decreased amount, abnormal ZP:0003015 pancreas bilateral symmetry, abnormal ZP:0003016 endocrine cell pancreas mislocalised, abnormal ZP:0003017 laminin complex somite decreased amount, abnormal ZP:0003018 pancreas primordium bilateral symmetry, abnormal ZP:0003019 cranial nerve II morphology, abnormal ZP:0003020 myotome decreased thickness, abnormal ZP:0003021 myotome U-shaped, abnormal ZP:0003022 post-vent region shortened, abnormal ZP:0003023 laminin complex neural tube decreased amount, abnormal ZP:0003024 forebrain midbrain boundary increased width, abnormal ZP:0003025 intestinal bulb primordium bilateral symmetry, abnormal ZP:0003026 myosin filament fast muscle cell disorganized, abnormal ZP:0003027 retinal ganglion cell ipsilateral to axon eye, abnormal ZP:0003028 fast muscle myoblast decreased length, abnormal ZP:0003029 actin filament organization disrupted, abnormal ZP:0003030 spermatogenesis disrupted, abnormal ZP:0003031 muscle organ morphogenesis delayed, abnormal ZP:0003032 extension quality, abnormal ZP:0003033 notochord structure, cavities, abnormal ZP:0003034 notochord lacks parts or has fewer parts of type rough endoplasmic reticulum cell, abnormal ZP:0003035 collagen type IV trimer notochord absent, abnormal ZP:0003036 muscle pioneer somite absent, abnormal ZP:0003037 testis structure, abnormal ZP:0003038 head swollen, abnormal ZP:0003039 axon Mauthner neuron mislocalised medially, abnormal ZP:0003040 basal part of cell neuroepithelial cell increased width, abnormal ZP:0003041 pharyngeal arch shape, abnormal ZP:0003042 epithelial cilium movement involved in extracellular fluid movement arrested, abnormal ZP:0003043 outer dynein arm assembly decreased occurrence, abnormal ZP:0003044 inner dynein arm assembly decreased occurrence, abnormal ZP:0003045 intestinal epithelial cell differentiation disrupted, abnormal ZP:0003046 brain increased occurrence cellular response to DNA damage stimulus, abnormal ZP:0003047 cardiac ventricle hypertrophic, abnormal ZP:0003048 cardiac ventricle hyperplastic, abnormal ZP:0003049 pronephric duct has fewer parts of type motile cilium inner dynein arm pronephric duct, abnormal ZP:0003050 pronephric duct has fewer parts of type motile cilium outer dynein arm pronephric duct, abnormal ZP:0003051 motile cilium posterior pronephric duct immobile, abnormal ZP:0003052 sarcomere cardiac muscle cell increased amount, abnormal ZP:0003053 muscle contraction disrupted, abnormal ZP:0003054 visceral muscle development disrupted, abnormal ZP:0003055 regulation of blood pressure disrupted, abnormal ZP:0003056 larval locomotory behavior absent, abnormal ZP:0003057 skeletal myofibril assembly disrupted, abnormal ZP:0003058 growth decreased occurrence, abnormal ZP:0003059 peripheral nervous system neuron axonogenesis increased rate, abnormal ZP:0003060 cardiac myofibril assembly disrupted, abnormal ZP:0003061 ventricular cardiac myofibril assembly disrupted, abnormal ZP:0003062 heart contraction amplitude, abnormal ZP:0003063 cardiac ventricle contractility, abnormal ZP:0003064 heart decreased strength, abnormal ZP:0003065 somite grey, abnormal ZP:0003066 atrium contractility, abnormal ZP:0003067 skeletal muscle quality, abnormal ZP:0003068 sensory neuron morphology, abnormal ZP:0003069 sensory neuron mislocalised, abnormal ZP:0003070 Z disc skeletal muscle cell disorganized, abnormal ZP:0003071 A band skeletal muscle cell disorganized, abnormal ZP:0003072 Rohon-Beard neuron morphology, abnormal ZP:0003073 cardiac muscle cell decreased thickness, abnormal ZP:0003074 cardiac muscle cell decreased contractility, abnormal ZP:0003075 myofibril cardiac muscle cell decreased size, abnormal ZP:0003076 myofibril cardiac muscle cell decreased amount, abnormal ZP:0003077 Z disc cardiac muscle cell disorganized, abnormal ZP:0003078 A band cardiac muscle cell disorganized, abnormal ZP:0003079 brain development process quality, abnormal ZP:0003080 hatching disrupted, abnormal ZP:0003081 developmental growth delayed, abnormal ZP:0003082 yolk increased volume, abnormal ZP:0003083 extension edematous, abnormal ZP:0003084 neuromast absent, abnormal ZP:0003085 neuromast decreased amount, abnormal ZP:0003086 caudal fin hypoplastic, abnormal ZP:0003087 whole organism apoptotic, abnormal ZP:0003088 Meckel's cartilage stubby, abnormal ZP:0003089 splanchnocranium morphology, abnormal ZP:0003090 palatoquadrate cartilage bent, abnormal ZP:0003091 ceratohyal cartilage orientation basibranchial, abnormal ZP:0003092 ventral region epithelium hypertrophic, abnormal ZP:0003093 ceratobranchial cartilage decreased length, abnormal ZP:0003094 subintestinal vein hypoplastic, abnormal ZP:0003095 subintestinal vein aplastic, abnormal ZP:0003096 muscle esophagus decreased size, abnormal ZP:0003097 gill morphology, abnormal ZP:0003098 sagitta mislocalised, abnormal ZP:0003099 pharyngeal arch morphology, abnormal ZP:0003100 epithelium pneumatic duct morphology, abnormal ZP:0003101 epithelial cell pneumatic duct disoriented, abnormal ZP:0003102 epithelial cell pneumatic duct increased variability of size, abnormal ZP:0003103 epithelial cell pneumatic duct decreased amount, abnormal ZP:0003104 mucus secreting cell esophageal epithelium decreased amount, abnormal ZP:0003105 otic vesicle protrusion absent, abnormal ZP:0003106 joint Meckel's cartilage absent, abnormal ZP:0003107 palatoquadrate cartilage malformed, abnormal ZP:0003109 joint pharyngeal arch 1 absent, abnormal ZP:0003110 mesoderm hypoplastic, abnormal ZP:0003111 notochord hypoplastic, abnormal ZP:0003112 muscle hypoplastic, abnormal ZP:0003113 gastrulation disrupted, abnormal ZP:0003114 Kupffer's vesicle morphology, abnormal ZP:0003115 intermediate cell mass of mesoderm increased size, abnormal ZP:0003117 cytolysis increased occurrence, abnormal ZP:0003118 erythrocyte differentiation arrested, abnormal ZP:0003119 erythrocyte maturation arrested, abnormal ZP:0003120 gall bladder increased size, abnormal ZP:0003121 spleen increased size, abnormal ZP:0003122 nucleate erythrocyte kidney apoptotic, abnormal ZP:0003123 nucleate erythrocyte morphology, abnormal ZP:0003124 nucleate erythrocyte broken, abnormal ZP:0003125 nucleate erythrocyte increased fragility, abnormal ZP:0003126 nucleus nucleate erythrocyte condensed, abnormal ZP:0003127 microtubule nucleate erythrocyte disorganized, abnormal ZP:0003128 plasma membrane nucleate erythrocyte morphology, abnormal ZP:0003129 plasma membrane nucleate erythrocyte pointleted, abnormal ZP:0003130 cell projection membrane nucleate erythrocyte present, abnormal ZP:0003131 telencephalon development disrupted, abnormal ZP:0003132 whole organism hypoplastic, abnormal ZP:0003133 post-vent region structure, abnormal ZP:0003134 axonal defasciculation increased occurrence, abnormal ZP:0003135 motor neuron axon guidance disrupted, abnormal ZP:0003136 branchiomotor neuron axon guidance disrupted, abnormal ZP:0003137 neuron differentiation disrupted, abnormal ZP:0003138 midbrain-hindbrain boundary development disrupted, abnormal ZP:0003139 retinal ganglion cell layer decreased size, abnormal ZP:0003140 retinal ganglion cell layer apoptotic, abnormal ZP:0003141 neuron projection retinal ganglion cell layer mislocalised, abnormal ZP:0003142 neuron spinal cord decreased amount, abnormal ZP:0003143 axon cranial nerve VI decreased length, abnormal ZP:0003144 cranial nerve II decreased size, abnormal ZP:0003145 axon cranial nerve II decreased amount, abnormal ZP:0003146 axon cranial nerve X decreased length, abnormal ZP:0003147 axon cranial nerve IX decreased length, abnormal ZP:0003148 axon cranial nerve V decreased length, abnormal ZP:0003149 axon cranial nerve V defasciculated, abnormal ZP:0003150 pharyngeal pouch morphology, abnormal ZP:0003151 facial ganglion decreased size, abnormal ZP:0003152 trigeminal motor nucleus decreased size, abnormal ZP:0003153 somite border morphology, abnormal ZP:0003154 axon lateral line nerve decreased length, abnormal ZP:0003155 axon Rohon-Beard neuron decreased length, abnormal ZP:0003156 axon Rohon-Beard neuron decreased amount, abnormal ZP:0003158 intestine decreased length, abnormal ZP:0003159 intestine decreased thickness, abnormal ZP:0003161 intestine smooth muscle contraction arrested, abnormal ZP:0003162 peristalsis disrupted, abnormal ZP:0003163 smooth muscle intestine non-contractile, abnormal ZP:0003164 atrium decreased size, abnormal ZP:0003165 intersegmental vessel decreased length, abnormal ZP:0003168 GTPase activity decreased process quality, abnormal ZP:0003170 brain development delayed, abnormal ZP:0003171 camera-type eye development disrupted, abnormal ZP:0003172 lens composition, abnormal ZP:0003173 diencephalon decreased size, abnormal ZP:0003174 somite unstructured, abnormal ZP:0003175 cell proliferation in midbrain decreased rate, abnormal ZP:0003176 midbrain hindbrain boundary physical object quality, abnormal ZP:0003177 neuron midbrain decreased amount, abnormal ZP:0003178 pigment granule maturation disrupted, abnormal ZP:0003179 Kupffer's vesicle has fewer parts of type cilium epithelial cell, abnormal ZP:0003180 melanocyte structure, abnormal ZP:0003182 sprouting angiogenesis disrupted, abnormal ZP:0003183 intersegmental vessel disorganized, abnormal ZP:0003184 dorsal longitudinal anastomotic vessel aplastic, abnormal ZP:0003185 renal system process disrupted, abnormal ZP:0003186 pronephros decreased functionality, abnormal ZP:0003187 neuron spinal cord disorganized, abnormal ZP:0003188 spindle cell structure, abnormal ZP:0003189 response to endoplasmic reticulum stress increased process quality, abnormal ZP:0003190 fin decreased size, abnormal ZP:0003191 liver increased size, abnormal ZP:0003192 liver fatty, abnormal ZP:0003193 postero-ventral region pharyngeal arch 1 decreased size, abnormal ZP:0003194 endoplasmic reticulum hepatocyte dilated, abnormal ZP:0003195 lipid droplet hepatocyte increased amount, abnormal ZP:0003196 glycogen granule hepatocyte decreased amount, abnormal ZP:0003197 locomotion disrupted, abnormal ZP:0003198 regulation of transmission of nerve impulse decreased process quality, abnormal ZP:0003199 cell brain decreased amount, abnormal ZP:0003200 fourth ventricle hydrocephalic, abnormal ZP:0003202 nucleus brain apoptotic, abnormal ZP:0003203 olfactory system apoptotic, abnormal ZP:0003204 forebrain cell migration delayed, abnormal ZP:0003205 neuron differentiation decreased rate, abnormal ZP:0003206 axonogenesis involved in innervation disrupted, abnormal ZP:0003207 forebrain neural keel physical object quality, abnormal ZP:0003208 motor neuron spinal cord truncated, abnormal ZP:0003209 motor neuron spinal cord branchiness, abnormal ZP:0003210 whole organism decreased mobility, abnormal ZP:0003211 hatching delayed, abnormal ZP:0003212 hatching gland development disrupted, abnormal ZP:0003213 hatching gland structure, abnormal ZP:0003214 hatching gland cell mislocalised, abnormal ZP:0003215 secretory granule hatching gland cell morphology, abnormal ZP:0003216 secretory granule hatching gland cell movement quality, abnormal ZP:0003217 cell lacks parts or has fewer parts of type filopodium cell, abnormal ZP:0003218 filamentous actin cell disorganized, abnormal ZP:0003219 cilium or flagellum-dependent cell motility arrested, abnormal ZP:0003220 muscle pioneer decreased amount, abnormal ZP:0003221 otolith morphology, abnormal ZP:0003222 regulation of neurogenesis disrupted, abnormal ZP:0003223 primary neuron increased amount, abnormal ZP:0003224 axon hindbrain decreased length, abnormal ZP:0003225 axon hindbrain disorganized, abnormal ZP:0003226 forebrain decreased width, abnormal ZP:0003227 axon forebrain decreased size, abnormal ZP:0003228 axon forebrain disorganized, abnormal ZP:0003229 midbrain shape, abnormal ZP:0003230 whole organism pigmented, abnormal ZP:0003231 cardiac ventricle deformed, abnormal ZP:0003232 pericardial cavity edematous, abnormal ZP:0003233 midbrain hindbrain boundary quality, abnormal ZP:0003234 glomerular filtration disrupted, abnormal ZP:0003235 mesonephric podocyte structure, abnormal ZP:0003236 rhombomere 4 development disrupted, abnormal ZP:0003237 hindbrain tangential cell migration disrupted, abnormal ZP:0003238 protein localization to nucleus process quality, abnormal ZP:0003239 facial nerve motor nucleus mislocalised anteriorly, abnormal ZP:0003240 nucleus facial nerve motor nucleus physical object quality, abnormal ZP:0003242 protein phosphorylation increased occurrence, abnormal ZP:0003243 non-canonical Wnt signaling pathway disrupted, abnormal ZP:0003244 protein initiator methionine removal decreased occurrence, abnormal ZP:0003245 mesoderm development disrupted, abnormal ZP:0003246 embryonic heart tube morphogenesis process quality, abnormal ZP:0003247 heart valve morphogenesis arrested, abnormal ZP:0003248 cardiac ventricle morphogenesis decreased process quality, abnormal ZP:0003249 cardiac muscle progenitor cell migration to the midline involved in heart field formation decreased process quality, abnormal ZP:0003250 endocardial cushion formation disrupted, abnormal ZP:0003251 cardiocyte differentiation process quality, abnormal ZP:0003252 heart contraction decreased process quality, abnormal ZP:0003253 cardiac ventricle malformed, abnormal ZP:0003254 cardiac ventricle bifurcated, abnormal ZP:0003255 otic vesicle lacks all parts of type otolith, abnormal ZP:0003256 somite obtuse, abnormal ZP:0003257 heart tube mislocalised radially, abnormal ZP:0003258 atrium bifurcated, abnormal ZP:0003259 post-vent region increased accumulation blood, abnormal ZP:0003260 ventricular system decreased volume, abnormal ZP:0003261 atrioventricular canal distended, abnormal ZP:0003262 myocardium split medially, abnormal ZP:0003263 endocardium split medially, abnormal ZP:0003264 cardiac muscle cell atrial myocardium shape, abnormal ZP:0003265 ventricular endocardium physical object quality, abnormal ZP:0003266 ventricular endocardium increased distance ventricular myocardium, abnormal ZP:0003267 muscle attachment process quality, abnormal ZP:0003268 embryonic neurocranium morphogenesis disrupted, abnormal ZP:0003269 cartilage morphogenesis decreased process quality, abnormal ZP:0003270 median fin fold decreased length, abnormal ZP:0003271 median fin fold increased thickness, abnormal ZP:0003272 median fin fold rough, abnormal ZP:0003273 median fin fold deformed, abnormal ZP:0003274 axis increased length, abnormal ZP:0003275 fin degenerate, abnormal ZP:0003276 fin edge shape, abnormal ZP:0003277 pectoral fin bud hypoplastic, abnormal ZP:0003278 dorsal root ganglion hypoplastic, abnormal ZP:0003279 dorsal root ganglion lacks parts or has fewer parts of type neuron, abnormal ZP:0003280 cephalic musculature morphology, abnormal ZP:0003281 ceratohyal bone inverted, abnormal ZP:0003282 ventral transverse aplastic, abnormal ZP:0003283 horizontal myoseptum aplastic, abnormal ZP:0003284 pectoral fin skeleton decreased size, abnormal ZP:0003285 pectoral fin skeleton aplastic, abnormal ZP:0003286 mesenchyme caudal fin hypoplastic, abnormal ZP:0003287 ventral fin fold increased size, abnormal ZP:0003288 ventral fin fold duplicated, abnormal ZP:0003289 myoseptum quality, abnormal ZP:0003290 whole organism lacks all parts of type ceratobranchial 5 tooth, abnormal ZP:0003291 whole organism has fewer parts of type pharyngeal pouch, abnormal ZP:0003292 whole organism lacks all parts of type ceratobranchial 2 cartilage, abnormal ZP:0003293 whole organism lacks all parts of type ceratobranchial 3 cartilage, abnormal ZP:0003294 whole organism lacks all parts of type ceratobranchial 4 cartilage, abnormal ZP:0003295 whole organism lacks all parts of type ceratobranchial 5 cartilage, abnormal ZP:0003296 whole organism lacks parts or has fewer parts of type dermal bone, abnormal ZP:0003297 pharyngeal pouch disorganized, abnormal ZP:0003298 pectoral fin rough, abnormal ZP:0003299 pectoral fin truncated, abnormal ZP:0003300 Meckel's cartilage shortened, abnormal ZP:0003301 lateral line curved, abnormal ZP:0003302 ceratobranchial cartilage malformed, abnormal ZP:0003303 ceratobranchial 2 cartilage absent, abnormal ZP:0003304 ceratobranchial 3 cartilage absent, abnormal ZP:0003305 ceratobranchial 4 cartilage absent, abnormal ZP:0003306 ceratobranchial 5 cartilage absent, abnormal ZP:0003307 neurocranium decreased thickness, abnormal ZP:0003308 neurocranium decreased width, abnormal ZP:0003309 ventral larval melanophore stripe has fewer parts of type melanocyte, abnormal ZP:0003310 lateral larval melanophore stripe lacks all parts of type melanocyte, abnormal ZP:0003311 dorsal longitudinal fasciculus hypoplastic, abnormal ZP:0003312 melanocyte degenerate, abnormal ZP:0003313 slow muscle cell multinucleate, abnormal ZP:0003314 Rohon-Beard neuron absent, abnormal ZP:0003315 Rohon-Beard neuron aplastic, abnormal ZP:0003316 xanthophore desaturated yellow, abnormal ZP:0003317 xanthophore decreased amount, abnormal ZP:0003318 xanthophore decreased pigmentation, abnormal ZP:0003319 iridophore low saturation, abnormal ZP:0003320 iridophore decreased pigmentation, abnormal ZP:0003321 secondary motor neuron morphology, abnormal ZP:0003322 secondary motor neuron defasciculated, abnormal ZP:0003323 swimming behavior process quality, abnormal ZP:0003324 motor neuron spinal cord decreased length, abnormal ZP:0003325 motor neuron spinal cord decreased branchiness, abnormal ZP:0003326 neuromuscular junction motor neuron disorganized, abnormal ZP:0003327 cerebellum development disrupted, abnormal ZP:0003328 cerebellum decreased volume, abnormal ZP:0003329 forebrain decreased volume, abnormal ZP:0003330 axon target recognition disrupted, abnormal ZP:0003331 optic tract disorganized, abnormal ZP:0003332 basement membrane optic tectum deformed, abnormal ZP:0003333 extracellular matrix optic tectum deformed, abnormal ZP:0003334 radial glial cell optic tectum deformed, abnormal ZP:0003335 photoreceptor cell outer segment organization decreased process quality, abnormal ZP:0003336 pronephric duct cystic, abnormal ZP:0003337 retina has fewer parts of type eye photoreceptor cell, abnormal ZP:0003338 photoreceptor outer segment eye photoreceptor cell decreased length, abnormal ZP:0003339 photoreceptor outer segment eye photoreceptor cell disorganized, abnormal ZP:0003340 axoneme eye photoreceptor cell decreased length, abnormal ZP:0003342 photoreceptor outer segment membrane eye photoreceptor cell disorganized, abnormal ZP:0003343 photoreceptor outer segment retinal cone cell decreased length, abnormal ZP:0003344 photoreceptor outer segment retinal cone cell malformed, abnormal ZP:0003345 photoreceptor outer segment retinal rod cell decreased length, abnormal ZP:0003346 photoreceptor outer segment retinal rod cell malformed, abnormal ZP:0003347 caudal vein dilated, abnormal ZP:0003348 caudal vein plexus morphology, abnormal ZP:0003349 blood vasculature broken, abnormal ZP:0003350 axon motor neuron morphology, abnormal ZP:0003351 notochord cell development disrupted, abnormal ZP:0003352 notochord cell vacuolation disrupted, abnormal ZP:0003353 tail bud protruding, abnormal ZP:0003354 actin cytoskeleton epidermis disorganized, abnormal ZP:0003355 cell epidermis size, abnormal ZP:0003356 notochord malformed, abnormal ZP:0003357 basement membrane notochord increased thickness, abnormal ZP:0003358 vacuole notochord circular, abnormal ZP:0003359 caveola notochord decreased mass density, abnormal ZP:0003360 caveola notochord decreased amount, abnormal ZP:0003361 cell notochord circular, abnormal ZP:0003362 cell notochord vacuolated, abnormal ZP:0003363 notochord increased distance cell cell notochord, abnormal ZP:0003364 retinal pigmented epithelium disorganized, abnormal ZP:0003365 pigment granule retinal pigmented epithelium movement quality, abnormal ZP:0003366 caveola somite absent, abnormal ZP:0003367 myofibril somite absent, abnormal ZP:0003368 nervous system decreased size, abnormal ZP:0003369 nervous system vacuolated, abnormal ZP:0003370 caveola nervous system absent, abnormal ZP:0003371 ventricular system structure, abnormal ZP:0003372 cranial vasculature spatial pattern, abnormal ZP:0003373 post-vent vasculature spatial pattern, abnormal ZP:0003374 caveola peridermal cell absent, abnormal ZP:0003375 pigment granule melanocyte movement quality, abnormal ZP:0003376 sarcoplasmic reticulum muscle cell disorganized, abnormal ZP:0003377 myofibril muscle cell disorganized, abnormal ZP:0003378 posterior lateral line neuromast deposition process quality, abnormal ZP:0003379 posterior lateral line neuromast spatial pattern, abnormal ZP:0003380 posterior lateral line primordium shape, abnormal ZP:0003381 posterior lateral line primordium organization quality, abnormal ZP:0003382 animal organ regeneration disrupted, abnormal ZP:0003383 lens necrotic, abnormal ZP:0003384 forebrain atrophied, abnormal ZP:0003385 regenerating tissue liver hypoplastic, abnormal ZP:0003386 midbrain atrophied, abnormal ZP:0003387 retina necrotic, abnormal ZP:0003388 whole organism ploidy, abnormal ZP:0003389 whole organism polyploid, abnormal ZP:0003390 whole organism aneuploid, abnormal ZP:0003391 condensed chromosome whole organism spatial pattern, abnormal ZP:0003392 condensed chromosome whole organism tangled, abnormal ZP:0003393 whole organism attached to nucleus nucleus whole organism, abnormal ZP:0003394 trunk atrophied, abnormal ZP:0003395 spindle post-vent region positional polarity, abnormal ZP:0003396 neural tube apoptotic, abnormal ZP:0003397 ciliary marginal zone poorly differentiated, abnormal ZP:0003398 cell death increased frequency, abnormal ZP:0003399 rRNA catabolic process disrupted, abnormal ZP:0003400 amyloid precursor protein metabolic process disrupted, abnormal ZP:0003401 white matter brain damaged, abnormal ZP:0003402 ventricular zone damaged, abnormal ZP:0003403 astrocyte ventricular zone increased amount, abnormal ZP:0003404 cerebral spinal fluid increased volume, abnormal ZP:0003405 lysosome CNS neuron (sensu Vertebrata) increased size, abnormal ZP:0003406 intersegmental vessel immature, abnormal ZP:0003407 intersegmental vessel lacks all parts of type angiogenic sprout, abnormal ZP:0003408 histone H3-K36 methylation disrupted, abnormal ZP:0003409 bone development disrupted, abnormal ZP:0003410 brain increased size, abnormal ZP:0003411 motor neuron spinal cord sparse, abnormal ZP:0003412 Meckel's cartilage deformed, abnormal ZP:0003413 ceratohyal cartilage deformed, abnormal ZP:0003414 cartilage element malformed, abnormal ZP:0003415 ceratobranchial cartilage deformed, abnormal ZP:0003416 motor neuron branched, abnormal ZP:0003417 motor neuron truncated, abnormal ZP:0003418 leukocyte migration involved in inflammatory response increased occurrence, abnormal ZP:0003419 inflammatory response increased occurrence, abnormal ZP:0003420 cell death increased rate, abnormal ZP:0003421 apoptotic chromosome condensation increased occurrence, abnormal ZP:0003422 neutrophil chemotaxis disrupted, abnormal ZP:0003423 epithelial cell proliferation increased rate, abnormal ZP:0003424 yolk present, abnormal ZP:0003425 neutrophil dorsal fin fold mislocalised, abnormal ZP:0003426 epidermis malformed, abnormal ZP:0003427 hemidesmosome epidermis decreased amount, abnormal ZP:0003428 neutrophil epidermis mislocalised, abnormal ZP:0003429 integument texture, abnormal ZP:0003430 integument rugose, abnormal ZP:0003431 epidermis caudal fin hyperplastic, abnormal ZP:0003432 ventral fin fold malformed, abnormal ZP:0003433 leukocyte ventral fin fold mislocalised, abnormal ZP:0003434 neutrophil ventral fin fold mislocalised, abnormal ZP:0003435 autophagy increased occurrence, abnormal ZP:0003436 musculoskeletal movement, spinal reflex action disrupted, abnormal ZP:0003437 trunk morphology, abnormal ZP:0003438 trunk hypoplastic, abnormal ZP:0003439 skeletal muscle cell morphology, abnormal ZP:0003441 mitochondrion skeletal muscle cell morphology, abnormal ZP:0003446 posterior lateral line development decreased process quality, abnormal ZP:0003447 posterior lateral line neuromast development decreased process quality, abnormal ZP:0003448 posterior lateral line neuromast has fewer parts of type neuromast hair cell, abnormal ZP:0003449 posterior lateral line primordium decreased area, abnormal ZP:0003450 epithelial cell morphogenesis heterochronic, abnormal ZP:0003451 negative regulation of TOR signaling disrupted, abnormal ZP:0003454 anterior region diencephalon disorganized, abnormal ZP:0003457 dorsal region ventral telencephalon increased width, abnormal ZP:0003458 dorsal region ventral telencephalon disorganized, abnormal ZP:0003459 dorsal telencephalon increased size, abnormal ZP:0003460 dorsal telencephalon disorganized, abnormal ZP:0003462 telencephalic white matter composition, abnormal ZP:0003463 telencephalic ventricle morphology, abnormal ZP:0003465 blood vessel increased diameter, abnormal ZP:0003466 CNS neuron (sensu Vertebrata) mislocalised, abnormal ZP:0003467 larval locomotory behavior decreased process quality, abnormal ZP:0003468 collateral sprouting process quality, abnormal ZP:0003469 regulation of actin cytoskeleton reorganization decreased process quality, abnormal ZP:0003470 cardiac ventricle decreased contractility, abnormal ZP:0003471 cardiac muscle cell cardiac ventricle circular, abnormal ZP:0003472 cardiac muscle cell cardiac ventricle decreased size, abnormal ZP:0003473 filamentous actin ventricular myocardium mislocalised, abnormal ZP:0003474 heart rudiment development disrupted, abnormal ZP:0003475 cellular pigmentation decreased occurrence, abnormal ZP:0003476 heart primordium decreased size, abnormal ZP:0003477 heart primordium decreased width, abnormal ZP:0003478 heart primordium lacks parts or has fewer parts of type cardiac muscle cell, abnormal ZP:0003479 bulbus arteriosus malformed, abnormal ZP:0003480 bulbus arteriosus cylindrical, abnormal ZP:0003481 whole organism lacks parts or has fewer parts of type pharyngeal arch, abnormal ZP:0003482 cranial neural crest disrupted neural crest cell development, abnormal ZP:0003483 cranial neural crest cell apoptotic, abnormal ZP:0003484 regulation of transcription elongation from RNA polymerase II promoter process quality, abnormal ZP:0003485 blood morphology, abnormal ZP:0003486 intermediate cell mass of mesoderm physical object quality, abnormal ZP:0003487 median fin fold edge shape, abnormal ZP:0003488 fin erose, abnormal ZP:0003489 trunk musculature morphology, abnormal ZP:0003490 caudal fin has extra parts of type iridophore, abnormal ZP:0003491 post-vent region has extra parts of type ventral larval melanophore stripe iridophore, abnormal ZP:0003492 dorsal larval melanophore stripe has extra parts of type iridophore, abnormal ZP:0003493 yolk larval melanophore stripe has extra parts of type iridophore, abnormal ZP:0003494 median fin shape, abnormal ZP:0003495 median fin decreased area, abnormal ZP:0003496 iridophore irregular spatial pattern, abnormal ZP:0003497 iridophore increased amount, abnormal ZP:0003498 iridophore degree of pigmentation, abnormal ZP:0003499 iridophore displaced to median fin, abnormal ZP:0003500 tRNA transcription disrupted, abnormal ZP:0003501 enteric nervous system complexity, abnormal ZP:0003502 exocrine pancreas quality, abnormal ZP:0003503 pharyngeal arch decreased size, abnormal ZP:0003504 intestine surface feature shape, abnormal ZP:0003505 smooth muscle contractile fiber intestine organization quality, abnormal ZP:0003506 intestinal epithelium flat, abnormal ZP:0003507 intestinal epithelium degenerate, abnormal ZP:0003508 intestinal epithelium positional polarity, abnormal ZP:0003509 intestinal epithelium undifferentiated, abnormal ZP:0003510 intestinal epithelium has fewer parts of type anterior region microvillus epithelial cell, abnormal ZP:0003511 microvillus intestinal epithelium decreased size, abnormal ZP:0003512 epithelial cell intestinal epithelium cuboid, abnormal ZP:0003513 exocrine cell undifferentiated, abnormal ZP:0003515 germ cell migration decreased process quality, abnormal ZP:0003519 primordial germ cell mislocalised medially, abnormal ZP:0003520 regulation of ossification disrupted, abnormal ZP:0003521 pancreas development process quality, abnormal ZP:0003522 retinoic acid catabolic process disrupted, abnormal ZP:0003524 centrum ossified, abnormal ZP:0003525 pancreas increased length, abnormal ZP:0003526 pancreas mislocalised anteriorly, abnormal ZP:0003527 basibranchial malformed, abnormal ZP:0003529 hypural malformed, abnormal ZP:0003530 frontal bone decreased length, abnormal ZP:0003531 frontal bone fused with parietal bone, abnormal ZP:0003532 mouth decreased size, abnormal ZP:0003533 supraorbital bone morphology, abnormal ZP:0003534 rhombomere 5 decreased width, abnormal ZP:0003535 rhombomere 4 increased size, abnormal ZP:0003536 rhombomere 4 decreased size, abnormal ZP:0003538 pectoral fin malformed, abnormal ZP:0003539 cartilage element pectoral fin mislocalised, abnormal ZP:0003540 vertebra malformed, abnormal ZP:0003541 vertebra fused with vertebra, abnormal ZP:0003542 optic cup decreased size, abnormal ZP:0003543 mandibular arch skeleton decreased width, abnormal ZP:0003544 palatoquadrate arch protruding, abnormal ZP:0003545 ventral mandibular arch protruding, abnormal ZP:0003546 ceratohyal cartilage fused with ceratohyal cartilage, abnormal ZP:0003547 ethmoid cartilage malformed, abnormal ZP:0003548 ethmoid cartilage arrow-shaped, abnormal ZP:0003549 hyosymplectic cartilage composition, abnormal ZP:0003550 parachordal cartilage decreased size, abnormal ZP:0003551 parachordal cartilage malformed, abnormal ZP:0003552 pectoral fin endoskeletal disc hyperplastic, abnormal ZP:0003553 trabecula cranii aplastic, abnormal ZP:0003554 basihyal cartilage malformed, abnormal ZP:0003555 bone element malformed, abnormal ZP:0003556 epibranchial ganglion disorganized, abnormal ZP:0003557 neuron epibranchial ganglion decreased amount, abnormal ZP:0003558 vertebral column ossified, abnormal ZP:0003559 neurocranium malformed, abnormal ZP:0003560 pharyngeal arch 3-7 malformed, abnormal ZP:0003561 extracellular matrix inter-frontal joint decreased amount, abnormal ZP:0003562 inter-parietal joint open, abnormal ZP:0003563 extracellular matrix inter-parietal joint decreased amount, abnormal ZP:0003564 frontal-parietal joint closed, abnormal ZP:0003565 extracellular matrix frontal-parietal joint decreased amount, abnormal ZP:0003566 osteoblast star shaped, abnormal ZP:0003567 rough endoplasmic reticulum osteoblast decreased amount, abnormal ZP:0003568 sprouting angiogenesis decreased occurrence, abnormal ZP:0003569 dorsal/ventral axis specification disrupted, abnormal ZP:0003570 notochord development delayed, abnormal ZP:0003571 convergent extension involved in axis elongation delayed, abnormal ZP:0003572 heart contraction decreased occurrence, abnormal ZP:0003573 blood decreased fluid flow, abnormal ZP:0003574 intermediate cell mass of mesoderm distended, abnormal ZP:0003575 forebrain morphology, abnormal ZP:0003576 neural keel apoptotic, abnormal ZP:0003577 pronephric duct fused with medial side medial side pronephric duct, abnormal ZP:0003578 bulbus arteriosus morphology, abnormal ZP:0003579 trunk has fewer parts of type somite, abnormal ZP:0003580 trunk vasculature increased accumulation blood, abnormal ZP:0003581 parachordal vessel morphology, abnormal ZP:0003582 parachordal vessel hypoplastic, abnormal ZP:0003583 post-vent vasculature increased accumulation blood, abnormal ZP:0003585 vasculature increased accumulation blood, abnormal ZP:0003587 spinal cord neural keel apoptotic, abnormal ZP:0003588 ocular blood vessel decreased size, abnormal ZP:0003589 gut endothelial cell morphology, abnormal ZP:0003591 phagolysosome assembly arrested, abnormal ZP:0003594 axial chorda mesoderm decreased size, abnormal ZP:0003598 cell notochord decreased size, abnormal ZP:0003600 head hypotrophic, abnormal ZP:0003601 retinal ganglion cell layer hyperplastic, abnormal ZP:0003602 medial region forebrain aplastic, abnormal ZP:0003603 optic stalk morphology, abnormal ZP:0003604 retinal pigmented epithelium hyperplastic, abnormal ZP:0003605 retina fused with retina, abnormal ZP:0003606 pectoral fin cartilage disorganized, abnormal ZP:0003607 optic primordium fused with optic primordium, abnormal ZP:0003608 whole organism lacks parts or has fewer parts of type pectoral fin, abnormal ZP:0003609 head bulbous, abnormal ZP:0003610 Meckel's cartilage increased thickness, abnormal ZP:0003611 optic fissure present, abnormal ZP:0003612 atrioventricular canal aplastic, abnormal ZP:0003613 ceratohyal cartilage increased thickness, abnormal ZP:0003614 pectoral fin endoskeletal disc hypoplastic, abnormal ZP:0003615 trabecula cranii malformed, abnormal ZP:0003616 pectoral fin fold decreased size, abnormal ZP:0003617 pectoral fin fold variability of size, abnormal ZP:0003618 pars superior ear morphology, abnormal ZP:0003619 optic furrow open, abnormal ZP:0003620 glucose import decreased rate, abnormal ZP:0003621 head opaque, abnormal ZP:0003622 regulation of cholesterol storage disrupted, abnormal ZP:0003623 programmed cell death increased occurrence, abnormal ZP:0003624 actin cytoskeleton organization disrupted, abnormal ZP:0003625 thrombocyte blood island absent, abnormal ZP:0003626 thrombocyte blood island decreased amount, abnormal ZP:0003627 segmental plate increased width, abnormal ZP:0003628 lateral mesoderm increased width, abnormal ZP:0003629 actinotrichium absent, abnormal ZP:0003630 kidney development disrupted, abnormal ZP:0003631 pronephros malformed, abnormal ZP:0003632 mitotic sister chromatid cohesion process quality, abnormal ZP:0003634 cerebellum necrotic, abnormal ZP:0003635 somite structure, abnormal ZP:0003636 caudal fin aplastic, abnormal ZP:0003637 whole organism deformed, abnormal ZP:0003638 spindle cell morphology, abnormal ZP:0003639 heart development quality, abnormal ZP:0003640 dorsal aorta lacks parts or has fewer parts of type blood vessel endothelial cell, abnormal ZP:0003641 heart non-functional, abnormal ZP:0003642 heart tube position, abnormal ZP:0003643 posterior cardinal vein lacks parts or has fewer parts of type blood vessel endothelial cell, abnormal ZP:0003644 cranial vasculature degenerate, abnormal ZP:0003645 intersegmental vessel lacks parts or has fewer parts of type blood vessel endothelial cell, abnormal ZP:0003646 endocardium collapsed, abnormal ZP:0003647 vascular endothelium broken, abnormal ZP:0003648 trunk vasculature hemorrhagic, abnormal ZP:0003649 dorsal longitudinal anastomotic vessel broken, abnormal ZP:0003650 blood vessel endothelial cell decreased amount, abnormal ZP:0003651 erythrocyte differentiation decreased occurrence, abnormal ZP:0003652 polysome whole organism decreased amount, abnormal ZP:0003654 epidermal basal stratum malformed, abnormal ZP:0003655 median fin absent, abnormal ZP:0003656 median fin broken, abnormal ZP:0003657 median fin ruffled, abnormal ZP:0003658 neuromuscular junction development disrupted, abnormal ZP:0003659 skeletal muscle acetylcholine-gated channel clustering disrupted, abnormal ZP:0003660 axon motor neuron truncated, abnormal ZP:0003661 axon motor neuron branchiness, abnormal ZP:0003662 canonical Wnt signaling pathway increased process quality, abnormal ZP:0003663 brain decreased width, abnormal ZP:0003664 neuromere forebrain disheveled, abnormal ZP:0003665 compartment boundary third ventricle inconspicuous, abnormal ZP:0003666 larval development arrested, abnormal ZP:0003667 pre-miRNA processing disrupted, abnormal ZP:0003668 forerunner cell group decreased amount, abnormal ZP:0003669 sarcomerogenesis disrupted, abnormal ZP:0003670 sarcomere cardiac ventricle immature, abnormal ZP:0003671 sarcomere cardiac ventricle decreased amount, abnormal ZP:0003675 intersegmental artery malformed, abnormal ZP:0003677 intersegmental artery decreased process quality branching involved in blood vessel morphogenesis, abnormal ZP:0003678 head hemorrhagic, abnormal ZP:0003680 dorsal longitudinal anastomotic vessel hypoplastic, abnormal ZP:0003682 convergent extension involved in neural plate elongation disrupted, abnormal ZP:0003683 cell cycle process disrupted, abnormal ZP:0003684 polster increased distance notochord, abnormal ZP:0003685 neuronal stem cell spinal cord increased amount, abnormal ZP:0003686 oligodendrocyte spinal cord decreased amount, abnormal ZP:0003687 whole organism increased angle to anterior-most region posterior-most region whole organism, abnormal ZP:0003688 oligodendrocyte decreased amount, abnormal ZP:0003689 cranial nerve X position, abnormal ZP:0003690 axis specification disrupted, abnormal ZP:0003691 oocyte differentiation process quality, abnormal ZP:0003692 oocyte morphogenesis process quality, abnormal ZP:0003693 oocyte animal/vegetal axis specification process quality, abnormal ZP:0003694 blastodisc absent, abnormal ZP:0003695 nucleus oocyte stage II mislocalised, abnormal ZP:0003696 mitochondrion oocyte stage II mislocalised, abnormal ZP:0003697 endoplasmic reticulum oocyte stage II mislocalised, abnormal ZP:0003699 cortical granule oocyte stage II mislocalised, abnormal ZP:0003700 cortical granule oocyte stage III mislocalised, abnormal ZP:0003701 oocyte stage I physical object quality, abnormal ZP:0003702 nucleus oocyte stage I mislocalised, abnormal ZP:0003703 mitochondrion oocyte stage I mislocalised, abnormal ZP:0003704 endoplasmic reticulum oocyte stage I mislocalised, abnormal ZP:0003705 microtubule oocyte stage I mislocalised, abnormal ZP:0003706 mitochondrial cloud oocyte stage I increased size, abnormal ZP:0003707 mitochondrial cloud oocyte stage I mislocalised, abnormal ZP:0003708 unfertilized egg decreased size, abnormal ZP:0003709 unfertilized egg malformed, abnormal ZP:0003710 cytoplasm unfertilized egg mislocalised, abnormal ZP:0003711 chorion unfertilized egg malformed, abnormal ZP:0003712 otolith morphogenesis disrupted, abnormal ZP:0003713 caudal fin upper lobe fused with caudal fin lower lobe, abnormal ZP:0003715 atrial myocardium decreased contractility, abnormal ZP:0003716 ventricular myocardium decreased contractility, abnormal ZP:0003717 actin cytoskeleton EVL disorganized, abnormal ZP:0003718 actin cytoskeleton yolk syncytial layer disorganized, abnormal ZP:0003719 axon trigeminal ganglion decreased amount, abnormal ZP:0003720 axon motor neuron branched, abnormal ZP:0003721 EVL structure, abnormal ZP:0003722 cell EVL shape, abnormal ZP:0003723 lipid phosphatase activity disrupted, abnormal ZP:0003724 phosphatidylinositol dephosphorylation decreased occurrence, abnormal ZP:0003725 semicircular canal formation disrupted, abnormal ZP:0003726 epithelial cell inner ear disorganized, abnormal ZP:0003727 epithelial cell inner ear aggregated, abnormal ZP:0003728 head domed, abnormal ZP:0003729 head mislocalised ventrally, abnormal ZP:0003730 intersegmental vessel shape, abnormal ZP:0003731 locomotory behavior having decreased processual parts skeletal muscle contraction, abnormal ZP:0003732 axon motor neuron decreased length, abnormal ZP:0003733 peripheral neuron branchiness, abnormal ZP:0003734 embryonic heart tube morphogenesis disrupted, abnormal ZP:0003735 cardiac muscle progenitor cell migration to the midline involved in heart field formation delayed, abnormal ZP:0003736 pigmentation arrested, abnormal ZP:0003737 cardiac muscle cell differentiation decreased occurrence, abnormal ZP:0003738 cardiac cell fate specification process quality, abnormal ZP:0003739 heart tube hypoplastic, abnormal ZP:0003740 heart tube aplastic, abnormal ZP:0003741 somite border trunk disorganized, abnormal ZP:0003742 somite border post-vent region disorganized, abnormal ZP:0003743 myocardial precursor decreased amount, abnormal ZP:0003744 pigment cell absent, abnormal ZP:0003745 neural crest cell absent, abnormal ZP:0003746 angiogenesis delayed, abnormal ZP:0003747 sprouting angiogenesis delayed, abnormal ZP:0003748 negative regulation of angiogenesis increased occurrence, abnormal ZP:0003749 intersegmental vessel hypoplastic, abnormal ZP:0003750 caudal vein plexus decreased thickness, abnormal ZP:0003751 caudal vein plexus complexity, abnormal ZP:0003752 endothelial tip cell caudal vein plexus absent, abnormal ZP:0003753 endothelial tip cell caudal vein plexus decreased amount, abnormal ZP:0003754 neutrophil chemotaxis process quality, abnormal ZP:0003756 rhombomere 5 increased width, abnormal ZP:0003757 rhombomere 3 increased width, abnormal ZP:0003758 neutrophil whole organism decreased amount, abnormal ZP:0003760 animal organ development disrupted, abnormal ZP:0003761 mandibular arch skeleton immature, abnormal ZP:0003762 oligodendrocyte development disrupted, abnormal ZP:0003763 ventral spinal cord interneuron differentiation disrupted, abnormal ZP:0003764 cell differentiation in hindbrain disrupted, abnormal ZP:0003765 abducens nucleus development disrupted, abnormal ZP:0003766 oligodendrocyte differentiation disrupted, abnormal ZP:0003767 glioblast (sensu Vertebrata) hindbrain decreased amount, abnormal ZP:0003768 GABAergic neuron spinal cord amount, abnormal ZP:0003769 motor neuron cranial nerve VI decreased amount, abnormal ZP:0003770 spinal cord interneuron cellular quality, abnormal ZP:0003771 Kolmer-Agduhr neuron lateral floor plate cellular quality, abnormal ZP:0003772 motor neuron lacks parts or has fewer parts of type axon motor neuron, abnormal ZP:0003773 posterior-most region pharyngeal arch hypoplastic, abnormal ZP:0003774 DNA replication disrupted, abnormal ZP:0003776 cell cycle disrupted, abnormal ZP:0003777 multicellular organism development arrested, abnormal ZP:0003778 cell death increased process quality, abnormal ZP:0003779 caudal fin curved ventral, abnormal ZP:0003780 cell whole organism polyploid, abnormal ZP:0003781 cell whole organism tetraploid, abnormal ZP:0003782 cell whole organism endopolyploid, abnormal ZP:0003783 head increased process quality cell death, abnormal ZP:0003784 anterior neural tube decreased width, abnormal ZP:0003785 cell increased size, abnormal ZP:0003786 chromosome cell polyploid, abnormal ZP:0003787 chromosome cell undivided, abnormal ZP:0003788 granulocyte decreased amount, abnormal ZP:0003789 macrophage decreased amount, abnormal ZP:0003790 erythroid lineage cell increased variability of size, abnormal ZP:0003791 myeloid lineage restricted progenitor cell increased size, abnormal ZP:0003792 myeloid lineage restricted progenitor cell decreased amount, abnormal ZP:0003793 regulation of cyclin-dependent protein serine/threonine kinase activity decreased process quality, abnormal ZP:0003794 re-entry into mitotic cell cycle increased occurrence, abnormal ZP:0003795 cell proliferation in hindbrain ventricular zone increased occurrence, abnormal ZP:0003796 neuron differentiation increased occurrence, abnormal ZP:0003797 regulation of neural precursor cell proliferation decreased process quality, abnormal ZP:0003798 spinal cord has extra parts of type primary motor neuron, abnormal ZP:0003799 spinal cord has extra parts of type primary interneuron, abnormal ZP:0003800 spinal cord has extra parts of type neuron, abnormal ZP:0003801 proliferative region mislocalised, abnormal ZP:0003802 whole organism opaque, abnormal ZP:0003803 primary neuron proliferative, abnormal ZP:0003804 voltage-gated calcium channel activity disrupted, abnormal ZP:0003805 brain morphogenesis disrupted, abnormal ZP:0003806 optic vesicle malformed, abnormal ZP:0003807 forebrain condensed, abnormal ZP:0003808 neural rod disorganized, abnormal ZP:0003809 neural rod Y-shaped, abnormal ZP:0003810 neural rod collapsed, abnormal ZP:0003811 epithelium ventricular system morphology, abnormal ZP:0003812 neurocranial trabecula fused with neurocranial trabecula, abnormal ZP:0003813 otic vesicle has extra parts of type otolith, abnormal ZP:0003814 cilium pronephros decreased length, abnormal ZP:0003815 anterior-posterior axis whole organism curved lateral, abnormal ZP:0003816 post-vent region necrotic, abnormal ZP:0003817 myoblast fusion disrupted, abnormal ZP:0003818 melanophore stripe disorganized, abnormal ZP:0003819 fast muscle cell increased amount, abnormal ZP:0003820 fast muscle cell mononucleate, abnormal ZP:0003821 CaP motoneuron has fewer parts of type filopodium CaP motoneuron, abnormal ZP:0003822 CaP motoneuron has fewer parts of type neuron projection primary motor neuron, abnormal ZP:0003823 neuron projection CaP motoneuron decreased length, abnormal ZP:0003824 neuron projection CaP motoneuron decreased branchiness, abnormal ZP:0003825 CaP motoneuron decreased process quality collateral sprouting, abnormal ZP:0003826 eye discolored, abnormal ZP:0003827 integument colorless, abnormal ZP:0003828 blood vessel endothelial cell migration disrupted, abnormal ZP:0003829 branching morphogenesis of an epithelial tube disrupted, abnormal ZP:0003830 caudal fin decreased thickness, abnormal ZP:0003831 posterior region trunk decreased size, abnormal ZP:0003832 intersegmental vessel dilated, abnormal ZP:0003833 intersegmental vessel decreased functionality, abnormal ZP:0003834 lipid metabolic process disrupted, abnormal ZP:0003835 central nervous system myelination disrupted, abnormal ZP:0003836 regulation of fatty acid beta-oxidation disrupted, abnormal ZP:0003837 mitochondrion brain swollen, abnormal ZP:0003838 lipid droplet brain increased amount, abnormal ZP:0003839 neuroblast (sensu Vertebrata) brain increased amount, abnormal ZP:0003840 neuroblast (sensu Vertebrata) brain hyperplastic, abnormal ZP:0003841 mitochondrion spinal cord swollen, abnormal ZP:0003842 liver color, abnormal ZP:0003843 mitochondrion liver swollen, abnormal ZP:0003844 lipid droplet liver increased amount, abnormal ZP:0003845 mitochondrial crista liver decreased mass density, abnormal ZP:0003846 kinocilium neuromast absent, abnormal ZP:0003847 kinocilium neuromast decreased length, abnormal ZP:0003848 kidney morphology, abnormal ZP:0003849 mitochondrion kidney swollen, abnormal ZP:0003850 glial cell (sensu Vertebrata) ventricular zone increased size, abnormal ZP:0003851 mitochondrion whole organism decreased functionality, abnormal ZP:0003852 lipid droplet intestine increased amount, abnormal ZP:0003853 grey matter morphology, abnormal ZP:0003854 axon sensory neuron disorganized, abnormal ZP:0003855 hepatocyte increased size, abnormal ZP:0003856 mitochondrion Mauthner neuron swollen, abnormal ZP:0003857 chondrocyte differentiation arrested, abnormal ZP:0003858 extracellular matrix constituent secretion decreased occurrence, abnormal ZP:0003859 pectoral fin cartilage malformed, abnormal ZP:0003860 pharyngeal arch cartilage immature, abnormal ZP:0003861 extracellular matrix pharyngeal arch cartilage decreased volume, abnormal ZP:0003862 auditory capsule malformed, abnormal ZP:0003863 caudal vein plexus malformed, abnormal ZP:0003864 subintestinal vein malformed, abnormal ZP:0003865 nucleate erythrocyte position, abnormal ZP:0003866 nucleate erythrocyte mislocalised, abnormal ZP:0003867 immature eye morphology, abnormal ZP:0003868 rRNA processing disrupted, abnormal ZP:0003869 regulation of mitotic cell cycle disrupted, abnormal ZP:0003870 exit from mitosis delayed, abnormal ZP:0003871 lens opacity, abnormal ZP:0003872 liver necrotic, abnormal ZP:0003873 nucleolus liver morphology, abnormal ZP:0003874 nucleolus liver increased size, abnormal ZP:0003875 ciliary marginal zone decreased size, abnormal ZP:0003876 nucleolus ciliary marginal zone morphology, abnormal ZP:0003877 nucleolus ciliary marginal zone increased size, abnormal ZP:0003878 lens epithelium increased thickness, abnormal ZP:0003879 nucleolus retinal ganglion cell morphology, abnormal ZP:0003880 nucleolus retinal ganglion cell increased size, abnormal ZP:0003881 cysteine-type peptidase activity decreased process quality, abnormal ZP:0003882 peptidyl-serine phosphorylation increased occurrence, abnormal ZP:0003883 otolith mineralization disrupted, abnormal ZP:0003884 branchiostegal ray disorganized, abnormal ZP:0003885 chondrocyte branchiostegal ray spheroid, abnormal ZP:0003886 collagen type II trimer Meckel's cartilage increased amount, abnormal ZP:0003887 ventral mandibular arch retracted, abnormal ZP:0003888 collagen type II trimer neurocranial trabecula increased amount, abnormal ZP:0003889 collagen type II trimer cranial cartilage increased amount, abnormal ZP:0003890 chondrocyte cranial cartilage increased size, abnormal ZP:0003891 chondrocyte cranial cartilage hyperplastic, abnormal ZP:0003892 neurocranium blunt, abnormal ZP:0003893 apical region Muller cell molecular quality, abnormal ZP:0003894 endocytosis arrested, abnormal ZP:0003895 protein localization arrested, abnormal ZP:0003896 cell population proliferation quality, abnormal ZP:0003897 inner ear morphogenesis paedomorphic growth, abnormal ZP:0003898 median fin fold increased size, abnormal ZP:0003899 median fin fold undulate, abnormal ZP:0003900 epithelium median fin fold undulate, abnormal ZP:0003901 otic vesicle quality, abnormal ZP:0003902 inner ear structure, abnormal ZP:0003903 optic tectum quality, abnormal ZP:0003904 caudal fin has extra parts of type lepidotrichium, abnormal ZP:0003905 epithelium ventral fin fold undulate, abnormal ZP:0003906 muscle pioneer increased amount, abnormal ZP:0003907 whole organism sterile, abnormal ZP:0003908 head increased volume, abnormal ZP:0003909 pectoral fin increased size, abnormal ZP:0003910 pectoral fin undulate, abnormal ZP:0003911 pectoral fin has extra parts of type lepidotrichium, abnormal ZP:0003912 anal fin absent, abnormal ZP:0003913 anal fin aplastic, abnormal ZP:0003914 dorsal fin has extra parts of type lepidotrichium, abnormal ZP:0003915 pelvic fin has extra parts of type lepidotrichium, abnormal ZP:0003916 pupil quality, abnormal ZP:0003917 pupil size, abnormal ZP:0003918 pupil decreased length, abnormal ZP:0003919 pupil decreased size, abnormal ZP:0003920 pupil decreased width, abnormal ZP:0003921 lepidotrichium increased amount, abnormal ZP:0003922 dorsolateral septum aplastic, abnormal ZP:0003923 slow muscle cell increased amount, abnormal ZP:0003924 urea transport decreased rate, abnormal ZP:0003925 oligodendrocyte progenitor proliferation increased occurrence, abnormal ZP:0003926 atrioventricular valve decreased functionality, abnormal ZP:0003927 oligodendrocyte increased amount, abnormal ZP:0003931 lipid localization disrupted, abnormal ZP:0003932 chondrocyte morphogenesis disrupted, abnormal ZP:0003933 liver circular, abnormal ZP:0003934 collagen type II trimer cartilage element aggregated, abnormal ZP:0003935 pharyngeal arch 3-7 increased size, abnormal ZP:0003936 chondrocyte pharyngeal arch 3-7 disorganized, abnormal ZP:0003937 midbrain hindbrain boundary decreased size, abnormal ZP:0003938 forebrain malformed, abnormal ZP:0003939 ethmoid cartilage morphology, abnormal ZP:0003940 cartilage element neurocranium decreased size, abnormal ZP:0003941 pharyngeal arch 3-7 disorganized, abnormal ZP:0003942 chondrocyte trabecular layer decreased amount, abnormal ZP:0003943 leukocyte differentiation disrupted, abnormal ZP:0003944 pronephric capsular space distended, abnormal ZP:0003945 photoreceptor outer segment photoreceptor cell decreased amount, abnormal ZP:0003946 brain deformed, abnormal ZP:0003947 cerebellum aplastic, abnormal ZP:0003948 cytochrome-c oxidase activity decreased occurrence, abnormal ZP:0003949 spinal cord motor neuron differentiation disrupted, abnormal ZP:0003950 digestive tract development arrested, abnormal ZP:0003951 secondary motor neuron spatial pattern, abnormal ZP:0003952 secondary motor neuron decreased amount, abnormal ZP:0003953 axon secondary motor neuron decreased size, abnormal ZP:0003954 forebrain ventricle dilated, abnormal ZP:0003955 ventral mandibular arch hypoplastic, abnormal ZP:0003957 mitotic spindle organization process quality, abnormal ZP:0003958 mitotic cell cycle, embryonic increased duration, abnormal ZP:0003959 post-vent region apoptotic, abnormal ZP:0003960 endochondral ossification decreased process quality, abnormal ZP:0003961 chondrocyte differentiation decreased process quality, abnormal ZP:0003962 branchiomeric skeletal muscle development decreased process quality, abnormal ZP:0003963 histone H2A monoubiquitination disrupted, abnormal ZP:0003964 direct ossification decreased process quality, abnormal ZP:0003965 cleithrum poorly ossified, abnormal ZP:0003966 opercle poorly ossified, abnormal ZP:0003967 parasphenoid poorly ossified, abnormal ZP:0003968 pharyngeal pouch cellular quality, abnormal ZP:0003969 head lacks all parts of type Meckel's cartilage, abnormal ZP:0003970 head lacks all parts of type neurocranial trabecula, abnormal ZP:0003971 head lacks all parts of type palatoquadrate cartilage, abnormal ZP:0003972 head lacks all parts of type ceratohyal cartilage, abnormal ZP:0003973 head lacks all parts of type ethmoid cartilage, abnormal ZP:0003974 head lacks all parts of type hyosymplectic cartilage, abnormal ZP:0003975 head lacks all parts of type parachordal cartilage, abnormal ZP:0003976 head lacks all parts of type sternohyoid, abnormal ZP:0003977 head lacks all parts of type ventral intermandibularis anterior, abnormal ZP:0003978 head lacks all parts of type ventral intermandibularis posterior, abnormal ZP:0003979 head lacks all parts of type adductor mandibulae, abnormal ZP:0003980 head lacks all parts of type interhyoideus, abnormal ZP:0003981 head lacks all parts of type hyohyoideus, abnormal ZP:0003982 pectoral fin lacks all parts of type scapulocoracoid, abnormal ZP:0003983 pectoral fin lacks all parts of type mesocoracoid cartilage, abnormal ZP:0003984 pharyngeal arch apoptotic, abnormal ZP:0003985 chondrocyte pharyngeal arch undifferentiated, abnormal ZP:0003986 chondrocyte neurocranial trabecula undifferentiated, abnormal ZP:0003987 pharyngeal arch cartilage poorly ossified, abnormal ZP:0003988 sternohyoid decreased size, abnormal ZP:0003989 melanocyte increased branchiness, abnormal ZP:0003990 xanthophore decreased size, abnormal ZP:0003991 xanthophore decreased branchiness, abnormal ZP:0003992 proximal region pronephric duct increased length, abnormal ZP:0003993 pronephric distal early tubule absent, abnormal ZP:0003994 whole organism structure, abnormal ZP:0003995 seminoma testis present, abnormal ZP:0003996 lymphoid neoplasms whole organism neoplastic, malignant, abnormal ZP:0003997 cerebellum decreased size, abnormal ZP:0003998 cerebellum disorganized, abnormal ZP:0003999 brain degeneration, abnormal ZP:0004000 retinal ganglion cell layer decayed, abnormal ZP:0004001 neuron retinal ganglion cell layer degenerate, abnormal ZP:0004002 diencephalon apoptotic, abnormal ZP:0004003 nucleus diencephalon aggregated, abnormal ZP:0004004 cell diencephalon decreased amount, abnormal ZP:0004005 eye size, abnormal ZP:0004006 eye degeneration, abnormal ZP:0004007 nucleus eye aggregated, abnormal ZP:0004008 cranial nerve II decreased width, abnormal ZP:0004009 head size, abnormal ZP:0004010 retinal inner plexiform layer decayed, abnormal ZP:0004011 neuron retinal inner plexiform layer degenerate, abnormal ZP:0004012 fast muscle myoblast binucleate, abnormal ZP:0004013 fast muscle myoblast unfused from fast muscle myoblast, abnormal ZP:0004014 cell proliferation in hindbrain disrupted, abnormal ZP:0004015 hindbrain morphogenesis delayed, abnormal ZP:0004016 hindbrain decreased width, abnormal ZP:0004020 optic fissure unfused from optic fissure, abnormal ZP:0004021 otolith increased amount, abnormal ZP:0004022 somite development disrupted, abnormal ZP:0004023 cardiac ventricle tubular, abnormal ZP:0004024 atrium elongated, abnormal ZP:0004025 atrium tubular, abnormal ZP:0004026 atrium separated from sinus venosus, abnormal ZP:0004027 myofibril myotome irregular spatial pattern, abnormal ZP:0004028 muscle cell disorganized, abnormal ZP:0004029 nucleus skeletal muscle myoblast circular, abnormal ZP:0004030 trunk immature, abnormal ZP:0004031 erythroblast binucleate, abnormal ZP:0004032 margin constricted, abnormal ZP:0004033 yolk broken, abnormal ZP:0004034 yolk syncytial layer morphology, abnormal ZP:0004035 nucleus yolk syncytial layer decreased amount, abnormal ZP:0004036 filamentous actin yolk syncytial layer absent, abnormal ZP:0004037 blastomere displaced to dorsal region blastoderm, abnormal ZP:0004038 whole organism lacks parts or has fewer parts of type presumptive endoderm, abnormal ZP:0004039 endocardial cushion quality, abnormal ZP:0004040 hindbrain distended, abnormal ZP:0004041 whole organism malformed, abnormal ZP:0004042 positive regulation of cytosolic calcium ion concentration occurrence, abnormal ZP:0004043 yolk constricted, abnormal ZP:0004044 nucleus internal yolk syncytial layer aggregated, abnormal ZP:0004045 head immature, abnormal ZP:0004046 angiogenesis process quality, abnormal ZP:0004047 vacuole organization process quality, abnormal ZP:0004049 endothelial tube morphogenesis process quality, abnormal ZP:0004050 blood vessel endothelial cell yolk increased distribution, abnormal ZP:0004051 sinus venosus dilated, abnormal ZP:0004052 caudal vein morphology, abnormal ZP:0004053 endothelial cell caudal vein morphology, abnormal ZP:0004054 posterior cardinal vein decreased thickness, abnormal ZP:0004055 posterior cardinal vein dilated, abnormal ZP:0004056 posterior cardinal vein increased diameter, abnormal ZP:0004057 endothelial cell posterior cardinal vein increased distribution, abnormal ZP:0004058 intersegmental vein unlumenized, abnormal ZP:0004059 intersegmental artery unlumenized, abnormal ZP:0004060 cranial vasculature morphology, abnormal ZP:0004061 vacuole intersegmental vessel absent, abnormal ZP:0004062 caudal vein plexus dilated, abnormal ZP:0004063 myocardium distended, abnormal ZP:0004064 myocardium decreased distance endocardium, abnormal ZP:0004065 vascular endothelium apoptotic, abnormal ZP:0004066 primordial midbrain channel dilated, abnormal ZP:0004067 trunk vasculature dilated, abnormal ZP:0004068 dorsal longitudinal anastomotic vessel unlumenized, abnormal ZP:0004069 subintestinal vein dilated, abnormal ZP:0004070 subintestinal vein increased diameter, abnormal ZP:0004071 inner optic circle unlumenized, abnormal ZP:0004072 endothelial cell increased distribution, abnormal ZP:0004073 neural crest formation disrupted, abnormal ZP:0004074 neural crest cell differentiation disrupted, abnormal ZP:0004075 BMP signaling pathway disrupted, abnormal ZP:0004076 hindbrain bulbous, abnormal ZP:0004077 mitotic cell cycle process quality, abnormal ZP:0004078 cell migration arrested, abnormal ZP:0004079 intraciliary transport disrupted, abnormal ZP:0004082 hindbrain has fewer parts of type branchiomotor neuron, abnormal ZP:0004083 cilium otic vesicle decreased length, abnormal ZP:0004084 cilium otic vesicle decreased amount, abnormal ZP:0004085 eye photoreceptor cell retinal photoreceptor layer apoptotic, abnormal ZP:0004086 mitotic spindle pronephric duct direction, abnormal ZP:0004087 photoreceptor outer segment retina absent, abnormal ZP:0004088 anterior side whole organism disorganized, abnormal ZP:0004089 axoneme neural tube absent, abnormal ZP:0004090 retinal outer nuclear layer perforate, abnormal ZP:0004091 eye photoreceptor cell retinal outer nuclear layer apoptotic, abnormal ZP:0004092 cilium posterior neural tube decreased amount, abnormal ZP:0004093 photoreceptor outer segment eye photoreceptor cell absent, abnormal ZP:0004094 nucleus eye photoreceptor cell decreased length, abnormal ZP:0004095 cilium eye photoreceptor cell absent, abnormal ZP:0004096 photoreceptor connecting cilium eye photoreceptor cell absent, abnormal ZP:0004097 photoreceptor inner segment membrane eye photoreceptor cell disorganized, abnormal ZP:0004098 photoreceptor inner segment membrane eye photoreceptor cell displaced, abnormal ZP:0004099 blue sensitive photoreceptor cell morphology, abnormal ZP:0004100 retinal cone cell morphology, abnormal ZP:0004101 retinal cone cell decreased length, abnormal ZP:0004102 retinal rod cell morphology, abnormal ZP:0004103 retinal rod cell pigmented, abnormal ZP:0004104 spliceosomal tri-snRNP complex assembly disrupted, abnormal ZP:0004105 mRNA splicing, via spliceosome disrupted, abnormal ZP:0004106 myeloid leukocyte differentiation disrupted, abnormal ZP:0004107 regulation of apoptotic process disrupted, abnormal ZP:0004108 central nervous system apoptotic, abnormal ZP:0004109 spinal cord degenerate, abnormal ZP:0004110 myeloid leukocyte decreased amount, abnormal ZP:0004111 pigment cell development disrupted, abnormal ZP:0004112 ovary morphology, abnormal ZP:0004113 whole organism female sterile, abnormal ZP:0004114 melanophore stripe trunk absent, abnormal ZP:0004115 pigment cell (sensu Vertebrata) trunk decreased amount, abnormal ZP:0004116 iridophore trunk decreased amount, abnormal ZP:0004117 xanthophore hypodermis decreased amount, abnormal ZP:0004118 iridophore hypodermis decreased amount, abnormal ZP:0004119 pigment cell (sensu Vertebrata) decreased amount, abnormal ZP:0004120 cell population proliferation absent, abnormal ZP:0004121 chordate embryonic development delayed, abnormal ZP:0004122 liver and biliary system decreased functionality, abnormal ZP:0004123 exocrine pancreas decreased thickness, abnormal ZP:0004124 exocrine pancreas degenerate, abnormal ZP:0004125 intrahepatic bile duct unbranched, abnormal ZP:0004126 intrahepatic bile duct absent, abnormal ZP:0004127 intrahepatic bile duct apoptotic, abnormal ZP:0004128 intrahepatic bile duct degenerate, abnormal ZP:0004129 epithelial cell intrahepatic bile duct decreased amount, abnormal ZP:0004130 endoderm shape, abnormal ZP:0004131 endoderm structure, abnormal ZP:0004133 glomerular filtration decreased process quality, abnormal ZP:0004134 glomerulus morphogenesis disrupted, abnormal ZP:0004135 glomerular capillary formation disrupted, abnormal ZP:0004136 dorsal aorta distended, abnormal ZP:0004137 renal glomerulus pronephros malformed, abnormal ZP:0004138 capillary loop nephron pronephros closure incomplete, abnormal ZP:0004139 capillary loop nephron pronephros decreased amount, abnormal ZP:0004140 mesangial cell pronephros decreased amount, abnormal ZP:0004141 dorsal-ventral axis whole organism decreased length, abnormal ZP:0004142 pronephric podocyte attached to dorsal aorta, abnormal ZP:0004143 cell projection pronephric podocyte folded, abnormal ZP:0004144 pronephric podocyte inserted into cell projection pronephric capsular space, abnormal ZP:0004145 lamina densa surrounding cell projection pronephric podocyte, abnormal ZP:0004146 pronephric glomerular basement membrane increased thickness, abnormal ZP:0004147 pronephric glomerular basement membrane decreased permeability, abnormal ZP:0004148 intersegmental vessel branched, abnormal ZP:0004149 neural crest cell migration delayed, abnormal ZP:0004150 eye increased distance eye, abnormal ZP:0004151 neuron dorsal root ganglion displaced, abnormal ZP:0004152 trigeminal ganglion decreased amount, abnormal ZP:0004153 neuron posterior lateral line decreased amount, abnormal ZP:0004154 neuron sympathetic nervous system decreased amount, abnormal ZP:0004155 pharyngeal arch 2 structure, abnormal ZP:0004156 pharyngeal arch 2 displaced, abnormal ZP:0004157 pharyngeal arch 1 structure, abnormal ZP:0004158 pharyngeal arch 1 displaced, abnormal ZP:0004159 otolith position, abnormal ZP:0004160 pharyngeal arch 3-7 skeleton aplastic, abnormal ZP:0004161 nervous system apoptotic, abnormal ZP:0004162 erythrocyte maturation decreased process quality, abnormal ZP:0004163 blood chromatic property, abnormal ZP:0004164 angiogenesis decreased process quality, abnormal ZP:0004165 establishment of blood-brain barrier decreased process quality, abnormal ZP:0004166 brain vasculature increased permeability, abnormal ZP:0004167 central artery malformed, abnormal ZP:0004168 phospholipase activity disrupted, abnormal ZP:0004169 peptidase activity disrupted, abnormal ZP:0004170 bile acid secretion disrupted, abnormal ZP:0004171 glucose homeostasis disrupted, abnormal ZP:0004172 liver and biliary system malformed, abnormal ZP:0004173 trunk female organism increased size, abnormal ZP:0004174 hepatic duct physical object quality, abnormal ZP:0004175 intestine fatty, abnormal ZP:0004176 hepatocyte decreased functionality, abnormal ZP:0004178 gut absent, abnormal ZP:0004179 gut decreased thickness, abnormal ZP:0004182 hyosymplectic cartilage decreased amount, abnormal ZP:0004185 ovarian follicle development premature, abnormal ZP:0004186 oocyte maturation increased occurrence, abnormal ZP:0004187 oocyte maturity, abnormal ZP:0004188 ovarian follicle maturity, abnormal ZP:0004189 neuron differentiation delayed, abnormal ZP:0004190 retina development in camera-type eye delayed, abnormal ZP:0004191 retinal ganglion cell layer immature, abnormal ZP:0004192 retinal neural layer poorly differentiated, abnormal ZP:0004193 central region retinal neural layer proliferative, abnormal ZP:0004194 retinal inner nuclear layer immature, abnormal ZP:0004195 optic tectum apoptotic, abnormal ZP:0004196 retinal outer nuclear layer immature, abnormal ZP:0004197 translation decreased process quality, abnormal ZP:0004199 chondrocyte differentiation disrupted, abnormal ZP:0004200 optic cup morphogenesis involved in camera-type eye development disrupted, abnormal ZP:0004201 somite obtuse angle to somite, abnormal ZP:0004202 muscle pioneer myotome increased amount, abnormal ZP:0004203 fast muscle cell myotome increased amount, abnormal ZP:0004204 muscle pioneer absent, abnormal ZP:0004205 muscle pioneer mislocalised, abnormal ZP:0004206 pectoral fin folded, abnormal ZP:0004207 ceratohyal cartilage physical object quality, abnormal ZP:0004208 ceratohyal cartilage ossified, abnormal ZP:0004209 hyosymplectic cartilage physical object quality, abnormal ZP:0004210 hyosymplectic cartilage ossified, abnormal ZP:0004211 chondrocyte pharyngeal arch 3-7 irregular spatial pattern, abnormal ZP:0004212 sprouting angiogenesis increased occurrence, abnormal ZP:0004214 intersegmental vessel has extra parts of type vascular sprouts, abnormal ZP:0004216 vascular sprouts disorganized, abnormal ZP:0004218 basement membrane renal glomerulus increased thickness, abnormal ZP:0004221 podocyte malformed, abnormal ZP:0004222 podocyte variant shape, abnormal ZP:0004223 podocyte increased variability of size, abnormal ZP:0004224 brain hypoplastic, abnormal ZP:0004225 midbrain hindbrain boundary apoptotic, abnormal ZP:0004226 olfactory region hypoplastic, abnormal ZP:0004227 optic primordium malformed, abnormal ZP:0004228 head truncated, abnormal ZP:0004229 Meckel's cartilage shape, abnormal ZP:0004230 ceratohyal cartilage obtuse angle to ceratohyal cartilage, abnormal ZP:0004231 cranial cartilage hypoplastic, abnormal ZP:0004232 chondrocyte cranial cartilage circular, abnormal ZP:0004233 chondrocyte cranial cartilage disorganized, abnormal ZP:0004234 neuron brain necrotic, abnormal ZP:0004235 lateral line truncated, abnormal ZP:0004236 erythroblast decreased amount, abnormal ZP:0004237 photoreceptor outer segment layer aplastic, abnormal ZP:0004238 myofibril slow muscle cell decreased diameter, abnormal ZP:0004239 myofibril slow muscle cell decreased amount, abnormal ZP:0004240 Z disc slow muscle cell malformed, abnormal ZP:0004242 erythroid lineage cell intermediate cell mass of mesoderm decreased amount, abnormal ZP:0004243 erythroid lineage cell blood island decreased amount, abnormal ZP:0004244 erythroid progenitor cell lateral plate mesoderm decreased amount, abnormal ZP:0004245 trunk curvature, abnormal ZP:0004246 response to ionizing radiation disrupted, abnormal ZP:0004247 melanocyte integument morphology, abnormal ZP:0004248 melanocyte trunk aggregated, abnormal ZP:0004249 face development disrupted, abnormal ZP:0004250 capillary pharyngeal arch hypoplastic, abnormal ZP:0004251 palatoquadrate cartilage deformed, abnormal ZP:0004252 aortic arch hypoplastic, abnormal ZP:0004253 neuromuscular junction development decreased occurrence, abnormal ZP:0004254 synaptic growth at neuromuscular junction disrupted, abnormal ZP:0004255 skeletal muscle acetylcholine-gated channel clustering arrested, abnormal ZP:0004256 skeletal muscle acetylcholine-gated channel clustering decreased occurrence, abnormal ZP:0004257 neuromuscular junction myotome decreased amount, abnormal ZP:0004258 peripheral neuron quality, abnormal ZP:0004259 growth cone CaP motoneuron malformed, abnormal ZP:0004260 axon primary motor neuron morphology, abnormal ZP:0004261 adaxial cell disorganized, abnormal ZP:0004263 primitive hemopoiesis disrupted, abnormal ZP:0004264 necrotic cell death increased occurrence, abnormal ZP:0004265 whole organism undulate, abnormal ZP:0004266 axis elongation decreased process quality, abnormal ZP:0004267 notochord shortened, abnormal ZP:0004272 regulation of smoothened signaling pathway process quality, abnormal ZP:0004273 spinal cord dorsal/ventral patterning process quality, abnormal ZP:0004274 forebrain regionalization process quality, abnormal ZP:0004275 adenohypophysis development process quality, abnormal ZP:0004276 forebrain development process quality, abnormal ZP:0004277 dorsal/ventral axon guidance disrupted, abnormal ZP:0004278 axon extension involved in axon guidance process quality, abnormal ZP:0004279 postoptic commissure absent, abnormal ZP:0004280 glial cell diencephalon mislocalised, abnormal ZP:0004281 ventral region midbrain physical object quality, abnormal ZP:0004282 axon caudal commissure mislocalised, abnormal ZP:0004283 cranial nerve II decreased length, abnormal ZP:0004284 cranial nerve II misrouted, abnormal ZP:0004285 lateral floor plate physical object quality, abnormal ZP:0004286 ventral mandibular arch increased width, abnormal ZP:0004287 adenohypophysis physical object quality, abnormal ZP:0004288 dorsoventral diencephalic tract morphology, abnormal ZP:0004289 axon tract of the postoptic commissure mislocalised laterally, abnormal ZP:0004290 phagocytosis, engulfment decreased occurrence, abnormal ZP:0004291 locomotion increased occurrence, abnormal ZP:0004292 neural precursor cell proliferation disrupted, abnormal ZP:0004293 lysosome hindbrain increased size, abnormal ZP:0004294 cerebellum absent, abnormal ZP:0004295 lysosome forebrain increased size, abnormal ZP:0004296 retina absent, abnormal ZP:0004297 lysosome retina increased size, abnormal ZP:0004298 axon caudal commissure deformed, abnormal ZP:0004299 axon cranial nerve II deformed, abnormal ZP:0004300 optic tectum absent, abnormal ZP:0004301 axon cranial nerve IV deformed, abnormal ZP:0004302 mandibular arch skeleton absent, abnormal ZP:0004303 skeletal muscle contraction arrested, abnormal ZP:0004304 potassium channel activity decreased occurrence, abnormal ZP:0004305 neuromuscular synaptic transmission arrested, abnormal ZP:0004306 skeletal myofibril assembly decreased occurrence, abnormal ZP:0004307 hatching gland quality, abnormal ZP:0004308 slow muscle cell somite morphology, abnormal ZP:0004309 fast muscle cell somite degenerate, abnormal ZP:0004310 skeletal muscle cell myotome atrophied, abnormal ZP:0004311 acetylcholine-gated channel complex skeletal muscle absent, abnormal ZP:0004312 potassium channel complex skeletal muscle decreased amount, abnormal ZP:0004313 slow muscle cell membrane potential, abnormal ZP:0004314 myosin complex slow muscle cell decreased object quality, abnormal ZP:0004315 myosin complex fast muscle cell decreased object quality, abnormal ZP:0004316 mRNA splicing, via spliceosome process quality, abnormal ZP:0004317 posterior intestine apoptotic, abnormal ZP:0004318 intestinal epithelium smooth, abnormal ZP:0004319 hyaloid vessel hypoplastic, abnormal ZP:0004320 blood vessel endothelial cell hyaloid vessel aggregated, abnormal ZP:0004321 embryonic heart tube morphogenesis arrested, abnormal ZP:0004322 cardiac muscle progenitor cell migration to the midline involved in heart field formation arrested, abnormal ZP:0004323 embryonic heart tube development arrested, abnormal ZP:0004324 melanosome melanocyte decreased pigmentation, abnormal ZP:0004325 cardiac muscle cell absent, abnormal ZP:0004326 histone H4-R3 methylation decreased occurrence, abnormal ZP:0004328 prechordal plate formation decreased process quality, abnormal ZP:0004329 cell migration involved in mesendoderm migration decreased process quality, abnormal ZP:0004330 bleb anterior axial hypoblast increased amount, abnormal ZP:0004331 pronephric glomerulus permeability, abnormal ZP:0004332 rRNA processing decreased process quality, abnormal ZP:0004333 rRNA transcription decreased process quality, abnormal ZP:0004334 blood accumulation heart, abnormal ZP:0004335 heart decreased rate, abnormal ZP:0004336 pigmentation delayed, abnormal ZP:0004337 fin rough, abnormal ZP:0004339 intersegmental vessel has extra parts of type endothelial cell, abnormal ZP:0004342 photoreceptor cell morphogenesis process quality, abnormal ZP:0004343 retinal photoreceptor layer physical object quality, abnormal ZP:0004344 melanocyte distended, abnormal ZP:0004345 photoreceptor inner segment eye photoreceptor cell absent, abnormal ZP:0004346 photoreceptor inner segment eye photoreceptor cell malformed, abnormal ZP:0004347 nucleus eye photoreceptor cell circular, abnormal ZP:0004348 mitochondrion eye photoreceptor cell mislocalised, abnormal ZP:0004349 Golgi apparatus eye photoreceptor cell mislocalised, abnormal ZP:0004350 organelle eye photoreceptor cell mislocalised, abnormal ZP:0004351 organelle eye photoreceptor cell positional polarity, abnormal ZP:0004352 synapse eye photoreceptor cell malformed, abnormal ZP:0004353 retinal cone cell malformed, abnormal ZP:0004354 organelle retinal cone cell mislocalised, abnormal ZP:0004355 retinal rod cell malformed, abnormal ZP:0004356 photoreceptor outer segment retinal rod cell physical object quality, abnormal ZP:0004357 peptidyl-lysine trimethylation decreased occurrence, abnormal ZP:0004358 peptidyl-lysine monomethylation increased occurrence, abnormal ZP:0004359 determination of left/right asymmetry in diencephalon disrupted, abnormal ZP:0004360 histone methyltransferase activity (H3-K9 specific) magnitude, abnormal ZP:0004361 cilium Kupffer's vesicle decreased amount, abnormal ZP:0004362 shield distended, abnormal ZP:0004363 diencephalon structure, abnormal ZP:0004364 gut mislocalised radially, abnormal ZP:0004365 gut centered, abnormal ZP:0004366 lateral plate mesoderm structure, abnormal ZP:0004367 liver mislocalised radially, abnormal ZP:0004368 liver centered, abnormal ZP:0004369 pancreas mislocalised radially, abnormal ZP:0004370 pancreas centered, abnormal ZP:0004371 primitive heart tube mislocalised radially, abnormal ZP:0004372 primitive heart tube centered, abnormal ZP:0004373 caudal vein plexus decreased branchiness, abnormal ZP:0004374 sensory perception of touch process quality, abnormal ZP:0004375 pharyngeal arch cartilage morphology, abnormal ZP:0004376 neurocranium morphology, abnormal ZP:0004377 muscle fiber development disrupted, abnormal ZP:0004378 myofibril myotome decreased thickness, abnormal ZP:0004379 myofibril myotome undulate, abnormal ZP:0004380 myotome detached from myofibril myofibril myotome, abnormal ZP:0004381 myofibril fast muscle cell decreased amount, abnormal ZP:0004382 neuromast has fewer parts of type hair cell, abnormal ZP:0004383 locomotory behavior decreased occurrence, abnormal ZP:0004384 median fin fold structure, abnormal ZP:0004385 median fin fold immature, abnormal ZP:0004386 inner ear aplastic, abnormal ZP:0004387 pancreas development delayed, abnormal ZP:0004388 pancreas morphogenesis disrupted, abnormal ZP:0004389 pancreas decreased volume, abnormal ZP:0004390 cell migration involved in sprouting angiogenesis arrested, abnormal ZP:0004392 primordial hindbrain channel dilated, abnormal ZP:0004393 intersegmental vessel truncated, abnormal ZP:0004394 intersegmental vessel cellular adhesivity blood vessel endothelial cell blood vessel endothelial cell intersegmental vessel, abnormal ZP:0004395 endothelial tip cell intersegmental vessel positional polarity, abnormal ZP:0004396 endothelial tip cell circular, abnormal ZP:0004397 filopodium endothelial tip cell absent, abnormal ZP:0004398 filopodium endothelial tip cell decreased amount, abnormal ZP:0004399 EVL detached from external yolk syncytial layer, abnormal ZP:0004400 somite absent, abnormal ZP:0004401 neural crest cell migration decreased rate, abnormal ZP:0004402 anterior region neurocranium decreased size, abnormal ZP:0004403 anterior region neurocranium deformed, abnormal ZP:0004404 pharyngeal arch 2 decreased length, abnormal ZP:0004405 cranial neural crest cell position, abnormal ZP:0004406 neural crest cell position, abnormal ZP:0004407 response to auditory stimulus arrested, abnormal ZP:0004408 skeletal muscle contraction amplitude, abnormal ZP:0004409 skeletal muscle contraction increased frequency, abnormal ZP:0004410 musculoskeletal movement process quality, abnormal ZP:0004411 whole organism partially paralysed, abnormal ZP:0004412 CaP motoneuron functionality, abnormal ZP:0004413 central nervous system neuron development disrupted, abnormal ZP:0004414 axial mesoderm structural organization disrupted, abnormal ZP:0004415 dorsal-ventral axis brain decreased length, abnormal ZP:0004416 neuron brain disorganized, abnormal ZP:0004417 neuron brain decreased amount, abnormal ZP:0004418 germ ring increased thickness, abnormal ZP:0004419 midbrain decreased width, abnormal ZP:0004420 muscle cell migration arrested, abnormal ZP:0004421 adaxial cell position, abnormal ZP:0004422 myofibril slow muscle cell bent, abnormal ZP:0004423 myofibril slow muscle cell elongated, abnormal ZP:0004424 locomotory behavior increased process quality, abnormal ZP:0004425 locomotion increased speed, abnormal ZP:0004426 neuron caudal tuberculum disorganized, abnormal ZP:0004427 dopaminergic neuron caudal tuberculum mislocalised, abnormal ZP:0004428 telencephalon increased size, abnormal ZP:0004429 whole organism wholly anterioralized, abnormal ZP:0004430 axial vasculature has fewer parts of type intersegmental vessel, abnormal ZP:0004431 post-vent region wholly dorsalized, abnormal ZP:0004432 vasculature morphology, abnormal ZP:0004433 somitogenesis arrested, abnormal ZP:0004434 pigmentation process quality, abnormal ZP:0004435 somite 26 aplastic, abnormal ZP:0004436 ventral region retina aplastic, abnormal ZP:0004437 somite 20 aplastic, abnormal ZP:0004438 somite 30 aplastic, abnormal ZP:0004439 inner ear has fewer parts of type otolith, abnormal ZP:0004440 atrium position, abnormal ZP:0004441 atrium attached to bulbus arteriosus, abnormal ZP:0004442 somite 11 aplastic, abnormal ZP:0004443 somite 14 aplastic, abnormal ZP:0004444 somite 17 aplastic, abnormal ZP:0004445 somite 23 aplastic, abnormal ZP:0004446 somite 27 aplastic, abnormal ZP:0004447 somite 7 malformed, abnormal ZP:0004448 somite 12 aplastic, abnormal ZP:0004449 somite 15 aplastic, abnormal ZP:0004450 somite 18 aplastic, abnormal ZP:0004451 somite 21 aplastic, abnormal ZP:0004452 somite 24 aplastic, abnormal ZP:0004453 somite 28 aplastic, abnormal ZP:0004454 somite 8 aplastic, abnormal ZP:0004455 somite 10 aplastic, abnormal ZP:0004456 somite 13 aplastic, abnormal ZP:0004457 somite 16 aplastic, abnormal ZP:0004458 somite 19 aplastic, abnormal ZP:0004459 somite 22 aplastic, abnormal ZP:0004460 somite 25 aplastic, abnormal ZP:0004461 somite 29 aplastic, abnormal ZP:0004462 somite 6 malformed, abnormal ZP:0004463 somite 9 aplastic, abnormal ZP:0004464 somite border degenerate, abnormal ZP:0004465 multicellular organismal locomotion decreased rate, abnormal ZP:0004466 peripheral neuron decreased thickness, abnormal ZP:0004467 axon primary motor neuron branched, abnormal ZP:0004468 axon secondary motor neuron mislocalised, abnormal ZP:0004469 dorsal aorta malformed, abnormal ZP:0004470 caudal vein malformed, abnormal ZP:0004471 intersegmental vessel post-vent region decreased mass density, abnormal ZP:0004472 caudal vein plexus increased accumulation blood, abnormal ZP:0004473 blood vessel decreased width, abnormal ZP:0004474 podocyte structure, abnormal ZP:0004475 thrombocyte shape, abnormal ZP:0004476 cartilage condensation decreased occurrence, abnormal ZP:0004477 chondrocyte differentiation decreased occurrence, abnormal ZP:0004478 chondrocyte proliferation decreased occurrence, abnormal ZP:0004482 chondrocyte ceratobranchial cartilage decreased size, abnormal ZP:0004483 chondrocyte ceratobranchial cartilage immature, abnormal ZP:0004484 ammonium transport decreased rate, abnormal ZP:0004485 blood circulation decreased process quality, abnormal ZP:0004486 hemopoiesis process quality, abnormal ZP:0004487 dorsal aorta shortened, abnormal ZP:0004488 blood island increased occurrence apoptotic process, abnormal ZP:0004490 intersegmental vessel absent, abnormal ZP:0004491 blood cell absent, abnormal ZP:0004492 cell fate specification disrupted, abnormal ZP:0004493 dorsal aorta increased accumulation blood, abnormal ZP:0004494 posterior cardinal vein increased size, abnormal ZP:0004495 posterior cardinal vein increased accumulation blood, abnormal ZP:0004496 axial vasculature morphology, abnormal ZP:0004497 axial vasculature decreased functionality, abnormal ZP:0004498 contractile fiber somite disorganized, abnormal ZP:0004499 contractile fiber somite undulate, abnormal ZP:0004500 nervous system development process quality, abnormal ZP:0004501 hepatocyte differentiation disrupted, abnormal ZP:0004502 hepatocyte proliferation decreased occurrence, abnormal ZP:0004503 liver morphogenesis disrupted, abnormal ZP:0004504 hepatocyte apoptotic, abnormal ZP:0004505 hepatocyte decreased amount, abnormal ZP:0004506 hepatocyte decreased area, abnormal ZP:0004507 ball deformed, abnormal ZP:0004508 telencephalon hypoplastic, abnormal ZP:0004509 fin decreased thickness, abnormal ZP:0004510 midbrain aplastic, abnormal ZP:0004511 cell migration involved in gastrulation decreased occurrence, abnormal ZP:0004512 forebrain pointed, abnormal ZP:0004513 anterior-posterior axis whole organism bent, abnormal ZP:0004514 blastoderm increased thickness, abnormal ZP:0004515 telencephalon morphology, abnormal ZP:0004516 tegmentum opaque, abnormal ZP:0004517 lens absent, abnormal ZP:0004518 eye immature, abnormal ZP:0004519 forebrain increased size, abnormal ZP:0004520 spinal cord bent, abnormal ZP:0004521 caudal fin bent, abnormal ZP:0004522 caudal fin increased occurrence apoptotic process, abnormal ZP:0004523 head increased occurrence apoptotic process, abnormal ZP:0004524 nucleate erythrocyte blood absent, abnormal ZP:0004525 myocardium bent, abnormal ZP:0004526 cardiac muscle cell shape, abnormal ZP:0004527 trabecula communis aplastic, abnormal ZP:0004528 optokinetic behavior decreased occurrence, abnormal ZP:0004529 axon extension delayed, abnormal ZP:0004530 CaP motoneuron myotome hypoplastic, abnormal ZP:0004531 otic vesicle formation disrupted, abnormal ZP:0004532 anterior macula position, abnormal ZP:0004533 lateral semicircular canal aplastic, abnormal ZP:0004534 pectoral fin cartilage morphology, abnormal ZP:0004535 posterior macula position, abnormal ZP:0004536 otolith organ lacks parts or has fewer parts of type otolith, abnormal ZP:0004537 otolith organ has extra parts of type otolith, abnormal ZP:0004538 immature posterior macula aplastic, abnormal ZP:0004539 vestibuloauditory system functionality, abnormal ZP:0004540 chondrocranium cartilage decreased size, abnormal ZP:0004541 otolith composition, abnormal ZP:0004542 otolith mislocalised, abnormal ZP:0004543 median fin fold decreased size, abnormal ZP:0004544 fin undulate, abnormal ZP:0004545 vertebra decreased mass density, abnormal ZP:0004546 lepidotrichium increased thickness, abnormal ZP:0004547 lepidotrichium decreased mass density, abnormal ZP:0004548 actinotrichium malformed, abnormal ZP:0004550 cilium otic vesicle increased length, abnormal ZP:0004551 cilium pronephric duct increased length, abnormal ZP:0004552 heart tube bilateral symmetry, abnormal ZP:0004553 hindbrain elongated, abnormal ZP:0004554 lymph vessel development disrupted, abnormal ZP:0004555 optic tectum structure, abnormal ZP:0004556 forerunner cell group disorganized, abnormal ZP:0004557 atrioventricular valve development disrupted, abnormal ZP:0004558 cell proliferation involved in heart valve development disrupted, abnormal ZP:0004559 atrioventricular canal endocardium morphology, abnormal ZP:0004560 cell atrioventricular canal endocardium decreased amount, abnormal ZP:0004561 chemical synaptic transmission disrupted, abnormal ZP:0004562 optokinetic behavior absent, abnormal ZP:0004564 axon terminus retinal cone cell morphology, abnormal ZP:0004565 plasma membrane neuromast hair cell protruding, abnormal ZP:0004566 synaptic vesicle neuromast hair cell amount, abnormal ZP:0004567 blood lacks parts or has fewer parts of type nucleate erythrocyte, abnormal ZP:0004568 intermediate cell mass of mesoderm increased accumulation blood, abnormal ZP:0004569 epidermis aggregated, abnormal ZP:0004570 extension structure, abnormal ZP:0004571 post-vent region edematous, abnormal ZP:0004572 whole organism lacks parts or has fewer parts of type hemoglobin complex nucleate erythrocyte, abnormal ZP:0004573 lateral line development process quality, abnormal ZP:0004574 neuromast primordium migration process quality, abnormal ZP:0004575 neuromast deposition decreased process quality, abnormal ZP:0004576 somite decreased width, abnormal ZP:0004577 somite tight, abnormal ZP:0004578 somite has fewer parts of type muscle pioneer, abnormal ZP:0004579 somite has fewer parts of type fast muscle cell, abnormal ZP:0004580 neuromast decreased size, abnormal ZP:0004581 neuromast dispersed, abnormal ZP:0004582 caudal fin increased width, abnormal ZP:0004584 lateral larval melanophore stripe absent, abnormal ZP:0004585 lateral larval melanophore stripe has fewer parts of type melanocyte, abnormal ZP:0004586 muscle cell sparse, abnormal ZP:0004588 midbrain hindbrain boundary absent, abnormal ZP:0004593 notochord increased size, abnormal ZP:0004594 endocrine pancreas increased size, abnormal ZP:0004595 pancreatic B cell increased amount, abnormal ZP:0004596 determination of left/right asymmetry in diencephalon process quality, abnormal ZP:0004597 metapterygoid morphology, abnormal ZP:0004598 Meckel's cartilage aplastic/hypoplastic, abnormal ZP:0004599 cartilaginous joint mandibular arch skeleton morphology, abnormal ZP:0004600 palatoquadrate cartilage aplastic/hypoplastic, abnormal ZP:0004601 ammonium homeostasis disrupted, abnormal ZP:0004602 vH ionocyte flux, abnormal ZP:0004603 keratinocyte flux, abnormal ZP:0004604 eye hypoplastic, abnormal ZP:0004605 heart elongated, abnormal ZP:0004606 myofibril myocardium disorganized, abnormal ZP:0004607 sarcoplasmic reticulum skeletal muscle cell disorganized, abnormal ZP:0004608 sarcomere skeletal muscle cell decreased length, abnormal ZP:0004609 Z disc skeletal muscle cell irregular spatial pattern, abnormal ZP:0004610 H zone skeletal muscle cell absent, abnormal ZP:0004611 I band skeletal muscle cell absent, abnormal ZP:0004612 Z disc cardiac muscle cell irregular spatial pattern, abnormal ZP:0004613 H zone cardiac muscle cell absent, abnormal ZP:0004614 I band cardiac muscle cell absent, abnormal ZP:0004615 calmodulin-dependent protein kinase activity decreased rate, abnormal ZP:0004616 hindbrain swollen, abnormal ZP:0004617 notochord posterior region kinked, abnormal ZP:0004618 head absent, abnormal ZP:0004619 regulation of RNA splicing disrupted, abnormal ZP:0004620 adenohypophysis increased size, abnormal ZP:0004621 adenohypophysis disorganized, abnormal ZP:0004622 proximal pars anterior morphology, abnormal ZP:0004623 convergent extension delayed, abnormal ZP:0004624 cardiac conduction disrupted, abnormal ZP:0004625 prechordal plate structure, abnormal ZP:0004626 eye position, abnormal ZP:0004627 eye decreased amount, abnormal ZP:0004633 cell-cell junction endothelial cell absent, abnormal ZP:0004634 mitotic G1 phase arrested, abnormal ZP:0004635 DNA damage response, signal transduction by p53 class mediator resulting in cell cycle arrest increased occurrence, abnormal ZP:0004636 brain edematous, abnormal ZP:0004637 hematopoietic stem cell dorsal aorta decreased amount, abnormal ZP:0004638 hematopoietic stem cell blood island decreased amount, abnormal ZP:0004639 extension shortened, abnormal ZP:0004640 leukocyte decreased amount, abnormal ZP:0004641 embryonic camera-type eye development disrupted, abnormal ZP:0004642 optic vesicle apoptotic, abnormal ZP:0004643 ceratobranchial cartilage morphology, abnormal ZP:0004644 cranial neural crest cell mislocalised, abnormal ZP:0004645 optic stalk decreased length, abnormal ZP:0004646 optic stalk increased thickness, abnormal ZP:0004647 whole organism lacks all parts of type optic chiasm, abnormal ZP:0004648 bleb assembly increased occurrence, abnormal ZP:0004649 heart primordium morphology, abnormal ZP:0004650 liver primordium morphology, abnormal ZP:0004651 pancreas primordium morphology, abnormal ZP:0004652 bleb mesodermal cell increased amount, abnormal ZP:0004653 eye pigmented, abnormal ZP:0004654 xanthophore absent, abnormal ZP:0004655 protein phosphorylation decreased occurrence, abnormal ZP:0004656 cortical actin cytoskeleton organization disrupted, abnormal ZP:0004657 filopodium assembly disrupted, abnormal ZP:0004658 convergent extension decreased rate, abnormal ZP:0004659 polster mislocalised, abnormal ZP:0004660 whole organism lacks all parts of type parachordal vessel, abnormal ZP:0004661 cortical actin cytoskeleton whole organism disorganized, abnormal ZP:0004662 cortical actin cytoskeleton whole organism decreased mass density, abnormal ZP:0004663 forerunner cell group whole organism cellular motility, abnormal ZP:0004664 EVL whole organism cellular motility, abnormal ZP:0004665 yolk syncytial layer whole organism cellular motility, abnormal ZP:0004666 DEL whole organism cellular motility, abnormal ZP:0004667 blood vessel endothelial cell intersegmental vessel decreased amount, abnormal ZP:0004668 blood vessel unlumenized, abnormal ZP:0004669 medial fin morphogenesis process quality, abnormal ZP:0004670 median fin fold blistered, abnormal ZP:0004671 blood island blistered, abnormal ZP:0004672 epidermis morphogenesis disrupted, abnormal ZP:0004673 epidermis morphology, abnormal ZP:0004674 cell surface keratinocyte disorganized, abnormal ZP:0004675 dorsal aorta hypoplastic, abnormal ZP:0004676 retinal pigmented epithelium unpigmented, abnormal ZP:0004677 larval melanophore stripe low saturation, abnormal ZP:0004678 neoplasm orbit protruding, abnormal ZP:0004679 melanocyte broken, abnormal ZP:0004680 melanocyte aggregated, abnormal ZP:0004681 melanosome melanocyte degenerate, abnormal ZP:0004682 cell adhesion disrupted, abnormal ZP:0004683 medial fin development disrupted, abnormal ZP:0004684 protein localization to adherens junction arrested, abnormal ZP:0004685 median fin fold malformed, abnormal ZP:0004686 median fin fold edematous, abnormal ZP:0004687 basement membrane median fin fold punctate, abnormal ZP:0004689 epidermis median fin fold disorganized, abnormal ZP:0004690 epidermal cell median fin fold positional polarity, abnormal ZP:0004691 extension hypoplastic, abnormal ZP:0004692 fin necrotic, abnormal ZP:0004693 caudal fin has fewer parts of type lepidotrichium, abnormal ZP:0004694 pectoral fin structure, abnormal ZP:0004695 pectoral fin degenerate, abnormal ZP:0004696 pectoral fin edematous, abnormal ZP:0004697 pectoral fin has fewer parts of type lepidotrichium, abnormal ZP:0004698 anal fin has fewer parts of type lepidotrichium, abnormal ZP:0004699 dorsal fin has fewer parts of type lepidotrichium, abnormal ZP:0004700 epidermal cell shape, abnormal ZP:0004701 neuron optic tectum decreased amount, abnormal ZP:0004702 locomotory behavior decreased frequency, abnormal ZP:0004703 cell migration process quality, abnormal ZP:0004704 endocrine pancreas development disrupted, abnormal ZP:0004705 axon cranial nerve V immature, abnormal ZP:0004706 axon Mauthner neuron morphology, abnormal ZP:0004707 axon Rohon-Beard neuron truncated, abnormal ZP:0004708 atrioventricular valve constricted, abnormal ZP:0004709 skeletal muscle decreased size, abnormal ZP:0004710 skeletal muscle refractivity, abnormal ZP:0004711 myofibril skeletal muscle disorganized, abnormal ZP:0004713 Z disc skeletal muscle increased thickness, abnormal ZP:0004714 epithelial to mesenchymal transition occurrence, abnormal ZP:0004715 negative regulation of epithelial to mesenchymal transition disrupted, abnormal ZP:0004716 posterior lateral line neuromast development disrupted, abnormal ZP:0004717 negative regulation of epithelial cell proliferation disrupted, abnormal ZP:0004718 epidermis quality, abnormal ZP:0004719 integument quality, abnormal ZP:0004720 cell integument circular, abnormal ZP:0004721 epithelial cell increased amount, abnormal ZP:0004722 lamellipodium epithelial cell increased amount, abnormal ZP:0004723 epidermal cell morphology, abnormal ZP:0004724 mandibular muscle aplastic, abnormal ZP:0004725 whole organism mobility, abnormal ZP:0004726 myofibril skeletal muscle cell structure, abnormal ZP:0004727 myofibril skeletal muscle cell decreased width, abnormal ZP:0004728 macrophage mislocalised, abnormal ZP:0004729 neutrophil mislocalised, abnormal ZP:0004730 basement membrane assembly disrupted, abnormal ZP:0004735 integument detached from whole organism, abnormal ZP:0004736 dermis broken, abnormal ZP:0004737 retinal ganglion cell layer decreased thickness, abnormal ZP:0004738 retinal inner nuclear layer decreased thickness, abnormal ZP:0004739 retinal outer nuclear layer decreased thickness, abnormal ZP:0004740 regulation of transcription by RNA polymerase II disrupted, abnormal ZP:0004741 neuron development process quality, abnormal ZP:0004742 trigeminal ganglion decreased size, abnormal ZP:0004743 chromosome whole organism disorganized, abnormal ZP:0004744 chromosome whole organism condensed, abnormal ZP:0004745 eye mislocalised anteriorly, abnormal ZP:0004746 digestive tract development delayed, abnormal ZP:0004747 digestive tract development process quality, abnormal ZP:0004748 gut poorly differentiated, abnormal ZP:0004749 mid intestine epithelium morphology, abnormal ZP:0004750 visual perception disrupted, abnormal ZP:0004751 otic vesicle formation process quality, abnormal ZP:0004752 otic placode formation process quality, abnormal ZP:0004753 intermediate cell mass of mesoderm morphology, abnormal ZP:0004754 otic vesicle malformed, abnormal ZP:0004756 caudal vein aplastic, abnormal ZP:0004757 caudal vein plexus absent, abnormal ZP:0004758 post-vent vasculature morphology, abnormal ZP:0004759 cell differentiation disrupted, abnormal ZP:0004760 exocrine pancreas morphology, abnormal ZP:0004761 angiogenesis arrested, abnormal ZP:0004762 embryonic pectoral fin morphogenesis disrupted, abnormal ZP:0004763 scapulocoracoid morphology, abnormal ZP:0004764 scapulocoracoid increased size, abnormal ZP:0004765 ventral mandibular arch shortened, abnormal ZP:0004766 pharyngeal arch 2 shortened, abnormal ZP:0004767 negative regulation of heart rate disrupted, abnormal ZP:0004771 pectoral fin musculature aplastic, abnormal ZP:0004772 neuromast posterior lateral line decreased amount, abnormal ZP:0004773 myotome cellular quality, abnormal ZP:0004774 thymus lacks parts or has fewer parts of type lymphocyte, abnormal ZP:0004775 hypaxial myotome region aplastic, abnormal ZP:0004776 protein prenylation disrupted, abnormal ZP:0004777 melanosome organization disrupted, abnormal ZP:0004778 pigmentation increased occurrence, abnormal ZP:0004779 lens opaque, abnormal ZP:0004780 retinal neural layer lacks parts or has fewer parts of type retinal outer plexiform layer, abnormal ZP:0004781 spinal cord increased curvature, abnormal ZP:0004782 iridophore eye decreased amount, abnormal ZP:0004783 retinal pigmented epithelium irregular spatial pattern, abnormal ZP:0004784 retinal pigmented epithelium hypertrophic, abnormal ZP:0004785 retinal pigmented epithelium irregular thickness, abnormal ZP:0004786 melanosome retinal pigmented epithelium decreased amount, abnormal ZP:0004787 retinal outer nuclear layer apoptotic, abnormal ZP:0004788 retinal outer nuclear layer has fewer parts of type photoreceptor cell, abnormal ZP:0004789 photoreceptor outer segment layer disheveled, abnormal ZP:0004790 photoreceptor cell morphology, abnormal ZP:0004791 photoreceptor cell disorganized, abnormal ZP:0004792 pigmented epithelial cell vacuolated, abnormal ZP:0004793 retinal ganglion cell apoptotic, abnormal ZP:0004794 cation transport arrested, abnormal ZP:0004795 cation transport decreased occurrence, abnormal ZP:0004796 adenohypophysis morphogenesis process quality, abnormal ZP:0004797 somatotropin secreting cell differentiation process quality, abnormal ZP:0004798 prolactin secreting cell differentiation process quality, abnormal ZP:0004799 corticotropin hormone secreting cell differentiation process quality, abnormal ZP:0004800 central nervous system has fewer parts of type white matter, abnormal ZP:0004801 facial nerve motor nucleus absent, abnormal ZP:0004802 motor nucleus of vagal nerve absent, abnormal ZP:0004803 optic chiasm malformed, abnormal ZP:0004804 cranial nerve IX absent, abnormal ZP:0004805 abducens motor nucleus absent, abnormal ZP:0004806 central canal quality, abnormal ZP:0004807 central canal morphology, abnormal ZP:0004808 adenohypophyseal placode decreased size, abnormal ZP:0004809 lateral floor plate composition, abnormal ZP:0004810 trigeminal motor nucleus absent, abnormal ZP:0004811 ethmoid cartilage decreased width, abnormal ZP:0004812 somatotropin secreting cell decreased amount, abnormal ZP:0004813 prolactin secreting cell decreased amount, abnormal ZP:0004814 adrenocorticotropic hormone secreting cell decreased amount, abnormal ZP:0004815 axon primary motor neuron misrouted, abnormal ZP:0004816 retinal ganglion cell displaced to axon diencephalon, abnormal ZP:0004817 cell proliferation in midbrain decreased occurrence, abnormal ZP:0004818 optic tectum physical object quality, abnormal ZP:0004819 ventral mandibular arch quality, abnormal ZP:0004820 developmental pigmentation delayed, abnormal ZP:0004821 embryonic morphogenesis paedomorphic growth, abnormal ZP:0004822 inner ear hypoplastic, abnormal ZP:0004823 head orientation trunk, abnormal ZP:0004824 taxis arrested, abnormal ZP:0004825 swim bladder formation growth quality of occurrent, abnormal ZP:0004826 myotome disorganized, abnormal ZP:0004827 myotome vacuolated, abnormal ZP:0004828 myoseptum perforate, abnormal ZP:0004829 sarcomere muscle cell disorganized, abnormal ZP:0004830 sarcomere muscle cell collapsed, abnormal ZP:0004831 melanocyte lateral larval melanophore stripe decreased amount, abnormal ZP:0004832 skeletal muscle degenerate, abnormal ZP:0004833 endothelial cell development disrupted, abnormal ZP:0004834 spinal cord development disrupted, abnormal ZP:0004835 ventral spinal cord interneuron specification disrupted, abnormal ZP:0004836 auditory receptor cell fate specification process quality, abnormal ZP:0004837 generation of neurons increased rate, abnormal ZP:0004838 taste bud formation decreased process quality, abnormal ZP:0004839 endothelial cell artery morphology, abnormal ZP:0004840 cell brain circular, abnormal ZP:0004841 cell brain dispersed, abnormal ZP:0004842 neuron central nervous system disorganized, abnormal ZP:0004843 epiphysis has extra parts of type neuron, abnormal ZP:0004844 hindbrain has fewer parts of type radial glial cell, abnormal ZP:0004845 hindbrain has fewer parts of type dorsal region neuron, abnormal ZP:0004846 radial glial cell hindbrain increased amount, abnormal ZP:0004847 radial glial cell hindbrain disorganized, abnormal ZP:0004848 midbrain hindbrain boundary increased size, abnormal ZP:0004849 retinal neural layer morphology, abnormal ZP:0004850 retinal neural layer undifferentiated, abnormal ZP:0004851 pericardium distended, abnormal ZP:0004852 polster increased size, abnormal ZP:0004853 somite 5 increased length, abnormal ZP:0004854 glial cell spinal cord decreased amount, abnormal ZP:0004856 primary motor neuron spinal cord increased amount, abnormal ZP:0004857 GABAergic neuron spinal cord decreased amount, abnormal ZP:0004858 cell notochord spherical, abnormal ZP:0004859 pronephric duct increased size, abnormal ZP:0004860 somite increased length, abnormal ZP:0004861 habenula cellular quality, abnormal ZP:0004862 neuron habenula morphology, abnormal ZP:0004863 hair cell posterior macula increased amount, abnormal ZP:0004864 trigeminal ganglion has extra parts of type sensory neuron, abnormal ZP:0004865 sensory neuron trigeminal ganglion apoptotic, abnormal ZP:0004866 integument has fewer parts of type pigment cell, abnormal ZP:0004867 semicircular canal spatial pattern, abnormal ZP:0004868 tela chorioidea morphology, abnormal ZP:0004869 tela chorioidea mislocalised, abnormal ZP:0004870 medial longitudinal fasciculus increased width, abnormal ZP:0004871 caudal tuberculum morphology, abnormal ZP:0004872 hair cell anterior macula increased amount, abnormal ZP:0004873 somite 2 increased length, abnormal ZP:0004874 somite 3 increased length, abnormal ZP:0004875 somite 4 increased length, abnormal ZP:0004877 rhombomere morphology, abnormal ZP:0004878 rhombomere increased size, abnormal ZP:0004879 primary neuron rhombomere increased amount, abnormal ZP:0004880 taste bud physical quality, abnormal ZP:0004881 thyroid primordium increased size, abnormal ZP:0004882 thyroid primordium increased volume, abnormal ZP:0004883 thyroid primordium mislocalised, abnormal ZP:0004884 thyroid primordium disorganized, abnormal ZP:0004885 thyroid primordium physical object quality, abnormal ZP:0004886 thyroid primordium mislocalised ventrally, abnormal ZP:0004887 whole organism has extra parts of type anterior-posterior axis Rohon-Beard neuron, abnormal ZP:0004888 whole organism has extra parts of type anterior-posterior axis primary motor neuron, abnormal ZP:0004889 whole organism has extra parts of type medial-lateral axis Rohon-Beard neuron, abnormal ZP:0004890 trunk has fewer parts of type anterior region melanocyte, abnormal ZP:0004891 melanocyte trunk absent, abnormal ZP:0004892 post-vent region lacks all parts of type pigment cell, abnormal ZP:0004893 posterior lateral line placode has extra parts of type sensory neuron, abnormal ZP:0004894 cell posterior lateral line primordium decreased amount, abnormal ZP:0004895 myofibril pectoral fin disheveled, abnormal ZP:0004896 myoblast pectoral fin decreased amount, abnormal ZP:0004897 roof plate spinal cord region malformed, abnormal ZP:0004898 roof plate spinal cord region separated from roof plate spinal cord region, abnormal ZP:0004899 cell projection roof plate spinal cord region absent, abnormal ZP:0004900 optic cup has fewer parts of type radial glial cell, abnormal ZP:0004901 intersegmental vessel increased mass density, abnormal ZP:0004902 intersegmental vessel has extra parts of type blood vessel, abnormal ZP:0004903 anterior lateral line placode has extra parts of type sensory neuron, abnormal ZP:0004904 rhombic lip cellular motility, abnormal ZP:0004905 epithelium pharyngeal arch 3 physical object quality, abnormal ZP:0004906 pharyngeal vasculature separated from thyroid primordium, abnormal ZP:0004907 CoSA increased amount, abnormal ZP:0004908 VeLD decreased amount, abnormal ZP:0004909 hindbrain interneuron increased amount, abnormal ZP:0004910 CiD increased amount, abnormal ZP:0004911 pectoral fin fold morphology, abnormal ZP:0004912 hindbrain neural keel concave, abnormal ZP:0004913 Mauthner neuron increased amount, abnormal ZP:0004914 axon Mauthner neuron fasciculation, abnormal ZP:0004915 axon primary neuron fasciculation, abnormal ZP:0004917 neuroepithelial cell circular, abnormal ZP:0004918 retinal ganglion cell dead, abnormal ZP:0004919 angiogenesis decreased occurrence, abnormal ZP:0004920 ion homeostasis disrupted, abnormal ZP:0004921 somatic stem cell epidermis decreased amount, abnormal ZP:0004922 vasculature neurohypophysis malformed, abnormal ZP:0004923 NaK ionocyte decreased amount, abnormal ZP:0004924 vH ionocyte decreased amount, abnormal ZP:0004925 sprouting angiogenesis arrested, abnormal ZP:0004926 granulocyte differentiation disrupted, abnormal ZP:0004927 artery aplastic, abnormal ZP:0004928 cardiac ventricle decreased strength, abnormal ZP:0004929 posterior cardinal vein morphology, abnormal ZP:0004930 posterior cardinal vein aplastic, abnormal ZP:0004931 intersegmental artery decreased length, abnormal ZP:0004932 granulocyte immature, abnormal ZP:0004933 proctodeum apoptotic, abnormal ZP:0004934 ventricular zone forebrain apoptotic, abnormal ZP:0004935 presumptive telencephalon necrotic, abnormal ZP:0004936 slow muscle cell somite decreased amount, abnormal ZP:0004937 muscle cell increased occurrence apoptotic process, abnormal ZP:0004938 muscle cell increased occurrence cell death, abnormal ZP:0004939 apoptotic process decreased occurrence, abnormal ZP:0004940 delamination involved in gastrulation with mouth forming second disrupted, abnormal ZP:0004941 Kupffer's vesicle development disrupted, abnormal ZP:0004942 heart mislocalised radially, abnormal ZP:0004943 hypoblast decreased thickness, abnormal ZP:0004944 whole organism lacks all parts of type Kupffer's vesicle, abnormal ZP:0004945 epithelial cell differentiation process quality, abnormal ZP:0004947 otic placode split, abnormal ZP:0004949 inner ear duplicated, abnormal ZP:0004950 inner ear split, abnormal ZP:0004951 integument physical object quality, abnormal ZP:0004952 pharyngeal arch 2 skeleton quality, abnormal ZP:0004953 cranial cartilage mislocalised posteriorly, abnormal ZP:0004954 pharyngeal arch cartilage mislocalised posteriorly, abnormal ZP:0004955 auditory capsule decreased size, abnormal ZP:0004956 ceratobranchial cartilage bent, abnormal ZP:0004957 pharyngeal arch 1 aplastic, abnormal ZP:0004958 otic vesicle protrusion morphology, abnormal ZP:0004959 pillar of the semicircular canal aplastic, abnormal ZP:0004960 epiphysis decreased size, abnormal ZP:0004961 apoptotic DNA fragmentation increased rate, abnormal ZP:0004962 apoptotic process increased rate, abnormal ZP:0004963 immature eye apoptotic, abnormal ZP:0004964 blood vessel endothelial cell proliferation involved in sprouting angiogenesis disrupted, abnormal ZP:0004965 canonical Wnt signaling pathway involved in neural crest cell differentiation disrupted, abnormal ZP:0004966 cell-cell junction organization disrupted, abnormal ZP:0004967 negative regulation of Notch signaling pathway disrupted, abnormal ZP:0004968 pigment cell differentiation disrupted, abnormal ZP:0004969 caudal fin morphology, abnormal ZP:0004970 trunk neural crest cell positional polarity, abnormal ZP:0004971 trunk neural crest cell decreased amount, abnormal ZP:0004972 axon habenula misrouted, abnormal ZP:0004973 interpeduncular nucleus tegmentum structure, abnormal ZP:0004974 blood vessel endothelial cell apoptotic, abnormal ZP:0004975 axon CaP motoneuron branched, abnormal ZP:0004976 cardiac ventricle development disrupted, abnormal ZP:0004977 blood circulation decreased occurrence, abnormal ZP:0004978 cardiac ventricle shape, abnormal ZP:0004979 sarcomere ventricular myocardium sparse, abnormal ZP:0004980 ball size, abnormal ZP:0004981 nucleate erythrocyte blood decreased amount, abnormal ZP:0004982 hindbrain apoptotic, abnormal ZP:0004983 hindbrain edematous, abnormal ZP:0004984 hindbrain aplastic, abnormal ZP:0004985 midbrain hindbrain boundary amorphous, abnormal ZP:0004986 extension degenerate, abnormal ZP:0004987 heart tube decreased thickness, abnormal ZP:0004988 heart tube collapsed, abnormal ZP:0004989 forebrain midbrain boundary amorphous, abnormal ZP:0004990 fin development disrupted, abnormal ZP:0004991 cell migration involved in heart development decreased rate, abnormal ZP:0004992 fin morphology, abnormal ZP:0004993 heart constricted, abnormal ZP:0004994 post-vent region curved lateral, abnormal ZP:0004995 atrioventricular canal increased length, abnormal ZP:0004996 melanocyte scale decreased amount, abnormal ZP:0004997 iridophore spatial pattern, abnormal ZP:0004998 swim bladder development process quality, abnormal ZP:0004999 habenular commissure aplastic, abnormal ZP:0005000 xanthophore low saturation, abnormal ZP:0005001 xanthophore increased distribution, abnormal ZP:0005002 axon retinal ganglion cell irregular spatial pattern, abnormal ZP:0005003 axon retinal ganglion cell aggregated, abnormal ZP:0005004 axon retinal ganglion cell displaced, abnormal ZP:0005005 retinal ganglion cell displaced to axon ipsilateral side eye, abnormal ZP:0005006 neuron-neuron synaptic transmission process quality, abnormal ZP:0005007 posterior lateral line neuromast hair cell development process quality, abnormal ZP:0005008 neuromast hair cell physical object quality, abnormal ZP:0005009 nucleate erythrocyte increased amount, abnormal ZP:0005010 hair cell quality, abnormal ZP:0005011 hair cell morphology, abnormal ZP:0005012 axis curved, abnormal ZP:0005013 cilium ciliated olfactory receptor neuron paralysed, abnormal ZP:0005014 ciliated olfactory receptor neuron increased rate cilium-dependent cell motility, abnormal ZP:0005015 ciliated olfactory receptor neuron decreased process quality cilium-dependent cell motility, abnormal ZP:0005016 startle response occurrence, abnormal ZP:0005017 hypothalamus development disrupted, abnormal ZP:0005018 afferent axon development in posterior lateral line nerve decreased occurrence, abnormal ZP:0005019 melanocyte dispersed, abnormal ZP:0005020 muscle pioneer somite decreased amount, abnormal ZP:0005021 heart tube elongated, abnormal ZP:0005022 post-vent region coiled, abnormal ZP:0005023 nucleus slow muscle cell decreased amount, abnormal ZP:0005024 skeletal muscle cell somite disorganized, abnormal ZP:0005025 nucleus skeletal muscle cell shape, abnormal ZP:0005026 establishment or maintenance of epithelial cell apical/basal polarity process quality, abnormal ZP:0005027 retinal inner nuclear layer distributed, abnormal ZP:0005028 third ventricle absent, abnormal ZP:0005029 third ventricle decreased volume, abnormal ZP:0005030 neuroblast (sensu Vertebrata) neural tube mislocalised, abnormal ZP:0005031 outer limiting membrane aplastic, abnormal ZP:0005032 retinal outer nuclear layer distributed, abnormal ZP:0005033 retinal cone cell mislocalised, abnormal ZP:0005034 retinal rod cell mislocalised, abnormal ZP:0005035 retinal rod cell disorganized, abnormal ZP:0005036 retinal rod cell deformed, abnormal ZP:0005037 retinal rod cell increased distribution, abnormal ZP:0005038 photoreceptor outer segment retinal rod cell decreased volume, abnormal ZP:0005039 Muller cell mislocalised, abnormal ZP:0005040 centrosome neuroepithelial cell mislocalised, abnormal ZP:0005041 retinal ganglion cell disorganized, abnormal ZP:0005042 retinal ganglion cell increased distribution, abnormal ZP:0005043 actin filament polymerization increased occurrence, abnormal ZP:0005044 eye neoplastic, abnormal ZP:0005047 caudal fin falciform, abnormal ZP:0005048 myeloid lineage restricted progenitor cell mislocalised, abnormal ZP:0005049 cardiovascular system morphology, abnormal ZP:0005050 cardiovascular system non-functional, abnormal ZP:0005051 gut edematous, abnormal ZP:0005053 intersegmental artery attached to intersegmental vessel, abnormal ZP:0005054 intersegmental vessel irregular spatial pattern, abnormal ZP:0005055 dorsal longitudinal anastomotic vessel irregular spatial pattern, abnormal ZP:0005056 subintestinal vein irregular spatial pattern, abnormal ZP:0005057 supraintestinal artery irregular spatial pattern, abnormal ZP:0005058 thoracic duct decreased size, abnormal ZP:0005059 chemical synaptic transmission amplitude, abnormal ZP:0005060 chemical synaptic transmission decreased intensity, abnormal ZP:0005061 visual perception decreased occurrence, abnormal ZP:0005062 retinal ganglion cell structure, abnormal ZP:0005063 axon retinal ganglion cell defasciculated, abnormal ZP:0005064 cell proliferation in hindbrain increased occurrence, abnormal ZP:0005065 cell proliferation in forebrain increased occurrence, abnormal ZP:0005066 forebrain neuron development decreased process quality, abnormal ZP:0005067 cell proliferation in midbrain increased occurrence, abnormal ZP:0005068 Rohon-Beard neuron spinal cord decreased amount, abnormal ZP:0005069 neuron cerebellum decreased amount, abnormal ZP:0005070 forebrain has fewer parts of type neuron, abnormal ZP:0005071 Meckel's cartilage decreased distance ceratohyal cartilage, abnormal ZP:0005072 neuron projection motor neuron decreased size, abnormal ZP:0005073 motor neuron perpendicular to neuron projection spinal cord, abnormal ZP:0005074 establishment of mitotic spindle orientation decreased process quality, abnormal ZP:0005075 secondary neural tube formation decreased process quality, abnormal ZP:0005076 neuroepithelial cell neural keel disorganized, abnormal ZP:0005077 neuroepithelial cell neural rod disorganized, abnormal ZP:0005078 central canal branched, abnormal ZP:0005079 central canal disorganized, abnormal ZP:0005080 neuroepithelial cell neural tube disorganized, abnormal ZP:0005082 mitotic spindle neuroepithelial cell direction, abnormal ZP:0005083 exocrine pancreas development delayed, abnormal ZP:0005084 anterior pancreatic bud decreased size, abnormal ZP:0005085 pancreatic duct aplastic, abnormal ZP:0005086 exocrine cell absent, abnormal ZP:0005087 calcium ion transport disrupted, abnormal ZP:0005088 embryonic digestive tract morphogenesis disrupted, abnormal ZP:0005089 cardiac ventricle orientation atrium, abnormal ZP:0005090 heart rudiment morphology, abnormal ZP:0005091 pancreatic bud mislocalised, abnormal ZP:0005092 anterior lateral plate mesoderm morphology, abnormal ZP:0005093 regulation of cell cycle arrest disrupted, abnormal ZP:0005094 mitotic cell cycle arrest increased occurrence, abnormal ZP:0005095 somite lacks parts or has fewer parts of type fast muscle cell, abnormal ZP:0005096 pharyngeal arch 3-7 skeleton decreased length, abnormal ZP:0005097 mouth open, abnormal ZP:0005098 cranium has extra parts of type cranial cartilage, abnormal ZP:0005099 branchiostegal ray 3 shape, abnormal ZP:0005100 branchiostegal ray 3 aplastic, abnormal ZP:0005101 palatoquadrate cartilage curved lateral, abnormal ZP:0005102 palatoquadrate cartilage curved medial, abnormal ZP:0005103 cartilage element mislocalised, abnormal ZP:0005104 osteoblast decreased amount, abnormal ZP:0005105 nucleate erythrocyte increased accumulation ventral wall of dorsal aorta, abnormal ZP:0005107 muscle misaligned with myofibril myofibril muscle, abnormal ZP:0005108 T-tubule muscle broken, abnormal ZP:0005109 muscle misaligned with T-tubule T-tubule muscle, abnormal ZP:0005110 sarcolemma muscle broken, abnormal ZP:0005111 myofibril muscle cell damaged, abnormal ZP:0005113 axis elongation disrupted, abnormal ZP:0005114 anterior/posterior axis specification disrupted, abnormal ZP:0005115 gut lateralized, abnormal ZP:0005116 heart mislocalised laterally, abnormal ZP:0005117 liver mislocalised laterally, abnormal ZP:0005118 pancreas mislocalised laterally, abnormal ZP:0005119 head increased distance post-vent region, abnormal ZP:0005120 anterior-posterior axis trunk shortened, abnormal ZP:0005121 branching morphogenesis of a nerve disrupted, abnormal ZP:0005122 peripheral nervous system neuron axonogenesis disrupted, abnormal ZP:0005123 cranial nerve morphology, abnormal ZP:0005124 pancreas development decreased process quality, abnormal ZP:0005125 swim bladder decreased size, abnormal ZP:0005126 epithelium swim bladder decreased size, abnormal ZP:0005127 parasphenoid shape, abnormal ZP:0005128 parasphenoid decreased length, abnormal ZP:0005129 hepatic duct morphology, abnormal ZP:0005130 hepatic duct decreased size, abnormal ZP:0005131 hepatic duct aplastic, abnormal ZP:0005132 intestine decreased width, abnormal ZP:0005133 palatoquadrate cartilage shape, abnormal ZP:0005134 ethmoid cartilage decreased length, abnormal ZP:0005135 esophageal epithelium decreased size, abnormal ZP:0005136 trabecula cranii shape, abnormal ZP:0005137 extrapancreatic duct physical object quality, abnormal ZP:0005138 palate shape, abnormal ZP:0005139 palate square, abnormal ZP:0005140 hepatocyte mislocalised, abnormal ZP:0005141 pectoral fin morphogenesis arrested, abnormal ZP:0005142 pectoral fin field morphology, abnormal ZP:0005145 mesodermal cell migration decreased occurrence, abnormal ZP:0005146 paraxial mesodermal cell differentiation process quality, abnormal ZP:0005147 paraxial mesodermal cell differentiation decreased process quality, abnormal ZP:0005148 tail bud increased size, abnormal ZP:0005149 tail bud cellular quality, abnormal ZP:0005150 tail bud decreased cellular motility, abnormal ZP:0005151 segmental plate poorly differentiated, abnormal ZP:0005152 segmental plate decreased cellular motility, abnormal ZP:0005153 somite trunk absent, abnormal ZP:0005155 post-vent region has extra parts of type somite, abnormal ZP:0005156 protein N-linked glycosylation decreased occurrence, abnormal ZP:0005157 lipooligosaccharide catabolic process increased occurrence, abnormal ZP:0005158 secondary motor neuron spinal cord increased amount, abnormal ZP:0005159 ethmoid cartilage shape, abnormal ZP:0005160 cartilage development process quality, abnormal ZP:0005161 pharyngeal arch 3-7 skeleton hypoplastic, abnormal ZP:0005162 cleithrum ossified, abnormal ZP:0005163 opercle ossified, abnormal ZP:0005164 osteoblast opercle poorly differentiated, abnormal ZP:0005165 maxilla ossified, abnormal ZP:0005166 branchiostegal ray ossified, abnormal ZP:0005167 osteoblast branchiostegal ray poorly differentiated, abnormal ZP:0005168 mouth ventrally rotated head, abnormal ZP:0005169 parasphenoid ossified, abnormal ZP:0005170 entopterygoid ossified, abnormal ZP:0005171 vertebra ossified, abnormal ZP:0005172 ceratobranchial 5 bone ossified, abnormal ZP:0005173 palatoquadrate cartilage hypoplastic, abnormal ZP:0005174 hyosymplectic cartilage hypoplastic, abnormal ZP:0005175 notochordal ossification ossified, abnormal ZP:0005176 cell population proliferation decreased process quality, abnormal ZP:0005177 neuron projection morphogenesis disrupted, abnormal ZP:0005178 Kupffer's vesicle deformed, abnormal ZP:0005179 forerunner cell group shape, abnormal ZP:0005180 forerunner cell group increased width, abnormal ZP:0005181 forerunner cell group malformed, abnormal ZP:0005182 bile ductule liver and biliary system increased amount, abnormal ZP:0005183 intrahepatic bile duct liver and biliary system decreased amount, abnormal ZP:0005184 prechordal plate mislocalised posteriorly, abnormal ZP:0005185 liver decreased functionality, abnormal ZP:0005186 anatomical axis whole organism curved, abnormal ZP:0005187 mesoderm head increased width, abnormal ZP:0005188 exocrine pancreas mislocalised, abnormal ZP:0005189 retinal inner plexiform layer disorganized, abnormal ZP:0005190 synapse retinal inner plexiform layer disorganized, abnormal ZP:0005191 intestine mislocalised, abnormal ZP:0005192 photoreceptor inner segment layer disorganized, abnormal ZP:0005193 cell intrahepatic bile duct decreased amount, abnormal ZP:0005194 multicellular organism growth decreased rate, abnormal ZP:0005195 adipose tissue development disrupted, abnormal ZP:0005196 adipose tissue increased mass, abnormal ZP:0005197 fat cell hypertrophic, abnormal ZP:0005198 lipid droplet fat cell increased size, abnormal ZP:0005199 DNA methylation on cytosine decreased occurrence, abnormal ZP:0005200 intermediate cell mass of mesoderm apoptotic, abnormal ZP:0005201 blood vasculature decreased amount, abnormal ZP:0005202 lens apoptotic, abnormal ZP:0005203 retina distended, abnormal ZP:0005204 pioneer neuron olfactory placode absent, abnormal ZP:0005205 pioneer neuron olfactory placode decreased amount, abnormal ZP:0005206 optic tract branchiness, abnormal ZP:0005207 cell population proliferation decreased rate, abnormal ZP:0005208 pharyngeal muscle development disrupted, abnormal ZP:0005209 semicircular canal morphogenesis arrested, abnormal ZP:0005210 pharynx development hypotrophic growth, abnormal ZP:0005211 cardiac ventricle increased width, abnormal ZP:0005212 cardiac ventricle shortened, abnormal ZP:0005213 neural crest cell hindbrain decreased amount, abnormal ZP:0005214 pharynx malformed, abnormal ZP:0005215 heart straight, abnormal ZP:0005216 neural crest cell midbrain decreased amount, abnormal ZP:0005217 notochord mislocalised anteriorly, abnormal ZP:0005218 bulbus arteriosus decreased length, abnormal ZP:0005219 bulbus arteriosus immature, abnormal ZP:0005220 smooth muscle bulbus arteriosus morphology, abnormal ZP:0005221 levator arcus palatini aplastic, abnormal ZP:0005222 macula hypoplastic, abnormal ZP:0005223 macula decreased amount, abnormal ZP:0005224 mesenchyme decreased size, abnormal ZP:0005225 semicircular canal hypoplastic, abnormal ZP:0005226 atrium increased width, abnormal ZP:0005227 atrium decreased angle to cardiac ventricle, abnormal ZP:0005228 dilatator operculi aplastic, abnormal ZP:0005229 mouth closure incomplete, abnormal ZP:0005230 mouth mislocalised posteriorly, abnormal ZP:0005231 thymus hypoplastic, abnormal ZP:0005232 thymus aplastic, abnormal ZP:0005233 pharyngeal pouch malformed, abnormal ZP:0005234 pharyngeal pouch aplastic, abnormal ZP:0005235 pharyngeal pouch decreased amount, abnormal ZP:0005236 Meckel's cartilage inverted, abnormal ZP:0005237 Meckel's cartilage mislocalised ventrally, abnormal ZP:0005238 glossopharyngeal ganglion absent, abnormal ZP:0005239 muscle pharyngeal arch aplastic, abnormal ZP:0005240 parachordal cartilage mislocalised posteriorly, abnormal ZP:0005241 pharyngeal arch cartilage fused with pharyngeal arch cartilage, abnormal ZP:0005242 epibranchial ganglion increased size, abnormal ZP:0005243 epibranchial ganglion fused with epibranchial ganglion, abnormal ZP:0005244 neural crest cell pharyngeal arch 2 absent, abnormal ZP:0005245 neural crest cell pharyngeal arch 2 decreased amount, abnormal ZP:0005246 neural crest cell pharyngeal arch 1 present, abnormal ZP:0005247 neural crest cell pharyngeal arch 1 decreased amount, abnormal ZP:0005248 neural crest cell pharyngeal arch 3-7 absent, abnormal ZP:0005249 pharyngeal arch 3-7 fused with neural crest cell neural crest cell pharyngeal arch 3-7, abnormal ZP:0005250 aortic arch decreased amount, abnormal ZP:0005251 constrictor dorsalis morphology, abnormal ZP:0005252 cardiac muscle cell circular, abnormal ZP:0005253 gonad morphology, abnormal ZP:0005254 gonad apoptotic, abnormal ZP:0005255 whole organism lacks all parts of type sperm, abnormal ZP:0005256 sperm decreased amount, abnormal ZP:0005257 germ line cell absent, abnormal ZP:0005258 germ line cell apoptotic, abnormal ZP:0005259 germ line cell decreased amount, abnormal ZP:0005260 olfactory placode morphology, abnormal ZP:0005261 basibranchial decreased size, abnormal ZP:0005262 basibranchial undulate, abnormal ZP:0005263 palatoquadrate cartilage mislocalised posteriorly, abnormal ZP:0005264 ceratohyal cartilage displaced, abnormal ZP:0005265 hyosymplectic cartilage mislocalised posteriorly, abnormal ZP:0005266 cranial cartilage shape, abnormal ZP:0005267 cranial cartilage malformed, abnormal ZP:0005268 basihyal cartilage undulate, abnormal ZP:0005269 compact myelin hindbrain decreased amount, abnormal ZP:0005270 oligodendrocyte hindbrain morphology, abnormal ZP:0005271 axon spinal cord decreased length, abnormal ZP:0005272 oligodendrocyte spinal cord morphology, abnormal ZP:0005274 epiboly disrupted, abnormal ZP:0005275 blood mislocalised, abnormal ZP:0005276 blood vessel endothelial cell dorsal aorta apoptotic, abnormal ZP:0005277 blood vessel endothelial cell posterior cardinal vein apoptotic, abnormal ZP:0005278 blood vasculature degenerate, abnormal ZP:0005279 head color, abnormal ZP:0005280 intersegmental vessel decreased diameter, abnormal ZP:0005281 intersegmental vessel absent blood circulation, abnormal ZP:0005282 endothelial cell apoptotic, abnormal ZP:0005283 blood vessel development delayed, abnormal ZP:0005284 hemopoiesis decreased occurrence, abnormal ZP:0005285 neuron apoptotic process increased occurrence, abnormal ZP:0005286 G1 to G0 transition disrupted, abnormal ZP:0005287 angioblastic mesenchymal cell lateral plate mesoderm cellular motility, abnormal ZP:0005288 axial vasculature apoptotic, abnormal ZP:0005289 axial vasculature decreased diameter, abnormal ZP:0005290 motor neuron head disorganized, abnormal ZP:0005291 proliferative region neural tube decreased functionality, abnormal ZP:0005292 caudal vein plexus apoptotic, abnormal ZP:0005293 proliferative region caudal vein plexus decreased functionality, abnormal ZP:0005294 neural crest cell pharyngeal arch 3-7 decreased amount, abnormal ZP:0005295 optic vein morphology, abnormal ZP:0005296 inner optic circle morphology, abnormal ZP:0005297 atrioventricular valve amorphous, abnormal ZP:0005298 endocardial ring amorphous, abnormal ZP:0005299 posterior neural tube apoptotic, abnormal ZP:0005300 egg activation disrupted, abnormal ZP:0005301 meiotic sister chromatid cohesion involved in meiosis II disrupted, abnormal ZP:0005302 oocyte microtubule cytoskeleton organization disrupted, abnormal ZP:0005303 ribonucleoprotein complex assembly disrupted, abnormal ZP:0005304 embryonic camera-type eye development delayed, abnormal ZP:0005305 actin cytoskeleton reorganization disrupted, abnormal ZP:0005306 sperm aster formation disrupted, abnormal ZP:0005307 meiotic metaphase II plate congression disrupted, abnormal ZP:0005309 sister chromosome movement towards spindle pole involved in meiotic sister chromatid segregation disrupted, abnormal ZP:0005311 astral microtubule blastomere disorganized, abnormal ZP:0005312 aster blastomere mislocalised, abnormal ZP:0005313 actin filament blastomere branched, abnormal ZP:0005314 cortical actin cytoskeleton blastomere morphology, abnormal ZP:0005315 blastomere disrupted astral microtubule organization, abnormal ZP:0005316 cortical microtubule cytoskeleton blastomere disorganized, abnormal ZP:0005317 cleavage furrow blastomere absent, abnormal ZP:0005318 P granule blastomere decreased size, abnormal ZP:0005319 mitotic spindle blastomere disorganized, abnormal ZP:0005320 sinus venosus decreased functionality, abnormal ZP:0005321 meiotic spindle unfertilized egg bent, abnormal ZP:0005322 microtubule bundle unfertilized egg absent, abnormal ZP:0005323 atrioventricular valve decreased diameter, abnormal ZP:0005324 endocardial ring decreased size, abnormal ZP:0005325 erythroid lineage cell decreased amount, abnormal ZP:0005326 interkinetic nuclear migration disrupted, abnormal ZP:0005327 presumptive neural retina decreased thickness, abnormal ZP:0005328 microtubule cytoskeleton presumptive neural retina disorganized, abnormal ZP:0005329 whole organism semi-lethal (sensu genetics), abnormal ZP:0005330 intersegmental vessel arrested, abnormal ZP:0005331 intersegmental vessel variability of size, abnormal ZP:0005332 endothelial tip cell intersegmental vessel shape, abnormal ZP:0005334 anterior region head truncated, abnormal ZP:0005335 EVL lacks parts or has fewer parts of type bicellular tight junction EVL, abnormal ZP:0005336 bicellular tight junction EVL decreased amount, abnormal ZP:0005337 blood island increased size, abnormal ZP:0005338 male gonad development delayed, abnormal ZP:0005339 male gonad development postdisplaced growth, abnormal ZP:0005340 female gonad development arrested, abnormal ZP:0005341 female gonad development aplastic growth, abnormal ZP:0005342 female organism absent, abnormal ZP:0005343 ovary aplastic, abnormal ZP:0005344 ovarian follicle stage I aplastic, abnormal ZP:0005345 primordial germ cell shape, abnormal ZP:0005346 primordial germ cell decreased cellular motility, abnormal ZP:0005347 primordial germ cell lacks all parts of type bleb primordial germ cell, abnormal ZP:0005348 primordial germ cell decreased occurrence cell motility, abnormal ZP:0005349 somitogenesis increased duration, abnormal ZP:0005350 proctodeum mislocalised anteriorly, abnormal ZP:0005351 anterior-posterior axis somite increased length, abnormal ZP:0005352 trunk has fewer parts of type myotome, abnormal ZP:0005353 anal fin mislocalised anteriorly, abnormal ZP:0005354 dorsal fin mislocalised anteriorly, abnormal ZP:0005355 vertebral column has fewer parts of type vertebra, abnormal ZP:0005357 cell proliferation involved in compound eye morphogenesis increased occurrence, abnormal ZP:0005358 retina lacks all parts of type amacrine cell, abnormal ZP:0005359 retina has fewer parts of type amacrine cell, abnormal ZP:0005360 proliferative region retina increased size, abnormal ZP:0005361 cranial nerve II decreased thickness, abnormal ZP:0005362 cranial nerve II hypoplastic, abnormal ZP:0005364 ciliary marginal zone increased size, abnormal ZP:0005367 auditory capsule morphology, abnormal ZP:0005369 left-right axis whole organism increased width, abnormal ZP:0005370 retinal pigmented epithelium forebrain mislocalized adaxially, abnormal ZP:0005371 macula utricle increased occurrence cell death, abnormal ZP:0005372 caudal fin upturned, abnormal ZP:0005373 macula saccule increased occurrence cell death, abnormal ZP:0005374 Kupffer's vesicle decreased volume, abnormal ZP:0005375 Kupffer's vesicle unlumenized, abnormal ZP:0005376 epithelial cell Kupffer's vesicle apical-basal polarity, abnormal ZP:0005377 forerunner cell group spatial pattern, abnormal ZP:0005378 forerunner cell group circular, abnormal ZP:0005379 forerunner cell group mislocalised, abnormal ZP:0005380 forerunner cell group orientation forerunner cell group, abnormal ZP:0005381 forerunner cell group detached from forerunner cell group, abnormal ZP:0005382 pseudopodium forerunner cell group direction, abnormal ZP:0005383 heart tube positional polarity, abnormal ZP:0005384 post-vent region undulate, abnormal ZP:0005385 ventricular system increased accumulation cerebral spinal fluid, abnormal ZP:0005386 caudal vein plexus perforate, abnormal ZP:0005387 JNK cascade disrupted, abnormal ZP:0005388 Wnt signaling pathway disrupted, abnormal ZP:0005389 heart split, abnormal ZP:0005390 chondrocyte differentiation process quality, abnormal ZP:0005391 retinal ganglion cell axon guidance arrested, abnormal ZP:0005392 embryonic cranial skeleton morphogenesis process quality, abnormal ZP:0005393 embryonic skeletal joint morphogenesis process quality, abnormal ZP:0005394 face morphogenesis process quality, abnormal ZP:0005395 floor plate hypoplastic, abnormal ZP:0005396 inner ear wholly anterioralized, abnormal ZP:0005397 inner ear has extra parts of type anterior macula, abnormal ZP:0005398 optic chiasm aplastic, abnormal ZP:0005399 posterior macula aplastic, abnormal ZP:0005400 horizontal myoseptum hypoplastic, abnormal ZP:0005401 head retracted, abnormal ZP:0005402 neural tube decreased thickness, abnormal ZP:0005403 joint mandibular arch skeleton malformed, abnormal ZP:0005404 pharyngeal arch 2 skeleton hypoplastic, abnormal ZP:0005405 joint pharyngeal arch 2 skeleton malformed, abnormal ZP:0005406 chondrocyte pharyngeal arch 3-7 absent, abnormal ZP:0005407 pars superior ear has extra parts of type anterior crista, abnormal ZP:0005408 axon primary motor neuron disorganized, abnormal ZP:0005409 axon primary motor neuron decreased amount, abnormal ZP:0005410 axon secondary motor neuron absent, abnormal ZP:0005411 cell body secondary motor neuron decreased amount, abnormal ZP:0005412 axon retinal ganglion cell disorganized, abnormal ZP:0005413 retinal ganglion cell displaced to axon eye, abnormal ZP:0005414 regulation of BMP signaling pathway disrupted, abnormal ZP:0005415 cardiac ventricle morphology, abnormal ZP:0005416 atrium deformed, abnormal ZP:0005417 cilium or flagellum-dependent cell motility disrupted, abnormal ZP:0005418 smoothened signaling pathway disrupted, abnormal ZP:0005419 axoneme assembly disrupted, abnormal ZP:0005421 Kupffer's vesicle altered number of axonemal microtubule ciliated cell, abnormal ZP:0005422 axoneme Kupffer's vesicle disorganized, abnormal ZP:0005423 gut position, abnormal ZP:0005424 liver position, abnormal ZP:0005425 liver inverted, abnormal ZP:0005426 pancreas position, abnormal ZP:0005427 pancreas inverted, abnormal ZP:0005428 heart tube inverted, abnormal ZP:0005429 heart tube symmetry, abnormal ZP:0005430 heart tube straight, abnormal ZP:0005431 nervous system necrotic, abnormal ZP:0005432 atrium inverted, abnormal ZP:0005433 lateral floor plate aplastic, abnormal ZP:0005434 medial floor plate morphology, abnormal ZP:0005435 roof of mouth development disrupted, abnormal ZP:0005436 trabecula communis cleft, abnormal ZP:0005437 sensory perception of sound decreased occurrence, abnormal ZP:0005438 hair cell macula utricle decreased amount, abnormal ZP:0005439 hair cell lateral crista decreased amount, abnormal ZP:0005440 hair cell posterior macula absent, abnormal ZP:0005441 hair cell posterior macula decreased amount, abnormal ZP:0005442 semicircular canal immature, abnormal ZP:0005443 hair cell posterior crista decreased amount, abnormal ZP:0005444 hair cell anterior crista decreased amount, abnormal ZP:0005445 sagitta decreased size, abnormal ZP:0005446 sagitta immature, abnormal ZP:0005447 integument ionocyte morphology, abnormal ZP:0005448 hair cell macula saccule decreased amount, abnormal ZP:0005449 neuromast hair cell has fewer parts of type stereocilium neuromast hair cell, abnormal ZP:0005450 neuromast hair cell has fewer parts of type kinocilium neuromast hair cell, abnormal ZP:0005451 kinocilium neuromast hair cell truncated, abnormal ZP:0005452 establishment or maintenance of epithelial cell apical/basal polarity disrupted, abnormal ZP:0005453 ventral region diencephalon structure, abnormal ZP:0005454 centrosome neural rod mislocalised, abnormal ZP:0005455 axoneme neural rod irregular spatial pattern, abnormal ZP:0005456 centrosome neural tube mislocalised, abnormal ZP:0005457 protein localization to adherens junction disrupted, abnormal ZP:0005459 DEL position, abnormal ZP:0005460 cerebellar central artery disorganized, abnormal ZP:0005461 inner optic circle decreased amount, abnormal ZP:0005462 primary motor neuron branched, abnormal ZP:0005463 intersegmental artery disrupted sprouting angiogenesis, abnormal ZP:0005464 subintestinal vein disrupted sprouting angiogenesis, abnormal ZP:0005466 respiratory burst decreased process quality, abnormal ZP:0005467 neuron-neuron synaptic transmission decreased process quality, abnormal ZP:0005468 sensory perception of sound decreased process quality, abnormal ZP:0005469 regulation of proton-transporting ATPase activity, rotational mechanism decreased process quality, abnormal ZP:0005470 synaptic vesicle maturation decreased process quality, abnormal ZP:0005471 regulation of cellular pH reduction decreased process quality, abnormal ZP:0005472 synaptic vesicle lumen acidification decreased process quality, abnormal ZP:0005473 vacuolar proton-transporting V-type ATPase, V1 domain neuromast hair cell mislocalised, abnormal ZP:0005474 synaptic vesicle lumen neuromast hair cell decreased acidity, abnormal ZP:0005475 dorsal telencephalon morphology, abnormal ZP:0005477 xanthoblast axis mislocalised medially, abnormal ZP:0005479 melanoblast axis mislocalised medially, abnormal ZP:0005480 glomerular capillary pronephros dilated, abnormal ZP:0005481 anatomical axis whole organism curved dorsal, abnormal ZP:0005482 cell projection pronephric podocyte absent, abnormal ZP:0005483 pericardium broken, abnormal ZP:0005484 neuron differentiation decreased occurrence, abnormal ZP:0005485 neuron brain undifferentiated, abnormal ZP:0005486 hindbrain has fewer parts of type neuron, abnormal ZP:0005488 tail bud umbonate, abnormal ZP:0005489 cardiac ventricle elliptic, abnormal ZP:0005490 cardiac ventricle immature, abnormal ZP:0005491 cardiac ventricle curvature, abnormal ZP:0005492 cardiac muscle cell cardiac ventricle shape, abnormal ZP:0005493 bulbus arteriosus increased length, abnormal ZP:0005494 atrium malformed, abnormal ZP:0005495 atrium decreased contractility, abnormal ZP:0005496 atrium non-contractile, abnormal ZP:0005497 atrium decreased strength, abnormal ZP:0005498 myofibril atrium disorganized, abnormal ZP:0005499 cardiac jelly distended, abnormal ZP:0005500 digestive tract mesoderm development disrupted, abnormal ZP:0005501 anterior/posterior axis specification process quality, abnormal ZP:0005502 cerebellum morphogenesis disrupted, abnormal ZP:0005503 cerebellum structural organization disrupted, abnormal ZP:0005504 midbrain-hindbrain boundary maturation disrupted, abnormal ZP:0005505 forebrain anterior/posterior pattern specification disrupted, abnormal ZP:0005506 forebrain dorsal/ventral pattern formation disrupted, abnormal ZP:0005507 cerebellar granule cell precursor proliferation increased occurrence, abnormal ZP:0005508 chemokine production disrupted, abnormal ZP:0005509 DNA hypomethylation chronic, abnormal ZP:0005510 canonical Wnt signaling pathway disrupted, abnormal ZP:0005511 canonical Wnt signaling pathway decreased process quality, abnormal ZP:0005512 endodermal digestive tract morphogenesis disrupted, abnormal ZP:0005513 DNA demethylation increased occurrence, abnormal ZP:0005514 negative regulation of canonical Wnt signaling pathway disrupted, abnormal ZP:0005515 cardiac ventricle mislocalised radially, abnormal ZP:0005516 dorsal aorta decreased process quality blood circulation, abnormal ZP:0005517 blood dorsal aorta decreased fluid flow, abnormal ZP:0005518 pharynx immature, abnormal ZP:0005519 postoptic commissure morphology, abnormal ZP:0005520 dorsal region cerebellum curved, abnormal ZP:0005521 dorsal region cerebellum increased size, abnormal ZP:0005522 ventral region cerebellum decreased thickness, abnormal ZP:0005523 diencephalon flattened, abnormal ZP:0005524 forebrain wholly dorsalized, abnormal ZP:0005525 liver has extra parts of type hepatocyte, abnormal ZP:0005526 liver primordium increased size, abnormal ZP:0005527 liver primordium aplastic, abnormal ZP:0005528 neuromast has extra parts of type neuromast hair cell, abnormal ZP:0005530 caudal commissure morphology, abnormal ZP:0005531 abnormal(ly) disrupted neutrophil aggregation ZP:0005532 optic tectum flattened, abnormal ZP:0005533 ventral fin fold morphology, abnormal ZP:0005534 anterior commissure morphology, abnormal ZP:0005535 anterior region neuroectoderm decreased size, abnormal ZP:0005536 posterior lateral line primordium morphology, abnormal ZP:0005537 atrioventricular canal obstructed, abnormal ZP:0005538 endocardium hyperplastic, abnormal ZP:0005539 intestine immature, abnormal ZP:0005540 intestine poorly differentiated, abnormal ZP:0005541 fin bud immature, abnormal ZP:0005542 pancreatic bud decreased size, abnormal ZP:0005543 atrioventricular canal endocardium fused with atrioventricular canal endocardium, abnormal ZP:0005544 optic nerve head decreased thickness, abnormal ZP:0005545 presumptive atrium heart tube mislocalised radially, abnormal ZP:0005546 atrioventricular valve malformed, abnormal ZP:0005547 hepatocyte increased amount, abnormal ZP:0005548 heart morphogenesis occurrence, abnormal ZP:0005549 excretion disrupted, abnormal ZP:0005550 post-anal tail morphogenesis process quality, abnormal ZP:0005551 cell proliferation involved in kidney development increased occurrence, abnormal ZP:0005552 cilium Kupffer's vesicle spatial pattern, abnormal ZP:0005553 cilium Kupffer's vesicle immobile, abnormal ZP:0005554 brush border pronephric duct irregular spatial pattern, abnormal ZP:0005555 brush border pronephric duct decreased size, abnormal ZP:0005556 cilium pronephros immobile, abnormal ZP:0005557 axoneme pronephros structure, abnormal ZP:0005558 testis hyperplastic, abnormal ZP:0005559 germ cell tumor testis increased amount, abnormal ZP:0005560 germ cell tumor testis proliferative, abnormal ZP:0005561 spermatogonium testis increased amount, abnormal ZP:0005562 kinocilium lateral line decreased length, abnormal ZP:0005563 kinocilium lateral line decreased amount, abnormal ZP:0005564 pronephric glomerulus increased size, abnormal ZP:0005565 pronephric tubule dilated, abnormal ZP:0005566 cornea development in camera-type eye disrupted, abnormal ZP:0005567 extracellular matrix assembly disrupted, abnormal ZP:0005568 symplectic quality, abnormal ZP:0005569 posterior lateral line primordium split, abnormal ZP:0005570 cell posterior lateral line primordium increased length, abnormal ZP:0005571 primordial germ cell cellular motility, abnormal ZP:0005572 primordial germ cell positional polarity, abnormal ZP:0005576 somite spatial pattern, abnormal ZP:0005578 intersegmental artery structure, abnormal ZP:0005579 blood vessel endothelial cell intersegmental artery increased amount, abnormal ZP:0005582 intersegmental vessel mislocalised, abnormal ZP:0005584 angiogenic sprout increased amount, abnormal ZP:0005585 blood vessel endothelial cell increased amount, abnormal ZP:0005586 motor neuron increased amount, abnormal ZP:0005587 Rohon-Beard neuron increased amount, abnormal ZP:0005588 definitive hemopoiesis decreased process quality, abnormal ZP:0005589 signal transduction by p53 class mediator increased process quality, abnormal ZP:0005590 fin regeneration arrested, abnormal ZP:0005591 cardiac muscle cell proliferation arrested, abnormal ZP:0005592 heart trabecula formation arrested, abnormal ZP:0005593 cardiac conduction process quality, abnormal ZP:0005594 neuron dorsal root ganglion absent, abnormal ZP:0005595 myocardium lacks all parts of type trabecular layer, abnormal ZP:0005596 neuron sympathetic nervous system absent, abnormal ZP:0005597 alpha-(1->6)-fucosyltransferase activity disrupted, abnormal ZP:0005598 spinal cord lacks all parts of type neuron projection motor neuron, abnormal ZP:0005599 eye physical object quality, abnormal ZP:0005600 fourth ventricle swollen, abnormal ZP:0005601 retina lacks parts or has fewer parts of type Muller cell, abnormal ZP:0005602 retina lacks parts or has fewer parts of type retinal ganglion cell, abnormal ZP:0005603 somite has fewer parts of type slow muscle cell, abnormal ZP:0005604 muscle cell somite decreased length, abnormal ZP:0005605 whole organism lacks all parts of type neuron projection dorsal root ganglion, abnormal ZP:0005606 splanchnocranium lacks all parts of type mandibular arch skeleton, abnormal ZP:0005607 hindbrain commissure decreased amount, abnormal ZP:0005608 motor neuron position, abnormal ZP:0005609 motor neuron disorganized, abnormal ZP:0005610 photoreceptor cell decreased amount, abnormal ZP:0005611 primitive erythrocyte differentiation arrested, abnormal ZP:0005612 hemoglobin complex blood absent, abnormal ZP:0005613 erythroblast immature, abnormal ZP:0005614 nucleus nucleate erythrocyte broken, abnormal ZP:0005615 palatoquadrate arch malformed, abnormal ZP:0005616 ventral mandibular arch decreased length, abnormal ZP:0005617 cilium posterior neural tube disorganized, abnormal ZP:0005618 cilium posterior neural tube distended, abnormal ZP:0005619 transcription, DNA-templated decreased occurrence, abnormal ZP:0005620 negative regulation of apoptotic process disrupted, abnormal ZP:0005621 positive regulation of cell cycle disrupted, abnormal ZP:0005622 eye disrupted cell division, abnormal ZP:0005623 liver apoptotic, abnormal ZP:0005624 liver development process quality, abnormal ZP:0005625 alkaline phosphatase activity process quality, abnormal ZP:0005626 endoderm development discontinuous, abnormal ZP:0005627 morphogenesis of embryonic epithelium process quality, abnormal ZP:0005628 basal protein localization disrupted, abnormal ZP:0005629 pancreas quality, abnormal ZP:0005630 digestive system hypoplastic, abnormal ZP:0005631 whole organism decreased acidity, abnormal ZP:0005632 whole organism organismal quality, abnormal ZP:0005633 brush border whole organism structure, abnormal ZP:0005634 mandibular arch skeleton structure, abnormal ZP:0005635 sodium ion transport disrupted, abnormal ZP:0005636 cellular calcium ion homeostasis disrupted, abnormal ZP:0005637 epidermal cell differentiation disrupted, abnormal ZP:0005638 water homeostasis disrupted, abnormal ZP:0005639 pore complex epidermis absent, abnormal ZP:0005640 integument ionocyte integument absent, abnormal ZP:0005641 pore complex epidermis decreased amount, abnormal ZP:0005642 head development process quality, abnormal ZP:0005644 notochord curled, abnormal ZP:0005645 epithelium hyperplastic, abnormal ZP:0005646 caudal fin actinotrichium malformed, abnormal ZP:0005647 cellular pigmentation process quality, abnormal ZP:0005648 melanin biosynthetic process arrested, abnormal ZP:0005649 retinal pigmented epithelium color, abnormal ZP:0005650 pigment granule retinal pigmented epithelium decreased amount, abnormal ZP:0005651 melanocyte integument decreased amount, abnormal ZP:0005652 melanocyte unpigmented, abnormal ZP:0005653 cardiac conduction system development process quality, abnormal ZP:0005654 cardiac muscle tissue morphogenesis process quality, abnormal ZP:0005655 heart contraction asynchronous, abnormal ZP:0005656 ventricular myocardium contractility, abnormal ZP:0005657 cardiac muscle cell malformed, abnormal ZP:0005658 carbonate dehydratase activity decreased occurrence, abnormal ZP:0005659 respiratory gaseous exchange by respiratory system process quality, abnormal ZP:0005660 intrahepatic bile duct development arrested, abnormal ZP:0005661 nucleus liver increased size, abnormal ZP:0005662 lipid droplet liver present, abnormal ZP:0005663 gall bladder decreased functionality, abnormal ZP:0005664 bile ductule degenerate, abnormal ZP:0005665 bile ductule unlumenized, abnormal ZP:0005666 intrahepatic bile duct decreased branchiness, abnormal ZP:0005667 mitochondrion hepatocyte structure, abnormal ZP:0005668 mitochondrial crista hepatocyte condensed, abnormal ZP:0005673 lateral dorsal aorta morphology, abnormal ZP:0005676 trunk vasculature disorganized, abnormal ZP:0005678 solid lens vesicle decreased size, abnormal ZP:0005679 circulatory system process disrupted, abnormal ZP:0005680 pigment cell morphology, abnormal ZP:0005681 heart contraction delayed, abnormal ZP:0005682 cell brain necrotic, abnormal ZP:0005683 heart swollen, abnormal ZP:0005684 posterior intestine morphology, abnormal ZP:0005685 myoblast fusion involved in skeletal muscle regeneration disrupted, abnormal ZP:0005686 fast muscle cell disorganized, abnormal ZP:0005687 fast muscle cell disheveled, abnormal ZP:0005688 fast muscle cell decreased diameter, abnormal ZP:0005689 fast muscle cell has fewer parts of type nucleus fast muscle cell, abnormal ZP:0005690 margin disorganized, abnormal ZP:0005691 dorsal aorta decreased diameter, abnormal ZP:0005692 adaxial cell absent, abnormal ZP:0005693 adaxial cell decreased amount, abnormal ZP:0005694 head muscle hypoplastic, abnormal ZP:0005695 fast muscle cell absent, abnormal ZP:0005696 post-vent region sigmoid, abnormal ZP:0005697 pharyngeal arch 2 skeleton shape, abnormal ZP:0005698 chondrocranium cartilage hypoplastic, abnormal ZP:0005699 activation of innate immune response decreased process quality, abnormal ZP:0005700 pattern recognition receptor signaling pathway decreased process quality, abnormal ZP:0005701 caudal vein plexus aplastic, abnormal ZP:0005702 angiogenic sprout caudal vein plexus decreased amount, abnormal ZP:0005703 caudal fin decreased pigmentation, abnormal ZP:0005704 axis whole organism decreased pigmentation, abnormal ZP:0005705 endothelial cell proliferation decreased rate, abnormal ZP:0005706 primordial hindbrain channel absent, abnormal ZP:0005707 primordial hindbrain channel aplastic, abnormal ZP:0005708 intersegmental vein decreased amount, abnormal ZP:0005709 intersegmental artery increased amount, abnormal ZP:0005710 lymph vasculature trunk aplastic, abnormal ZP:0005711 trunk vasculature branchiness, abnormal ZP:0005712 lymphangioblast cord absent, abnormal ZP:0005713 vascular lymphangioblast absent, abnormal ZP:0005714 vascular lymphangioblast cellular motility, abnormal ZP:0005715 vascular lymphangioblast decreased amount, abnormal ZP:0005716 somite misaligned with myofibril myofibril somite, abnormal ZP:0005717 somite border amorphous, abnormal ZP:0005718 feeding behavior decreased process quality, abnormal ZP:0005719 anterior commissure morphogenesis disrupted, abnormal ZP:0005720 posterior commissure morphogenesis disrupted, abnormal ZP:0005721 medial longitudinal fasciculus structure, abnormal ZP:0005722 muscle organ development disrupted, abnormal ZP:0005723 axon motor neuron misrouted, abnormal ZP:0005725 actin cap epiblast position, abnormal ZP:0005726 mitotic spindle epiblast position, abnormal ZP:0005727 tail bud mislocalised, abnormal ZP:0005728 tail bud opaque, abnormal ZP:0005729 inner ear increased size, abnormal ZP:0005730 otolith organ has fewer parts of type otolith, abnormal ZP:0005731 head position, abnormal ZP:0005732 head mislocalised posteriorly, abnormal ZP:0005733 somite border hypoplastic, abnormal ZP:0005734 muscle morphology, abnormal ZP:0005735 ventral region retina mislocalized adaxially, abnormal ZP:0005737 type B pancreatic cell differentiation decreased occurrence, abnormal ZP:0005738 pancreatic A cell differentiation increased occurrence, abnormal ZP:0005739 endocrine pancreas development decreased process quality, abnormal ZP:0005740 type B pancreatic cell proliferation disrupted, abnormal ZP:0005741 endocrine pancreas decreased size, abnormal ZP:0005742 endocrine pancreas has fewer parts of type pancreatic B cell, abnormal ZP:0005743 endocrine pancreas has extra parts of type pancreatic A cell, abnormal ZP:0005744 endocrine pancreas has fewer parts of type endodermal cell, abnormal ZP:0005745 posterior pancreatic bud decreased size, abnormal ZP:0005748 posterior pancreatic bud has fewer parts of type pancreatic B cell, abnormal ZP:0005749 posterior pancreatic bud has extra parts of type pancreatic A cell, abnormal ZP:0005752 axon MiP motor neuron mislocalised, abnormal ZP:0005754 endocrine cell extrapancreatic duct decreased amount, abnormal ZP:0005755 post-vent region increased size, abnormal ZP:0005756 pharyngeal arch non-functional, abnormal ZP:0005758 subintestinal vein morphology, abnormal ZP:0005760 neuromuscular synaptic transmission decreased process quality, abnormal ZP:0005763 slow muscle cell morphology, abnormal ZP:0005764 pancreas absent, abnormal ZP:0005765 lens morphogenesis in camera-type eye process quality, abnormal ZP:0005766 anaphase-promoting complex-dependent catabolic process decreased rate, abnormal ZP:0005767 proteasome-mediated ubiquitin-dependent protein catabolic process decreased rate, abnormal ZP:0005768 lens fiber cell differentiation process quality, abnormal ZP:0005769 nucleus lens circular, abnormal ZP:0005770 nucleus lens mislocalised anteriorly, abnormal ZP:0005771 nucleus lens decreased amount, abnormal ZP:0005772 midbrain hindbrain boundary hemorrhagic, abnormal ZP:0005773 cell division rate, abnormal ZP:0005774 EVL increased permeability, abnormal ZP:0005775 EVL moderately well differentiated, abnormal ZP:0005776 actin filament EVL disorganized, abnormal ZP:0005777 bicellular tight junction EVL irregular spatial pattern, abnormal ZP:0005778 cell junction EVL immature, abnormal ZP:0005779 extracellular space DEL decreased area, abnormal ZP:0005780 camera-type eye development arrested, abnormal ZP:0005781 retinal bipolar neuron differentiation delayed, abnormal ZP:0005782 axon retina malformed, abnormal ZP:0005783 pneumatic duct morphology, abnormal ZP:0005784 neutrophil aggregation disrupted, abnormal ZP:0005785 neutrophil intermediate cell mass of mesoderm absent, abnormal ZP:0005786 opercle decreased thickness, abnormal ZP:0005787 cytosolic small ribosomal subunit whole organism decreased amount, abnormal ZP:0005788 neutrophil anterior lateral mesoderm absent, abnormal ZP:0005789 granulocyte position, abnormal ZP:0005790 integument disorganized, abnormal ZP:0005791 caudal fin disorganized, abnormal ZP:0005794 cellular sodium ion homeostasis disrupted, abnormal ZP:0005796 visual perception arrested, abnormal ZP:0005797 response to light stimulus arrested, abnormal ZP:0005798 developmental growth decreased rate, abnormal ZP:0005799 cilium peripheral olfactory organ decreased length, abnormal ZP:0005800 eye elliptic, abnormal ZP:0005801 cilium olfactory pit decreased amount, abnormal ZP:0005802 retinal photoreceptor layer structure, abnormal ZP:0005803 retinal photoreceptor layer apoptotic, abnormal ZP:0005804 cilium pronephric duct morphology, abnormal ZP:0005805 retina electrical conductivity, abnormal ZP:0005806 central region retina apoptotic, abnormal ZP:0005807 retina lacks all parts of type central region eye photoreceptor cell, abnormal ZP:0005808 retina has fewer parts of type central region eye photoreceptor cell, abnormal ZP:0005809 retina lacks all parts of type central region retinal cone cell, abnormal ZP:0005810 photoreceptor outer segment retina decreased size, abnormal ZP:0005811 photoreceptor outer segment retina disorganized, abnormal ZP:0005812 anterior-posterior axis whole organism curled, abnormal ZP:0005813 cilium whole organism morphology, abnormal ZP:0005814 retinal outer nuclear layer wholeness, abnormal ZP:0005815 photoreceptor cell degenerate, abnormal ZP:0005816 eye photoreceptor cell apoptotic, abnormal ZP:0005817 eye photoreceptor cell decreased amount, abnormal ZP:0005818 nucleus eye photoreceptor cell condensed, abnormal ZP:0005819 cilium Kupffer's vesicle decreased volume, abnormal ZP:0005820 cell Kupffer's vesicle mislocalised, abnormal ZP:0005821 blood accumulation yolk, abnormal ZP:0005822 forerunner cell group distributed, abnormal ZP:0005823 hindbrain molecular quality, abnormal ZP:0005824 oligodendrocyte hindbrain decreased amount, abnormal ZP:0005825 gut orientation left-right axis whole organism, abnormal ZP:0005826 intersegmental artery attached to intersegmental artery, abnormal ZP:0005827 eye edematous, abnormal ZP:0005828 orbital region increased accumulation blood, abnormal ZP:0005829 mitochondrial chromosome whole organism decreased amount, abnormal ZP:0005830 dorsal-ventral axis head decreased length, abnormal ZP:0005831 cerebellar central artery hemorrhagic, abnormal ZP:0005832 cerebellum degenerate, abnormal ZP:0005833 basihyal bone decreased size, abnormal ZP:0005834 optic tectum degenerate, abnormal ZP:0005835 left/right pattern formation occurrence, abnormal ZP:0005836 motile cilium Kupffer's vesicle decreased length, abnormal ZP:0005837 motile cilium Kupffer's vesicle decreased amount, abnormal ZP:0005838 cell Kupffer's vesicle decreased amount, abnormal ZP:0005839 motile cilium pronephric duct decreased length, abnormal ZP:0005841 cilium olfactory placode paralysed, abnormal ZP:0005842 cilium pronephros partially paralysed, abnormal ZP:0005843 pronephric tubule distended, abnormal ZP:0005844 motile cilium pronephric duct decreased amount, abnormal ZP:0005845 axoneme olfactory epithelium swollen, abnormal ZP:0005847 photoreceptor outer segment photoreceptor cell decreased length, abnormal ZP:0005848 intraciliary transport particle photoreceptor cell mislocalised, abnormal ZP:0005849 photoreceptor connecting cilium photoreceptor cell swollen, abnormal ZP:0005850 photoreceptor outer segment membrane photoreceptor cell disorganized, abnormal ZP:0005851 photoreceptor outer segment membrane photoreceptor cell vacuolated, abnormal ZP:0005852 mitotic spindle assembly process quality, abnormal ZP:0005853 caudal fin increased thickness, abnormal ZP:0005854 whole organism lacks parts or has fewer parts of type circulating cell blood cell, abnormal ZP:0005855 hematopoietic system accumulation cell anterior region ball, abnormal ZP:0005856 erythroblast increased size, abnormal ZP:0005857 nucleus erythroblast increased size, abnormal ZP:0005858 blood vessel has fewer parts of type blood cell, abnormal ZP:0005859 blood vessel lacks parts or has fewer parts of type blood nucleate erythrocyte, abnormal ZP:0005860 hematopoietic stem cell absent, abnormal ZP:0005861 nucleate erythrocyte accumulation intermediate cell mass of mesoderm, abnormal ZP:0005862 nucleate erythrocyte accumulation common cardinal vein, abnormal ZP:0005863 motor neuron spinal cord disorganized, abnormal ZP:0005864 brain amorphous, abnormal ZP:0005865 midbrain hindbrain boundary dorso-ventrally flattened, abnormal ZP:0005866 paraxial mesoderm formation disrupted, abnormal ZP:0005867 cell migration involved in mesendoderm migration disrupted, abnormal ZP:0005868 polster mislocalised posteriorly, abnormal ZP:0005869 tail bud truncated, abnormal ZP:0005870 anterior region forebrain aplastic, abnormal ZP:0005871 paraxial mesoderm increased distance adaxial cell adaxial cell paraxial mesoderm, abnormal ZP:0005872 segmental plate curved, abnormal ZP:0005873 anterior region head flattened, abnormal ZP:0005874 hindbrain neural keel increased width, abnormal ZP:0005875 midbrain hindbrain boundary neural keel increased width, abnormal ZP:0005876 glucagon secreting cell decreased amount, abnormal ZP:0005877 retinal photoreceptor layer aplastic, abnormal ZP:0005878 photoreceptor outer segment photoreceptor outer segment layer deformed, abnormal ZP:0005879 photoreceptor outer segment photoreceptor outer segment layer decreased amount, abnormal ZP:0005880 Muller cell apical-basal polarity, abnormal ZP:0005881 perikaryon Muller cell mislocalised, abnormal ZP:0005882 pigmentation abnormal, abnormal ZP:0005883 embryonic pectoral fin morphogenesis process quality, abnormal ZP:0005884 otic vesicle morphogenesis process quality, abnormal ZP:0005885 apical ectodermal ridge pectoral fin bud physical object quality, abnormal ZP:0005886 intersegmental vessel non-functional, abnormal ZP:0005887 epibranchial placode decreased size, abnormal ZP:0005888 axis elongation arrested, abnormal ZP:0005890 brain vasculature morphology, abnormal ZP:0005891 brain vasculature dilated, abnormal ZP:0005892 heart shape, abnormal ZP:0005896 anterior cerebral vein dilated, abnormal ZP:0005897 cranial vasculature dilated, abnormal ZP:0005898 cranial vasculature attachment quality cranial vasculature, abnormal ZP:0005900 intersegmental vessel increased width, abnormal ZP:0005901 myocardium decreased thickness, abnormal ZP:0005905 primordial midbrain channel increased size, abnormal ZP:0005909 subintestinal vein disorganized, abnormal ZP:0005911 prosencephalic artery dilated, abnormal ZP:0005912 mesencephalic vein spatial pattern, abnormal ZP:0005918 brain vasculature broken, abnormal ZP:0005919 epithelium brain vasculature decreased thickness, abnormal ZP:0005920 integument blistered, abnormal ZP:0005921 endothelial cell morphology, abnormal ZP:0005922 actin cytoskeleton skeletal muscle cell retracted, abnormal ZP:0005924 retinal ganglion cell layer hypoplastic, abnormal ZP:0005925 retinal inner nuclear layer hypoplastic, abnormal ZP:0005926 retina lacks parts or has fewer parts of type retinal inner plexiform layer, abnormal ZP:0005927 retina lacks parts or has fewer parts of type retinal outer plexiform layer, abnormal ZP:0005928 whole organism lacks all parts of type cranial nerve II, abnormal ZP:0005929 regulation of heart contraction disrupted, abnormal ZP:0005930 blood accumulation pericardium, abnormal ZP:0005931 sinus venosus hypoplastic, abnormal ZP:0005932 myocardium sinus venosus poorly differentiated, abnormal ZP:0005933 lipid metabolic process process quality, abnormal ZP:0005934 liver and biliary system morphology, abnormal ZP:0005935 bile ductule obstructed, abnormal ZP:0005936 bile ductule aplastic, abnormal ZP:0005937 bile ductule dilated, abnormal ZP:0005938 bile ductule lumenized, abnormal ZP:0005939 bile ductule decreased amount, abnormal ZP:0005940 intrahepatic bile duct length, abnormal ZP:0005941 intrahepatic bile duct decreased thickness, abnormal ZP:0005942 intrahepatic bile duct distributed, abnormal ZP:0005943 granular layer corpus cerebelli decreased size, abnormal ZP:0005944 molecular layer corpus cerebelli decreased size, abnormal ZP:0005945 granular layer valvula cerebelli decreased size, abnormal ZP:0005946 molecular layer valvula cerebelli decreased size, abnormal ZP:0005947 motile cilium Kupffer's vesicle movement quality, abnormal ZP:0005948 cilium olfactory pit decreased length, abnormal ZP:0005949 cilium macula decreased length, abnormal ZP:0005951 chondrocyte pharyngeal arch cartilage decreased amount, abnormal ZP:0005952 cilium anterior lateral line neuromast decreased length, abnormal ZP:0005953 photoreceptor outer segment eye photoreceptor cell decreased amount, abnormal ZP:0005954 collateral sprouting decreased process quality, abnormal ZP:0005955 neuron spinal cord degenerate, abnormal ZP:0005956 axon collateral primary motor neuron decreased branchiness, abnormal ZP:0005957 calcium ion import increased rate, abnormal ZP:0005958 peroxisome yolk decreased amount, abnormal ZP:0005959 peroxisome pronephric duct decreased amount, abnormal ZP:0005960 peroxisome hepatocyte decreased amount, abnormal ZP:0005962 homologous chromosome pairing at meiosis disrupted, abnormal ZP:0005963 male meiosis I disrupted, abnormal ZP:0005964 meiotic metaphase I plate congression disrupted, abnormal ZP:0005965 chiasma assembly disrupted, abnormal ZP:0005966 male organism male sterile, abnormal ZP:0005967 male organism triploid, abnormal ZP:0005968 male organism decreased male fertility, abnormal ZP:0005969 female organism lethal (sensu genetics), abnormal ZP:0005970 female organism aneuploid, abnormal ZP:0005971 testis increased weight, abnormal ZP:0005972 testis apoptotic, abnormal ZP:0005973 whole organism increased size, abnormal ZP:0005974 whole organism brood viability, abnormal ZP:0005975 spermatocyte increased amount, abnormal ZP:0005976 spermatocyte decreased amount, abnormal ZP:0005977 recombination nodule spermatocyte absent, abnormal ZP:0005978 sperm absent, abnormal ZP:0005979 spermatogonium increased amount, abnormal ZP:0005980 eye morphogenesis process quality, abnormal ZP:0005982 germ cell migration cellular spatiotemporal quality, abnormal ZP:0005983 rod bipolar cell disorganized, abnormal ZP:0005984 cone retinal bipolar cell disorganized, abnormal ZP:0005985 response to light intensity decreased occurrence, abnormal ZP:0005986 pigmentation decreased intensity, abnormal ZP:0005987 keratinocyte epidermis morphology, abnormal ZP:0005988 neuromast action potential, abnormal ZP:0005989 neuromast non-functional, abnormal ZP:0005990 neuromast hair cell mislocalised, abnormal ZP:0005991 positive phototaxis decreased occurrence, abnormal ZP:0005993 retinal photoreceptor layer morphology, abnormal ZP:0005994 retina has fewer parts of type retinal cone cell, abnormal ZP:0005995 photoreceptor cell retina degenerate, abnormal ZP:0005996 retinal outer plexiform layer irregular thickness, abnormal ZP:0005997 retinal outer plexiform layer has fewer parts of type synapse neuron, abnormal ZP:0005998 photoreceptor outer segment eye photoreceptor cell morphology, abnormal ZP:0005999 UV sensitive photoreceptor cell decreased amount, abnormal ZP:0006000 blue sensitive photoreceptor cell decreased amount, abnormal ZP:0006001 green sensitive photoreceptor cell decreased amount, abnormal ZP:0006002 red sensitive photoreceptor cell decreased amount, abnormal ZP:0006003 retinal cone cell degenerate, abnormal ZP:0006004 retinal rod cell degenerate, abnormal ZP:0006005 photoreceptor outer segment retinal rod cell morphology, abnormal ZP:0006006 Muller cell morphology, abnormal ZP:0006007 nucleus retinal bipolar neuron displaced, abnormal ZP:0006008 axon retinal bipolar neuron displaced, abnormal ZP:0006009 ON-bipolar cell morphology, abnormal ZP:0006010 axon ON-bipolar cell increased amount, abnormal ZP:0006011 axon ON-bipolar cell increased length, abnormal ZP:0006012 ON-bipolar cell located in axon retinal ganglion cell layer, abnormal ZP:0006013 dendrite ON-bipolar cell increased amount, abnormal ZP:0006014 dendrite ON-bipolar cell increased length, abnormal ZP:0006015 ON-bipolar cell located in dendrite retinal outer nuclear layer, abnormal ZP:0006016 epidermis atrophied, abnormal ZP:0006017 locomotor rhythm decreased process quality, abnormal ZP:0006019 cell lens apoptotic, abnormal ZP:0006020 trunk curved lateral, abnormal ZP:0006021 erythrocyte development disrupted, abnormal ZP:0006022 heart primordium position, abnormal ZP:0006023 erythroblast intermediate cell mass of mesoderm increased amount, abnormal ZP:0006024 forebrain aplastic, abnormal ZP:0006025 digestive system position, abnormal ZP:0006026 optic tectum aplastic, abnormal ZP:0006027 optic primordium decreased size, abnormal ZP:0006028 ribosome whole organism decreased amount, abnormal ZP:0006029 pharyngeal arch 3-7 immature, abnormal ZP:0006030 nucleate erythrocyte apoptotic, abnormal ZP:0006031 anterior region whole organism necrotic, abnormal ZP:0006032 hemoglobin complex blood cell decreased amount, abnormal ZP:0006034 blood vessel endothelial cell posterior cardinal vein decreased amount, abnormal ZP:0006035 blood vasculature head decreased amount, abnormal ZP:0006036 angioblastic mesenchymal cell mislocalised, abnormal ZP:0006037 angioblastic mesenchymal cell apoptotic, abnormal ZP:0006038 angioblastic mesenchymal cell decreased amount, abnormal ZP:0006039 erythrocyte differentiation delayed, abnormal ZP:0006040 endocrine pancreas disorganized, abnormal ZP:0006041 heart looping decreased process quality, abnormal ZP:0006042 cardioblast cell fate specification decreased process quality, abnormal ZP:0006043 atrial cardiac muscle cell differentiation decreased occurrence, abnormal ZP:0006044 ventricular cardiac muscle cell differentiation decreased occurrence, abnormal ZP:0006045 heart contraction decreased frequency, abnormal ZP:0006046 cardiac ventricle decreased length, abnormal ZP:0006047 cardiac ventricle has fewer parts of type cardiac muscle cell, abnormal ZP:0006048 heart has fewer parts of type cardiac muscle cell, abnormal ZP:0006049 atrium decreased length, abnormal ZP:0006050 atrium has fewer parts of type cardiac muscle cell, abnormal ZP:0006051 whole organism lacks all parts of type blood, abnormal ZP:0006052 cranial cartilage decreased object quality, abnormal ZP:0006053 posterior lateral plate mesoderm physical object quality, abnormal ZP:0006055 cell cycle process temporally extended, abnormal ZP:0006056 neuron maturation delayed, abnormal ZP:0006057 retinal cone cell differentiation disrupted, abnormal ZP:0006058 retinal rod cell differentiation disrupted, abnormal ZP:0006059 retinal outer plexiform layer structure, abnormal ZP:0006060 horizontal cell immature, abnormal ZP:0006061 retinal bipolar neuron immature, abnormal ZP:0006062 presumptive atrium heart tube increased size, abnormal ZP:0006063 presumptive cardiac ventricle heart tube decreased size, abnormal ZP:0006064 branching involved in blood vessel morphogenesis disrupted, abnormal ZP:0006065 sprouting angiogenesis premature, abnormal ZP:0006066 intersegmental artery increased branchiness, abnormal ZP:0006067 axial vasculature has extra parts of type intersegmental vessel, abnormal ZP:0006068 intersegmental vessel spatial pattern, abnormal ZP:0006069 ocular blood vessel structure, abnormal ZP:0006070 ocular blood vessel increased amount, abnormal ZP:0006071 ocular blood vessel kinked, abnormal ZP:0006072 myelination in peripheral nervous system decreased occurrence, abnormal ZP:0006073 myelination of anterior lateral line nerve axons decreased occurrence, abnormal ZP:0006074 neuromast increased amount, abnormal ZP:0006075 neuromast trunk increased amount, abnormal ZP:0006076 inner dynein arm olfactory placode absent, abnormal ZP:0006077 outer dynein arm olfactory placode absent, abnormal ZP:0006078 cilium spinal cord decreased length, abnormal ZP:0006079 pronephros distended, abnormal ZP:0006080 pronephros lacks parts or has fewer parts of type microvillus epithelial cell, abnormal ZP:0006081 brush border pronephros absent, abnormal ZP:0006082 inner dynein arm pronephros absent, abnormal ZP:0006083 outer dynein arm pronephros absent, abnormal ZP:0006084 parapineal organ right side of whole organism, abnormal ZP:0006085 pronephric glomerulus decreased thickness, abnormal ZP:0006086 basibranchial absent, abnormal ZP:0006087 opercular flap absent, abnormal ZP:0006088 dorsal region neural tube necrotic, abnormal ZP:0006089 ventral mandibular arch absent, abnormal ZP:0006090 mesenchyme condensation cell pharyngeal arch decreased amount, abnormal ZP:0006091 palatoquadrate cartilage absent, abnormal ZP:0006092 hyosymplectic cartilage absent, abnormal ZP:0006093 basihyal cartilage absent, abnormal ZP:0006094 xanthoblast decreased amount, abnormal ZP:0006095 oculomotor nerve formation decreased process quality, abnormal ZP:0006096 axon cranial nerve III mislocalised, abnormal ZP:0006097 cranial nerve III process quality axon extension, abnormal ZP:0006098 smoothened signaling pathway process quality, abnormal ZP:0006099 adaxial cell physical object quality, abnormal ZP:0006100 cilium pronephric duct absent, abnormal ZP:0006101 cilium pronephric duct deformed, abnormal ZP:0006102 photoreceptor outer segment layer retina absent, abnormal ZP:0006103 cilium neuromast absent, abnormal ZP:0006104 heart tube mislocalised, abnormal ZP:0006105 renal glomerulus kidney cystic, abnormal ZP:0006106 nucleus retinal outer nuclear layer decreased amount, abnormal ZP:0006107 cilium multi-ciliated epithelial cell absent, abnormal ZP:0006108 renal duct increased size, abnormal ZP:0006109 Muller cell absent, abnormal ZP:0006110 yolk physical object quality, abnormal ZP:0006111 zymogen granule pancreas decreased amount, abnormal ZP:0006112 intrahepatic bile duct increased width, abnormal ZP:0006113 intrahepatic bile duct sparse, abnormal ZP:0006114 intrahepatic bile duct separated from intrahepatic bile duct, abnormal ZP:0006115 intrahepatic bile duct increased accumulation vesicle intrahepatic bile duct, abnormal ZP:0006116 cytoplasm intrahepatic bile duct composition, abnormal ZP:0006117 smooth endoplasmic reticulum intrahepatic bile duct dilated, abnormal ZP:0006118 Golgi apparatus enterocyte dilated, abnormal ZP:0006119 mesendoderm development disrupted, abnormal ZP:0006121 DNA methylation decreased occurrence, abnormal ZP:0006122 DNA methylation on cytosine within a CG sequence decreased occurrence, abnormal ZP:0006123 lens capsule absent, abnormal ZP:0006124 yolk accumulation blood, abnormal ZP:0006125 parachordal vessel aplastic, abnormal ZP:0006126 atrial ventricular junction remodeling disrupted, abnormal ZP:0006127 developmental growth involved in morphogenesis disrupted, abnormal ZP:0006128 heart tube condensed, abnormal ZP:0006129 P granule primordial germ cell size, abnormal ZP:0006130 myofibril muscle decreased diameter, abnormal ZP:0006131 alpha-tubulin acetylation disrupted, abnormal ZP:0006132 granuloma formation decreased occurrence, abnormal ZP:0006133 cell retinal ganglion cell layer decreased amount, abnormal ZP:0006134 cell retinal inner nuclear layer decreased amount, abnormal ZP:0006136 cell retinal outer nuclear layer decreased amount, abnormal ZP:0006140 midbrain hindbrain boundary poorly differentiated, abnormal ZP:0006141 epidermis development disrupted, abnormal ZP:0006142 neutrophil chemotaxis increased rate, abnormal ZP:0006144 median fin fold morphology, abnormal ZP:0006145 median fin fold decreased thickness, abnormal ZP:0006146 median fin fold degenerate, abnormal ZP:0006147 epidermis increased thickness, abnormal ZP:0006148 epidermis disorganized, abnormal ZP:0006149 chorion accumulation keratinocyte, abnormal ZP:0006150 olfactory epithelium morphology, abnormal ZP:0006151 keratinocyte epidermal basal stratum aggregated, abnormal ZP:0006152 keratinocyte mislocalised, abnormal ZP:0006153 keratinocyte disorganized, abnormal ZP:0006154 leukocyte aggregated, abnormal ZP:0006155 neutrophil increased amount, abnormal ZP:0006156 visual behavior decreased rate, abnormal ZP:0006157 melanocyte differentiation process quality, abnormal ZP:0006158 phototaxis arrested, abnormal ZP:0006159 detection of light stimulus involved in visual perception process quality, abnormal ZP:0006160 cholinergic neuron retinal neural layer decreased amount, abnormal ZP:0006161 retinal inner nuclear layer perforate, abnormal ZP:0006162 melanocyte increased area, abnormal ZP:0006163 heart contraction occurrence, abnormal ZP:0006164 cardiac muscle contraction arrested, abnormal ZP:0006165 posterior lateral line neuromast deposition disrupted, abnormal ZP:0006166 integument tail bud aggregated, abnormal ZP:0006167 yolk protruding out of whole organism, abnormal ZP:0006168 ruffle EVL absent, abnormal ZP:0006169 keratinocyte aggregated, abnormal ZP:0006170 detection of visible light disrupted, abnormal ZP:0006171 photoreceptor outer segment photoreceptor outer segment layer absent, abnormal ZP:0006172 photoreceptor outer segment retinal cone cell absent, abnormal ZP:0006173 double-strand break repair via homologous recombination decreased frequency, abnormal ZP:0006174 somitomeric trunk muscle development disrupted, abnormal ZP:0006175 skeletal muscle cell proliferation increased rate, abnormal ZP:0006176 striated muscle cell differentiation disrupted, abnormal ZP:0006177 somite decreased occurrence cell population proliferation, abnormal ZP:0006178 fast muscle cell somite disorganized, abnormal ZP:0006179 medial rectus aplastic, abnormal ZP:0006180 cephalic musculature decreased process quality skeletal muscle tissue development, abnormal ZP:0006181 ventral rectus aplastic, abnormal ZP:0006182 trunk musculature refractivity, abnormal ZP:0006183 sternohyoid aplastic, abnormal ZP:0006184 fast muscle cell shape, abnormal ZP:0006185 myofibril fast muscle cell position, abnormal ZP:0006186 melanocyte stimulating hormone secreting cell absent, abnormal ZP:0006187 melanocyte stimulating hormone secreting cell decreased amount, abnormal ZP:0006188 adrenocorticotropic hormone secreting cell absent, abnormal ZP:0006189 neuron differentiation premature, abnormal ZP:0006190 hindbrain physical object quality, abnormal ZP:0006191 dorsal region diencephalon physical object quality, abnormal ZP:0006192 midbrain physical object quality, abnormal ZP:0006193 T cell thymus absent, abnormal ZP:0006194 trunk altered number of intersegmental vessel, abnormal ZP:0006195 cytoplasmic microtubule organization process quality, abnormal ZP:0006196 filopodium assembly process quality, abnormal ZP:0006197 axon extension decreased occurrence, abnormal ZP:0006198 microtubule severing decreased occurrence, abnormal ZP:0006199 Meckel's cartilage fused with ventral region dorsal region palatoquadrate cartilage, abnormal ZP:0006200 hyosymplectic cartilage fused with dorsal region ventral region ceratohyal cartilage, abnormal ZP:0006201 interhyal cartilage aplastic, abnormal ZP:0006202 whole organism lacks parts or has fewer parts of type cartilage element, abnormal ZP:0006203 whole organism lacks parts or has fewer parts of type pharyngeal arch 3-7, abnormal ZP:0006204 myofibril trunk musculature decreased size, abnormal ZP:0006205 anterior-posterior axis whole organism decreased thickness, abnormal ZP:0006206 eye colorless, abnormal ZP:0006207 pharyngeal arch cartilage deformed, abnormal ZP:0006208 myofibril muscle cell decreased amount, abnormal ZP:0006209 axon primary motor neuron decreased length, abnormal ZP:0006210 neuron projection primary motor neuron decreased amount, abnormal ZP:0006211 branching involved in blood vessel morphogenesis process quality, abnormal ZP:0006212 central nervous system myelination occurrence, abnormal ZP:0006213 oligodendrocyte progenitor proliferation disrupted, abnormal ZP:0006214 cardiac ventricle collapsed, abnormal ZP:0006215 sinus venosus collapsed, abnormal ZP:0006216 bulbus arteriosus collapsed, abnormal ZP:0006217 melanocyte head decreased amount, abnormal ZP:0006218 xanthophore head decreased amount, abnormal ZP:0006219 melanoblast head decreased amount, abnormal ZP:0006220 xanthophore trunk decreased amount, abnormal ZP:0006221 melanoblast trunk decreased amount, abnormal ZP:0006222 oligodendrocyte morphology, abnormal ZP:0006223 glial cell (sensu Vertebrata) absent, abnormal ZP:0006224 establishment of endothelial barrier disrupted, abnormal ZP:0006225 tectal ventricle decreased volume, abnormal ZP:0006226 ventricular system lumenized, abnormal ZP:0006227 hyaloid vessel broken, abnormal ZP:0006228 bicellular tight junction neuroepithelial cell increased permeability, abnormal ZP:0006229 centrosome pronephric duct decreased amount, abnormal ZP:0006230 locomotion involved in locomotory behavior arrested, abnormal ZP:0006231 axon hindbrain decreased amount, abnormal ZP:0006232 axon eye decreased amount, abnormal ZP:0006233 axon forebrain decreased amount, abnormal ZP:0006234 axon midbrain decreased amount, abnormal ZP:0006235 third ventricle decreased size, abnormal ZP:0006236 telencephalic ventricle decreased size, abnormal ZP:0006242 myofibril muscle disorganized, abnormal ZP:0006245 long-chain fatty acid metabolic process disrupted, abnormal ZP:0006246 hepaticobiliary system process disrupted, abnormal ZP:0006247 gall bladder disrupted lipid storage, abnormal ZP:0006248 bile canaliculus spheroid, abnormal ZP:0006249 bile canaliculus decreased branchiness, abnormal ZP:0006250 bile ductule sparse, abnormal ZP:0006251 rough endoplasmic reticulum hepatocyte increased amount, abnormal ZP:0006252 response to bacterium disrupted, abnormal ZP:0006253 response to bacterium increased process quality, abnormal ZP:0006254 photoreceptor cell development disrupted, abnormal ZP:0006255 lens position, abnormal ZP:0006256 cell lens disorganized, abnormal ZP:0006257 cell lens poorly differentiated, abnormal ZP:0006258 liver spheroid, abnormal ZP:0006259 liver increased pigmentation, abnormal ZP:0006260 blood vessel liver morphology, abnormal ZP:0006261 retinal photoreceptor layer lacks parts or has fewer parts of type retinal cone cell, abnormal ZP:0006262 retinal photoreceptor layer lacks all parts of type retinal cone cell, abnormal ZP:0006263 retinal photoreceptor layer lacks all parts of type retinal rod cell, abnormal ZP:0006264 retinal photoreceptor layer has fewer parts of type retinal rod cell, abnormal ZP:0006265 eye photoreceptor cell retinal photoreceptor layer disorganized, abnormal ZP:0006266 eye photoreceptor cell retinal photoreceptor layer immature, abnormal ZP:0006267 retinal cone cell retinal photoreceptor layer disorganized, abnormal ZP:0006268 retinal rod cell retinal photoreceptor layer disorganized, abnormal ZP:0006269 retina lacks all parts of type photoreceptor outer segment layer, abnormal ZP:0006270 cranium increased width, abnormal ZP:0006271 cranium shortened, abnormal ZP:0006272 whole organism buoyancy, abnormal ZP:0006273 trunk swollen, abnormal ZP:0006274 ciliary marginal zone hyperplastic, abnormal ZP:0006275 goblet cell mid intestine decreased amount, abnormal ZP:0006276 lens epithelium disorganized, abnormal ZP:0006277 columnar/cuboidal epithelial cell lens epithelium morphology, abnormal ZP:0006278 columnar/cuboidal epithelial cell lens epithelium shape, abnormal ZP:0006279 columnar/cuboidal epithelial cell lens epithelium disorganized, abnormal ZP:0006280 intestine decreased volume, abnormal ZP:0006281 mucus layer intestine decreased thickness, abnormal ZP:0006282 leukocyte intestine increased amount, abnormal ZP:0006283 hepatic sinusoid decreased size, abnormal ZP:0006284 intestinal villus damage, abnormal ZP:0006285 endoplasmic reticulum lumen pancreatic acinar cell distended, abnormal ZP:0006286 goblet cell increased amount, abnormal ZP:0006287 goblet cell mislocalised, abnormal ZP:0006288 goblet cell disorganized, abnormal ZP:0006289 goblet cell detached from intestinal epithelium, abnormal ZP:0006290 condensed nuclear chromosome goblet cell increased amount, abnormal ZP:0006291 cytoskeleton goblet cell disorganized, abnormal ZP:0006292 exocytic vesicle goblet cell morphology, abnormal ZP:0006293 autophagosome enteroendocrine cell increased amount, abnormal ZP:0006294 hepatocyte necrotic, abnormal ZP:0006295 hepatocyte vacuolated, abnormal ZP:0006296 hepatocyte fatty, abnormal ZP:0006297 nucleus hepatocyte mislocalised, abnormal ZP:0006298 mitochondrion hepatocyte morphology, abnormal ZP:0006299 endoplasmic reticulum lumen hepatocyte vacuolated, abnormal ZP:0006300 endoplasmic reticulum lumen hepatocyte swollen, abnormal ZP:0006302 intestinal epithelial cell shape, abnormal ZP:0006303 intestinal epithelial cell apoptotic, abnormal ZP:0006304 intestinal epithelial cell disorganized, abnormal ZP:0006305 intestinal epithelial cell detached from intestinal epithelium, abnormal ZP:0006306 intestinal epithelial cell increased process quality autophagy of mitochondrion, abnormal ZP:0006307 cytoplasm intestinal epithelial cell immature, abnormal ZP:0006308 mitochondrion intestinal epithelial cell morphology, abnormal ZP:0006309 mitochondrion intestinal epithelial cell decreased amount, abnormal ZP:0006310 autophagosome intestinal epithelial cell increased amount, abnormal ZP:0006311 endoplasmic reticulum intestinal epithelial cell distended, abnormal ZP:0006312 endoplasmic reticulum lumen intestinal epithelial cell vacuolated, abnormal ZP:0006313 endoplasmic reticulum lumen intestinal epithelial cell distended, abnormal ZP:0006314 Golgi apparatus intestinal epithelial cell distended, abnormal ZP:0006315 brush border intestinal epithelial cell morphology, abnormal ZP:0006316 brush border intestinal epithelial cell decreased thickness, abnormal ZP:0006317 brush border intestinal epithelial cell atrophied, abnormal ZP:0006318 intestinal epithelial cell increased occurrence autophagy, abnormal ZP:0006319 intestinal epithelial cell decreased process quality cell population proliferation, abnormal ZP:0006320 cortical actin cytoskeleton intestinal epithelial cell decreased thickness, abnormal ZP:0006321 vesicle intestinal epithelial cell increased amount, abnormal ZP:0006322 vesicle intestinal epithelial cell increased size, abnormal ZP:0006323 intestinal epithelial cell increased process quality positive regulation of autophagy in response to ER overload, abnormal ZP:0006324 caudal vein plexus edematous, abnormal ZP:0006325 axis specification arrested, abnormal ZP:0006326 spinal cord decreased width, abnormal ZP:0006327 caudal fin multiple, abnormal ZP:0006328 neural tube distended, abnormal ZP:0006329 sodium ion transport decreased process quality, abnormal ZP:0006330 ammonium transport decreased process quality, abnormal ZP:0006331 cell cycle process arrested, abnormal ZP:0006332 endoplasmic reticulum unfolded protein response increased occurrence, abnormal ZP:0006333 photoreceptor cell differentiation disrupted, abnormal ZP:0006334 extracellular matrix constituent secretion disrupted, abnormal ZP:0006335 cell eye apoptotic, abnormal ZP:0006336 fin kinked, abnormal ZP:0006338 retinal photoreceptor layer absent, abnormal ZP:0006340 neuroepithelial cell retinal pigmented epithelium disorganized, abnormal ZP:0006341 pronephric duct decreased thickness, abnormal ZP:0006342 nucleus retina condensed, abnormal ZP:0006343 endoplasmic reticulum intestinal epithelium dilated, abnormal ZP:0006344 endoplasmic reticulum intestinal epithelium distended, abnormal ZP:0006345 cell junction intestinal epithelium loose, abnormal ZP:0006346 intestinal villus decreased length, abnormal ZP:0006347 intestinal villus disorganized, abnormal ZP:0006348 intestinal villus decreased amount, abnormal ZP:0006349 Bruch's membrane aplastic, abnormal ZP:0006350 chondrocyte deformed, abnormal ZP:0006351 chondrocyte increased accumulation vacuole cytoplasm chondrocyte, abnormal ZP:0006352 extracellular matrix chondrocyte decreased mass density, abnormal ZP:0006353 endoplasmic reticulum hepatocyte morphology, abnormal ZP:0006354 endoplasmic reticulum hepatocyte vacuolated, abnormal ZP:0006355 endoplasmic reticulum eye photoreceptor cell dilated, abnormal ZP:0006356 retinal rod cell aplastic, abnormal ZP:0006357 Muller cell disoriented, abnormal ZP:0006358 swimming decreased speed, abnormal ZP:0006359 brain decreased volume, abnormal ZP:0006360 brain has fewer parts of type cell, abnormal ZP:0006361 dopaminergic neuron diencephalon spatial pattern, abnormal ZP:0006362 positive regulation of gene expression disrupted, abnormal ZP:0006363 heart deformed, abnormal ZP:0006364 axon extension involved in axon guidance decreased process quality, abnormal ZP:0006365 axon CaP motoneuron increased branchiness, abnormal ZP:0006366 nuclear division disrupted, abnormal ZP:0006367 mitotic spindle organization disrupted, abnormal ZP:0006368 centriole replication disrupted, abnormal ZP:0006369 embryonic cleavage disrupted, abnormal ZP:0006370 centrosome duplication disrupted, abnormal ZP:0006371 yolk syncytial layer increased size, abnormal ZP:0006372 blastomere size, abnormal ZP:0006373 blastomere decreased amount, abnormal ZP:0006374 nucleus blastomere increased size, abnormal ZP:0006375 centrosome blastomere decreased amount, abnormal ZP:0006376 whole organism tetraploid, abnormal ZP:0006377 chromosome whole organism increased amount, abnormal ZP:0006378 centriole sperm composition, abnormal ZP:0006379 photoreceptor cell morphogenesis disrupted, abnormal ZP:0006380 photoreceptor cell outer segment organization disrupted, abnormal ZP:0006381 retinal cone cell development disrupted, abnormal ZP:0006382 determination of heart left/right asymmetry process quality, abnormal ZP:0006383 retinal ganglion cell layer absent, abnormal ZP:0006384 midbrain hindbrain boundary blurry, abnormal ZP:0006385 extension decreased width, abnormal ZP:0006386 eye opaque, abnormal ZP:0006387 retinal inner nuclear layer absent, abnormal ZP:0006388 lateral mesoderm bilateral symmetry, abnormal ZP:0006389 retinal outer nuclear layer absent, abnormal ZP:0006390 photoreceptor outer segment retinal rod cell absent, abnormal ZP:0006391 cranium quality, abnormal ZP:0006392 prechordal plate malformed, abnormal ZP:0006393 neural plate malformed, abnormal ZP:0006394 eye development process quality, abnormal ZP:0006395 somitogenesis process quality, abnormal ZP:0006396 extension disorganized, abnormal ZP:0006397 forebrain bulbous, abnormal ZP:0006398 palate malformed, abnormal ZP:0006399 somite cuboid, abnormal ZP:0006400 intersegmental vessel branchiness, abnormal ZP:0006401 cranial neural crest pharyngeal arch mislocalised, abnormal ZP:0006402 neurocranial trabecula decreased length, abnormal ZP:0006403 parachordal cartilage morphology, abnormal ZP:0006404 cranial cartilage decreased size, abnormal ZP:0006405 cranial ganglion decreased size, abnormal ZP:0006406 cranial neural crest cell rhombomere 6 decreased amount, abnormal ZP:0006407 fourth ventricle edematous, abnormal ZP:0006408 olfactory pit decreased size, abnormal ZP:0006409 mouth malformed, abnormal ZP:0006410 oral cavity mislocalised posteriorly, abnormal ZP:0006411 trigeminal motor nucleus fused with trigeminal motor nucleus, abnormal ZP:0006412 neural tube closure disrupted, abnormal ZP:0006413 protein localization to centrosome disrupted, abnormal ZP:0006414 cranial ganglion irregular spatial pattern, abnormal ZP:0006415 myoblast fusion decreased occurrence, abnormal ZP:0006416 fast muscle cell circular, abnormal ZP:0006417 pancreatic bud morphology, abnormal ZP:0006419 hypobranchial bone aplastic, abnormal ZP:0006420 ceratobranchial bone increased width, abnormal ZP:0006421 ceratohyal bone morphology, abnormal ZP:0006422 ceratohyal bone shape, abnormal ZP:0006423 symplectic decreased length, abnormal ZP:0006424 pharyngeal arch 2 skeleton decreased length, abnormal ZP:0006425 pharyngeal arch 2 skeleton increased width, abnormal ZP:0006426 pharyngeal arch 2 skeleton bifurcated, abnormal ZP:0006427 hyosymplectic cartilage shape, abnormal ZP:0006428 interhyal cartilage shape, abnormal ZP:0006429 hypobranchial cartilage decreased size, abnormal ZP:0006430 hypobranchial 1 cartilage aplastic, abnormal ZP:0006431 hypobranchial 2 cartilage aplastic, abnormal ZP:0006441 sensory neuron spinal cord decreased amount, abnormal ZP:0006442 glial cell proliferation decreased process quality, abnormal ZP:0006443 retinal rod cell development decreased process quality, abnormal ZP:0006444 retinal neural layer has fewer parts of type retinal rod cell, abnormal ZP:0006445 eye lacks all parts of type lens, abnormal ZP:0006448 establishment of anatomical structure orientation disrupted, abnormal ZP:0006449 embryonic morphogenesis disrupted, abnormal ZP:0006450 liver cystic, abnormal ZP:0006451 endoplasmic reticulum liver disoriented, abnormal ZP:0006452 endoplasmic reticulum liver swollen, abnormal ZP:0006453 whole organism curved lateral, abnormal ZP:0006454 trunk malformed, abnormal ZP:0006455 endoderm aplastic, abnormal ZP:0006456 cilium Kupffer's vesicle increased amount, abnormal ZP:0006457 cilium macula saccule decreased length, abnormal ZP:0006458 cilium macula saccule decreased amount, abnormal ZP:0006459 cell macula saccule decreased amount, abnormal ZP:0006460 spinal cord interneuron morphology, abnormal ZP:0006461 skeletal muscle decreased functionality, abnormal ZP:0006462 motor neuron absent, abnormal ZP:0006463 central nervous system degeneration, abnormal ZP:0006464 retinal pigmented epithelium distance retinal outer nuclear layer, abnormal ZP:0006465 photoreceptor outer segment retinal cone cell decreased amount, abnormal ZP:0006466 protein phosphorylation disrupted, abnormal ZP:0006467 chordate embryonic development disrupted, abnormal ZP:0006468 heart decreased thickness, abnormal ZP:0006469 notochord formation process quality, abnormal ZP:0006470 notochord cell differentiation process quality, abnormal ZP:0006471 notochord coiled, abnormal ZP:0006472 vacuole notochord increased amount, abnormal ZP:0006473 hindbrain decreased length, abnormal ZP:0006474 whole organism wholly posterioralized, abnormal ZP:0006475 anterior/posterior pattern specification process quality, abnormal ZP:0006476 pelvic fin mislocalised posteriorly, abnormal ZP:0006477 exocrine pancreas increased size, abnormal ZP:0006478 optic nerve development delayed, abnormal ZP:0006479 positive phototaxis decreased frequency, abnormal ZP:0006480 retinal ganglion cell retina decreased amount, abnormal ZP:0006481 axon retinal ganglion cell morphology, abnormal ZP:0006482 dorsal aorta obstructed, abnormal ZP:0006483 dorsal aorta mislocalised dorsally, abnormal ZP:0006484 blood vessel endothelial cell dorsal aorta positional polarity, abnormal ZP:0006485 posterior cardinal vein duplicated, abnormal ZP:0006486 posterior cardinal vein deformed, abnormal ZP:0006487 posterior cardinal vein mislocalised dorsally, abnormal ZP:0006488 blood vessel endothelial cell posterior cardinal vein structure, abnormal ZP:0006489 axial vasculature decreased area, abnormal ZP:0006490 ventral wall of dorsal aorta deformed, abnormal ZP:0006491 bicellular tight junction blood vessel endothelial cell increased amount, abnormal ZP:0006492 bicellular tight junction blood vessel endothelial cell mislocalised, abnormal ZP:0006493 detection of mechanical stimulus involved in sensory perception of sound process quality, abnormal ZP:0006494 vestibular reflex absent, abnormal ZP:0006495 stereocilium bundle auditory receptor cell splayed, abnormal ZP:0006496 afferent neuron has extra parts of type neuron projection afferent neuron, abnormal ZP:0006497 afferent neuron process quality neuron projection development, abnormal ZP:0006498 neuron projection afferent neuron complexity, abnormal ZP:0006499 neuron projection afferent neuron transient, abnormal ZP:0006500 blood vessel development process quality, abnormal ZP:0006501 blood vessel morphogenesis process quality, abnormal ZP:0006502 cilium assembly disrupted, abnormal ZP:0006503 cell brain morphology, abnormal ZP:0006504 floor plate patchy, abnormal ZP:0006506 motile cilium floor plate decreased amount, abnormal ZP:0006507 lens increased amount, abnormal ZP:0006508 motile cilium otic vesicle absent, abnormal ZP:0006509 somite hemorrhagic, abnormal ZP:0006510 ventral mesenchyme physical object quality, abnormal ZP:0006511 central canal decreased size, abnormal ZP:0006512 lateral dorsal aorta decreased diameter, abnormal ZP:0006513 posterior region myoseptum morphology, abnormal ZP:0006514 axoneme whole organism absent, abnormal ZP:0006518 adenohypophysis aplastic, abnormal ZP:0006519 trabecula cranii morphology, abnormal ZP:0006520 otolith deformed, abnormal ZP:0006521 pharyngeal vasculature hemorrhagic, abnormal ZP:0006522 kinocilium auditory receptor cell absent, abnormal ZP:0006523 thoracic duct decreased length, abnormal ZP:0006524 TOR signaling disrupted, abnormal ZP:0006525 photoreceptor outer segment retina decreased length, abnormal ZP:0006526 photoreceptor outer segment eye photoreceptor cell disheveled, abnormal ZP:0006527 vesicle membrane eye photoreceptor cell present, abnormal ZP:0006529 gall bladder quality, abnormal ZP:0006530 heart primordium increased size, abnormal ZP:0006531 tail bud deformed, abnormal ZP:0006532 yolk protruding, abnormal ZP:0006533 epidermis separated from muscle, abnormal ZP:0006534 immature eye decreased size, abnormal ZP:0006535 muscle malformed, abnormal ZP:0006536 epidermal cell permeable, abnormal ZP:0006537 epidermal cell separated from epidermal cell, abnormal ZP:0006538 bicellular tight junction epidermal cell decreased length, abnormal ZP:0006539 ossification decreased process quality, abnormal ZP:0006540 bone mineralization decreased process quality, abnormal ZP:0006541 integument ball physical object quality, abnormal ZP:0006542 integument extension physical object quality, abnormal ZP:0006543 postcranial axial skeleton cartilaginous, abnormal ZP:0006544 integument gill physical object quality, abnormal ZP:0006545 corpuscles of Stannius cellular quality, abnormal ZP:0006546 convergent extension involved in organogenesis disrupted, abnormal ZP:0006550 whole organism decreased width, abnormal ZP:0006551 regulation of transcription, DNA-templated disrupted, abnormal ZP:0006552 regulation of glucose metabolic process disrupted, abnormal ZP:0006553 midbrain-hindbrain boundary structural organization disrupted, abnormal ZP:0006554 nucleate erythrocyte maturation disrupted, abnormal ZP:0006555 eye pigmentation delayed, abnormal ZP:0006556 hematopoietic multipotent progenitor cell intermediate cell mass of mesoderm decreased amount, abnormal ZP:0006557 liver immature, abnormal ZP:0006558 erythroid lineage cell increased size, abnormal ZP:0006564 statoacoustic (VIII) ganglion decreased size, abnormal ZP:0006566 mechanosensory behavior arrested, abnormal ZP:0006567 protein localization to cell surface arrested, abnormal ZP:0006568 detection of mechanical stimulus involved in sensory perception of touch arrested, abnormal ZP:0006569 voltage-gated sodium channel complex Rohon-Beard neuron mislocalised, abnormal ZP:0006570 protein sumoylation disrupted, abnormal ZP:0006571 collagen fibril organization process quality, abnormal ZP:0006572 embryonic camera-type eye morphogenesis process quality, abnormal ZP:0006573 eye distended, abnormal ZP:0006575 anterior region sclera decreased thickness, abnormal ZP:0006576 posterior region sclera decreased thickness, abnormal ZP:0006577 fibroblast sclera decreased amount, abnormal ZP:0006578 neutrophil homeostasis disrupted, abnormal ZP:0006579 neutrophil spatial pattern, abnormal ZP:0006580 swim bladder increased length, abnormal ZP:0006581 swim bladder increased volume, abnormal ZP:0006582 anterior macula morphology, abnormal ZP:0006583 inner ear collapsed, abnormal ZP:0006584 macula crowded, abnormal ZP:0006585 intermediate mesoderm morphology, abnormal ZP:0006586 G2/M transition of mitotic cell cycle delayed, abnormal ZP:0006587 mitotic cell cycle delayed, abnormal ZP:0006589 gastrulation decreased rate, abnormal ZP:0006590 embryonic cleavage delayed, abnormal ZP:0006591 epiboly involved in gastrulation with mouth forming second decreased rate, abnormal ZP:0006592 intrinsic apoptotic signaling pathway increased process quality, abnormal ZP:0006593 blastoderm cell increased size, abnormal ZP:0006594 blastoderm cell decreased amount, abnormal ZP:0006595 blastoderm cell cellular adhesivity blastoderm cell, abnormal ZP:0006596 nucleus blastoderm cell increased size, abnormal ZP:0006597 nucleus blastoderm cell decreased amount, abnormal ZP:0006598 cardiac ventricle hypotrophic, abnormal ZP:0006599 dorsal aorta absent, abnormal ZP:0006600 yolk concave, abnormal ZP:0006601 caudal vein absent, abnormal ZP:0006602 common cardinal vein decreased width, abnormal ZP:0006604 posterior cardinal vein increased thickness, abnormal ZP:0006605 trunk vasculature hypoplastic, abnormal ZP:0006606 striated muscle myosin thick filament cardiac muscle cell disorganized, abnormal ZP:0006607 striated muscle thin filament cardiac muscle cell disorganized, abnormal ZP:0006608 myofibril cardiac muscle cell sparse, abnormal ZP:0006609 sarcomere cardiac muscle cell increased length, abnormal ZP:0006610 defense response to bacterium disrupted, abnormal ZP:0006611 hypophysis quality, abnormal ZP:0006613 cell cycle decreased rate, abnormal ZP:0006614 swimming decreased rate, abnormal ZP:0006615 regulation of ventricular cardiac muscle cell membrane repolarization process quality, abnormal ZP:0006616 cardiac conduction arrested, abnormal ZP:0006617 cardiac conduction increased duration, abnormal ZP:0006618 cardiac conduction decreased rate, abnormal ZP:0006619 nucleate erythrocyte blood increased amount, abnormal ZP:0006620 cardiac ventricle action potential, abnormal ZP:0006621 cardiac ventricle functionality, abnormal ZP:0006622 whole organism semi-viable, abnormal ZP:0006623 vertebral artery present, abnormal ZP:0006624 parachordal vessel present, abnormal ZP:0006625 pharyngeal arch disorganized, abnormal ZP:0006626 epithelial cilium movement involved in extracellular fluid movement disrupted, abnormal ZP:0006627 tubulin-glutamic acid ligase activity disrupted, abnormal ZP:0006628 cilium Kupffer's vesicle non-functional, abnormal ZP:0006629 axonemal microtubule pronephric duct increased amount, abnormal ZP:0006630 axonemal microtubule pronephric duct decreased size, abnormal ZP:0006631 axoneme pronephric duct morphology, abnormal ZP:0006632 inner ear altered number of otolith, abnormal ZP:0006633 ventral mandibular arch increased thickness, abnormal ZP:0006634 somite increased size, abnormal ZP:0006635 whole organism elongated, abnormal ZP:0006636 caudal fin lower lobe absent, abnormal ZP:0006637 blood accumulation cranial vasculature, abnormal ZP:0006638 blood accumulation trunk vasculature, abnormal ZP:0006639 intersegmental vein absent, abnormal ZP:0006640 intersegmental vein decreased length, abnormal ZP:0006641 liver development decreased rate, abnormal ZP:0006642 eye photoreceptor cell differentiation disrupted, abnormal ZP:0006643 antero-ventral region hindbrain apoptotic, abnormal ZP:0006644 serotonergic neuron hindbrain decreased amount, abnormal ZP:0006645 retinal inner nuclear layer malformed, abnormal ZP:0006646 neuron retinal inner nuclear layer decreased amount, abnormal ZP:0006647 neuron retina decreased amount, abnormal ZP:0006648 whole organism increased pigmentation, abnormal ZP:0006649 retinal outer nuclear layer malformed, abnormal ZP:0006650 melanosome melanocyte increased distribution, abnormal ZP:0006651 mesoderm cellular motility, abnormal ZP:0006652 hypophyseal fenestra increased width, abnormal ZP:0006653 anterior neural plate decreased length, abnormal ZP:0006654 mRNA polyadenylation disrupted, abnormal ZP:0006655 iridophore post-vent region decreased amount, abnormal ZP:0006656 ventral mandibular arch shape, abnormal ZP:0006657 hematopoietic stem cell apoptotic, abnormal ZP:0006658 heart contraction decreased magnitude, abnormal ZP:0006659 heart increased accumulation blood, abnormal ZP:0006660 common cardinal vein decreased size, abnormal ZP:0006661 blood vasculature obstructed, abnormal ZP:0006662 aortic arch constricted, abnormal ZP:0006663 cell-cell junction blood vessel endothelial cell decreased length, abnormal ZP:0006664 multicellular organism growth disrupted, abnormal ZP:0006665 caudal fin truncated, abnormal ZP:0006666 neuromast hair cell posterior lateral line decreased amount, abnormal ZP:0006667 growth cone motor neuron increased size, abnormal ZP:0006668 swimming disrupted, abnormal ZP:0006669 axon neuron decreased length, abnormal ZP:0006670 axon neuron decreased branchiness, abnormal ZP:0006671 glutamatergic neuron decreased amount, abnormal ZP:0006672 forebrain neuron development disrupted, abnormal ZP:0006673 locomotion involved in locomotory behavior increased occurrence, abnormal ZP:0006674 neuron brain apoptotic, abnormal ZP:0006676 retina lacks parts or has fewer parts of type dopaminergic neuron, abnormal ZP:0006677 adrenergic neuron olfactory bulb decreased amount, abnormal ZP:0006678 periventricular nucleus of caudal tuberculum has fewer parts of type dopaminergic neuron, abnormal ZP:0006679 pretectum lacks parts or has fewer parts of type dopaminergic neuron, abnormal ZP:0006680 adrenergic neuron pretectum decreased amount, abnormal ZP:0006681 ventral thalamus has fewer parts of type dopaminergic neuron, abnormal ZP:0006682 preoptic area lacks parts or has fewer parts of type dopaminergic neuron, abnormal ZP:0006683 adrenergic neuron preoptic area decreased amount, abnormal ZP:0006684 adrenergic neuron caudal tuberculum decreased amount, abnormal ZP:0006686 neuron fate commitment disrupted, abnormal ZP:0006687 pancreas primordium has fewer parts of type endocrine cell, abnormal ZP:0006688 pancreatic bud has fewer parts of type endocrine cell, abnormal ZP:0006689 pancreatic bud has fewer parts of type pancreatic B cell, abnormal ZP:0006691 pancreatic bud has fewer parts of type pancreatic A cell, abnormal ZP:0006692 VeLD increased amount, abnormal ZP:0006694 eye development delayed, abnormal ZP:0006695 optic vesicle morphology, abnormal ZP:0006696 nucleus retinal inner nuclear layer apoptotic, abnormal ZP:0006697 cell retinal inner nuclear layer degenerate, abnormal ZP:0006698 retinal pigmented epithelium discolored, abnormal ZP:0006699 axon cranial nerve II decreased length, abnormal ZP:0006700 axon cranial nerve II defasciculated, abnormal ZP:0006701 whole organism colorless, abnormal ZP:0006702 ciliary marginal zone damaged, abnormal ZP:0006703 retinal inner plexiform layer decreased thickness, abnormal ZP:0006704 nucleus retinal ganglion cell apoptotic, abnormal ZP:0006711 left/right axis specification disrupted, abnormal ZP:0006712 floor plate morphology, abnormal ZP:0006713 cilium pronephric duct immobile, abnormal ZP:0006714 inner dynein arm pronephric duct absent, abnormal ZP:0006715 outer dynein arm pronephric duct absent, abnormal ZP:0006716 cilium olfactory bulb immobile, abnormal ZP:0006717 anatomical axis trunk curved, abnormal ZP:0006718 trunk unpigmented, abnormal ZP:0006719 cell cycle arrest disrupted, abnormal ZP:0006720 regulation of cell cycle process disrupted, abnormal ZP:0006721 cell retina decreased amount, abnormal ZP:0006722 mandibular arch skeleton physical object quality, abnormal ZP:0006723 cranium morphology, abnormal ZP:0006724 myelination in peripheral nervous system disrupted, abnormal ZP:0006725 endoplasmic reticulum unfolded protein response increased process quality, abnormal ZP:0006726 myelination of posterior lateral line nerve axons decreased process quality, abnormal ZP:0006727 axon spinal cord morphology, abnormal ZP:0006728 node of Ranvier spinal cord morphology, abnormal ZP:0006729 node of Ranvier spinal cord decreased amount, abnormal ZP:0006730 mitochondrion liver decreased size, abnormal ZP:0006731 endoplasmic reticulum liver broken, abnormal ZP:0006732 endoplasmic reticulum lumen liver morphology, abnormal ZP:0006733 mitochondrial crista liver increased width, abnormal ZP:0006734 bile canaliculus liver disorganized, abnormal ZP:0006735 node of Ranvier posterior lateral line nerve morphology, abnormal ZP:0006736 node of Ranvier posterior lateral line nerve decreased amount, abnormal ZP:0006737 endoplasmic reticulum oligodendrocyte swollen, abnormal ZP:0006738 endoplasmic reticulum myelinating Schwann cell swollen, abnormal ZP:0006739 neuron death increased occurrence, abnormal ZP:0006740 hindbrain degenerate, abnormal ZP:0006741 telencephalon degenerate, abnormal ZP:0006742 diencephalon degenerate, abnormal ZP:0006743 dorsal region neural tube degenerate, abnormal ZP:0006744 macrophage absent, abnormal ZP:0006747 maintenance of blood-brain barrier disrupted, abnormal ZP:0006748 glucose import decreased process quality, abnormal ZP:0006749 brain vasculature decreased functionality, abnormal ZP:0006750 adherens junction blood vessel endothelium decreased object quality, abnormal ZP:0006751 bicellular tight junction blood vessel endothelium decreased object quality, abnormal ZP:0006752 blood vessel permeable, abnormal ZP:0006753 lymph vasculature trunk absent, abnormal ZP:0006754 endothelial cell trunk decreased amount, abnormal ZP:0006755 cerebellar central artery absent, abnormal ZP:0006756 anterior mesencephalic central artery absent, abnormal ZP:0006757 middle mesencephalic central artery absent, abnormal ZP:0006758 posterior mesencephalic central artery absent, abnormal ZP:0006759 filopodium vascular sprouts absent, abnormal ZP:0006760 cloacal chamber cystic, abnormal ZP:0006761 protein localization to cilium disrupted, abnormal ZP:0006762 caudal fin upper lobe rough, abnormal ZP:0006763 caudal fin lower lobe rough, abnormal ZP:0006764 spliceosomal complex assembly disrupted, abnormal ZP:0006765 epithelial cell thymus decreased thickness, abnormal ZP:0006766 U6 snRNP whole organism decreased amount, abnormal ZP:0006767 head decreased circumference, abnormal ZP:0006768 splanchnocranium malformed, abnormal ZP:0006769 osteoblast differentiation predisplaced growth, abnormal ZP:0006770 chondrocyte development premature, abnormal ZP:0006771 proteoglycan biosynthetic process disrupted, abnormal ZP:0006772 eye protruding, abnormal ZP:0006773 extracellular matrix cranium decreased volume, abnormal ZP:0006774 perichondral bone cranium hyperplastic, abnormal ZP:0006775 splanchnocranium structure, abnormal ZP:0006776 chondrocranium structure, abnormal ZP:0006777 anterior region neurocranium hypoplastic, abnormal ZP:0006778 perichondral bone hyperplastic, abnormal ZP:0006779 perichondral bone has extra parts of type osteoblast, abnormal ZP:0006780 atrium decreased functionality, abnormal ZP:0006781 bone mineralization increased process quality, abnormal ZP:0006782 cleithrum nodular, abnormal ZP:0006783 axial fin skeleton mineralized, abnormal ZP:0006784 vertebra fused with centrum centrum, abnormal ZP:0006785 myotome morphology, abnormal ZP:0006786 skeletal muscle cell apoptotic, abnormal ZP:0006787 slow muscle cell mislocalised, abnormal ZP:0006788 cardiovascular system hypertrophic, abnormal ZP:0006789 DNA replication checkpoint disrupted, abnormal ZP:0006790 mitotic prophase temporally extended, abnormal ZP:0006791 S phase increased occurrence, abnormal ZP:0006792 startle response sporadic, abnormal ZP:0006794 tonic skeletal muscle contraction sporadic, abnormal ZP:0006796 axis whole organism shortened, abnormal ZP:0006797 dorsal region retinal pigmented epithelium aplastic, abnormal ZP:0006798 exocrine pancreas undifferentiated, abnormal ZP:0006799 thrombocyte differentiation disrupted, abnormal ZP:0006800 blood decreased volume, abnormal ZP:0006801 yolk vacuolated, abnormal ZP:0006802 common cardinal vein congested, abnormal ZP:0006803 intestine edematous, abnormal ZP:0006806 Wnt signaling pathway, calcium modulating pathway disrupted, abnormal ZP:0006807 convergent extension involved in somitogenesis disrupted, abnormal ZP:0006808 mitotic sister chromatid segregation arrested, abnormal ZP:0006809 mitotic prometaphase increased duration, abnormal ZP:0006811 mitotic metaphase plate congression process quality, abnormal ZP:0006814 spindle assembly checkpoint increased occurrence, abnormal ZP:0006815 intrinsic apoptotic signaling pathway by p53 class mediator increased occurrence, abnormal ZP:0006816 brain immature, abnormal ZP:0006817 proliferative region increased occurrence intrinsic apoptotic signaling pathway by p53 class mediator, abnormal ZP:0006818 optic primordium immature, abnormal ZP:0006819 caudal fin shortened, abnormal ZP:0006820 caudal fin increased occurrence intrinsic apoptotic signaling pathway by p53 class mediator, abnormal ZP:0006821 whole organism increased occurrence intrinsic apoptotic signaling pathway by p53 class mediator, abnormal ZP:0006822 head increased occurrence intrinsic apoptotic signaling pathway by p53 class mediator, abnormal ZP:0006823 trunk increased occurrence intrinsic apoptotic signaling pathway by p53 class mediator, abnormal ZP:0006824 blood vessel decreased amount, abnormal ZP:0006825 lens non-functional, abnormal ZP:0006826 eye deformed, abnormal ZP:0006827 iridophore absent, abnormal ZP:0006828 blood island distended, abnormal ZP:0006829 hematopoietic stem cell increased amount, abnormal ZP:0006830 monocyte increased amount, abnormal ZP:0006831 leukocyte proportionality to nucleate erythrocyte, abnormal ZP:0006832 pancreatic epsilon cell decreased amount, abnormal ZP:0006833 protein glycosylation decreased process quality, abnormal ZP:0006834 myoseptum increased width, abnormal ZP:0006835 myoseptum damaged, abnormal ZP:0006836 sarcolemma muscle damaged, abnormal ZP:0006837 skeletal muscle cell disorganized, abnormal ZP:0006838 skeletal muscle cell sparse, abnormal ZP:0006839 prechordal plate mislocalised, abnormal ZP:0006840 lens rough, abnormal ZP:0006841 calcium ion homeostasis disrupted, abnormal ZP:0006842 muscle post-vent region shortened, abnormal ZP:0006843 leucine metabolic process disrupted, abnormal ZP:0006844 spinal cord curved, abnormal ZP:0006845 synaptic transmission, cholinergic amplitude, abnormal ZP:0006846 nucleate erythrocyte cardiovascular system absent, abnormal ZP:0006847 intersegmental vessel brochidodromous, abnormal ZP:0006848 ceratohyal cartilage straight, abnormal ZP:0006849 blood vessel endothelial cell delamination involved in blood vessel lumen ensheathment disrupted, abnormal ZP:0006850 endothelial tube lumen extension involved in blood vessel lumen ensheathment disrupted, abnormal ZP:0006851 cardiac ventricle elongated, abnormal ZP:0006852 common cardinal vein decreased length, abnormal ZP:0006853 common cardinal vein disrupted blood vessel endothelial cell migration, abnormal ZP:0006854 intersegmental vessel absent blood vessel lumenization, abnormal ZP:0006855 cardiac jelly physical quality, abnormal ZP:0006856 atrial endocardium structure, abnormal ZP:0006857 cell-cell junction atrial endocardium decreased size, abnormal ZP:0006858 cell-cell junction atrial endocardium decreased amount, abnormal ZP:0006859 developmental growth process quality, abnormal ZP:0006860 angioblast cell migration from lateral mesoderm to midline disrupted, abnormal ZP:0006861 artery development disrupted, abnormal ZP:0006862 blood vessel endothelial cell intersegmental vessel slender, abnormal ZP:0006863 axial blood vessel malformed, abnormal ZP:0006864 mitotic cell cycle arrested, abnormal ZP:0006865 chromosome segregation process quality, abnormal ZP:0006866 mitotic cell cycle arrest increased duration, abnormal ZP:0006867 exocrine pancreas decreased length, abnormal ZP:0006868 exocrine pancreas retracted, abnormal ZP:0006869 spindle ciliary marginal zone structure, abnormal ZP:0006870 spindle ciliary marginal zone increased amount, abnormal ZP:0006871 spindle ciliary marginal zone apical-basal polarity, abnormal ZP:0006872 ciliary marginal zone orientation spindle retinal pigmented epithelium, abnormal ZP:0006873 dorsal aorta decreased size, abnormal ZP:0006874 lateral dorsal aorta decreased thickness, abnormal ZP:0006875 lateral dorsal aorta unlumenized, abnormal ZP:0006876 myeloid cell development disrupted, abnormal ZP:0006877 blood island has fewer parts of type myeloid cell, abnormal ZP:0006878 olfactory placode decreased size, abnormal ZP:0006879 cilium olfactory placode aggregated, abnormal ZP:0006880 ventricular system edematous, abnormal ZP:0006881 whole organism color, abnormal ZP:0006882 whole organism curled, abnormal ZP:0006883 head structure, abnormal ZP:0006884 cilium olfactory pit truncated, abnormal ZP:0006885 cilium olfactory pit shortened, abnormal ZP:0006887 photoreceptor outer segment layer decreased size, abnormal ZP:0006888 centriole eye photoreceptor cell displaced, abnormal ZP:0006889 cilium or flagellum-dependent cell motility decreased rate, abnormal ZP:0006890 epithelial cilium movement involved in extracellular fluid movement decreased frequency, abnormal ZP:0006891 establishment of epithelial cell apical/basal polarity disrupted, abnormal ZP:0006892 cilium movement involved in cell motility disrupted, abnormal ZP:0006893 cilium Kupffer's vesicle functionality, abnormal ZP:0006894 cilium floor plate functionality, abnormal ZP:0006895 optic vesicle decreased size, abnormal ZP:0006896 tail bud increased length, abnormal ZP:0006897 pronephric duct morphology, abnormal ZP:0006898 mesodermal cell paraxial mesoderm disoriented, abnormal ZP:0006899 cilium cloacal chamber functionality, abnormal ZP:0006900 motile cilium olfactory epithelium decreased speed, abnormal ZP:0006901 cilium neural tube functionality, abnormal ZP:0006902 pronephric glomerulus dilated, abnormal ZP:0006903 cilium pronephric tubule functionality, abnormal ZP:0006904 cilium pronephric tubule decreased amount, abnormal ZP:0006905 pronephric proximal straight tubule dilated, abnormal ZP:0006906 motile cilium posterior pronephric duct decreased speed, abnormal ZP:0006907 neural crest apoptotic, abnormal ZP:0006908 trigeminal ganglion disorganized, abnormal ZP:0006909 calmodulin-dependent protein kinase activity decreased occurrence, abnormal ZP:0006910 regulation of cardiac muscle contraction by calcium ion signaling decreased process quality, abnormal ZP:0006911 regulation of collagen biosynthetic process process quality, abnormal ZP:0006912 cell migration involved in kidney development disrupted, abnormal ZP:0006913 cell proliferation involved in pronephros development increased occurrence, abnormal ZP:0006914 protein autophosphorylation decreased occurrence, abnormal ZP:0006915 ventricular cardiac muscle cell action potential decreased process quality, abnormal ZP:0006916 notochord physical object quality, abnormal ZP:0006917 distal region pronephric duct obstructed, abnormal ZP:0006918 anterior region pronephros structure, abnormal ZP:0006919 anterior region pronephros truncated, abnormal ZP:0006920 inner ear increased distance posterior-most region anterior-most region pronephric duct, abnormal ZP:0006921 cilium cloacal chamber decreased length, abnormal ZP:0006922 cilium cloacal chamber decreased amount, abnormal ZP:0006923 digestive system morphology, abnormal ZP:0006924 pronephric duct opening decreased size, abnormal ZP:0006925 renal glomerulus cystic, abnormal ZP:0006926 angiogenesis increased occurrence, abnormal ZP:0006927 blood vasculature hindbrain branched, abnormal ZP:0006928 brain vasculature branched, abnormal ZP:0006929 cranial vasculature increased diameter, abnormal ZP:0006930 cranial vasculature branchiness, abnormal ZP:0006931 cell intersegmental vessel increased amount, abnormal ZP:0006932 aortic arch dilated, abnormal ZP:0006933 aortic arch increased diameter, abnormal ZP:0006934 locomotory behavior decreased process quality, abnormal ZP:0006935 axon extension decreased process quality, abnormal ZP:0006936 sensory perception of touch decreased process quality, abnormal ZP:0006937 neuronal stem cell population maintenance decreased process quality, abnormal ZP:0006938 spinal cord decreased size, abnormal ZP:0006939 spinal cord has fewer parts of type motor neuron, abnormal ZP:0006940 spinal cord lacks parts or has fewer parts of type secondary motor neuron, abnormal ZP:0006941 neuronal stem cell spinal cord apoptotic, abnormal ZP:0006942 integument edematous, abnormal ZP:0006943 ciliary marginal zone apoptotic, abnormal ZP:0006944 intestinal epithelium morphology, abnormal ZP:0006945 axon motor neuron disorganized, abnormal ZP:0006946 symplectic increased length, abnormal ZP:0006947 symplectic in contact with Meckel's cartilage, abnormal ZP:0006948 caudal fin ruffled, abnormal ZP:0006949 pharyngeal arch 4 skeleton decreased size, abnormal ZP:0006950 joint pharyngeal arch absent, abnormal ZP:0006951 ceratohyal cartilage fused with hyosymplectic cartilage, abnormal ZP:0006952 basihyal cartilage shape, abnormal ZP:0006953 basihyal cartilage hyperplastic, abnormal ZP:0006954 cardiac muscle cell differentiation arrested, abnormal ZP:0006955 cardiac muscle cell differentiation process quality, abnormal ZP:0006957 heart aplastic, abnormal ZP:0006958 bulbus arteriosus decreased size, abnormal ZP:0006959 bulbus arteriosus aplastic, abnormal ZP:0006960 heart tube shortened, abnormal ZP:0006961 atrium physical object quality, abnormal ZP:0006962 presumptive atrium heart tube decreased volume, abnormal ZP:0006963 presumptive cardiac ventricle heart tube decreased volume, abnormal ZP:0006964 cardiac muscle cell undifferentiated, abnormal ZP:0006965 Kupffer's vesicle decreased functionality, abnormal ZP:0006966 bicellular tight junction Kupffer's vesicle disorganized, abnormal ZP:0006967 motor neuron migration abnormal, abnormal ZP:0006968 glycolytic process increased rate, abnormal ZP:0006969 neuroblast proliferation increased rate, abnormal ZP:0006970 aerobic respiration decreased rate, abnormal ZP:0006971 respiratory electron transport chain process quality, abnormal ZP:0006972 cilium pronephric duct malformed, abnormal ZP:0006973 mitochondrion motor neuron mislocalised, abnormal ZP:0006974 axon motor neuron unbranched, abnormal ZP:0006975 axon terminus motor neuron decreased amount, abnormal ZP:0006976 glial cell spatial pattern, abnormal ZP:0006977 glial cell malformed, abnormal ZP:0006978 neutrophil blood island increased amount, abnormal ZP:0006979 vasculogenesis decreased process quality, abnormal ZP:0006980 erythrocyte maturation disrupted, abnormal ZP:0006981 primitive erythrocyte differentiation disrupted, abnormal ZP:0006982 blood heart absent, abnormal ZP:0006983 blood blood vessel absent, abnormal ZP:0006984 pharyngeal arch deformed, abnormal ZP:0006985 head protruding, abnormal ZP:0006987 trunk kinked, abnormal ZP:0006988 outer dynein arm ciliated olfactory receptor neuron absent, abnormal ZP:0006989 somite rostral/caudal axis specification disrupted, abnormal ZP:0006990 tail bud increased width, abnormal ZP:0006991 somite anterior-posterior polarity, abnormal ZP:0006992 anterior-posterior axis somite condensed, abnormal ZP:0006993 medial-lateral axis somite increased width, abnormal ZP:0006994 medial-lateral axis whole organism increased width, abnormal ZP:0006996 sinus venosus edematous, abnormal ZP:0006997 skeletal muscle morphology, abnormal ZP:0006998 epidermis trunk morphology, abnormal ZP:0006999 epidermis post-vent region morphology, abnormal ZP:0007000 post-vent vasculature increased accumulation postero-ventral region nucleate erythrocyte, abnormal ZP:0007001 vasculature degenerate, abnormal ZP:0007002 chondrocyte ventral mandibular arch decreased amount, abnormal ZP:0007003 pharyngeal arch cartilage fragile, abnormal ZP:0007004 mitotic cell cycle, embryonic arrested, abnormal ZP:0007005 neuron projection optic tectum mislocalised, abnormal ZP:0007006 neuron projection optic tectum disorganized, abnormal ZP:0007007 retinal inner plexiform layer deformed, abnormal ZP:0007008 stratum fibrosum et griseum superficiale increased width, abnormal ZP:0007009 axon stratum fibrosum et griseum superficiale mislocalised, abnormal ZP:0007010 neuron projection amacrine cell morphology, abnormal ZP:0007011 dendrite retinal ganglion cell morphology, abnormal ZP:0007012 axon retinal bipolar neuron morphology, abnormal ZP:0007013 head damaged, abnormal ZP:0007014 muscle cell cellular homeostasis disrupted, abnormal ZP:0007015 myosin complex somite border aggregated, abnormal ZP:0007016 slow muscle cell quality, abnormal ZP:0007017 slow muscle cell broken, abnormal ZP:0007018 slow muscle cell non-functional, abnormal ZP:0007019 actin filament slow muscle cell irregular spatial pattern, abnormal ZP:0007020 myosin filament slow muscle cell irregular spatial pattern, abnormal ZP:0007021 type III intermediate filament slow muscle cell irregular spatial pattern, abnormal ZP:0007023 Z disc cardiac muscle increased width, abnormal ZP:0007024 Z disc cardiac muscle disorganized, abnormal ZP:0007025 sarcomere cardiac muscle cell decreased thickness, abnormal ZP:0007026 sarcomere cardiac muscle cell decreased amount, abnormal ZP:0007027 heart jogging process quality, abnormal ZP:0007028 embryonic heart tube left/right pattern formation process quality, abnormal ZP:0007029 left/right pattern formation process quality, abnormal ZP:0007030 determination of digestive tract left/right asymmetry process quality, abnormal ZP:0007031 Kupffer's vesicle decreased width, abnormal ZP:0007032 Kupffer's vesicle functionality, abnormal ZP:0007033 Kupffer's vesicle lacks parts or has fewer parts of type motile cilium Kupffer's vesicle, abnormal ZP:0007034 Kupffer's vesicle process quality cilium movement, abnormal ZP:0007035 motile cilium Kupffer's vesicle immobile, abnormal ZP:0007036 motile cilium Kupffer's vesicle malformed, abnormal ZP:0007037 Kupffer's vesicle lacks parts or has fewer parts of type motile cilium axonemal central pair Kupffer's vesicle, abnormal ZP:0007038 ciliated cell Kupffer's vesicle decreased length, abnormal ZP:0007039 ciliated cell Kupffer's vesicle decreased amount, abnormal ZP:0007040 heart rudiment split bilaterally, abnormal ZP:0007041 heart rudiment displaced to right side whole organism, abnormal ZP:0007042 heart rudiment displaced to axis whole organism, abnormal ZP:0007043 musculature system caudal fin decreased thickness, abnormal ZP:0007045 cardiac muscle cell ventricular myocardium decreased amount, abnormal ZP:0007046 cell-cell junction maintenance disrupted, abnormal ZP:0007047 aconitate hydratase activity decreased process quality, abnormal ZP:0007048 cytochrome-c oxidase activity decreased process quality, abnormal ZP:0007049 nucleate erythrocyte heart decreased amount, abnormal ZP:0007050 myelination of lateral line nerve axons disrupted, abnormal ZP:0007051 melanocyte dilated, abnormal ZP:0007052 myelinating Schwann cell decreased amount, abnormal ZP:0007053 neural rod decreased length, abnormal ZP:0007054 otic placode increased distance otic placode, abnormal ZP:0007055 neuroepithelial cell apical-basal polarity, abnormal ZP:0007056 apical surface neuroepithelial cell morphology, abnormal ZP:0007058 lamellipodium anterior axial hypoblast decreased amount, abnormal ZP:0007059 filopodium anterior axial hypoblast decreased amount, abnormal ZP:0007060 endodermal cell gut disorganized, abnormal ZP:0007061 lateral plate mesoderm morphology, abnormal ZP:0007062 lateral plate mesoderm apoptotic, abnormal ZP:0007063 actin filament bundle lateral plate mesoderm increased size, abnormal ZP:0007064 mesodermal cell lateral plate mesoderm disorganized, abnormal ZP:0007065 liver mislocalised ventrally, abnormal ZP:0007066 hepatocyte liver apoptotic, abnormal ZP:0007067 liver primordium mislocalised posteriorly, abnormal ZP:0007068 actin filament bundle endodermal cell increased size, abnormal ZP:0007069 cell proliferation in hindbrain decreased rate, abnormal ZP:0007070 cerebellar granule cell differentiation disrupted, abnormal ZP:0007071 neurotransmitter biosynthetic process process quality, abnormal ZP:0007072 musculoskeletal movement, spinal reflex action decreased rate, abnormal ZP:0007073 secondary motor neuron floor plate decreased amount, abnormal ZP:0007074 cerebellar granule cell cerebellum decreased amount, abnormal ZP:0007075 pancreas spheroid, abnormal ZP:0007076 pectoral fin musculature decreased tonicity, abnormal ZP:0007077 pancreatic duct disrupted cell migration, abnormal ZP:0007079 pancreatic ductal cell located in hepatic duct, abnormal ZP:0007080 muscle organ morphogenesis disrupted, abnormal ZP:0007081 skeletal muscle cell myotome disorganized, abnormal ZP:0007082 sarcomere skeletal muscle cell disorganized, abnormal ZP:0007083 trunk disorganized, abnormal ZP:0007084 post-vent region disorganized, abnormal ZP:0007085 endocrine cell endocrine pancreas undifferentiated, abnormal ZP:0007086 epidermis ventral fin fold morphology, abnormal ZP:0007087 endoplasmic reticulum unfolded protein response process quality, abnormal ZP:0007088 locomotory behavior decreased speed, abnormal ZP:0007089 posterior lateral line nerve decreased thickness, abnormal ZP:0007090 myelin sheath posterior lateral line nerve morphology, abnormal ZP:0007091 myelin sheath posterior lateral line nerve decreased thickness, abnormal ZP:0007092 compact myelin posterior lateral line nerve absent, abnormal ZP:0007093 inner ear swollen, abnormal ZP:0007095 vertebra mineralized, abnormal ZP:0007096 otic vesicle protrusion disorganized, abnormal ZP:0007097 regulation of blood vessel endothelial cell migration disrupted, abnormal ZP:0007098 branching involved in lymph vessel morphogenesis disrupted, abnormal ZP:0007099 venous endothelial cell migration involved in lymph vessel development disrupted, abnormal ZP:0007100 cellular response to growth factor stimulus increased occurrence, abnormal ZP:0007101 dorsal aorta has extra parts of type endothelial tip cell, abnormal ZP:0007102 blood vasculature gut increased amount, abnormal ZP:0007103 posterior cardinal vein lacks parts or has fewer parts of type endothelial tip cell, abnormal ZP:0007104 intersegmental artery absent, abnormal ZP:0007106 blood vasculature pectoral fin increased amount, abnormal ZP:0007109 thoracic duct hypotrophic, abnormal ZP:0007110 lymphangiogenic sprout decreased amount, abnormal ZP:0007111 median fin fold hypoplastic, abnormal ZP:0007112 ventral region caudal fin hypoplastic, abnormal ZP:0007113 ventral fin fold hypoplastic, abnormal ZP:0007114 post-vent region has extra parts of type muscle, abnormal ZP:0007115 protein kinase activity decreased occurrence, abnormal ZP:0007116 epithelial structure maintenance disrupted, abnormal ZP:0007117 formation of anatomical boundary delayed, abnormal ZP:0007118 actin cytoskeleton somite disorganized, abnormal ZP:0007119 epithelial cell somite morphology, abnormal ZP:0007120 lamellipodium cell decreased amount, abnormal ZP:0007121 spinal cord physical object quality, abnormal ZP:0007123 post-vent region decreased thickness, abnormal ZP:0007124 skeletal muscle contractility, abnormal ZP:0007125 skeletal muscle decreased force, abnormal ZP:0007126 striated muscle thin filament skeletal muscle decreased length, abnormal ZP:0007127 sarcomere skeletal muscle decreased length, abnormal ZP:0007128 filamentous actin skeletal muscle cell aggregated, abnormal ZP:0007129 epidermis post-vent region irregular spatial pattern, abnormal ZP:0007130 cloacal septation disrupted, abnormal ZP:0007131 brain decreased mass, abnormal ZP:0007132 brain infiltrative, abnormal ZP:0007133 cerebellum organization quality, abnormal ZP:0007134 fourth ventricle composition, abnormal ZP:0007135 retinal photoreceptor layer lacks all parts of type photoreceptor outer segment photoreceptor cell, abnormal ZP:0007136 renal system cystic, abnormal ZP:0007137 anterior-posterior axis whole organism increased curvature, abnormal ZP:0007138 photoreceptor outer segment layer disorganized, abnormal ZP:0007139 erythrocyte homeostasis disrupted, abnormal ZP:0007140 homeostasis of number of cells within a tissue disrupted, abnormal ZP:0007141 nucleate erythrocyte dorsal aorta decreased amount, abnormal ZP:0007142 nucleate erythrocyte common cardinal vein decreased amount, abnormal ZP:0007143 integument increased accumulation epidermal cell, abnormal ZP:0007144 ventral fin fold increased accumulation epidermal cell, abnormal ZP:0007145 whole organism monstrous, abnormal ZP:0007146 nucleate erythrocyte increased volume, abnormal ZP:0007147 nucleate erythrocyte deformed, abnormal ZP:0007148 nucleus nucleate erythrocyte swollen, abnormal ZP:0007149 plasma membrane nucleate erythrocyte broken, abnormal ZP:0007150 plasma membrane nucleate erythrocyte deformed, abnormal ZP:0007151 mitotic sister chromatid segregation disrupted, abnormal ZP:0007152 nucleus retina morphology, abnormal ZP:0007153 nucleus retina variability of size, abnormal ZP:0007154 chromosome gastrula cell morphology, abnormal ZP:0007155 M phase increased duration, abnormal ZP:0007156 retina morphogenesis in camera-type eye delayed, abnormal ZP:0007157 hematopoietic stem cell proliferation decreased rate, abnormal ZP:0007158 blood island has fewer parts of type hematopoietic stem cell, abnormal ZP:0007159 T cell absent, abnormal ZP:0007160 embryonic neurocranium morphogenesis process quality, abnormal ZP:0007161 neural crest cell mislocalised, abnormal ZP:0007162 intestinal epithelial structure maintenance decreased process quality, abnormal ZP:0007163 intestine well differentiated, abnormal ZP:0007165 intestinal epithelium has fewer parts of type epithelial cell, abnormal ZP:0007166 slow-twitch skeletal muscle fiber contraction decreased process quality, abnormal ZP:0007167 taxis decreased process quality, abnormal ZP:0007168 axis curved ventral, abnormal ZP:0007169 slow muscle cell has fewer parts of type myofibril slow muscle cell, abnormal ZP:0007170 striated muscle thin filament slow muscle cell disorganized, abnormal ZP:0007171 myofibril slow muscle cell decreased size, abnormal ZP:0007172 sarcomere slow muscle cell malformed, abnormal ZP:0007173 sarcomere slow muscle cell decreased amount, abnormal ZP:0007174 animal organ morphogenesis disrupted, abnormal ZP:0007176 melanosome transport decreased rate, abnormal ZP:0007177 startle response decreased process quality, abnormal ZP:0007178 cellular respiration decreased process quality, abnormal ZP:0007179 midbrain hindbrain boundary inconspicuous, abnormal ZP:0007180 contractile fiber muscle disorganized, abnormal ZP:0007181 mitochondrion muscle cell broken, abnormal ZP:0007182 nucleate erythrocyte accumulation heart, abnormal ZP:0007183 sarcomere heart malformed, abnormal ZP:0007184 Z disc heart malformed, abnormal ZP:0007185 telencephalon cellular quality, abnormal ZP:0007186 postero-dorsal region telencephalon cellular quality, abnormal ZP:0007187 heparan sulfate proteoglycan biosynthetic process process quality, abnormal ZP:0007188 chondroitin sulfate biosynthetic process increased occurrence, abnormal ZP:0007189 tooth mineralization delayed, abnormal ZP:0007190 chondroitin sulfate proteoglycan biosynthetic process increased occurrence, abnormal ZP:0007191 sulfation increased occurrence, abnormal ZP:0007192 pharyngeal arch 3-7 skeleton increased thickness, abnormal ZP:0007193 pharyngeal arch 3-7 skeleton increased width, abnormal ZP:0007194 dorsal region diencephalon flattened, abnormal ZP:0007195 dorsal region midbrain flattened, abnormal ZP:0007196 optic tract structure, abnormal ZP:0007197 dorsomedial optic tract composition, abnormal ZP:0007198 distal region pectoral fin degenerate, abnormal ZP:0007199 cell pectoral fin circular, abnormal ZP:0007200 mandibular arch skeleton increased width, abnormal ZP:0007201 mandibular arch skeleton increased mass, abnormal ZP:0007202 mandibular arch skeleton sloped downward, abnormal ZP:0007203 ventral mandibular arch morphology, abnormal ZP:0007204 pharyngeal arch 2 skeleton increased thickness, abnormal ZP:0007205 chondrocyte pharyngeal arch cartilage organization quality, abnormal ZP:0007206 pectoral fin fold aplastic, abnormal ZP:0007207 distal region pectoral fin fold aplastic, abnormal ZP:0007208 chondrocyte shape, abnormal ZP:0007209 axon retinal ganglion cell branched, abnormal ZP:0007210 axon retinal ganglion cell organization quality, abnormal ZP:0007211 skeletal system development disrupted, abnormal ZP:0007212 ossification decreased occurrence, abnormal ZP:0007213 chondrocyte intercalation involved in growth plate cartilage morphogenesis arrested, abnormal ZP:0007214 pectoral fin development arrested, abnormal ZP:0007215 olfactory placode hypoplastic, abnormal ZP:0007216 apical ectodermal ridge pectoral fin bud aplastic, abnormal ZP:0007217 pectoral girdle decreased size, abnormal ZP:0007218 ceratobranchial 5 tooth decreased length, abnormal ZP:0007219 ceratobranchial 5 tooth increased thickness, abnormal ZP:0007220 ceratobranchial 5 tooth increased width, abnormal ZP:0007221 ceratobranchial 5 tooth ossified, abnormal ZP:0007222 ceratobranchial 5 tooth mislocalised posteriorly, abnormal ZP:0007223 ceratobranchial 5 tooth increased distance ceratobranchial 5 tooth, abnormal ZP:0007224 ceratobranchial 5 tooth decreased concentration enameloid, abnormal ZP:0007225 distal surface ceratobranchial 5 tooth split, abnormal ZP:0007226 ventral tooth row has extra parts of type ceratobranchial 5 tooth, abnormal ZP:0007227 dorsal tooth row has fewer parts of type ceratobranchial 5 tooth, abnormal ZP:0007228 pharyngeal epithelium decreased thickness, abnormal ZP:0007229 Meckel's cartilage increased size, abnormal ZP:0007230 mandibular arch skeleton mislocalised posteriorly, abnormal ZP:0007231 ceratobranchial 5 bone apoptotic, abnormal ZP:0007232 pectoral fin endoskeletal disc absent, abnormal ZP:0007233 cartilage element increased thickness, abnormal ZP:0007234 ceratobranchial 4 cartilage decreased size, abnormal ZP:0007235 neurocranium decreased length, abnormal ZP:0007236 neurocranium increased thickness, abnormal ZP:0007237 dermal bone hypoplastic, abnormal ZP:0007238 pharyngeal arch 3-7 increased width, abnormal ZP:0007239 fin fold pectoral fin bud absent, abnormal ZP:0007240 chondrocyte circular, abnormal ZP:0007241 axon retinal ganglion cell fasciculation, abnormal ZP:0007242 hair cell absent, abnormal ZP:0007243 hair cell decreased amount, abnormal ZP:0007244 pronuclear fusion disrupted, abnormal ZP:0007245 pronuclear migration disrupted, abnormal ZP:0007246 female pronucleus blastomere movement quality, abnormal ZP:0007247 blastomere misaligned with female pronucleus aster blastomere, abnormal ZP:0007248 blastomere detached from centrosome male pronucleus blastomere, abnormal ZP:0007249 blood increased accumulation yolk, abnormal ZP:0007250 cell-cell junction heart structure, abnormal ZP:0007251 desmosome heart decreased amount, abnormal ZP:0007253 pancreatic epsilon cell increased amount, abnormal ZP:0007254 ghrelin secreting cell increased amount, abnormal ZP:0007255 glucagon secreting cell increased amount, abnormal ZP:0007256 pharynx decreased width, abnormal ZP:0007257 pigment granule whole organism decreased amount, abnormal ZP:0007258 ceratobranchial 3 cartilage aplastic, abnormal ZP:0007259 ceratobranchial 4 cartilage aplastic, abnormal ZP:0007260 ceratobranchial 5 cartilage aplastic, abnormal ZP:0007261 cell brain degenerate, abnormal ZP:0007262 hindbrain increased size, abnormal ZP:0007263 cell eye degenerate, abnormal ZP:0007264 startle response process quality, abnormal ZP:0007265 otolith development disrupted, abnormal ZP:0007266 whole organism lacks all parts of type lateral crista, abnormal ZP:0007268 cilium movement increased rate, abnormal ZP:0007269 regulation of cilium beat frequency disrupted, abnormal ZP:0007270 cilium pronephros disoriented, abnormal ZP:0007271 cilium pronephros disorganized, abnormal ZP:0007272 cilium pronephros shortened, abnormal ZP:0007273 blood vessel development arrested, abnormal ZP:0007274 endothelial cell proliferation decreased occurrence, abnormal ZP:0007275 head mesenchyme position, abnormal ZP:0007276 ventral aorta has fewer parts of type vascular associated smooth muscle cell, abnormal ZP:0007277 primordial hindbrain channel fragile, abnormal ZP:0007278 head increased accumulation blood, abnormal ZP:0007279 ventricular system hemorrhagic, abnormal ZP:0007280 ventricular system increased accumulation blood, abnormal ZP:0007281 cranial vasculature immature, abnormal ZP:0007282 blood vessel endothelial cell cranial vasculature morphology, abnormal ZP:0007283 cranial vasculature separated from blood vessel endothelial cell mesenchymal cell head mesenchyme, abnormal ZP:0007284 pharyngeal vasculature has fewer parts of type vascular associated smooth muscle cell, abnormal ZP:0007285 mid cerebral vein fragile, abnormal ZP:0007286 primordial midbrain channel fragile, abnormal ZP:0007287 central artery morphology, abnormal ZP:0007288 central artery irregular spatial pattern, abnormal ZP:0007289 central artery unlumenized, abnormal ZP:0007290 cytoplasm blood vessel endothelial cell decreased thickness, abnormal ZP:0007291 eye disorganized, abnormal ZP:0007292 retinal cone cell retinal photoreceptor layer disheveled, abnormal ZP:0007293 kinocilium inner ear decreased length, abnormal ZP:0007294 nucleus photoreceptor inner segment layer condensed, abnormal ZP:0007295 photoreceptor outer segment layer malformed, abnormal ZP:0007296 nucleus photoreceptor outer segment layer condensed, abnormal ZP:0007297 photoreceptor outer segment membrane photoreceptor outer segment layer disorganized, abnormal ZP:0007298 cell photoreceptor outer segment layer decreased amount, abnormal ZP:0007299 photoreceptor cell degeneration, abnormal ZP:0007300 catalase activity decreased process quality, abnormal ZP:0007301 central nervous system neuron axonogenesis disrupted, abnormal ZP:0007302 post-anal tail morphogenesis arrested, abnormal ZP:0007303 vascular endothelial growth factor signaling pathway cellular spatiotemporal quality, abnormal ZP:0007304 sensory perception of touch arrested, abnormal ZP:0007305 head development arrested, abnormal ZP:0007306 regulation of superoxide dismutase activity disrupted, abnormal ZP:0007307 regulation of hypoxia-inducible factor-1alpha signaling pathway disrupted, abnormal ZP:0007308 regulation of reactive oxygen species metabolic process disrupted, abnormal ZP:0007309 proliferative region brain increased size, abnormal ZP:0007310 spinal cord curved ventral, abnormal ZP:0007311 primary motor neuron spinal cord decreased amount, abnormal ZP:0007312 dopaminergic neuron diencephalon distributed, abnormal ZP:0007313 dopaminergic neuron diencephalon mislocalised ventrally, abnormal ZP:0007314 brainstem and spinal white matter disorganized, abnormal ZP:0007315 dopaminergic neuron pretectum decreased amount, abnormal ZP:0007316 ansulate commissure aplastic, abnormal ZP:0007317 dopaminergic neuron caudal tuberculum dead, abnormal ZP:0007318 dopaminergic neuron caudal tuberculum disheveled, abnormal ZP:0007319 caudal fin shape, abnormal ZP:0007320 head low brightness, abnormal ZP:0007321 white matter shape, abnormal ZP:0007322 peripheral neuron decreased amount, abnormal ZP:0007323 axon dopaminergic neuron absent, abnormal ZP:0007324 axon dopaminergic neuron decreased length, abnormal ZP:0007325 axon dopaminergic neuron broken, abnormal ZP:0007326 cranial ganglion absent, abnormal ZP:0007329 median fin fold aplastic, abnormal ZP:0007331 whole organism lacks all parts of type melanocyte, abnormal ZP:0007333 neuromast hair cell absent, abnormal ZP:0007334 hematopoietic stem cell caudal vein plexus decreased amount, abnormal ZP:0007335 parachordal vessel disorganized, abnormal ZP:0007336 parachordal vessel agenesis, abnormal ZP:0007337 motile cilium otic vesicle decreased amount, abnormal ZP:0007338 heart right side of anterior-posterior axis whole organism, abnormal ZP:0007339 heart rudiment bilateral, abnormal ZP:0007340 heart rudiment right side of anterior-posterior axis whole organism, abnormal ZP:0007341 liver right side of anterior-posterior axis whole organism, abnormal ZP:0007342 somite loose, abnormal ZP:0007343 kinocilium auditory receptor cell decreased amount, abnormal ZP:0007344 cilium renal tubule curled, abnormal ZP:0007349 pharyngeal endoderm increased amount, abnormal ZP:0007350 pharyngeal arch increased amount, abnormal ZP:0007351 Kupffer's vesicle aplastic, abnormal ZP:0007353 nucleate erythrocyte decreased size, abnormal ZP:0007354 nucleate erythrocyte undifferentiated, abnormal ZP:0007356 diencephalon lacks all parts of type dopaminergic neuron, abnormal ZP:0007357 diencephalon has fewer parts of type dopaminergic neuron, abnormal ZP:0007358 dopaminergic neuron diencephalon disorganized, abnormal ZP:0007359 retinal inner nuclear layer lacks all parts of type amacrine cell, abnormal ZP:0007360 retinal inner nuclear layer has fewer parts of type amacrine cell, abnormal ZP:0007361 pretectum lacks all parts of type dopaminergic neuron, abnormal ZP:0007362 pretectum has fewer parts of type dopaminergic neuron, abnormal ZP:0007363 locus coeruleus has fewer parts of type dopaminergic neuron, abnormal ZP:0007364 pathway-restricted SMAD protein phosphorylation disrupted, abnormal ZP:0007365 margin increased thickness, abnormal ZP:0007366 hypoblast has extra parts of type somatic stem cell, abnormal ZP:0007367 epithelial cell fin disorganized, abnormal ZP:0007368 epithelial cell notochord circular, abnormal ZP:0007369 epithelial cell notochord disorganized, abnormal ZP:0007370 integument apoptotic, abnormal ZP:0007371 epithelial cell integument circular, abnormal ZP:0007372 epithelial cell integument disorganized, abnormal ZP:0007373 caudal fin collapsed, abnormal ZP:0007374 cell ventral fin fold circular, abnormal ZP:0007375 integument trunk rough, abnormal ZP:0007376 pectoral fin apoptotic, abnormal ZP:0007377 startle response arrested, abnormal ZP:0007378 inhibitory postsynaptic potential process quality, abnormal ZP:0007379 regulation of synaptic transmission, glycinergic process quality, abnormal ZP:0007380 sensory perception of sound arrested, abnormal ZP:0007381 chemosensory behavior decreased occurrence, abnormal ZP:0007382 glial cell migration arrested, abnormal ZP:0007383 fin regeneration decreased occurrence, abnormal ZP:0007384 developmental pigmentation arrested, abnormal ZP:0007385 posterior lateral line nerve has extra parts of type posterior lateral line neuromast, abnormal ZP:0007386 posterior lateral line nerve has fewer parts of type glial cell, abnormal ZP:0007387 trunk has extra parts of type posterior lateral line neuromast, abnormal ZP:0007388 trunk has fewer parts of type melanophore stripe melanocyte, abnormal ZP:0007389 melanophore stripe post-vent region decreased pigmentation, abnormal ZP:0007390 post-vent region has fewer parts of type melanophore stripe melanocyte, abnormal ZP:0007391 melanocyte post-vent region poorly differentiated, abnormal ZP:0007392 blastema decreased size, abnormal ZP:0007393 sympathetic chain ganglion absent, abnormal ZP:0007394 glial cell decreased amount, abnormal ZP:0007395 lymphangiogenesis decreased occurrence, abnormal ZP:0007396 lymph vessel endothelium aplastic, abnormal ZP:0007397 BMP signaling pathway process quality, abnormal ZP:0007398 scale aplastic, abnormal ZP:0007399 scale decreased amount, abnormal ZP:0007400 gill raker decreased size, abnormal ZP:0007401 gill raker aplastic, abnormal ZP:0007402 ceratobranchial 5 tooth aplastic, abnormal ZP:0007403 ceratobranchial 5 tooth decreased amount, abnormal ZP:0007404 whole organism lacks all parts of type fin, abnormal ZP:0007405 endochondral bone pectoral fin size, abnormal ZP:0007406 anal fin lepidotrichium aplastic, abnormal ZP:0007407 caudal fin lepidotrichium aplastic, abnormal ZP:0007408 lepidotrichium morphology, abnormal ZP:0007409 lepidotrichium malformed, abnormal ZP:0007410 eye morphogenesis disrupted, abnormal ZP:0007415 retinal pigmented epithelium decreased thickness, abnormal ZP:0007418 posterior crista increased size, abnormal ZP:0007419 posterior crista disorganized, abnormal ZP:0007420 anterior crista increased size, abnormal ZP:0007421 anterior crista disorganized, abnormal ZP:0007425 pillar of the lateral semicircular canal shape, abnormal ZP:0007426 brain V-shaped, abnormal ZP:0007427 protein kinase activity increased occurrence, abnormal ZP:0007428 receptor-mediated endocytosis arrested, abnormal ZP:0007429 stem cell population maintenance disrupted, abnormal ZP:0007430 renal absorption arrested, abnormal ZP:0007431 retinal ganglion cell layer hypotrophic, abnormal ZP:0007432 neuron retinal ganglion cell layer increased amount, abnormal ZP:0007433 neuron retinal ganglion cell layer sparse, abnormal ZP:0007434 retinal neural layer decreased thickness, abnormal ZP:0007435 cell retinal neural layer decreased mass density, abnormal ZP:0007436 eye refractivity, abnormal ZP:0007437 eye increased diameter, abnormal ZP:0007438 eye variability of size, abnormal ZP:0007439 retinal inner nuclear layer hypotrophic, abnormal ZP:0007440 endosome pronephric duct absent, abnormal ZP:0007441 recycling endosome membrane pronephric duct absent, abnormal ZP:0007442 retina increased area, abnormal ZP:0007443 visual system decreased functionality, abnormal ZP:0007444 ciliary zone hypertrophic, abnormal ZP:0007445 neuronal stem cell ciliary marginal zone decreased amount, abnormal ZP:0007446 retinal outer nuclear layer hypotrophic, abnormal ZP:0007447 optic nerve head increased size, abnormal ZP:0007448 optic nerve head increased diameter, abnormal ZP:0007449 vitreous increased size, abnormal ZP:0007450 aqueous humor anterior segment eye increased pressure, abnormal ZP:0007451 posterior segment eye increased depth, abnormal ZP:0007452 photoreceptor cell outer segment organization delayed, abnormal ZP:0007453 axoneme retinal photoreceptor layer absent, abnormal ZP:0007454 cilium lateral crista decreased variability of size, abnormal ZP:0007455 cilium anterior macula absent, abnormal ZP:0007456 cilium olfactory epithelium decreased length, abnormal ZP:0007457 cilium olfactory epithelium decreased amount, abnormal ZP:0007458 cilium posterior lateral line neuromast absent, abnormal ZP:0007459 cilium posterior lateral line neuromast decreased length, abnormal ZP:0007460 cilium posterior lateral line neuromast decreased amount, abnormal ZP:0007461 photoreceptor connecting cilium photoreceptor outer segment layer decreased length, abnormal ZP:0007462 myotome development disrupted, abnormal ZP:0007463 postcranial axial skeleton behavioral quality of a process skeletal system development, abnormal ZP:0007464 axis whole organism decreased length, abnormal ZP:0007465 cranial vault dorso-ventrally flattened, abnormal ZP:0007467 ventral mandibular arch exserted, abnormal ZP:0007468 integument ionocyte decreased amount, abnormal ZP:0007469 NCC ionocyte increased amount, abnormal ZP:0007470 ceratohyal cartilage increased angle to ceratohyal cartilage, abnormal ZP:0007471 axon trigeminal ganglion decreased length, abnormal ZP:0007472 roof plate formation disrupted, abnormal ZP:0007473 roof plate midbrain region increased width, abnormal ZP:0007476 neuron hyperplastic, abnormal ZP:0007477 pigment granule dispersal disrupted, abnormal ZP:0007478 hepatic duct decreased length, abnormal ZP:0007479 hepatic duct disorganized, abnormal ZP:0007480 hepatic duct decreased amount, abnormal ZP:0007481 intersegmental vessel disrupted membrane raft distribution, abnormal ZP:0007482 endothelial tip cell disrupted membrane raft distribution, abnormal ZP:0007484 response to light stimulus decreased strength, abnormal ZP:0007485 retina decreased pigmentation, abnormal ZP:0007486 anterior-most region telencephalon truncated, abnormal ZP:0007487 pharyngeal arch 3-7 skeleton increased size, abnormal ZP:0007488 cranial cartilage apoptotic, abnormal ZP:0007489 perichondrium increased thickness, abnormal ZP:0007490 perichondrium rough, abnormal ZP:0007491 cell perichondrium increased size, abnormal ZP:0007492 chondrocyte color, abnormal ZP:0007493 nucleus chondrocyte shape, abnormal ZP:0007494 plasma membrane chondrocyte undulate, abnormal ZP:0007496 cell population proliferation occurrence, abnormal ZP:0007497 brain wholly posterioralized, abnormal ZP:0007498 posterior lateral line truncated, abnormal ZP:0007499 pectoral fin hypoplastic, abnormal ZP:0007500 skeletal muscle contraction decreased process quality, abnormal ZP:0007501 SCF-dependent proteasomal ubiquitin-dependent protein catabolic process decreased occurrence, abnormal ZP:0007502 cardiac muscle contraction decreased process quality, abnormal ZP:0007503 determination of left/right symmetry decreased process quality, abnormal ZP:0007504 motile cilium assembly decreased process quality, abnormal ZP:0007505 determination of heart left/right asymmetry decreased process quality, abnormal ZP:0007506 determination of intestine left/right asymmetry decreased process quality, abnormal ZP:0007507 gut symmetry, abnormal ZP:0007508 liver symmetry, abnormal ZP:0007509 post-vent vasculature increased branchiness, abnormal ZP:0007510 blood vessel inner optic circle increased branchiness, abnormal ZP:0007511 cranial blood vessel increased branchiness, abnormal ZP:0007512 Schwann cell proliferation decreased process quality, abnormal ZP:0007513 eurydendroid cell differentiation disrupted, abnormal ZP:0007514 oligodendrocyte cell fate specification disrupted, abnormal ZP:0007515 peripheral nervous system myelin formation decreased occurrence, abnormal ZP:0007516 Schwann cell migration decreased process quality, abnormal ZP:0007517 lateral line nerve glial cell migration decreased process quality, abnormal ZP:0007518 lateral line system has extra parts of type posterior lateral line neuromast, abnormal ZP:0007519 eurydendroid cell cerebellum decreased amount, abnormal ZP:0007520 posterior lateral line nerve located in epidermis, abnormal ZP:0007521 posterior lateral line nerve lateral to basement membrane epidermis, abnormal ZP:0007522 posterior lateral line nerve lacks parts or has fewer parts of type myelinating Schwann cell, abnormal ZP:0007523 neuron dorsal root ganglion mislocalised, abnormal ZP:0007526 contractile fiber somite decreased amount, abnormal ZP:0007527 blood circulation delayed, abnormal ZP:0007528 muscle pioneer trunk decreased amount, abnormal ZP:0007530 fast muscle cell trunk decreased amount, abnormal ZP:0007532 contractile fiber post-vent region patchy, abnormal ZP:0007533 slow muscle cell post-vent region decreased amount, abnormal ZP:0007534 axon regeneration decreased process quality, abnormal ZP:0007535 sensory epithelium regeneration decreased process quality, abnormal ZP:0007536 skeletal muscle cell increased length, abnormal ZP:0007537 Muller cell cellular potency, abnormal ZP:0007538 positive regulation of deoxyribonuclease activity decreased process quality, abnormal ZP:0007539 lens fiber cell differentiation decreased process quality, abnormal ZP:0007540 lens nucleate quality, abnormal ZP:0007541 chromatin lens damaged, abnormal ZP:0007543 pharyngeal arch hypoplastic, abnormal ZP:0007544 digestive system malformed, abnormal ZP:0007545 endocardial ring malformed, abnormal ZP:0007546 cartilage development decreased process quality, abnormal ZP:0007547 spinal cord increased process quality apoptotic DNA fragmentation, abnormal ZP:0007548 eye increased process quality apoptotic DNA fragmentation, abnormal ZP:0007549 cartilage element pharyngeal arch immature, abnormal ZP:0007550 cartilage element chondrocranium cartilage immature, abnormal ZP:0007551 endoplasmic reticulum chondrocyte increased size, abnormal ZP:0007552 endoplasmic reticulum chondrocyte disorganized, abnormal ZP:0007553 endoplasmic reticulum lumen chondrocyte distended, abnormal ZP:0007554 respiratory electron transport chain disrupted, abnormal ZP:0007555 nucleus nucleate erythrocyte increased size, abnormal ZP:0007556 myotome decreased width, abnormal ZP:0007557 muscle cell myotome increased length, abnormal ZP:0007558 I band skeletal muscle cell disorganized, abnormal ZP:0007559 branched-chain amino acid metabolic process disrupted, abnormal ZP:0007560 central nervous system functionality, abnormal ZP:0007561 spinal cord hypoplastic, abnormal ZP:0007562 epithelial cell pronephros morphology, abnormal ZP:0007563 pronephric glomerulus structure, abnormal ZP:0007564 cilium Kupffer's vesicle decreased functionality, abnormal ZP:0007565 cilium central canal decreased length, abnormal ZP:0007566 cilium central canal decreased functionality, abnormal ZP:0007567 vesicle-mediated transport process quality, abnormal ZP:0007568 cytoplasm liver and biliary system composition, abnormal ZP:0007569 epithelial cell liver and biliary system structure, abnormal ZP:0007570 cytoplasm enterocyte composition, abnormal ZP:0007571 Golgi stack enterocyte dilated, abnormal ZP:0007572 stereocilium hair cell anterior macula malformed, abnormal ZP:0007573 stereocilium hair cell anterior macula decreased amount, abnormal ZP:0007574 hatching decreased occurrence, abnormal ZP:0007576 Z disc skeletal muscle absent, abnormal ZP:0007577 T-tubule skeletal muscle absent, abnormal ZP:0007578 T-tubule skeletal muscle disorganized, abnormal ZP:0007579 muscle cell displaced to nucleus central region muscle cell, abnormal ZP:0007580 spinal cord has fewer parts of type CNS neuron (sensu Vertebrata), abnormal ZP:0007582 endothelial tip cell intersegmental vessel increased width, abnormal ZP:0007583 vascular sprouts has extra parts of type endothelial tip cell, abnormal ZP:0007585 convergent extension involved in gastrulation delayed, abnormal ZP:0007586 sympathetic ganglion development disrupted, abnormal ZP:0007587 angioblast cell migration from lateral mesoderm to midline delayed, abnormal ZP:0007588 angioblastic mesenchymal cell vascular cord mislocalised laterally, abnormal ZP:0007589 angioblastic mesenchymal cell vascular cord decreased amount, abnormal ZP:0007590 cell median fin fold circular, abnormal ZP:0007591 ventral fin fold rough, abnormal ZP:0007592 mitochondrial electron transport, NADH to ubiquinone decreased rate, abnormal ZP:0007593 T-tubule fast muscle cell unlumenized, abnormal ZP:0007594 blood vessel morphogenesis delayed, abnormal ZP:0007595 ventral aorta morphology, abnormal ZP:0007596 ceratobranchial cartilage decreased distance ceratobranchial cartilage, abnormal ZP:0007597 ceratobranchial cartilage dislocated ceratobranchial cartilage, abnormal ZP:0007598 pharyngeal vasculature morphology, abnormal ZP:0007599 aortic arch 5 unlumenized, abnormal ZP:0007600 aortic arch 6 unlumenized, abnormal ZP:0007601 primary head sinus morphology, abnormal ZP:0007603 epithalamus development process quality, abnormal ZP:0007604 forebrain neuron differentiation decreased process quality, abnormal ZP:0007605 cell pretectum mislocalised, abnormal ZP:0007607 dorsal thalamus fused with pretectum, abnormal ZP:0007608 cell dorsal thalamus mislocalised, abnormal ZP:0007610 GABAergic neuron dorsal thalamus mislocalised posteriorly, abnormal ZP:0007611 goblet cell cellular quality, abnormal ZP:0007612 goblet cell immature, abnormal ZP:0007613 secretory granule goblet cell decreased amount, abnormal ZP:0007614 intermediate cell mass of mesoderm decreased size, abnormal ZP:0007615 pharynx hemorrhagic, abnormal ZP:0007616 vasculature hemorrhagic, abnormal ZP:0007617 whole organism fragile, abnormal ZP:0007618 cell post-vent region apoptotic, abnormal ZP:0007619 cardiac muscle cell heart disorganized, abnormal ZP:0007620 muscle deformed, abnormal ZP:0007621 sarcomere skeletal muscle cell morphology, abnormal ZP:0007622 M band skeletal muscle cell morphology, abnormal ZP:0007623 midbrain hindbrain boundary decreased distance otic vesicle, abnormal ZP:0007624 otic vesicle increased distance otic vesicle, abnormal ZP:0007625 cilium pronephros paralysed, abnormal ZP:0007626 pronephros decreased process quality cilium-dependent cell motility, abnormal ZP:0007627 leukocyte chemotaxis process quality, abnormal ZP:0007628 leukocyte morphology, abnormal ZP:0007629 leukocyte cellular motility, abnormal ZP:0007630 pseudopodium leukocyte increased amount, abnormal ZP:0007631 anterior region forebrain non-functional, abnormal ZP:0007632 notochord absent, abnormal ZP:0007633 glandular epithelial cell development heterochronic, abnormal ZP:0007634 feeding behavior quality, abnormal ZP:0007635 metabolic process increased rate, abnormal ZP:0007636 regulation of phosphatidylinositol 3-kinase signaling disrupted, abnormal ZP:0007637 TOR signaling occurrence, abnormal ZP:0007638 epithelial cell proliferation decreased rate, abnormal ZP:0007639 whole organism increased acidity, abnormal ZP:0007640 intestine increased diameter, abnormal ZP:0007641 goblet cell intestine present, abnormal ZP:0007642 intestinal epithelium flattened, abnormal ZP:0007643 brush border intestinal epithelium increased height, abnormal ZP:0007644 epithelial cell intestinal epithelium increased amount, abnormal ZP:0007645 oocyte development delayed, abnormal ZP:0007646 RNA 3' uridylation increased occurrence, abnormal ZP:0007647 embryonic pectoral fin morphogenesis arrested, abnormal ZP:0007648 cell division decreased occurrence, abnormal ZP:0007649 hepatocyte proliferation disrupted, abnormal ZP:0007651 brain decreased occurrence branching morphogenesis of a nerve, abnormal ZP:0007652 telencephalon disorganized, abnormal ZP:0007653 neuron telencephalon decreased amount, abnormal ZP:0007654 dorsal region neural plate apoptotic, abnormal ZP:0007655 neuron neural tube decreased amount, abnormal ZP:0007656 neuronal stem cell apoptotic, abnormal ZP:0007657 axon motor neuron decreased amount, abnormal ZP:0007658 lymph vessel morphogenesis disrupted, abnormal ZP:0007659 whole organism lacks all parts of type lymphangioblast cord, abnormal ZP:0007660 intersegmental vessel increased amount, abnormal ZP:0007661 neural crest cell development decreased process quality, abnormal ZP:0007662 embryonic camera-type eye morphogenesis decreased process quality, abnormal ZP:0007663 cornea disorganized, abnormal ZP:0007664 cranial neural crest physical object quality, abnormal ZP:0007665 neurocranial trabecula absent, abnormal ZP:0007666 yolk increased accumulation blood, abnormal ZP:0007667 atrium increased accumulation blood, abnormal ZP:0007668 ventricular myocardium hypoplastic, abnormal ZP:0007669 cilium movement disrupted, abnormal ZP:0007670 axonemal dynein complex Kupffer's vesicle decreased amount, abnormal ZP:0007671 cilium Kupffer's vesicle decreased coordination, abnormal ZP:0007672 axoneme Kupffer's vesicle structure, abnormal ZP:0007673 neuronal action potential ictal, abnormal ZP:0007674 swimming process quality, abnormal ZP:0007675 anterior region pronephros dilated, abnormal ZP:0007676 motile cilium pronephros immobile, abnormal ZP:0007677 ciliary rootlet ciliated cell absent, abnormal ZP:0007678 fucose biosynthetic process disrupted, abnormal ZP:0007679 glycosylation decreased occurrence, abnormal ZP:0007680 dorsolateral motor nucleus of vagal nerve mislocalised medially, abnormal ZP:0007681 dorsolateral motor nucleus of vagal nerve fused with dorsolateral motor nucleus of vagal nerve, abnormal ZP:0007682 secondary motor neuron irregular spatial pattern, abnormal ZP:0007683 axon secondary motor neuron morphology, abnormal ZP:0007684 cardiac muscle cell atrioventricular canal morphology, abnormal ZP:0007685 otolith inner ear malformed, abnormal ZP:0007686 sagitta malformed, abnormal ZP:0007687 glomerulus development disrupted, abnormal ZP:0007688 pronephric duct malformed, abnormal ZP:0007689 pronephric glomerulus aplastic, abnormal ZP:0007690 pronephric tubule aplastic, abnormal ZP:0007691 intersegmental vessel decreased thickness, abnormal ZP:0007692 trunk vasculature malformed, abnormal ZP:0007693 skeletal muscle cell vacuolated, abnormal ZP:0007694 intercalated disc cardiac muscle cell decreased thickness, abnormal ZP:0007695 intercalated disc cardiac muscle cell decreased amount, abnormal ZP:0007696 sarcomere cardiac muscle cell mislocalised, abnormal ZP:0007697 nucleus retina increased size, abnormal ZP:0007698 nucleus retina variability of shape, abnormal ZP:0007699 sarcomere skeletal muscle decreased thickness, abnormal ZP:0007700 Z disc skeletal muscle increased width, abnormal ZP:0007701 lipid storage disrupted, abnormal ZP:0007702 cell migration delayed, abnormal ZP:0007703 hindbrain-spinal cord boundary formation disrupted, abnormal ZP:0007704 hindbrain increased length, abnormal ZP:0007709 trunk mesenchyme distended, abnormal ZP:0007711 pancreas primordium mislocalised posteriorly, abnormal ZP:0007719 pancreatic bud mislocalised posteriorly, abnormal ZP:0007725 podocyte mislocalised posteriorly, abnormal ZP:0007726 respiratory burst involved in inflammatory response disrupted, abnormal ZP:0007727 iris perforate, abnormal ZP:0007728 pupil morphology, abnormal ZP:0007729 detection of muscle stretch process quality, abnormal ZP:0007730 sarcomere organization decreased process quality, abnormal ZP:0007731 myotome detached from myofibril vertical myoseptum, abnormal ZP:0007732 Z disc skeletal muscle cell decreased amount, abnormal ZP:0007733 Z disc cardiac muscle cell malformed, abnormal ZP:0007734 skeletal muscle cell differentiation disrupted, abnormal ZP:0007735 respiratory system development disrupted, abnormal ZP:0007736 retinal neural layer absent, abnormal ZP:0007737 gill filament malformed, abnormal ZP:0007738 epithelium gill filament disorganized, abnormal ZP:0007739 chondrocyte gill filament absent, abnormal ZP:0007740 skeletal muscle cell curved, abnormal ZP:0007741 nucleus skeletal muscle cell increased amount, abnormal ZP:0007742 nucleus skeletal muscle cell increased diameter, abnormal ZP:0007743 planar cell polarity pathway involved in axis elongation disrupted, abnormal ZP:0007744 medial-lateral axis neural plate distended, abnormal ZP:0007745 whole organism increased width, abnormal ZP:0007746 anterior-posterior axis whole organism condensed, abnormal ZP:0007747 whole organism oblong, abnormal ZP:0007748 anterior-posterior axis whole organism elongated, abnormal ZP:0007749 post-vent region increased thickness, abnormal ZP:0007750 odontogenesis paedomorphic growth, abnormal ZP:0007751 cartilage development delayed, abnormal ZP:0007752 embryonic skeletal joint morphogenesis disrupted, abnormal ZP:0007753 intermandibularis disorganized, abnormal ZP:0007754 ceratobranchial 5 tooth immature, abnormal ZP:0007755 ceratobranchial 5 tooth detached from ceratobranchial 5 bone, abnormal ZP:0007756 cartilage tissue Meckel's cartilage decreased amount, abnormal ZP:0007757 bony projection palatoquadrate arch decreased length, abnormal ZP:0007758 ventral mandibular arch notched, abnormal ZP:0007759 mesenchyme pharyngeal arch morphology, abnormal ZP:0007760 joint pharyngeal arch increased amount, abnormal ZP:0007761 hyosymplectic cartilage notched, abnormal ZP:0007762 chondroblast pharyngeal arch cartilage disorganized, abnormal ZP:0007763 joint mislocalised, abnormal ZP:0007764 sternohyoid decreased length, abnormal ZP:0007765 sternohyoid detached from bone tissue, abnormal ZP:0007766 head muscle detached from bone element, abnormal ZP:0007767 hyohyoideus inverted, abnormal ZP:0007768 extracellular matrix chondroblast absent, abnormal ZP:0007769 epidermis blistered, abnormal ZP:0007770 anterior-posterior axis whole organism increased length, abnormal ZP:0007771 lens cellularity, abnormal ZP:0007772 retina process quality cell population proliferation, abnormal ZP:0007773 mandibular arch skeleton shortened, abnormal ZP:0007774 midbrain elongated, abnormal ZP:0007775 retina degeneration, abnormal ZP:0007776 myoseptum partially broken, abnormal ZP:0007777 otolith formation disrupted, abnormal ZP:0007779 defecation disrupted, abnormal ZP:0007780 cortical granule exocytosis disrupted, abnormal ZP:0007781 positive regulation of cortical granule exocytosis by positive regulation of cytosolic calcium ion concentration disrupted, abnormal ZP:0007782 intestinal epithelial structure maintenance disrupted, abnormal ZP:0007783 microtubule blastomere disorganized, abnormal ZP:0007784 chorion soft, abnormal ZP:0007785 microtubule marginal blastomere disorganized, abnormal ZP:0007786 microtubule marginal blastomere sparse, abnormal ZP:0007787 intestinal bulb lacks parts or has fewer parts of type intestinal villus, abnormal ZP:0007788 muscle intestinal bulb degenerate, abnormal ZP:0007789 blastodisc decreased size, abnormal ZP:0007790 intestinal villus mid intestine increased circumference, abnormal ZP:0007791 muscle mid intestine degenerate, abnormal ZP:0007792 intestinal villus intestinal bulb epithelium increased circumference, abnormal ZP:0007793 goblet cell intestinal bulb epithelium decreased amount, abnormal ZP:0007794 goblet cell mid intestine epithelium decreased amount, abnormal ZP:0007795 startle response increased process quality, abnormal ZP:0007796 visual behavior decreased process quality, abnormal ZP:0007797 swimming decreased occurrence, abnormal ZP:0007798 light adaption decreased process quality, abnormal ZP:0007799 regulation of dopamine receptor signaling pathway decreased process quality, abnormal ZP:0007800 calcium ion import process quality, abnormal ZP:0007801 liver decreased mass, abnormal ZP:0007802 melanocyte myoseptum disorganized, abnormal ZP:0007803 Meckel's cartilage disoriented, abnormal ZP:0007804 ceratohyal cartilage fused with hypobranchial cartilage, abnormal ZP:0007805 ethmoid cartilage curled, abnormal ZP:0007806 ethmoid cartilage retracted, abnormal ZP:0007807 subintestinal vein absent, abnormal ZP:0007808 subintestinal vein decreased amount, abnormal ZP:0007809 hematopoietic progenitor cell differentiation decreased functionality, abnormal ZP:0007810 erythroid progenitor cell decreased amount, abnormal ZP:0007811 thrombocyte increased amount, abnormal ZP:0007812 hemoglobin complex erythroid lineage cell decreased amount, abnormal ZP:0007814 myeloid lineage restricted progenitor cell increased amount, abnormal ZP:0007815 angiogenic sprout decreased length, abnormal ZP:0007816 angiogenic sprout decreased amount, abnormal ZP:0007817 astrocyte hindbrain decreased amount, abnormal ZP:0007818 facial nerve motor nucleus mislocalised laterally, abnormal ZP:0007820 vagal lobe aplastic, abnormal ZP:0007821 abducens motor nucleus aplastic, abnormal ZP:0007822 pars anterior physical object quality, abnormal ZP:0007823 floor plate rhombomere region increased width, abnormal ZP:0007824 adenohypophysis wholly anterioralized, abnormal ZP:0007825 trigeminal motor nucleus aplastic, abnormal ZP:0007826 trigeminal motor nucleus mislocalised laterally, abnormal ZP:0007827 prolactin secreting cell increased amount, abnormal ZP:0007828 thyroid stimulating hormone secreting cell increased amount, abnormal ZP:0007829 posterior intestine undulate, abnormal ZP:0007830 posterior intestine distended, abnormal ZP:0007831 posterior intestine cystic, abnormal ZP:0007832 mesenchyme posterior intestine distended, abnormal ZP:0007833 mesenchymal cell posterior intestine morphology, abnormal ZP:0007834 mesenchymal cell posterior intestine increased amount, abnormal ZP:0007835 mesenchymal cell posterior intestine degenerate, abnormal ZP:0007836 smooth muscle cell posterior intestine irregular spatial pattern, abnormal ZP:0007837 posterior intestine epithelium morphology, abnormal ZP:0007838 posterior intestine epithelium disorganized, abnormal ZP:0007839 posterior intestine epithelium stratification, abnormal ZP:0007840 basement membrane posterior intestine epithelium morphology, abnormal ZP:0007841 myosin complex smooth muscle morphology, abnormal ZP:0007842 regulation of myeloid leukocyte differentiation disrupted, abnormal ZP:0007843 blood vasculature morphology, abnormal ZP:0007844 posterior lateral mesoderm morphology, abnormal ZP:0007845 spinal cord decreased thickness, abnormal ZP:0007846 pancreatic B cell mislocalised, abnormal ZP:0007847 peripheral nervous system neuron axonogenesis decreased occurrence, abnormal ZP:0007848 double-strand break repair via single-strand annealing decreased frequency, abnormal ZP:0007849 cysteine-type peptidase activity increased process quality, abnormal ZP:0007850 regulation of autophagy disrupted, abnormal ZP:0007851 melanocyte apoptotic process increased occurrence, abnormal ZP:0007852 retinal neural layer detached from retinal pigmented epithelium, abnormal ZP:0007853 chromatin retinal neural layer condensed, abnormal ZP:0007854 liver hyperplastic, abnormal ZP:0007855 chromatin retinal pigmented epithelium condensed, abnormal ZP:0007856 melanocyte retinal pigmented epithelium immature, abnormal ZP:0007857 melanocyte head decreased pigmentation, abnormal ZP:0007858 iridophore head decreased amount, abnormal ZP:0007859 melanosome melanophore stripe morphology, abnormal ZP:0007860 photoreceptor outer segment layer collapsed, abnormal ZP:0007861 photoreceptor outer segment layer displaced to photoreceptor outer segment membrane vacuolar lumen photoreceptor outer segment layer, abnormal ZP:0007862 retinal rod cell photoreceptor outer segment layer vacuolated, abnormal ZP:0007863 retinal rod cell photoreceptor outer segment layer collapsed, abnormal ZP:0007864 larval melanophore stripe decreased pigmentation, abnormal ZP:0007865 melanocyte larval melanophore stripe decreased pigmentation, abnormal ZP:0007866 vacuole dorsal larval melanophore stripe increased amount, abnormal ZP:0007867 melanosome dorsal larval melanophore stripe decreased amount, abnormal ZP:0007868 nucleus retinal rod cell mislocalised, abnormal ZP:0007869 Muller cell hypertrophic, abnormal ZP:0007870 regulation of cell projection assembly process quality, abnormal ZP:0007871 anterior axial hypoblast decreased cellular motility, abnormal ZP:0007872 bleb anterior axial hypoblast increased size, abnormal ZP:0007873 cardiac ventricle quality, abnormal ZP:0007874 myofibril cardiac ventricle decreased thickness, abnormal ZP:0007875 sarcomere cardiac ventricle irregular spatial pattern, abnormal ZP:0007876 Z disc cardiac ventricle morphology, abnormal ZP:0007877 atrium collapsed, abnormal ZP:0007878 myocardium uncoordinated, abnormal ZP:0007879 melanosome transport increased duration, abnormal ZP:0007880 anatomical axis whole organism asymmetrical, abnormal ZP:0007881 cell division disrupted, abnormal ZP:0007882 mRNA splicing, via endonucleolytic cleavage and ligation process quality, abnormal ZP:0007883 forerunner cell group position, abnormal ZP:0007884 shield morphology, abnormal ZP:0007885 dolichol-linked oligosaccharide biosynthetic process disrupted, abnormal ZP:0007886 oligosaccharide-lipid intermediate biosynthetic process disrupted, abnormal ZP:0007887 head development abnormal, abnormal ZP:0007888 midbrain hindbrain boundary neural tube cleft, abnormal ZP:0007889 trunk shortened, abnormal ZP:0007890 ventricular system morphology, abnormal ZP:0007891 digestive system inverted, abnormal ZP:0007892 digestive system centered, abnormal ZP:0007893 epithalamus bilateral, abnormal ZP:0007894 epithalamus inverted, abnormal ZP:0007895 epithalamus aplastic, abnormal ZP:0007896 negative regulation of TOR signaling increased occurrence, abnormal ZP:0007897 pectoral fin deformed, abnormal ZP:0007898 cell pectoral fin decreased size, abnormal ZP:0007899 cell pectoral fin condensed, abnormal ZP:0007900 basihyal cartilage deformed, abnormal ZP:0007901 hypobranchial cartilage decreased thickness, abnormal ZP:0007902 chromosome cell disorganized, abnormal ZP:0007903 mitotic spindle cell deformed, abnormal ZP:0007904 central nervous system development process quality, abnormal ZP:0007905 embryonic camera-type eye formation disrupted, abnormal ZP:0007908 posterior lateral line neuromast has fewer parts of type kinocilium neuromast, abnormal ZP:0007909 stereocilium posterior lateral line neuromast decreased length, abnormal ZP:0007910 kinocilium posterior lateral line neuromast decreased length, abnormal ZP:0007911 pharyngeal pouch decreased length, abnormal ZP:0007912 pharyngeal pouch increased width, abnormal ZP:0007913 pharyngeal epithelium disorganized, abnormal ZP:0007914 pharyngeal arch 3-7 lacks all parts of type ceratobranchial 2 cartilage, abnormal ZP:0007915 pharyngeal arch 3-7 lacks all parts of type ceratobranchial 3 cartilage, abnormal ZP:0007916 pharyngeal arch 3-7 lacks all parts of type ceratobranchial 4 cartilage, abnormal ZP:0007917 pharyngeal arch 3-7 lacks all parts of type ceratobranchial 1 cartilage, abnormal ZP:0007918 pharyngeal arch 3-7 lacks all parts of type ceratobranchial 5 cartilage, abnormal ZP:0007919 cranial neural crest cell decreased amount, abnormal ZP:0007920 Kupffer's vesicle hypoplastic, abnormal ZP:0007921 cilium Kupffer's vesicle increased length, abnormal ZP:0007923 somite apoptotic, abnormal ZP:0007924 thigmotaxis decreased functionality, abnormal ZP:0007926 heart apoptotic, abnormal ZP:0007927 Z disc heart blurry, abnormal ZP:0007928 sarcolemma heart edematous, abnormal ZP:0007929 somite shortened, abnormal ZP:0007930 myocardium degenerate, abnormal ZP:0007931 presumptive mesoderm decreased length, abnormal ZP:0007933 mitochondrion cardiac muscle cell vacuolated, abnormal ZP:0007934 midbrain hemorrhagic, abnormal ZP:0007935 heart dysplastic, abnormal ZP:0007936 myofibril skeletal muscle undulate, abnormal ZP:0007937 myofibril skeletal muscle loose, abnormal ZP:0007940 osteoblast differentiation process quality, abnormal ZP:0007941 intramembranous ossification decreased rate, abnormal ZP:0007942 endochondral ossification decreased occurrence, abnormal ZP:0007943 osteoclast differentiation delayed, abnormal ZP:0007944 osteoblast proliferation disrupted, abnormal ZP:0007945 swim bladder morphogenesis disrupted, abnormal ZP:0007946 swim bladder formation disrupted, abnormal ZP:0007947 swim bladder hypoplastic, abnormal ZP:0007948 mesenchyme swim bladder decreased size, abnormal ZP:0007949 mesenchyme swim bladder disorganized, abnormal ZP:0007950 smooth muscle swim bladder aplastic, abnormal ZP:0007951 mesothelial cell swim bladder decreased amount, abnormal ZP:0007952 mesenchyme gut decreased size, abnormal ZP:0007953 neuron gut absent, abnormal ZP:0007954 opercle fused with subopercle, abnormal ZP:0007955 opercle fused with interopercle, abnormal ZP:0007956 dorsal-ventral axis opercle decreased length, abnormal ZP:0007957 opercle has fewer parts of type antero-ventral margin bone tissue, abnormal ZP:0007958 opercle has fewer parts of type antero-ventral margin osteoblast, abnormal ZP:0007959 postero-ventral margin opercle decreased length, abnormal ZP:0007960 opercle has fewer parts of type postero-ventral margin osteoblast, abnormal ZP:0007961 interopercle fused with subopercle, abnormal ZP:0007962 osteoblast Meckel's cartilage decreased amount, abnormal ZP:0007963 osteoclast pharyngeal arch 7 skeleton undifferentiated, abnormal ZP:0007964 osteoclast pharyngeal arch 7 skeleton poorly differentiated, abnormal ZP:0007965 anterior chamber swim bladder absent, abnormal ZP:0007966 ceratohyal cartilage cartilaginous, abnormal ZP:0007967 osteoblast ceratohyal cartilage absent, abnormal ZP:0007968 pneumatic duct decreased size, abnormal ZP:0007969 intramembranous bone has extra parts of type branchiostegal ray, abnormal ZP:0007970 gut epithelium decreased size, abnormal ZP:0007971 swim bladder bud hypoplastic, abnormal ZP:0007972 regulation of transcription from RNA polymerase II promoter in response to stress disrupted, abnormal ZP:0007973 cardiac ventricle increased distance atrium, abnormal ZP:0007974 somite immature, abnormal ZP:0007975 blood coagulation disrupted, abnormal ZP:0007976 intersegmental vein physical quality, abnormal ZP:0007977 whole organism kinked, abnormal ZP:0007978 caudal vein plexus branchiness, abnormal ZP:0007980 thrombocyte decreased functionality, abnormal ZP:0007981 posterior kidney cystic, abnormal ZP:0007982 skeletal muscle tissue development process quality, abnormal ZP:0007983 muscle cell myotome decreased length, abnormal ZP:0007984 nucleate erythrocyte pericardium decreased amount, abnormal ZP:0007985 heart mislocalised medially, abnormal ZP:0007986 myocardium position, abnormal ZP:0007987 phosphatidylinositol dephosphorylation disrupted, abnormal ZP:0007988 trunk musculature decreased size, abnormal ZP:0007989 skeletal muscle cell hypotrophic, abnormal ZP:0007990 skeletal muscle cell decreased functionality, abnormal ZP:0007991 skeletal muscle cell separated from skeletal muscle cell, abnormal ZP:0007992 nucleus skeletal muscle cell increased size, abnormal ZP:0007993 sarcoplasmic reticulum skeletal muscle cell morphology, abnormal ZP:0007994 T-tubule skeletal muscle cell morphology, abnormal ZP:0007995 T-tubule skeletal muscle cell disorganized, abnormal ZP:0007996 perinuclear region of cytoplasm skeletal muscle cell disorganized, abnormal ZP:0007997 ceratobranchial 3 cartilage decreased length, abnormal ZP:0007998 ceratobranchial 4 cartilage decreased length, abnormal ZP:0007999 ceratobranchial 5 cartilage decreased length, abnormal ZP:0008000 T cell differentiation arrested, abnormal ZP:0008001 alpha-beta T cell differentiation arrested, abnormal ZP:0008002 thymus increased occurrence apoptotic process, abnormal ZP:0008003 T cell aplastic/hypoplastic, abnormal ZP:0008004 alpha-beta T cell aplastic/hypoplastic, abnormal ZP:0008007 voltage-gated sodium channel complex spinal cord decreased amount, abnormal ZP:0008008 voltage-gated sodium channel complex posterior lateral line nerve decreased amount, abnormal ZP:0008009 node of Ranvier posterior lateral line nerve increased length, abnormal ZP:0008010 head muscle absent, abnormal ZP:0008011 olfactory pit obstructed, abnormal ZP:0008012 cilium olfactory pit non-functional, abnormal ZP:0008013 cilium olfactory pit decreased functionality, abnormal ZP:0008014 gall bladder lacks parts or has fewer parts of type cell, abnormal ZP:0008015 intrahepatic bile duct decreased functionality, abnormal ZP:0008016 extrahepatic duct decreased amount, abnormal ZP:0008017 endocardial ring absent, abnormal ZP:0008018 cardiac muscle cell apoptotic, abnormal ZP:0008019 cardiac muscle cell elongated, abnormal ZP:0008021 yolk autofluorescence, abnormal ZP:0008022 whole organism autofluorescence, abnormal ZP:0008023 post-vent vasculature autofluorescence, abnormal ZP:0008024 nucleate erythrocyte autofluorescence, abnormal ZP:0008025 cell lens nucleate quality, abnormal ZP:0008026 eye lacks all parts of type retinal photoreceptor layer, abnormal ZP:0008027 atrium lacks parts or has fewer parts of type sarcomere cardiac muscle cell, abnormal ZP:0008028 atrium lacks parts or has fewer parts of type Z disc cardiac muscle cell, abnormal ZP:0008029 ventricular myocardium decreased size, abnormal ZP:0008030 ventricular myocardium decreased volume, abnormal ZP:0008031 ventricular myocardium decreased occurrence cardiac chamber ballooning, abnormal ZP:0008032 skeletal muscle lacks parts or has fewer parts of type myofibril slow muscle cell, abnormal ZP:0008033 myofibril skeletal muscle morphology, abnormal ZP:0008034 contractile fiber skeletal muscle decreased size, abnormal ZP:0008035 myofibril cardiac muscle disorganized, abnormal ZP:0008036 slow muscle cell decreased diameter, abnormal ZP:0008037 nucleus slow muscle cell circular, abnormal ZP:0008038 Z disc cardiac muscle cell decreased size, abnormal ZP:0008039 Z disc cardiac muscle cell increased width, abnormal ZP:0008040 Z disc cardiac muscle cell broken, abnormal ZP:0008041 whole organism circular, abnormal ZP:0008042 optokinetic behavior process quality, abnormal ZP:0008043 optomotor response disrupted, abnormal ZP:0008044 lens increased distance retinal pigmented epithelium, abnormal ZP:0008045 lens increased distance iridophore, abnormal ZP:0008046 eye degree of pigmentation, abnormal ZP:0008047 neoplasm eye protruding, abnormal ZP:0008048 retinal pigmented epithelium spatial pattern, abnormal ZP:0008049 retinal pigmented epithelium organization quality, abnormal ZP:0008050 retinal pigmented epithelium dislocated lens, abnormal ZP:0008051 optic chiasm absent, abnormal ZP:0008052 retinal ganglion cell ipsilateral to axon ipsilateral region brain, abnormal ZP:0008053 habenula development process quality, abnormal ZP:0008054 regulation of dendrite morphogenesis process quality, abnormal ZP:0008055 dendrite ventral habenular nucleus increased volume, abnormal ZP:0008056 axonogenesis neotenous growth, abnormal ZP:0008057 anterior region notochord undifferentiated, abnormal ZP:0008058 medial longitudinal fasciculus morphology, abnormal ZP:0008059 axon medial longitudinal fasciculus branched, abnormal ZP:0008060 vertical myoseptum morphology, abnormal ZP:0008061 retinal ganglion cell poorly differentiated, abnormal ZP:0008062 cell body retinal ganglion cell mislocalised, abnormal ZP:0008063 apoptotic process delayed, abnormal ZP:0008064 skeletal muscle tissue development decreased process quality, abnormal ZP:0008065 myotome structure, abnormal ZP:0008066 myotome decreased size, abnormal ZP:0008067 myotome dystrophic, abnormal ZP:0008068 extracellular matrix myotome structure, abnormal ZP:0008069 skeletal muscle cell retracted, abnormal ZP:0008070 skeletal muscle cell dystrophic, abnormal ZP:0008071 skeletal muscle cell detached from myofibril muscle tendon junction myotome, abnormal ZP:0008072 skeletal muscle cell detached from myofibril myofibril skeletal muscle cell, abnormal ZP:0008073 M band skeletal muscle cell disorganized, abnormal ZP:0008074 myeloid leukocyte differentiation process quality, abnormal ZP:0008075 thrombocyte differentiation process quality, abnormal ZP:0008076 T cell differentiation delayed, abnormal ZP:0008077 neutrophil differentiation process quality, abnormal ZP:0008078 hematopoietic stem cell migration process quality, abnormal ZP:0008079 cranial ganglion has fewer parts of type sensory neuron, abnormal ZP:0008080 hindbrain lacks all parts of type fourth ventricle, abnormal ZP:0008081 hindbrain has fewer parts of type serotonergic neuron, abnormal ZP:0008082 blood island aplastic, abnormal ZP:0008083 forebrain has fewer parts of type dopaminergic neuron, abnormal ZP:0008084 midbrain deformed, abnormal ZP:0008085 locus coeruleus has fewer parts of type norepinephrine secreting cell, abnormal ZP:0008086 exocrine pancreas increased amount, abnormal ZP:0008087 parapineal organ aplastic, abnormal ZP:0008088 anterior pancreatic bud increased amount, abnormal ZP:0008089 sympathetic nervous system has fewer parts of type norepinephrine secreting cell, abnormal ZP:0008090 neuron hindbrain commissure decreased amount, abnormal ZP:0008091 hepatocyte morphology, abnormal ZP:0008092 cilium Kupffer's vesicle symmetry, abnormal ZP:0008093 portion of organism substance Kupffer's vesicle decreased fluid flow, abnormal ZP:0008094 portion of organism substance Kupffer's vesicle circling direction, abnormal ZP:0008095 cell Kupffer's vesicle shape, abnormal ZP:0008096 cell Kupffer's vesicle structure, abnormal ZP:0008097 cell Kupffer's vesicle cellular quality, abnormal ZP:0008098 pancreas symmetry, abnormal ZP:0008099 apical side cell increased width, abnormal ZP:0008100 apical surface cell increased size, abnormal ZP:0008102 convergent extension process quality, abnormal ZP:0008103 somite broad, abnormal ZP:0008104 cilium pronephric tubule increased length, abnormal ZP:0008105 rhodopsin metabolic process disrupted, abnormal ZP:0008106 photoreceptor inner segment layer structure, abnormal ZP:0008107 cilium olfactory pit disorganized, abnormal ZP:0008108 filamentous actin somite disorganized, abnormal ZP:0008110 brain morphogenesis decreased process quality, abnormal ZP:0008111 tectal ventricle hydrocephalic, abnormal ZP:0008112 ventral wall of dorsal aorta morphology, abnormal ZP:0008113 eye agenesis, abnormal ZP:0008114 forebrain agenesis, abnormal ZP:0008115 midbrain agenesis, abnormal ZP:0008116 vertical myoseptum obtuse angle to vertical myoseptum, abnormal ZP:0008117 myofibril myotome disorganized, abnormal ZP:0008118 motor neuron spatial pattern, abnormal ZP:0008119 motor neuron defasciculated, abnormal ZP:0008120 swimming behavior behavioral quality of a process, abnormal ZP:0008121 skeletal muscle cell has extra parts of type membrane skeletal muscle cell, abnormal ZP:0008122 sarcoplasmic reticulum skeletal muscle cell dilated, abnormal ZP:0008123 sarcoplasmic reticulum skeletal muscle cell swollen, abnormal ZP:0008124 T-tubule skeletal muscle cell dilated, abnormal ZP:0008125 cell lens morphology, abnormal ZP:0008126 cell lens decreased length, abnormal ZP:0008127 cell lens vacuolated, abnormal ZP:0008128 synapse assembly disrupted, abnormal ZP:0008129 detection of light stimulus involved in visual perception disrupted, abnormal ZP:0008130 postsynaptic density assembly disrupted, abnormal ZP:0008131 synapse retinal outer plexiform layer disorganized, abnormal ZP:0008132 kinocilium auditory receptor cell bent, abnormal ZP:0008133 retinal cone cell detached from cytoskeleton of presynaptic active zone postsynaptic density retinal outer plexiform layer, abnormal ZP:0008134 posterior cardinal vein absent, abnormal ZP:0008135 fibroblast growth factor receptor signaling pathway decreased process quality, abnormal ZP:0008136 cell-cell adhesion mediated by cadherin decreased process quality, abnormal ZP:0008137 endodermal cell mislocalised, abnormal ZP:0008138 glycosphingolipid biosynthetic process process quality, abnormal ZP:0008139 hindbrain increased occurrence cell death, abnormal ZP:0008140 midbrain increased occurrence cell death, abnormal ZP:0008141 caudal fin curved dorsal, abnormal ZP:0008142 intersegmental vessel decreased process quality sprouting angiogenesis, abnormal ZP:0008143 ethmoid cartilage immature, abnormal ZP:0008144 pharyngeal arch 3 deformed, abnormal ZP:0008145 pharyngeal arch 4 deformed, abnormal ZP:0008146 pharyngeal arch 5 deformed, abnormal ZP:0008147 pharyngeal arch 2 inverted, abnormal ZP:0008148 nucleus yolk syncytial layer increased size, abnormal ZP:0008149 nucleus yolk syncytial layer decreased size, abnormal ZP:0008150 nucleus yolk syncytial layer mislocalised, abnormal ZP:0008151 nucleus yolk syncytial layer dispersed, abnormal ZP:0008152 marginal blastomere necrotic, abnormal ZP:0008153 somitogenesis decreased process quality, abnormal ZP:0008154 neural tube formation decreased process quality, abnormal ZP:0008155 convergent extension involved in gastrulation decreased process quality, abnormal ZP:0008156 neural tube has extra parts of type central canal, abnormal ZP:0008157 cell neural tube disorganized, abnormal ZP:0008158 Meckel's cartilage decreased width, abnormal ZP:0008159 Meckel's cartilage sharp, abnormal ZP:0008160 ceratohyal cartilage mislocalised dorsally, abnormal ZP:0008162 dorsal longitudinal anastomotic vessel immature, abnormal ZP:0008163 neural crest cell migration decreased occurrence, abnormal ZP:0008164 pigment cell post-vent region decreased amount, abnormal ZP:0008165 trunk neural crest cell morphology, abnormal ZP:0008166 neural crest cell increased amount, abnormal ZP:0008167 retinal neural layer stratification, abnormal ZP:0008168 eye spherical, abnormal ZP:0008169 oral cavity decreased size, abnormal ZP:0008170 nerve midbrain hindbrain boundary sparse, abnormal ZP:0008172 glial cell (sensu Vertebrata) decreased amount, abnormal ZP:0008173 regulation of synapse structure or activity disrupted, abnormal ZP:0008174 synaptic vesicle hair cell decreased amount, abnormal ZP:0008175 neuromast hair cell decreased functionality, abnormal ZP:0008176 endoderm decreased amount, abnormal ZP:0008177 positive regulation of apoptotic process disrupted, abnormal ZP:0008178 brain hydrophilic, abnormal ZP:0008179 proctodeum atretic, abnormal ZP:0008180 pronephric duct increased thickness, abnormal ZP:0008181 cilium pronephric duct curved, abnormal ZP:0008182 pronephros obstructed, abnormal ZP:0008183 cloacal chamber dilated, abnormal ZP:0008184 cilium cloacal chamber absent, abnormal ZP:0008185 cilium cloacal chamber decreased mobility, abnormal ZP:0008186 heart tube left side of axis, abnormal ZP:0008187 renal glomerulus dilated, abnormal ZP:0008188 posterior pronephric duct bent, abnormal ZP:0008189 otolith absent, abnormal ZP:0008190 cilium or flagellum-dependent cell motility increased rate, abnormal ZP:0008191 axonemal microtubule pronephros increased amount, abnormal ZP:0008192 axonemal microtubule pronephros displaced, abnormal ZP:0008193 cilium pronephric tubule decreased length, abnormal ZP:0008194 glomerular visceral epithelial cell development disrupted, abnormal ZP:0008195 glomerular basement membrane disorganized, abnormal ZP:0008196 orbit edematous, abnormal ZP:0008197 cell projection podocyte disorganized, abnormal ZP:0008200 female sex determination arrested, abnormal ZP:0008201 ovary absent, abnormal ZP:0008202 testis neoplastic, abnormal ZP:0008203 testis degeneration, abnormal ZP:0008204 testis has fewer parts of type spermatocyte, abnormal ZP:0008205 spermatocyte apoptotic, abnormal ZP:0008206 cartilage condensation disrupted, abnormal ZP:0008207 cranial cartilage pharyngeal arch decreased size, abnormal ZP:0008209 brain bulbous, abnormal ZP:0008210 cardiac muscle cell differentiation disrupted, abnormal ZP:0008211 extracellular matrix atrium increased size, abnormal ZP:0008212 cardiac muscle cell atrium decreased amount, abnormal ZP:0008213 cardiac muscle cell atrioventricular canal mislocalised, abnormal ZP:0008214 heart electrical conductivity, abnormal ZP:0008215 fin musculature disorganized, abnormal ZP:0008216 cephalic musculature hypoplastic, abnormal ZP:0008217 cephalic musculature malformed, abnormal ZP:0008218 atrium orientation cardiac ventricle, abnormal ZP:0008219 myotome irregular spatial pattern, abnormal ZP:0008220 muscle tendon junction myotome structure, abnormal ZP:0008221 muscle tendon junction myotome irregular spatial pattern, abnormal ZP:0008222 muscle tendon junction myotome decreased thickness, abnormal ZP:0008223 myofibril myotome distributed, abnormal ZP:0008224 myofibril myotome decreased amount, abnormal ZP:0008225 whole organism uncoordinated, abnormal ZP:0008226 skeletal muscle cell decreased mass, abnormal ZP:0008227 slow muscle cell undulate, abnormal ZP:0008228 slow muscle cell misaligned with slow muscle cell, abnormal ZP:0008229 fast muscle cell variant shape, abnormal ZP:0008230 pharynx lacks parts or has fewer parts of type pharyngeal arch 3-7, abnormal ZP:0008231 melanophore stripe decreased thickness, abnormal ZP:0008232 trunk vasculature increased branchiness, abnormal ZP:0008233 cardiac muscle myosin thick filament assembly disrupted, abnormal ZP:0008234 slow muscle cell disrupted myofibril assembly, abnormal ZP:0008235 sarcomere fast muscle cell disorganized, abnormal ZP:0008236 Z disc fast muscle cell disorganized, abnormal ZP:0008237 M band fast muscle cell disorganized, abnormal ZP:0008238 fast muscle cell disrupted sarcomere organization, abnormal ZP:0008239 fast muscle cell disrupted striated muscle myosin thick filament assembly, abnormal ZP:0008240 fast muscle cell disrupted muscle thin filament assembly, abnormal ZP:0008241 sarcomere cardiac muscle cell absent, abnormal ZP:0008242 shield increased size, abnormal ZP:0008244 trunk truncated, abnormal ZP:0008245 post-vent region branched, abnormal ZP:0008246 outflow tract morphogenesis decreased process quality, abnormal ZP:0008247 transforming growth factor beta receptor signaling pathway decreased process quality, abnormal ZP:0008248 cardiac ventricle physical object quality, abnormal ZP:0008249 cardiac ventricle has fewer parts of type ventricular endocardium, abnormal ZP:0008250 bulbus arteriosus lacks all parts of type smooth muscle myoblast, abnormal ZP:0008251 whole organism lacks all parts of type ventral aorta, abnormal ZP:0008252 presumptive bulbus arteriosus hypoplastic, abnormal ZP:0008253 presumptive cardiac ventricle heart tube decreased length, abnormal ZP:0008254 pharyngeal vasculature hypoplastic, abnormal ZP:0008255 pharyngeal vasculature malformed, abnormal ZP:0008257 hematopoietic stem cell differentiation increased occurrence, abnormal ZP:0008258 endothelial to hematopoietic transition increased occurrence, abnormal ZP:0008259 blood increased accumulation blood island, abnormal ZP:0008260 blood increased accumulation post-vent region, abnormal ZP:0008261 blood increased accumulation vasculature, abnormal ZP:0008262 caudal vein disorganized, abnormal ZP:0008263 caudal vein functionality, abnormal ZP:0008264 posterior cardinal vein functionality, abnormal ZP:0008265 mouth structure, abnormal ZP:0008266 central artery hemorrhagic, abnormal ZP:0008267 hematopoietic stem cell ventral wall of dorsal aorta increased amount, abnormal ZP:0008268 optic choroid vascular plexus hemorrhagic, abnormal ZP:0008269 ventral fin fold aplastic, abnormal ZP:0008270 renal filtration decreased process quality, abnormal ZP:0008272 cilium pronephric duct kinked, abnormal ZP:0008273 cilium pronephric duct shortened, abnormal ZP:0008274 pronephric duct lacks parts or has fewer parts of type epithelial cell microvillus epithelial cell, abnormal ZP:0008275 caudal fin curvature, abnormal ZP:0008277 ventral fin fold edematous, abnormal ZP:0008278 dorsal compartment pharyngeal pouch 1 morphology, abnormal ZP:0008279 segmentation decreased rate, abnormal ZP:0008280 anatomical axis whole organism decreased length, abnormal ZP:0008281 neuromast development disrupted, abnormal ZP:0008282 lateral line morphology, abnormal ZP:0008283 regulation of neuron apoptotic process disrupted, abnormal ZP:0008284 neuron brain absent, abnormal ZP:0008285 axon central nervous system decreased amount, abnormal ZP:0008286 neuronal stem cell decreased amount, abnormal ZP:0008287 pronephric glomerulus physical object quality, abnormal ZP:0008288 pronephric podocyte morphology, abnormal ZP:0008289 cell projection pronephric podocyte disorganized, abnormal ZP:0008290 apical junction complex neural tube structure, abnormal ZP:0008291 photoreceptor cell decreased adhesivity, abnormal ZP:0008292 cilium movement amplitude, abnormal ZP:0008294 tubulin-glycine ligase activity arrested, abnormal ZP:0008295 epiphysis bilateral symmetry, abnormal ZP:0008296 cilium olfactory placode decreased length, abnormal ZP:0008297 cilium olfactory placode malformed, abnormal ZP:0008298 cilium olfactory placode decreased amount, abnormal ZP:0008300 cilium pronephros direction, abnormal ZP:0008301 cilium pronephros inverted, abnormal ZP:0008303 inner ear lacks parts or has fewer parts of type otolith, abnormal ZP:0008304 retinoid metabolic process disrupted, abnormal ZP:0008305 presumptive neural retina decreased size, abnormal ZP:0008306 forerunner cell group stratification, abnormal ZP:0008307 fourth ventricle increased accumulation cerebral spinal fluid, abnormal ZP:0008310 skeletal system morphogenesis disrupted, abnormal ZP:0008311 telencephalon wholly dorsalized, abnormal ZP:0008312 retina fused with cranial nerve II, abnormal ZP:0008313 gill absent, abnormal ZP:0008314 semicircular canal quality, abnormal ZP:0008315 pharyngeal arch 3 skeleton absent, abnormal ZP:0008316 palatoquadrate arch morphology, abnormal ZP:0008317 ventral mandibular arch fused with palatoquadrate arch, abnormal ZP:0008318 pharyngeal arch 2 skeleton inverted, abnormal ZP:0008319 palatoquadrate cartilage quality, abnormal ZP:0008320 ceratohyal cartilage quality, abnormal ZP:0008321 ceratohyal cartilage kinked, abnormal ZP:0008322 brain morphogenesis process quality, abnormal ZP:0008323 MAP kinase activity disrupted, abnormal ZP:0008324 MAP kinase activity increased occurrence, abnormal ZP:0008325 angiogenic sprout dorsal aorta immature, abnormal ZP:0008326 vascular sprouts posterior cardinal vein absent, abnormal ZP:0008327 vascular sprouts posterior cardinal vein decreased amount, abnormal ZP:0008328 inner ear morphogenesis decreased process quality, abnormal ZP:0008329 camera-type eye morphogenesis decreased process quality, abnormal ZP:0008330 kidney morphogenesis decreased process quality, abnormal ZP:0008331 Kupffer's vesicle lacks all parts of type cilium ciliated epithelial cell, abnormal ZP:0008332 pronephric duct lacks parts or has fewer parts of type cilium ciliated epithelial cell, abnormal ZP:0008333 pronephros dilated, abnormal ZP:0008334 gamma-delta T cell differentiation arrested, abnormal ZP:0008335 ventral wall of dorsal aorta decreased process quality hematopoietic stem cell differentiation, abnormal ZP:0008336 gamma-delta T cell aplastic/hypoplastic, abnormal ZP:0008337 pronephric duct morphogenesis disrupted, abnormal ZP:0008338 epithelial tube formation disrupted, abnormal ZP:0008339 pronephric duct structure, abnormal ZP:0008342 phosphatidylcholine-retinol O-acyltransferase activity disrupted, abnormal ZP:0008344 collagen fibril organization decreased process quality, abnormal ZP:0008345 collagen metabolic process disrupted, abnormal ZP:0008346 fin shape, abnormal ZP:0008347 fin decreased length, abnormal ZP:0008348 fin has fewer parts of type lepidotrichium, abnormal ZP:0008349 fibrillar collagen trimer fin disorganized, abnormal ZP:0008350 fibrillar collagen trimer centrum disorganized, abnormal ZP:0008351 postcranial axial skeleton increased curvature, abnormal ZP:0008352 lepidotrichium caudal fin decreased size, abnormal ZP:0008353 ventral fin fold decreased length, abnormal ZP:0008354 ventral fin fold undulate, abnormal ZP:0008355 lepidotrichium anal fin decreased size, abnormal ZP:0008356 lepidotrichium dorsal fin decreased size, abnormal ZP:0008357 pelvic fin decreased size, abnormal ZP:0008358 vertebra shape, abnormal ZP:0008359 vertebra increased mass density, abnormal ZP:0008360 lepidotrichium undulate, abnormal ZP:0008361 lepidotrichium broken, abnormal ZP:0008362 lepidotrichium fused with lepidotrichium, abnormal ZP:0008363 osteoblast cuboid, abnormal ZP:0008364 post-anal tail morphogenesis delayed, abnormal ZP:0008365 liver development arrested, abnormal ZP:0008366 liver development having decreased processual parts cell population proliferation, abnormal ZP:0008367 swim bladder development having decreased processual parts cell population proliferation, abnormal ZP:0008368 liver increased variability of size, abnormal ZP:0008369 gall bladder morphology, abnormal ZP:0008370 gall bladder absent, abnormal ZP:0008371 extrahepatic duct morphology, abnormal ZP:0008372 extrahepatic duct decreased size, abnormal ZP:0008373 neuron brain increased amount, abnormal ZP:0008374 diencephalon hypoplastic, abnormal ZP:0008375 forebrain asymmetrical, abnormal ZP:0008376 midbrain hypoplastic, abnormal ZP:0008377 white matter spatial pattern, abnormal ZP:0008378 cardiac ventricle mislocalised, abnormal ZP:0008379 yolk lacks parts or has fewer parts of type granulocyte, abnormal ZP:0008380 yolk lacks parts or has fewer parts of type macrophage, abnormal ZP:0008381 blood island lacks parts or has fewer parts of type granulocyte, abnormal ZP:0008382 blood island lacks parts or has fewer parts of type macrophage, abnormal ZP:0008383 histone methyltransferase activity (H4-K20 specific) disrupted, abnormal ZP:0008384 shield increased width, abnormal ZP:0008385 ossification increased magnitude, abnormal ZP:0008386 skeletal system morphology, abnormal ZP:0008387 exit from mitosis decreased occurrence, abnormal ZP:0008388 retinal neural layer structure, abnormal ZP:0008389 apical region retinal neural layer increased area, abnormal ZP:0008390 cell retinal neural layer aggregated, abnormal ZP:0008391 heart decreased object quality, abnormal ZP:0008392 adherens junction retina increased size, abnormal ZP:0008393 adherens junction retina distributed, abnormal ZP:0008394 stomodeum shape, abnormal ZP:0008395 proximal region neurocranial trabecula decreased length, abnormal ZP:0008396 proximal region neurocranial trabecula truncated, abnormal ZP:0008397 chondrocyte neurocranial trabecula circular, abnormal ZP:0008398 chondrocyte neurocranial trabecula disorganized, abnormal ZP:0008399 ethmoid cartilage has fewer parts of type chondrocyte, abnormal ZP:0008400 ethmoid cartilage decreased occurrence chondrocyte proliferation, abnormal ZP:0008401 chondrocyte ethmoid cartilage shape, abnormal ZP:0008402 chondrocyte ethmoid cartilage disorganized, abnormal ZP:0008403 postero-lateral region parachordal cartilage aplastic, abnormal ZP:0008404 cranial neural crest cell lateralized, abnormal ZP:0008405 dorsal region cranial neural crest cell mislocalised laterally, abnormal ZP:0008406 hindbrain structure, abnormal ZP:0008407 determination of left/right symmetry arrested, abnormal ZP:0008408 response to wounding decreased process quality, abnormal ZP:0008409 cilium Kupffer's vesicle absent, abnormal ZP:0008410 cilium floor plate decreased amount, abnormal ZP:0008411 motile cilium central canal immobile, abnormal ZP:0008412 ventral fin fold absent, abnormal ZP:0008413 pharyngeal arch decreased process quality chondrocyte differentiation, abnormal ZP:0008414 pharyngeal arch decreased process quality transforming growth factor beta receptor signaling pathway, abnormal ZP:0008415 pharyngeal arch decreased occurrence cell population proliferation, abnormal ZP:0008416 chondrocyte pharyngeal arch differentiated, abnormal ZP:0008417 floor plate deformed, abnormal ZP:0008418 post-vent region hemorrhagic, abnormal ZP:0008419 dopamine metabolic process disrupted, abnormal ZP:0008420 pronephros deformed, abnormal ZP:0008421 mid cerebral vein immature, abnormal ZP:0008422 cell lymphangioblast cord decreased amount, abnormal ZP:0008423 somite border curvature, abnormal ZP:0008424 Kupffer's vesicle non-functional, abnormal ZP:0008425 Kupffer's vesicle has fewer parts of type cilium inner dynein arm Kupffer's vesicle, abnormal ZP:0008426 ciliary basal body floor plate mislocalised, abnormal ZP:0008427 anterior-most region head decreased size, abnormal ZP:0008428 anterior-most region head antero-posteriorly flattened, abnormal ZP:0008429 anterior-most region head shortened, abnormal ZP:0008430 cranial neural crest morphology, abnormal ZP:0008431 cranial neural crest lacks all parts of type antero-ventral region cranial neural crest cell, abnormal ZP:0008432 cranial neural crest has fewer parts of type medial region cranial neural crest cell, abnormal ZP:0008433 ethmoid cartilage notched, abnormal ZP:0008434 ethmoid cartilage perforate, abnormal ZP:0008435 ethmoid cartilage shortened, abnormal ZP:0008436 trabecula communis hypoplastic, abnormal ZP:0008437 trabecula communis deformed, abnormal ZP:0008438 palate cleft, abnormal ZP:0008439 epithelial cell notochord irregular spatial pattern, abnormal ZP:0008440 epithelial cell notochord variant shape, abnormal ZP:0008441 epithelial cell notochord variability of size, abnormal ZP:0008442 cellular sodium ion homeostasis decreased process quality, abnormal ZP:0008443 detection of mechanical stimulus involved in sensory perception of sound decreased process quality, abnormal ZP:0008444 angular vestibuloocular reflex decreased process quality, abnormal ZP:0008445 hair cell lateral crista morphology, abnormal ZP:0008446 hair cell anterior macula has extra parts of type multivesicular body hair cell anterior macula, abnormal ZP:0008447 vesicle hair cell anterior macula increased diameter, abnormal ZP:0008448 sodium:potassium-exchanging ATPase complex hair cell mislocalised, abnormal ZP:0008449 stereocilium bundle hair cell decreased width, abnormal ZP:0008450 neuromast hair cell cellular quality, abnormal ZP:0008451 neuromast hair cell functionality, abnormal ZP:0008452 skeletal muscle contraction decreased force, abnormal ZP:0008454 swimming behavior decreased occurrence, abnormal ZP:0008456 myoseptum decreased thickness, abnormal ZP:0008458 convergent extension involved in gastrulation decreased magnitude, abnormal ZP:0008459 tissue development disrupted, abnormal ZP:0008460 embryonic organ development disrupted, abnormal ZP:0008461 musculature system disorganized, abnormal ZP:0008462 keratinocyte detached from whole organism, abnormal ZP:0008463 midbrain increased size, abnormal ZP:0008464 heart primordium bifurcated, abnormal ZP:0008465 prechordal plate position, abnormal ZP:0008466 organizer inducing center increased width, abnormal ZP:0008467 brain morphogenesis arrested, abnormal ZP:0008468 muscle tendon junction muscle disorganized, abnormal ZP:0008469 myofibril muscle degenerate, abnormal ZP:0008470 sarcolemma muscle collapsed, abnormal ZP:0008471 phosphatidylinositol-4,5-bisphosphate 5-phosphatase activity decreased occurrence, abnormal ZP:0008472 cellular response to heat increased duration, abnormal ZP:0008473 neural precursor cell proliferation decreased occurrence, abnormal ZP:0008474 cellular response to epinephrine stimulus delayed, abnormal ZP:0008475 renal filtration disrupted, abnormal ZP:0008476 Kupffer's vesicle has fewer parts of type cilium ciliated epithelial cell, abnormal ZP:0008477 neuron forebrain electrical conductivity, abnormal ZP:0008478 anterior region pronephros cystic, abnormal ZP:0008479 retina deformed, abnormal ZP:0008480 neuromast immature, abnormal ZP:0008481 heart tube displaced to right side whole organism, abnormal ZP:0008482 heart tube displaced to central region whole organism, abnormal ZP:0008483 anterior-posterior axis whole organism asymmetrical, abnormal ZP:0008484 ethmoid cartilage absent, abnormal ZP:0008485 pronephric tubule increased width, abnormal ZP:0008486 cilium pronephric tubule disorganized, abnormal ZP:0008487 pharyngeal arch 3-7 lacks parts or has fewer parts of type cartilage tissue, abnormal ZP:0008488 white matter cystic, abnormal ZP:0008489 white matter increased accumulation astrocyte, abnormal ZP:0008490 anterior region cranial vault flattened, abnormal ZP:0008491 growth plate cartilage chondrocyte proliferation disrupted, abnormal ZP:0008492 ventral mandibular arch deformed, abnormal ZP:0008493 hyosymplectic cartilage decreased length, abnormal ZP:0008494 locomotion irregular rhythm, abnormal ZP:0008495 semicircular canal morphogenesis process quality, abnormal ZP:0008496 lateral line development delayed, abnormal ZP:0008497 posterior lateral line neuromast primordium migration delayed, abnormal ZP:0008498 equilibrioception delayed, abnormal ZP:0008499 hair cell anterior macula decreased amount, abnormal ZP:0008500 neuromast physical object quality, abnormal ZP:0008501 pronephric podocyte structure, abnormal ZP:0008502 pronephric podocyte disorganized, abnormal ZP:0008503 pronephric glomerular basement membrane disorganized, abnormal ZP:0008504 lens fiber cell fate commitment disrupted, abnormal ZP:0008505 lens epithelial cell proliferation increased occurrence, abnormal ZP:0008506 lens physical object quality, abnormal ZP:0008507 lens pigmented, abnormal ZP:0008508 actin filament lens spatial pattern, abnormal ZP:0008509 actin filament lens decreased amount, abnormal ZP:0008510 cell lens shape, abnormal ZP:0008511 cornea composition, abnormal ZP:0008512 cornea nucleate quality, abnormal ZP:0008513 pupil absent, abnormal ZP:0008514 lens epithelium composition, abnormal ZP:0008515 lens epithelium structure, abnormal ZP:0008516 lens epithelium has extra parts of type epithelial cell, abnormal ZP:0008517 lens epithelium has extra parts of type nucleus epithelial cell, abnormal ZP:0008518 nucleus lens epithelium increased size, abnormal ZP:0008519 nucleus lens epithelium disorganized, abnormal ZP:0008520 epithelial cell lens epithelium nucleate quality, abnormal ZP:0008521 epithelial cell lens epithelium immature, abnormal ZP:0008522 epithelial cell lens epithelium swollen, abnormal ZP:0008523 locomotory behavior process quality, abnormal ZP:0008524 swimming occurrence, abnormal ZP:0008525 motor neuron axon guidance decreased process quality, abnormal ZP:0008526 axon motor neuron mislocalised, abnormal ZP:0008527 vasculature yolk decreased amount, abnormal ZP:0008528 pharyngeal arch 3-7 deformed, abnormal ZP:0008529 posterior-most region somite decreased amount, abnormal ZP:0008530 vertical myoseptum structure, abnormal ZP:0008531 vertical myoseptum decreased length, abnormal ZP:0008532 post-vent region decreased flexibility, abnormal ZP:0008533 hindbrain development delayed, abnormal ZP:0008534 EVL constricted, abnormal ZP:0008535 rhombomere 5 decreased thickness, abnormal ZP:0008536 rhombomere 3 decreased thickness, abnormal ZP:0008537 cell detached from post-vent region, abnormal ZP:0008538 hemostasis delayed, abnormal ZP:0008539 yolk hemorrhagic, abnormal ZP:0008540 regulation of vascular endothelial growth factor receptor signaling pathway process quality, abnormal ZP:0008541 retina edematous, abnormal ZP:0008542 ocular blood vessel retinal inner plexiform layer mislocalised, abnormal ZP:0008543 pronephric podocyte physical object quality, abnormal ZP:0008544 blood vessel trunk vasculature increased amount, abnormal ZP:0008545 optic artery increased permeability, abnormal ZP:0008546 hyaloid vessel branched, abnormal ZP:0008547 hyaloid vessel malformed, abnormal ZP:0008548 optic choroid vascular plexus branched, abnormal ZP:0008549 optic choroid vascular plexus malformed, abnormal ZP:0008550 cranial blood vessel increased amount, abnormal ZP:0008551 ocular blood vessel branched, abnormal ZP:0008552 nucleate erythrocyte optical quality, abnormal ZP:0008553 endoplasmic reticulum to Golgi vesicle-mediated transport decreased process quality, abnormal ZP:0008554 melanosome organization decreased process quality, abnormal ZP:0008555 collagen biosynthetic process decreased process quality, abnormal ZP:0008556 extracellular matrix constituent secretion decreased process quality, abnormal ZP:0008557 collagen trimer notochord mislocalised, abnormal ZP:0008558 extracellular matrix notochord decreased thickness, abnormal ZP:0008559 chondrocyte Meckel's cartilage malformed, abnormal ZP:0008560 fibrillar collagen trimer cranial cartilage decreased mass, abnormal ZP:0008561 extracellular matrix cranial cartilage decreased mass, abnormal ZP:0008562 chondroblast spatial pattern, abnormal ZP:0008563 endoplasmic reticulum chondrocyte distended, abnormal ZP:0008564 melanosome melanocyte circular, abnormal ZP:0008565 melanosome melanocyte immature, abnormal ZP:0008566 caudal artery increased accumulation thrombocyte, abnormal ZP:0008567 thrombocyte aggregated, abnormal ZP:0008571 retinal outer plexiform layer aplastic, abnormal ZP:0008572 retinal outer nuclear layer aplastic, abnormal ZP:0008573 photoreceptor outer segment photoreceptor cell aplastic/hypoplastic, abnormal ZP:0008574 nucleus photoreceptor cell shape, abnormal ZP:0008576 Golgi cisterna photoreceptor cell hypoplastic, abnormal ZP:0008577 horizontal cell absent, abnormal ZP:0008579 EVL cellular motility, abnormal ZP:0008580 deep blastomere circular, abnormal ZP:0008581 deep blastomere cellular adhesivity, abnormal ZP:0008582 portion of tissue cardiac ventricle increased thickness, abnormal ZP:0008583 portion of tissue atrium decreased thickness, abnormal ZP:0008584 pericardium hypertrophic, abnormal ZP:0008585 cellular response to DNA damage stimulus disrupted, abnormal ZP:0008586 cardiac muscle contraction decreased rate, abnormal ZP:0008587 cardiac muscle contraction decreased strength, abnormal ZP:0008588 brain atrophied, abnormal ZP:0008589 brain decreased occurrence cell population proliferation, abnormal ZP:0008590 brain disrupted axon extension, abnormal ZP:0008591 brain disrupted innervation, abnormal ZP:0008592 ventricular system brain decreased volume, abnormal ZP:0008593 neuron brain mislocalised, abnormal ZP:0008594 heart primordium decreased occurrence cell population proliferation, abnormal ZP:0008595 midbrain decreased occurrence cell population proliferation, abnormal ZP:0008596 tectal ventricle decreased width, abnormal ZP:0008597 atrium shortened, abnormal ZP:0008598 plasma membrane neuron structure, abnormal ZP:0008599 spinal cord interneuron increased amount, abnormal ZP:0008600 microtubule cytoskeleton organization disrupted, abnormal ZP:0008601 efferent axon development in posterior lateral line nerve disrupted, abnormal ZP:0008602 spinal cord structure, abnormal ZP:0008603 mitochondrion spinal cord vacuolated, abnormal ZP:0008604 axon spinal cord discolored, abnormal ZP:0008605 axon spinal cord decreased amount, abnormal ZP:0008606 compact myelin spinal cord decreased amount, abnormal ZP:0008607 synaptic vesicle enteric nervous system mislocalised, abnormal ZP:0008608 microtubule cytoskeleton enteric nervous system disorganized, abnormal ZP:0008609 microtubule cytoskeleton neuron disorganized, abnormal ZP:0008610 fin absent, abnormal ZP:0008611 caudal fin absent, abnormal ZP:0008612 mesoderm caudal fin immature, abnormal ZP:0008613 mesoderm anal fin immature, abnormal ZP:0008614 pelvic fin absent, abnormal ZP:0008615 pectoral fin distal radial fused with pectoral fin distal radial, abnormal ZP:0008617 retinal ganglion cell retinal ganglion cell layer increased amount, abnormal ZP:0008618 retinal photoreceptor layer poorly differentiated, abnormal ZP:0008619 nucleus retina mislocalised, abnormal ZP:0008620 eye photoreceptor cell shape, abnormal ZP:0008621 retinal ganglion cell increased amount, abnormal ZP:0008622 retinal ganglion cell mislocalised, abnormal ZP:0008623 notochord broken, abnormal ZP:0008624 post-vent region increased amount, abnormal ZP:0008625 pectoral fin physical object quality, abnormal ZP:0008626 primitive erythrocyte differentiation decreased occurrence, abnormal ZP:0008627 whole organism has fewer parts of type hemoglobin complex nucleate erythrocyte, abnormal ZP:0008628 neuroectoderm apoptotic, abnormal ZP:0008629 nucleate erythrocyte hypoplastic, abnormal ZP:0008630 collagen biosynthetic process increased rate, abnormal ZP:0008632 chondrocyte Meckel's cartilage length, abnormal ZP:0008633 chondrocyte Meckel's cartilage obtuse, abnormal ZP:0008634 chondrocyte ceratohyal cartilage obtuse, abnormal ZP:0008635 chondrocyte pharyngeal arch cartilage malformed, abnormal ZP:0008636 chondrocyte malformed, abnormal ZP:0008637 chondrocyte undifferentiated, abnormal ZP:0008638 endoplasmic reticulum lumen chondrocyte swollen, abnormal ZP:0008639 Golgi apparatus chondrocyte decreased size, abnormal ZP:0008640 Golgi apparatus chondrocyte disorganized, abnormal ZP:0008641 actin filament chondrocyte disorganized, abnormal ZP:0008643 neural crest cell migration increased rate, abnormal ZP:0008644 parachordal vessel absent, abnormal ZP:0008645 cellular response to light stimulus increased intensity, abnormal ZP:0008646 ON-bipolar cell functionality, abnormal ZP:0008647 axon terminus ON-bipolar cell morphology, abnormal ZP:0008648 pigmentation occurrence, abnormal ZP:0008649 membrane depolarization increased occurrence, abnormal ZP:0008650 melanocyte membrane potential, abnormal ZP:0008651 xanthophore spatial pattern, abnormal ZP:0008652 midbrain hindbrain boundary decreased width, abnormal ZP:0008653 tegmentum increased size, abnormal ZP:0008654 tegmentum deformed, abnormal ZP:0008655 mouth prominent, abnormal ZP:0008656 rhombomere deformed, abnormal ZP:0008657 optic cup prominent, abnormal ZP:0008658 caudal vein plexus decreased occurrence blood circulation, abnormal ZP:0008659 release of sequestered calcium ion into cytosol decreased occurrence, abnormal ZP:0008660 rhombomere hindbrain condensed, abnormal ZP:0008661 somite trunk increased width, abnormal ZP:0008662 developmental growth neotenous growth, abnormal ZP:0008663 atrioventricular canal increased width, abnormal ZP:0008664 fin bud decreased size, abnormal ZP:0008665 sprouting angiogenesis sporadic, abnormal ZP:0008666 central region dorsal aorta decreased width, abnormal ZP:0008667 common cardinal vein increased accumulation blood cell, abnormal ZP:0008668 central region posterior cardinal vein decreased width, abnormal ZP:0008669 caudal vein plexus increased accumulation blood cell, abnormal ZP:0008670 dorsal longitudinal anastomotic vessel non-functional, abnormal ZP:0008671 central region subintestinal vein decreased width, abnormal ZP:0008672 fin vasculature decreased functionality, abnormal ZP:0008673 central region pectoral fin blood vessel decreased width, abnormal ZP:0008674 melatonin biosynthetic process disrupted, abnormal ZP:0008675 circadian sleep/wake cycle, sleep decreased duration, abnormal ZP:0008676 circadian sleep/wake cycle, sleep disrupted, abnormal ZP:0008677 spleen decreased size, abnormal ZP:0008678 spleen agenesis, abnormal ZP:0008679 pharyngeal arch 5 immature, abnormal ZP:0008680 presumptive cardiac ventricle heart tube mislocalised, abnormal ZP:0008681 cell body intrahepatic bile duct increased size, abnormal ZP:0008682 lateral mesodermal cell differentiation disrupted, abnormal ZP:0008683 intermediate mesodermal cell differentiation disrupted, abnormal ZP:0008684 hemangioblast cell differentiation disrupted, abnormal ZP:0008685 pronephros morphology, abnormal ZP:0008686 common cardinal vein increased diameter, abnormal ZP:0008687 presumptive endoderm increased width, abnormal ZP:0008688 pharyngeal endoderm increased width, abnormal ZP:0008689 pronephric tubule decreased diameter, abnormal ZP:0008690 pronephric proximal convoluted tubule morphology, abnormal ZP:0008691 anterior lateral mesoderm morphology, abnormal ZP:0008692 epiphysis apoptotic, abnormal ZP:0008693 telencephalon apoptotic, abnormal ZP:0008694 caudal artery poorly differentiated, abnormal ZP:0008695 caudal vein poorly differentiated, abnormal ZP:0008696 whole organism hemorrhagic, abnormal ZP:0008697 nucleate erythrocyte increased accumulation caudal artery, abnormal ZP:0008698 nucleate erythrocyte increased accumulation dorsal aorta, abnormal ZP:0008699 whole organism swollen, abnormal ZP:0008700 trunk shape, abnormal ZP:0008701 hemoglobin complex blood decreased amount, abnormal ZP:0008702 melanocyte yolk decreased amount, abnormal ZP:0008703 melanosome retinal pigmented epithelium immature, abnormal ZP:0008704 melanosome retinal pigmented epithelium decreased circumference, abnormal ZP:0008705 retinal pigmented epithelium displaced to melanosome retinal pigmented epithelium, abnormal ZP:0008706 retinal pigmented epithelium displaced to melanosome central region retinal pigmented epithelium, abnormal ZP:0008707 retinal pigmented epithelium displaced to melanosome dorsal region retinal pigmented epithelium, abnormal ZP:0008708 retinal pigmented epithelium displaced to melanosome retina, abnormal ZP:0008709 retinal pigmented epithelium displaced to melanosome optic choroid, abnormal ZP:0008710 retinal pigmented epithelium lacks all parts of type cell projection melanosome retinal pigmented epithelium, abnormal ZP:0008711 lipid biosynthetic process process quality, abnormal ZP:0008712 nucleus notochord morphology, abnormal ZP:0008713 endoplasmic reticulum notochord increased size, abnormal ZP:0008714 Golgi apparatus notochord morphology, abnormal ZP:0008715 myofibril somite unstructured, abnormal ZP:0008716 blood vessel inner optic circle decreased size, abnormal ZP:0008717 blood vessel inner optic circle elliptic, abnormal ZP:0008718 ocular blood vessel deformed, abnormal ZP:0008719 protein glycosylation disrupted, abnormal ZP:0008720 voluntary musculoskeletal movement disrupted, abnormal ZP:0008721 head morphogenesis disrupted, abnormal ZP:0008722 notochord disorganized, abnormal ZP:0008723 vertical myoseptum curved, abnormal ZP:0008724 myotome decreased mass, abnormal ZP:0008725 basement membrane myotome morphology, abnormal ZP:0008726 myofibril myotome spatial pattern, abnormal ZP:0008727 myofibril myotome decreased length, abnormal ZP:0008728 myofibril myotome refractivity, abnormal ZP:0008729 myoseptum disorganized, abnormal ZP:0008730 myoseptum increased distance myoseptum, abnormal ZP:0008732 contractile fiber trunk disorganized, abnormal ZP:0008733 neural tube disorganized, abnormal ZP:0008734 muscle cell irregular spatial pattern, abnormal ZP:0008735 chondrocyte development disrupted, abnormal ZP:0008736 neuromuscular junction development delayed, abnormal ZP:0008737 somite curved, abnormal ZP:0008738 clathrin-sculpted acetylcholine transport vesicle somite mislocalised medially, abnormal ZP:0008739 hyosymplectic cartilage disorganized, abnormal ZP:0008740 melanocyte apoptotic, abnormal ZP:0008741 neuron fate determination disrupted, abnormal ZP:0008742 anatomical compartment boundary somite shape, abnormal ZP:0008743 myofibril muscle misrouted, abnormal ZP:0008744 voluntary musculoskeletal movement arrested, abnormal ZP:0008745 T-tubule myotome mislocalised, abnormal ZP:0008746 T-tubule myotome decreased amount, abnormal ZP:0008747 myofibril skeletal muscle cell disoriented, abnormal ZP:0008748 myofibril skeletal muscle cell undulate, abnormal ZP:0008749 myofibril skeletal muscle cell increased variability of size, abnormal ZP:0008750 muscle cell apoptotic, abnormal ZP:0008751 collagen trimer skeletal muscle cell spatial pattern, abnormal ZP:0008752 mitochondrion skeletal muscle cell increased amount, abnormal ZP:0008753 mitochondrion skeletal muscle cell swollen, abnormal ZP:0008754 endoplasmic reticulum skeletal muscle cell dilated, abnormal ZP:0008755 mitochondrial crista skeletal muscle cell structure, abnormal ZP:0008756 sarcolemma skeletal muscle cell structure, abnormal ZP:0008757 intersegmental vessel has extra parts of type filopodium endothelial tip cell, abnormal ZP:0008758 intersegmental vessel process quality sprouting angiogenesis, abnormal ZP:0008759 intersegmental vessel detached from endothelial tip cell dorsal aorta, abnormal ZP:0008761 pharynx has fewer parts of type goblet cell, abnormal ZP:0008762 goblet cell pharynx decreased amount, abnormal ZP:0008763 retinal photoreceptor layer decreased size, abnormal ZP:0008764 retinal pigmented epithelium increased size, abnormal ZP:0008765 nuclear pore retina mislocalised, abnormal ZP:0008766 nuclear pore retina disorganized, abnormal ZP:0008767 nuclear pore retina decreased amount, abnormal ZP:0008768 cranial nerve II decreased diameter, abnormal ZP:0008769 nuclear pore posterior intestine decreased amount, abnormal ZP:0008770 enterocyte intestinal bulb decreased amount, abnormal ZP:0008771 retinal outer plexiform layer decreased size, abnormal ZP:0008772 intestine apoptotic, abnormal ZP:0008773 intestine has fewer parts of type goblet cell, abnormal ZP:0008774 nuclear pore intestine mislocalised, abnormal ZP:0008775 nuclear pore intestine disorganized, abnormal ZP:0008776 intestinal epithelium surface feature shape, abnormal ZP:0008778 nuclear pore intestinal epithelium decreased amount, abnormal ZP:0008779 cell intestinal epithelium disorganized, abnormal ZP:0008780 enteroendocrine cell intestinal epithelium decreased amount, abnormal ZP:0008781 intestinal bulb epithelium decreased thickness, abnormal ZP:0008782 intestinal bulb epithelium surface feature shape, abnormal ZP:0008783 nuclear pore intestinal bulb epithelium absent, abnormal ZP:0008784 goblet cell posterior intestine epithelium absent, abnormal ZP:0008785 nucleus enterocyte shape, abnormal ZP:0008786 nucleus enterocyte mislocalised, abnormal ZP:0008787 caudal artery malformed, abnormal ZP:0008788 heart hemorrhagic, abnormal ZP:0008789 intersegmental vessel fused with intersegmental vessel, abnormal ZP:0008790 filopodium intersegmental vessel decreased length, abnormal ZP:0008791 dorsal longitudinal anastomotic vessel shape, abnormal ZP:0008792 filopodium endothelial tip cell decreased length, abnormal ZP:0008793 motor neuron spinal cord morphology, abnormal ZP:0008794 axon neuron truncated, abnormal ZP:0008795 anterior region whole organism truncated, abnormal ZP:0008796 pronephric duct distended, abnormal ZP:0008797 sodium:potassium-exchanging ATPase complex pronephric duct mislocalised, abnormal ZP:0008798 cilium pronephric duct increased behavioural activity, abnormal ZP:0008799 actin cytoskeleton pronephric duct disorganized, abnormal ZP:0008800 otolith organ increased amount, abnormal ZP:0008801 collateral sprouting in absence of injury premature, abnormal ZP:0008802 regulation of collateral sprouting in absence of injury process quality, abnormal ZP:0008803 branching morphogenesis of a nerve sporadic, abnormal ZP:0008804 branching morphogenesis of a nerve increased occurrence, abnormal ZP:0008805 motor neuron spinal cord malformed, abnormal ZP:0008806 primary motor neuron spinal cord malformed, abnormal ZP:0008807 cranial nerve VII malformed, abnormal ZP:0008808 cranial nerve V malformed, abnormal ZP:0008809 axon MiP motor neuron increased branchiness, abnormal ZP:0008810 axon RoP motor neuron mislocalised, abnormal ZP:0008811 axon RoP motor neuron increased branchiness, abnormal ZP:0008812 axon motor neuron increased amount, abnormal ZP:0008813 axon collateral CaP motoneuron increased amount, abnormal ZP:0008814 axon collateral CaP motoneuron mislocalised proximally, abnormal ZP:0008815 epithelial cell differentiation disrupted, abnormal ZP:0008816 basal plate midbrain region decreased size, abnormal ZP:0008817 intestinal bulb morphology, abnormal ZP:0008818 zona limitans intrathalamica decreased size, abnormal ZP:0008819 goblet cell intestinal epithelium absent, abnormal ZP:0008820 enterocyte intestinal epithelium absent, abnormal ZP:0008821 epithelial cell mid intestine epithelium cuboid, abnormal ZP:0008822 epithelial cell posterior intestine epithelium cuboid, abnormal ZP:0008823 enteroendocrine cell absent, abnormal ZP:0008824 mesodermal cell decreased amount, abnormal ZP:0008825 lymph vasculature inverted, abnormal ZP:0008826 regulation of growth hormone secretion disrupted, abnormal ZP:0008827 branchiomeric skeletal muscle development process quality, abnormal ZP:0008828 abductor hyohyoid has fewer parts of type skeletal muscle cell, abnormal ZP:0008829 adductor operculi has fewer parts of type skeletal muscle cell, abnormal ZP:0008830 dilatator operculi has fewer parts of type skeletal muscle cell, abnormal ZP:0008831 levator operculi has fewer parts of type skeletal muscle cell, abnormal ZP:0008832 adductor hyohyoid has fewer parts of type skeletal muscle cell, abnormal ZP:0008833 pronephric duct opening morphology, abnormal ZP:0008834 neuromast increased size, abnormal ZP:0008835 neuromast increased area, abnormal ZP:0008837 parapineal organ inverted, abnormal ZP:0008841 ryanodine-sensitive calcium-release channel activity decreased occurrence, abnormal ZP:0008842 voltage-gated calcium channel activity decreased occurrence, abnormal ZP:0008843 muscle contraction decreased intensity, abnormal ZP:0008844 protein oxidation increased occurrence, abnormal ZP:0008845 fast-twitch skeletal muscle fiber contraction process quality, abnormal ZP:0008846 fast-twitch skeletal muscle fiber contraction decreased occurrence, abnormal ZP:0008848 locomotion involved in locomotory behavior occurrence, abnormal ZP:0008850 fast muscle cell trunk musculature decreased contractility, abnormal ZP:0008853 fast muscle cell myotome decreased functionality, abnormal ZP:0008855 fast muscle cell post-vent region decreased contractility, abnormal ZP:0008857 longitudinal sarcoplasmic reticulum skeletal muscle swollen, abnormal ZP:0008858 sarcoplasmic reticulum membrane skeletal muscle dilated, abnormal ZP:0008859 sarcoplasmic reticulum fast muscle cell absent, abnormal ZP:0008860 sarcoplasmic reticulum fast muscle cell disorganized, abnormal ZP:0008864 neural tube formation occurrence, abnormal ZP:0008865 midbrain-hindbrain boundary morphogenesis occurrence, abnormal ZP:0008866 ventricular system development occurrence, abnormal ZP:0008867 midbrain-hindbrain boundary development occurrence, abnormal ZP:0008868 cranium deformed, abnormal ZP:0008869 neuroectoderm deformed, abnormal ZP:0008870 T cell differentiation disrupted, abnormal ZP:0008871 thymus cellularity, abnormal ZP:0008872 thymus lacks parts or has fewer parts of type pro-T cell, abnormal ZP:0008873 pro-T cell decreased amount, abnormal ZP:0008874 blood vasculature hemorrhagic, abnormal ZP:0008875 trunk vasculature spatial pattern, abnormal ZP:0008877 P granule primordial germ cell physical object quality, abnormal ZP:0008878 P granule primordial germ cell decreased amount, abnormal ZP:0008879 primordial germ cell increased distance P granule mitochondrion primordial germ cell, abnormal ZP:0008880 exocrine pancreas disorganized, abnormal ZP:0008881 double-strand break repair via homologous recombination increased frequency, abnormal ZP:0008882 double-strand break repair via nonhomologous end joining decreased frequency, abnormal ZP:0008884 vasculogenesis paedomorphic growth, abnormal ZP:0008885 filopodium assembly paedomorphic growth, abnormal ZP:0008886 intersegmental vein decreased size, abnormal ZP:0008887 filopodium intersegmental vein decreased length, abnormal ZP:0008888 response to cytokine decreased process quality, abnormal ZP:0008889 anatomical structure aplastic, abnormal ZP:0008890 tail bud increased amount, abnormal ZP:0008891 notochord increased amount, abnormal ZP:0008892 whole organism radial symmetry, abnormal ZP:0008893 glomerular basement membrane increased permeability, abnormal ZP:0008894 neural crest formation process quality, abnormal ZP:0008895 bone mineralization process quality, abnormal ZP:0008896 heart tubular, abnormal ZP:0008897 facial nerve motor nucleus has fewer parts of type motor neuron, abnormal ZP:0008898 motor neuron cranial nerve position, abnormal ZP:0008899 motor neuron cranial nerve disorganized, abnormal ZP:0008900 anterior-posterior axis whole organism kinked, abnormal ZP:0008901 anterior-posterior axis trunk curved, abnormal ZP:0008902 vertebra increased distance vertebra, abnormal ZP:0008903 vertebra has fewer parts of type neural spine, abnormal ZP:0008904 vertebra has fewer parts of type hemal spine, abnormal ZP:0008905 cranial neural crest disorganized, abnormal ZP:0008906 cranial neural crest has fewer parts of type cranial neural crest cell, abnormal ZP:0008907 facial ganglion hypoplastic, abnormal ZP:0008908 axon facial ganglion decreased length, abnormal ZP:0008909 axon facial ganglion decreased amount, abnormal ZP:0008910 pharyngeal arch decreased amount, abnormal ZP:0008911 neural spine decreased size, abnormal ZP:0008912 hemal spine decreased size, abnormal ZP:0008913 somite border malformed, abnormal ZP:0008914 pharyngeal arch 3-7 absent, abnormal ZP:0008916 otolith increased variability of size, abnormal ZP:0008918 external yolk syncytial layer immature, abnormal ZP:0008919 actin filament whole organism disorganized, abnormal ZP:0008920 protein secretion disrupted, abnormal ZP:0008921 hypochord development disrupted, abnormal ZP:0008922 rough endoplasmic reticulum hypochord increased size, abnormal ZP:0008923 rough endoplasmic reticulum notochord increased size, abnormal ZP:0008924 otolith organ altered number of otolith, abnormal ZP:0008925 otolith aplastic, abnormal ZP:0008926 transmission of nerve impulse process quality, abnormal ZP:0008927 blood cell intermediate cell mass of mesoderm decreased amount, abnormal ZP:0008928 midbrain degenerate, abnormal ZP:0008929 notochord immature, abnormal ZP:0008930 fourth ventricle dilated, abnormal ZP:0008931 tectal ventricle dilated, abnormal ZP:0008933 neural tube closure arrested, abnormal ZP:0008934 glial cell differentiation decreased occurrence, abnormal ZP:0008935 caudal vein absent blood circulation, abnormal ZP:0008936 ceratobranchial cartilage hypoplastic, abnormal ZP:0008937 dorsal longitudinal anastomotic vessel absent blood circulation, abnormal ZP:0008939 epithelial cell pronephros shortened, abnormal ZP:0008941 cilium olfactory epithelium shortened, abnormal ZP:0008942 pronephric tubule increased size, abnormal ZP:0008943 pronephric proximal convoluted tubule closed, abnormal ZP:0008944 multi-ciliated epithelial cell accumulation pronephric duct, abnormal ZP:0008948 cilium multi-ciliated epithelial cell disorganized, abnormal ZP:0008950 definitive hemopoiesis arrested, abnormal ZP:0008951 midbrain disorganized, abnormal ZP:0008952 axon nervous system spatial pattern, abnormal ZP:0008953 cranial nerve III decreased size, abnormal ZP:0008954 cranial nerve X morphology, abnormal ZP:0008955 cranial nerve IV decreased size, abnormal ZP:0008956 cranial nerve VII decreased size, abnormal ZP:0008957 cranial nerve VII disorganized, abnormal ZP:0008958 cranial nerve V decreased size, abnormal ZP:0008959 cranial nerve V disorganized, abnormal ZP:0008960 cardiac ventricle decreased volume, abnormal ZP:0008961 heart insufficient, abnormal ZP:0008962 nucleate erythrocyte decreased fluid flow, abnormal ZP:0008963 cranial ganglion morphology, abnormal ZP:0008964 glial cell lateral line decreased amount, abnormal ZP:0008965 T cell differentiation in thymus disrupted, abnormal ZP:0008966 T cell decreased amount, abnormal ZP:0008967 muscle contraction decreased rate, abnormal ZP:0008968 sarcomere organization process quality, abnormal ZP:0008969 fast muscle cell myotome physical object quality, abnormal ZP:0008970 dopaminergic neuron diencephalon irregular spatial pattern, abnormal ZP:0008971 axon optic tectum decreased amount, abnormal ZP:0008972 neuromuscular synaptic transmission amplitude, abnormal ZP:0008973 neuromuscular synaptic transmission process quality, abnormal ZP:0008974 receptor clustering process quality, abnormal ZP:0008975 post-vent region mislocalised, abnormal ZP:0008976 ventricular zone increased size, abnormal ZP:0008977 cell ventricular zone increased mass density, abnormal ZP:0008978 pharyngeal arch decreased length, abnormal ZP:0008979 cell pharyngeal arch increased mass density, abnormal ZP:0008980 atrioventricular valve non-functional, abnormal ZP:0008981 blood cell aggregated, abnormal ZP:0008982 regulation of neurotransmitter levels disrupted, abnormal ZP:0008983 response to light stimulus decreased duration, abnormal ZP:0008984 oxygen metabolic process decreased rate, abnormal ZP:0008985 ball increased circumference, abnormal ZP:0008986 dorsal region brain physical object quality, abnormal ZP:0008987 axon secondary motor neuron branchiness, abnormal ZP:0008988 regulation of hydrogen peroxide metabolic process disrupted, abnormal ZP:0008989 neutrophil differentiation disrupted, abnormal ZP:0008990 macrophage differentiation disrupted, abnormal ZP:0008991 mononuclear phagocyte rostral blood island aggregated, abnormal ZP:0008992 mononuclear phagocyte rostral blood island decreased amount, abnormal ZP:0008993 neutrophil rostral blood island decreased amount, abnormal ZP:0008994 myeloid cell aggregated, abnormal ZP:0008995 cranial nerve X mislocalised, abnormal ZP:0008996 thymus has fewer parts of type pro-T cell, abnormal ZP:0008997 lymphangioblast cord malformed, abnormal ZP:0008998 pronephric glomerulus disorganized, abnormal ZP:0008999 retina layer formation decreased process quality, abnormal ZP:0009000 retinal cone cell differentiation delayed, abnormal ZP:0009001 retina morphogenesis in camera-type eye decreased process quality, abnormal ZP:0009002 brain increased occurrence apoptotic process, abnormal ZP:0009003 lens increased occurrence apoptotic process, abnormal ZP:0009004 retinal inner nuclear layer increased occurrence cell population proliferation, abnormal ZP:0009005 retina increased occurrence cell population proliferation, abnormal ZP:0009006 optic cup increased occurrence apoptotic process, abnormal ZP:0009007 retinal outer nuclear layer increased occurrence cell population proliferation, abnormal ZP:0009008 solid lens vesicle decreased occurrence apoptotic process, abnormal ZP:0009009 vasculature development arrested, abnormal ZP:0009010 notochord curved, abnormal ZP:0009011 caudal vein plexus irregular spatial pattern, abnormal ZP:0009012 vasculature irregular spatial pattern, abnormal ZP:0009013 neurogenesis process quality, abnormal ZP:0009014 primary neuron decreased amount, abnormal ZP:0009015 median fin fold collapsed, abnormal ZP:0009016 epidermis damaged, abnormal ZP:0009017 telomerase activity process quality, abnormal ZP:0009018 telomerase activity decreased occurrence, abnormal ZP:0009020 telomere maintenance via telomerase decreased occurrence, abnormal ZP:0009021 cell cycle arrest increased occurrence, abnormal ZP:0009022 spermatogonial cell division decreased occurrence, abnormal ZP:0009024 determination of adult lifespan decreased duration, abnormal ZP:0009025 fertilization having decreased processual parts fertilization, abnormal ZP:0009026 animal organ senescence premature, abnormal ZP:0009027 chromosome breakage increased occurrence, abnormal ZP:0009028 hematopoietic stem cell homeostasis disrupted, abnormal ZP:0009029 regulation of signal transduction by p53 class mediator increased process quality, abnormal ZP:0009030 spinal cord curvature, abnormal ZP:0009031 retinal photoreceptor layer atrophied, abnormal ZP:0009032 male organism decreased fertility, abnormal ZP:0009033 male organism has fewer parts of type renal tubule head kidney, abnormal ZP:0009034 male organism has fewer parts of type hematopoietic multipotent progenitor cell head kidney, abnormal ZP:0009035 gut male organism increased thickness, abnormal ZP:0009036 gut male organism apoptotic, abnormal ZP:0009037 gut male organism degenerate, abnormal ZP:0009038 gut male organism senescent, abnormal ZP:0009039 gut male organism inflamed, abnormal ZP:0009040 liver male organism degenerate, abnormal ZP:0009041 trunk musculature male organism degenerate, abnormal ZP:0009042 head kidney male organism apoptotic, abnormal ZP:0009043 head kidney male organism degenerate, abnormal ZP:0009044 head kidney male organism senescent, abnormal ZP:0009045 renal tubule male organism apoptotic, abnormal ZP:0009046 intestinal epithelium male organism dysplastic, abnormal ZP:0009047 intestinal villus male organism decreased length, abnormal ZP:0009048 blood cell male organism decreased amount, abnormal ZP:0009049 hematopoietic multipotent progenitor cell male organism apoptotic, abnormal ZP:0009050 female organism decreased fertility, abnormal ZP:0009051 chromosome, telomeric region integument decreased length, abnormal ZP:0009052 testis degenerate, abnormal ZP:0009053 testis senescent, abnormal ZP:0009054 testis atrophied, abnormal ZP:0009055 testis decreased occurrence telomere maintenance, abnormal ZP:0009056 sperm testis decreased amount, abnormal ZP:0009057 germ line cell testis apoptotic, abnormal ZP:0009058 chromosome, telomeric region caudal fin decreased length, abnormal ZP:0009059 whole organism decreased female fertility, abnormal ZP:0009060 whole organism decreased male fertility, abnormal ZP:0009062 neural tube closure incomplete, abnormal ZP:0009063 ventral wall of dorsal aorta apoptotic, abnormal ZP:0009064 chromosome, telomeric region gut epithelium decreased length, abnormal ZP:0009065 chromosome, telomeric region gut epithelium decreased variability of size, abnormal ZP:0009066 blood cell apoptotic, abnormal ZP:0009067 developmental process arrested, abnormal ZP:0009068 spinal cord oligodendrocyte cell differentiation disrupted, abnormal ZP:0009069 dorsal/ventral neural tube patterning disrupted, abnormal ZP:0009070 smoothened signaling pathway involved in dorsal/ventral neural tube patterning disrupted, abnormal ZP:0009071 neuronal cell body cranial nerve VII mislocalised anteriorly, abnormal ZP:0009072 neuronal cell body rhombomere 5 mislocalised, abnormal ZP:0009073 neuronal cell body rhombomere 7 mislocalised, abnormal ZP:0009074 neuronal cell body rhombomere 4 mislocalised, abnormal ZP:0009075 whole organism decreased fertility, abnormal ZP:0009076 posterior region whole organism morphology, abnormal ZP:0009077 neural tube wholly ventralized, abnormal ZP:0009078 striated muscle tissue development disrupted, abnormal ZP:0009079 myoseptum curved, abnormal ZP:0009080 myofibril muscle loose, abnormal ZP:0009083 endocardium aplastic, abnormal ZP:0009084 locomotion involved in locomotory behavior process quality, abnormal ZP:0009085 neural crest physical object quality, abnormal ZP:0009086 extraocular musculature decreased amount, abnormal ZP:0009087 ventricular system malformed, abnormal ZP:0009088 pharyngeal musculature decreased amount, abnormal ZP:0009090 otic vesicle has fewer parts of type otolith, abnormal ZP:0009091 ventral side eye decreased pigmentation, abnormal ZP:0009093 epithelium sensory system decreased thickness, abnormal ZP:0009094 whole organism rough, abnormal ZP:0009097 otolith broken, abnormal ZP:0009099 neuroepithelial cell dislocated dorsal side ventricular system, abnormal ZP:0009100 phagolysosome assembly disrupted, abnormal ZP:0009101 vesicle-mediated transport disrupted, abnormal ZP:0009102 retinal neural layer apoptotic, abnormal ZP:0009103 liver discolored, abnormal ZP:0009104 retinal pigmented epithelium swollen, abnormal ZP:0009105 microvillus retinal pigmented epithelium decreased amount, abnormal ZP:0009106 vesicle retinal pigmented epithelium present, abnormal ZP:0009107 melanosome retinal pigmented epithelium shape, abnormal ZP:0009108 melanocyte retinal pigmented epithelium colored, abnormal ZP:0009109 melanocyte retinal pigmented epithelium colorless, abnormal ZP:0009110 integument colored, abnormal ZP:0009111 melanosome integument shape, abnormal ZP:0009112 melanosome integument decreased amount, abnormal ZP:0009113 melanocyte integument colored, abnormal ZP:0009114 melanocyte integument colorless, abnormal ZP:0009115 intestine discolored, abnormal ZP:0009116 vesicle intestine increased amount, abnormal ZP:0009117 vesicle intestine decreased size, abnormal ZP:0009118 photoreceptor outer segment layer decreased length, abnormal ZP:0009119 hepatocyte disorganized, abnormal ZP:0009120 vesicle hepatocyte present, abnormal ZP:0009121 vesicle macrophage increased size, abnormal ZP:0009122 vesicle macrophage variant shape, abnormal ZP:0009123 iridophore reflectivity, abnormal ZP:0009124 smoothened signaling pathway increased process quality, abnormal ZP:0009130 cell proliferation involved in heart morphogenesis decreased rate, abnormal ZP:0009131 retinal ganglion cell decreased functionality, abnormal ZP:0009132 retina shape, abnormal ZP:0009133 optic tectum swollen, abnormal ZP:0009134 lens epithelium vacuolated, abnormal ZP:0009136 photoreceptor connecting cilium photoreceptor outer segment layer decreased variability of size, abnormal ZP:0009137 head lacks parts or has fewer parts of type otic placode, abnormal ZP:0009138 bile ductule intrahepatic bile duct decreased amount, abnormal ZP:0009139 1-phosphatidylinositol-4-phosphate 5-kinase activity decreased occurrence, abnormal ZP:0009140 muscle cell proliferation increased occurrence, abnormal ZP:0009141 muscle has fewer parts of type sarcoplasmic reticulum muscle cell, abnormal ZP:0009142 muscle precursor cell decreased amount, abnormal ZP:0009143 brainstem and spinal white matter decreased amount, abnormal ZP:0009144 photoreceptor outer segment photoreceptor cell decreased size, abnormal ZP:0009145 retinal cone cell cellular quality, abnormal ZP:0009146 retinal rod cell cellular quality, abnormal ZP:0009147 optic tract composition, abnormal ZP:0009148 cranial nerve II composition, abnormal ZP:0009149 optic tectum composition, abnormal ZP:0009150 amacrine cell mislocalised, abnormal ZP:0009151 primary motor neuron has fewer parts of type neuron projection primary motor neuron, abnormal ZP:0009152 neuron projection primary motor neuron decreased branchiness, abnormal ZP:0009153 primary motor neuron decreased process quality collateral sprouting, abnormal ZP:0009154 acetylcholine receptor activity disrupted, abnormal ZP:0009155 mitochondrial matrix trunk musculature absent, abnormal ZP:0009156 striated muscle thin filament trunk musculature decreased amount, abnormal ZP:0009157 trunk musculature misaligned with myofibril myofibril trunk musculature, abnormal ZP:0009158 sarcomere trunk musculature morphology, abnormal ZP:0009159 actin filament bundle trunk musculature disorganized, abnormal ZP:0009160 myoseptum U-shaped, abnormal ZP:0009162 cell proliferation involved in heart morphogenesis decreased occurrence, abnormal ZP:0009163 cell adhesion involved in heart morphogenesis decreased process quality, abnormal ZP:0009164 cardiac muscle cell cardiac ventricle decreased area, abnormal ZP:0009165 heart tube increased fragility, abnormal ZP:0009167 mastication decreased process quality, abnormal ZP:0009168 esophagus lacks parts or has fewer parts of type skeletal muscle cell, abnormal ZP:0009169 skeletal muscle cell esophagus poorly differentiated, abnormal ZP:0009172 pectoral fin musculature decreased size, abnormal ZP:0009173 pectoral fin musculature disorganized, abnormal ZP:0009174 musculoskeletal movement arrested, abnormal ZP:0009175 basement membrane notochord distributed, abnormal ZP:0009176 whole organism behavioural inactive, abnormal ZP:0009177 perichordal connective tissue decreased thickness, abnormal ZP:0009178 perichordal connective tissue disorganized, abnormal ZP:0009179 slow muscle cell misaligned with myofibril myofibril slow muscle cell, abnormal ZP:0009180 fast muscle cell misaligned with myofibril myofibril fast muscle cell, abnormal ZP:0009181 axon primary motor neuron shape, abnormal ZP:0009182 neuron projection motor neuron morphology, abnormal ZP:0009183 neuron projection motor neuron decreased amount, abnormal ZP:0009184 heart contraction decreased volume, abnormal ZP:0009185 heart contraction decreased fluid flow, abnormal ZP:0009186 otic vesicle development arrested, abnormal ZP:0009187 dorsal region cerebellum morphology, abnormal ZP:0009188 postero-dorsal region optic tectum morphology, abnormal ZP:0009189 whole organism disorganized, abnormal ZP:0009190 G1/S transition of mitotic cell cycle decreased rate, abnormal ZP:0009191 ethmoid cartilage increased length, abnormal ZP:0009192 trabecula communis increased length, abnormal ZP:0009193 pronephros apoptotic, abnormal ZP:0009194 olfactory bulb apoptotic, abnormal ZP:0009195 olfactory placode apoptotic, abnormal ZP:0009196 vertebra 1 malformed, abnormal ZP:0009197 vertebra 2 malformed, abnormal ZP:0009198 ventral fin fold apoptotic, abnormal ZP:0009199 nucleate erythrocyte development decreased occurrence, abnormal ZP:0009200 action potential disrupted, abnormal ZP:0009201 basement membrane vertical myoseptum malformed, abnormal ZP:0009202 myoseptum myotome mislocalised, abnormal ZP:0009203 muscle cell myotome retracted, abnormal ZP:0009204 sarcolemma skeletal muscle cell broken, abnormal ZP:0009205 slow muscle cell retracted, abnormal ZP:0009206 tectal ventricle morphology, abnormal ZP:0009207 neuromast deposition disrupted, abnormal ZP:0009208 parachordal vessel decreased size, abnormal ZP:0009209 cysteine-type endopeptidase activity increased rate, abnormal ZP:0009210 chromatin central nervous system condensed, abnormal ZP:0009211 spinal cord opaque, abnormal ZP:0009213 urea cycle disrupted, abnormal ZP:0009214 epidermis morphogenesis decreased process quality, abnormal ZP:0009215 epidermis separated from epidermal cell epidermal cell epidermis, abnormal ZP:0009216 epidermal cell increased variability of size, abnormal ZP:0009217 neuromuscular junction development decreased process quality, abnormal ZP:0009218 axonal transport of mitochondrion decreased occurrence, abnormal ZP:0009219 yolk distended, abnormal ZP:0009220 somite irregular spatial pattern, abnormal ZP:0009221 RoP motor neuron decreased length, abnormal ZP:0009222 RoP motor neuron immature, abnormal ZP:0009223 axon motor neuron absent, abnormal ZP:0009224 presynaptic active zone motor neuron decreased area, abnormal ZP:0009225 neuromuscular junction muscle cell decreased area, abnormal ZP:0009226 myofibril skeletal muscle cell decreased thickness, abnormal ZP:0009227 CaP motoneuron disorganized, abnormal ZP:0009228 CaP motoneuron branchiness, abnormal ZP:0009229 mitochondrion neuron circular, abnormal ZP:0009230 mitochondrion neuron mislocalised, abnormal ZP:0009231 neuron decreased process quality mitochondrion localization, abnormal ZP:0009232 protein lipidation disrupted, abnormal ZP:0009233 Wnt protein secretion disrupted, abnormal ZP:0009234 neural tube shortened, abnormal ZP:0009235 TOR signaling increased occurrence, abnormal ZP:0009237 diencephalon bilateral symmetry, abnormal ZP:0009238 motile cilium pronephric duct increased length, abnormal ZP:0009239 pancreas primordium mislocalised, abnormal ZP:0009240 dorsal root ganglion position, abnormal ZP:0009241 caudal fin skeleton deformed, abnormal ZP:0009242 trunk neural crest cell mislocalised, abnormal ZP:0009243 hypophysis disorganized, abnormal ZP:0009244 adenohypophysis morphology, abnormal ZP:0009245 somatotropin secreting cell spatial pattern, abnormal ZP:0009246 prolactin secreting cell spatial pattern, abnormal ZP:0009247 cilium movement arrested, abnormal ZP:0009248 induction of programmed cell death increased occurrence, abnormal ZP:0009249 brain decreased object quality, abnormal ZP:0009250 neuroepithelial cell hindbrain decreased amount, abnormal ZP:0009251 heart displaced to right side whole organism, abnormal ZP:0009252 heart displaced to medial side whole organism, abnormal ZP:0009253 cell ventricular zone apoptotic, abnormal ZP:0009254 somite border disorganized, abnormal ZP:0009255 Mauthner neuron decreased amount, abnormal ZP:0009256 dopaminergic neuron central nervous system apoptotic, abnormal ZP:0009257 epidermis median fin fold morphology, abnormal ZP:0009258 anal fin increased length, abnormal ZP:0009259 endothelial cell decreased amount, abnormal ZP:0009260 neuron remodeling disrupted, abnormal ZP:0009261 peripheral olfactory organ morphology, abnormal ZP:0009262 synaptic vesicle olfactory receptor cell decreased amount, abnormal ZP:0009263 axon terminus olfactory receptor cell morphology, abnormal ZP:0009264 axon terminus olfactory receptor cell increased size, abnormal ZP:0009267 posterior cardinal vein decreased width, abnormal ZP:0009268 cranium hemorrhagic, abnormal ZP:0009269 intersegmental vessel deformed, abnormal ZP:0009270 myocardium decreased size, abnormal ZP:0009271 atrial myocardium decreased size, abnormal ZP:0009274 endocardium development decreased process quality, abnormal ZP:0009275 median fin fold attenuate, abnormal ZP:0009276 notochord delaminated, abnormal ZP:0009277 caudal vein structure, cavities, abnormal ZP:0009278 blood vessel endothelial cell caudal vein disorganized, abnormal ZP:0009279 atrium has fewer parts of type atrial endocardium, abnormal ZP:0009280 posterior cardinal vein decreased diameter, abnormal ZP:0009281 integument trunk distended, abnormal ZP:0009282 caudal vein plexus disorganized, abnormal ZP:0009283 myocardium attached to endocardium, abnormal ZP:0009284 bleb assembly disrupted, abnormal ZP:0009285 filamentous actin margin decreased amount, abnormal ZP:0009286 bleb margin absent, abnormal ZP:0009287 cell projection prechordal plate decreased amount, abnormal ZP:0009288 cell projection hypoblast decreased amount, abnormal ZP:0009289 hindbrain cellular quality, abnormal ZP:0009290 neuron hindbrain disorganized, abnormal ZP:0009291 swim bladder malformed, abnormal ZP:0009292 forebrain truncated, abnormal ZP:0009293 basibranchial aplastic, abnormal ZP:0009294 glial cell trigeminal ganglion increased amount, abnormal ZP:0009295 diencephalic white matter lacks parts or has fewer parts of type postoptic commissure, abnormal ZP:0009296 telencephalic white matter lacks parts or has fewer parts of type anterior commissure, abnormal ZP:0009297 whole organism lacks parts or has fewer parts of type facial nerve motor nucleus, abnormal ZP:0009298 whole organism lacks parts or has fewer parts of type motor nucleus of vagal nerve, abnormal ZP:0009299 whole organism lacks parts or has fewer parts of type cranial nerve X, abnormal ZP:0009300 whole organism lacks parts or has fewer parts of type cranial nerve VII, abnormal ZP:0009301 whole organism lacks parts or has fewer parts of type cranial nerve V, abnormal ZP:0009302 whole organism lacks parts or has fewer parts of type trigeminal motor nucleus, abnormal ZP:0009303 cranial neural crest increased size, abnormal ZP:0009304 axial mesoderm increased width, abnormal ZP:0009305 axial mesoderm sigmoid, abnormal ZP:0009306 glial cell posterior lateral line ganglion increased amount, abnormal ZP:0009307 white matter lacks parts or has fewer parts of type supraoptic tract, abnormal ZP:0009308 MiP motor neuron decreased amount, abnormal ZP:0009309 primary motor neuron increased branchiness, abnormal ZP:0009310 synapse maturation disrupted, abnormal ZP:0009311 dendrite dorsal habenular nucleus decreased volume, abnormal ZP:0009312 dendrite habenula absent, abnormal ZP:0009313 dendrite habenula decreased volume, abnormal ZP:0009314 dendrite ventral habenular nucleus decreased volume, abnormal ZP:0009315 ectoderm delaminated, abnormal ZP:0009316 yolk protruding out of ball, abnormal ZP:0009317 retrograde axonal transport decreased occurrence, abnormal ZP:0009318 lysosome localization decreased process quality, abnormal ZP:0009319 regulation of JNK cascade decreased process quality, abnormal ZP:0009321 central nervous system physical object quality, abnormal ZP:0009322 peripheral nervous system physical object quality, abnormal ZP:0009323 axon medial longitudinal fasciculus decreased length, abnormal ZP:0009324 lysosome posterior lateral line mislocalised, abnormal ZP:0009325 axon posterior lateral line decreased length, abnormal ZP:0009326 axon terminus posterior lateral line swollen, abnormal ZP:0009327 posterior lateral line has extra parts of type axon terminus lysosome posterior lateral line, abnormal ZP:0009328 neuromuscular junction myotome decreased size, abnormal ZP:0009329 myotome misaligned with slow muscle cell slow muscle cell myotome, abnormal ZP:0009330 slow muscle cell curved, abnormal ZP:0009331 axon extension involved in axon guidance arrested, abnormal ZP:0009332 heart trabecula formation disrupted, abnormal ZP:0009333 endocardium atrioventricular canal increased length, abnormal ZP:0009334 cardiac muscle cell atrioventricular canal increased amount, abnormal ZP:0009335 cardiac jelly mislocalised, abnormal ZP:0009336 endocardium far from myocardium, abnormal ZP:0009337 trabecular layer morphology, abnormal ZP:0009338 atrioventricular valve increased length, abnormal ZP:0009339 pectoral fin morphogenesis process quality, abnormal ZP:0009340 calcium- and calmodulin-dependent protein kinase complex Kupffer's vesicle mislocalised posteriorly, abnormal ZP:0009341 epidermis structure, abnormal ZP:0009342 epidermis vacuolated, abnormal ZP:0009343 basement membrane integument structure, abnormal ZP:0009344 eye photoreceptor cell development process quality, abnormal ZP:0009345 inner ear receptor cell development process quality, abnormal ZP:0009346 stereocilium bundle anterior crista malformed, abnormal ZP:0009347 photoreceptor connecting cilium eye photoreceptor cell physical object quality, abnormal ZP:0009348 ceratohyal cartilage orientation axis, abnormal ZP:0009349 morphogenesis of an epithelial sheet disrupted, abnormal ZP:0009350 cardiac muscle cell proliferation disrupted, abnormal ZP:0009351 trunk vasculature broken, abnormal ZP:0009352 subintestinal vein structure, abnormal ZP:0009353 subintestinal vein decreased functionality, abnormal ZP:0009354 nucleate erythrocyte aggregated, abnormal ZP:0009355 nucleate erythrocyte fluid flow rate, abnormal ZP:0009356 blood vessel lumenization decreased process quality, abnormal ZP:0009357 endocardium dilated, abnormal ZP:0009358 subintestinal vein disheveled, abnormal ZP:0009359 dorsal convergence decreased duration, abnormal ZP:0009360 shield increased thickness, abnormal ZP:0009361 anterior-posterior axis axis elongated, abnormal ZP:0009362 anterior-posterior axis axis shortened, abnormal ZP:0009363 anatomical axis trunk increased curvature, abnormal ZP:0009364 post-vent region increased width, abnormal ZP:0009366 spinal cord has extra parts of type dorsal region glioblast (sensu Vertebrata), abnormal ZP:0009367 whole organism lacks all parts of type dorsal longitudinal anastomotic vessel, abnormal ZP:0009368 oligodendrocyte mislocalised medially, abnormal ZP:0009369 neuroblast (sensu Vertebrata) increased amount, abnormal ZP:0009370 glioblast (sensu Vertebrata) increased amount, abnormal ZP:0009371 axonogenesis increased occurrence, abnormal ZP:0009372 cranial nerve I fasciculation, abnormal ZP:0009373 frontonasal suture morphogenesis arrested, abnormal ZP:0009374 intersegmental lymph vessel aplastic, abnormal ZP:0009375 dorsal longitudinal lymphatic vessel aplastic, abnormal ZP:0009376 neuromuscular synaptic transmission decreased occurrence, abnormal ZP:0009377 high voltage-gated calcium channel activity decreased process quality, abnormal ZP:0009378 response to external stimulus arrested, abnormal ZP:0009379 swimming decreased process quality, abnormal ZP:0009380 swimming behavior absent, abnormal ZP:0009382 slow muscle cell non-contractile, abnormal ZP:0009383 axon terminus motor neuron physical object quality, abnormal ZP:0009384 retinal inner plexiform layer decreased size, abnormal ZP:0009385 oocyte maturation decreased occurrence, abnormal ZP:0009386 germ cell development disrupted, abnormal ZP:0009387 female organism female sterile, abnormal ZP:0009388 testis increased size, abnormal ZP:0009389 testis increased accumulation primordial germ cell, abnormal ZP:0009390 germ cell tumor testis present, abnormal ZP:0009391 oocyte stage IV absent, abnormal ZP:0009392 spermatocyte absent, abnormal ZP:0009393 synchronous neurotransmitter secretion decreased occurrence, abnormal ZP:0009394 calcium ion import disrupted, abnormal ZP:0009395 vH ionocyte decreased functionality, abnormal ZP:0009396 lens morphogenesis in camera-type eye delayed, abnormal ZP:0009397 striated muscle contraction disrupted, abnormal ZP:0009398 heart increased width, abnormal ZP:0009399 heart tube increased width, abnormal ZP:0009400 actin filament myotome absent, abnormal ZP:0009401 sarcomere myotome disorganized, abnormal ZP:0009402 Z disc myotome structure, abnormal ZP:0009403 myosin filament myotome absent, abnormal ZP:0009404 chloride transport disrupted, abnormal ZP:0009405 erythrocyte maturation delayed, abnormal ZP:0009406 hemoglobin complex erythroid progenitor cell decreased amount, abnormal ZP:0009407 anterior side head collapsed, abnormal ZP:0009408 cilium assembly process quality, abnormal ZP:0009409 ciliated epithelial cell Kupffer's vesicle physical object quality, abnormal ZP:0009410 motile cilium pronephric duct direction, abnormal ZP:0009411 pronephric tubule increased diameter, abnormal ZP:0009412 filamentous actin ciliated epithelial cell decreased mass, abnormal ZP:0009413 apical cortex ciliated epithelial cell composition, abnormal ZP:0009414 mandibular arch skeleton dysplastic, abnormal ZP:0009415 atrium mislocalised, abnormal ZP:0009416 cilium olfactory placode structure, abnormal ZP:0009417 cilium olfactory placode immobile, abnormal ZP:0009418 cilium spinal cord decreased mobility, abnormal ZP:0009419 inner dynein arm ciliated cell decreased amount, abnormal ZP:0009420 outer dynein arm ciliated cell decreased amount, abnormal ZP:0009421 caudal vein plexus immature, abnormal ZP:0009422 notochord collapsed, abnormal ZP:0009423 hemal spine caudal vertebra decreased amount, abnormal ZP:0009424 vertebra deformed, abnormal ZP:0009425 neural spine decreased amount, abnormal ZP:0009426 vertebral column curved lateral, abnormal ZP:0009427 mesenchymal cell proliferation decreased rate, abnormal ZP:0009428 vascular sprouts increased amount, abnormal ZP:0009429 pronephric duct collapsed, abnormal ZP:0009430 intraciliary transport particle photoreceptor cell spatial pattern, abnormal ZP:0009431 metallopeptidase activity disrupted, abnormal ZP:0009432 heart contraction rate, abnormal ZP:0009433 yolk width, abnormal ZP:0009434 melanosome integument decreased size, abnormal ZP:0009435 melanosome integument variant shape, abnormal ZP:0009436 melanosome integument decreased pigmentation, abnormal ZP:0009437 phosphate ion homeostasis disrupted, abnormal ZP:0009438 fast muscle myoblast morphology, abnormal ZP:0009439 fast muscle myoblast irregular spatial pattern, abnormal ZP:0009440 voltage-gated sodium channel activity decreased rate, abnormal ZP:0009441 neuronal action potential process quality, abnormal ZP:0009442 neuron apoptotic process decreased occurrence, abnormal ZP:0009443 Rohon-Beard neuron alive, abnormal ZP:0009444 Rohon-Beard neuron increased age, abnormal ZP:0009446 chondrocyte Meckel's cartilage circular, abnormal ZP:0009448 mitotic spindle neural plate decreased functionality, abnormal ZP:0009449 neuron medial longitudinal fasciculus decreased amount, abnormal ZP:0009450 neuron rhombomere decreased amount, abnormal ZP:0009451 axon anterior commissure organization quality, abnormal ZP:0009452 neural tube decreased size, abnormal ZP:0009453 cell neural tube decreased amount, abnormal ZP:0009454 Rohon-Beard neuron decreased branchiness, abnormal ZP:0009455 platelet formation disrupted, abnormal ZP:0009456 cranial nerve development disrupted, abnormal ZP:0009457 glial cell hindbrain decreased amount, abnormal ZP:0009458 adherens junction assembly disrupted, abnormal ZP:0009459 caudal vein increased permeability, abnormal ZP:0009460 caudal vein plexus broken, abnormal ZP:0009461 dorsal longitudinal anastomotic vessel increased permeability, abnormal ZP:0009462 blood vessel endothelial cell has fewer parts of type cell-cell junction blood vessel endothelial cell, abnormal ZP:0009463 adherens junction blood vessel endothelial cell immature, abnormal ZP:0009465 margin poorly differentiated, abnormal ZP:0009466 optic primordium shape, abnormal ZP:0009467 optic primordium hypoplastic, abnormal ZP:0009468 blastoderm thickness, abnormal ZP:0009469 nucleus lens epithelium mislocalised, abnormal ZP:0009470 pronephric podocyte shape, abnormal ZP:0009471 pronephric glomerular capsule dilated, abnormal ZP:0009472 pronephric glomerular basement membrane broken, abnormal ZP:0009473 basement membrane lens capsule decreased thickness, abnormal ZP:0009474 basement membrane lens capsule broken, abnormal ZP:0009475 neutral lipid metabolic process process quality, abnormal ZP:0009477 response to starvation process quality, abnormal ZP:0009478 response to starvation decreased process quality, abnormal ZP:0009479 hepaticobiliary system process decreased process quality, abnormal ZP:0009480 anatomical compartment boundary paraxial mesoderm disorganized, abnormal ZP:0009481 anatomical compartment boundary paraxial mesoderm distributed, abnormal ZP:0009482 anatomical axis whole organism shortened, abnormal ZP:0009483 whole organism dissociated from cell yolk, abnormal ZP:0009484 regulation of pH process quality, abnormal ZP:0009485 sodium ion homeostasis process quality, abnormal ZP:0009486 thymus development delayed, abnormal ZP:0009487 thymocyte migration disrupted, abnormal ZP:0009488 ventral region retina morphology, abnormal ZP:0009489 ceratobranchial bone deformed, abnormal ZP:0009490 ceratohyal bone deformed, abnormal ZP:0009492 retinal inner plexiform layer morphology, abnormal ZP:0009493 locomotion process quality, abnormal ZP:0009494 abductor hyohyoid lacks parts or has fewer parts of type skeletal muscle cell, abnormal ZP:0009495 adductor operculi physical object quality, abnormal ZP:0009496 myoblast adductor operculi decreased amount, abnormal ZP:0009497 myoblast dilatator operculi decreased amount, abnormal ZP:0009498 levator operculi physical object quality, abnormal ZP:0009499 myoblast levator operculi decreased amount, abnormal ZP:0009500 adductor hyohyoid lacks parts or has fewer parts of type skeletal muscle cell, abnormal ZP:0009501 muscle organ development arrested, abnormal ZP:0009502 somite dispersed, abnormal ZP:0009503 thyroid follicle decreased size, abnormal ZP:0009504 thyroid follicle poorly differentiated, abnormal ZP:0009505 hemoglobin complex intermediate cell mass of mesoderm absent, abnormal ZP:0009506 nucleate erythrocyte proportionality to nucleus cytoplasm nucleate erythrocyte, abnormal ZP:0009507 cerebellar Purkinje cell differentiation disrupted, abnormal ZP:0009508 cerebellar granule cell decreased amount, abnormal ZP:0009509 Purkinje cell decreased amount, abnormal ZP:0009510 hypophysis has fewer parts of type vasculature blood vessel endothelial cell, abnormal ZP:0009511 vasculature neurohypophysis hypoplastic, abnormal ZP:0009512 hyaloid vessel structure, abnormal ZP:0009513 hyaloid vessel decreased diameter, abnormal ZP:0009514 enteroendocrine cell differentiation disrupted, abnormal ZP:0009515 goblet cell posterior intestine decreased amount, abnormal ZP:0009516 goblet cell intestinal bulb decreased amount, abnormal ZP:0009517 intestine distended, abnormal ZP:0009518 goblet cell decreased amount, abnormal ZP:0009519 goblet cell poorly differentiated, abnormal ZP:0009520 chondrocyte hypertrophy premature, abnormal ZP:0009521 hypertrophic chondrocyte increased amount, abnormal ZP:0009525 spinal cord deformed, abnormal ZP:0009526 determination of bilateral symmetry decreased process quality, abnormal ZP:0009527 pectoral fin development process quality, abnormal ZP:0009528 skeletal muscle cell differentiation process quality, abnormal ZP:0009529 motile cilium Kupffer's vesicle absent, abnormal ZP:0009531 motile cilium pronephric duct absent, abnormal ZP:0009533 pectoral fin bilateral symmetry, abnormal ZP:0009534 exocrine pancreas absent, abnormal ZP:0009535 exocrine pancreas bilateral symmetry, abnormal ZP:0009536 cerebellar central artery branchiness, abnormal ZP:0009537 retinal bipolar neuron decreased functionality, abnormal ZP:0009538 intestine lacks all parts of type goblet cell, abnormal ZP:0009539 blood accumulation sinus venosus, abnormal ZP:0009540 apical-basal axis relative to substrate whole organism increased curvature, abnormal ZP:0009541 protoneuromast disorganized, abnormal ZP:0009542 signal transduction in response to DNA damage decreased process quality, abnormal ZP:0009543 myofibril muscle morphology, abnormal ZP:0009544 sarcolemma muscle perforate, abnormal ZP:0009545 neutrophil activation involved in immune response disrupted, abnormal ZP:0009546 collateral sprouting decreased occurrence, abnormal ZP:0009547 upper region head flattened, abnormal ZP:0009548 main axon Rohon-Beard neuron decreased length, abnormal ZP:0009549 ceratobranchial cartilage increased width, abnormal ZP:0009550 hypophyseal fenestra absent, abnormal ZP:0009551 hypophyseal fenestra decreased size, abnormal ZP:0009552 neural precursor cell proliferation increased rate, abnormal ZP:0009553 retina vasculature development in camera-type eye disrupted, abnormal ZP:0009554 vascular sprouts morphology, abnormal ZP:0009555 ocular blood vessel morphology, abnormal ZP:0009556 thigmotropism decreased occurrence, abnormal ZP:0009557 whole organism increased contractility, abnormal ZP:0009558 mandibular arch skeleton movement quality, abnormal ZP:0009559 neuroblast decreased amount, abnormal ZP:0009560 steroid biosynthetic process disrupted, abnormal ZP:0009561 cortisol biosynthetic process disrupted, abnormal ZP:0009562 motor neuron migration disrupted, abnormal ZP:0009565 neuroectoderm increased width, abnormal ZP:0009569 endocardial cushion development arrested, abnormal ZP:0009570 endocardial cushion development disrupted, abnormal ZP:0009571 heart lacks all parts of type endocardial cushion, abnormal ZP:0009572 locomotion arrested, abnormal ZP:0009573 atrial cardiac muscle cell differentiation disrupted, abnormal ZP:0009574 endocrine pancreas lacks parts or has fewer parts of type insulin secreting cell, abnormal ZP:0009575 endocrine pancreas lacks parts or has fewer parts of type glucagon secreting cell, abnormal ZP:0009576 endocrine pancreas lacks parts or has fewer parts of type somatostatin secreting cell, abnormal ZP:0009577 posterior pancreatic bud lacks parts or has fewer parts of type insulin secreting cell, abnormal ZP:0009578 posterior pancreatic bud lacks parts or has fewer parts of type somatostatin secreting cell, abnormal ZP:0009579 Kolmer-Agduhr neuron increased amount, abnormal ZP:0009580 axon pectoral fin motor nerve decreased amount, abnormal ZP:0009581 axon motor neuron mislocalised posteriorly, abnormal ZP:0009582 axon CaP motoneuron absent, abnormal ZP:0009583 secondary motor neuron absent, abnormal ZP:0009584 axon secondary motor neuron disorganized, abnormal ZP:0009585 neuron posterior lateral line ganglion decreased amount, abnormal ZP:0009586 somite border somite 1 amorphous, abnormal ZP:0009587 somite border somite 2 amorphous, abnormal ZP:0009588 somite border somite 3 amorphous, abnormal ZP:0009590 positive regulation of transcription, DNA-templated disrupted, abnormal ZP:0009591 neuron locus coeruleus decreased amount, abnormal ZP:0009592 neuromuscular synaptic transmission increased duration, abnormal ZP:0009593 acetylcholine receptor activity increased duration, abnormal ZP:0009594 acetylcholine receptor activity physiological state, abnormal ZP:0009595 fast-twitch skeletal muscle fiber contraction decreased rate, abnormal ZP:0009596 behavioral response to nicotine decreased occurrence, abnormal ZP:0009597 membrane repolarization decreased rate, abnormal ZP:0009598 mouth morphology, abnormal ZP:0009599 muscle cell increased permeability, abnormal ZP:0009600 pharyngeal arch 3-7 skeleton malformed, abnormal ZP:0009601 neuron peripheral nervous system decreased amount, abnormal ZP:0009602 whole organism lacks all parts of type neuron dorsal root ganglion, abnormal ZP:0009603 pharyngeal arch 2 skeleton malformed, abnormal ZP:0009604 phagocytosis decreased occurrence, abnormal ZP:0009605 blood vessel endothelial cell common cardinal vein increased amount, abnormal ZP:0009606 erythroid progenitor cell increased amount, abnormal ZP:0009607 microglial cell absent, abnormal ZP:0009608 leukocyte absent, abnormal ZP:0009609 myeloid cell absent, abnormal ZP:0009610 erythroid lineage cell increased amount, abnormal ZP:0009611 neutrophil absent, abnormal ZP:0009613 odontogenesis delayed, abnormal ZP:0009614 muscle cell differentiation decreased occurrence, abnormal ZP:0009615 striated muscle cell differentiation delayed, abnormal ZP:0009616 striated muscle cell differentiation process quality, abnormal ZP:0009617 adaxial cell immature, abnormal ZP:0009618 somite has extra parts of type muscle precursor cell, abnormal ZP:0009619 segmental plate has fewer parts of type anterior region adaxial cell, abnormal ZP:0009620 pectoral girdle morphology, abnormal ZP:0009621 myoseptum aplastic, abnormal ZP:0009623 pectoral fin variability of size, abnormal ZP:0009624 fin fold pectoral fin bud disorganized, abnormal ZP:0009625 retinal cone cell irregular spatial pattern, abnormal ZP:0009626 brain lacks all parts of type midbrain hindbrain boundary, abnormal ZP:0009628 hindbrain cellular adhesivity cell cell hindbrain, abnormal ZP:0009629 macula morphology, abnormal ZP:0009630 lateral longitudinal fasciculus decreased size, abnormal ZP:0009631 medial longitudinal fasciculus decreased size, abnormal ZP:0009632 rhombomere 5 shape, abnormal ZP:0009633 rhombomere 3 shape, abnormal ZP:0009634 post-vent region cystic, abnormal ZP:0009635 post-vent region cellular adhesivity cell cell post-vent region, abnormal ZP:0009636 locus ceruleus development disrupted, abnormal ZP:0009637 parasympathetic nervous system development disrupted, abnormal ZP:0009639 pars intermedia physical object quality, abnormal ZP:0009640 epibranchial placode morphology, abnormal ZP:0009642 osteoblast proliferation increased occurrence, abnormal ZP:0009643 pigmentation decreased process quality, abnormal ZP:0009645 cell retinal ganglion cell layer increased amount, abnormal ZP:0009646 cell retinal inner nuclear layer increased amount, abnormal ZP:0009647 dorsal region retina disorganized, abnormal ZP:0009648 cell retina increased amount, abnormal ZP:0009649 muscle pioneer somite increased amount, abnormal ZP:0009651 postero-ventral margin opercle increased length, abnormal ZP:0009652 inner limiting membrane disorganized, abnormal ZP:0009653 inner limiting membrane broken, abnormal ZP:0009654 osteoblast Meckel's cartilage increased amount, abnormal ZP:0009655 iris increased size, abnormal ZP:0009656 neuronal stem cell ciliary marginal zone increased amount, abnormal ZP:0009657 cell retinal outer nuclear layer increased amount, abnormal ZP:0009658 retinal outer nuclear layer displaced to photoreceptor cell ciliary marginal zone, abnormal ZP:0009659 slow muscle cell absent, abnormal ZP:0009660 fast muscle cell mislocalised, abnormal ZP:0009661 photoreceptor cell mislocalised, abnormal ZP:0009662 axon terminus Muller cell physical object quality, abnormal ZP:0009663 negative regulation of neurogenesis decreased occurrence, abnormal ZP:0009664 neuron rhombomere 2 mislocalised, abnormal ZP:0009665 neuron rhombomere 4 mislocalised, abnormal ZP:0009666 hypothalamus morphology, abnormal ZP:0009667 cranial neural crest apoptotic, abnormal ZP:0009668 palatoquadrate cartilage morphology, abnormal ZP:0009669 hyosymplectic cartilage morphology, abnormal ZP:0009670 chondrocyte ceratobranchial cartilage decreased amount, abnormal ZP:0009671 vertebral artery aplastic, abnormal ZP:0009672 vasculature lacks parts or has fewer parts of type intersegmental vessel, abnormal ZP:0009673 eye swollen, abnormal ZP:0009674 eye mislocalised laterally, abnormal ZP:0009675 maxilla shape, abnormal ZP:0009676 maxilla fused with maxilla, abnormal ZP:0009677 pharyngeal arch 2 skeleton disorganized, abnormal ZP:0009678 branchiostegal ray 1 aplastic, abnormal ZP:0009679 branchiostegal ray 3 decreased size, abnormal ZP:0009680 palatoquadrate cartilage structure, abnormal ZP:0009681 hyosymplectic cartilage structure, abnormal ZP:0009682 ceratobranchial 2 cartilage aplastic, abnormal ZP:0009683 ceratobranchial 1 cartilage truncated, abnormal ZP:0009684 ceratobranchial 5 cartilage truncated, abnormal ZP:0009685 endochondral bone aplastic, abnormal ZP:0009688 axon VaP motor neuron mislocalised, abnormal ZP:0009689 axon CaP motoneuron mislocalised, abnormal ZP:0009693 opercle increased variability, abnormal ZP:0009694 opercle distended, abnormal ZP:0009695 opercle fused with branchiostegal ray 3, abnormal ZP:0009696 branchiostegal ray fan-shaped, abnormal ZP:0009697 bone tissue cranium mislocalised, abnormal ZP:0009698 myotome decreased volume, abnormal ZP:0009699 branchiostegal ray 3 increased variability, abnormal ZP:0009700 ceratohyal cartilage split, abnormal ZP:0009701 myofibril skeletal muscle cell decreased diameter, abnormal ZP:0009705 skin morphogenesis process quality, abnormal ZP:0009706 scale increased size, abnormal ZP:0009707 scale patchy, abnormal ZP:0009708 dorsal aorta morphogenesis disrupted, abnormal ZP:0009709 blood decreased viscosity, abnormal ZP:0009710 circulating cell blood absent, abnormal ZP:0009711 circulating cell blood decreased amount, abnormal ZP:0009712 lateral dorsal aorta dilated, abnormal ZP:0009713 Kolmer-Agduhr neuron lateral floor plate undifferentiated, abnormal ZP:0009714 atrioventricular valve absent, abnormal ZP:0009716 cephalic musculature aplastic, abnormal ZP:0009718 heme biosynthetic process arrested, abnormal ZP:0009719 monocyte differentiation increased occurrence, abnormal ZP:0009720 macrophage differentiation increased occurrence, abnormal ZP:0009721 nucleate erythrocyte present, abnormal ZP:0009722 myeloid cell increased amount, abnormal ZP:0009724 eye perforate, abnormal ZP:0009726 ventral region retinal pigmented epithelium absent, abnormal ZP:0009728 post-vent region wholly ventralized, abnormal ZP:0009731 hindbrain structural organization disrupted, abnormal ZP:0009732 hindbrain deformed, abnormal ZP:0009733 choroid plexus fourth ventricle increased size, abnormal ZP:0009734 otic vesicle development disrupted, abnormal ZP:0009735 thymus lacks all parts of type lymphocyte, abnormal ZP:0009736 thymus has fewer parts of type lymphocyte, abnormal ZP:0009737 epithelium thymus morphology, abnormal ZP:0009738 digestive system process disrupted, abnormal ZP:0009739 mouth closed, abnormal ZP:0009740 neuron posterior intestine absent, abnormal ZP:0009741 neuron projection posterior lateral line primordium absent, abnormal ZP:0009747 heart tube shape, abnormal ZP:0009748 atrium shape, abnormal ZP:0009753 atrial myocardium increased size, abnormal ZP:0009754 atrial myocardium increased width, abnormal ZP:0009755 atrial myocardium dilated, abnormal ZP:0009756 atrial myocardium distended, abnormal ZP:0009757 atrial myocardium bulbous, abnormal ZP:0009758 ventricular myocardium decreased width, abnormal ZP:0009759 ventricular myocardium shortened, abnormal ZP:0009760 blood vessel endothelial cell intersegmental artery decreased amount, abnormal ZP:0009761 foregut morphogenesis disrupted, abnormal ZP:0009762 ball constricted, abnormal ZP:0009763 liver mislocalised posteriorly, abnormal ZP:0009764 pancreas mislocalised posteriorly, abnormal ZP:0009765 whole organism spherical, abnormal ZP:0009766 corpuscles of Stannius decreased size, abnormal ZP:0009767 corpuscles of Stannius mislocalised posteriorly, abnormal ZP:0009768 exocrine pancreas mislocalised posteriorly, abnormal ZP:0009769 endocrine pancreas mislocalised posteriorly, abnormal ZP:0009770 pronephric proximal convoluted tubule increased length, abnormal ZP:0009771 pronephric proximal straight tubule decreased length, abnormal ZP:0009772 pronephric distal early tubule decreased length, abnormal ZP:0009773 posterior pronephric duct decreased length, abnormal ZP:0009774 pronephric distal late tubule decreased length, abnormal ZP:0009775 neural crest cell mislocalised posteriorly, abnormal ZP:0009776 mesoderm formation disrupted, abnormal ZP:0009777 brain poorly differentiated, abnormal ZP:0009778 presumptive neural plate wholly anterioralized, abnormal ZP:0009779 axis mislocalised posteriorly, abnormal ZP:0009780 forebrain prominent, abnormal ZP:0009781 forebrain distended, abnormal ZP:0009782 somite aplastic, abnormal ZP:0009784 mesoderm trunk decreased size, abnormal ZP:0009785 mesoderm post-vent region decreased size, abnormal ZP:0009786 presumptive mesoderm wholly dorsalized, abnormal ZP:0009787 neural crest cell morphology, abnormal ZP:0009788 nucleus brain decreased amount, abnormal ZP:0009789 nucleus spinal cord decreased amount, abnormal ZP:0009790 central canal unlumenized, abnormal ZP:0009791 neurogenic placode morphology, abnormal ZP:0009793 heart tube fused with heart tube, abnormal ZP:0009794 iron ion transport disrupted, abnormal ZP:0009795 habenular commissure absent, abnormal ZP:0009796 habenular commissure decreased thickness, abnormal ZP:0009797 habenular commissure discontinuous, abnormal ZP:0009798 habenular commissure decreased process quality axon extension involved in axon guidance, abnormal ZP:0009799 fin morphogenesis process quality, abnormal ZP:0009800 caudal fin lepidotrichium undivided, abnormal ZP:0009801 joint caudal fin lepidotrichium absent, abnormal ZP:0009802 pectoral fin lepidotrichium undivided, abnormal ZP:0009803 joint pectoral fin lepidotrichium absent, abnormal ZP:0009804 lepidotrichium undivided, abnormal ZP:0009805 joint lepidotrichium absent, abnormal ZP:0009806 posterior side notochord disorganized, abnormal ZP:0009807 melanocyte disorganized, abnormal ZP:0009809 lens vacuolated, abnormal ZP:0009810 GABAergic neuron retina mislocalised, abnormal ZP:0009811 ventral region optic tectum morphology, abnormal ZP:0009812 ventrolateral optic tract quality, abnormal ZP:0009813 ventrolateral optic tract agenesis, abnormal ZP:0009814 axial vasculature hemorrhagic, abnormal ZP:0009815 optic fissure morphology, abnormal ZP:0009816 optic fissure mislocalised, abnormal ZP:0009817 ceratohyal cartilage mislocalised medially, abnormal ZP:0009818 ceratohyal cartilage overlap with ceratohyal cartilage, abnormal ZP:0009819 ceratobranchial 2 cartilage mislocalised anteriorly, abnormal ZP:0009820 ceratobranchial 2 cartilage orientation ceratobranchial 2 cartilage, abnormal ZP:0009821 ceratobranchial 1 cartilage mislocalised anteriorly, abnormal ZP:0009822 ceratobranchial 1 cartilage orientation ceratobranchial 1 cartilage, abnormal ZP:0009823 hypobranchial cartilage decreased width, abnormal ZP:0009824 hypobranchial cartilage notched, abnormal ZP:0009825 Muller cell disorganized, abnormal ZP:0009826 liver development decreased process quality, abnormal ZP:0009827 epiphysis has fewer parts of type photoreceptor cell, abnormal ZP:0009828 anterior pancreatic bud hypoplastic, abnormal ZP:0009829 anterior pancreatic bud aplastic, abnormal ZP:0009830 musculoskeletal movement decreased occurrence, abnormal ZP:0009834 primary motor neuron decreased process quality axon extension, abnormal ZP:0009836 secondary motor neuron decreased process quality axon extension, abnormal ZP:0009837 lymphatic endothelial cell differentiation disrupted, abnormal ZP:0009838 neuron hypothalamus decreased amount, abnormal ZP:0009839 somatic stem cell neuromast immature, abnormal ZP:0009840 kinocilium neuromast hair cell absent, abnormal ZP:0009841 hyomandibula bifurcated, abnormal ZP:0009842 hyomandibula cylindrical, abnormal ZP:0009843 trabecula cranii unfused from posterior region neurocranium, abnormal ZP:0009844 chondrocyte trabecula cranii disorganized, abnormal ZP:0009845 spinal cord oligodendrocyte cell differentiation delayed, abnormal ZP:0009846 spinal cord oligodendrocyte cell fate specification process quality, abnormal ZP:0009847 oligodendrocyte differentiation decreased frequency, abnormal ZP:0009848 spinal cord has fewer parts of type oligodendrocyte, abnormal ZP:0009849 spinal cord has extra parts of type oligodendrocyte, abnormal ZP:0009850 endocrine pancreas physical object quality, abnormal ZP:0009851 bicellular tight junction glial cell absent, abnormal ZP:0009852 myelinating Schwann cell mislocalised, abnormal ZP:0009854 floor plate disorganized, abnormal ZP:0009855 floor plate undifferentiated, abnormal ZP:0009857 hypochord decreased length, abnormal ZP:0009858 hypochord disorganized, abnormal ZP:0009859 hypochord aplastic, abnormal ZP:0009860 axial chorda mesoderm decreased width, abnormal ZP:0009863 paraxial mesoderm increased area, abnormal ZP:0009864 paraxial mesoderm fused with left side right side paraxial mesoderm, abnormal ZP:0009866 extrahepatic duct absent, abnormal ZP:0009867 embryonic retina morphogenesis in camera-type eye decreased process quality, abnormal ZP:0009868 retinal blood vessel morphogenesis decreased process quality, abnormal ZP:0009869 whole organism lacks all parts of type nucleate erythrocyte, abnormal ZP:0009870 optic fissure increased width, abnormal ZP:0009871 hyaloid artery constricted, abnormal ZP:0009872 hyaloid vein dilated, abnormal ZP:0009873 ocular blood vessel dilated, abnormal ZP:0009874 ocular blood vessel increased permeability, abnormal ZP:0009875 ocular blood vessel increased diameter, abnormal ZP:0009876 anterior axial hypoblast morphology, abnormal ZP:0009877 prechordal plate poorly differentiated, abnormal ZP:0009878 ventral mesenchyme distended, abnormal ZP:0009879 protein autophosphorylation arrested, abnormal ZP:0009881 posterior region gut increased thickness, abnormal ZP:0009882 primitive heart tube bilateral symmetry, abnormal ZP:0009883 mesoderm post-vent region decreased amount, abnormal ZP:0009884 notochord posterior region absent, abnormal ZP:0009885 osteoclast differentiation premature, abnormal ZP:0009886 eye structure, abnormal ZP:0009887 eye curved lateral, abnormal ZP:0009888 eye protruding into diencephalon, abnormal ZP:0009889 optic stalk mislocalised, abnormal ZP:0009890 optic stalk distended, abnormal ZP:0009891 optic stalk kinked, abnormal ZP:0009892 retinal pigmented epithelium displaced, abnormal ZP:0009893 retina protruding, abnormal ZP:0009894 retina displaced, abnormal ZP:0009895 somite orientation somite, abnormal ZP:0009896 optic tectum proliferative, abnormal ZP:0009897 osteoclast opercular flap differentiated, abnormal ZP:0009898 osteoclast caudal fin skeleton differentiated, abnormal ZP:0009899 osteoclast neural arch differentiated, abnormal ZP:0009901 osteoclast Meckel's cartilage differentiated, abnormal ZP:0009902 osteoclast pharyngeal arch 7 skeleton differentiated, abnormal ZP:0009903 ventral mandibular arch proliferative, abnormal ZP:0009904 photoreceptor outer segment layer protruding, abnormal ZP:0009905 skeletal muscle cell has fewer parts of type myosin filament skeletal muscle cell, abnormal ZP:0009906 cardiac muscle cell has fewer parts of type myosin filament cardiac muscle cell, abnormal ZP:0009907 intercalated disc cardiac muscle cell malformed, abnormal ZP:0009908 melanocyte migration arrested, abnormal ZP:0009909 gut decreased contractility, abnormal ZP:0009910 gut distended, abnormal ZP:0009911 melanocyte head absent, abnormal ZP:0009912 melanocyte head mislocalised, abnormal ZP:0009913 melanocyte ventral larval melanophore stripe decreased amount, abnormal ZP:0009914 melanocyte shape, abnormal ZP:0009915 melanocyte circular, abnormal ZP:0009917 melanocyte increased occurrence apoptotic process, abnormal ZP:0009918 melanosome melanocyte low saturation, abnormal ZP:0009919 melanoblast increased amount, abnormal ZP:0009920 ependymal cell spinal cord proliferative, abnormal ZP:0009921 convergent extension involved in axis elongation process quality, abnormal ZP:0009922 myofibril cardiac ventricle disorganized, abnormal ZP:0009923 optic vesicle mislocalised, abnormal ZP:0009924 axis thickness, abnormal ZP:0009925 pronephric duct aplastic, abnormal ZP:0009926 rhombomere 3 fused with left side right side rhombomere 3, abnormal ZP:0009927 neuron spinal cord neural rod absent, abnormal ZP:0009928 heart looping decreased occurrence, abnormal ZP:0009929 posterior lateral line lacks parts or has fewer parts of type neuromast, abnormal ZP:0009930 neuron projection posterior lateral line mislocalised, abnormal ZP:0009931 neuron posterior lateral line decreased branchiness, abnormal ZP:0009932 caudal fin decreased process quality blood circulation, abnormal ZP:0009933 trunk lacks parts or has fewer parts of type neuromast, abnormal ZP:0009934 nucleate erythrocyte differentiation disrupted, abnormal ZP:0009935 solid lens vesicle morphology, abnormal ZP:0009936 endothelial cell migration disrupted, abnormal ZP:0009938 presumptive endocardium heart primordium aplastic, abnormal ZP:0009939 epithelium ventricular endocardium aplastic, abnormal ZP:0009940 trunk vasculature decreased size, abnormal ZP:0009941 post-vent vasculature decreased size, abnormal ZP:0009942 medial longitudinal fasciculus defasciculated, abnormal ZP:0009943 interhyal cartilage fused with ceratohyal cartilage, abnormal ZP:0009944 interhyal cartilage fused with hyosymplectic cartilage, abnormal ZP:0009946 polster increased length, abnormal ZP:0009947 prechordal plate shape, abnormal ZP:0009948 prechordal plate increased size, abnormal ZP:0009949 rhombomere 5 development disrupted, abnormal ZP:0009950 rhombomere 6 development disrupted, abnormal ZP:0009951 semicircular canal formation process quality, abnormal ZP:0009952 rhombomere 6 aplastic, abnormal ZP:0009953 anterior/posterior compartment boundary rhombomere 6 absent, abnormal ZP:0009954 rhombomere 6 arrested rhombomere boundary formation, abnormal ZP:0009955 anterior/posterior compartment boundary rhombomere 5 absent, abnormal ZP:0009956 rhombomere 5 arrested rhombomere boundary formation, abnormal ZP:0009957 anterior/posterior compartment boundary rhombomere 7 absent, abnormal ZP:0009958 cartilage element pharyngeal arch malformed, abnormal ZP:0009959 cartilage element pharyngeal arch 3 increased thickness, abnormal ZP:0009960 cartilage element pharyngeal arch 3 truncated, abnormal ZP:0009961 axon hindbrain commissure decussate, abnormal ZP:0009962 neural crest hindbrain process quality neural crest cell migration, abnormal ZP:0009963 xanthophore differentiation disrupted, abnormal ZP:0009964 sensory neuron dorsal root ganglion mislocalised dorsally, abnormal ZP:0009965 pterinosome head decreased amount, abnormal ZP:0009966 pterinosome trunk absent, abnormal ZP:0009967 melanocyte trunk increased amount, abnormal ZP:0009968 melanocyte trunk decreased size, abnormal ZP:0009969 melanocyte trunk mislocalised, abnormal ZP:0009970 xanthophore trunk colorless, abnormal ZP:0009971 xanthophore trunk absent, abnormal ZP:0009973 neuron neural crest derived presumptive enteric nervous system decreased amount, abnormal ZP:0009974 melanocyte melanophore stripe increased amount, abnormal ZP:0009975 neural crest cell delaminated, abnormal ZP:0009976 cranial nerve VI hypoplastic, abnormal ZP:0009977 cranial nerve X hypoplastic, abnormal ZP:0009978 cranial nerve VII hypoplastic, abnormal ZP:0009979 cranial nerve IX hypoplastic, abnormal ZP:0009980 ceratobranchial 5 tooth malformed, abnormal ZP:0009981 pharyngeal arch mislocalised laterally, abnormal ZP:0009982 adrenal gland development disrupted, abnormal ZP:0009983 pronephros morphogenesis disrupted, abnormal ZP:0009984 pronephros decreased size, abnormal ZP:0009985 interrenal primordium decreased size, abnormal ZP:0009986 coelom edematous, abnormal ZP:0009987 head muscle poorly differentiated, abnormal ZP:0009988 CaP motoneuron physical quality of a process axon guidance, abnormal ZP:0009989 axon CaP motoneuron truncated, abnormal ZP:0009990 axon CaP motoneuron branchiness, abnormal ZP:0009991 CaP motoneuron decreased process quality axon extension, abnormal ZP:0009992 Muller cell retinal neural layer decreased amount, abnormal ZP:0009993 retinal cone cell retinal photoreceptor layer decreased amount, abnormal ZP:0009994 anterior macula has fewer parts of type hair cell anterior macula, abnormal ZP:0009995 Muller cell proliferative, abnormal ZP:0009997 tail bud duplicated, abnormal ZP:0009999 caudal fin duplicated, abnormal ZP:0010000 scapulocoracoid pectoral fin fold absent, abnormal ZP:0010001 endochondral bone pectoral fin fold absent, abnormal ZP:0010002 unidimensional cell growth disrupted, abnormal ZP:0010003 cell projection hypoblast deviation, abnormal ZP:0010004 cell hypoblast circular, abnormal ZP:0010005 central canal bent, abnormal ZP:0010006 central canal kinked, abnormal ZP:0010007 anterior cerebral vein morphology, abnormal ZP:0010008 anterior cerebral vein decreased size, abnormal ZP:0010009 anterior region whole organism morphology, abnormal ZP:0010010 head increased width, abnormal ZP:0010011 head condensed, abnormal ZP:0010013 anterior-posterior axis trunk bifurcated, abnormal ZP:0010014 ceratohyal cartilage increased size, abnormal ZP:0010015 cranial cartilage decreased length, abnormal ZP:0010016 chondrocyte pharyngeal arch cartilage increased amount, abnormal ZP:0010017 chondrocyte pharyngeal arch cartilage decreased size, abnormal ZP:0010018 notochord posterior region bent, abnormal ZP:0010019 mid cerebral vein decreased size, abnormal ZP:0010020 ectodermal cell circular, abnormal ZP:0010021 cell projection ectodermal cell deviation, abnormal ZP:0010022 muscle cell differentiation process quality, abnormal ZP:0010023 mesodermal cell heart primordium decreased amount, abnormal ZP:0010024 cardiac muscle myoblast heart primordium decreased amount, abnormal ZP:0010025 proctodeum malformed, abnormal ZP:0010026 swim bladder disorganized, abnormal ZP:0010027 cerebellum physical object quality, abnormal ZP:0010028 anterior macula increased size, abnormal ZP:0010029 common cardinal vein increased width, abnormal ZP:0010030 pancreas primordium hypoplastic, abnormal ZP:0010031 segmental plate lacks all parts of type anterior region adaxial cell, abnormal ZP:0010032 macula fused with macula, abnormal ZP:0010033 tela chorioidea decreased size, abnormal ZP:0010034 tela chorioidea hypoplastic, abnormal ZP:0010035 cell tela chorioidea fragility, abnormal ZP:0010036 cell tela chorioidea decreased amount, abnormal ZP:0010037 lapillus decreased size, abnormal ZP:0010038 melanocyte caudal fin mislocalised, abnormal ZP:0010039 cell projection roof plate spinal cord region decreased length, abnormal ZP:0010040 ventricular system apoptotic, abnormal ZP:0010041 smooth muscle aplastic, abnormal ZP:0010042 pillar of the anterior semicircular canal shape, abnormal ZP:0010043 mesothelial cell distributed, abnormal ZP:0010044 mesothelial cell decreased amount, abnormal ZP:0010045 endocrine cell decreased amount, abnormal ZP:0010046 slow muscle cell decreased size, abnormal ZP:0010047 slow muscle cell aplastic, abnormal ZP:0010048 Muller cell decreased occurrence cell population proliferation, abnormal ZP:0010049 notochord development peramorphic growth, abnormal ZP:0010050 gut decreased curvature, abnormal ZP:0010051 liver orientation left-right axis whole organism, abnormal ZP:0010052 notochord decreased diameter, abnormal ZP:0010053 cell notochord decreased amount, abnormal ZP:0010054 pancreas orientation left-right axis whole organism, abnormal ZP:0010055 cloacal chamber morphology, abnormal ZP:0010056 pronephric duct opening closed, abnormal ZP:0010057 chordo neural hinge decreased size, abnormal ZP:0010058 epicardium hypoplastic, abnormal ZP:0010059 notochord decreased width, abnormal ZP:0010060 interneuron hindbrain increased amount, abnormal ZP:0010061 facial nerve motor nucleus increased amount, abnormal ZP:0010062 vagal lobe increased amount, abnormal ZP:0010063 trigeminal motor nucleus increased amount, abnormal ZP:0010064 rostrocaudal neural tube patterning disrupted, abnormal ZP:0010065 negative regulation of Wnt signaling pathway disrupted, abnormal ZP:0010066 eye morphogenesis arrested, abnormal ZP:0010068 forebrain morphogenesis disrupted, abnormal ZP:0010070 trigeminal neural crest distended, abnormal ZP:0010072 neuron trigeminal placode irregular spatial pattern, abnormal ZP:0010073 neuron hindbrain mislocalised, abnormal ZP:0010074 posterior lateral line neuromast primordium migration increased duration, abnormal ZP:0010075 posterior lateral line primordium has fewer parts of type posterior-most region cell, abnormal ZP:0010076 posterior lateral line primordium decreased process quality cell population proliferation, abnormal ZP:0010077 glucose metabolic process disrupted, abnormal ZP:0010078 determination of pancreatic left/right asymmetry process quality, abnormal ZP:0010079 determination of liver left/right asymmetry process quality, abnormal ZP:0010080 digestive system positional polarity, abnormal ZP:0010081 endocrine pancreas hypoplastic, abnormal ZP:0010082 endocrine pancreas decreased functionality, abnormal ZP:0010083 acinar cell decreased amount, abnormal ZP:0010084 whole organism lacks all parts of type telencephalon, abnormal ZP:0010085 whole organism lacks all parts of type eye, abnormal ZP:0010086 regulation of brain-derived neurotrophic factor receptor signaling pathway disrupted, abnormal ZP:0010087 pigment accumulation delayed, abnormal ZP:0010088 blood low saturation, abnormal ZP:0010089 olfactory placode composition, abnormal ZP:0010090 olfactory receptor cell olfactory placode absent, abnormal ZP:0010091 pharyngeal arch 3-7 skeleton has fewer parts of type pharyngeal arch cartilage, abnormal ZP:0010092 neuroblast head dispersed, abnormal ZP:0010093 trunk misaligned with larval melanophore stripe anterior-posterior axis whole organism, abnormal ZP:0010094 melanocyte trunk disorganized, abnormal ZP:0010095 neural tube shape, abnormal ZP:0010096 ceratohyal cartilage curved caudal, abnormal ZP:0010097 neuromast lateral line decreased amount, abnormal ZP:0010098 pharyngeal arch 2 disoriented, abnormal ZP:0010099 pharyngeal arch 2 mislocalised ventrally, abnormal ZP:0010100 pharyngeal arch 1 disoriented, abnormal ZP:0010101 pharyngeal arch 1 mislocalised ventrally, abnormal ZP:0010102 dopaminergic neuron ventral thalamus decreased amount, abnormal ZP:0010103 dopaminergic neuron preoptic area decreased amount, abnormal ZP:0010104 somite post-vent region apoptotic, abnormal ZP:0010105 posterior region somite border surface feature shape, abnormal ZP:0010111 whole organism lacks parts or has fewer parts of type intersegmental vessel, abnormal ZP:0010112 whole organism lacks parts or has fewer parts of type parachordal vessel, abnormal ZP:0010113 trunk vasculature lacks all parts of type parachordal vessel, abnormal ZP:0010114 axon VaP motor neuron increased branchiness, abnormal ZP:0010115 neuromast hair cell posterior lateral line neuromast absent, abnormal ZP:0010116 brain disoriented, abnormal ZP:0010117 epiphysis split, abnormal ZP:0010118 retinal ganglion cell layer mislocalised, abnormal ZP:0010119 hindbrain decreased thickness, abnormal ZP:0010120 cell hindbrain aggregated, abnormal ZP:0010121 cell hindbrain loose, abnormal ZP:0010122 lens disoriented, abnormal ZP:0010123 tail bud vacuolated, abnormal ZP:0010124 paraxial mesoderm tail bud disorganized, abnormal ZP:0010125 eye fused with brain, abnormal ZP:0010126 cell fourth ventricle mislocalised, abnormal ZP:0010127 fourth ventricle midbrain mislocalised anteriorly, abnormal ZP:0010128 cell midbrain loose, abnormal ZP:0010129 neural rod shape, abnormal ZP:0010130 cartilage element pectoral fin bud absent, abnormal ZP:0010131 cartilage element pectoral fin bud disorganized, abnormal ZP:0010132 retinal pigmented epithelium position, abnormal ZP:0010133 mesodermal cell paraxial mesoderm spherical, abnormal ZP:0010134 stereocilium bundle hair cell posterior macula decreased length, abnormal ZP:0010135 kinocilium hair cell posterior macula decreased length, abnormal ZP:0010136 kinocilium hair cell anterior macula decreased length, abnormal ZP:0010137 spinal cord interneuron disorganized, abnormal ZP:0010138 presumptive neural retina detached from adherens junction presumptive retinal pigmented epithelium, abnormal ZP:0010139 photoreceptor outer segment whole organism decreased length, abnormal ZP:0010140 neuroectoderm malformed, abnormal ZP:0010141 mesodermal cell axial mesoderm mislocalised, abnormal ZP:0010142 ventricular system composition, abnormal ZP:0010143 retinal inner plexiform layer structure, abnormal ZP:0010144 pillar of the semicircular canal structure, abnormal ZP:0010145 hindbrain interneuron disorganized, abnormal ZP:0010146 anterior neural keel increased width, abnormal ZP:0010147 hindbrain neural keel umbonate, abnormal ZP:0010148 posterior neural tube T-shaped, abnormal ZP:0010149 filopodium cell present, abnormal ZP:0010150 mesodermal cell mislocalised, abnormal ZP:0010151 Mauthner neuron mislocalised, abnormal ZP:0010152 Mauthner neuron displaced to posterior region rhombomere, abnormal ZP:0010153 posterior lateral line development disrupted, abnormal ZP:0010154 neuromast shape, abnormal ZP:0010156 neuron migration arrested, abnormal ZP:0010157 axon extension heterochronic, abnormal ZP:0010158 olfactory placode development delayed, abnormal ZP:0010159 mitotic cell cycle arrest delayed, abnormal ZP:0010160 dopaminergic neuron forebrain absent, abnormal ZP:0010161 posterior lateral line nerve aplastic, abnormal ZP:0010162 dorsal root ganglion morphology, abnormal ZP:0010163 neuromast mislocalised, abnormal ZP:0010164 primary olfactory fiber layer morphology, abnormal ZP:0010165 glomerular layer morphology, abnormal ZP:0010166 nerve opercular lateral line absent, abnormal ZP:0010167 posterior lateral line ganglion absent, abnormal ZP:0010168 ventral anterior lateral line nerve decreased size, abnormal ZP:0010169 atrial myocardium disorganized, abnormal ZP:0010170 atrial myocardium swollen, abnormal ZP:0010171 cardiac muscle cell atrial myocardium loose, abnormal ZP:0010172 ventricular myocardium increased width, abnormal ZP:0010173 cardiac muscle cell ventricular myocardium condensed, abnormal ZP:0010174 camera-type eye morphogenesis disrupted, abnormal ZP:0010175 medial region brain decreased size, abnormal ZP:0010176 prechordal plate hypoplastic, abnormal ZP:0010177 shield aplastic, abnormal ZP:0010178 shield decreased amount, abnormal ZP:0010179 eye decreased distance anterior region anterior region eye, abnormal ZP:0010180 ventral region forebrain constricted, abnormal ZP:0010181 immature eye malformed, abnormal ZP:0010183 neuronal stem cell population maintenance decreased occurrence, abnormal ZP:0010184 dorsal telencephalon has extra parts of type ventricular zone neuron, abnormal ZP:0010185 radial glial cell dorsal telencephalon cellular potency, abnormal ZP:0010186 endoderm formation disrupted, abnormal ZP:0010187 anterior axial hypoblast increased thickness, abnormal ZP:0010188 mesoderm morphology, abnormal ZP:0010189 mesoderm aplastic, abnormal ZP:0010190 polster absent, abnormal ZP:0010191 prechordal plate decreased size, abnormal ZP:0010192 prechordal plate aplastic, abnormal ZP:0010193 gut physical object quality, abnormal ZP:0010194 retina aplastic, abnormal ZP:0010195 retina stratification, abnormal ZP:0010196 presumptive dorsal mesoderm morphology, abnormal ZP:0010197 rhombomere 4 morphology, abnormal ZP:0010198 mesoderm head aplastic, abnormal ZP:0010199 mesoderm trunk aplastic, abnormal ZP:0010200 medial floor plate aplastic, abnormal ZP:0010201 facial placode morphology, abnormal ZP:0010202 glossopharyngeal placode morphology, abnormal ZP:0010203 mandibular neural crest fused with hyoid neural crest, abnormal ZP:0010204 hatching gland cell absent, abnormal ZP:0010205 xanthophore head colored, abnormal ZP:0010206 xanthophore trunk colored, abnormal ZP:0010207 pterinosome xanthophore morphology, abnormal ZP:0010208 mitotic S phase arrested, abnormal ZP:0010209 central nervous system has fewer parts of type myelin sheath oligodendrocyte, abnormal ZP:0010210 spinal cord has fewer parts of type cell projection radial glial cell, abnormal ZP:0010211 spinal cord has fewer parts of type dorsal region oligodendrocyte, abnormal ZP:0010212 spinal cord has extra parts of type ventral region oligodendrocyte, abnormal ZP:0010213 spinal cord has extra parts of type grey matter oligodendrocyte, abnormal ZP:0010214 spinal cord has fewer parts of type white matter oligodendrocyte, abnormal ZP:0010215 head opacity, abnormal ZP:0010216 oligodendrocyte distributed, abnormal ZP:0010217 plasma membrane oligodendrocyte disorganized, abnormal ZP:0010218 axon oligodendrocyte misrouted, abnormal ZP:0010219 axon oligodendrocyte split, abnormal ZP:0010220 axonal growth cone oligodendrocyte collapsed, abnormal ZP:0010221 neurectodermal cell increased amount, abnormal ZP:0010222 cell projection radial glial cell disorganized, abnormal ZP:0010223 cranial vasculature perforate, abnormal ZP:0010224 ethmoid cartilage unfused from ethmoid cartilage, abnormal ZP:0010225 palate hypoplastic, abnormal ZP:0010226 lip decreased size, abnormal ZP:0010227 regulation of canonical Wnt signaling pathway disrupted, abnormal ZP:0010228 floor plate undulate, abnormal ZP:0010230 adaxial cell mislocalised, abnormal ZP:0010231 dermomyotome increased amount, abnormal ZP:0010232 fast muscle cell immature, abnormal ZP:0010233 immunoglobulin heavy chain V-D-J recombination disrupted, abnormal ZP:0010234 T cell head kidney absent, abnormal ZP:0010235 B cell head kidney absent, abnormal ZP:0010236 granulocyte increased amount, abnormal ZP:0010237 retina lacks all parts of type Muller cell, abnormal ZP:0010238 optic vesicle morphogenesis process quality, abnormal ZP:0010239 adenohypophysis development disrupted, abnormal ZP:0010240 retinal neural layer quality, abnormal ZP:0010241 adenohypophysis decreased amount, abnormal ZP:0010243 whole organism sigmoid, abnormal ZP:0010244 trunk vasculature non-functional, abnormal ZP:0010245 post-vent vasculature structure, abnormal ZP:0010246 thoracic duct immature, abnormal ZP:0010247 ossification increased occurrence, abnormal ZP:0010248 segmental plate increased cellular motility, abnormal ZP:0010249 postcranial axial skeleton ossified, abnormal ZP:0010250 embryonic axis specification disrupted, abnormal ZP:0010251 endodermal cell endoderm increased amount, abnormal ZP:0010252 epiphysis oblong, abnormal ZP:0010253 forerunner cell group increased amount, abnormal ZP:0010254 prechordal plate quality, abnormal ZP:0010255 ventral region diencephalon decreased size, abnormal ZP:0010257 head sharpness, abnormal ZP:0010258 nucleus of the tract of the postoptic commissure absent, abnormal ZP:0010259 dorsal rectus morphology, abnormal ZP:0010260 ventral rectus morphology, abnormal ZP:0010262 dorsal oblique extraocular muscle morphology, abnormal ZP:0010263 ventral oblique extraocular muscle morphology, abnormal ZP:0010264 corneal epithelium increased thickness, abnormal ZP:0010265 cell cycle rate, abnormal ZP:0010266 forebrain neuron differentiation disrupted, abnormal ZP:0010267 neuron differentiation arrested, abnormal ZP:0010268 serotonin metabolic process disrupted, abnormal ZP:0010269 defense response to fungus process quality, abnormal ZP:0010270 retinal rod cell differentiation delayed, abnormal ZP:0010271 retinal rod cell differentiation process quality, abnormal ZP:0010272 oncogene-induced cell senescence decreased occurrence, abnormal ZP:0010274 nucleus retinal neural layer apoptotic, abnormal ZP:0010275 ventricular zone telencephalon increased width, abnormal ZP:0010276 eye adjacent to eye, abnormal ZP:0010277 gut neoplastic, abnormal ZP:0010278 hepatocellular carcinoma liver present, abnormal ZP:0010279 peripheral nervous system neoplastic, malignant, abnormal ZP:0010280 neurofibrosarcoma peripheral nervous system increased amount, abnormal ZP:0010281 cranial nerve I defasciculated, abnormal ZP:0010282 motor neuron vagal lobe decreased amount, abnormal ZP:0010283 gill neoplastic, abnormal ZP:0010284 glomerular layer decreased size, abnormal ZP:0010285 integument neoplastic, abnormal ZP:0010286 paraventricular organ absent neurotransmitter metabolic process, abnormal ZP:0010287 posterior cardinal vein structure, abnormal ZP:0010288 posterior intestine neoplastic, abnormal ZP:0010292 sarcoma trunk present, abnormal ZP:0010293 post-vent region neoplastic, abnormal ZP:0010294 optic nerve head decreased size, abnormal ZP:0010295 axon optic nerve head absent, abnormal ZP:0010296 supraoptic tract decreased thickness, abnormal ZP:0010297 supraoptic tract fasciculation, abnormal ZP:0010298 anterior swim bladder bud absent, abnormal ZP:0010299 anterior swim bladder bud decreased size, abnormal ZP:0010300 cardiac muscle cell decreased process quality cell population proliferation, abnormal ZP:0010301 neutrophil decreased process quality phagocytosis, abnormal ZP:0010303 positive regulation of vascular endothelial growth factor signaling pathway decreased occurrence, abnormal ZP:0010304 intersegmental vessel has fewer parts of type blood vessel endothelial cell, abnormal ZP:0010305 atrioventricular canal decreased size, abnormal ZP:0010306 posterior side hypothalamus morphology, abnormal ZP:0010307 optic tectum hypoplastic, abnormal ZP:0010308 splanchnocranium decreased length, abnormal ZP:0010309 interhyal cartilage absent, abnormal ZP:0010310 Kupffer's vesicle bilateral, abnormal ZP:0010311 Kupffer's vesicle inverted, abnormal ZP:0010312 Kupffer's vesicle dislocated yolk, abnormal ZP:0010313 anterior region brain decreased size, abnormal ZP:0010314 median fin fold increased amount, abnormal ZP:0010315 median fin fold duplicated, abnormal ZP:0010317 somite 1 decreased size, abnormal ZP:0010318 somite 5 decreased size, abnormal ZP:0010319 tail bud shape, abnormal ZP:0010320 tail bud increased thickness, abnormal ZP:0010321 tail bud wholly anterioralized, abnormal ZP:0010322 tail bud everted, abnormal ZP:0010323 blood island increased amount, abnormal ZP:0010324 blood island increased width, abnormal ZP:0010325 extension increased size, abnormal ZP:0010326 lateral plate mesoderm increased width, abnormal ZP:0010327 neural plate decreased thickness, abnormal ZP:0010328 primitive heart tube bilateral, abnormal ZP:0010329 primitive heart tube inverted, abnormal ZP:0010330 ventral region pronephros increased width, abnormal ZP:0010331 caudal vein truncated, abnormal ZP:0010332 somite 11 increased size, abnormal ZP:0010333 somite 11 fused with dorso-medial margin dorso-medial margin somite 11, abnormal ZP:0010334 somite 14 increased size, abnormal ZP:0010335 somite 14 fused with dorso-medial margin dorso-medial margin somite 14, abnormal ZP:0010336 somite 2 decreased size, abnormal ZP:0010337 somite 3 decreased size, abnormal ZP:0010338 somite 12 increased size, abnormal ZP:0010339 somite 12 fused with dorso-medial margin dorso-medial margin somite 12, abnormal ZP:0010340 somite 15 increased size, abnormal ZP:0010341 somite 15 fused with dorso-medial margin dorso-medial margin somite 15, abnormal ZP:0010342 somite 4 decreased size, abnormal ZP:0010343 somite 13 increased size, abnormal ZP:0010344 somite 13 fused with dorso-medial margin dorso-medial margin somite 13, abnormal ZP:0010345 caudal fin increased amount, abnormal ZP:0010346 ventral fin fold multiple, abnormal ZP:0010347 head decreased thickness, abnormal ZP:0010349 ventral region trunk increased thickness, abnormal ZP:0010350 somite trunk decreased size, abnormal ZP:0010351 post-vent region folded, abnormal ZP:0010352 somite post-vent region increased size, abnormal ZP:0010353 somite post-vent region decreased size, abnormal ZP:0010354 notochord posterior region has fewer parts of type cell, abnormal ZP:0010355 Kupffer's vesicle development arrested, abnormal ZP:0010356 gall bladder mislocalised radially, abnormal ZP:0010357 pancreatic bud mislocalised radially, abnormal ZP:0010358 atrium increased thickness, abnormal ZP:0010359 forebrain neuron development extra or missing processual parts neuron fate specification, abnormal ZP:0010360 medial longitudinal catecholaminergic tract increased size, abnormal ZP:0010361 cellular pigmentation disrupted, abnormal ZP:0010363 intersegmental vein truncated, abnormal ZP:0010364 cell-cell junction blood vessel endothelium mislocalised, abnormal ZP:0010366 pronephros development process quality, abnormal ZP:0010367 pronephric glomerulus hypoplastic, abnormal ZP:0010369 fibroblast growth factor receptor signaling pathway process quality, abnormal ZP:0010370 regulation of bone remodeling occurrence, abnormal ZP:0010371 pharyngeal arch 3-7 skeleton disorganized, abnormal ZP:0010372 heart rudiment decreased size, abnormal ZP:0010373 opercle bilateral symmetry, abnormal ZP:0010374 semicircular canal truncated, abnormal ZP:0010375 locus coeruleus aplastic, abnormal ZP:0010376 oral epithelium has fewer parts of type taste bud, abnormal ZP:0010377 rhombomere 1 morphology, abnormal ZP:0010378 ventral mandibular arch bilateral symmetry, abnormal ZP:0010379 alar plate midbrain region morphology, abnormal ZP:0010380 chondrocranium bilateral symmetry, abnormal ZP:0010381 midbrain neural rod morphology, abnormal ZP:0010382 midbrain neural rod increased thickness, abnormal ZP:0010383 midbrain neural rod prominent, abnormal ZP:0010384 midbrain hindbrain boundary neural rod morphology, abnormal ZP:0010385 embryonic medial fin morphogenesis decreased process quality, abnormal ZP:0010388 median fin fold decreased height, abnormal ZP:0010401 endocardium morphogenesis disrupted, abnormal ZP:0010402 pineal gland development disrupted, abnormal ZP:0010403 endocrine cell pancreas decreased amount, abnormal ZP:0010404 somite fused with medial side medial side somite, abnormal ZP:0010405 caudal fin physical object quality, abnormal ZP:0010406 post-vent region increased distance somite somite post-vent region, abnormal ZP:0010407 melanocyte displaced to ventral surface neural tube, abnormal ZP:0010408 midbrain-hindbrain boundary initiation process quality, abnormal ZP:0010409 optic nerve development disrupted, abnormal ZP:0010410 midbrain-hindbrain boundary development arrested, abnormal ZP:0010411 neuron cranial ganglion decreased amount, abnormal ZP:0010412 epiphysis decreased width, abnormal ZP:0010413 retinal neural layer closure incomplete, abnormal ZP:0010414 otic vesicle physical object quality, abnormal ZP:0010415 diencephalon distended, abnormal ZP:0010416 retinal pigmented epithelium closure incomplete, abnormal ZP:0010417 pronephric duct absent, abnormal ZP:0010418 pronephric duct physical object quality, abnormal ZP:0010419 pronephric duct lacks all parts of type brush border epithelial cell, abnormal ZP:0010420 central region pronephric duct distended, abnormal ZP:0010421 epithelial cell pronephric duct flattened, abnormal ZP:0010422 pronephros absent, abnormal ZP:0010423 pronephros physical object quality, abnormal ZP:0010424 caudal commissure increased size, abnormal ZP:0010425 optic tectum malformed, abnormal ZP:0010426 cell optic tectum degenerate, abnormal ZP:0010427 cell optic tectum refractile, abnormal ZP:0010428 trochlear motor nucleus has fewer parts of type neuron, abnormal ZP:0010429 commissura cerebelli aplastic, abnormal ZP:0010430 oculomotor nucleus has fewer parts of type neuron, abnormal ZP:0010431 optic chiasm ipsilateral to cranial nerve II cranial nerve II optic chiasm, abnormal ZP:0010432 cranial nerve IV aplastic, abnormal ZP:0010433 ansulate commissure decreased size, abnormal ZP:0010434 thyroid follicle aplastic, abnormal ZP:0010435 forebrain midbrain boundary decreased distance hindbrain commissure, abnormal ZP:0010436 anterior region pronephric tubule malformed, abnormal ZP:0010437 gut epithelium edematous, abnormal ZP:0010438 regulation of cellular response to stress increased process quality, abnormal ZP:0010439 otic vesicle has fewer parts of type hair cell, abnormal ZP:0010440 Kolmer-Agduhr neuron spinal cord undifferentiated, abnormal ZP:0010441 internal gill bud decreased length, abnormal ZP:0010442 internal gill bud decreased amount, abnormal ZP:0010443 neurocranium lacks all parts of type neurocranial trabecula, abnormal ZP:0010444 pronephric distal late tubule decreased object quality, abnormal ZP:0010445 mandibular muscle refractivity, abnormal ZP:0010446 striated muscle myosin thick filament myotome absent, abnormal ZP:0010447 striated muscle myosin thick filament myotome decreased amount, abnormal ZP:0010448 striated muscle thin filament myotome decreased amount, abnormal ZP:0010449 Z disc myotome disorganized, abnormal ZP:0010450 M band myotome disorganized, abnormal ZP:0010451 nucleus skeletal muscle cell circular, abnormal ZP:0010452 myofibril skeletal muscle cell decreased amount, abnormal ZP:0010453 striated muscle myosin thick filament slow muscle cell disorganized, abnormal ZP:0010454 striated muscle myosin thick filament fast muscle cell disorganized, abnormal ZP:0010455 striated muscle thin filament fast muscle cell disorganized, abnormal ZP:0010457 intracellularly ATP-gated chloride channel activity increased occurrence, abnormal ZP:0010458 exocrine pancreas development process quality, abnormal ZP:0010459 gut swollen, abnormal ZP:0010460 gut epithelium flattened, abnormal ZP:0010461 intestinal villus flattened, abnormal ZP:0010462 enterocyte decreased height, abnormal ZP:0010463 microvillus enterocyte decreased length, abnormal ZP:0010464 prechordal plate formation disrupted, abnormal ZP:0010465 ventral region central nervous system decreased length, abnormal ZP:0010466 polster decreased size, abnormal ZP:0010467 polster elongated, abnormal ZP:0010468 polster anterior-posterior polarity, abnormal ZP:0010469 polster flattened, abnormal ZP:0010470 posterior region prechordal plate decreased length, abnormal ZP:0010471 posterior region prechordal plate increased width, abnormal ZP:0010472 notochord protruding, abnormal ZP:0010473 optic stalk fused with optic stalk, abnormal ZP:0010474 axial mesoderm decreased length, abnormal ZP:0010475 mandibular arch skeleton deformed, abnormal ZP:0010476 axial hypoblast decreased length, abnormal ZP:0010477 axial hypoblast increased width, abnormal ZP:0010478 regulation of heart contraction increased duration, abnormal ZP:0010479 whole organism has fewer parts of type nucleate erythrocyte, abnormal ZP:0010481 ectodermal cell fate commitment disrupted, abnormal ZP:0010482 hindbrain condensed, abnormal ZP:0010483 pronephros increased width, abnormal ZP:0010484 dorsal region retina cellular quality, abnormal ZP:0010485 cloacal chamber cellular quality, abnormal ZP:0010486 rhombomere 5 increased length, abnormal ZP:0010487 caudal fin increased accumulation blood cell, abnormal ZP:0010488 ventral fin fold flattened, abnormal ZP:0010489 ventral fin fold edge shape, abnormal ZP:0010490 postero-ventral region ventral fin fold hypoplastic, abnormal ZP:0010491 neuroectoderm degenerate, abnormal ZP:0010492 anal fin hypoplastic, abnormal ZP:0010493 Meckel's cartilage position, abnormal ZP:0010494 Meckel's cartilage overlap with Meckel's cartilage, abnormal ZP:0010495 ceratohyal cartilage fused with ceratobranchial 1 cartilage, abnormal ZP:0010496 cell division decreased rate, abnormal ZP:0010497 ceratobranchial bone malformed, abnormal ZP:0010498 chondrocyte palatoquadrate cartilage decreased amount, abnormal ZP:0010499 chondrocyte increased size, abnormal ZP:0010501 retina increased duration cell cycle process, abnormal ZP:0010502 retina increased duration S phase, abnormal ZP:0010503 behavioral fear response arrested, abnormal ZP:0010504 dopamine biosynthetic process from tyrosine decreased occurrence, abnormal ZP:0010505 multicellular organismal response to stress arrested, abnormal ZP:0010507 lateral plate mesoderm asymmetrical, abnormal ZP:0010508 heart primordium fused with left side right side heart primordium, abnormal ZP:0010509 trigeminal ganglion dispersed, abnormal ZP:0010510 smoothened signaling pathway decreased occurrence, abnormal ZP:0010511 optic nerve formation disrupted, abnormal ZP:0010512 striated muscle cell development arrested, abnormal ZP:0010514 somite lacks all parts of type muscle pioneer, abnormal ZP:0010515 third ventricle increased size, abnormal ZP:0010516 horizontal myoseptum morphology, abnormal ZP:0010517 anterior commissure decreased size, abnormal ZP:0010518 pharyngeal arch 3-7 mislocalised ventrally, abnormal ZP:0010519 axon MiP motor neuron decreased amount, abnormal ZP:0010521 gastrulation physical quality of a process, abnormal ZP:0010522 cell migration involved in gastrulation increased rate, abnormal ZP:0010523 Wnt signaling pathway process quality, abnormal ZP:0010524 neural tube patterning disrupted, abnormal ZP:0010527 neuroendocrine cell poorly differentiated, abnormal ZP:0010528 dopaminergic neuron disorganized, abnormal ZP:0010529 photopic photoreceptor cell retina absent, abnormal ZP:0010530 smooth muscle tissue development disrupted, abnormal ZP:0010531 smooth muscle tunica interna swim bladder absent, abnormal ZP:0010532 visceral peritoneum disorganized, abnormal ZP:0010533 adenohypophysis development paedomorphic growth, abnormal ZP:0010534 otic vesicle apoptotic, abnormal ZP:0010535 otic vesicle oblong, abnormal ZP:0010536 lateral crista absent, abnormal ZP:0010537 mandibular muscle hypoplastic, abnormal ZP:0010538 cranial nerve VIII increased length, abnormal ZP:0010539 cranial nerve VIII decreased thickness, abnormal ZP:0010540 macula shape, abnormal ZP:0010541 posterior crista absent, abnormal ZP:0010542 anterior crista absent, abnormal ZP:0010543 posterior-most region posterior lateral line neuromast absent, abnormal ZP:0010544 posterior lateral line primordium apoptotic, abnormal ZP:0010545 mandibular arch skeleton circular, abnormal ZP:0010546 neurohypophysis quality, abnormal ZP:0010547 adenohypophysis poorly differentiated, abnormal ZP:0010548 secretory granule adenohypophysis mislocalised, abnormal ZP:0010549 peptide hormone secreting cell structure, abnormal ZP:0010550 somatotropin secreting cell absent, abnormal ZP:0010551 prolactin secreting cell mislocalised, abnormal ZP:0010552 thyroid stimulating hormone secreting cell absent, abnormal ZP:0010553 DNA methylation on cytosine increased occurrence, abnormal ZP:0010554 lens poorly differentiated, abnormal ZP:0010555 dorsal region retinal pigmented epithelium absent, abnormal ZP:0010556 nucleus exocrine pancreas condensed, abnormal ZP:0010557 gut endothelial cell intestinal epithelium absent, abnormal ZP:0010558 hepatocyte degenerate, abnormal ZP:0010559 hepatocyte aggregated, abnormal ZP:0010560 hepatocyte mislocalised posteriorly, abnormal ZP:0010562 pigment accumulation process quality, abnormal ZP:0010563 dendrite retinal ganglion cell mislocalised, abnormal ZP:0010564 retinal ganglion cell displaced to dendrite retinal inner nuclear layer, abnormal ZP:0010565 retinal ganglion cell displaced to dendrite retinal inner plexiform layer, abnormal ZP:0010566 retinal ganglion cell displaced to dendrite retinal outer plexiform layer, abnormal ZP:0010567 neuron projection retinal ganglion cell mislocalised, abnormal ZP:0010568 retinal ganglion cell displaced to neuron projection optic tectum, abnormal ZP:0010569 retinal ganglion cell process quality dendrite guidance, abnormal ZP:0010570 retinal ganglion cell process quality neuron projection guidance, abnormal ZP:0010571 Wnt signaling pathway decreased process quality, abnormal ZP:0010572 hypothalamus cell differentiation disrupted, abnormal ZP:0010573 fin development decreased process quality, abnormal ZP:0010574 regulation of cell proliferation involved in tissue homeostasis decreased process quality, abnormal ZP:0010575 posterior region hypothalamus decreased size, abnormal ZP:0010576 axon hypothalamus decreased amount, abnormal ZP:0010577 neuron hypothalamus morphology, abnormal ZP:0010578 posterior lateral line nerve truncated, abnormal ZP:0010579 neuromast has fewer parts of type neuromast hair cell, abnormal ZP:0010580 paraxial mesoderm decreased size, abnormal ZP:0010581 posterior lateral line neuromast mislocalised anteriorly, abnormal ZP:0010582 posterior lateral line primordium increased length, abnormal ZP:0010583 posterior lateral line primordium self-renewal, abnormal ZP:0010584 anal fin decreased length, abnormal ZP:0010585 dorsal fin decreased length, abnormal ZP:0010586 caudal fin lepidotrichium hypoplastic, abnormal ZP:0010587 pectoral fin lepidotrichium hypoplastic, abnormal ZP:0010588 anterior-posterior axis eye decreased length, abnormal ZP:0010589 dorsal-ventral axis eye decreased length, abnormal ZP:0010590 retinal inner nuclear layer disorganized, abnormal ZP:0010591 basibranchial hypoplastic, abnormal ZP:0010593 medial rectus increased thickness, abnormal ZP:0010594 cornea morphology, abnormal ZP:0010595 oral cavity malformed, abnormal ZP:0010596 iris morphology, abnormal ZP:0010597 ventral mandibular arch mislocalised ventrally, abnormal ZP:0010598 pharyngeal arch 2 skeleton mislocalised ventrally, abnormal ZP:0010599 ceratohyal cartilage position, abnormal ZP:0010600 basihyal cartilage hypoplastic, abnormal ZP:0010601 corneal epithelium disorganized, abnormal ZP:0010602 hyaloid vessel disorganized, abnormal ZP:0010603 anterior segment eye structure, abnormal ZP:0010604 anterior segment eye increased accumulation cell, abnormal ZP:0010605 cell anterior segment eye disorganized, abnormal ZP:0010606 ocular blood vessel has extra parts of type hyaloid vessel, abnormal ZP:0010607 heart valve aplastic, abnormal ZP:0010608 spinal cord malformed, abnormal ZP:0010609 maxilla hyperplastic, abnormal ZP:0010610 Meckel's cartilage flat, abnormal ZP:0010611 palatoquadrate cartilage increased variability of size, abnormal ZP:0010612 ceratohyal cartilage shortened, abnormal ZP:0010613 axon development disrupted, abnormal ZP:0010614 neuromuscular junction myotome physical object quality, abnormal ZP:0010615 axon motor neuron bifurcated, abnormal ZP:0010616 presynaptic active zone motor neuron physical object quality, abnormal ZP:0010617 CaP motoneuron morphology, abnormal ZP:0010618 bulbus arteriosus amorphous, abnormal ZP:0010619 epithalamus development disrupted, abnormal ZP:0010621 cell migration in diencephalon disrupted, abnormal ZP:0010622 retina has extra parts of type retinal rod cell, abnormal ZP:0010623 pineal complex morphology, abnormal ZP:0010625 retinal rod cell increased amount, abnormal ZP:0010627 whole organism lacks parts or has fewer parts of type melanocyte, abnormal ZP:0010628 whole organism lacks parts or has fewer parts of type melanoblast, abnormal ZP:0010629 melanocyte aplastic, abnormal ZP:0010630 swim bladder inflation decreased process quality, abnormal ZP:0010631 pharyngeal system development decreased process quality, abnormal ZP:0010632 axis whole organism curved, abnormal ZP:0010633 pharyngeal pouch arrested, abnormal ZP:0010634 pharyngeal arch arrested, abnormal ZP:0010635 pharyngeal arch fused with mesenchyme condensation cell mesenchyme condensation cell pharyngeal arch, abnormal ZP:0010637 sarcomere cardiac muscle cell decreased length, abnormal ZP:0010638 melanin biosynthetic process from tyrosine disrupted, abnormal ZP:0010639 iridophore morphology, abnormal ZP:0010640 melanoblast unpigmented, abnormal ZP:0010641 fin regeneration hypotrophic growth, abnormal ZP:0010642 intermediate cell mass of mesoderm vacuolated, abnormal ZP:0010643 regenerating fin decreased length, abnormal ZP:0010644 rhombomere morphogenesis disrupted, abnormal ZP:0010645 hindbrain constricted, abnormal ZP:0010646 midbrain hindbrain boundary closure incomplete, abnormal ZP:0010647 axon Mauthner neuron decreased length, abnormal ZP:0010648 hematopoietic stem cell migration disrupted, abnormal ZP:0010649 ossification involved in bone maturation arrested, abnormal ZP:0010650 hematopoietic stem cell proliferation decreased occurrence, abnormal ZP:0010651 head kidney lacks parts or has fewer parts of type hematopoietic multipotent progenitor cell, abnormal ZP:0010652 head kidney has fewer parts of type hemoglobin complex hematopoietic multipotent progenitor cell, abnormal ZP:0010653 blood cell head kidney decreased amount, abnormal ZP:0010654 hemoglobin complex whole organism decreased amount, abnormal ZP:0010655 hematopoietic stem cell increased accumulation ventral wall of dorsal aorta, abnormal ZP:0010656 pro-T cell absent, abnormal ZP:0010657 lymphoid progenitor cell decreased amount, abnormal ZP:0010658 zinc ion homeostasis disrupted, abnormal ZP:0010659 swimming decreased distance swimming behavior, abnormal ZP:0010660 pancreatic bud has extra parts of type pancreatic epsilon cell, abnormal ZP:0010661 epiphysis cellular quality, abnormal ZP:0010662 median fin fold cellular quality, abnormal ZP:0010663 heart cellular quality, abnormal ZP:0010664 pectoral fin cellular quality, abnormal ZP:0010665 stomodeum cellular quality, abnormal ZP:0010666 cardiac muscle cell cardiac ventricle increased size, abnormal ZP:0010667 cardiac muscle cell cardiac ventricle elongated, abnormal ZP:0010668 fin agenesis, abnormal ZP:0010669 pectoral girdle aplastic, abnormal ZP:0010670 trunk curled, abnormal ZP:0010671 pectoral fin curved dorsal, abnormal ZP:0010672 myocardium disorganized, abnormal ZP:0010673 pectoral fin lepidotrichium decreased amount, abnormal ZP:0010674 atrioventricular valve structure, abnormal ZP:0010675 mitochondrion cardiac muscle cell increased amount, abnormal ZP:0010676 mitochondrion cardiac muscle cell swollen, abnormal ZP:0010677 cardiac muscle cell dissociated from bicellular tight junction bicellular tight junction cardiac muscle cell, abnormal ZP:0010678 telencephalon protruding, abnormal ZP:0010680 amacrine cell differentiation disrupted, abnormal ZP:0010681 retinal ganglion cell layer sparse, abnormal ZP:0010682 compartment boundary retinal ganglion cell layer rough, abnormal ZP:0010683 retina hypoplastic, abnormal ZP:0010684 retina lacks parts or has fewer parts of type photoreceptor cell, abnormal ZP:0010685 retina lacks parts or has fewer parts of type amacrine cell, abnormal ZP:0010686 cranial nerve II truncated, abnormal ZP:0010687 cranial nerve II sparse, abnormal ZP:0010688 cranial nerve II fasciculation, abnormal ZP:0010689 cranial nerve decreased size, abnormal ZP:0010690 lateral line nerve decreased size, abnormal ZP:0010691 retinal ganglion cell lacks parts or has fewer parts of type neuron projection retinal ganglion cell, abnormal ZP:0010692 neuron projection retinal ganglion cell physical object quality, abnormal ZP:0010693 cell-cell junction heart decreased amount, abnormal ZP:0010694 adherens junction heart composition, abnormal ZP:0010695 adherens junction heart decreased amount, abnormal ZP:0010696 endothelial cell heart morphology, abnormal ZP:0010697 skeletal muscle cell differentiated, abnormal ZP:0010698 bone tissue decreased mass density, abnormal ZP:0010699 brain symmetry, abnormal ZP:0010700 endocrine pancreas inverted, abnormal ZP:0010701 pronephric duct lacks all parts of type motile cilium pronephric duct, abnormal ZP:0010702 motile cilium peripheral olfactory organ decreased length, abnormal ZP:0010703 motile cilium peripheral olfactory organ decreased mobility, abnormal ZP:0010704 pronephric duct disorganized, abnormal ZP:0010705 motile cilium pronephric duct uncoordinated, abnormal ZP:0010706 motile cilium pronephric duct decreased mobility, abnormal ZP:0010707 pronephros morphogenesis process quality, abnormal ZP:0010708 pronephros lacks all parts of type pronephric glomerulus, abnormal ZP:0010709 pronephric glomerulus split bilaterally, abnormal ZP:0010710 centrum irregular spatial pattern, abnormal ZP:0010711 centrum malformed, abnormal ZP:0010712 centrum disorganized, abnormal ZP:0010713 vertebral column deviation, abnormal ZP:0010714 notochord outer sheath cell disorganized, abnormal ZP:0010715 notochord outer sheath cell deformed, abnormal ZP:0010716 activation of cysteine-type endopeptidase activity involved in apoptotic process increased process quality, abnormal ZP:0010718 cardioblast migration to the midline involved in heart rudiment formation disrupted, abnormal ZP:0010721 ventral mandibular arch disorganized, abnormal ZP:0010722 pharyngeal arch 1 decreased length, abnormal ZP:0010723 pharyngeal arch 1 disrupted embryonic morphogenesis, abnormal ZP:0010724 cardioblast migration to the midline involved in heart rudiment formation decreased process quality, abnormal ZP:0010725 heart tube increased amount, abnormal ZP:0010726 heart tube mislocalised laterally, abnormal ZP:0010727 mitotic cell cycle temporally extended, abnormal ZP:0010728 pronephric glomerulus morphogenesis process quality, abnormal ZP:0010729 centrum fused with centrum, abnormal ZP:0010730 osteoblast vertebral column mislocalised, abnormal ZP:0010731 whole organism lacks all parts of type ventral region brain, abnormal ZP:0010732 hypochord undulate, abnormal ZP:0010733 dorsal fin decreased size, abnormal ZP:0010734 blood ventricular system mislocalised, abnormal ZP:0010735 cranial blood vessel decreased branchiness, abnormal ZP:0010736 intestine increased occurrence peristalsis, abnormal ZP:0010737 retinal pigmented epithelium broken, abnormal ZP:0010739 melanosome retinal pigmented epithelium displaced, abnormal ZP:0010740 retinal pigmented epithelium has fewer parts of type cell melanosome retinal pigmented epithelium, abnormal ZP:0010741 basement membrane assembly involved in embryonic body morphogenesis process quality, abnormal ZP:0010742 collagen type IV trimer whole organism physical object quality, abnormal ZP:0010743 pericyte cranial blood vessel decreased amount, abnormal ZP:0010744 liver has fewer parts of type hepatocyte, abnormal ZP:0010745 skeletal muscle broken, abnormal ZP:0010746 response to light stimulus decreased process quality, abnormal ZP:0010747 retinal cone cell increased process quality cell death, abnormal ZP:0010749 thigmotropism decreased process quality, abnormal ZP:0010750 sarcoplasmic reticulum skeletal muscle swollen, abnormal ZP:0010751 muscle cell broken, abnormal ZP:0010752 slow muscle cell process quality muscle contraction, abnormal ZP:0010753 fast muscle cell process quality muscle contraction, abnormal ZP:0010754 lymphoid lineage cell migration into thymus disrupted, abnormal ZP:0010755 lymphocyte ventral wall of dorsal aorta decreased amount, abnormal ZP:0010756 centriole peripheral olfactory organ physical object quality, abnormal ZP:0010757 ciliary basal body peripheral olfactory organ physical object quality, abnormal ZP:0010758 skeletal muscle cell myotome morphology, abnormal ZP:0010759 whole organism lacks all parts of type macrophage, abnormal ZP:0010760 lymphoid lineage cell migration into thymus involved in thymus epithelium morphogenesis disrupted, abnormal ZP:0010761 cranial suture morphogenesis process quality, abnormal ZP:0010762 scale malformed, abnormal ZP:0010763 pectoral girdle alignment pectoral fin, abnormal ZP:0010764 parietal bone malformed, abnormal ZP:0010765 parasphenoid malformed, abnormal ZP:0010766 premaxilla malformed, abnormal ZP:0010767 dermatocranium decreased occurrence ossification involved in bone remodeling, abnormal ZP:0010768 dermatocranium increased occurrence bone resorption, abnormal ZP:0010769 preopercular sensory canal malformed, abnormal ZP:0010770 inter-frontal joint branched, abnormal ZP:0010771 cranial vault malformed, abnormal ZP:0010772 cranial vault increased occurrence bone resorption, abnormal ZP:0010773 cone photoresponse recovery process quality, abnormal ZP:0010774 retinal cone cell photosensitive, abnormal ZP:0010775 retinal cone cell increased process quality detection of light stimulus involved in visual perception, abnormal ZP:0010776 myotube cell development disrupted, abnormal ZP:0010777 muscle trunk musculature morphology, abnormal ZP:0010778 muscle cell trunk musculature disorganized, abnormal ZP:0010779 myoseptum muscle decreased thickness, abnormal ZP:0010780 myotome broken, abnormal ZP:0010781 muscle broken, abnormal ZP:0010782 posterior lateral line primordium process quality actin filament bundle organization, abnormal ZP:0010783 brain aplastic, abnormal ZP:0010784 apoptotic process increased process quality, abnormal ZP:0010785 posterior lateral line neuromast deposition decreased process quality, abnormal ZP:0010788 blood accumulation caudal vein plexus, abnormal ZP:0010789 caudal artery morphology, abnormal ZP:0010790 caudal artery immature, abnormal ZP:0010791 dorsal aorta disrupted blood circulation, abnormal ZP:0010792 axial vasculature disrupted blood circulation, abnormal ZP:0010793 cranial vasculature lacks parts or has fewer parts of type central artery, abnormal ZP:0010794 cranial vasculature disrupted blood circulation, abnormal ZP:0010795 central artery immature, abnormal ZP:0010796 central artery disrupted blood vessel lumenization, abnormal ZP:0010797 post-vent vasculature disrupted blood circulation, abnormal ZP:0010798 joint fin irregular spatial pattern, abnormal ZP:0010799 caudal fin increased length, abnormal ZP:0010800 pectoral fin increased length, abnormal ZP:0010801 dorsal fin increased length, abnormal ZP:0010802 pelvic fin increased length, abnormal ZP:0010803 lepidotrichium structure, abnormal ZP:0010804 lepidotrichium increased length, abnormal ZP:0010805 mitotic S phase temporally extended, abnormal ZP:0010806 microglial cell activation increased process quality, abnormal ZP:0010807 mitochondrial electron transport, ubiquinol to cytochrome c decreased rate, abnormal ZP:0010808 mitochondrion muscle increased size, abnormal ZP:0010809 mitochondrion muscle decreased functionality, abnormal ZP:0010811 CaP motoneuron increased duration motor neuron axon guidance, abnormal ZP:0010812 Mauthner neuron process quality action potential, abnormal ZP:0010813 Mauthner neuron increased occurrence action potential, abnormal ZP:0010814 Mauthner neuron temporal distribution quality action potential, abnormal ZP:0010815 Mauthner neuron process quality transmission of nerve impulse, abnormal ZP:0010816 microglia development arrested, abnormal ZP:0010817 mRNA splicing, via spliceosome decreased process quality, abnormal ZP:0010818 inner ear receptor cell stereocilium organization disrupted, abnormal ZP:0010819 stereocilium bundle auditory receptor cell shape, abnormal ZP:0010820 inflammatory response increased process quality, abnormal ZP:0010821 yolk syncytial layer edematous, abnormal ZP:0010822 blood island lacks all parts of type leukocyte, abnormal ZP:0010823 eye damaged, abnormal ZP:0010825 integument damaged, abnormal ZP:0010826 leukocyte accumulation anatomical region heart, abnormal ZP:0010827 striated muscle thin filament skeletal muscle disorganized, abnormal ZP:0010828 Z disc slow muscle cell disorganized, abnormal ZP:0010829 pronephric duct morphogenesis decreased process quality, abnormal ZP:0010830 Kupffer's vesicle has fewer parts of type motile cilium Kupffer's vesicle, abnormal ZP:0010831 Kupffer's vesicle decreased process quality motile cilium assembly, abnormal ZP:0010832 otic vesicle decreased volume, abnormal ZP:0010833 otic vesicle has fewer parts of type motile cilium otic vesicle, abnormal ZP:0010834 motile cilium otic vesicle decreased length, abnormal ZP:0010835 otic vesicle decreased process quality motile cilium assembly, abnormal ZP:0010836 motile cilium pronephric duct disorganized, abnormal ZP:0010837 peripheral olfactory organ disorganized, abnormal ZP:0010838 eye atrophied, abnormal ZP:0010839 caudal fin atrophied, abnormal ZP:0010840 axis whole organism truncated, abnormal ZP:0010841 determination of intestine left/right asymmetry process quality, abnormal ZP:0010842 dermal bone decreased process quality ossification, abnormal ZP:0010843 ceratohyal cartilage decreased angle to ceratohyal cartilage, abnormal ZP:0010845 oxidative DNA demethylation process quality, abnormal ZP:0010846 erythroid progenitor cell intermediate cell mass of mesoderm decreased amount, abnormal ZP:0010847 polychromatophilic erythroblast increased amount, abnormal ZP:0010848 erythroid progenitor cell increased accumulation intermediate cell mass of mesoderm, abnormal ZP:0010849 trunk lacks all parts of type anterior region thoracic duct, abnormal ZP:0010850 tooth 4V delayed odontogenesis, abnormal ZP:0010851 tooth 3V absent, abnormal ZP:0010853 notochord cell differentiation disrupted, abnormal ZP:0010854 somite development process quality, abnormal ZP:0010855 axial chorda mesoderm disrupted cell fate commitment, abnormal ZP:0010856 floor plate spinal cord region patchy, abnormal ZP:0010857 muscle displaced to axis, abnormal ZP:0010858 dorsal side spinal cord apoptotic, abnormal ZP:0010859 olfactory epithelium lacks parts or has fewer parts of type microvillous olfactory receptor neuron olfactory epithelium, abnormal ZP:0010860 microvillous olfactory receptor neuron olfactory epithelium disorganized, abnormal ZP:0010861 neural crest cell apoptotic, abnormal ZP:0010862 xanthophore dead, abnormal ZP:0010863 pectoral girdle aplastic/hypoplastic, abnormal ZP:0010864 palatoquadrate cartilage shortened, abnormal ZP:0010865 sternohyoid displaced, abnormal ZP:0010866 brain shortened, abnormal ZP:0010867 caudal fin necrotic, abnormal ZP:0010868 whole organism increased process quality apoptotic process, abnormal ZP:0010869 slow muscle cell shortened, abnormal ZP:0010870 fast muscle cell disoriented, abnormal ZP:0010871 fast muscle cell shortened, abnormal ZP:0010872 primary motor neuron morphology, abnormal ZP:0010873 Kupffer's vesicle decreased area, abnormal ZP:0010874 basolateral plasma membrane Kupffer's vesicle physical object quality, abnormal ZP:0010876 otic placode formation increased process quality, abnormal ZP:0010877 otolith development arrested, abnormal ZP:0010878 otic vesicle has extra parts of type hair cell, abnormal ZP:0010879 primary neuron neural plate increased amount, abnormal ZP:0010880 lapillus hypotrophic, abnormal ZP:0010881 statoacoustic (VIII) ganglion increased size, abnormal ZP:0010882 statoacoustic (VIII) ganglion hyperplastic, abnormal ZP:0010883 sagitta hypotrophic, abnormal ZP:0010884 hair cell anterior macula absent, abnormal ZP:0010885 auditory epithelial support cell absent, abnormal ZP:0010886 vascular sprouts pleuroperitoneal cavity increased amount, abnormal ZP:0010887 brain increased process quality apoptotic process, abnormal ZP:0010888 eye increased process quality apoptotic process, abnormal ZP:0010890 angioblast cell migration premature, abnormal ZP:0010891 intersegmental vessel position, abnormal ZP:0010892 vascular sprouts mislocalised, abnormal ZP:0010893 pronephric glomerulus development disrupted, abnormal ZP:0010894 pronephric glomerulus decreased size, abnormal ZP:0010895 cell projection pronephric podocyte morphology, abnormal ZP:0010896 cell projection pronephric podocyte irregular spatial pattern, abnormal ZP:0010897 cell projection pronephric podocyte increased area, abnormal ZP:0010898 pronephric glomerular capillary hypotrophic, abnormal ZP:0010899 fin bud hypoplastic, abnormal ZP:0010901 cell pectoral fin skeleton decreased amount, abnormal ZP:0010902 cleithrum pectoral fin decreased length, abnormal ZP:0010903 scapulocoracoid pectoral fin decreased size, abnormal ZP:0010904 pectoral fin actinotrichium decreased size, abnormal ZP:0010905 macula utricle has extra parts of type immature hair cell anterior macula, abnormal ZP:0010906 macula utricle has extra parts of type tether cell, abnormal ZP:0010907 macula utricle has extra parts of type hair cell, abnormal ZP:0010908 otic vesicle lacks parts or has fewer parts of type auditory epithelial support cell, abnormal ZP:0010909 otic vesicle has extra parts of type tether cell, abnormal ZP:0010910 macula has extra parts of type hair cell, abnormal ZP:0010911 posterior crista has extra parts of type hair cell, abnormal ZP:0010912 posterior macula increased size, abnormal ZP:0010913 axial mesoderm formation process quality, abnormal ZP:0010914 paraxial mesoderm formation process quality, abnormal ZP:0010915 dorso-medial region anatomical structure disorganized, abnormal ZP:0010916 spinal cord bifurcated, abnormal ZP:0010917 angioblast cell migration delayed, abnormal ZP:0010918 dorsal aorta broken, abnormal ZP:0010919 vein broken, abnormal ZP:0010920 angiogenic sprout absent, abnormal ZP:0010921 caudal fin wholly dorsalized, abnormal ZP:0010922 dorsal aorta increased size, abnormal ZP:0010923 dorsal aorta process quality sprouting angiogenesis, abnormal ZP:0010924 somite 1 morphology, abnormal ZP:0010925 somite 2 morphology, abnormal ZP:0010926 somite 3 morphology, abnormal ZP:0010927 somite 4 morphology, abnormal ZP:0010928 interstitial matrix trunk morphology, abnormal ZP:0010929 interrenal primordium morphology, abnormal ZP:0010930 interrenal primordium position, abnormal ZP:0010931 interrenal primordium unfused from left side right side interrenal primordium, abnormal ZP:0010932 interrenal vessel absent, abnormal ZP:0010933 interrenal angiogenic sprout absent, abnormal ZP:0010934 artery absent, abnormal ZP:0010935 vein morphology, abnormal ZP:0010936 interrenal primordium centered, abnormal ZP:0010937 pronephric glomerular capillary absent, abnormal ZP:0010938 adrenal gland development lacking processual parts cell migration, abnormal ZP:0010939 pronephric glomerulus unfused from right side left side pronephric glomerulus, abnormal ZP:0010940 vascular endothelium increased size, abnormal ZP:0010941 vascular endothelium mislocalised, abnormal ZP:0010942 pronephric glomerular capillary increased size, abnormal ZP:0010943 interrenal angiogenic sprout mislocalised laterally, abnormal ZP:0010944 embryonic pectoral fin morphogenesis decreased process quality, abnormal ZP:0010945 axial mesoderm development decreased process quality, abnormal ZP:0010946 paraxial mesoderm development process quality, abnormal ZP:0010947 paraxial mesoderm development decreased process quality, abnormal ZP:0010948 somite 1 fused with somite 2, abnormal ZP:0010949 lateral plate mesoderm physical object quality, abnormal ZP:0010950 anterior region notochord apoptotic, abnormal ZP:0010951 rhombomere 5 decreased distance somite 1, abnormal ZP:0010952 whole organism lacks all parts of type pectoral fin cartilage, abnormal ZP:0010953 whole organism lacks all parts of type pharyngeal pouch 3, abnormal ZP:0010954 whole organism lacks all parts of type pharyngeal pouch 4, abnormal ZP:0010955 whole organism lacks all parts of type pectoral fin, abnormal ZP:0010956 head has fewer parts of type notochord cell notochord, abnormal ZP:0010957 pectoral fin field physical object quality, abnormal ZP:0010958 neural crest pharyngeal arch 3-7 apoptotic, abnormal ZP:0010959 cartilage element cranium shortened, abnormal ZP:0010960 sarcomere caudal fin musculature disorganized, abnormal ZP:0010961 muscle cell caudal fin malformed, abnormal ZP:0010962 muscle cell caudal fin deformed, abnormal ZP:0010963 muscle cell malformed, abnormal ZP:0010964 muscle cell deformed, abnormal ZP:0010965 stereocilium bundle anterior macula bent, abnormal ZP:0010966 stereocilium bundle anterior macula splayed, abnormal ZP:0010968 Kupffer's vesicle has fewer parts of type cilium Kupffer's vesicle, abnormal ZP:0010969 pronephric duct has fewer parts of type cilium pronephric duct, abnormal ZP:0010971 intestinal epithelium stratified, abnormal ZP:0010973 invadopodium intestinal epithelium present, abnormal ZP:0010974 basal lamina intestinal epithelium degenerate, abnormal ZP:0010975 intestinal epithelial cell mislocalised, abnormal ZP:0010980 hair cell anterior macula increased occurrence apoptotic process, abnormal ZP:0010981 posterior lateral line primordium decreased size, abnormal ZP:0010982 posterior lateral line primordium disorganized, abnormal ZP:0010983 posterior lateral line primordium lacks parts or has fewer parts of type protoneuromast, abnormal ZP:0010984 ribbon synapse photoreceptor cell malformed, abnormal ZP:0010985 pharyngeal arch 2 hypoplastic, abnormal ZP:0010986 pharyngeal arch 1 hypoplastic, abnormal ZP:0010987 otic vesicle morphogenesis decreased process quality, abnormal ZP:0010988 otic vesicle has fewer parts of type immature macula, abnormal ZP:0010990 otic vesicle decreased process quality neuron differentiation, abnormal ZP:0010991 neuroblast (sensu Vertebrata) otic vesicle poorly differentiated, abnormal ZP:0010992 breeding tubercle jaw flap decreased size, abnormal ZP:0010993 jaw row breeding tubercle decreased size, abnormal ZP:0010994 jaw row breeding tubercle decreased amount, abnormal ZP:0010995 motor neuron process quality collateral sprouting, abnormal ZP:0010996 axon Rohon-Beard neuron decreased branchiness, abnormal ZP:0010997 ceratobranchial cartilage aplastic/hypoplastic, abnormal ZP:0010998 optokinetic behavior decreased process quality, abnormal ZP:0010999 myelination premature, abnormal ZP:0011000 oligodendrocyte decreased process quality cell migration, abnormal ZP:0011001 Mauthner neuron decreased diameter, abnormal ZP:0011002 Mauthner neuron increased process quality myelination, abnormal ZP:0011003 myelin sheath Mauthner neuron increased thickness, abnormal ZP:0011004 neuron increased process quality myelination, abnormal ZP:0011005 myelin sheath neuron increased thickness, abnormal ZP:0011006 regulation of smooth muscle contraction process quality, abnormal ZP:0011007 tonic smooth muscle contraction present, abnormal ZP:0011009 regulation of intestinal epithelial structure maintenance disrupted, abnormal ZP:0011010 enteric musculature intestine morphology, abnormal ZP:0011011 intestinal epithelium cystic, abnormal ZP:0011012 focal adhesion intestinal epithelium degenerate, abnormal ZP:0011013 basal lamina intestinal epithelium damaged, abnormal ZP:0011014 interrenal primordium bilateral, abnormal ZP:0011015 mesoderm migration involved in gastrulation disrupted, abnormal ZP:0011016 actin polymerization or depolymerization process quality, abnormal ZP:0011017 regulation of cytosolic calcium ion concentration disrupted, abnormal ZP:0011018 mitochondrial calcium ion homeostasis disrupted, abnormal ZP:0011019 filamentous actin mesodermal cell oriented, abnormal ZP:0011020 renal water transport decreased process quality, abnormal ZP:0011021 embryonic heart tube left/right pattern formation decreased process quality, abnormal ZP:0011022 pronephros morphogenesis decreased process quality, abnormal ZP:0011023 central canal has fewer parts of type cilium ependymal cell, abnormal ZP:0011024 pronephric tubule has fewer parts of type microvillus pronephric tubule, abnormal ZP:0011025 actin cytoskeleton pronephric tubule decreased object quality, abnormal ZP:0011026 motile cilium pronephric tubule decreased length, abnormal ZP:0011027 motile cilium pronephric tubule disoriented, abnormal ZP:0011028 ciliary basal body pronephric tubule disorganized, abnormal ZP:0011029 apical part of cell pronephric tubule physical object quality, abnormal ZP:0011030 pronephric podocyte lacks parts or has fewer parts of type slit diaphragm pronephric podocyte, abnormal ZP:0011031 cell projection pronephric podocyte malformed, abnormal ZP:0011032 apical part of cell pronephric podocyte malformed, abnormal ZP:0011033 pronephric capsular space dilated, abnormal ZP:0011034 cilium ependymal cell decreased length, abnormal ZP:0011035 cilium ependymal cell disoriented, abnormal ZP:0011036 erythrocyte development process quality, abnormal ZP:0011038 endoderm disrupted cell migration involved in gastrulation, abnormal ZP:0011039 extension malformed, abnormal ZP:0011040 germ ring constricted, abnormal ZP:0011041 heart agenesis, abnormal ZP:0011042 hypoblast movement quality, abnormal ZP:0011043 presumptive endoderm process quality cell migration involved in gastrulation, abnormal ZP:0011044 ventral fin fold abnormal, abnormal ZP:0011045 pharyngeal endoderm malformed, abnormal ZP:0011046 notochord posterior region malformed, abnormal ZP:0011047 blood cell increased accumulation trunk, abnormal ZP:0011048 mesodermal cell accumulation margin, abnormal ZP:0011049 endodermal cell movement quality, abnormal ZP:0011050 retinal outer plexiform layer decreased thickness, abnormal ZP:0011051 retinal cone cell quality, abnormal ZP:0011054 retinal cone cell lacks parts or has fewer parts of type cone cell pedicle ribbon synapse retinal cone cell, abnormal ZP:0011055 axon microtubule bundle Rohon-Beard neuron loose, abnormal ZP:0011058 central canal hindbrain increased amount, abnormal ZP:0011059 cell hindbrain disoriented, abnormal ZP:0011061 fourth ventricle separated from fourth ventricle, abnormal ZP:0011063 rhombomere 3 increased variability establishment of mitotic spindle orientation, abnormal ZP:0011065 rhombomere 4 increased variability establishment of mitotic spindle orientation, abnormal ZP:0011066 eye decreased process quality cell population proliferation, abnormal ZP:0011067 eye increased process quality intrinsic apoptotic signaling pathway, abnormal ZP:0011068 ciliary marginal zone decreased process quality cell population proliferation, abnormal ZP:0011069 forebrain dorsal/ventral pattern formation process quality, abnormal ZP:0011070 floor plate development decreased process quality, abnormal ZP:0011071 retina development in camera-type eye process quality, abnormal ZP:0011072 commissural neuron axon guidance process quality, abnormal ZP:0011073 spinal cord has fewer parts of type anterior region primary motor neuron, abnormal ZP:0011074 lens eye deformed, abnormal ZP:0011075 forebrain process quality axon guidance, abnormal ZP:0011077 somite lacks all parts of type horizontal myoseptum, abnormal ZP:0011078 cleithrum hypoplastic, abnormal ZP:0011079 caudal commissure absent, abnormal ZP:0011081 caudal fin lacks all parts of type primary motor neuron, abnormal ZP:0011083 anterior commissure absent, abnormal ZP:0011084 trunk lacks all parts of type posterior region primary motor neuron, abnormal ZP:0011085 adenohypophyseal placode transformed to lens, abnormal ZP:0011086 lateral floor plate absent, abnormal ZP:0011087 medial floor plate broken, abnormal ZP:0011088 primary motor neuron absent, abnormal ZP:0011089 retinal ganglion cell process quality axon guidance, abnormal ZP:0011090 neuroblast (sensu Vertebrata) otic vesicle physical object quality, abnormal ZP:0011091 notochord mislocalised laterally, abnormal ZP:0011092 filamentous actin somite deformed, abnormal ZP:0011093 myelin sheath peripheral neuron neoplastic, abnormal ZP:0011095 abducens motor nucleus fused with abducens motor nucleus, abnormal ZP:0011100 cerebellum development decreased process quality, abnormal ZP:0011101 midbrain-hindbrain boundary development decreased process quality, abnormal ZP:0011102 somite development decreased process quality, abnormal ZP:0011103 somite poorly differentiated, abnormal ZP:0011104 whole organism lacks all parts of type midbrain hindbrain boundary, abnormal ZP:0011105 whole organism lacks all parts of type cerebellum, abnormal ZP:0011106 axon VaP motor neuron branchiness, abnormal ZP:0011107 iridophore dorsal larval melanophore stripe mislocalised anteriorly, abnormal ZP:0011108 iridophore ventral larval melanophore stripe increased amount, abnormal ZP:0011109 blood island morphology, abnormal ZP:0011110 blood island has extra parts of type erythroid lineage cell, abnormal ZP:0011115 oligodendrocyte differentiation process quality, abnormal ZP:0011116 embryonic cleavage process quality, abnormal ZP:0011117 regulation of nodal signaling pathway process quality, abnormal ZP:0011118 pharyngeal pouch 1 physical object quality, abnormal ZP:0011119 stomodeum mislocalised ventrally, abnormal ZP:0011120 palatoquadrate cartilage fused with Meckel's cartilage, abnormal ZP:0011121 hyosymplectic cartilage fused with ceratohyal cartilage, abnormal ZP:0011122 ventral region pharyngeal arch 3 physical object quality, abnormal ZP:0011123 mesenchymal cell pharyngeal arch 3 physical object quality, abnormal ZP:0011124 ventral region pharyngeal arch 4 physical object quality, abnormal ZP:0011125 mesenchymal cell pharyngeal arch 4 physical object quality, abnormal ZP:0011126 ventral region pharyngeal arch 2 physical object quality, abnormal ZP:0011127 mesenchymal cell pharyngeal arch 2 physical object quality, abnormal ZP:0011128 ventral region pharyngeal arch 1 physical object quality, abnormal ZP:0011129 mesenchymal cell pharyngeal arch 1 physical object quality, abnormal ZP:0011130 ventral intermandibularis anterior physical object quality, abnormal ZP:0011131 ventral intermandibularis posterior physical object quality, abnormal ZP:0011132 interhyoideus decreased length, abnormal ZP:0011133 interhyoideus physical object quality, abnormal ZP:0011134 hyohyoideus decreased length, abnormal ZP:0011135 anterior commissure morphogenesis process quality, abnormal ZP:0011136 supraoptic tract process quality axon extension, abnormal ZP:0011137 dorso-rostral cluster process quality axon extension, abnormal ZP:0011138 axon retinal ganglion cell decreased branchiness, abnormal ZP:0011139 retinal ganglion cell decreased process quality collateral sprouting in absence of injury, abnormal ZP:0011140 hindbrain morphogenesis process quality, abnormal ZP:0011141 posterior region hindbrain physical object quality, abnormal ZP:0011142 rhombomere 6 increased length, abnormal ZP:0011143 spinal cord has fewer parts of type anterior region spinal cord interneuron, abnormal ZP:0011144 spinal cord has fewer parts of type anterior region motor neuron, abnormal ZP:0011145 intermandibularis decreased length, abnormal ZP:0011146 rhombomere 7 increased length, abnormal ZP:0011147 rhombomere 7 physical object quality, abnormal ZP:0011148 neuron projection dorso-rostral cluster physical object quality, abnormal ZP:0011149 locomotor rhythm process quality, abnormal ZP:0011150 head decreased pigmentation, abnormal ZP:0011151 opsin transport decreased process quality, abnormal ZP:0011152 retinal outer nuclear layer increased process quality apoptotic process, abnormal ZP:0011153 retinal outer nuclear layer increased process quality cell death, abnormal ZP:0011154 neuron projection cranial nerve physical object quality, abnormal ZP:0011155 angiogenic sprout physical object quality, abnormal ZP:0011156 intersegmental vessel process quality blood vessel lumenization, abnormal ZP:0011158 Schwann cell migration process quality, abnormal ZP:0011159 posterior lateral line nerve has fewer parts of type axon myelinating Schwann cell, abnormal ZP:0011160 posterior lateral line nerve arrested myelination, abnormal ZP:0011161 posterior lateral line nerve decreased process quality myelination, abnormal ZP:0011162 immature Schwann cell decreased velocity, abnormal ZP:0011163 motor neuron has extra parts of type axon myelinating Schwann cell, abnormal ZP:0011164 motor neuron arrested myelination, abnormal ZP:0011165 motor neuron decreased process quality myelination, abnormal ZP:0011166 myelinating Schwann cell loose, abnormal ZP:0011167 atrioventricular valve formation process quality, abnormal ZP:0011168 atrioventricular canal development process quality, abnormal ZP:0011169 atrioventricular canal malformed, abnormal ZP:0011170 otic vesicle development process quality, abnormal ZP:0011171 otic vesicle split, abnormal ZP:0011172 hyomandibula hypoplastic, abnormal ZP:0011173 pharyngeal pouch 1 increased process quality apoptotic process, abnormal ZP:0011174 pharyngeal pouch 2 increased process quality apoptotic process, abnormal ZP:0011175 facial ganglion absent, abnormal ZP:0011176 neurogenic placode increased process quality apoptotic process, abnormal ZP:0011177 ventral anterior lateral line ganglion absent, abnormal ZP:0011178 middle lateral line ganglion absent, abnormal ZP:0011179 pharyngeal arch 3 hypoplastic, abnormal ZP:0011180 pharyngeal arch 4 hypoplastic, abnormal ZP:0011181 neurogenic field increased process quality apoptotic process, abnormal ZP:0011182 vagal ganglion decreased size, abnormal ZP:0011183 vagal ganglion lacks parts or has fewer parts of type vagal ganglion, abnormal ZP:0011184 neuroectoderm wholly dorsalized, abnormal ZP:0011185 retinal pigmented epithelium process quality melanosome localization, abnormal ZP:0011186 lapillus decreased width, abnormal ZP:0011187 lapillus adjacent to sagitta, abnormal ZP:0011188 sagitta decreased width, abnormal ZP:0011190 angioblast cell migration process quality, abnormal ZP:0011192 tonic skeletal muscle contraction process quality, abnormal ZP:0011193 glomerular filtration process quality, abnormal ZP:0011194 intersegmental vessel disrupted sprouting angiogenesis, abnormal ZP:0011195 lens disrupted collagen fibril organization, abnormal ZP:0011196 Golgi apparatus photoreceptor cell physical object quality, abnormal ZP:0011197 negative regulation of oxidative stress-induced intrinsic apoptotic signaling pathway disrupted, abnormal ZP:0011198 epithelial cell pronephros physical object quality, abnormal ZP:0011199 cilium multi-ciliated epithelial cell physical object quality, abnormal ZP:0011200 telomere maintenance via telomerase process quality, abnormal ZP:0011201 chromosome, telomeric region whole organism physical object quality, abnormal ZP:0011202 retinal cone cell process quality chemical synaptic transmission, abnormal ZP:0011203 cone cell pedicle retinal cone cell morphology, abnormal ZP:0011204 brain vasculature malformed, abnormal ZP:0011205 cerebellum hypoplastic, abnormal ZP:0011206 diencephalon increased process quality apoptotic process, abnormal ZP:0011207 fourth ventricle increased process quality apoptotic process, abnormal ZP:0011208 rhombomere 3 process quality establishment of mitotic spindle orientation, abnormal ZP:0011209 rhombomere 4 process quality establishment of mitotic spindle orientation, abnormal ZP:0011210 brain decreased length, abnormal ZP:0011211 posterior region mesoderm increased length, abnormal ZP:0011212 cell migration to the midline involved in heart development disrupted, abnormal ZP:0011213 optic stalk physical object quality, abnormal ZP:0011214 supraoptic commissure physical object quality, abnormal ZP:0011215 anterior commissure physical object quality, abnormal ZP:0011216 anterior commissure process quality axon extension, abnormal ZP:0011217 cell migration involved in somitogenic axis elongation disrupted, abnormal ZP:0011218 adherens junction tail bud morphology, abnormal ZP:0011219 thoracic duct morphology, abnormal ZP:0011220 rhombomere boundary formation process quality, abnormal ZP:0011221 rhombomere 5 process quality rhombomere boundary formation, abnormal ZP:0011222 rhombomere 3 process quality rhombomere boundary formation, abnormal ZP:0011223 fourth ventricle development process quality, abnormal ZP:0011224 hindbrain process quality neural keel formation, abnormal ZP:0011225 rhombomere 3 process quality neural keel formation, abnormal ZP:0011226 rhombomere 4 process quality neural keel formation, abnormal ZP:0011227 interrenal gland mislocalised, abnormal ZP:0011228 interrenal gland decreased occurrence steroid biosynthetic process, abnormal ZP:0011229 interrenal primordium disrupted cell migration, abnormal ZP:0011230 splanchnocranium aplastic, abnormal ZP:0011231 anterior region neurocranium aplastic, abnormal ZP:0011232 myotome development process quality, abnormal ZP:0011233 fast muscle cell morphology, abnormal ZP:0011234 neuromast hair cell process quality synapse organization, abnormal ZP:0011235 neuromast hair cell process quality cellular response to mechanical stimulus, abnormal ZP:0011236 ribbon synapse neuromast hair cell morphology, abnormal ZP:0011237 splanchnocranium hyperplastic, abnormal ZP:0011238 ceratobranchial cartilage hyperplastic, abnormal ZP:0011239 diencephalic nucleus displaced to axon lateral region hindbrain, abnormal ZP:0011240 diencephalic nucleus displaced to axon medial region hindbrain, abnormal ZP:0011241 hypocretin-secreting neuron displaced to axon medial region hindbrain, abnormal ZP:0011242 otic vesicle development decreased process quality, abnormal ZP:0011245 otic placode physical object quality, abnormal ZP:0011246 lateral crista physical object quality, abnormal ZP:0011248 pectoral fin bud absent, abnormal ZP:0011249 pectoral girdle absent, abnormal ZP:0011250 pharyngeal arch absent, abnormal ZP:0011251 dopaminergic neuron displaced to axon medial region hindbrain, abnormal ZP:0011253 anterior-posterior axis whole organism truncated, abnormal ZP:0011255 cell accumulation dorsal side tail bud, abnormal ZP:0011256 pectoral fin cartilage absent, abnormal ZP:0011257 dorsal side whole organism decreased thickness, abnormal ZP:0011258 blood accumulation head, abnormal ZP:0011259 blood accumulation post-vent region, abnormal ZP:0011260 atrioventricular canal shape, abnormal ZP:0011261 NADH oxidation decreased rate, abnormal ZP:0011262 trunk decreased occurrence blood circulation, abnormal ZP:0011263 intestine disrupted epithelial tube morphogenesis, abnormal ZP:0011264 anatomical space intestine increased amount, abnormal ZP:0011265 anatomical space intestine trabecular, abnormal ZP:0011266 epiphysis split bilaterally, abnormal ZP:0011267 parapineal organ process quality determination of left/right asymmetry in nervous system, abnormal ZP:0011268 epiphysis morphology, abnormal ZP:0011269 neural tube open, abnormal ZP:0011270 hypothalamus has fewer parts of type serotonin secreting cell, abnormal ZP:0011271 hypothalamus increased duration mitotic S phase, abnormal ZP:0011272 vH ionocyte process quality regulation of pH, abnormal ZP:0011274 olfactory epithelium organization quality, abnormal ZP:0011275 olfactory bulb glomerulus malformed, abnormal ZP:0011276 olfactory bulb glomerulus aplastic/hypoplastic, abnormal ZP:0011277 cell detached from neural tube, abnormal ZP:0011278 olfactory nerve formation process quality, abnormal ZP:0011279 cranial nerve I morphology, abnormal ZP:0011280 axon cranial nerve I mislocalised, abnormal ZP:0011281 olfactory epithelium shape, abnormal ZP:0011282 olfactory epithelium decreased size, abnormal ZP:0011283 olfactory bulb glomerulus morphology, abnormal ZP:0011284 cell-cell adhesion disrupted, abnormal ZP:0011285 posterior side dorsal fin fold decreased size, abnormal ZP:0011286 posterior side dorsal fin fold split medially, abnormal ZP:0011287 hindbrain neural keel shape, abnormal ZP:0011288 neuroepithelial cell displaced to fourth ventricle, abnormal ZP:0011289 heart development process quality, abnormal ZP:0011290 blood circulation decreased functionality, abnormal ZP:0011291 blood vessel hindbrain absent, abnormal ZP:0011292 blood vessel midbrain hindbrain boundary absent, abnormal ZP:0011293 dorsal region brain vasculature absent, abnormal ZP:0011294 heart decreased length, abnormal ZP:0011295 anterior cardinal vein absent, abnormal ZP:0011296 blood vessel optic tectum absent, abnormal ZP:0011297 blood vessel pharyngeal arch absent, abnormal ZP:0011299 somite amorphous, abnormal ZP:0011301 ventral spinal cord interneuron differentiation decreased occurrence, abnormal ZP:0011302 spinal cord oligodendrocyte cell differentiation decreased occurrence, abnormal ZP:0011303 spinal cord has fewer parts of type spinal cord interneuron, abnormal ZP:0011304 spinal cord has fewer parts of type Kolmer-Agduhr neuron, abnormal ZP:0011305 whole organism lacks all parts of type swim bladder, abnormal ZP:0011306 mandibular arch skeleton degenerate, abnormal ZP:0011307 somite antero-posteriorly flattened, abnormal ZP:0011309 central nervous system disorganized, abnormal ZP:0011310 neural crest increased size, abnormal ZP:0011311 whole organism elliptic, abnormal ZP:0011312 posterior region whole organism wholly dorsalized, abnormal ZP:0011313 posterior region whole organism truncated, abnormal ZP:0011314 eye displaced, abnormal ZP:0011315 locus coeruleus lacks parts or has fewer parts of type neuron, abnormal ZP:0011316 pharyngeal arch has fewer parts of type neuron, abnormal ZP:0011317 pharyngeal pouch decreased occurrence protein localization to plasma membrane, abnormal ZP:0011318 musculoskeletal movement irregular rhythm, abnormal ZP:0011319 musculoskeletal movement decreased coordination, abnormal ZP:0011320 musculoskeletal movement episodic, abnormal ZP:0011321 optic tectum increased frequency neuronal action potential, abnormal ZP:0011322 optic tectum irregular rhythm neuronal action potential, abnormal ZP:0011323 optic tectum decreased process quality regulation of neuronal action potential, abnormal ZP:0011324 whole organism process quality mitotic cell cycle, abnormal ZP:0011325 whole organism increased process quality cell population proliferation, abnormal ZP:0011326 cloaca morphology, abnormal ZP:0011327 embryonic digestive tract morphogenesis process quality, abnormal ZP:0011328 endoderm decreased process quality cell population proliferation, abnormal ZP:0011329 endoderm process quality cell migration, abnormal ZP:0011330 cell endoderm decreased amount, abnormal ZP:0011331 gut shape, abnormal ZP:0011332 liver primordium aplastic/hypoplastic, abnormal ZP:0011333 pancreas primordium aplastic/hypoplastic, abnormal ZP:0011334 endodermal cell delayed cell migration, abnormal ZP:0011335 endodermal cell process quality cell migration, abnormal ZP:0011336 cell migration to the midline involved in heart development delayed, abnormal ZP:0011337 cell migration to the midline involved in heart development process quality, abnormal ZP:0011338 endothelial cell ventral wall of dorsal aorta apoptotic, abnormal ZP:0011339 heart rudiment process quality cardioblast anterior-lateral migration, abnormal ZP:0011340 presumptive endocardium decreased process quality BMP signaling pathway involved in heart development, abnormal ZP:0011341 blood vessel morphogenesis decreased process quality, abnormal ZP:0011342 caudal vein plexus increased occurrence sprouting angiogenesis, abnormal ZP:0011343 angiogenic sprout caudal vein plexus increased amount, abnormal ZP:0011344 ventral wall of dorsal aorta has fewer parts of type hematopoietic stem cell, abnormal ZP:0011345 cell projection cardiac muscle cell transient, abnormal ZP:0011346 hindbrain increased process quality apoptotic process, abnormal ZP:0011347 midbrain increased process quality apoptotic process, abnormal ZP:0011348 horizontal myoseptum increased process quality apoptotic process, abnormal ZP:0011349 head increased process quality apoptotic process, abnormal ZP:0011350 trunk increased process quality apoptotic process, abnormal ZP:0011351 retroarticular absent, abnormal ZP:0011352 mesenchyme pharyngeal arch 1 decreased area, abnormal ZP:0011354 retinal ganglion cell decreased process quality neuron remodeling, abnormal ZP:0011355 axon retinal ganglion cell physical object quality, abnormal ZP:0011356 axon retinal ganglion cell increased branchiness, abnormal ZP:0011357 retinal ganglion cell has extra parts of type axon presynaptic active zone retinal ganglion cell, abnormal ZP:0011358 axon collateral retinal ganglion cell increased length, abnormal ZP:0011359 axon collateral retinal ganglion cell physical object quality, abnormal ZP:0011360 retinal ganglion cell occurrence collateral sprouting in absence of injury, abnormal ZP:0011361 retinal ganglion cell increased occurrence collateral sprouting in absence of injury, abnormal ZP:0011362 heart lacks all parts of type cell ventricular epicardium, abnormal ZP:0011363 proepicardial cluster absent, abnormal ZP:0011364 telencephalon lacks parts or has fewer parts of type dopaminergic neuron, abnormal ZP:0011365 heart decreased duration cardiac muscle cell action potential, abnormal ZP:0011366 whole organism spotted, abnormal ZP:0011367 whole organism desaturated yellow, abnormal ZP:0011368 whole organism has fewer parts of type melanocyte, abnormal ZP:0011369 whole organism lacks all parts of type xanthophore, abnormal ZP:0011370 whole organism has fewer parts of type xanthophore, abnormal ZP:0011371 head has fewer parts of type xanthophore, abnormal ZP:0011372 xanthophore head irregular spatial pattern, abnormal ZP:0011373 trunk lacks all parts of type xanthophore, abnormal ZP:0011374 trunk has fewer parts of type ventro-lateral region xanthophore, abnormal ZP:0011375 trunk has fewer parts of type dermis melanocyte, abnormal ZP:0011376 trunk lacks all parts of type dermis xanthophore, abnormal ZP:0011377 melanophore stripe trunk malformed, abnormal ZP:0011378 iridophore trunk mislocalised, abnormal ZP:0011379 anal fin spotted, abnormal ZP:0011380 anal fin has fewer parts of type melanophore stripe, abnormal ZP:0011381 melanophore stripe anal fin patchy, abnormal ZP:0011382 melanophore stripe low saturation, abnormal ZP:0011383 melanophore stripe irregular spatial pattern, abnormal ZP:0011384 melanophore stripe spotted, abnormal ZP:0011385 melanophore stripe absent, abnormal ZP:0011386 melanophore stripe patchy, abnormal ZP:0011387 xanthophore area density, abnormal ZP:0011388 dopaminergic neuron disrupted neuron development, abnormal ZP:0011389 hindbrain disrupted anterior/posterior pattern specification, abnormal ZP:0011390 axon hindbrain morphology, abnormal ZP:0011391 axon hindbrain mislocalised, abnormal ZP:0011392 radial glial cell hindbrain morphology, abnormal ZP:0011393 glial cell (sensu Vertebrata) floor plate spinal cord region amount, abnormal ZP:0011394 glial cell (sensu Vertebrata) floor plate spinal cord region increased size, abnormal ZP:0011395 endothelial cell migration delayed, abnormal ZP:0011396 filopodium assembly increased occurrence, abnormal ZP:0011397 regulation of blood vessel remodeling process quality, abnormal ZP:0011398 caudal vein plexus has extra parts of type endothelial cell filopodium endothelial cell, abnormal ZP:0011399 subintestinal vein has extra parts of type angiogenic sprout, abnormal ZP:0011400 glial cell projection trunk mislocalised, abnormal ZP:0011401 enteric neuron decreased amount, abnormal ZP:0011402 cellular calcium ion homeostasis process quality, abnormal ZP:0011403 skeletal myofibril assembly decreased process quality, abnormal ZP:0011404 skeletal muscle myofibril myotome malformed, abnormal ZP:0011405 skeletal muscle myofibril myotome disorganized, abnormal ZP:0011406 skeletal muscle myofibril myotome increased fragility, abnormal ZP:0011407 sarcolemma skeletal muscle cell increased permeability, abnormal ZP:0011408 trigeminal sensory neuron mislocalised, abnormal ZP:0011409 trigeminal sensory neuron process quality cell migration, abnormal ZP:0011410 lipid transport disrupted, abnormal ZP:0011411 lipid droplet liver decreased amount, abnormal ZP:0011412 liver decreased occurrence cell population proliferation, abnormal ZP:0011413 lipid droplet gall bladder decreased amount, abnormal ZP:0011414 lipid droplet intestine decreased amount, abnormal ZP:0011415 posterior lateral line nerve development process quality, abnormal ZP:0011416 spinal cord molecular quality, abnormal ZP:0011417 anatomical region motor nucleus of vagal nerve decreased size, abnormal ZP:0011418 somite 4 increased duration somitogenesis, abnormal ZP:0011419 intestinal bulb hypoplastic, abnormal ZP:0011420 vertebra 2 absent, abnormal ZP:0011421 intestine lacks all parts of type intestinal villus, abnormal ZP:0011422 intestine lacks all parts of type columnar/cuboidal epithelial cell, abnormal ZP:0011423 intestinal epithelium aplastic, abnormal ZP:0011424 Kupffer's vesicle increased diameter, abnormal ZP:0011425 Kupffer's vesicle process quality calcium-mediated signaling, abnormal ZP:0011426 optic cup flattened, abnormal ZP:0011427 hyaloid vessel delayed vasculature development, abnormal ZP:0011428 hyaloid vessel process quality vasculature development, abnormal ZP:0011429 spinal cord has fewer parts of type radial glial cell, abnormal ZP:0011430 central canal increased size, abnormal ZP:0011431 endoderm mislocalised, abnormal ZP:0011432 pancreatic bud split medially, abnormal ZP:0011433 extracellular matrix cell increased size, abnormal ZP:0011434 extracellular matrix cell organization quality, abnormal ZP:0011435 endothelial cell mislocalised, abnormal ZP:0011436 macula utricle physical object quality, abnormal ZP:0011437 anterior region otic vesicle physical object quality, abnormal ZP:0011438 lateral crista primordium physical object quality, abnormal ZP:0011439 posterior crista primordium physical object quality, abnormal ZP:0011440 semicircular canal physical object quality, abnormal ZP:0011441 posterior crista physical object quality, abnormal ZP:0011442 anterior crista physical object quality, abnormal ZP:0011443 primordial germ cell apoptotic, abnormal ZP:0011444 thoracic duct decreased process quality lymphangiogenesis, abnormal ZP:0011445 postoptic commissure defasciculated, abnormal ZP:0011446 postoptic commissure disrupted commissural neuron axon guidance, abnormal ZP:0011447 forebrain disrupted commissural neuron axon guidance, abnormal ZP:0011448 cranial nerve II disrupted commissural neuron axon guidance, abnormal ZP:0011449 anterior commissure defasciculated, abnormal ZP:0011450 anterior commissure disrupted commissural neuron axon guidance, abnormal ZP:0011454 anterior region endoderm increased width, abnormal ZP:0011455 anterior region endoderm perforate, abnormal ZP:0011456 endoderm process quality convergent extension, abnormal ZP:0011457 larval locomotory behavior increased rate, abnormal ZP:0011458 axon primary motor neuron increased branchiness, abnormal ZP:0011460 cellular senescence increased process quality, abnormal ZP:0011461 autophagosome maturation process quality, abnormal ZP:0011462 cell accumulation autophagosome perinuclear region of cytoplasm cell, abnormal ZP:0011463 cell accumulation autolysosome perinuclear region of cytoplasm cell, abnormal ZP:0011464 astrocyte postoptic commissure mislocalised, abnormal ZP:0011465 astrocyte forebrain morphology, abnormal ZP:0011466 astrocyte anterior commissure mislocalised, abnormal ZP:0011467 caudal fin lacks parts or has fewer parts of type dorsal root ganglion, abnormal ZP:0011468 pharyngeal arch 1 has fewer parts of type chondrocyte, abnormal ZP:0011469 chondrocyte pharyngeal arch 1 shape, abnormal ZP:0011470 pharyngeal arch 3-7 increased process quality cell death, abnormal ZP:0011471 glial cell (sensu Vertebrata) hindbrain mislocalised, abnormal ZP:0011472 spinal cord lacks all parts of type radial glial cell ventricular zone, abnormal ZP:0011473 cranial nerve II absent, abnormal ZP:0011474 trunk has fewer parts of type glial cell (sensu Vertebrata) nerve, abnormal ZP:0011475 trunk has fewer parts of type axon motor neuron, abnormal ZP:0011476 nerve trunk truncated, abnormal ZP:0011477 spinal cord has extra parts of type radial glial cell ventricular zone, abnormal ZP:0011478 neural tube has extra parts of type radial glial cell, abnormal ZP:0011479 neural tube increased process quality apoptotic process, abnormal ZP:0011480 forebrain ventricle has extra parts of type astrocyte, abnormal ZP:0011481 CoSA decreased amount, abnormal ZP:0011482 VeLD process quality axon guidance, abnormal ZP:0011483 Kolmer-Agduhr neuron process quality axon guidance, abnormal ZP:0011484 radial glial cell has fewer parts of type aster radial glial cell, abnormal ZP:0011485 Kupffer's vesicle increased distance nucleus apical plasma membrane Kupffer's vesicle, abnormal ZP:0011487 Kupffer's vesicle detached from ciliary basal body apical plasma membrane Kupffer's vesicle, abnormal ZP:0011488 cell ectoderm shape, abnormal ZP:0011489 ectoderm orientation cell ectoderm, abnormal ZP:0011490 floor plate process quality establishment of planar polarity, abnormal ZP:0011491 cell notochord shape, abnormal ZP:0011492 notochord orientation cell notochord, abnormal ZP:0011493 extracellular matrix cell decreased size, abnormal ZP:0011494 pronephric glomerulus development process quality, abnormal ZP:0011495 turning behavior process quality, abnormal ZP:0011496 exploration behavior process quality, abnormal ZP:0011497 locomotory exploration behavior process quality, abnormal ZP:0011498 forebrain deformed, abnormal ZP:0011499 glial cell (sensu Vertebrata) nerve branched, abnormal ZP:0011500 myofibril assembly delayed, abnormal ZP:0011501 myofibril somite morphology, abnormal ZP:0011502 myofibril somite loose, abnormal ZP:0011503 vasculature development process quality, abnormal ZP:0011504 basal communicating artery detached from primordial midbrain channel, abnormal ZP:0011505 posterior margin midbrain increased width, abnormal ZP:0011506 central region optic tectum proliferative, abnormal ZP:0011507 optic tectum increased occurrence apoptotic process, abnormal ZP:0011508 optic tectum increased occurrence cell proliferation in midbrain, abnormal ZP:0011509 optic tectum process quality regulation of neurogenesis, abnormal ZP:0011511 postoptic commissure has fewer parts of type astrocyte, abnormal ZP:0011512 anterior commissure has fewer parts of type astrocyte, abnormal ZP:0011513 central nervous system morphogenesis decreased process quality, abnormal ZP:0011514 neural crest poorly differentiated, abnormal ZP:0011515 neuroectoderm retina necrotic, abnormal ZP:0011516 head lacks parts or has fewer parts of type pharyngeal arch cartilage, abnormal ZP:0011517 neural tube necrotic, abnormal ZP:0011518 pharyngeal arch necrotic, abnormal ZP:0011519 pharyngeal arch 1 fused with pharyngeal arch 2, abnormal ZP:0011520 chondrocyte mislocalised, abnormal ZP:0011521 pancreas molecular quality, abnormal ZP:0011522 intestine molecular quality, abnormal ZP:0011524 myelin sheath lateral line nerve absent, abnormal ZP:0011527 aortic arch malformed, abnormal ZP:0011528 cell projection organization disrupted, abnormal ZP:0011529 pseudopodium organization disrupted, abnormal ZP:0011530 epiboly involved in gastrulation with mouth forming second process quality, abnormal ZP:0011531 convergent extension involved in axis elongation decreased process quality, abnormal ZP:0011532 dorsal convergence decreased process quality, abnormal ZP:0011533 cell-cell adhesion involved in gastrulation decreased occurrence, abnormal ZP:0011534 DEL circular, abnormal ZP:0011535 DEL detached from EVL, abnormal ZP:0011536 axis whole organism increased width, abnormal ZP:0011537 filamentous actin blastoderm increased amount, abnormal ZP:0011538 neutrophil migration increased occurrence, abnormal ZP:0011539 enteric nervous system delayed neuron migration, abnormal ZP:0011540 enteric nervous system decreased rate neuron migration, abnormal ZP:0011541 enteric nervous system decreased occurrence cell division, abnormal ZP:0011542 caudal fin malformed, abnormal ZP:0011543 ventral wall of dorsal aorta increased process quality apoptotic process, abnormal ZP:0011544 ventral wall of dorsal aorta decreased process quality Notch signaling pathway, abnormal ZP:0011545 cell posterior lateral mesoderm shape, abnormal ZP:0011546 endothelial cell decreased process quality Notch signaling pathway, abnormal ZP:0011547 neural tube decreased width, abnormal ZP:0011548 neural tube asymmetrical, abnormal ZP:0011549 ventricular system closed, abnormal ZP:0011550 intersegmental vein hypoplastic, abnormal ZP:0011551 cranial vasculature aplastic, abnormal ZP:0011552 cranial vasculature process quality angiogenesis, abnormal ZP:0011553 intersegmental vessel process quality angiogenesis, abnormal ZP:0011554 pronephric glomerulus morphogenesis decreased process quality, abnormal ZP:0011555 slit diaphragm pronephric podocyte malformed, abnormal ZP:0011556 pronephric glomerular capsule cystic, abnormal ZP:0011557 eye process quality pigmentation, abnormal ZP:0011558 dorsal aorta decreased distance caudal vein, abnormal ZP:0011559 posterior cardinal vein increased occurrence endothelial cell apoptotic process, abnormal ZP:0011560 cytokinesis process quality, abnormal ZP:0011561 cortical granule exocytosis decreased process quality, abnormal ZP:0011562 blastomere has extra parts of type nucleus blastomere, abnormal ZP:0011563 oocyte accumulation secretory granule oocyte, abnormal ZP:0011564 oocyte stage III has extra parts of type cortical granule oocyte stage III, abnormal ZP:0011565 lysosome oocyte stage III broken, abnormal ZP:0011566 cytoplasm unfertilized egg opaque, abnormal ZP:0011567 egg chorion unfertilized egg elevation, abnormal ZP:0011568 egg chorion fertilized egg elevation, abnormal ZP:0011569 spinal cord lacks parts or has fewer parts of type oligodendrocyte, abnormal ZP:0011570 spinal cord lacks all parts of type primary motor neuron, abnormal ZP:0011571 JNK cascade decreased process quality, abnormal ZP:0011572 convergent extension involved in neural plate elongation process quality, abnormal ZP:0011573 mediolateral intercalation process quality, abnormal ZP:0011574 hypoblast process quality convergent extension, abnormal ZP:0011575 caudal fin folded, abnormal ZP:0011576 hindbrain increased process quality cell death, abnormal ZP:0011577 intersegmental vein increased amount, abnormal ZP:0011578 intersegmental artery decreased amount, abnormal ZP:0011579 post-vent region absent blood circulation, abnormal ZP:0011580 caudal vein plexus increased size, abnormal ZP:0011581 post-vent vasculature malformed, abnormal ZP:0011582 mandibular arch skeleton flattened, abnormal ZP:0011583 memory decreased process quality, abnormal ZP:0011584 intersegmental vein arrested, abnormal ZP:0011585 intersegmental vein shortened, abnormal ZP:0011586 intersegmental vein lacks parts or has fewer parts of type endothelial cell, abnormal ZP:0011587 intersegmental vein delayed sprouting angiogenesis, abnormal ZP:0011588 intersegmental vein disrupted sprouting angiogenesis, abnormal ZP:0011589 intersegmental vein disrupted blood circulation, abnormal ZP:0011590 intersegmental vein decreased occurrence cell population proliferation, abnormal ZP:0011591 motor neuron morphology, abnormal ZP:0011592 motor neuron broken, abnormal ZP:0011593 germ cell migration premature, abnormal ZP:0011594 establishment of mitotic spindle orientation process quality, abnormal ZP:0011595 cilium mesoderm aplastic, abnormal ZP:0011596 neural plate process quality establishment of mitotic spindle orientation, abnormal ZP:0011597 pronephros lacks parts or has fewer parts of type multi-ciliated epithelial cell cilium multi-ciliated epithelial cell, abnormal ZP:0011598 neural tube lacks all parts of type axoneme neural tube, abnormal ZP:0011599 xanthophore differentiation delayed, abnormal ZP:0011600 melanophore stripe malformed, abnormal ZP:0011601 midbrain hindbrain boundary increased angle to basal side epithelium brain, abnormal ZP:0011602 cell midbrain hindbrain boundary increased length, abnormal ZP:0011603 neuroepithelial cell decreased accumulation actin filament apical region midbrain hindbrain boundary, abnormal ZP:0011604 ceratohyal cartilage shape, abnormal ZP:0011605 retina disrupted cell population proliferation, abnormal ZP:0011606 pectoral fin shortened, abnormal ZP:0011607 optic fissure unfused from anatomical margin anatomical margin optic fissure, abnormal ZP:0011608 exonucleolytic trimming to generate mature 3'-end of 5.8S rRNA from tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA) disrupted, abnormal ZP:0011609 fourth ventricle increased volume, abnormal ZP:0011610 integument discolored, abnormal ZP:0011611 large ribosomal subunit whole organism decreased amount, abnormal ZP:0011612 cytosolic ribosome whole organism decreased amount, abnormal ZP:0011613 forebrain ventricle increased volume, abnormal ZP:0011614 posterior chamber swim bladder uninflated, abnormal ZP:0011615 gut has fewer parts of type enteric neuron, abnormal ZP:0011616 optic tectum increased distance optic tectum, abnormal ZP:0011617 blood island has fewer parts of type neutrophil, abnormal ZP:0011618 thigmotaxis decreased strength, abnormal ZP:0011619 acetylcholine-gated channel complex skeletal muscle cell position, abnormal ZP:0011620 slow muscle cell decreased magnitude neuromuscular synaptic transmission, abnormal ZP:0011621 acetylcholine-gated channel complex fast muscle cell non-functional, abnormal ZP:0011622 fast muscle cell arrested neuromuscular synaptic transmission, abnormal ZP:0011623 vesicle localization process quality, abnormal ZP:0011624 eye decreased area, abnormal ZP:0011625 cell head apoptotic, abnormal ZP:0011626 cell trunk apoptotic, abnormal ZP:0011627 pigment cell decreased perimeter, abnormal ZP:0011628 cell projection pigment cell increased amount, abnormal ZP:0011629 vesicle neuron decreased speed, abnormal ZP:0011630 renal tubule dilated, abnormal ZP:0011631 renal glomerulus disorganized, abnormal ZP:0011632 renal glomerulus distended, abnormal ZP:0011633 photoreceptor outer segment photoreceptor cell absent, abnormal ZP:0011635 kidney development process quality, abnormal ZP:0011636 photoreceptor inner segment retinal cone cell physical object quality, abnormal ZP:0011637 retinal cone cell has extra parts of type photoreceptor inner segment cytoplasmic vesicle retinal cone cell, abnormal ZP:0011638 Golgi apparatus retinal cone cell morphology, abnormal ZP:0011639 Golgi apparatus retinal cone cell disorganized, abnormal ZP:0011640 Golgi apparatus retinal cone cell broken, abnormal ZP:0011641 retinal cone cell process quality autophagy, abnormal ZP:0011642 retinal cone cell process quality lysosome organization, abnormal ZP:0011643 retinal cone cell process quality endosomal transport, abnormal ZP:0011644 retinal cone cell decreased process quality maintenance of Golgi location, abnormal ZP:0011645 ribosomal protein S6 kinase activity increased occurrence, abnormal ZP:0011646 protein kinase B signaling decreased occurrence, abnormal ZP:0011647 ventral spinal cord development process quality, abnormal ZP:0011648 ventral region spinal cord poorly differentiated, abnormal ZP:0011649 spinal cord decreased process quality smoothened signaling pathway, abnormal ZP:0011650 neural tube decreased process quality smoothened signaling pathway, abnormal ZP:0011651 epithelium pronephric duct morphology, abnormal ZP:0011652 ventral mesoderm increased occurrence cell population proliferation, abnormal ZP:0011653 eye photoreceptor cell differentiation delayed, abnormal ZP:0011655 axon optic cup misrouted, abnormal ZP:0011656 ciliary marginal zone disrupted cell population proliferation, abnormal ZP:0011657 hemopoiesis delayed, abnormal ZP:0011658 heart formation delayed, abnormal ZP:0011659 caudal fin increased process quality apoptotic process, abnormal ZP:0011660 pharynx increased process quality apoptotic process, abnormal ZP:0011661 palatoquadrate arch hypoplastic, abnormal ZP:0011662 ventral mandibular arch decreased process quality cell population proliferation, abnormal ZP:0011663 axon posterior lateral line nerve mislocalised, abnormal ZP:0011664 intestine has fewer parts of type enteroendocrine cell, abnormal ZP:0011665 intestine increased process quality cell population proliferation, abnormal ZP:0011666 ATP biosynthetic process disrupted, abnormal ZP:0011667 mitochondrion myocardium disorganized, abnormal ZP:0011668 mitochondrial crista myocardium decreased amount, abnormal ZP:0011669 mitochondrion skeletal muscle structure, abnormal ZP:0011670 mitochondrion skeletal muscle vacuolated, abnormal ZP:0011671 mitochondrial crista skeletal muscle decreased amount, abnormal ZP:0011672 medial rectus decreased thickness, abnormal ZP:0011673 adductor mandibulae decreased thickness, abnormal ZP:0011674 adductor mandibulae disrupted regulation of myofibril size, abnormal ZP:0011675 muscle cell adductor mandibulae decreased size, abnormal ZP:0011676 interhyoideus decreased thickness, abnormal ZP:0011677 interhyoideus disrupted regulation of myofibril size, abnormal ZP:0011678 muscle cell interhyoideus decreased size, abnormal ZP:0011679 dorsal aorta disorganized, abnormal ZP:0011680 radial glial cell hindbrain mislocalised, abnormal ZP:0011681 cranial nerve II increased thickness, abnormal ZP:0011682 posterior cardinal vein disorganized, abnormal ZP:0011683 trunk decreased process quality pigmentation, abnormal ZP:0011684 vascular sprouts intersegmental vessel mislocalised, abnormal ZP:0011685 retinal ganglion cell increased accumulation axon ventral region retina, abnormal ZP:0011686 whole organism lacks parts or has fewer parts of type hyosymplectic cartilage, abnormal ZP:0011687 pharyngeal endoderm apoptotic, abnormal ZP:0011688 pharyngeal arch 6 skeleton decreased size, abnormal ZP:0011689 pharyngeal arch 5 skeleton decreased size, abnormal ZP:0011690 pineal complex process quality circadian regulation of gene expression, abnormal ZP:0011691 iridophore differentiation decreased occurrence, abnormal ZP:0011692 eye has fewer parts of type iridophore, abnormal ZP:0011693 caudal fin has fewer parts of type iridophore, abnormal ZP:0011694 trunk lacks parts or has fewer parts of type melanophore stripe, abnormal ZP:0011695 trunk has fewer parts of type melanophore stripe, abnormal ZP:0011696 trunk lacks all parts of type dermis iridophore, abnormal ZP:0011697 anal fin has fewer parts of type iridophore, abnormal ZP:0011698 melanocyte increased process quality cell death, abnormal ZP:0011699 cell midbrain hindbrain boundary increased width, abnormal ZP:0011700 cell midbrain hindbrain boundary increased area, abnormal ZP:0011701 inner ear receptor cell stereocilium organization decreased process quality, abnormal ZP:0011702 stereocilium bundle hair cell direction, abnormal ZP:0011703 cell projection hypoblast direction, abnormal ZP:0011704 cell projection hypoblast physical object quality, abnormal ZP:0011705 liver increased process quality apoptotic process, abnormal ZP:0011706 forebrain flattened, abnormal ZP:0011707 retina has fewer parts of type retinal ganglion cell, abnormal ZP:0011708 neuromast displaced, abnormal ZP:0011709 cranial nerve II has fewer parts of type axon retinal ganglion cell, abnormal ZP:0011710 optic tectum has fewer parts of type neuron projection retinal ganglion cell, abnormal ZP:0011711 head altered number of neuromast, abnormal ZP:0011712 anterior region floor plate deformed, abnormal ZP:0011713 hypothalamus deformed, abnormal ZP:0011714 fourth ventricle deformed, abnormal ZP:0011715 cranial nerve III absent, abnormal ZP:0011716 cranial nerve II immature, abnormal ZP:0011717 optic tectum mislocalised anteriorly, abnormal ZP:0011718 cranial nerve IV absent, abnormal ZP:0011719 dorsal thalamus deformed, abnormal ZP:0011720 pectoral fin aplastic/hypoplastic, abnormal ZP:0011721 pericardial cavity inflated, abnormal ZP:0011722 retinal ganglion cell immature, abnormal ZP:0011723 neuron projection retinal ganglion cell immature, abnormal ZP:0011725 ectodermal placode development decreased process quality, abnormal ZP:0011728 head lacks all parts of type glossopharyngeal ganglion, abnormal ZP:0011729 head lacks all parts of type vagal ganglion 1, abnormal ZP:0011730 head lacks all parts of type vagal ganglion 2, abnormal ZP:0011731 head lacks all parts of type vagal ganglion 3, abnormal ZP:0011733 facial placode poorly differentiated, abnormal ZP:0011735 glossopharyngeal placode poorly differentiated, abnormal ZP:0011736 glossopharyngeal placode decreased occurrence neurogenesis, abnormal ZP:0011737 vagal placode 1 poorly differentiated, abnormal ZP:0011738 vagal placode 1 decreased occurrence neurogenesis, abnormal ZP:0011739 vagal placode 2 poorly differentiated, abnormal ZP:0011740 vagal placode 2 decreased occurrence neurogenesis, abnormal ZP:0011741 vagal placode 3 poorly differentiated, abnormal ZP:0011742 vagal placode 3 decreased occurrence neurogenesis, abnormal ZP:0011743 vagal placode 4 poorly differentiated, abnormal ZP:0011745 neuroblast (sensu Vertebrata) vagal placode 4 mislocalised ventrally, abnormal ZP:0011747 heart primordium decreased process quality cell population proliferation, abnormal ZP:0011748 pharyngeal pouch absent, abnormal ZP:0011749 pharyngeal pouch process quality pharyngeal system development, abnormal ZP:0011750 blood island has fewer parts of type macrophage, abnormal ZP:0011751 caudal fin has fewer parts of type axon caudal fin, abnormal ZP:0011752 forebrain shape, abnormal ZP:0011753 blood vessel endothelial cell proliferation involved in sprouting angiogenesis increased occurrence, abnormal ZP:0011754 angiogenic sprout intersegmental vessel increased amount, abnormal ZP:0011755 angiogenic sprout mislocalised, abnormal ZP:0011756 bulbus arteriosus development process quality, abnormal ZP:0011757 atrium morphology, abnormal ZP:0011758 whole organism lacks parts or has fewer parts of type portion of tissue, abnormal ZP:0011759 melanocyte process quality neural crest cell migration, abnormal ZP:0011760 myelination decreased process quality, abnormal ZP:0011762 photoreceptor cell pineal complex increased amount, abnormal ZP:0011763 parapineal organ process quality epithalamus development, abnormal ZP:0011764 parapineal organ process quality determination of left/right asymmetry in diencephalon, abnormal ZP:0011766 pronephric duct branched, abnormal ZP:0011767 pronephric duct undulate, abnormal ZP:0011768 pronephric duct in contact with pronephric duct, abnormal ZP:0011769 habenula decreased process quality cytoskeleton organization, abnormal ZP:0011770 filamentous actin habenula disorganized, abnormal ZP:0011775 tooth mineralization decreased process quality, abnormal ZP:0011776 opercle decreased area bone mineralization, abnormal ZP:0011777 tooth 4V absent tooth mineralization, abnormal ZP:0011778 tooth 4V disrupted tooth mineralization, abnormal ZP:0011779 ceratobranchial cartilage absent ossification, abnormal ZP:0011780 ceratobranchial cartilage disrupted ossification, abnormal ZP:0011781 dental epithelium lacks parts or has fewer parts of type tooth placode, abnormal ZP:0011784 trunk neural crest cell migration decreased process quality, abnormal ZP:0011785 swim bladder dysplastic, abnormal ZP:0011786 posterior region whole organism curved, abnormal ZP:0011787 cranial neural crest condensed, abnormal ZP:0011788 cranial neural crest cell broadly articulated with cranial neural crest cell, abnormal ZP:0011789 trunk neural crest cell shape, abnormal ZP:0011790 trunk neural crest cell disorganized, abnormal ZP:0011791 trunk neural crest cell broadly articulated with trunk neural crest cell, abnormal ZP:0011792 trunk neural crest cell disrupted contact inhibition, abnormal ZP:0011793 oligodendrocyte loose, abnormal ZP:0011794 cardiac muscle cell has fewer parts of type cell projection cardiac muscle cell, abnormal ZP:0011795 liver neoplastic, spontaneous, abnormal ZP:0011796 adenoma liver present, abnormal ZP:0011797 intestine neoplastic, spontaneous, abnormal ZP:0011798 adenoma intestine present, abnormal ZP:0011799 adenomatous polyp intestine present, abnormal ZP:0011800 posterior lateral line lacks all parts of type myelinating Schwann cell, abnormal ZP:0011801 posterior lateral line arrested myelination in peripheral nervous system, abnormal ZP:0011802 thoracic duct agenesis, abnormal ZP:0011803 cell notochord malformed, abnormal ZP:0011804 DEL increased thickness, abnormal ZP:0011805 skeletal muscle disorganized, abnormal ZP:0011806 Notch signaling pathway decreased occurrence, abnormal ZP:0011807 presumptive neural retina molecular quality, abnormal ZP:0011808 pigment cell mislocalised, abnormal ZP:0011809 anal fin has fewer parts of type melanocyte, abnormal ZP:0011810 melanophore stripe decreased pigmentation, abnormal ZP:0011811 cholesterol homeostasis process quality, abnormal ZP:0011812 posterior cardinal vein fatty, abnormal ZP:0011813 vascular endothelium posterior cardinal vein increased permeability, abnormal ZP:0011814 posterior region notochord malformed, abnormal ZP:0011815 atrium decreased thickness, abnormal ZP:0011816 myotome condensed, abnormal ZP:0011817 myotome deformed, abnormal ZP:0011818 presumptive atrium heart tube elongated, abnormal ZP:0011819 ventricular myocardium disorganized, abnormal ZP:0011820 skeletal muscle structure, cavities, abnormal ZP:0011821 endocytosis decreased process quality, abnormal ZP:0011822 nodal signaling pathway decreased process quality, abnormal ZP:0011823 shield absent, abnormal ZP:0011824 secondary lysosome EVL increased amount, abnormal ZP:0011825 cell EVL morphology, abnormal ZP:0011826 blastoderm separated from yolk, abnormal ZP:0011827 cardiac ventricle has extra parts of type cell, abnormal ZP:0011828 atrium has extra parts of type cell, abnormal ZP:0011829 brain lacks parts or has fewer parts of type ventricular system, abnormal ZP:0011830 primary motor neuron brain spatial pattern, abnormal ZP:0011831 primary motor neuron brain decreased amount, abnormal ZP:0011832 spinal cord has fewer parts of type primary motor neuron, abnormal ZP:0011833 primary motor neuron spinal cord spatial pattern, abnormal ZP:0011834 head increased occurrence cell death, abnormal ZP:0011835 trunk increased occurrence apoptotic process, abnormal ZP:0011836 primary motor neuron irregular spatial pattern, abnormal ZP:0011837 posterior cardinal vein lacks parts or has fewer parts of type lymphangiogenic sprout, abnormal ZP:0011838 lymphatic system cranial vasculature decreased functionality, abnormal ZP:0011839 intestine decreased process quality lymphangiogenesis, abnormal ZP:0011840 lymph vasculature absent, abnormal ZP:0011841 facial lymphatic vessel decreased process quality lymphangiogenesis, abnormal ZP:0011842 endothelial cell lymph vessel endothelium decreased amount, abnormal ZP:0011843 lymphangioblast lymphangioblast cord decreased amount, abnormal ZP:0011844 lipoprotein biosynthetic process disrupted, abnormal ZP:0011845 MAP kinase kinase activity disrupted, abnormal ZP:0011846 dorsal aorta development disrupted, abnormal ZP:0011847 cranial blood vessel morphology, abnormal ZP:0011848 oligodendrocyte development process quality, abnormal ZP:0011849 central nervous system myelination decreased process quality, abnormal ZP:0011850 oligodendrocyte hindbrain poorly differentiated, abnormal ZP:0011852 spinal cord has fewer parts of type oligodendrocyte spinal cord, abnormal ZP:0011853 oligodendrocyte spinal cord mislocalised dorsally, abnormal ZP:0011854 oligodendrocyte spinal cord poorly differentiated, abnormal ZP:0011855 spinal cord dorsal to oligodendrocyte dorsal longitudinal fasciculus, abnormal ZP:0011856 spinal cord far from oligodendrocyte dorsal longitudinal fasciculus, abnormal ZP:0011857 dorsal longitudinal fasciculus decreased process quality axon ensheathment in central nervous system, abnormal ZP:0011858 oligodendrocyte mislocalised dorsally, abnormal ZP:0011859 axon trigeminal ganglion decreased branchiness, abnormal ZP:0011860 trigeminal ganglion decreased occurrence collateral sprouting, abnormal ZP:0011861 early endosome Rohon-Beard neuron mislocalised, abnormal ZP:0011862 Rohon-Beard neuron decreased occurrence anterograde axonal transport, abnormal ZP:0011863 growth cone Rohon-Beard neuron decreased volume, abnormal ZP:0011864 growth cone Rohon-Beard neuron decreased branchiness, abnormal ZP:0011865 Rohon-Beard neuron decreased occurrence collateral sprouting, abnormal ZP:0011866 Rohon-Beard neuron increased rate axon extension, abnormal ZP:0011867 Rohon-Beard neuron decreased occurrence retrograde transport, endosome to plasma membrane, abnormal ZP:0011869 lens detached from retina, abnormal ZP:0011870 retinal neural layer malformed, abnormal ZP:0011871 ciliated cell pronephric duct irregular density, abnormal ZP:0011872 cloaca cystic, abnormal ZP:0011873 trunk neural crest cell migration delayed, abnormal ZP:0011874 neural crest cell migration involved in autonomic nervous system development disrupted, abnormal ZP:0011875 retina has fewer parts of type cell, abnormal ZP:0011876 retina process quality mitotic cell cycle, abnormal ZP:0011877 retina decreased process quality apoptotic process, abnormal ZP:0011878 retina decreased process quality exit from mitosis, abnormal ZP:0011879 vagal neural crest decreased size, abnormal ZP:0011880 cranial neural crest decreased size, abnormal ZP:0011881 enteric neuron decreased length, abnormal ZP:0011882 enteric neuron mislocalised, abnormal ZP:0011883 slow muscle cell detached from vertical myoseptum, abnormal ZP:0011884 iridophore eye morphology, abnormal ZP:0011885 melanophore stripe trunk decreased amount, abnormal ZP:0011886 melanophore stripe distributed, abnormal ZP:0011887 optic nerve development decreased process quality, abnormal ZP:0011888 embryonic camera-type eye development decreased process quality, abnormal ZP:0011889 cranial nerve II decreased volume, abnormal ZP:0011890 fin increased length, abnormal ZP:0011891 caudal fin asymmetrical, abnormal ZP:0011892 caudal fin drooping, abnormal ZP:0011893 lepidotrichium increased branchiness, abnormal ZP:0011894 lepidotrichium segment length, abnormal ZP:0011895 lepidotrichium segment increased amount, abnormal ZP:0011896 lepidotrichium segment increased variability of size, abnormal ZP:0011897 blood increased process quality apoptotic process, abnormal ZP:0011898 mitochondrion whole organism morphology, abnormal ZP:0011899 Golgi apparatus whole organism morphology, abnormal ZP:0011900 whole organism increased occurrence autophagy, abnormal ZP:0011901 nucleate erythrocyte has extra parts of type autophagosome nucleate erythrocyte, abnormal ZP:0011902 nucleate erythrocyte has extra parts of type autolysosome nucleate erythrocyte, abnormal ZP:0011903 nucleate erythrocyte increased occurrence autophagy, abnormal ZP:0011904 muscle increased distance muscle cell, abnormal ZP:0011905 muscle cell skeletal muscle loose, abnormal ZP:0011906 skeletal muscle cell undulate, abnormal ZP:0011907 fast muscle cell decreased width, abnormal ZP:0011908 blood circulation decreased speed, abnormal ZP:0011909 heart disrupted calcium-mediated signaling, abnormal ZP:0011910 endocardial cushion lacks parts or has fewer parts of type cardiac muscle cell, abnormal ZP:0011911 cell whole organism decreased amount, abnormal ZP:0011912 brain agenesis, abnormal ZP:0011913 liver arrested cell cycle, abnormal ZP:0011914 inner ear increased process quality cell death, abnormal ZP:0011915 mandibular arch skeleton increased process quality cell death, abnormal ZP:0011916 nucleus hepatocyte increased size, abnormal ZP:0011917 hepatocyte decreased process quality DNA methylation, abnormal ZP:0011919 pronephric tubule decreased process quality ciliary basal body organization, abnormal ZP:0011920 ciliary basal body pronephric tubule mislocalised, abnormal ZP:0011921 pronephric tubule separated from ciliary basal body apical plasma membrane pronephric tubule, abnormal ZP:0011922 ceratohyal cartilage misaligned with ceratohyal cartilage, abnormal ZP:0011923 pharyngeal arch cartilage misaligned with pharyngeal arch cartilage, abnormal ZP:0011924 skeletal muscle cell increased process quality apoptotic process, abnormal ZP:0011925 cleavage in ITS2 between 5.8S rRNA and LSU-rRNA of tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA) disrupted, abnormal ZP:0011926 nuclear pore retinal inner nuclear layer malformed, abnormal ZP:0011927 endoplasmic reticulum retinal inner nuclear layer morphology, abnormal ZP:0011928 nuclear pore liver malformed, abnormal ZP:0011929 liver decreased process quality poly(A)+ mRNA export from nucleus, abnormal ZP:0011930 pancreas decreased process quality poly(A)+ mRNA export from nucleus, abnormal ZP:0011931 retinal pigmented epithelium distended, abnormal ZP:0011932 nuclear pore retina malformed, abnormal ZP:0011933 retina increased process quality apoptotic process, abnormal ZP:0011934 retina decreased process quality poly(A)+ mRNA export from nucleus, abnormal ZP:0011935 nuclear pore intestine malformed, abnormal ZP:0011936 intestine decreased process quality poly(A)+ mRNA export from nucleus, abnormal ZP:0011937 nuclear pore retinal outer nuclear layer malformed, abnormal ZP:0011938 endoplasmic reticulum retinal outer nuclear layer morphology, abnormal ZP:0011939 nuclear pore retinal ganglion cell malformed, abnormal ZP:0011940 endoplasmic reticulum retinal ganglion cell morphology, abnormal ZP:0011941 hypothalamus has extra parts of type posterior side dopaminergic neuron, abnormal ZP:0011942 lens shape, abnormal ZP:0011943 atrial cardiac muscle cell action potential increased duration, abnormal ZP:0011944 atrioventricular ring aplastic, abnormal ZP:0011945 blood accumulation cardiac ventricle, abnormal ZP:0011946 heart vasculature non-functional, abnormal ZP:0011947 vasculature malformed, abnormal ZP:0011948 posterior lateral line molecular quality, abnormal ZP:0011949 posterior side yolk decreased size, abnormal ZP:0011950 semicircular canal absent, abnormal ZP:0011951 hindbrain increased occurrence cell proliferation in hindbrain ventricular zone, abnormal ZP:0011952 whole organism viable, abnormal ZP:0011953 mRNA processing process quality, abnormal ZP:0011954 head muscle malformed, abnormal ZP:0011955 skeletal muscle cell loose, abnormal ZP:0011956 endothelial cell increased rate cell population proliferation, abnormal ZP:0011957 Notch signaling pathway increased occurrence, abnormal ZP:0011958 neurogenesis decreased occurrence, abnormal ZP:0011959 negative regulation of neurogenesis increased occurrence, abnormal ZP:0011960 neural crest cell migration involved in heart formation process quality, abnormal ZP:0011961 common cardinal vein decreased process quality blood circulation, abnormal ZP:0011962 slow muscle cell somite disorganized, abnormal ZP:0011963 fast muscle cell somite decreased amount, abnormal ZP:0011964 posterior lateral line nerve misrouted, abnormal ZP:0011965 muscle fin musculature hypoplastic, abnormal ZP:0011966 muscle trunk musculature hypoplastic, abnormal ZP:0011967 fast muscle cell myotome decreased amount, abnormal ZP:0011968 muscle hypaxial myotome region hypoplastic, abnormal ZP:0011969 muscle hypaxial myotome region malformed, abnormal ZP:0011970 myoseptum hypoplastic, abnormal ZP:0011971 whole organism lacks all parts of type horizontal myoseptum, abnormal ZP:0011972 melanophore stripe trunk branched, abnormal ZP:0011973 melanophore stripe trunk curved, abnormal ZP:0011974 posterior lateral line primordium misrouted, abnormal ZP:0011975 sternohyoid hypoplastic, abnormal ZP:0011976 somite decreased diameter, abnormal ZP:0011977 skeletal muscle cell irregular spatial pattern, abnormal ZP:0011978 skeletal muscle cell decussate, abnormal ZP:0011979 skeletal muscle cell misaligned with skeletal muscle cell, abnormal ZP:0011980 macrophage aplastic, abnormal ZP:0011981 protein localization to synapse disrupted, abnormal ZP:0011982 synaptic vesicle recycling via endosome disrupted, abnormal ZP:0011983 terminal bouton hair cell anterior macula increased amount, abnormal ZP:0011984 terminal bouton neuromast hair cell increased amount, abnormal ZP:0011985 kinocilium neuromast hair cell decreased length, abnormal ZP:0011987 integument ball calcified, abnormal ZP:0011988 eye calcified, abnormal ZP:0011989 heart calcified, abnormal ZP:0011990 notochord calcified, abnormal ZP:0011991 notochord severe intensity bone mineralization, abnormal ZP:0011992 bulbus arteriosus calcified, abnormal ZP:0011993 cleithrum calcified, abnormal ZP:0011994 pectoral fin cartilage calcified, abnormal ZP:0011995 osteoclast integument mislocalised, abnormal ZP:0011996 hemal arch fused with hemal arch, abnormal ZP:0011997 cranium calcified, abnormal ZP:0011998 osteoclast cranium mislocalised, abnormal ZP:0011999 neural arch fused with neural arch, abnormal ZP:0012001 neural tube calcified, abnormal ZP:0012002 vertebra increased occurrence bone mineralization, abnormal ZP:0012003 vertebra increased occurrence bone resorption, abnormal ZP:0012004 osteoclast vertebra mislocalised, abnormal ZP:0012005 ventricular system calcified, abnormal ZP:0012006 ceratohyal cartilage increased occurrence bone mineralization, abnormal ZP:0012007 ceratohyal cartilage premature perichondral ossification, abnormal ZP:0012008 bone tissue ceratohyal cartilage mislocalised, abnormal ZP:0012009 ethmoid cartilage calcified, abnormal ZP:0012010 notochord outer sheath cell mineralized, abnormal ZP:0012011 notochord outer sheath cell increased occurrence bone mineralization, abnormal ZP:0012012 skeletal muscle cell accumulation mitochondrion skeletal muscle cell, abnormal ZP:0012013 Z disc skeletal muscle cell morphology, abnormal ZP:0012014 skeletal muscle myofibril skeletal muscle cell disorganized, abnormal ZP:0012015 skeletal muscle myofibril skeletal muscle cell broken, abnormal ZP:0012016 autophagosome slow muscle cell increased amount, abnormal ZP:0012017 intersegmental vessel has extra parts of type filopodium intersegmental vessel, abnormal ZP:0012018 intersegmental vessel lacks parts or has fewer parts of type dorsal region cell junction endothelial cell, abnormal ZP:0012019 cell junction intersegmental vessel morphology, abnormal ZP:0012020 intersegmental vessel dissociated from endothelial tip cell vascular sprouts intersegmental vessel, abnormal ZP:0012021 pronephros process quality cilium movement, abnormal ZP:0012022 motile cilium pronephros paralysed, abnormal ZP:0012023 motile cilium pronephros decreased coordination, abnormal ZP:0012024 whole organism lacks all parts of type ventral fin fold, abnormal ZP:0012025 anterior-posterior axis whole organism undulate, abnormal ZP:0012026 cloaca malformed, abnormal ZP:0012027 whole organism hydrocephalic, abnormal ZP:0012028 thoracic duct malformed, abnormal ZP:0012029 facial nerve motor nucleus accumulation rhombomere 4, abnormal ZP:0012030 facial nerve motor nucleus arrested cell migration, abnormal ZP:0012031 cell midbrain hindbrain boundary decreased length, abnormal ZP:0012032 spinal cord has fewer parts of type radial glial cell ventricular zone, abnormal ZP:0012033 glial cell (sensu Vertebrata) spinal cord mislocalised, abnormal ZP:0012034 neuron spinal cord mislocalised, abnormal ZP:0012035 neuroepithelial cell decreased accumulation actin filament basal region midbrain hindbrain boundary, abnormal ZP:0012036 mitochondrion organization process quality, abnormal ZP:0012037 myelination of posterior lateral line nerve axons arrested, abnormal ZP:0012038 myelination of posterior lateral line nerve axons disrupted, abnormal ZP:0012039 heart lacks all parts of type trabecular layer, abnormal ZP:0012040 myelin sheath posterior lateral line nerve physical object quality, abnormal ZP:0012041 inner ear edematous, abnormal ZP:0012042 mitochondrion myocardium elongated, abnormal ZP:0012043 mitochondrial crista myocardium increased branchiness, abnormal ZP:0012044 sprouting angiogenesis growth quality of occurrent, abnormal ZP:0012045 lymphangioblast decreased amount, abnormal ZP:0012046 dorsal-ventral axis whole organism absent, abnormal ZP:0012047 post-vent region bifurcated, abnormal ZP:0012048 bulbus arteriosus formation process quality, abnormal ZP:0012049 bulbus arteriosus elongated, abnormal ZP:0012050 bulbus arteriosus has extra parts of type cardiac muscle cell, abnormal ZP:0012051 thigmotaxis increased duration, abnormal ZP:0012053 ventral spinal cord interneuron specification decreased process quality, abnormal ZP:0012054 hindbrain has fewer parts of type oligodendrocyte, abnormal ZP:0012055 hindbrain has fewer parts of type glioblast (sensu Vertebrata), abnormal ZP:0012056 spinal cord lacks all parts of type CiA, abnormal ZP:0012057 abducens motor nucleus has fewer parts of type motor neuron abducens motor nucleus, abnormal ZP:0012058 hindbrain interneuron process quality neuron fate specification, abnormal ZP:0012059 prolactin secreting cell development decreased process quality, abnormal ZP:0012060 adenohypophysis has extra parts of type follicle stimulating hormone secreting cell, abnormal ZP:0012061 adenohypophysis has fewer parts of type prolactin secreting cell, abnormal ZP:0012062 adenohypophysis has fewer parts of type adrenocorticotropic hormone secreting cell, abnormal ZP:0012063 adenohypophysis increased occurrence apoptotic process, abnormal ZP:0012064 adenohypophysis decreased occurrence corticotropin hormone secreting cell differentiation, abnormal ZP:0012065 prolactin secreting cell rostral pars anterior dispersed, abnormal ZP:0012066 ossification process quality, abnormal ZP:0012067 adipose tissue development premature, abnormal ZP:0012069 levator arcus palatini increased width, abnormal ZP:0012070 levator arcus palatini shortened, abnormal ZP:0012071 adductor operculi increased width, abnormal ZP:0012072 adductor operculi shortened, abnormal ZP:0012073 dilatator operculi increased width, abnormal ZP:0012074 dilatator operculi shortened, abnormal ZP:0012075 adductor hyohyoid increased width, abnormal ZP:0012076 adductor hyohyoid shortened, abnormal ZP:0012077 sternohyoid increased width, abnormal ZP:0012078 sternohyoid shortened, abnormal ZP:0012079 head muscle increased width, abnormal ZP:0012080 head muscle shortened, abnormal ZP:0012081 ventral intermandibularis anterior increased width, abnormal ZP:0012082 ventral intermandibularis anterior shortened, abnormal ZP:0012083 ventral intermandibularis posterior increased width, abnormal ZP:0012084 ventral intermandibularis posterior shortened, abnormal ZP:0012085 adductor mandibulae increased width, abnormal ZP:0012086 adductor mandibulae shortened, abnormal ZP:0012087 interhyoideus increased width, abnormal ZP:0012088 interhyoideus shortened, abnormal ZP:0012089 hyohyoideus absent, abnormal ZP:0012091 glial cell absent, abnormal ZP:0012092 lens increased diameter, abnormal ZP:0012093 sodium ion homeostasis disrupted, abnormal ZP:0012095 autophagy decreased process quality, abnormal ZP:0012096 myosin filament organization disrupted, abnormal ZP:0012097 myoseptum morphology, abnormal ZP:0012098 myoseptum unstructured, abnormal ZP:0012099 mitochondrion muscle morphology, abnormal ZP:0012100 muscle separated from striated muscle thin filament myosin filament muscle, abnormal ZP:0012101 sarcoplasmic reticulum muscle dilated, abnormal ZP:0012102 muscle cell degenerate, abnormal ZP:0012103 nucleus muscle cell morphology, abnormal ZP:0012104 nucleus muscle cell increased amount, abnormal ZP:0012105 fast muscle cell undulate, abnormal ZP:0012106 magnesium ion homeostasis disrupted, abnormal ZP:0012107 musculoskeletal movement, spinal reflex action increased occurrence, abnormal ZP:0012108 interneuromast cell increased process quality Notch signaling pathway, abnormal ZP:0012109 interneuromast cell increased process quality fibroblast growth factor receptor signaling pathway, abnormal ZP:0012110 interneuromast cell increased process quality canonical Wnt signaling pathway, abnormal ZP:0012111 DNA methylation disrupted, abnormal ZP:0012112 DNA methylation on cytosine within a CG sequence disrupted, abnormal ZP:0012113 lipid homeostasis disrupted, abnormal ZP:0012114 Meckel's cartilage circular, abnormal ZP:0012115 ceratohyal cartilage curved, abnormal ZP:0012116 telencephalon physical object quality, abnormal ZP:0012117 cardiac muscle cell action potential increased duration, abnormal ZP:0012118 blood island has extra parts of type hematopoietic stem cell, abnormal ZP:0012119 keratinocyte integument decreased amount, abnormal ZP:0012120 mucus secreting cell integument decreased amount, abnormal ZP:0012121 melanophore stripe caudal fin spotted, abnormal ZP:0012122 melanophore stripe caudal fin absent, abnormal ZP:0012123 melanocyte caudal fin decreased amount, abnormal ZP:0012124 anal fin has fewer parts of type xanthophore, abnormal ZP:0012125 melanophore stripe anal fin spotted, abnormal ZP:0012126 melanophore stripe anal fin absent, abnormal ZP:0012127 melanophore stripe anal fin undulate, abnormal ZP:0012128 melanocyte anal fin decreased amount, abnormal ZP:0012129 melanophore stripe increased width, abnormal ZP:0012130 melanophore stripe undulate, abnormal ZP:0012131 melanophore stripe disheveled, abnormal ZP:0012132 melanocyte distributed, abnormal ZP:0012133 iridophore dispersed, abnormal ZP:0012134 otic vesicle decreased length, abnormal ZP:0012135 kinocilium otic vesicle increased amount, abnormal ZP:0012136 kinocilium posterior crista deformed, abnormal ZP:0012137 kinocilium posterior crista decreased amount, abnormal ZP:0012138 kinocilium hair cell anterior macula deformed, abnormal ZP:0012139 kinocilium hair cell anterior macula decreased amount, abnormal ZP:0012140 hindbrain lacks all parts of type radial glial cell, abnormal ZP:0012141 developmental growth decreased process quality, abnormal ZP:0012142 opercle decreased process quality bone mineralization, abnormal ZP:0012143 branchiostegal ray decreased process quality bone mineralization, abnormal ZP:0012144 ceratohyal bone decreased process quality bone mineralization, abnormal ZP:0012145 quadrate decreased process quality bone mineralization, abnormal ZP:0012146 hyomandibula decreased process quality bone mineralization, abnormal ZP:0012147 vertebra decreased process quality bone mineralization, abnormal ZP:0012148 cranial vault decreased process quality bone mineralization, abnormal ZP:0012149 determination of stomach left/right asymmetry disrupted, abnormal ZP:0012150 transcriptional activation by promoter-enhancer looping decreased process quality, abnormal ZP:0012151 hypothalamus lacks parts or has fewer parts of type dopaminergic neuron, abnormal ZP:0012152 diencephalon lacks parts or has fewer parts of type dopaminergic neuron, abnormal ZP:0012153 pectoral fin bud decreased process quality embryonic pectoral fin morphogenesis, abnormal ZP:0012154 sympathetic nervous system lacks parts or has fewer parts of type sympathetic neuron, abnormal ZP:0012155 dopaminergic neuron disrupted axon development, abnormal ZP:0012156 cell junction diencephalon morphology, abnormal ZP:0012157 cell diencephalon disorganized, abnormal ZP:0012158 cell accumulation forebrain ventricle, abnormal ZP:0012159 smoothened signaling pathway decreased process quality, abnormal ZP:0012160 GABAergic neuron differentiation disrupted, abnormal ZP:0012161 hindbrain lacks all parts of type oligodendrocyte, abnormal ZP:0012162 diencephalon decreased process quality neuron differentiation, abnormal ZP:0012163 forebrain lacks all parts of type oligodendrocyte, abnormal ZP:0012164 forebrain has fewer parts of type oligodendrocyte, abnormal ZP:0012165 forebrain lacks all parts of type GABAergic neuron, abnormal ZP:0012166 forebrain has fewer parts of type GABAergic neuron, abnormal ZP:0012167 forebrain increased occurrence apoptotic process, abnormal ZP:0012168 midbrain increased occurrence apoptotic process, abnormal ZP:0012169 pectoral fin bud decreased depth, abnormal ZP:0012170 ventral telencephalon decreased process quality neuron differentiation, abnormal ZP:0012171 mesenchyme pectoral fin decreased occurrence cell population proliferation, abnormal ZP:0012172 GABAergic neuron decreased amount, abnormal ZP:0012173 microglial cell brain decreased amount, abnormal ZP:0012174 macrophage brain decreased amount, abnormal ZP:0012175 macrophage central nervous system decreased amount, abnormal ZP:0012176 macrophage integument decreased amount, abnormal ZP:0012177 integument lacks parts or has fewer parts of type macrophage cell projection macrophage, abnormal ZP:0012178 anatomical region hemal arch decreased size, abnormal ZP:0012179 macrophage head morphology, abnormal ZP:0012180 neutrophil head increased amount, abnormal ZP:0012181 vertebra morphology, abnormal ZP:0012182 vertebra increased volume, abnormal ZP:0012183 vertebra increased area, abnormal ZP:0012184 blood vessel mislocalised, abnormal ZP:0012185 macrophage has fewer parts of type cell projection macrophage, abnormal ZP:0012186 hair cell saccule decreased amount, abnormal ZP:0012187 skeletal muscle myofibril muscle disorganized, abnormal ZP:0012188 myoseptum muscle disorganized, abnormal ZP:0012189 whole organism lacks parts or has fewer parts of type pectoral fin bud, abnormal ZP:0012190 NCC ionocyte head increased amount, abnormal ZP:0012191 hemal arch hypoplastic, abnormal ZP:0012192 rib hypoplastic, abnormal ZP:0012193 basipterygium hypoplastic, abnormal ZP:0012194 neural arch hypoplastic, abnormal ZP:0012195 dorsal fin lepidotrichium absent, abnormal ZP:0012196 anal fin lepidotrichium decreased amount, abnormal ZP:0012197 caudal fin lepidotrichium decreased amount, abnormal ZP:0012198 pectoral fin lepidotrichium aplastic, abnormal ZP:0012199 pelvic fin lepidotrichium hypoplastic, abnormal ZP:0012200 motile cilium Kupffer's vesicle decreased fluid flow, abnormal ZP:0012201 musculoskeletal movement decreased process quality, abnormal ZP:0012202 skeletal muscle paralysed, abnormal ZP:0012203 striated muscle cell misaligned with striated muscle cell, abnormal ZP:0012204 myofibril striated muscle cell disorganized, abnormal ZP:0012205 striated muscle cell misaligned with Z disc Z disc striated muscle cell, abnormal ZP:0012206 myofilament striated muscle cell disorganized, abnormal ZP:0012207 striated muscle cell detached from myofilament myoseptum, abnormal ZP:0012208 skeletal muscle cell detached from somite border, abnormal ZP:0012209 retinal cone cell development decreased process quality, abnormal ZP:0012210 melanocyte occurrence cellular pigment accumulation, abnormal ZP:0012211 melanocyte decreased occurrence cellular response to light intensity, abnormal ZP:0012212 retinal cone cell lacks all parts of type photoreceptor outer segment retinal cone cell, abnormal ZP:0012213 eye far from eye, abnormal ZP:0012214 cardiac muscle cell proliferation decreased rate, abnormal ZP:0012215 pectoral fin development delayed, abnormal ZP:0012216 pectoral fin immature, abnormal ZP:0012217 liver decreased process quality cell population proliferation, abnormal ZP:0012218 caudal fin decreased process quality cell population proliferation, abnormal ZP:0012219 trunk decreased process quality cell population proliferation, abnormal ZP:0012220 Meckel's cartilage disrupted cartilage development, abnormal ZP:0012221 palatoquadrate cartilage disrupted cartilage development, abnormal ZP:0012222 peripheral olfactory organ has fewer parts of type ciliated olfactory receptor neuron, abnormal ZP:0012223 thoracic duct has fewer parts of type endothelial cell, abnormal ZP:0012224 mitochondrial respiratory chain complex I whole organism decreased amount, abnormal ZP:0012225 caudal vein plexus increased process quality apoptotic process, abnormal ZP:0012227 precaudal vertebra curved, abnormal ZP:0012228 caudal vertebra curved, abnormal ZP:0012229 dorsal-ventral axis whole organism curved, abnormal ZP:0012230 medial-lateral axis whole organism curved, abnormal ZP:0012231 vertebra angle vertebra, abnormal ZP:0012232 vertebral column curved, abnormal ZP:0012233 dorsal-ventral axis whole organism shortened, abnormal ZP:0012234 cilium neural tube disorganized, abnormal ZP:0012235 pharyngeal arch decreased width, abnormal ZP:0012236 dorsal aorta decreased thickness, abnormal ZP:0012237 dorsal aorta lacks parts or has fewer parts of type endothelial cell, abnormal ZP:0012241 ventral wall of dorsal aorta decreased process quality cell population proliferation, abnormal ZP:0012242 vertical myoseptum decreased size, abnormal ZP:0012243 vertical myoseptum disorganized, abnormal ZP:0012244 post-vent region decreased width, abnormal ZP:0012245 skeletal muscle cell elongated, abnormal ZP:0012246 striated muscle myosin thick filament skeletal muscle cell disorganized, abnormal ZP:0012247 skeletal muscle cell orientation myofibril skeletal muscle cell, abnormal ZP:0012248 Z disc skeletal muscle cell structure, abnormal ZP:0012249 M band skeletal muscle cell decreased amount, abnormal ZP:0012250 photoreceptor cell absent, abnormal ZP:0012251 cardiac muscle cell structure, abnormal ZP:0012252 intercalated disc cardiac muscle cell absent, abnormal ZP:0012253 caudal fin has fewer parts of type melanophore stripe, abnormal ZP:0012254 melanophore stripe anal fin decreased width, abnormal ZP:0012255 melanocyte confluent with xanthophore, abnormal ZP:0012256 response to auditory stimulus process quality, abnormal ZP:0012257 trunk neural crest cell migration process quality, abnormal ZP:0012258 trunk neural crest cell elongated, abnormal ZP:0012259 muscle tendon junction muscle morphology, abnormal ZP:0012260 T-tubule muscle dilated, abnormal ZP:0012261 mitochondrion muscle cell increased size, abnormal ZP:0012262 mitochondrion muscle cell aggregated, abnormal ZP:0012263 mitochondrial intermembrane space muscle cell dilated, abnormal ZP:0012264 myofibril muscle cell kinked, abnormal ZP:0012265 muscle cell separated from myofibril muscle tendon junction muscle cell, abnormal ZP:0012266 muscle cell misaligned with myofibril myofibril muscle cell, abnormal ZP:0012267 mitochondrial crista muscle cell decreased amount, abnormal ZP:0012268 parachordal vessel malformed, abnormal ZP:0012269 basement membrane renal glomerulus morphology, abnormal ZP:0012270 endothelial cell renal glomerulus swollen, abnormal ZP:0012271 thoracic duct has fewer parts of type endothelial cell lymphatic system, abnormal ZP:0012272 neuromast development process quality, abnormal ZP:0012273 posterior lateral line has fewer parts of type neuromast, abnormal ZP:0012274 caudal fin lacks all parts of type neuromast, abnormal ZP:0012275 trunk has fewer parts of type posterior region neuromast, abnormal ZP:0012276 posterior lateral line primordium increased process quality cell death, abnormal ZP:0012277 thyroxine 5-deiodinase activity decreased process quality, abnormal ZP:0012281 hindbrain increased occurrence neurogenesis, abnormal ZP:0012282 lateral region facial lymphatic vessel decreased length, abnormal ZP:0012284 phototaxis disrupted, abnormal ZP:0012285 response to mechanical stimulus decreased process quality, abnormal ZP:0012286 axonal transport of mitochondrion decreased process quality, abnormal ZP:0012287 axon posterior lateral line nerve decreased size, abnormal ZP:0012288 axon posterior lateral line nerve degeneration, abnormal ZP:0012289 posterior lateral line nerve has fewer parts of type axon mitochondrion posterior lateral line nerve, abnormal ZP:0012290 caudal fin has fewer parts of type axon mitochondrion neuron, abnormal ZP:0012291 mitochondrion neuron mobility, abnormal ZP:0012292 otolith development process quality, abnormal ZP:0012293 otic vesicle lacks parts or has fewer parts of type otolith, abnormal ZP:0012294 neuron optic recess mislocalised, abnormal ZP:0012295 hematopoietic stem cell intermediate cell mass of mesoderm decreased amount, abnormal ZP:0012296 sternohyoid disorganized, abnormal ZP:0012297 spinal cord increased process quality apoptotic process, abnormal ZP:0012298 telencephalon hydrocephalic, abnormal ZP:0012300 muscle contraction decreased force, abnormal ZP:0012301 skeletal muscle thin filament assembly disrupted, abnormal ZP:0012302 trunk musculature decreased functionality, abnormal ZP:0012303 inclusion body muscle cell increased amount, abnormal ZP:0012304 M band muscle cell morphology, abnormal ZP:0012305 muscle cell increased distance skeletal muscle myofibril skeletal muscle myofibril muscle cell, abnormal ZP:0012306 MAPK cascade disrupted, abnormal ZP:0012309 intersegmental vessel trunk morphology, abnormal ZP:0012311 trigeminal nerve morphogenesis decreased process quality, abnormal ZP:0012312 axon trigeminal ganglion misrouted, abnormal ZP:0012313 trigeminal sensory neuron decreased occurrence extracellular matrix disassembly, abnormal ZP:0012314 trigeminal sensory neuron decreased process quality sensory neuron axon guidance, abnormal ZP:0012315 blood island has extra parts of type neutrophil, abnormal ZP:0012316 vasculature has fewer parts of type circulating cell neutrophil, abnormal ZP:0012317 neuromast deposition process quality, abnormal ZP:0012318 neural crest accumulation axis, abnormal ZP:0012319 trunk lacks all parts of type posterior region neuromast, abnormal ZP:0012320 blood cell accumulation bulbus arteriosus, abnormal ZP:0012322 auditory receptor cell decreased functionality, abnormal ZP:0012323 xanthophore differentiation premature, abnormal ZP:0012324 barbel absent, abnormal ZP:0012325 ventral mandibular arch hypertrophic, abnormal ZP:0012326 xanthophore increased amount, abnormal ZP:0012327 sleep process quality, abnormal ZP:0012329 cerebellum vasculature development disrupted, abnormal ZP:0012330 neuron cranial nerve V decreased amount, abnormal ZP:0012331 Rohon-Beard neuron has fewer parts of type dendritic filopodium Rohon-Beard neuron, abnormal ZP:0012332 neuron projection Rohon-Beard neuron malformed, abnormal ZP:0012333 neuron projection Rohon-Beard neuron decreased branchiness, abnormal ZP:0012334 Rohon-Beard neuron decreased process quality collateral sprouting, abnormal ZP:0012335 startle response delayed, abnormal ZP:0012336 sensory perception of sound disrupted, abnormal ZP:0012337 sensory perception of mechanical stimulus disrupted, abnormal ZP:0012338 posterior lateral line neuromast morphology, abnormal ZP:0012339 posterior lateral line neuromast decreased functionality, abnormal ZP:0012340 stereocilium posterior lateral line neuromast decreased amount, abnormal ZP:0012341 kinocilium posterior lateral line neuromast decreased amount, abnormal ZP:0012342 neuromuscular junction skeletal muscle decreased size, abnormal ZP:0012343 neuromuscular junction skeletal muscle broken, abnormal ZP:0012344 neuromuscular junction skeletal muscle decreased amount, abnormal ZP:0012345 skeletal muscle cell decreased width, abnormal ZP:0012346 skeletal muscle cell atrophied, abnormal ZP:0012347 skeletal muscle myofibril skeletal muscle cell disoriented, abnormal ZP:0012348 iridophore ridged, abnormal ZP:0012349 neuron projection dorsal root ganglion morphology, abnormal ZP:0012350 Rohon-Beard neuron process quality neuronal action potential, abnormal ZP:0012351 CaP motoneuron process quality neuronal action potential, abnormal ZP:0012352 neuron projection CaP motoneuron morphology, abnormal ZP:0012353 neuron projection CaP motoneuron displaced, abnormal ZP:0012354 CaP motoneuron process quality membrane repolarization, abnormal ZP:0012355 caudal vein plexus structure, abnormal ZP:0012356 trunk vasculature disrupted blood circulation, abnormal ZP:0012357 axial blood vessel disrupted blood circulation, abnormal ZP:0012358 spinal cord disrupted spinal cord oligodendrocyte cell fate specification, abnormal ZP:0012359 spinal cord disrupted regulation of oligodendrocyte progenitor proliferation, abnormal ZP:0012360 neuron spinal cord increased amount, abnormal ZP:0012361 glioblast (sensu Vertebrata) increased occurrence cell division, abnormal ZP:0012362 dorsal-ventral axis notochord increased size, abnormal ZP:0012363 dorsal-ventral axis myotome increased size, abnormal ZP:0012364 skeletal muscle myofibril skeletal muscle organization quality, abnormal ZP:0012365 Z disc skeletal muscle cell spatial pattern, abnormal ZP:0012366 trunk has fewer parts of type dermis iridophore, abnormal ZP:0012367 melanophore stripe lacks parts or has fewer parts of type melanocyte, abnormal ZP:0012368 esophagus malformed, abnormal ZP:0012369 esophageal epithelium disorganized, abnormal ZP:0012370 esophageal epithelium disrupted epithelial cell differentiation, abnormal ZP:0012371 primary islet absent, abnormal ZP:0012372 photoreceptor cell differentiation decreased process quality, abnormal ZP:0012373 retinal ganglion cell layer has fewer parts of type retinal ganglion cell, abnormal ZP:0012374 optic stalk shape, abnormal ZP:0012375 optic stalk decreased size, abnormal ZP:0012376 cranial nerve II physical object quality, abnormal ZP:0012377 adenohypophysis formation decreased process quality, abnormal ZP:0012378 hypothalamus has fewer parts of type posterior side dopaminergic neuron, abnormal ZP:0012379 blood vasculature lacks all parts of type hypophyseal artery, abnormal ZP:0012380 blood vasculature lacks all parts of type hypophyseal capillary, abnormal ZP:0012381 neurohypophysis decreased occurrence vasculogenesis, abnormal ZP:0012382 neurohypophysis decreased occurrence innervation, abnormal ZP:0012383 adenohypophysis decreased object quality, abnormal ZP:0012384 pharyngeal pouch decreased speed cell migration, abnormal ZP:0012385 rhombomere 6 decreased size, abnormal ZP:0012386 facial nerve motor nucleus decreased process quality motor neuron migration, abnormal ZP:0012387 rhombomere 3 increased size, abnormal ZP:0012388 amacrine cell differentiation decreased process quality, abnormal ZP:0012389 camera-type eye photoreceptor cell differentiation delayed, abnormal ZP:0012390 retinal inner nuclear layer physical object quality, abnormal ZP:0012391 retinal inner nuclear layer poorly differentiated, abnormal ZP:0012392 retinal inner nuclear layer has fewer parts of type horizontal cell retinal inner nuclear layer, abnormal ZP:0012393 retinal inner plexiform layer malformed, abnormal ZP:0012394 retinal inner plexiform layer has fewer parts of type dendrite retinal ganglion cell, abnormal ZP:0012395 retinal outer nuclear layer poorly differentiated, abnormal ZP:0012396 amacrine cell poorly differentiated, abnormal ZP:0012397 retinal cone cell undifferentiated, abnormal ZP:0012398 retinal rod cell undifferentiated, abnormal ZP:0012399 Muller cell poorly differentiated, abnormal ZP:0012400 retinal ganglion cell decreased occurrence dendrite morphogenesis, abnormal ZP:0012401 retinal bipolar neuron poorly differentiated, abnormal ZP:0012402 pharyngeal vasculature has fewer parts of type blood vessel endothelial cell, abnormal ZP:0012403 pharyngeal vasculature decreased process quality vasculogenesis, abnormal ZP:0012404 pharyngeal vasculature decreased process quality angioblast cell differentiation, abnormal ZP:0012405 pharyngeal vasculature decreased occurrence blood vessel endothelial cell differentiation, abnormal ZP:0012406 pharyngeal vasculature decreased process quality pharyngeal arch artery morphogenesis, abnormal ZP:0012407 lymphangiogenic sprout facial lymphatic vessel aplastic, abnormal ZP:0012408 pharynx increased amount, abnormal ZP:0012409 pharynx increased width, abnormal ZP:0012410 pharyngeal epithelium absent, abnormal ZP:0012411 pharyngeal pouch increased speed cell migration, abnormal ZP:0012413 spinal cord lacks parts or has fewer parts of type motor neuron, abnormal ZP:0012414 retina has fewer parts of type blue sensitive photoreceptor cell, abnormal ZP:0012415 retina process quality dorsal/ventral pattern formation, abnormal ZP:0012416 optic tectum decreased process quality innervation, abnormal ZP:0012417 neuromuscular junction motor neuron increased volume, abnormal ZP:0012418 neuromuscular junction motor neuron physical object quality, abnormal ZP:0012419 determination of left/right asymmetry in diencephalon decreased process quality, abnormal ZP:0012420 lateral plate mesoderm decreased process quality determination of left/right asymmetry in lateral mesoderm, abnormal ZP:0012421 lateral semicircular canal development disrupted, abnormal ZP:0012422 anterior macula decreased distance posterior macula, abnormal ZP:0012423 inner ear lacks all parts of type lateral crista, abnormal ZP:0012424 inner ear lacks all parts of type lateral semicircular canal, abnormal ZP:0012425 blood vessel morphology, abnormal ZP:0012426 nodal signaling pathway involved in determination of left/right asymmetry disrupted, abnormal ZP:0012427 convergent extension involved in nephron morphogenesis process quality, abnormal ZP:0012428 habenula disrupted determination of left/right symmetry, abnormal ZP:0012429 habenula process quality neurogenesis, abnormal ZP:0012430 epithalamus disrupted determination of left/right symmetry, abnormal ZP:0012431 trunk wholly dorsalized, abnormal ZP:0012432 medial floor plate increased width, abnormal ZP:0012433 melanocyte process quality developmental pigmentation, abnormal ZP:0012434 neurogenesis decreased process quality, abnormal ZP:0012435 interneuron increased amount, abnormal ZP:0012436 atrium lacks all parts of type ventricular endocardium, abnormal ZP:0012437 endocardium aggregated, abnormal ZP:0012438 endocardium decreased anterior-posterior diameter, abnormal ZP:0012439 cell-cell junction endocardium mislocalised, abnormal ZP:0012440 endocardium decreased process quality cell-cell junction organization, abnormal ZP:0012441 endocardium process quality cardiac muscle cell differentiation, abnormal ZP:0012442 endothelial cell endocardium aggregated, abnormal ZP:0012443 endothelial cell endocardium obtuse, abnormal ZP:0012444 ventricular endocardium aggregated, abnormal ZP:0012445 presumptive endocardium decreased process quality morphogenesis of an epithelial sheet, abnormal ZP:0012446 ventral wall of dorsal aorta lacks all parts of type hematopoietic stem cell, abnormal ZP:0012447 pronephric glomerulus morphogenesis arrested, abnormal ZP:0012448 presumptive pronephric mesoderm malformed, abnormal ZP:0012449 pronephric glomerulus poorly differentiated, abnormal ZP:0012450 hindbrain decreased occurrence cell proliferation in hindbrain ventricular zone, abnormal ZP:0012451 hindbrain premature neurogenesis, abnormal ZP:0012452 spinal cord lacks all parts of type oligodendrocyte, abnormal ZP:0012453 enteric nervous system development decreased process quality, abnormal ZP:0012454 intestinal epithelial cell differentiation process quality, abnormal ZP:0012455 swim bladder decreased volume, abnormal ZP:0012456 posterior intestine decreased occurrence peristalsis, abnormal ZP:0012457 enteric nervous system lacks all parts of type enteric neuron, abnormal ZP:0012458 enteric nervous system has fewer parts of type enteric neuron, abnormal ZP:0012459 intestinal epithelium lacks parts or has fewer parts of type goblet cell, abnormal ZP:0012460 intestinal epithelium lacks parts or has fewer parts of type enteroendocrine cell, abnormal ZP:0012461 intestinal epithelium process quality Notch signaling pathway, abnormal ZP:0012462 enteroendocrine cell intestinal epithelium undifferentiated, abnormal ZP:0012463 anterior region intestine lumen increased diameter, abnormal ZP:0012464 rhombomere 6 has fewer parts of type cranial motor neuron, abnormal ZP:0012465 rhombomere 7 has fewer parts of type cranial motor neuron, abnormal ZP:0012466 rhombomere 4 has extra parts of type cranial motor neuron, abnormal ZP:0012467 ventral aorta separated from bulbus arteriosus, abnormal ZP:0012468 hypobranchial artery morphology, abnormal ZP:0012469 hypobranchial artery dysplastic, abnormal ZP:0012470 thyroid follicle position, abnormal ZP:0012471 thyroid follicle mislocalised, abnormal ZP:0012472 cell thyroid follicle decreased amount, abnormal ZP:0012473 thyroid primordium morphology, abnormal ZP:0012474 thyroid primordium distended, abnormal ZP:0012475 aortic arch absent, abnormal ZP:0012476 parachordal vessel incomplete structure, abnormal ZP:0012477 neuron cell-cell adhesion disrupted, abnormal ZP:0012478 glial cell projection trunk truncated, abnormal ZP:0012479 glial cell projection trunk disorganized, abnormal ZP:0012480 glial cell projection trunk kinked, abnormal ZP:0012481 branchiomotor neuron decreased cellular motility, abnormal ZP:0012482 branchiomotor neuron detached from medial longitudinal fasciculus, abnormal ZP:0012483 branchiomotor neuron decreased velocity neuron migration, abnormal ZP:0012484 neural plate morphogenesis process quality, abnormal ZP:0012485 cardioblast migration to the midline involved in heart field formation process quality, abnormal ZP:0012486 prechordal plate aplastic/hypoplastic, abnormal ZP:0012487 neural keel malformed, abnormal ZP:0012488 neural plate process quality cell motility, abnormal ZP:0012489 anterior region notochord absent, abnormal ZP:0012490 neural tube cellular spatiotemporal quality cell division, abnormal ZP:0012491 pancreatic bud lacks all parts of type pancreatic B cell, abnormal ZP:0012492 prechordal plate formation process quality, abnormal ZP:0012493 prechordal plate process quality mesodermal cell migration, abnormal ZP:0012494 thymus morphology, abnormal ZP:0012495 thymus has fewer parts of type T cell, abnormal ZP:0012496 thymus has extra parts of type fat cell, abnormal ZP:0012497 thymic epithelium has fewer parts of type epithelial cell, abnormal ZP:0012498 eye field cell fate commitment involved in camera-type eye formation disrupted, abnormal ZP:0012499 cellular response to light stimulus disrupted, abnormal ZP:0012500 cranial nerve II shape, abnormal ZP:0012502 axis malformed, abnormal ZP:0012503 neuromuscular junction trunk morphology, abnormal ZP:0012504 cell proliferation in forebrain disrupted, abnormal ZP:0012505 epithelial cell proliferation disrupted, abnormal ZP:0012506 olfactory bulb morphology, abnormal ZP:0012507 ciliated olfactory receptor neuron decreased amount, abnormal ZP:0012508 microvillous olfactory receptor neuron decreased amount, abnormal ZP:0012510 postoptic commissure has fewer parts of type axon postoptic commissure, abnormal ZP:0012511 postoptic commissure has fewer parts of type medial region glial cell (sensu Vertebrata), abnormal ZP:0012512 postoptic commissure decreased process quality commissural neuron axon guidance, abnormal ZP:0012513 forebrain lacks all parts of type anterior commissure, abnormal ZP:0012514 forebrain increased process quality Roundabout signaling pathway involved in axon guidance, abnormal ZP:0012515 anterior commissure has fewer parts of type axon anterior commissure, abnormal ZP:0012516 anterior commissure has fewer parts of type medial region glial cell (sensu Vertebrata), abnormal ZP:0012517 anterior commissure decreased process quality commissural neuron axon guidance, abnormal ZP:0012518 pharyngeal pouch process quality adherens junction organization, abnormal ZP:0012519 pharyngeal pouch decreased occurrence apical protein localization, abnormal ZP:0012520 optic vesicle morphogenesis disrupted, abnormal ZP:0012521 pharyngeal pouch process quality epithelial cell migration, abnormal ZP:0012522 pineal complex has extra parts of type photoreceptor cell, abnormal ZP:0012523 parapineal organ malformed, abnormal ZP:0012524 parapineal organ has fewer parts of type cell, abnormal ZP:0012525 axial mesoderm development disrupted, abnormal ZP:0012526 floor plate split, abnormal ZP:0012527 spinal cord lacks all parts of type posterior region primary motor neuron, abnormal ZP:0012528 notochord aplastic/hypoplastic, abnormal ZP:0012529 sclerotome absent, abnormal ZP:0012530 whole organism lacks all parts of type notochord, abnormal ZP:0012531 pineal complex decreased size, abnormal ZP:0012532 pronephric glomerulus increased amount, abnormal ZP:0012534 pronephric glomerulus mislocalised laterally, abnormal ZP:0012535 pronephric glomerular capillary attached to common cardinal vein, abnormal ZP:0012536 pronephric glomerular capillary detached from membrane pronephric glomerular basement membrane, abnormal ZP:0012537 glomerular endothelium fenestra pronephric glomerular capillary closed, abnormal ZP:0012538 anatomical region secondary motor neuron discontinuous, abnormal ZP:0012539 anatomical region secondary motor neuron split, abnormal ZP:0012540 podocyte mislocalised laterally, abnormal ZP:0012541 pharyngeal pouch 2 malformed, abnormal ZP:0012542 pharyngeal arch 6 absent, abnormal ZP:0012543 pharyngeal arch 7 absent, abnormal ZP:0012544 pharyngeal arch 2 fused with pharyngeal arch 3, abnormal ZP:0012545 trigeminal sensory neuron decreased amount, abnormal ZP:0012546 DNA methylation decreased process quality, abnormal ZP:0012547 habenula process quality determination of left/right symmetry, abnormal ZP:0012548 pineal complex molecular quality, abnormal ZP:0012549 parapineal organ hyperplastic, abnormal ZP:0012550 pharyngeal arch increased process quality apoptotic process, abnormal ZP:0012551 chondrocranium shape, abnormal ZP:0012552 chondrocranium decreased size, abnormal ZP:0012553 gut constricted, abnormal ZP:0012554 dorsal root ganglion has fewer parts of type neuron, abnormal ZP:0012555 axon dorsal root ganglion morphology, abnormal ZP:0012556 dendrite motor neuron morphology, abnormal ZP:0012557 dendrite motor neuron decreased length, abnormal ZP:0012558 node of Ranvier motor neuron increased width, abnormal ZP:0012559 myelin sheath motor neuron loose, abnormal ZP:0012560 motor neuron process quality axon extension, abnormal ZP:0012561 myelinating Schwann cell structure, abnormal ZP:0012562 retina has fewer parts of type UV sensitive photoreceptor cell, abnormal ZP:0012563 cell parapineal organ mislocalised, abnormal ZP:0012564 cell parapineal organ decreased amount, abnormal ZP:0012565 UV sensitive photoreceptor cell morphology, abnormal ZP:0012566 UV sensitive photoreceptor cell deformed, abnormal ZP:0012567 UV sensitive photoreceptor cell has extra parts of type cone cell pedicle UV sensitive photoreceptor cell, abnormal ZP:0012568 axon UV sensitive photoreceptor cell bifurcated, abnormal ZP:0012569 trunk lacks all parts of type dermis melanocyte, abnormal ZP:0012570 locomotion involved in locomotory behavior decreased speed, abnormal ZP:0012571 striated muscle thin filament myotome disoriented, abnormal ZP:0012572 skeletal muscle decreased strength, abnormal ZP:0012573 hyohyoideus misaligned away from hyohyoideus, abnormal ZP:0012574 striated muscle thin filament fast muscle cell increased variability of size, abnormal ZP:0012575 myofibril fast muscle cell malformed, abnormal ZP:0012576 sarcomere fast muscle cell malformed, abnormal ZP:0012577 Z disc fast muscle cell increased width, abnormal ZP:0012578 eye red, abnormal ZP:0012580 anal fin lacks all parts of type melanocyte, abnormal ZP:0012582 habenula process quality determination of left/right asymmetry in diencephalon, abnormal ZP:0012583 neuron projection habenula displaced, abnormal ZP:0012585 cilium neural tube decreased length, abnormal ZP:0012586 protein kinase B signaling decreased process quality, abnormal ZP:0012587 trunk vasculature process quality angiogenesis, abnormal ZP:0012588 cornea malformed, abnormal ZP:0012589 corneal endothelium malformed, abnormal ZP:0012590 anterior segment eye morphology, abnormal ZP:0012591 anterior segment eye hypoplastic, abnormal ZP:0012592 mesenchymal cell anterior segment eye morphology, abnormal ZP:0012593 common lymphoid progenitor decreased amount, abnormal ZP:0012594 ependymal cell decreased process quality cell population proliferation, abnormal ZP:0012595 compact layer of ventricle has fewer parts of type apical region cardiac myofibril compact layer of ventricle, abnormal ZP:0012596 compact layer of ventricle has extra parts of type basal cortex cardiac myofibril compact layer of ventricle, abnormal ZP:0012597 compact layer of ventricle decreased process quality ventricular cardiac myofibril assembly, abnormal ZP:0012598 cardiac myofibril compact layer of ventricle increased diameter, abnormal ZP:0012599 behavior process quality, abnormal ZP:0012600 learning process quality, abnormal ZP:0012601 learning decreased process quality, abnormal ZP:0012602 circadian rhythm rhythm quality, abnormal ZP:0012603 locomotory exploration behavior increased process quality, abnormal ZP:0012604 dopaminergic neuron caudal tuberculum disorganized, abnormal ZP:0012605 cell head necrotic, abnormal ZP:0012606 motor neuron branchiness, abnormal ZP:0012607 atrium hypertrophic, abnormal ZP:0012608 cardiac muscle cell atrium increased size, abnormal ZP:0012609 cardiac muscle cell disrupted sarcomere organization, abnormal ZP:0012611 osteoblast differentiation decreased occurrence, abnormal ZP:0012612 intramembranous ossification decreased occurrence, abnormal ZP:0012613 thrombocyte differentiation decreased occurrence, abnormal ZP:0012614 cellular response to oxidative stress increased occurrence, abnormal ZP:0012615 definitive hemopoiesis occurrence, abnormal ZP:0012616 centrum decreased occurrence bone mineralization, abnormal ZP:0012617 opercle decreased volume, abnormal ZP:0012618 opercle decreased occurrence bone mineralization, abnormal ZP:0012619 ceratohyal bone decreased occurrence bone mineralization, abnormal ZP:0012620 cranium decreased occurrence bone mineralization, abnormal ZP:0012621 hematopoietic system has fewer parts of type nucleate erythrocyte, abnormal ZP:0012622 hematopoietic system has fewer parts of type thrombocyte, abnormal ZP:0012623 hematopoietic stem cell mislocalised, abnormal ZP:0012624 habenula development decreased process quality, abnormal ZP:0012625 dorsal habenular nucleus poorly differentiated, abnormal ZP:0012626 midbrain hindbrain boundary hypoplastic, abnormal ZP:0012627 optic vesicle formation decreased process quality, abnormal ZP:0012628 optic vesicle decreased process quality regionalization, abnormal ZP:0012629 optic vesicle increased occurrence apoptotic process, abnormal ZP:0012630 cell optic vesicle mislocalised, abnormal ZP:0012631 ovarian follicle development delayed, abnormal ZP:0012632 spermatogenesis delayed, abnormal ZP:0012633 vitellogenesis delayed, abnormal ZP:0012634 sex determination process quality, abnormal ZP:0012635 female gonad development delayed, abnormal ZP:0012636 ovary decreased size, abnormal ZP:0012637 ovary immature, abnormal ZP:0012638 testis decreased size, abnormal ZP:0012639 ovulation decreased occurrence, abnormal ZP:0012640 multi-ciliated epithelial cell pronephros aggregated, abnormal ZP:0012641 pronephric proximal straight tubule distended, abnormal ZP:0012642 pronephric distal late tubule decreased size, abnormal ZP:0012643 vertebral column increased curvature, abnormal ZP:0012646 dendrite Mauthner neuron increased branchiness, abnormal ZP:0012647 Mauthner neuron process quality dendrite morphogenesis, abnormal ZP:0012648 axon spinal cord increased branchiness, abnormal ZP:0012649 melanophore stripe has fewer parts of type melanocyte, abnormal ZP:0012650 melanosome melanocyte decreased amount, abnormal ZP:0012651 optic vesicle unstructured, abnormal ZP:0012652 optic vesicle looseness, abnormal ZP:0012653 optic vesicle edge shape, abnormal ZP:0012654 cell optic vesicle mislocalised medially, abnormal ZP:0012655 axon cerebellum morphology, abnormal ZP:0012656 axon cerebellum degenerate, abnormal ZP:0012657 hematopoietic progenitor cell differentiation process quality, abnormal ZP:0012658 sclerotome development process quality, abnormal ZP:0012659 dorsal aorta development process quality, abnormal ZP:0012660 thymus development process quality, abnormal ZP:0012661 hematopoietic stem cell differentiation process quality, abnormal ZP:0012662 Golgi organization disrupted, abnormal ZP:0012663 lipid digestion disrupted, abnormal ZP:0012664 Golgi apparatus exocrine pancreas dilated, abnormal ZP:0012665 Golgi apparatus cholangiocyte dilated, abnormal ZP:0012666 myelin maintenance decreased process quality, abnormal ZP:0012667 spinal cord decreased process quality myelination, abnormal ZP:0012668 cell projection oligodendrocyte decreased amount, abnormal ZP:0012669 myelin sheath oligodendrocyte decreased length, abnormal ZP:0012670 myelin sheath oligodendrocyte decreased amount, abnormal ZP:0012671 respiratory burst involved in defense response decreased process quality, abnormal ZP:0012672 macrophage heart decreased amount, abnormal ZP:0012673 macrophage head decreased amount, abnormal ZP:0012674 blood island increased process quality cell death, abnormal ZP:0012675 macrophage blood island absent, abnormal ZP:0012676 macrophage head absent, abnormal ZP:0012677 macrophage immature, abnormal ZP:0012678 myeloid cell increased process quality cell death, abnormal ZP:0012679 swimming behavior increased duration, abnormal ZP:0012680 female organism increased female fertility, abnormal ZP:0012681 otolith detached from otolith organ, abnormal ZP:0012682 posterior crista otic vesicle absent, abnormal ZP:0012683 posterior crista otic vesicle apoptotic, abnormal ZP:0012684 anterior crista otic vesicle absent, abnormal ZP:0012685 gut decreased process quality peristalsis, abnormal ZP:0012687 glucose import disrupted, abnormal ZP:0012688 hindbrain increased occurrence apoptotic process, abnormal ZP:0012689 telencephalon displaced, abnormal ZP:0012690 lateral longitudinal fasciculus decreased thickness, abnormal ZP:0012691 lateral longitudinal fasciculus fasciculation, abnormal ZP:0012692 otic vesicle has fewer parts of type auditory epithelial support cell, abnormal ZP:0012693 cell periderm decreased amount, abnormal ZP:0012694 peridermal cell increased size, abnormal ZP:0012696 epidermal basal stratum increased occurrence cell population proliferation, abnormal ZP:0012697 periderm increased occurrence cell population proliferation, abnormal ZP:0012698 cell increased accumulation lysosome periderm, abnormal ZP:0012699 cell increased accumulation endosome periderm, abnormal ZP:0012700 cell increased accumulation vesicle periderm, abnormal ZP:0012701 peridermal cell morphology, abnormal ZP:0012702 peridermal cell increased amount, abnormal ZP:0012703 peridermal cell decreased size, abnormal ZP:0012704 peridermal cell spherical, abnormal ZP:0012705 basolateral plasma membrane peridermal cell decreased area, abnormal ZP:0012706 apical plasma membrane peridermal cell decreased area, abnormal ZP:0012707 cell projection membrane peridermal cell absent, abnormal ZP:0012708 epidermal cell spherical, abnormal ZP:0012709 lymphocyte differentiation decreased process quality, abnormal ZP:0012710 myeloid cell development process quality, abnormal ZP:0012711 otic vesicle lacks all parts of type tether cell, abnormal ZP:0012712 pancreas degenerate, abnormal ZP:0012713 pancreas lacks parts or has fewer parts of type pancreatic acinar cell, abnormal ZP:0012714 neutrophil pancreas mislocalised, abnormal ZP:0012715 pancreatic acinar cell decreased amount, abnormal ZP:0012716 neuromast hair cell decreased efficacy calcium ion import, abnormal ZP:0012717 posterior macula separated from tether cell sagitta, abnormal ZP:0012718 sagitta arrested otolith tethering, abnormal ZP:0012719 acellular anatomical structure utricle physical object quality, abnormal ZP:0012720 otic vesicle delayed otolith formation, abnormal ZP:0012721 otic vesicle delayed otolith tethering, abnormal ZP:0012722 BMP signaling pathway increased process quality, abnormal ZP:0012723 nodal signaling pathway increased process quality, abnormal ZP:0012724 pronephric proximal tubule morphogenesis decreased process quality, abnormal ZP:0012725 glomerular visceral epithelial cell migration decreased process quality, abnormal ZP:0012726 pronephric proximal convoluted tubule malformed, abnormal ZP:0012727 pronephric podocyte mislocalised laterally, abnormal ZP:0012728 pronephros arrested epithelial cilium movement involved in extracellular fluid movement, abnormal ZP:0012729 cell migration involved in sprouting angiogenesis decreased process quality, abnormal ZP:0012730 liver right side of gut, abnormal ZP:0012731 pancreas left side of gut, abnormal ZP:0012732 macula adjacent to macula, abnormal ZP:0012733 posterior macula has extra parts of type hair cell, abnormal ZP:0012734 epiboly decreased duration, abnormal ZP:0012735 whole organism has fewer parts of type cell, abnormal ZP:0012736 whole organism has extra parts of type cell, abnormal ZP:0012737 whole organism altered number of cell, abnormal ZP:0012738 posterior macula decreased size, abnormal ZP:0012739 posterior macula has fewer parts of type hair cell, abnormal ZP:0012740 shield poorly differentiated, abnormal ZP:0012741 germ ring poorly differentiated, abnormal ZP:0012742 sympathetic nervous system development process quality, abnormal ZP:0012743 filopodium cranial neural crest decreased length, abnormal ZP:0012744 filopodium cranial neural crest decreased amount, abnormal ZP:0012745 cardiac muscle cell decreased volume, abnormal ZP:0012746 cranial neural crest misrouted, abnormal ZP:0012747 cranial neural crest process quality neural crest cell migration, abnormal ZP:0012748 sympathetic nervous system decreased size, abnormal ZP:0012749 sympathetic nervous system malformed, abnormal ZP:0012750 pharyngeal arch 1 absent, abnormal ZP:0012751 pharyngeal arch 1 process quality neural crest cell migration, abnormal ZP:0012752 cranial neural crest pharyngeal arch 1 misrouted, abnormal ZP:0012753 pectoral fin bud increased occurrence cell death, abnormal ZP:0012754 pectoral fin bud decreased occurrence cell population proliferation, abnormal ZP:0012755 pectoral fin field decreased size, abnormal ZP:0012756 pectoral fin field distributed, abnormal ZP:0012757 scapulocoracoid absent, abnormal ZP:0012758 scapulocoracoid malformed, abnormal ZP:0012759 bony projection scapulocoracoid absent, abnormal ZP:0012760 bony projection scapulocoracoid mislocalised, abnormal ZP:0012761 pectoral fin endoskeletal disc aplastic, abnormal ZP:0012762 Notch signaling pathway decreased process quality, abnormal ZP:0012763 trunk vasculature process quality blood vessel morphogenesis, abnormal ZP:0012764 retinal cone cell increased amount, abnormal ZP:0012765 endodermal cell differentiation increased occurrence, abnormal ZP:0012766 hypoblast has extra parts of type endodermal cell, abnormal ZP:0012767 swimming behavior increased behavioural activity, abnormal ZP:0012768 interneuron somite decreased amount, abnormal ZP:0012769 glutamatergic neuron increased amount, abnormal ZP:0012770 glycinergic neuron decreased amount, abnormal ZP:0012782 pronephric duct morphogenesis process quality, abnormal ZP:0012815 central artery structure, abnormal ZP:0012852 posterior lateral line morphology, abnormal ZP:0012870 apoptotic process process quality, abnormal ZP:0012877 locomotory behavior occurrence, abnormal ZP:0012890 cardiac atrium development process quality, abnormal ZP:0012891 cardiac ventricle development process quality, abnormal ZP:0012926 intersegmental vein morphology, abnormal ZP:0012943 neural keel morphology, abnormal ZP:0012953 thigmotaxis occurrence, abnormal ZP:0012965 central nervous system structure, abnormal ZP:0012993 endocrine pancreas morphology, abnormal ZP:0013010 whole organism size, abnormal ZP:0013026 sarcomere atrium morphology, abnormal ZP:0013065 rhombomere 3 morphology, abnormal ZP:0013068 vasculature liver morphology, abnormal ZP:0013069 hepatocyte structure, abnormal ZP:0013119 Meckel's cartilage size, abnormal ZP:0013121 palatoquadrate cartilage size, abnormal ZP:0013123 ceratohyal cartilage size, abnormal ZP:0013124 ceratohyal cartilage length, abnormal ZP:0013125 ceratohyal cartilage distance Meckel's cartilage, abnormal ZP:0013137 cell division process quality, abnormal ZP:0013142 pharyngeal endoderm morphology, abnormal ZP:0013148 habenula symmetry, abnormal ZP:0013173 visual behavior process quality, abnormal ZP:0013176 peripheral nervous system development process quality, abnormal ZP:0013179 testis morphology, abnormal ZP:0013186 Sertoli cell present, abnormal ZP:0013224 ventral spinal nerve morphology, abnormal ZP:0013230 larval development process quality, abnormal ZP:0013249 lens fiber cell morphogenesis process quality, abnormal ZP:0013258 circadian rhythm process quality, abnormal ZP:0013259 pineal gland development process quality, abnormal ZP:0013279 phototaxis process quality, abnormal ZP:0013286 myofibril slow muscle cell morphology, abnormal ZP:0013297 rRNA processing process quality, abnormal ZP:0013360 angioblast cell differentiation process quality, abnormal ZP:0013369 whole organism male fertility, abnormal ZP:0013379 axoneme pronephros morphology, abnormal ZP:0013388 pronephric tubule shape, abnormal ZP:0013402 pericardium structure, abnormal ZP:0013456 photoreceptor outer segment layer morphology, abnormal ZP:0013470 axoneme pronephric duct structure, abnormal ZP:0013484 cilium otic vesicle morphology, abnormal ZP:0013486 fucosylation decreased process quality, abnormal ZP:0013488 embryonic heart tube development process quality, abnormal ZP:0013501 cardiac muscle morphology, abnormal ZP:0013527 perichondral bone absent, abnormal ZP:0013546 Kupffer's vesicle lumenized, abnormal ZP:0013554 male gonad development process quality, abnormal ZP:0013573 extrapancreatic duct morphology, abnormal ZP:0013590 notochord shape, abnormal ZP:0013611 erythrocyte maturation process quality, abnormal ZP:0013613 whole organism physical object quality, abnormal ZP:0013619 neural tube spatial pattern, abnormal ZP:0013651 renal glomerulus morphology, abnormal ZP:0013664 cardiac ventricle volume, abnormal ZP:0013670 canonical Wnt signaling pathway process quality, abnormal ZP:0013681 atrioventricular valve morphogenesis disrupted, abnormal ZP:0013685 mesencephalic vein morphology, abnormal ZP:0013689 motor neuron action potential, abnormal ZP:0013748 posterior lateral line nerve morphology, abnormal ZP:0013753 lens development in camera-type eye process quality, abnormal ZP:0013759 trigeminal ganglion morphology, abnormal ZP:0013760 melanophore stripe morphology, abnormal ZP:0013779 posterior lateral line neuromast position, abnormal ZP:0013799 ribosome biogenesis process quality, abnormal ZP:0013833 cardiac muscle cell morphology, abnormal ZP:0013848 cranial nerve VII spatial pattern, abnormal ZP:0013869 sarcomere slow muscle cell morphology, abnormal ZP:0013876 adrenal gland development process quality, abnormal ZP:0013877 interrenal gland position, abnormal ZP:0013878 interrenal gland decreased occurrence epithelial to mesenchymal transition, abnormal ZP:0013879 interrenal gland process quality animal organ morphogenesis, abnormal ZP:0013880 pronephric glomerulus separated from pronephric glomerulus, abnormal ZP:0013881 chromaffin cell mislocalised, abnormal ZP:0013882 interrenal angiogenic sprout decreased length, abnormal ZP:0013883 cardiac muscle progenitor cell migration to the midline involved in heart field formation decreased occurrence, abnormal ZP:0013884 heart split bilaterally, abnormal ZP:0013885 heart tube split bilaterally, abnormal ZP:0013886 myocardial precursor mislocalised laterally, abnormal ZP:0013887 enterocyte differentiation decreased occurrence, abnormal ZP:0013888 intestinal epithelium has fewer parts of type enterocyte, abnormal ZP:0013889 intestinal epithelium decreased occurrence endocytosis, abnormal ZP:0013890 digestive tract morphogenesis decreased process quality, abnormal ZP:0013891 intestinal epithelium malformed, abnormal ZP:0013892 intestinal epithelium has extra parts of type goblet cell, abnormal ZP:0013893 apical region intestinal epithelium physical object quality, abnormal ZP:0013894 intestinal epithelium process quality endocytosis, abnormal ZP:0013895 intestinal epithelium decreased process quality Notch signaling pathway, abnormal ZP:0013896 apical plasma membrane intestinal epithelium increased area, abnormal ZP:0013897 epithelial cell intestinal epithelium decreased height, abnormal ZP:0013898 recycling endosome enterocyte mislocalised radially, abnormal ZP:0013899 gut disrupted innervation, abnormal ZP:0013900 bone mineralization increased occurrence, abnormal ZP:0013901 integument mineralized, abnormal ZP:0013902 cranium increased occurrence bone mineralization, abnormal ZP:0013903 vertebral column increased occurrence bone mineralization, abnormal ZP:0013904 anatomical space vertebral column mineralized, abnormal ZP:0013905 islet increased amount, abnormal ZP:0013906 islet decreased size, abnormal ZP:0013907 antero-medial region endoderm decreased object quality, abnormal ZP:0013908 anterior region endoderm apoptotic, abnormal ZP:0013909 endoderm increased occurrence apoptotic process, abnormal ZP:0013910 pharyngeal endoderm mislocalised laterally, abnormal ZP:0013911 Notch signaling pathway decreased intensity, abnormal ZP:0013912 ventral mandibular arch atrophied, abnormal ZP:0013913 endoderm cellular quality, abnormal ZP:0013914 cerebellar neuron development disrupted, abnormal ZP:0013915 prechordal plate decreased speed, abnormal ZP:0013916 voltage-gated sodium channel activity decreased process quality, abnormal ZP:0013918 Golgi to plasma membrane protein transport disrupted, abnormal ZP:0013919 skeletal muscle action potential, abnormal ZP:0013920 Rohon-Beard neuron action potential, abnormal ZP:0013921 Rohon-Beard neuron accumulation voltage-gated sodium channel complex endoplasmic reticulum Rohon-Beard neuron, abnormal ZP:0013922 Rohon-Beard neuron accumulation voltage-gated sodium channel complex Golgi apparatus Rohon-Beard neuron, abnormal ZP:0013923 response to light stimulus process quality, abnormal ZP:0013924 spinal cord has fewer parts of type motor neuron synapse motor neuron, abnormal ZP:0013925 dorsal anterior lateral line nerve has fewer parts of type synapse dorsal anterior lateral line nerve, abnormal ZP:0013926 dorsal anterior lateral line nerve decreased process quality synapse assembly, abnormal ZP:0013927 motor neuron decreased process quality synapse assembly, abnormal ZP:0013931 optic vesicle constricted, abnormal ZP:0013932 retinal pigmented epithelium disconnected, abnormal ZP:0013933 retina folded, abnormal ZP:0013934 cornea pigmented, abnormal ZP:0013935 ventral region optic cup decreased depth, abnormal ZP:0013936 lens epithelium decreased occurrence cell population proliferation, abnormal ZP:0013937 ceratohyal cartilage pharyngeal arch 2 malformed, abnormal ZP:0013947 caudal fin increased size, abnormal ZP:0013954 whole organism degree of pigmentation, abnormal ZP:0013955 microtubule pronephric duct disorganized, abnormal ZP:0013959 fibroblast vertical myoseptum mislocalised, abnormal ZP:0013961 endodermal cell differentiation arrested, abnormal ZP:0013963 nodal signaling pathway decreased occurrence, abnormal ZP:0013965 hypoblast lacks all parts of type endodermal cell, abnormal ZP:0013971 caudal fin morphogenesis disrupted, abnormal ZP:0013972 fin fold actinotrichium decreased size, abnormal ZP:0013973 ventral fin fold has fewer parts of type fin fold actinotrichium, abnormal ZP:0013975 ocular blood vessel decreased amount, abnormal ZP:0013979 photoreceptor outer segment retinal cone cell disorganized, abnormal ZP:0013992 dorsal longitudinal anastomotic vessel decreased diameter, abnormal ZP:0013993 subintestinal vein increased occurrence sprouting angiogenesis, abnormal ZP:0013997 posterior cardinal vein broken, abnormal ZP:0013998 cranial vasculature physical object quality, abnormal ZP:0013999 aortic arch physical object quality, abnormal ZP:0014000 caudal vein decreased size, abnormal ZP:0014001 angiogenic sprout intersegmental vessel arrested, abnormal ZP:0014002 subintestinal vein decreased size, abnormal ZP:0014003 intersegmental vessel increased size, abnormal ZP:0014004 filopodium intersegmental vessel increased amount, abnormal ZP:0014007 intersegmental vessel decreased branchiness, abnormal ZP:0014008 trunk vasculature lacks parts or has fewer parts of type filopodium blood vessel endothelial cell, abnormal ZP:0014009 filopodium intersegmental vessel decreased size, abnormal ZP:0014010 blood vessel intestine decreased branchiness, abnormal ZP:0014012 angioblast cell migration from lateral mesoderm to midline process quality, abnormal ZP:0014020 chondroblast palatoquadrate cartilage disorganized, abnormal ZP:0014024 blood vessel increased branchiness, abnormal ZP:0014032 caudal vein plexus process quality blood vessel development, abnormal ZP:0014033 cell-cell junction blood vessel endothelial cell decreased amount, abnormal ZP:0014035 intersegmental vessel extends beyond somite, abnormal ZP:0014043 eye photoreceptor cell quality, abnormal ZP:0014044 iridophore intensity, abnormal ZP:0014050 trunk increased size, abnormal ZP:0014051 notochord has extra parts of type cell notochord, abnormal ZP:0014052 notochord posterior region bifurcated, abnormal ZP:0014053 determination of ventral identity disrupted, abnormal ZP:0014054 whole organism lacks parts or has fewer parts of type post-vent region, abnormal ZP:0014055 Meckel's cartilage decreased thickness, abnormal ZP:0014056 palatoquadrate cartilage decreased thickness, abnormal ZP:0014058 liver increased amount, abnormal ZP:0014061 otolith angular, abnormal ZP:0014062 otolith star shaped, abnormal ZP:0014066 abducens motor nucleus adjacent to abducens motor nucleus, abnormal ZP:0014067 trigeminal motor nucleus adjacent to trigeminal motor nucleus, abnormal ZP:0014087 desmosome heart structure, abnormal ZP:0014088 renal tubule morphology, abnormal ZP:0014089 gut endothelial cell decreased size, abnormal ZP:0014090 pharyngeal arch 3-7 hypoplastic, abnormal ZP:0014092 fin regeneration decreased rate, abnormal ZP:0014098 fast muscle myoblast mononucleate, abnormal ZP:0014099 hindbrain size, abnormal ZP:0014101 caudal vein edematous, abnormal ZP:0014102 thyroid follicle morphology, abnormal ZP:0014103 endocrine pancreas dispersed, abnormal ZP:0014104 brain vasculature structure, abnormal ZP:0014106 defense response to bacterium arrested, abnormal ZP:0014114 margin morphology, abnormal ZP:0014115 yolk syncytial layer disorganized, abnormal ZP:0014116 microvillus external yolk syncytial layer decreased length, abnormal ZP:0014117 microvillus external yolk syncytial layer decreased mass density, abnormal ZP:0014118 margin irregular spatial pattern, abnormal ZP:0014120 filamentous actin external yolk syncytial layer disorganized, abnormal ZP:0014133 cardiac ventricle increased volume, abnormal ZP:0014143 retinal pigmented epithelium colorless, abnormal ZP:0014156 cell brain apoptotic, abnormal ZP:0014182 common cardinal vein aplastic, abnormal ZP:0014185 liver vacuolated, abnormal ZP:0014189 epithelium development process quality, abnormal ZP:0014206 ventricular cardiac myofibril assembly process quality, abnormal ZP:0014207 striated muscle myosin thick filament cardiac ventricle absent, abnormal ZP:0014217 sodium ion transport increased occurrence, abnormal ZP:0014218 chloride transport decreased occurrence, abnormal ZP:0014219 calcium-independent cell-cell adhesion via plasma membrane cell-adhesion molecules disrupted, abnormal ZP:0014220 adherens junction maintenance disrupted, abnormal ZP:0014221 DEL increased accumulation cytoplasmic vesicle DEL, abnormal ZP:0014222 adherens junction EVL disorganized, abnormal ZP:0014223 adherens junction DEL disorganized, abnormal ZP:0014224 cell DEL circular, abnormal ZP:0014225 cell DEL disorganized, abnormal ZP:0014226 cell brain dead, abnormal ZP:0014238 otolith formation process quality, abnormal ZP:0014239 inner ear morphogenesis process quality, abnormal ZP:0014240 macula utricle decreased size, abnormal ZP:0014241 lateral crista aplastic, abnormal ZP:0014242 posterior crista aplastic, abnormal ZP:0014243 statoacoustic (VIII) ganglion malformed, abnormal ZP:0014244 anterior crista aplastic, abnormal ZP:0014245 macula saccule decreased size, abnormal ZP:0014246 pillar of the anterior semicircular canal aplastic, abnormal ZP:0014247 pillar of the lateral semicircular canal aplastic, abnormal ZP:0014248 pillar of the posterior semicircular canal aplastic, abnormal ZP:0014256 somite border spatial pattern, abnormal ZP:0014257 melanocyte black, abnormal ZP:0014258 midbrain opaque, abnormal ZP:0014260 intestinal villus gut epithelium absent, abnormal ZP:0014261 epithelial cell gut circular, abnormal ZP:0014262 smooth muscle cell gut disorganized, abnormal ZP:0014269 caudal fin development disrupted, abnormal ZP:0014275 fin regeneration decreased process quality, abnormal ZP:0014277 wound healing decreased process quality, abnormal ZP:0014282 heart primordium has fewer parts of type cardiac muscle cell, abnormal ZP:0014292 muscle cell undulate, abnormal ZP:0014293 muscle tendon junction myotome physical object quality, abnormal ZP:0014294 muscle cell increased length, abnormal ZP:0014309 endocrine cell posterior pancreatic bud decreased amount, abnormal ZP:0014312 neural crest absent, abnormal ZP:0014322 trigeminal ganglion apoptotic, abnormal ZP:0014323 peripheral neuron head decreased amount, abnormal ZP:0014324 cardiac chamber formation process quality, abnormal ZP:0014325 cranial blood vessel hemorrhagic, abnormal ZP:0014326 response to chemical disrupted, abnormal ZP:0014332 nucleus yolk syncytial layer shape, abnormal ZP:0014333 nucleus yolk syncytial layer dense, abnormal ZP:0014334 nucleus yolk syncytial layer irregular spatial pattern, abnormal ZP:0014335 margin blastoderm irregular spatial pattern, abnormal ZP:0014336 yolk syncytial layer fused with chromosome chromosome yolk syncytial layer, abnormal ZP:0014337 nucleus yolk syncytial layer undivided, abnormal ZP:0014338 sarcomere slow muscle cell absent, abnormal ZP:0014339 filamentous actin slow muscle cell dispersed, abnormal ZP:0014340 myofibril muscle cell absent, abnormal ZP:0014341 myofibril slow muscle cell undulate, abnormal ZP:0014347 cytoskeleton of presynaptic active zone neuromast hair cell decreased size, abnormal ZP:0014350 musculoskeletal movement decreased magnitude, abnormal ZP:0014353 locomotion involved in locomotory behavior decreased process quality, abnormal ZP:0014354 mesodermal to mesenchymal transition involved in gastrulation disrupted, abnormal ZP:0014355 mesodermal cell spatial pattern, abnormal ZP:0014356 bleb hypoblast increased amount, abnormal ZP:0014364 retina lacks all parts of type microvillus retinal pigmented epithelium, abnormal ZP:0014377 response to wounding disrupted, abnormal ZP:0014379 frontal bone decreased thickness, abnormal ZP:0014382 pronephric proximal convoluted tubule dilated, abnormal ZP:0014383 pronephric capsular space increased size, abnormal ZP:0014384 slow muscle cell trunk musculature decreased contractility, abnormal ZP:0014385 slow muscle cell post-vent region decreased contractility, abnormal ZP:0014389 endocardial progenitor cell migration to the midline involved in heart field formation disrupted, abnormal ZP:0014390 Wnt signaling pathway increased occurrence, abnormal ZP:0014392 regulation of RNA stability disrupted, abnormal ZP:0014394 angiogenic sprout intersegmental vessel decreased amount, abnormal ZP:0014398 pronephric podocyte fused with pronephric podocyte, abnormal ZP:0014399 anterior region pronephros deformed, abnormal ZP:0014400 pronephric tubule fused with anterior region anterior region pronephric tubule, abnormal ZP:0014401 pronephric glomerular capillary hypoplastic, abnormal ZP:0014402 pronephric glomerular capillary non-functional, abnormal ZP:0014408 nucleus yolk syncytial layer spatial pattern, abnormal ZP:0014409 microtubule yolk syncytial layer spatial pattern, abnormal ZP:0014412 myosin filament assembly arrested, abnormal ZP:0014413 axon motor neuron disoriented, abnormal ZP:0014440 embryo development decreased functionality, abnormal ZP:0014445 fin regeneration process quality, abnormal ZP:0014454 response to hypoxia decreased process quality, abnormal ZP:0014462 notochord granular, abnormal ZP:0014463 vesicle notochord inner cell decreased size, abnormal ZP:0014464 migratory slow muscle precursor cell decreased amount, abnormal ZP:0014466 dopaminergic neuron retina decreased amount, abnormal ZP:0014472 tail bud malformed, abnormal ZP:0014482 anterior-posterior axis whole organism morphology, abnormal ZP:0014491 heart tube medial orientation, abnormal ZP:0014492 anterior region neuroectoderm absent, abnormal ZP:0014495 whole organism increased permeability, abnormal ZP:0014497 erythrocyte differentiation decreased process quality, abnormal ZP:0014499 blood cell heart decreased amount, abnormal ZP:0014512 musculoskeletal movement increased occurrence, abnormal ZP:0014524 Kupffer's vesicle increased area, abnormal ZP:0014525 BMP signaling pathway involved in heart development decreased process quality, abnormal ZP:0014531 ventral mandibular arch open, abnormal ZP:0014532 chondrocranium cartilage absent, abnormal ZP:0014547 cardiac muscle cell proliferation decreased process quality, abnormal ZP:0014566 heart decreased width, abnormal ZP:0014571 slow muscle cell adaxial to somite, abnormal ZP:0014574 cardiac ventricle constricted, abnormal ZP:0014594 muscle structure development disrupted, abnormal ZP:0014595 fast muscle cell bent, abnormal ZP:0014596 rhombomere 5 decreased size, abnormal ZP:0014597 rhombomere 3 decreased size, abnormal ZP:0014599 mitochondrial calcium ion transmembrane transport disrupted, abnormal ZP:0014600 Kupffer's vesicle has fewer parts of type inner dynein arm ciliated cell, abnormal ZP:0014601 Kupffer's vesicle has fewer parts of type outer dynein arm ciliated cell, abnormal ZP:0014602 motile cilium Kupffer's vesicle decreased speed, abnormal ZP:0014603 motile cilium Kupffer's vesicle shortened, abnormal ZP:0014604 gut process quality left/right pattern formation, abnormal ZP:0014637 cortisol metabolic process increased process quality, abnormal ZP:0014638 cortisol metabolic process decreased process quality, abnormal ZP:0014639 hatching process quality, abnormal ZP:0014641 hatching premature, abnormal ZP:0014642 EVL temporally extended epiboly, abnormal ZP:0014643 yolk syncytial layer temporally extended epiboly, abnormal ZP:0014644 DEL arrested epiboly, abnormal ZP:0014645 DEL temporally extended epiboly, abnormal ZP:0014651 pronephric proximal straight tubule decreased size, abnormal ZP:0014653 regulation of cardiac muscle contraction by calcium ion signaling process quality, abnormal ZP:0014655 atrial cardiac muscle cell action potential process quality, abnormal ZP:0014656 troponin complex heart disorganized, abnormal ZP:0014657 muscle thin filament tropomyosin heart disorganized, abnormal ZP:0014658 sarcomere cardiac ventricle disorganized, abnormal ZP:0014659 sarcomere heart disorganized, abnormal ZP:0014660 cardiac ventricle decreased process quality heart contraction, abnormal ZP:0014661 cardiac myofibril heart disorganized, abnormal ZP:0014674 neutrophil migration decreased process quality, abnormal ZP:0014681 reactive oxygen species metabolic process process quality, abnormal ZP:0014682 head kidney decreased size, abnormal ZP:0014688 cleithrum absent, abnormal ZP:0014690 parachordal cartilage absent, abnormal ZP:0014692 mesoderm decreased amount, abnormal ZP:0014716 whole organism decreased process quality apoptotic process, abnormal ZP:0014717 whole organism decreased process quality cell population proliferation, abnormal ZP:0014727 bulbus arteriosus absent, abnormal ZP:0014734 mesoderm development process quality, abnormal ZP:0014736 median fin fold decreased width, abnormal ZP:0014746 muscle detached from tendon, abnormal ZP:0014747 muscle tendon junction somite border morphology, abnormal ZP:0014748 cardiac muscle cell action potential process quality, abnormal ZP:0014759 retina has fewer parts of type retinal rod cell, abnormal ZP:0014763 BMP signaling pathway decreased process quality, abnormal ZP:0014774 optic tectum increased process quality cell population proliferation, abnormal ZP:0014778 photoreceptor cell development process quality, abnormal ZP:0014779 lens nucleated, abnormal ZP:0014780 lens process quality enucleation, abnormal ZP:0014781 adult behavior process quality, abnormal ZP:0014785 posterior region trunk decreased length, abnormal ZP:0014803 palatoquadrate arch absent, abnormal ZP:0014804 palatoquadrate arch decreased size, abnormal ZP:0014805 interrenal gland decreased size, abnormal ZP:0014806 neuromuscular process controlling balance process quality, abnormal ZP:0014814 pronephric glomerular basement membrane increased permeability, abnormal ZP:0014815 left/right axis specification process quality, abnormal ZP:0014816 inner ear has extra parts of type otolith, abnormal ZP:0014817 cilium Kupffer's vesicle disorganized, abnormal ZP:0014818 Kupffer's vesicle has fewer parts of type cilium axonemal microtubule Kupffer's vesicle, abnormal ZP:0014819 growth decreased process quality, abnormal ZP:0014822 posterior lateral line neuromast mislocalised, abnormal ZP:0014826 oligodendrocyte decreased process quality cell division, abnormal ZP:0014830 hypothalamus absent, abnormal ZP:0014848 melanosome trunk increased area, abnormal ZP:0014851 optic cup deformed, abnormal ZP:0014852 ventricular system absent, abnormal ZP:0014858 endodermal cell fate specification decreased process quality, abnormal ZP:0014859 whole organism lacks all parts of type endoderm, abnormal ZP:0014860 branchiomotor neuron rhombomere 5 mislocalised anteriorly, abnormal ZP:0014865 blood desaturated red, abnormal ZP:0014867 EVL delayed epiboly, abnormal ZP:0014868 DEL delayed epiboly, abnormal ZP:0014884 spinal cord has fewer parts of type dorsal side oligodendrocyte, abnormal ZP:0014885 spinal cord process quality central nervous system myelination, abnormal ZP:0014890 retinal rod cell degeneration, abnormal ZP:0014891 chondrocyte decreased amount, abnormal ZP:0014897 axon fasciculus retroflexus misrouted, abnormal ZP:0014914 neuromast decreased occurrence cell population proliferation, abnormal ZP:0014916 posterior lateral line neuromast hair cell differentiation decreased occurrence, abnormal ZP:0014920 gut inverted, abnormal ZP:0014921 embryonic heart tube elongation decreased process quality, abnormal ZP:0014922 primitive heart tube decreased length, abnormal ZP:0014923 cardiac ventricle process quality heart contraction, abnormal ZP:0014924 cardiac muscle cell cardiac ventricle decreased volume, abnormal ZP:0014926 cranial neural crest cell decreased process quality cell population proliferation, abnormal ZP:0014927 mandibular arch skeleton quality, abnormal ZP:0014931 endocardial cushion agenesis, abnormal ZP:0014934 atrioventricular valve development process quality, abnormal ZP:0014948 cardioblast cell midline fusion disrupted, abnormal ZP:0014952 midbrain decreased volume, abnormal ZP:0014956 hemopoiesis quality, abnormal ZP:0014965 granulocyte spatial pattern, abnormal ZP:0014967 brain spatial pattern, abnormal ZP:0014969 cell migration quality, abnormal ZP:0014984 fin increased size, abnormal ZP:0014985 diencephalon spatial pattern, abnormal ZP:0014987 scale spatial pattern, abnormal ZP:0014988 pancreas spatial pattern, abnormal ZP:0014991 testis increased amount, abnormal ZP:0014992 pectoral fin musculature decreased amount, abnormal ZP:0014995 caudal fin spatial pattern, abnormal ZP:0014998 head spatial pattern, abnormal ZP:0015003 musculature system decreased amount, abnormal ZP:0015004 epidermal cell circular, abnormal ZP:0015012 testis absent, abnormal ZP:0015013 ovary increased amount, abnormal ZP:0015014 gonad decreased size, abnormal ZP:0015015 melanophore stripe decreased width, abnormal ZP:0015016 epidermal cell decreased amount, abnormal ZP:0015019 gonad absent, abnormal ZP:0015029 scale size, abnormal ZP:0015031 branchiostegal ray decreased amount, abnormal ZP:0015040 granulocyte absent, abnormal ZP:0015041 mitochondrion posterior lateral line nerve decreased amount, abnormal ZP:0015042 axon posterior lateral line nerve discolored, abnormal ZP:0015043 synaptic vesicle posterior lateral line nerve mislocalised, abnormal ZP:0015046 Muller cell increased amount, abnormal ZP:0015049 heart rudiment has fewer parts of type cardiac muscle cell, abnormal ZP:0015050 cardiac ventricle lacks all parts of type trabecular layer of ventricle, abnormal ZP:0015051 cardiac muscle cell cardiac ventricle irregular spatial pattern, abnormal ZP:0015053 fin mislocalised, abnormal ZP:0015054 ventral larval melanophore stripe duplicated, abnormal ZP:0015055 extension wholly ventralized, abnormal ZP:0015056 anal fin duplicated, abnormal ZP:0015066 cardiac muscle cell increased process quality apoptotic process, abnormal ZP:0015069 cardiac ventricle has extra parts of type cardiac muscle cell, abnormal ZP:0015070 heart has extra parts of type cardiac muscle cell, abnormal ZP:0015071 atrium has extra parts of type cardiac muscle cell, abnormal ZP:0015078 posterior lateral line primordium decreased process quality cell division, abnormal ZP:0015079 neuromast increased distance neuromast, abnormal ZP:0015080 neuromast decreased distance neuromast, abnormal ZP:0015081 lateral line primordium decreased size, abnormal ZP:0015084 posterior lateral line primordium decreased process quality adherens junction maintenance, abnormal ZP:0015093 gonad development quality, abnormal ZP:0015096 mature neutrophil decreased amount, abnormal ZP:0015099 mature neutrophil absent, abnormal ZP:0015106 muscle pioneer spatial pattern, abnormal ZP:0015114 cranium decreased length, abnormal ZP:0015115 scale absent, abnormal ZP:0015119 yolk structure, abnormal ZP:0015122 melanophore stripe spatial pattern, abnormal ZP:0015124 intersegmental vessel delayed sprouting angiogenesis, abnormal ZP:0015147 multi-ciliated epithelial cell pronephros decreased amount, abnormal ZP:0015151 otic placode absent, abnormal ZP:0015154 neuroectoderm increased size, abnormal ZP:0015155 non neural ectoderm decreased size, abnormal ZP:0015162 testis hypertrophic, abnormal ZP:0015171 muscle cell somite disorganized, abnormal ZP:0015172 melanocyte spindle-shaped, abnormal ZP:0015177 circadian sleep/wake cycle, wakefulness increased occurrence, abnormal ZP:0015180 response to absence of light increased occurrence, abnormal ZP:0015184 nucleate erythrocyte accumulation head, abnormal ZP:0015208 Notch signaling pathway increased process quality, abnormal ZP:0015240 otic vesicle decreased amount, abnormal ZP:0015243 otic placode decreased amount, abnormal ZP:0015250 hatching gland hypoplastic, abnormal ZP:0015258 primary motor neuron structure, abnormal ZP:0015259 pronephros edematous, abnormal ZP:0015260 cilium pronephros decreased amount, abnormal ZP:0015275 thymus increased size, abnormal ZP:0015279 cardiac muscle cell mislocalised, abnormal ZP:0015280 vasculogenesis arrested, abnormal ZP:0015281 axial vasculature aplastic, abnormal ZP:0015282 primitive hemopoiesis arrested, abnormal ZP:0015283 ventral wall of dorsal aorta lacks all parts of type nucleate erythrocyte, abnormal ZP:0015285 motile cilium pronephric duct immobile, abnormal ZP:0015286 heart tube decreased functionality, abnormal ZP:0015287 neural tube bilateral symmetry, abnormal ZP:0015293 heart tube absent, abnormal ZP:0015317 macrophage aggregated, abnormal ZP:0015318 ball decreased size, abnormal ZP:0015319 inner ear sharpness, abnormal ZP:0015320 inner ear lacks all parts of type lapillus, abnormal ZP:0015321 ball morphology, abnormal ZP:0015324 pillar of the lateral semicircular canal decreased size, abnormal ZP:0015326 inner ear symmetrical, abnormal ZP:0015327 posterior macula deformed, abnormal ZP:0015328 lateral crista hypotrophic, abnormal ZP:0015329 anterior macula deformed, abnormal ZP:0015330 inner ear degenerate, abnormal ZP:0015331 inner ear increased thickness, abnormal ZP:0015332 stereocilium bundle macula decreased amount, abnormal ZP:0015333 inner ear lacks all parts of type sagitta, abnormal ZP:0015334 inner ear flat, abnormal ZP:0015341 intestine neoplastic, abnormal ZP:0015349 sleep increased duration, abnormal ZP:0015352 cilium olfactory placode absent, abnormal ZP:0015353 retinal rod cell development disrupted, abnormal ZP:0015354 renal glomerulus increased size, abnormal ZP:0015355 posterior neural keel increased width, abnormal ZP:0015356 anterior neural keel flat, abnormal ZP:0015357 post-vent region spade-shaped, abnormal ZP:0015358 cell medial floor plate mislocalised, abnormal ZP:0015359 whole organism has fewer parts of type posterior region muscle, abnormal ZP:0015360 paraxial mesoderm disorganized, abnormal ZP:0015361 cell pronephros increased amount, abnormal ZP:0015362 mesoderm absent, abnormal ZP:0015363 keratin accumulating cell increased accumulation epidermis, abnormal ZP:0015366 corpuscles of Stannius increased size, abnormal ZP:0015368 pronephric distal early tubule increased length, abnormal ZP:0015373 caudal vein plexus increased diameter, abnormal ZP:0015374 axial vasculature unlumenized, abnormal ZP:0015375 axial vasculature perforate, abnormal ZP:0015376 splanchnocranium decreased size, abnormal ZP:0015379 posterior cardinal vein collapsed, abnormal ZP:0015380 cranial vasculature misrouted, abnormal ZP:0015381 anterior cardinal vein unfused from posterior cardinal vein, abnormal ZP:0015382 lateral dorsal aorta unfused from lateral dorsal aorta, abnormal ZP:0015387 sperm decreased cellular motility, abnormal ZP:0015391 fertilization decreased occurrence, abnormal ZP:0015392 integument translucent, abnormal ZP:0015395 iridophore eye absent, abnormal ZP:0015403 ocular blood vessel irregular spatial pattern, abnormal ZP:0015404 ocular blood vessel degenerate, abnormal ZP:0015407 heart process process quality, abnormal ZP:0015412 thigmotaxis behavioral quality of a process, abnormal ZP:0015413 response to nicotine decreased process quality, abnormal ZP:0015414 melanocyte sparse, abnormal ZP:0015426 blastoderm irregular spatial pattern, abnormal ZP:0015438 keratinocyte differentiation disrupted, abnormal ZP:0015439 cell population proliferation increased duration, abnormal ZP:0015440 epidermal cell increased amount, abnormal ZP:0015441 cardiac muscle tissue development disrupted, abnormal ZP:0015442 heart perforate, abnormal ZP:0015448 blood cell mislocalised, abnormal ZP:0015458 neuromast hair cell increased amount, abnormal ZP:0015470 primordial hindbrain channel arrested blood vessel development, abnormal ZP:0015473 intersegmental vessel arrested blood vessel development, abnormal ZP:0015475 common cardinal vein malformed, abnormal ZP:0015476 cranial vasculature structure, abnormal ZP:0015479 DEL translucent, abnormal ZP:0015480 actin filament yolk syncytial layer spatial pattern, abnormal ZP:0015481 cortical cytoskeleton yolk syncytial layer morphology, abnormal ZP:0015482 germ ring morphology, abnormal ZP:0015483 lamellipodium EVL increased amount, abnormal ZP:0015484 blastoderm cell EVL morphology, abnormal ZP:0015485 microtubule yolk syncytial layer disorganized, abnormal ZP:0015486 vesicle yolk syncytial layer present, abnormal ZP:0015489 marginal blastomere constricted, abnormal ZP:0015490 blastoderm decreased size, abnormal ZP:0015491 shield decreased size, abnormal ZP:0015492 shield malformed, abnormal ZP:0015493 blastoderm cell EVL circular, abnormal ZP:0015494 posterior lateral line decreased length, abnormal ZP:0015498 photoreceptor outer segment layer decreased thickness, abnormal ZP:0015499 photoreceptor outer segment retinal rod cell degenerate, abnormal ZP:0015503 blastomere shield mislocalised, abnormal ZP:0015514 mesencephalic vein malformed, abnormal ZP:0015522 sinoatrial node decreased functionality, abnormal ZP:0015525 retinal inner nuclear layer structure, abnormal ZP:0015527 oocyte anterior/posterior axis specification disrupted, abnormal ZP:0015528 intracellular mRNA localization disrupted, abnormal ZP:0015529 chorion micropyle formation disrupted, abnormal ZP:0015530 chorion malformed, abnormal ZP:0015531 oocyte physical object quality, abnormal ZP:0015532 oocyte positional polarity, abnormal ZP:0015533 unfertilized egg positional polarity, abnormal ZP:0015534 posterior region ovary neoplastic, abnormal ZP:0015535 mitochondrial cloud oocyte absent, abnormal ZP:0015553 iridophore decreased size, abnormal ZP:0015554 melanocyte punctiform, abnormal ZP:0015556 lymphocyte differentiation disrupted, abnormal ZP:0015563 anterior region neuroectoderm increased size, abnormal ZP:0015582 pronephros aplastic, abnormal ZP:0015584 blood vasculature liver aplastic, abnormal ZP:0015585 hepatocyte liver morphology, abnormal ZP:0015589 cellular response to DNA damage stimulus increased occurrence, abnormal ZP:0015594 endothelial cell trunk absent, abnormal ZP:0015595 neuromast hair cell differentiation involved in neuromast regeneration decreased occurrence, abnormal ZP:0015596 gut flattened, abnormal ZP:0015597 liver structure, abnormal ZP:0015598 liver low brightness, abnormal ZP:0015608 oocyte maturation process quality, abnormal ZP:0015609 pole plasm assembly process quality, abnormal ZP:0015610 pole plasm mRNA localization arrested, abnormal ZP:0015611 pole plasm mRNA localization process quality, abnormal ZP:0015612 oocyte stage II physical object quality, abnormal ZP:0015613 oocyte stage I symmetry, abnormal ZP:0015620 molecular layer corpus cerebelli malformed, abnormal ZP:0015621 axon granule cell decreased length, abnormal ZP:0015622 granule cell cerebellum decreased amount, abnormal ZP:0015623 Purkinje cell cerebellum decreased amount, abnormal ZP:0015632 myelination of posterior lateral line nerve axons decreased occurrence, abnormal ZP:0015633 posterior lateral line increased diameter, abnormal ZP:0015634 axon posterior lateral line defasciculated, abnormal ZP:0015635 Z disc cardiac muscle cell absent, abnormal ZP:0015636 fin fold actinotrichium disorganized, abnormal ZP:0015637 fin fold actinotrichium decreased mass density, abnormal ZP:0015639 caudal fin lepidotrichium malformed, abnormal ZP:0015640 interray vessel caudal fin disorganized, abnormal ZP:0015641 osteoblast caudal fin mislocalised, abnormal ZP:0015642 dorsal fin lepidotrichium undulate, abnormal ZP:0015643 anal fin lepidotrichium undulate, abnormal ZP:0015644 fin fold actinotrichium rough, abnormal ZP:0015645 caudal fin lepidotrichium fused with caudal fin lepidotrichium, abnormal ZP:0015646 caudal fin lepidotrichium undulate, abnormal ZP:0015647 fin fold actinotrichium lepidotrichium mislocalised, abnormal ZP:0015648 response to amphetamine arrested, abnormal ZP:0015654 skeletal muscle myofibril myotome morphology, abnormal ZP:0015656 brain folded, abnormal ZP:0015665 pelvic fin hypoplastic, abnormal ZP:0015666 pectoral fin lepidotrichium absent, abnormal ZP:0015667 pelvic fin lepidotrichium absent, abnormal ZP:0015668 pectoral fin bent, abnormal ZP:0015669 pectoral fin curved, abnormal ZP:0015670 otic vesicle protrusion aplastic, abnormal ZP:0015671 basihyal cartilage mislocalised posteriorly, abnormal ZP:0015672 melanocyte size, abnormal ZP:0015673 forebrain ventricle increased size, abnormal ZP:0015675 skeletal muscle acetylcholine-gated channel clustering process quality, abnormal ZP:0015681 pigment granule xanthophore composition, abnormal ZP:0015695 lymphocyte proliferation increased occurrence, abnormal ZP:0015696 fin neoplastic, abnormal ZP:0015697 head kidney neoplastic, abnormal ZP:0015698 common lymphoid progenitor head kidney increased amount, abnormal ZP:0015699 lymphocyte blood increased amount, abnormal ZP:0015700 lymphocyte head kidney increased amount, abnormal ZP:0015701 lymphocyte whole organism increased amount, abnormal ZP:0015702 lymphocyte whole organism neoplastic, malignant, abnormal ZP:0015703 erythroid lineage cell head kidney decreased amount, abnormal ZP:0015704 lymphoid progenitor cell whole organism increased amount, abnormal ZP:0015705 myeloid lineage restricted progenitor cell head kidney decreased amount, abnormal ZP:0015708 endoderm absent, abnormal ZP:0015721 epithelium pectoral fin degenerate, abnormal ZP:0015722 pectoral fin fold degenerate, abnormal ZP:0015723 pectoral fin necrotic, abnormal ZP:0015724 mating decreased efficiency, abnormal ZP:0015725 pelvic radial decreased amount, abnormal ZP:0015726 anal fin decreased size, abnormal ZP:0015727 dorsal fin lepidotrichium decreased length, abnormal ZP:0015728 dorsal fin lepidotrichium malformed, abnormal ZP:0015729 dorsal fin lepidotrichium decreased amount, abnormal ZP:0015730 dorsal fin pterygiophore decreased amount, abnormal ZP:0015731 anal fin pterygiophore decreased amount, abnormal ZP:0015732 anal fin lepidotrichium decreased length, abnormal ZP:0015733 melanophore stripe branched, abnormal ZP:0015734 pelvic fin lepidotrichium decreased length, abnormal ZP:0015735 pelvic fin lepidotrichium malformed, abnormal ZP:0015736 pectoral fin radial decreased amount, abnormal ZP:0015737 lepidotrichium segment decreased amount, abnormal ZP:0015738 pectoral fin skeleton has fewer parts of type lepidotrichium, abnormal ZP:0015739 axial fin skeleton has fewer parts of type lepidotrichium, abnormal ZP:0015740 pelvic fin has fewer parts of type lepidotrichium, abnormal ZP:0015741 pelvic fin skeleton has fewer parts of type lepidotrichium, abnormal ZP:0015742 dorsal fin hypoplastic, abnormal ZP:0015745 whole organism increased weight, abnormal ZP:0015777 vertical myoseptum irregular spatial pattern, abnormal ZP:0015778 somite border somite 11 amorphous, abnormal ZP:0015779 somite border somite 14 amorphous, abnormal ZP:0015780 somite border somite 17 amorphous, abnormal ZP:0015781 somite border somite 12 amorphous, abnormal ZP:0015782 somite border somite 15 amorphous, abnormal ZP:0015785 somite border somite 10 amorphous, abnormal ZP:0015786 somite border somite 13 amorphous, abnormal ZP:0015787 somite border somite 16 amorphous, abnormal ZP:0015788 reproductive behavior behavioral quality of a process, abnormal ZP:0015789 dentary structure, abnormal ZP:0015790 maxilla structure, abnormal ZP:0015791 gill malformed, abnormal ZP:0015792 opercular flap decreased size, abnormal ZP:0015793 premaxilla structure, abnormal ZP:0015794 supraorbital bone decreased size, abnormal ZP:0015795 mandibular arch skeleton increased length, abnormal ZP:0015796 orbital region decreased size, abnormal ZP:0015797 neurocranium structure, abnormal ZP:0015802 otolith physical object quality, abnormal ZP:0015803 hair cell inner ear decreased functionality, abnormal ZP:0015804 stereocilia tip link posterior lateral line neuromast absent, abnormal ZP:0015805 lysosome neuromast support cell increased amount, abnormal ZP:0015806 lysosome neuromast hair cell increased amount, abnormal ZP:0015807 stereocilium posterior lateral line neuromast decreased diameter, abnormal ZP:0015808 posterior lateral line neuromast physical object quality, abnormal ZP:0015811 apical ectodermal ridge pectoral fin bud absent, abnormal ZP:0015818 regulation of Notch signaling pathway disrupted, abnormal ZP:0015822 detection of light stimulus disrupted, abnormal ZP:0015823 entopterygoid decreased size, abnormal ZP:0015824 cranium structure, abnormal ZP:0015826 anterior region lens epithelium structure, abnormal ZP:0015828 blood cell increased amount, abnormal ZP:0015830 anterior lateral plate mesoderm decreased width, abnormal ZP:0015831 dorsal region forebrain aplastic, abnormal ZP:0015832 cell head undifferentiated, abnormal ZP:0015840 fast muscle cell myotome disorganized, abnormal ZP:0015846 response to mechanical stimulus disrupted, abnormal ZP:0015853 oocyte stage I absent, abnormal ZP:0015883 testis hypoplastic, abnormal ZP:0015885 spermatogonium absent, abnormal ZP:0015887 intracellular mRNA localization process quality, abnormal ZP:0015888 central nervous system myelination decreased occurrence, abnormal ZP:0015890 peripheral nervous system myelin maintenance process quality, abnormal ZP:0015891 oligodendrocyte physical object quality, abnormal ZP:0015895 cell projection oligodendrocyte mislocalised, abnormal ZP:0015896 detection of mechanical stimulus involved in sensory perception of touch disrupted, abnormal ZP:0015899 lapillus absent, abnormal ZP:0015907 female gonad development process quality, abnormal ZP:0015938 afferent neuron has extra parts of type dendritic branch afferent neuron, abnormal ZP:0015950 notochord mislocalised, abnormal ZP:0015977 central artery decreased amount, abnormal ZP:0015978 central artery absent, abnormal ZP:0015992 glomerular basement membrane decreased functionality, abnormal ZP:0016010 left side dorsal habenular nucleus physical object quality, abnormal ZP:0016013 leptotene arrested, abnormal ZP:0016014 meiotic prophase I increased duration, abnormal ZP:0016015 male meiosis I arrested, abnormal ZP:0016016 male meiosis I increased duration, abnormal ZP:0016017 sperm non-functional, abnormal ZP:0016018 condensed chromosome spermatocyte morphology, abnormal ZP:0016020 sperm sperm duct absent, abnormal ZP:0016023 zygotene arrested, abnormal ZP:0016024 meiotic prophase I non-progressive, abnormal ZP:0016025 Sertoli cell apoptotic, abnormal ZP:0016026 chromatin spermatocyte phosphorylation, abnormal ZP:0016027 Leydig cell apoptotic, abnormal ZP:0016038 extraocular musculature absent, abnormal ZP:0016039 median fin fold perforate, abnormal ZP:0016040 fin hypoplastic, abnormal ZP:0016041 pelvic fin aplastic, abnormal ZP:0016042 integument necrotic, abnormal ZP:0016043 extracellular matrix chondrocyte composition, abnormal ZP:0016049 otic epithelium decreased thickness, abnormal ZP:0016050 startle response decreased occurrence, abnormal ZP:0016051 semicircular canal formation delayed, abnormal ZP:0016052 motor neuron decreased length, abnormal ZP:0016070 heart rudiment absent, abnormal ZP:0016071 heart absent, abnormal ZP:0016075 whole organism transparent, abnormal ZP:0016083 liver development delayed, abnormal ZP:0016084 whole organism lacks parts or has fewer parts of type pharyngeal arch cartilage, abnormal ZP:0016085 whole organism lacks all parts of type pharyngeal arch 3-7 skeleton, abnormal ZP:0016086 trunk musculature degenerate, abnormal ZP:0016087 ceratohyal cartilage oriented, abnormal ZP:0016092 yolk condensed, abnormal ZP:0016093 yolk teardrop-shaped, abnormal ZP:0016094 anterior region trunk decreased thickness, abnormal ZP:0016095 posterior region trunk increased width, abnormal ZP:0016096 anterior region trunk kinked, abnormal ZP:0016097 dorsal-ventral axis head increased height, abnormal ZP:0016098 posterior region trunk bulbous, abnormal ZP:0016104 epithelial cell intrahepatic bile duct disorganized, abnormal ZP:0016121 parasphenoid bent, abnormal ZP:0016132 hepatocyte spatial pattern, abnormal ZP:0016133 hepatocyte apical-basal polarity, abnormal ZP:0016134 skeletal muscle contraction decreased magnitude, abnormal ZP:0016135 trunk musculature decreased contractility, abnormal ZP:0016136 trunk decreased angle to anterior-posterior axis whole organism, abnormal ZP:0016137 post-vent region decreased contractility, abnormal ZP:0016138 cell communication by electrical coupling arrested, abnormal ZP:0016139 slow muscle cell electrical conductivity, abnormal ZP:0016140 retinal rod cell retinal outer nuclear layer increased amount, abnormal ZP:0016141 ceratohyal cartilage disorganized, abnormal ZP:0016142 slow-twitch skeletal muscle fiber contraction amplitude, abnormal ZP:0016145 glucose import in response to insulin stimulus decreased process quality, abnormal ZP:0016147 cardiac ventricle increased thickness, abnormal ZP:0016148 interrenal gland hyperplastic, abnormal ZP:0016152 ventral wall of dorsal aorta has fewer parts of type nucleate erythrocyte, abnormal ZP:0016158 whole organism lacks all parts of type iridophore, abnormal ZP:0016159 cardiac muscle progenitor cell migration to the midline involved in heart field formation process quality, abnormal ZP:0016176 pharyngeal arch cartilage loose, abnormal ZP:0016177 prechordal plate apoptotic, abnormal ZP:0016178 hatching gland cell decreased size, abnormal ZP:0016179 anterior region prechordal plate apoptotic, abnormal ZP:0016180 regulation of muscle contraction disrupted, abnormal ZP:0016181 head curved dorsal, abnormal ZP:0016182 hindbrain neural rod decreased diameter, abnormal ZP:0016183 hindbrain flat, abnormal ZP:0016184 hindbrain neural rod flat, abnormal ZP:0016185 hindbrain neural rod decreased thickness, abnormal ZP:0016187 blood circulation decreased intensity, abnormal ZP:0016188 neuroepithelial cell apoptotic, abnormal ZP:0016189 medial longitudinal fasciculus fasciculation, abnormal ZP:0016190 hindbrain commissure decreased size, abnormal ZP:0016191 chromosome brain broken, abnormal ZP:0016192 chromosome spinal cord broken, abnormal ZP:0016193 chromosome neuroectoderm broken, abnormal ZP:0016194 proliferative region tail bud apoptotic, abnormal ZP:0016195 telencephalon mislocalised anteriorly, abnormal ZP:0016196 hindbrain has fewer parts of type grey matter, abnormal ZP:0016197 radial glial cell decreased amount, abnormal ZP:0016199 post-vent region degenerate, abnormal ZP:0016200 hypothalamus degenerate, abnormal ZP:0016201 thalamus degenerate, abnormal ZP:0016202 immature eye degenerate, abnormal ZP:0016207 olfactory epithelium hypoplastic, abnormal ZP:0016211 inner ear distended, abnormal ZP:0016212 inner ear morphogenesis delayed, abnormal ZP:0016213 auditory behavior decreased process quality, abnormal ZP:0016214 equilibrioception decreased process quality, abnormal ZP:0016218 nucleate erythrocyte colorless, abnormal ZP:0016228 forebrain hemorrhagic, abnormal ZP:0016229 chondrocyte structure, abnormal ZP:0016232 neurocranial trabecula kinked, abnormal ZP:0016235 palatoquadrate cartilage increased thickness, abnormal ZP:0016236 Meckel's cartilage kinked, abnormal ZP:0016237 ventral mandibular arch increased length, abnormal ZP:0016240 xanthophore increased fluorescence, abnormal ZP:0016246 xanthophore white, abnormal ZP:0016249 xanthophore pinnate, abnormal ZP:0016250 pterinosome xanthophore composition, abnormal ZP:0016251 xanthophore head desaturated yellow, abnormal ZP:0016252 xanthophore head granular, abnormal ZP:0016253 iris decreased size, abnormal ZP:0016254 xanthophore head brown, abnormal ZP:0016256 xanthophore brown, abnormal ZP:0016259 xanthophore shape, abnormal ZP:0016260 iridophore white, abnormal ZP:0016261 xanthophore composition, abnormal ZP:0016262 cell projection melanocyte decreased amount, abnormal ZP:0016263 central region melanocyte decreased pigmentation, abnormal ZP:0016264 melanocyte star shaped, abnormal ZP:0016265 ventral larval melanophore stripe decreased width, abnormal ZP:0016266 swim bladder lacks all parts of type dorsal region melanocyte, abnormal ZP:0016267 ventral larval melanophore stripe lacks all parts of type dorsal region melanocyte, abnormal ZP:0016268 ventral region ventral larval melanophore stripe patchy, abnormal ZP:0016269 yolk larval melanophore stripe has fewer parts of type iridophore, abnormal ZP:0016270 iridophore yolk larval melanophore stripe irregular spatial pattern, abnormal ZP:0016271 trunk increased accumulation ventro-lateral region melanocyte, abnormal ZP:0016272 trunk increased accumulation ventro-lateral region iridophore, abnormal ZP:0016273 post-vent region increased accumulation ventro-lateral region melanocyte, abnormal ZP:0016274 post-vent region increased accumulation ventro-lateral region iridophore, abnormal ZP:0016279 oral ectoderm mislocalised dorsally, abnormal ZP:0016280 cilium peripheral olfactory organ absent, abnormal ZP:0016281 cilium macula absent, abnormal ZP:0016286 mandibular arch skeleton apoptotic, abnormal ZP:0016287 pharyngeal arch 2 skeleton apoptotic, abnormal ZP:0016288 dorsal hyoid arch decreased size, abnormal ZP:0016289 ventral hyoid arch decreased size, abnormal ZP:0016290 pharyngeal arch 3-7 fused with pharyngeal arch 3-7, abnormal ZP:0016291 chondrocyte proliferation increased occurrence, abnormal ZP:0016294 dorsal hyoid arch shape, abnormal ZP:0016295 pharyngeal arch cartilage associated with pharyngeal arch cartilage, abnormal ZP:0016297 oral ectoderm mislocalised laterally, abnormal ZP:0016302 anterior region trunk bent, abnormal ZP:0016303 osteoblast cranium mislocalised, abnormal ZP:0016313 blood vessel increased amount, abnormal ZP:0016321 head increased accumulation epidermal cell, abnormal ZP:0016327 retinal cone cell disorganized, abnormal ZP:0016328 cranial ganglion maturation decreased process quality, abnormal ZP:0016329 glossopharyngeal ganglion poorly differentiated, abnormal ZP:0016330 vagal ganglion 1 poorly differentiated, abnormal ZP:0016331 vagal ganglion 2 poorly differentiated, abnormal ZP:0016332 vagal ganglion 3 poorly differentiated, abnormal ZP:0016333 axon upper rhombic lip decreased amount, abnormal ZP:0016334 cell motility disrupted, abnormal ZP:0016335 neutrophil decreased cellular motility, abnormal ZP:0016341 symplectic length, abnormal ZP:0016355 substrate-dependent cell migration, cell attachment to substrate disrupted, abnormal ZP:0016356 melanocyte spheroid, abnormal ZP:0016364 whole organism low brightness, abnormal ZP:0016365 swimming behavior increased occurrence, abnormal ZP:0016367 synapse assembly process quality, abnormal ZP:0016368 brain size, abnormal ZP:0016375 nucleolus liver increased amount, abnormal ZP:0016378 actin filament polymerization decreased occurrence, abnormal ZP:0016379 filamentous actin heart decreased amount, abnormal ZP:0016380 heart distended, abnormal ZP:0016381 myofibril myocardium structure, abnormal ZP:0016382 myofibril myocardium decreased length, abnormal ZP:0016383 myofibril heart disorganized, abnormal ZP:0016384 heart increased contractility, abnormal ZP:0016405 fat cell pleuroperitoneal cavity increased amount, abnormal ZP:0016407 response to light stimulus increased process quality, abnormal ZP:0016413 karyomere membrane fusion disrupted, abnormal ZP:0016414 nucleus blastomere lobate, abnormal ZP:0016415 karyomere blastomere life span, abnormal ZP:0016416 karyomere blastomere morphology, abnormal ZP:0016417 karyomere blastomere increased amount, abnormal ZP:0016418 pronucleus cell present, abnormal ZP:0016419 blastodisc morphology, abnormal ZP:0016434 lens broken, abnormal ZP:0016435 iris closed, abnormal ZP:0016436 lens capsule deformed, abnormal ZP:0016437 retina low brightness, abnormal ZP:0016438 retina rough, abnormal ZP:0016439 artery retina sinuous, abnormal ZP:0016440 retina spotted, abnormal ZP:0016441 retinal pigmented epithelium detached from pigmented epithelial cell, abnormal ZP:0016442 pigmented epithelial cell located in retinal inner plexiform layer, abnormal ZP:0016445 intestine low brightness, abnormal ZP:0016446 response to oxidative stress process quality, abnormal ZP:0016451 mRNA export from nucleus disrupted, abnormal ZP:0016452 chondroblast pharyngeal arch 3-7 skeleton absent, abnormal ZP:0016453 pharyngeal arch has fewer parts of type chondroblast nuclear pore chondroblast, abnormal ZP:0016454 chondroblast pharyngeal arch 2 decreased amount, abnormal ZP:0016455 chondroblast pharyngeal arch 1 decreased amount, abnormal ZP:0016456 chondrocyte pharyngeal arch 3-7 skeleton absent, abnormal ZP:0016457 chondrocyte pharyngeal arch 2 decreased amount, abnormal ZP:0016458 chondrocyte pharyngeal arch 1 decreased amount, abnormal ZP:0016459 intestine smooth, abnormal ZP:0016460 nuclear pore intestine aggregated, abnormal ZP:0016461 nuclear pore retina aggregated, abnormal ZP:0016462 nuclear pore optic tectum aggregated, abnormal ZP:0016463 nuclear pore pharyngeal arch aggregated, abnormal ZP:0016465 hepatocyte detached from liver, abnormal ZP:0016466 pelvic fin development disrupted, abnormal ZP:0016470 mesoderm pelvic fin bud present, abnormal ZP:0016471 pelvic fin skeleton absent, abnormal ZP:0016472 apical ectodermal ridge pelvic fin bud absent, abnormal ZP:0016474 peroxidase activity disrupted, abnormal ZP:0016484 olfactory pit increased size, abnormal ZP:0016485 adenohypophyseal placode increased size, abnormal ZP:0016493 head has fewer parts of type melanocyte, abnormal ZP:0016494 Meckel's cartilage curved ventral, abnormal ZP:0016495 ethmoid cartilage curved ventral, abnormal ZP:0016496 dorsal root ganglion lacks parts or has fewer parts of type glial cell (sensu Vertebrata), abnormal ZP:0016497 posterior lateral line separated from melanocyte, abnormal ZP:0016498 posterior lateral line has extra parts of type melanocyte, abnormal ZP:0016499 trunk has extra parts of type melanocyte, abnormal ZP:0016500 post-vent region has extra parts of type melanocyte, abnormal ZP:0016501 trunk has fewer parts of type dorsal region iridophore, abnormal ZP:0016502 retinal rod cell absent, abnormal ZP:0016508 collateral sprouting in absence of injury process quality, abnormal ZP:0016514 axon collateral RoP motor neuron mislocalised, abnormal ZP:0016515 axon collateral CaP motoneuron mislocalised, abnormal ZP:0016519 vertebral column malformed, abnormal ZP:0016524 retina hyperplastic, abnormal ZP:0016526 cell migration involved in heart jogging decreased process quality, abnormal ZP:0016527 endocardial precursor heart rudiment mislocalised, abnormal ZP:0016528 myocardial precursor heart rudiment mislocalised, abnormal ZP:0016533 keratin filament epidermal cell spatial pattern, abnormal ZP:0016546 habituation decreased process quality, abnormal ZP:0016550 pigment cell development decreased process quality, abnormal ZP:0016561 vertebral column morphology, abnormal ZP:0016567 central nervous system morphogenesis disrupted, abnormal ZP:0016568 rhombomere 4 morphogenesis disrupted, abnormal ZP:0016569 cell division absent, abnormal ZP:0016570 regulation of cell division disrupted, abnormal ZP:0016571 ectodermal placode development disrupted, abnormal ZP:0016572 anterior macula has fewer parts of type auditory receptor cell, abnormal ZP:0016573 anterior macula unstratified, abnormal ZP:0016574 reticular formation structure, abnormal ZP:0016575 pharyngeal endoderm decreased size, abnormal ZP:0016576 optic cup hypoplastic, abnormal ZP:0016577 solid lens vesicle protruding out of immature eye, abnormal ZP:0016578 protoneuromast absent, abnormal ZP:0016579 neuron increased size, abnormal ZP:0016580 dorsal region hindbrain disorganized, abnormal ZP:0016581 ventral region forebrain structure, abnormal ZP:0016582 microtubule neuron molecular quality, abnormal ZP:0016583 cell floor plate increased size, abnormal ZP:0016584 floor plate separated from cell cell floor plate, abnormal ZP:0016585 cell hypochord increased size, abnormal ZP:0016586 hypochord separated from cell cell hypochord, abnormal ZP:0016587 neuron central nervous system decreased amount, abnormal ZP:0016588 cell cycle lacking processual parts cytokinesis, abnormal ZP:0016589 nucleus whole organism increased size, abnormal ZP:0016590 cell cycle lacking processual parts DNA replication, abnormal ZP:0016591 interneuron axon guidance disrupted, abnormal ZP:0016592 axon hindbrain commissure disorganized, abnormal ZP:0016593 axon Mauthner neuron decreased amount, abnormal ZP:0016594 otic placode morphology, abnormal ZP:0016596 axon CaP motoneuron decreased branchiness, abnormal ZP:0016609 hepatocyte ballooning, abnormal ZP:0016626 atrial endocardium mislocalised, abnormal ZP:0016647 notochord separated from notochord inner cell notochord inner cell, abnormal ZP:0016648 vertebra immature, abnormal ZP:0016649 vertebral column discontinuous bone development, abnormal ZP:0016650 vertebral column disrupted bone development, abnormal ZP:0016651 notochord has extra parts of type anatomical space, abnormal ZP:0016652 notochord outer sheath cell proliferative, abnormal ZP:0016653 notochord inner cell decreased size, abnormal ZP:0016654 nucleus notochord spherical, abnormal ZP:0016655 nucleus notochord decondensed, abnormal ZP:0016656 cytoplasm notochord inner cell increased volume, abnormal ZP:0016657 notochord inner cell lacks parts or has fewer parts of type cytoplasm intermediate filament notochord inner cell, abnormal ZP:0016658 intermediate filament notochord inner cell morphology, abnormal ZP:0016659 anatomical space notochord mislocalised, abnormal ZP:0016660 cell notochord proliferative, abnormal ZP:0016668 palate morphology, abnormal ZP:0016669 palate decreased length, abnormal ZP:0016671 nucleus notochord increased amount, abnormal ZP:0016682 integument transparent, abnormal ZP:0016683 gold iridophore absent, abnormal ZP:0016684 silver iridophore absent, abnormal ZP:0016685 melanosome retinal pigmented epithelium absent, abnormal ZP:0016686 silver iridophore iris stroma absent, abnormal ZP:0016692 xanthophore color pattern, abnormal ZP:0016693 iridophore color pattern, abnormal ZP:0016694 dorsal-most region melanophore stripe color pattern, abnormal ZP:0016697 type B pancreatic cell proliferation increased occurrence, abnormal ZP:0016704 neurocranial trabecula morphology, abnormal ZP:0016711 angiogenic sprout intersegmental vessel decreased length, abnormal ZP:0016742 pectoral fin exserted, abnormal ZP:0016743 pectoral fin increased angle to trunk, abnormal ZP:0016745 exocrine pancreas disrupted cell migration, abnormal ZP:0016747 intersegmental vessel delayed angiogenesis, abnormal ZP:0016755 angiogenesis increased process quality, abnormal ZP:0016758 intersegmental vessel has extra parts of type filopodium endothelial cell, abnormal ZP:0016759 intersegmental vessel increased process quality sprouting angiogenesis, abnormal ZP:0016766 liver increased occurrence apoptotic process, abnormal ZP:0016769 common bile duct dilated, abnormal ZP:0016773 cranial vasculature absent, abnormal ZP:0016788 vertebra dysplastic, abnormal ZP:0016789 vertebra delayed bone mineralization, abnormal ZP:0016791 macrophage abnormal, abnormal ZP:0016792 melanocyte eye absent, abnormal ZP:0016794 photoreceptor cell abnormal, abnormal ZP:0016807 histone methylation decreased process quality, abnormal ZP:0016808 heart hypertrophic, abnormal ZP:0016823 optic vesicle has extra parts of type hair cell, abnormal ZP:0016824 heart lacks parts or has fewer parts of type mitochondrion heart, abnormal ZP:0016825 mitochondrion heart degenerate, abnormal ZP:0016826 mitochondrial crista heart deformed, abnormal ZP:0016836 ventral region presumptive ectoderm physical object quality, abnormal ZP:0016837 ventral region ectoderm physical object quality, abnormal ZP:0016841 melanoma post-vent region present, abnormal ZP:0016849 microglia development decreased occurrence, abnormal ZP:0016850 brain lacks all parts of type macrophage, abnormal ZP:0016851 brain has extra parts of type neutrophil, abnormal ZP:0016852 neutrophil brain mislocalised, abnormal ZP:0016853 brain has fewer parts of type microglial cell, abnormal ZP:0016854 macrophage activation increased process quality, abnormal ZP:0016855 whole organism has fewer parts of type macrophage, abnormal ZP:0016856 macrophage ball apoptotic, abnormal ZP:0016857 macrophage ball vacuolated, abnormal ZP:0016858 whole organism inflamed, abnormal ZP:0016859 macrophage ball mislocalised, abnormal ZP:0016860 macrophage ball aggregated, abnormal ZP:0016861 neutrophil adjacent to macrophage, abnormal ZP:0016862 fast muscle cell process quality skeletal myofibril assembly, abnormal ZP:0016863 T-tubule fast muscle cell disorganized, abnormal ZP:0016864 slow muscle cell process quality skeletal myofibril assembly, abnormal ZP:0016866 myofibril skeletal muscle cell irregular spatial pattern, abnormal ZP:0016879 splanchnocranium absent, abnormal ZP:0016893 intestinal epithelium hypertrophic, abnormal ZP:0016901 CaP motoneuron decreased length, abnormal ZP:0016907 visual behavior decreased occurrence, abnormal ZP:0016910 locomotion involved in locomotory behavior decreased occurrence, abnormal ZP:0016919 branchiomotor neuron decreased occurrence neuron migration, abnormal ZP:0016941 hindbrain neoplastic, abnormal ZP:0016942 eye increased pigmentation, abnormal ZP:0016958 intersegmental vein increased branchiness, abnormal ZP:0016987 glial cell vagal ganglion absent, abnormal ZP:0017002 cell integument aggregated, abnormal ZP:0017007 precaudal vertebra condensed, abnormal ZP:0017011 swim bladder development delayed, abnormal ZP:0017012 centrum decreased amount, abnormal ZP:0017013 vertebra decreased length, abnormal ZP:0017014 vertebra decreased amount, abnormal ZP:0017015 vertebra has extra parts of type hemal arch, abnormal ZP:0017016 vertebra has extra parts of type neural arch, abnormal ZP:0017024 trunk absent blood circulation, abnormal ZP:0017030 thyroid follicle absent, abnormal ZP:0017038 forebrain absent, abnormal ZP:0017046 caudal vein plexus has fewer parts of type endothelial cell, abnormal ZP:0017055 nucleate erythrocyte accumulation trunk, abnormal ZP:0017070 mitochondrial cloud oocyte stage I absent, abnormal ZP:0017075 radial glial cell spinal cord morphology, abnormal ZP:0017077 pronephric podocyte apoptotic, abnormal ZP:0017085 ventral wall of dorsal aorta has extra parts of type hematopoietic stem cell, abnormal ZP:0017087 myelinating Schwann cell posterior lateral line circular, abnormal ZP:0017097 lymphangiogenesis decreased process quality, abnormal ZP:0017105 male sex determination increased occurrence, abnormal ZP:0017108 melanosome localization process quality, abnormal ZP:0017113 cell cardiac ventricle spatial pattern, abnormal ZP:0017118 slit diaphragm pronephric glomerulus decreased amount, abnormal ZP:0017122 cardiac ventricle size, abnormal ZP:0017123 atrium size, abnormal ZP:0017127 vascular lymphangioblast increased amount, abnormal ZP:0017130 mandibular arch skeleton decreased amount, abnormal ZP:0017134 diencephalon mislocalised, abnormal ZP:0017145 neural plate apoptotic, abnormal ZP:0017146 neural crest cell fate specification disrupted, abnormal ZP:0017147 hindbrain increased width, abnormal ZP:0017148 neural crest decreased thickness, abnormal ZP:0017149 midbrain increased width, abnormal ZP:0017150 neural crest morphology, abnormal ZP:0017157 blood accumulation atrium, abnormal ZP:0017159 anatomical margin EVL scalloped, abnormal ZP:0017160 EVL detached from blastoderm cell blastoderm cell EVL, abnormal ZP:0017162 anatomical margin EVL disorganized, abnormal ZP:0017163 involution involved in gastrulation with mouth forming second delayed, abnormal ZP:0017178 retinoic acid receptor signaling pathway decreased occurrence, abnormal ZP:0017187 retinal inner nuclear layer lacks all parts of type Muller cell, abnormal ZP:0017188 retina decreased area, abnormal ZP:0017189 whole organism lacks parts or has fewer parts of type neuron projection retinal ganglion cell, abnormal ZP:0017190 photoreceptor cell shortened, abnormal ZP:0017191 horizontal cell decreased amount, abnormal ZP:0017192 neuron projection amacrine cell decreased amount, abnormal ZP:0017193 compartment boundary rhombomere disorganized, abnormal ZP:0017198 posterior region whole organism decreased size, abnormal ZP:0017200 vH ionocyte increased amount, abnormal ZP:0017201 vH ionocyte gill increased amount, abnormal ZP:0017215 actin filament somite disorganized, abnormal ZP:0017216 actin filament somite decondensed, abnormal ZP:0017217 focal adhesion somite decreased amount, abnormal ZP:0017233 hatching decreased rate, abnormal ZP:0017234 cardiac muscle cell heart decreased contractility, abnormal ZP:0017235 cell whole organism low brightness, abnormal ZP:0017236 cell whole organism spherical, abnormal ZP:0017238 pharyngeal musculature absent, abnormal ZP:0017239 levator arcus palatini undifferentiated, abnormal ZP:0017240 dilatator operculi undifferentiated, abnormal ZP:0017241 basal plate cartilage decreased length, abnormal ZP:0017242 basal plate cartilage increased width, abnormal ZP:0017243 hypobranchial cartilage absent, abnormal ZP:0017244 head arrested skeletal system development, abnormal ZP:0017245 cell pharyngeal arch cartilage undifferentiated, abnormal ZP:0017246 heart valve decreased functionality, abnormal ZP:0017251 liver hemorrhagic, abnormal ZP:0017252 liver increased accumulation nucleate erythrocyte, abnormal ZP:0017253 lateral crista primordium morphology, abnormal ZP:0017254 posterior crista primordium morphology, abnormal ZP:0017255 anterior crista primordium morphology, abnormal ZP:0017256 whole organism semi-fertile, abnormal ZP:0017258 ciliary marginal zone hypotrophic, abnormal ZP:0017259 ciliary marginal zone vacuolated, abnormal ZP:0017260 xanthophore unpigmented, abnormal ZP:0017263 endocardium absent, abnormal ZP:0017266 xanthophore whole organism absent, abnormal ZP:0017267 chondrocyte pharyngeal arch cartilage morphology, abnormal ZP:0017268 pharyngeal arch cartilage kinked, abnormal ZP:0017269 trabecula cranii right angle to ethmoid cartilage, abnormal ZP:0017278 myotome lacks all parts of type myofibril skeletal muscle cell, abnormal ZP:0017279 caudal fin lower lobe mislocalised, abnormal ZP:0017280 cerebral spinal fluid ventricular system decreased fluid flow, abnormal ZP:0017281 pronephric glomerulus distended, abnormal ZP:0017282 pronephric podocyte has fewer parts of type cell projection pronephric podocyte, abnormal ZP:0017283 cell pronephric glomerulus distributed, abnormal ZP:0017284 cell pronephric glomerulus flattened, abnormal ZP:0017285 cell pronephric glomerular basement membrane distributed, abnormal ZP:0017286 pronephric glomerulus flattened, abnormal ZP:0017287 glomerular capillary distended, abnormal ZP:0017288 pronephric glomerular basement membrane decreased thickness, abnormal ZP:0017289 pronephric glomerulus loose, abnormal ZP:0017290 prechordal plate absent, abnormal ZP:0017291 axial mesoderm absent, abnormal ZP:0017292 axial chorda mesoderm hypoplastic, abnormal ZP:0017293 neural keel hypoplastic, abnormal ZP:0017294 ventral-most region floor plate spinal cord region hypoplastic, abnormal ZP:0017295 ventral region diencephalon hypoplastic, abnormal ZP:0017296 ventral region midbrain hypoplastic, abnormal ZP:0017297 Kupffer's vesicle absent, abnormal ZP:0017298 midbrain-hindbrain boundary morphogenesis process quality, abnormal ZP:0017309 retinal inner nuclear layer increased occurrence cell death, abnormal ZP:0017311 cell ventral fin fold mislocalised, abnormal ZP:0017313 epithelium pronephric tubule flattened, abnormal ZP:0017314 retinal outer plexiform layer absent, abnormal ZP:0017315 pharyngeal endoderm aplastic, abnormal ZP:0017316 proctodeum absent, abnormal ZP:0017317 intestine absent, abnormal ZP:0017318 kidney morphogenesis disrupted, abnormal ZP:0017319 heart rudiment split, abnormal ZP:0017320 pronephric duct mislocalised laterally, abnormal ZP:0017321 erythroblast mislocalised laterally, abnormal ZP:0017322 forerunner cell group absent, abnormal ZP:0017325 melanosome melanocyte position, abnormal ZP:0017326 retinal rod cell decreased length, abnormal ZP:0017327 photoreceptor outer segment layer apoptotic, abnormal ZP:0017330 cell brain spherical, abnormal ZP:0017331 cell spinal cord spherical, abnormal ZP:0017332 axis condensed, abnormal ZP:0017333 integument head texture, abnormal ZP:0017334 cell fin circular, abnormal ZP:0017335 myotome has fewer parts of type myofibril skeletal muscle cell, abnormal ZP:0017337 melanocyte dorsal larval melanophore stripe mislocalised laterally, abnormal ZP:0017338 pharyngeal arch 3-7 skeleton necrotic, abnormal ZP:0017339 mandibular arch skeleton necrotic, abnormal ZP:0017340 pharyngeal arch 2 skeleton necrotic, abnormal ZP:0017341 melanocyte decreased thickness, abnormal ZP:0017342 melanocyte elongated, abnormal ZP:0017344 striated muscle thin filament muscle cell striated, abnormal ZP:0017345 hyoid muscle aplastic/hypoplastic, abnormal ZP:0017346 cranium dysplastic, abnormal ZP:0017347 head muscle dysplastic, abnormal ZP:0017348 interhyoideus displaced, abnormal ZP:0017349 muscle cell striated, abnormal ZP:0017350 muscle cell shortened, abnormal ZP:0017351 striated muscle myosin thick filament muscle cell striated, abnormal ZP:0017352 anterior commissure disorganized, abnormal ZP:0017353 chondrocyte Meckel's cartilage neoplastic, abnormal ZP:0017355 chondrocyte pharyngeal arch cartilage neoplastic, abnormal ZP:0017356 chondrocyte neurocranium neoplastic, abnormal ZP:0017358 cardiac ventricle aplastic, abnormal ZP:0017359 post-vent region has fewer parts of type yolk larval melanophore stripe melanocyte, abnormal ZP:0017360 ventral side caudal fin aplastic, abnormal ZP:0017363 diencephalon bilateral, abnormal ZP:0017364 determination of ventral identity process quality, abnormal ZP:0017365 ventricular system aplastic, abnormal ZP:0017366 somite post-vent region increased width, abnormal ZP:0017368 notochord trunk aplastic, abnormal ZP:0017369 trunk has fewer parts of type cell notochord, abnormal ZP:0017374 axon posterior lateral line nerve decreased length, abnormal ZP:0017376 somite trunk aplastic, abnormal ZP:0017378 presumptive paraxial mesoderm morphology, abnormal ZP:0017379 trunk lacks all parts of type somite, abnormal ZP:0017380 cell accumulation caudal fin, abnormal ZP:0017381 muscle trunk malformed, abnormal ZP:0017382 muscle trunk disorganized, abnormal ZP:0017386 segment polarity determination disrupted, abnormal ZP:0017390 desmosome assembly disrupted, abnormal ZP:0017391 desmosome epidermal cell decreased amount, abnormal ZP:0017392 desmosome epidermal cell malformed, abnormal ZP:0017393 gut decreased functionality, abnormal ZP:0017394 atrioventricular valve development arrested, abnormal ZP:0017395 atrioventricular ring immature, abnormal ZP:0017396 whole organism contractility, abnormal ZP:0017397 pronephric proximal straight tubule increased length, abnormal ZP:0017401 gliogenesis disrupted, abnormal ZP:0017402 pleuroperitoneal cavity edematous, abnormal ZP:0017403 anterior-posterior axis whole organism increased width, abnormal ZP:0017414 pronephric proximal tubule morphogenesis process quality, abnormal ZP:0017418 pronephric proximal convoluted tubule increased occurrence apoptotic process, abnormal ZP:0017424 pronephros decreased process quality renal absorption, abnormal ZP:0017426 eye photoreceptor cell lacks parts or has fewer parts of type photoreceptor outer segment eye photoreceptor cell, abnormal ZP:0017427 eye photoreceptor cell has fewer parts of type photoreceptor connecting cilium eye photoreceptor cell, abnormal ZP:0017428 apical region eye photoreceptor cell decreased length, abnormal ZP:0017429 apical region eye photoreceptor cell decreased area, abnormal ZP:0017430 eye photoreceptor cell decreased process quality establishment of apical/basal cell polarity, abnormal ZP:0017432 endosome pronephric duct increased size, abnormal ZP:0017433 endosome pronephric duct decreased amount, abnormal ZP:0017434 endocytic vesicle pronephric duct decreased amount, abnormal ZP:0017435 pronephros decreased process quality endocytosis, abnormal ZP:0017436 pronephros process quality endocytic recycling, abnormal ZP:0017441 macrophage activation involved in immune response disrupted, abnormal ZP:0017445 macrophage morphology, abnormal ZP:0017446 macrophage whole organism spatial pattern, abnormal ZP:0017447 macrophage trunk decreased cellular motility, abnormal ZP:0017448 anatomical region statoacoustic (VIII) ganglion decreased size, abnormal ZP:0017449 photoreceptor cell morphogenesis decreased process quality, abnormal ZP:0017450 camera-type eye photoreceptor cell differentiation decreased occurrence, abnormal ZP:0017452 photoreceptor inner segment photoreceptor cell physical object quality, abnormal ZP:0017454 blood coagulation, fibrin clot formation decreased occurrence, abnormal ZP:0017455 thrombocyte cellular adhesivity, abnormal ZP:0017456 intestine has extra parts of type neutrophil, abnormal ZP:0017457 neutrophil intestine increased amount, abnormal ZP:0017458 gut epithelium permeability, abnormal ZP:0017459 brush border gut epithelium decreased size, abnormal ZP:0017460 intestinal epithelial cell decreased height, abnormal ZP:0017461 intestinal epithelial cell cuboid, abnormal ZP:0017462 intestinal epithelial cell decreased process quality DNA methylation, abnormal ZP:0017463 intestinal epithelial cell increased process quality apoptotic process, abnormal ZP:0017464 hypoblast process quality calcium-mediated signaling, abnormal ZP:0017465 Kupffer's vesicle decreased process quality cilium movement, abnormal ZP:0017466 lymphoid progenitor cell thymus absent, abnormal ZP:0017480 cell retina circular, abnormal ZP:0017481 anatomical axis trunk decreased length, abnormal ZP:0017482 ventral region whole organism increased thickness, abnormal ZP:0017483 axis distended, abnormal ZP:0017484 cilium movement frequency, abnormal ZP:0017485 fast muscle cell arrested myoblast fusion, abnormal ZP:0017486 ventricular cardiac muscle cell action potential absent, abnormal ZP:0017487 ventricular cardiac muscle cell action potential increased duration, abnormal ZP:0017488 membrane repolarization during cardiac muscle cell action potential decreased process quality, abnormal ZP:0017489 midbrain hindbrain boundary disorganized, abnormal ZP:0017490 diencephalon disorganized, abnormal ZP:0017491 tegmentum disorganized, abnormal ZP:0017492 hematopoietic stem cell differentiation decreased occurrence, abnormal ZP:0017494 whole organism has fewer parts of type hematopoietic stem cell, abnormal ZP:0017495 optic tectum process quality transmission of nerve impulse, abnormal ZP:0017496 sleep decreased duration, abnormal ZP:0017506 locomotion involved in locomotory behavior increased process quality, abnormal ZP:0017507 melanosome assembly process quality, abnormal ZP:0017508 melanosome retinal pigmented epithelium morphology, abnormal ZP:0017509 photoreceptor outer segment photoreceptor cell morphology, abnormal ZP:0017510 photoreceptor outer segment photoreceptor cell structure, abnormal ZP:0017511 epidermal basal stratum decreased process quality epithelial cell morphogenesis, abnormal ZP:0017512 ecto-epithelial cell epidermal basal stratum oblong, abnormal ZP:0017513 spinal cord process quality generation of neurons, abnormal ZP:0017514 laminin complex median fin fold increased amount, abnormal ZP:0017515 median fin fold decreased occurrence epithelial cell proliferation, abnormal ZP:0017516 epidermal basal stratum decreased height, abnormal ZP:0017517 epidermal basal stratum increased process quality canonical Wnt signaling pathway, abnormal ZP:0017518 ecto-epithelial cell epidermal basal stratum elongated, abnormal ZP:0017523 cilium otic vesicle absent, abnormal ZP:0017532 neutrophil morphology, abnormal ZP:0017535 telencephalon development decreased process quality, abnormal ZP:0017537 cerebellum size, abnormal ZP:0017538 dorsal telencephalon has extra parts of type neuron, abnormal ZP:0017539 dorsal telencephalon decreased process quality Notch signaling pathway, abnormal ZP:0017540 dorsal telencephalon increased occurrence neurogenesis, abnormal ZP:0017541 neuron projection dorsal telencephalon decreased branchiness, abnormal ZP:0017542 dorsal telencephalon decreased occurrence neuron projection morphogenesis, abnormal ZP:0017543 neuronal stem cell dorsal telencephalon proliferative, abnormal ZP:0017544 neuron dorsal telencephalon immature, abnormal ZP:0017545 ventricular zone decreased process quality Notch signaling pathway, abnormal ZP:0017546 paraxial mesoderm decreased process quality Notch signaling pathway, abnormal ZP:0017547 paraxial mesoderm decreased process quality fibroblast growth factor receptor signaling pathway, abnormal ZP:0017548 axis elongation decreased rate, abnormal ZP:0017549 anterior region axis decreased thickness, abnormal ZP:0017550 caudal vein plexus process quality sprouting angiogenesis, abnormal ZP:0017551 caudal vein plexus has fewer parts of type blood vessel endothelial cell filopodium blood vessel endothelial cell, abnormal ZP:0017553 retinal ganglion cell layer increased thickness, abnormal ZP:0017554 retinal ganglion cell process quality asymmetric cell division, abnormal ZP:0017555 neuron development delayed, abnormal ZP:0017556 mandibular arch skeleton agenesis, abnormal ZP:0017557 pharyngeal arch 3-7 decreased amount, abnormal ZP:0017558 posterior lateral line neuromast primordium migration decreased process quality, abnormal ZP:0017559 visceral fat decreased volume, abnormal ZP:0017560 lipid droplet visceral fat morphology, abnormal ZP:0017561 lipid droplet visceral fat increased amount, abnormal ZP:0017562 visceral fat increased process quality cell population proliferation, abnormal ZP:0017563 visceral fat process quality collagen fibril organization, abnormal ZP:0017564 fat cell increased process quality cell population proliferation, abnormal ZP:0017565 endothelial cell lateral dorsal aorta increased amount, abnormal ZP:0017566 endocardial cushion absent, abnormal ZP:0017567 endocardium proliferative, abnormal ZP:0017568 subintestinal vein increased branchiness, abnormal ZP:0017569 anatomical axis trunk bent, abnormal ZP:0017570 pronephric duct development process quality, abnormal ZP:0017573 hypochord decreased process quality Notch signaling pathway, abnormal ZP:0017574 cell ventricular zone amount, abnormal ZP:0017575 cell ventricular zone decreased amount, abnormal ZP:0017576 exocrine pancreas fibrillary, abnormal ZP:0017577 exocrine pancreas lacks all parts of type central region pancreatic acinar cell, abnormal ZP:0017578 pancreatic duct obstructed, abnormal ZP:0017579 neuron forebrain increased amount, abnormal ZP:0017581 neural precursor cell proliferation decreased process quality, abnormal ZP:0017582 brain lacks parts or has fewer parts of type oligodendrocyte, abnormal ZP:0017583 peripheral nervous system lacks parts or has fewer parts of type myelinating Schwann cell, abnormal ZP:0017584 nervous system has fewer parts of type glioblast, abnormal ZP:0017585 somite border structure, abnormal ZP:0017586 astrocyte decreased amount, abnormal ZP:0017587 chondrocyte head maturity, abnormal ZP:0017588 chondrocyte head decreased amount, abnormal ZP:0017589 Meckel's cartilage premature endochondral ossification, abnormal ZP:0017590 mandibular arch skeleton atrophied, abnormal ZP:0017591 endothelial cell dorsal aorta aplastic, abnormal ZP:0017598 receptor signaling pathway via JAK-STAT increased occurrence, abnormal ZP:0017605 ovarian follicle rupture disrupted, abnormal ZP:0017606 ovulation disrupted, abnormal ZP:0017607 multi-organism reproductive process disrupted, abnormal ZP:0017609 oocyte stage V immobile, abnormal ZP:0017610 oocyte stage V non-functional, abnormal ZP:0017624 replacement tooth 4V immature, abnormal ZP:0017625 pronephric proximal tubule development decreased process quality, abnormal ZP:0017626 pronephros lacks all parts of type corpuscles of Stannius, abnormal ZP:0017627 pronephros lacks all parts of type pronephric proximal straight tubule, abnormal ZP:0017628 pronephric proximal convoluted tubule distended, abnormal ZP:0017629 pronephric proximal convoluted tubule mislocalised posteriorly, abnormal ZP:0017630 pronephric proximal convoluted tubule straight, abnormal ZP:0017633 autophagosome maturation arrested, abnormal ZP:0017634 tooth placode agenesis, abnormal ZP:0017635 nucleus eye shape, abnormal ZP:0017636 eye increased occurrence apoptotic process, abnormal ZP:0017637 eye delayed cell cycle, abnormal ZP:0017638 cell eye polyploid, abnormal ZP:0017639 cell eye decreased amount, abnormal ZP:0017640 behavior decreased occurrence, abnormal ZP:0017641 response to gravity decreased occurrence, abnormal ZP:0017642 synapse hindbrain interneuron decreased amount, abnormal ZP:0017643 Mauthner neuron process quality synapse assembly, abnormal ZP:0017644 dendrite Mauthner neuron complexity, abnormal ZP:0017645 synapse Mauthner neuron decreased amount, abnormal ZP:0017646 sclerotome morphology, abnormal ZP:0017647 vertebra cuneate, abnormal ZP:0017648 vertebral column rotated, abnormal ZP:0017649 posterior lateral line decreased process quality Schwann cell development, abnormal ZP:0017650 posterior lateral line arrested myelination of posterior lateral line nerve axons, abnormal ZP:0017651 posterior lateral line decreased occurrence myelination of posterior lateral line nerve axons, abnormal ZP:0017652 pronephric proximal straight tubule mislocalised posteriorly, abnormal ZP:0017653 pronephric distal early tubule mislocalised posteriorly, abnormal ZP:0017656 tooth 5V absent, abnormal ZP:0017665 blood plasma heart fatty, abnormal ZP:0017666 posterior lateral line decreased process quality peripheral nervous system myelin formation, abnormal ZP:0017667 posterior lateral line arrested peripheral nervous system axon ensheathment, abnormal ZP:0017671 nucleus hepatocyte broken, abnormal ZP:0017672 microvesicle hepatocyte increased amount, abnormal ZP:0017673 brain functionality, abnormal ZP:0017674 cell-cell adhesion involved in gastrulation decreased process quality, abnormal ZP:0017675 hatching gland mislocalised, abnormal ZP:0017676 posterior region hindbrain morphology, abnormal ZP:0017677 anterior region spinal cord morphology, abnormal ZP:0017678 trigeminal ganglion mislocalised laterally, abnormal ZP:0017679 neuron trigeminal ganglion disorganized, abnormal ZP:0017680 neuron trigeminal ganglion distributed, abnormal ZP:0017681 nervous system flattened, abnormal ZP:0017682 filopodium axial hypoblast decreased amount, abnormal ZP:0017683 Rohon-Beard neuron mislocalised, abnormal ZP:0017684 heart rudiment formation decreased process quality, abnormal ZP:0017685 pronephric nephron tubule development process quality, abnormal ZP:0017686 heart increased process quality apoptotic process, abnormal ZP:0017687 heart decreased process quality cell population proliferation, abnormal ZP:0017688 cell atrium spatial pattern, abnormal ZP:0017689 pectoral fin decreased process quality cell population proliferation, abnormal ZP:0017690 cardiac ventricle decreased process quality sarcomere organization, abnormal ZP:0017691 olfactory placode development process quality, abnormal ZP:0017692 hindbrain has extra parts of type dorsal region neuron, abnormal ZP:0017693 motor neuron hindbrain mislocalised dorsally, abnormal ZP:0017694 motor neuron hindbrain mislocalised anteriorly, abnormal ZP:0017695 midbrain has extra parts of type dorsal region neuron, abnormal ZP:0017696 cell neural tube increased amount, abnormal ZP:0017697 alar plate midbrain region separated from basal plate midbrain region, abnormal ZP:0017698 hindbrain interneuron irregular spatial pattern, abnormal ZP:0017699 hindbrain interneuron mislocalised, abnormal ZP:0017700 Mauthner neuron irregular spatial pattern, abnormal ZP:0017702 vascular lymphangioblast malformed, abnormal ZP:0017704 swimming increased frequency, abnormal ZP:0017705 swimming increased process quality, abnormal ZP:0017707 brain process quality transmission of nerve impulse, abnormal ZP:0017714 phosphatidylinositol 3-kinase signaling process quality, abnormal ZP:0017715 protein kinase B signaling process quality, abnormal ZP:0017717 head cellularity, abnormal ZP:0017718 forebrain increased process quality apoptotic process, abnormal ZP:0017719 brain increased process quality cell death, abnormal ZP:0017720 eye increased process quality cell death, abnormal ZP:0017721 liver decreased rate cell population proliferation, abnormal ZP:0017728 pronephric proximal tubule development process quality, abnormal ZP:0017729 pronephric proximal convoluted tubule decreased size, abnormal ZP:0017730 otic vesicle has fewer parts of type neuroblast (sensu Vertebrata) otic vesicle, abnormal ZP:0017732 otic vesicle increased process quality Notch signaling pathway, abnormal ZP:0017733 otic vesicle increased process quality fibroblast growth factor receptor signaling pathway, abnormal ZP:0017734 otic vesicle decreased occurrence neuroblast fate specification, abnormal ZP:0017735 otic vesicle decreased occurrence neurogenesis, abnormal ZP:0017737 statoacoustic (VIII) ganglion has extra parts of type neuroblast (sensu Vertebrata) statoacoustic (VIII) ganglion, abnormal ZP:0017738 statoacoustic (VIII) ganglion has fewer parts of type neuron statoacoustic (VIII) ganglion, abnormal ZP:0017739 statoacoustic (VIII) ganglion decreased rate neuron differentiation, abnormal ZP:0017740 ATP biosynthetic process decreased process quality, abnormal ZP:0017741 cardiac ventricle position, abnormal ZP:0017742 mitochondrial chromosome anatomical structure decreased amount, abnormal ZP:0017743 chondrocyte hypertrophy decreased process quality, abnormal ZP:0017744 dentary protruding, abnormal ZP:0017745 basihyal bone position, abnormal ZP:0017746 Meckel's cartilage increased angle to palatoquadrate cartilage, abnormal ZP:0017747 chondrocyte Meckel's cartilage increased amount, abnormal ZP:0017748 polysome head decreased amount, abnormal ZP:0017750 cytosolic ribosome head increased amount, abnormal ZP:0017751 intersegmental vessel delayed vasculature development, abnormal ZP:0017752 liver decreased process quality organ growth, abnormal ZP:0017753 pancreas decreased process quality organ growth, abnormal ZP:0017754 white matter optic tectum position, abnormal ZP:0017755 white matter optic tectum decreased size, abnormal ZP:0017756 white matter rhombic lip position, abnormal ZP:0017757 white matter rhombic lip decreased size, abnormal ZP:0017758 hindbrain decreased area, abnormal ZP:0017759 optic tectum decreased width, abnormal ZP:0017760 autophagosome neuron increased amount, abnormal ZP:0017761 cardioblast cell midline fusion delayed, abnormal ZP:0017762 mesoderm head absent, abnormal ZP:0017763 mesoderm trunk absent, abnormal ZP:0017769 hepatocyte swollen, abnormal ZP:0017783 neoplasm whole organism increased occurrence, abnormal ZP:0017788 podocyte disorganized, abnormal ZP:0017789 cell projection podocyte absent, abnormal ZP:0017791 barbel increased size, abnormal ZP:0017793 cilium pronephros curled, abnormal ZP:0017799 statoacoustic (VIII) ganglion occurrence neuron differentiation, abnormal ZP:0017803 cardiac muscle cell decreased velocity, abnormal ZP:0017804 cardiac muscle cell decreased process quality cell migration involved in heart formation, abnormal ZP:0017815 pharyngeal arch decreased object quality, abnormal ZP:0017816 pharyngeal arch cartilage has fewer parts of type ceratobranchial cartilage, abnormal ZP:0017817 pharyngeal arch cartilage lacks all parts of type ceratobranchial 3 cartilage, abnormal ZP:0017818 pharyngeal arch cartilage lacks all parts of type ceratobranchial 4 cartilage, abnormal ZP:0017819 pharyngeal arch cartilage lacks all parts of type ceratobranchial 5 cartilage, abnormal ZP:0017820 pharyngeal arch 3 decreased object quality, abnormal ZP:0017821 pharyngeal arch 4 decreased object quality, abnormal ZP:0017822 dorsal aorta in contact with lateral region common cardinal vein, abnormal ZP:0017823 dorsal aorta in contact with lateral region primary head sinus, abnormal ZP:0017824 trunk arrested blood circulation, abnormal ZP:0017825 axon spinal nerve decreased length, abnormal ZP:0017826 axon spinal nerve increased branchiness, abnormal ZP:0017828 glomerular filtration decreased functionality, abnormal ZP:0017829 renal glomerular capsule increased size, abnormal ZP:0017830 cilium movement process quality, abnormal ZP:0017831 neuron brain decreased branchiness, abnormal ZP:0017832 trunk disrupted neuron development, abnormal ZP:0017833 post-vent region disrupted neuron development, abnormal ZP:0017837 ceratobranchial 1 cartilage fused with ceratobranchial 2 cartilage, abnormal ZP:0017841 endocardium hypotrophic, abnormal ZP:0017842 pronephric nephron tubule development decreased process quality, abnormal ZP:0017843 distal region pronephros decreased object quality, abnormal ZP:0017844 melanosome melanocyte decreased size, abnormal ZP:0017853 pronephric distal early tubule poorly differentiated, abnormal ZP:0017856 caudal vein decreased thickness, abnormal ZP:0017857 embryonic organ development decreased rate, abnormal ZP:0017858 inner ear lacks all parts of type semicircular canal, abnormal ZP:0017859 whole organism has extra parts of type common myeloid progenitor, abnormal ZP:0017860 whole organism has fewer parts of type neutrophil, abnormal ZP:0017861 melanosome retinal pigmented epithelium decreased pigmentation, abnormal ZP:0017862 melanosome melanocyte unpigmented, abnormal ZP:0017863 cardiac muscle cell cardiac ventricle degenerate, abnormal ZP:0017864 collateral sprouting disrupted, abnormal ZP:0017866 membrane eye photoreceptor cell immature, abnormal ZP:0017876 neuron locus coeruleus absent, abnormal ZP:0017877 norepinephrine secreting cell pharyngeal arch absent, abnormal ZP:0017878 glomerular visceral epithelial cell development decreased process quality, abnormal ZP:0017879 pronephric glomerulus lacks all parts of type slit diaphragm pronephric podocyte, abnormal ZP:0017880 pronephric glomerulus lacks all parts of type pronephric glomerular capillary, abnormal ZP:0017881 stem cell population maintenance decreased occurrence, abnormal ZP:0017882 inner ear development decreased process quality, abnormal ZP:0017883 blood has fewer parts of type nucleate erythrocyte, abnormal ZP:0017884 retina has fewer parts of type somatic stem cell, abnormal ZP:0017885 skeletal muscle cell myotome malformed, abnormal ZP:0017886 heart valve morphogenesis disrupted, abnormal ZP:0017887 heart process quality blood circulation, abnormal ZP:0017888 heart valve morphology, abnormal ZP:0017889 pronephric glomerular capillary increased diameter, abnormal ZP:0017890 pronephros has fewer parts of type cell, abnormal ZP:0017891 optic chiasma development disrupted, abnormal ZP:0017892 spinal cord disrupted motor neuron axon guidance, abnormal ZP:0017893 neuroepithelial cell hindbrain neural tube morphology, abnormal ZP:0017894 neuroepithelial cell morphology, abnormal ZP:0017895 glomerular basement membrane morphology, abnormal ZP:0017902 neuroblast (sensu Vertebrata) ventricular zone increased amount, abnormal ZP:0017909 leukocyte increased amount, abnormal ZP:0017912 noradrenergic neuron development disrupted, abnormal ZP:0017913 trochlear motor nucleus decreased size, abnormal ZP:0017914 oculomotor nucleus decreased size, abnormal ZP:0017915 regulation of blood coagulation process quality, abnormal ZP:0017916 regulation of circulating fibrinogen levels process quality, abnormal ZP:0017917 heart obstructed, abnormal ZP:0017918 heart increased process quality blood coagulation, abnormal ZP:0017919 posterior cardinal vein increased occurrence blood coagulation, fibrin clot formation, abnormal ZP:0017920 caudal fin development delayed, abnormal ZP:0017922 locus coeruleus absent, abnormal ZP:0017923 locus ceruleus development process quality, abnormal ZP:0017924 ventricular system hydrocephalic, abnormal ZP:0017925 hematopoietic multipotent progenitor cell ventral wall of dorsal aorta decreased amount, abnormal ZP:0017932 integument broken, abnormal ZP:0017934 telencephalon absent, abnormal ZP:0017951 hematopoietic multipotent progenitor cell ventral wall of dorsal aorta increased amount, abnormal ZP:0017952 T cell increased amount, abnormal ZP:0017953 hematopoietic cell intermediate cell mass of mesoderm decreased amount, abnormal ZP:0017954 Kupffer's vesicle decreased frequency cilium movement, abnormal ZP:0017958 hematopoietic cell intermediate cell mass of mesoderm increased amount, abnormal ZP:0017959 primitive erythrocyte differentiation decreased process quality, abnormal ZP:0017960 nucleus of the caudal commissure decreased amount, abnormal ZP:0017961 blood island process quality cell cycle, abnormal ZP:0017962 blood island decreased process quality cell population proliferation, abnormal ZP:0017963 atrioventricular valve morphogenesis process quality, abnormal ZP:0017964 atrium decreased process quality heart contraction, abnormal ZP:0017965 atrioventricular canal constricted, abnormal ZP:0017966 atrial myocardium absent, abnormal ZP:0017967 atrioventricular valve process quality blood circulation, abnormal ZP:0017968 blood atrioventricular valve fluid flow rate, abnormal ZP:0017969 ventral trunk neural crest cell migration arrested, abnormal ZP:0017970 eye lacks all parts of type macrophage, abnormal ZP:0017971 head has fewer parts of type macrophage, abnormal ZP:0017972 head has fewer parts of type leukocyte, abnormal ZP:0017973 leukocyte head apoptotic, abnormal ZP:0017974 caudal vein blistered, abnormal ZP:0017975 yolk syncytial layer deformed, abnormal ZP:0017976 trunk colorless, abnormal ZP:0017980 cranial neural crest decreased amount, abnormal ZP:0017999 myeloid cell head kidney increased amount, abnormal ZP:0018013 brain increased process quality cell population proliferation, abnormal ZP:0018014 caudal fin increased process quality cell population proliferation, abnormal ZP:0018015 cell cycle rhythm quality, abnormal ZP:0018016 circadian rhythm disrupted, abnormal ZP:0018017 developmental growth increased rate, abnormal ZP:0018018 nucleus skeletal muscle circular, abnormal ZP:0018019 fin development process quality, abnormal ZP:0018020 caudal fin increased rate developmental growth, abnormal ZP:0018021 lepidotrichium segment increased length, abnormal ZP:0018022 photoreceptor outer segment layer decreased amount, abnormal ZP:0018023 cilium neuromast hair cell morphology, abnormal ZP:0018024 cilium neuromast hair cell decreased amount, abnormal ZP:0018025 thyroid gland development process quality, abnormal ZP:0018026 hypocretin-secreting neuron decreased amount, abnormal ZP:0018027 DEL decreased rate cell migration, abnormal ZP:0018028 DEL process quality cell migration, abnormal ZP:0018029 skeletal muscle myofibril skeletal muscle absent, abnormal ZP:0018030 vacuole muscle cell increased amount, abnormal ZP:0018031 optokinetic behavior amplitude, abnormal ZP:0018032 optokinetic behavior decreased frequency, abnormal ZP:0018033 vestibular reflex amplitude, abnormal ZP:0018047 myelin sheath spinal cord decreased amount, abnormal ZP:0018049 dorsal longitudinal anastomotic vessel incomplete structure, abnormal ZP:0018053 nitric oxide production involved in inflammatory response disrupted, abnormal ZP:0018057 renal system lacks parts or has fewer parts of type podocyte, abnormal ZP:0018058 GABAergic neuron hindbrain decreased amount, abnormal ZP:0018059 glutamatergic neuron hindbrain decreased amount, abnormal ZP:0018060 GABAergic neuron midbrain decreased amount, abnormal ZP:0018061 outer dynein arm Kupffer's vesicle decreased amount, abnormal ZP:0018062 motile cilium spinal cord immobile, abnormal ZP:0018063 hypophysis increased size, abnormal ZP:0018064 cell hypophysis increased amount, abnormal ZP:0018066 subintestinal vein decreased length, abnormal ZP:0018073 neuromast support cell decreased amount, abnormal ZP:0018081 retinal rod cell physical object quality, abnormal ZP:0018082 pronephros immature, abnormal ZP:0018083 renal glomerulus immature, abnormal ZP:0018084 microvillus glomerular basement membrane crowded, abnormal ZP:0018085 sarcomere post-vent region disorganized, abnormal ZP:0018086 slit diaphragm renal glomerulus decreased functionality, abnormal ZP:0018087 slit diaphragm glomerular basement membrane absent, abnormal ZP:0018088 podocyte foot glomerular basement membrane protruding, abnormal ZP:0018089 podocyte foot glomerular basement membrane irregularly shaped, abnormal ZP:0018091 median fin blistered, abnormal ZP:0018092 osteoblast differentiation disrupted, abnormal ZP:0018093 protein N-linked glycosylation disrupted, abnormal ZP:0018094 cell Meckel's cartilage decreased amount, abnormal ZP:0018095 mandibular arch skeleton truncated, abnormal ZP:0018096 cell palatoquadrate cartilage decreased amount, abnormal ZP:0018097 cell ceratohyal cartilage decreased amount, abnormal ZP:0018098 brain has extra parts of type neuronal stem cell, abnormal ZP:0018099 brain has extra parts of type astrocyte, abnormal ZP:0018100 brain has fewer parts of type neuron, abnormal ZP:0018101 brain decreased occurrence neuron differentiation, abnormal ZP:0018102 brain increased occurrence astrocyte differentiation, abnormal ZP:0018103 brain increased occurrence neural precursor cell proliferation, abnormal ZP:0018104 neuronal stem cell brain proliferative, abnormal ZP:0018105 trigeminal ganglion has fewer parts of type motor neuron, abnormal ZP:0018106 facial ganglion has fewer parts of type motor neuron, abnormal ZP:0018107 vagal ganglion has fewer parts of type motor neuron, abnormal ZP:0018108 cerebellum increased occurrence apoptotic process, abnormal ZP:0018109 carbohydrate metabolic process disrupted, abnormal ZP:0018110 cellular amino acid metabolic process disrupted, abnormal ZP:0018111 fatty acid metabolic process disrupted, abnormal ZP:0018112 cerebellum decreased occurrence cell proliferation in hindbrain, abnormal ZP:0018113 enteric neuron posterior intestine absent, abnormal ZP:0018114 enteric neuron intestine decreased amount, abnormal ZP:0018115 whole organism has extra parts of type posterior pancreatic bud, abnormal ZP:0018116 pancreatic bud lacks parts or has fewer parts of type cell, abnormal ZP:0018117 dorsal aorta increased diameter, abnormal ZP:0018127 photoreceptor outer segment photoreceptor outer segment layer morphology, abnormal ZP:0018136 Golgi vesicle transport process quality, abnormal ZP:0018137 brain increased occurrence Notch signaling pathway, abnormal ZP:0018138 vagal neural crest decreased distance hyoid neural crest, abnormal ZP:0018139 whole organism lacks parts or has fewer parts of type otic vesicle, abnormal ZP:0018140 anterior-posterior axis pharyngeal arch decreased length, abnormal ZP:0018142 pharyngeal arch 3-7 orientation anterior-posterior axis whole organism, abnormal ZP:0018143 chordoma intestine present, abnormal ZP:0018144 intestinal epithelium hyperplastic, abnormal ZP:0018145 chordoma vertebra present, abnormal ZP:0018146 hemoglobin biosynthetic process decreased process quality, abnormal ZP:0018147 T cell thymus decreased amount, abnormal ZP:0018148 posterior lateral line primordium increased occurrence apoptotic process, abnormal ZP:0018149 posterior lateral line primordium decreased occurrence cell population proliferation, abnormal ZP:0018150 neuromast posterior lateral line primordium decreased amount, abnormal ZP:0018151 heart unlumenized, abnormal ZP:0018152 cardiac jelly increased thickness, abnormal ZP:0018153 endocardium increased distance myocardium, abnormal ZP:0018154 semicircular canal development delayed, abnormal ZP:0018155 posterior lateral line primordium structure, abnormal ZP:0018156 establishment of blood-brain barrier disrupted, abnormal ZP:0018157 cranial vasculature porous, abnormal ZP:0018158 blood accumulation hindbrain, abnormal ZP:0018159 hair cell semicircular canal decreased amount, abnormal ZP:0018160 hair cell decreased functionality, abnormal ZP:0018161 neuromast hair cell degenerate, abnormal ZP:0018162 stereocilium bundle neuromast hair cell morphology, abnormal ZP:0018163 kinocilium neuromast hair cell morphology, abnormal ZP:0018164 neuron differentiation decreased process quality, abnormal ZP:0018165 head lacks all parts of type cleithrum, abnormal ZP:0018166 head lacks all parts of type opercle, abnormal ZP:0018167 head lacks all parts of type pharyngeal arch 3-7, abnormal ZP:0018168 neurocranial trabecula truncated, abnormal ZP:0018169 ethmoid cartilage truncated, abnormal ZP:0018170 brain has fewer parts of type neuronal stem cell, abnormal ZP:0018171 brain has fewer parts of type astrocyte, abnormal ZP:0018172 brain has extra parts of type neuron, abnormal ZP:0018173 brain increased occurrence neuron differentiation, abnormal ZP:0018174 brain decreased occurrence neural precursor cell proliferation, abnormal ZP:0018175 hindbrain decreased duration mitotic cell cycle, abnormal ZP:0018178 hematopoietic multipotent progenitor cell increased amount, abnormal ZP:0018186 whole organism lacks parts or has fewer parts of type eye, abnormal ZP:0018187 anatomical margin median fin fold protruding, abnormal ZP:0018188 cell apical ectodermal ridge median fin fold morphology, abnormal ZP:0018207 slow muscle cell somite undulate, abnormal ZP:0018208 anatomical margin pectoral fin fold increased thickness, abnormal ZP:0018209 fin fold actinotrichium increased thickness, abnormal ZP:0018210 fin fold actinotrichium bent, abnormal ZP:0018211 fin fold actinotrichium mislocalised, abnormal ZP:0018212 anatomical margin median fin fold increased thickness, abnormal ZP:0018223 otic vesicle has fewer parts of type cilium otic vesicle, abnormal ZP:0018224 lateral crista has fewer parts of type kinocilium lateral crista, abnormal ZP:0018225 spinal cord has fewer parts of type cilium ependymal cell, abnormal ZP:0018227 angioblastic mesenchymal cell ventral wall of dorsal aorta decreased amount, abnormal ZP:0018228 endothelial to hematopoietic transition decreased process quality, abnormal ZP:0018229 trunk vasculature decreased process quality blood vessel lumenization, abnormal ZP:0018230 Kupffer's vesicle decreased occurrence detection of nodal flow, abnormal ZP:0018231 dorsal aorta decreased process quality blood vessel lumenization, abnormal ZP:0018232 blood cell accumulation sinus venosus, abnormal ZP:0018233 monoamine oxidase activity increased process quality, abnormal ZP:0018234 central artery hindbrain absent, abnormal ZP:0018235 central artery hindbrain decreased amount, abnormal ZP:0018236 brain vasculature absent, abnormal ZP:0018237 dorsal root ganglion decreased process quality Wnt signaling pathway, abnormal ZP:0018238 primordial hindbrain channel decreased process quality Wnt signaling pathway, abnormal ZP:0018239 primordial hindbrain channel decreased process quality sprouting angiogenesis, abnormal ZP:0018240 primordial hindbrain channel decreased process quality endothelial tip cell fate specification, abnormal ZP:0018241 angiogenic sprout primordial hindbrain channel absent, abnormal ZP:0018242 endothelial cell decreased accumulation filamentous actin dorsal region primordial hindbrain channel, abnormal ZP:0018243 sympathetic neuron absent, abnormal ZP:0018249 aerobic respiration process quality, abnormal ZP:0018253 mitochondrial chromosome whole organism increased amount, abnormal ZP:0018255 lens decreased diameter, abnormal ZP:0018269 optic tectum decreased process quality generation of neurons, abnormal ZP:0018270 photoreceptor outer segment retinal cone cell increased length, abnormal ZP:0018271 photoreceptor outer segment retinal rod cell decreased size, abnormal ZP:0018272 photoreceptor outer segment retinal rod cell absence due to degeneration, abnormal ZP:0018273 photoreceptor disc membrane retinal rod cell disorganized, abnormal ZP:0018274 optic tectum decreased process quality mitotic cell cycle process, abnormal ZP:0018275 myofibril post-vent region disorganized, abnormal ZP:0018276 blood island size, abnormal ZP:0018281 mitochondrion slow muscle cell functionality, abnormal ZP:0018282 mitochondrion slow muscle cell decreased functionality, abnormal ZP:0018283 mitochondrial respirasome slow muscle cell decreased functionality, abnormal ZP:0018284 mitochondrial respirasome fast muscle cell decreased functionality, abnormal ZP:0018285 ventricular system brain edematous, abnormal ZP:0018286 germ ring decreased circumference, abnormal ZP:0018287 collagen network caudal fin disorganized, abnormal ZP:0018288 epithelium protruding, abnormal ZP:0018289 neutrophil epithelium increased amount, abnormal ZP:0018290 mitochondrial fission disrupted, abnormal ZP:0018291 mitochondrion spinal cord aggregated, abnormal ZP:0018292 neuron projection spinal cord decreased amount, abnormal ZP:0018293 mitochondrion motor neuron spatial pattern, abnormal ZP:0018294 mitochondrion motor neuron aggregated, abnormal ZP:0018295 motor neuron process quality bleb assembly, abnormal ZP:0018296 axon retinal ganglion cell shortened, abnormal ZP:0018297 dendrite retinal ganglion cell decreased amount, abnormal ZP:0018298 angioblast cell migration from lateral mesoderm to midline arrested, abnormal ZP:0018299 vascular lymphangioblast posterior cardinal vein absent, abnormal ZP:0018300 vascular lymphangioblast posterior cardinal vein decreased amount, abnormal ZP:0018301 thoracic duct aplastic/hypoplastic, abnormal ZP:0018302 nucleate erythrocyte blood morphology, abnormal ZP:0018303 nucleate erythrocyte blood circular, abnormal ZP:0018304 myeloid cell kidney dysplastic, abnormal ZP:0018305 erythroid lineage cell kidney morphology, abnormal ZP:0018306 hematopoietic multipotent progenitor cell kidney dysplastic, abnormal ZP:0018307 common myeloid progenitor head kidney increased amount, abnormal ZP:0018308 nucleate erythrocyte head kidney decreased amount, abnormal ZP:0018309 myeloid cell head kidney dysplastic, abnormal ZP:0018310 erythroid lineage cell head kidney morphology, abnormal ZP:0018311 hematopoietic multipotent progenitor cell head kidney increased amount, abnormal ZP:0018312 hematopoietic multipotent progenitor cell head kidney dysplastic, abnormal ZP:0018313 ribosome nucleate erythrocyte increased amount, abnormal ZP:0018335 nucleus neutrophil morphology, abnormal ZP:0018336 glossopharyngeal ganglion decreased size, abnormal ZP:0018337 glossopharyngeal ganglion lacks parts or has fewer parts of type axon glossopharyngeal ganglion, abnormal ZP:0018338 axon facial ganglion malformed, abnormal ZP:0018339 axon glossopharyngeal ganglion malformed, abnormal ZP:0018340 axon epibranchial ganglion morphology, abnormal ZP:0018341 axon vagal ganglion malformed, abnormal ZP:0018342 epibranchial ganglion process quality axon development, abnormal ZP:0018343 vagal ganglion decreased process quality fasciculation of sensory neuron axon, abnormal ZP:0018344 forebrain increased process quality cell death, abnormal ZP:0018345 midbrain increased process quality cell death, abnormal ZP:0018346 hindbrain decreased process quality mitotic cell cycle, abnormal ZP:0018347 cerebellum structure, abnormal ZP:0018348 epidermal cell aggregated, abnormal ZP:0018349 central nervous system decreased thickness, abnormal ZP:0018350 ball increased diameter, abnormal ZP:0018351 pancreas growth quality of occurrent growth, abnormal ZP:0018352 pancreas increased process quality growth, abnormal ZP:0018353 subintestinal vein delayed angiogenesis, abnormal ZP:0018354 cilium hair cell anterior macula decreased length, abnormal ZP:0018355 histone H3-K9 acetylation increased process quality, abnormal ZP:0018356 histone H3-K27 acetylation increased process quality, abnormal ZP:0018357 artery increased size, abnormal ZP:0018358 anatomical axis whole organism decreased size, abnormal ZP:0018359 erythrocyte differentiation increased process quality, abnormal ZP:0018360 respiratory gaseous exchange by respiratory system increased rate, abnormal ZP:0018361 skeletal muscle collagenous, abnormal ZP:0018362 muscle cell skeletal muscle disorganized, abnormal ZP:0018363 mitochondrion muscle cell morphology, abnormal ZP:0018364 muscle cell detached from mitochondrial outer membrane mitochondrial inner membrane muscle cell, abnormal ZP:0018365 mitochondrial matrix muscle cell morphology, abnormal ZP:0018366 vacuole muscle cell present, abnormal ZP:0018367 sarcoplasm muscle cell composition, abnormal ZP:0018368 sarcoplasmic reticulum muscle cell increased size, abnormal ZP:0018369 muscle cell misaligned with sarcomere sarcomere muscle cell, abnormal ZP:0018370 mitochondrial crista muscle cell morphology, abnormal ZP:0018371 mitochondrial crista muscle cell swollen, abnormal ZP:0018372 skeletal muscle myofibril muscle cell disorganized, abnormal ZP:0018373 lymphangioblast cord decreased length, abnormal ZP:0018374 heart tube present, abnormal ZP:0018375 heart tube linear, abnormal ZP:0018376 myocardium heart tube decreased thickness, abnormal ZP:0018377 mesenchyme pectoral fin flattened, abnormal ZP:0018378 mesenchyme pectoral fin absent cell population proliferation, abnormal ZP:0018379 pectoral fin upturned, abnormal ZP:0018382 sperm testis absent, abnormal ZP:0018386 male organism sterile, abnormal ZP:0018387 Sertoli cell disorganized, abnormal ZP:0018388 oocyte maturation disrupted, abnormal ZP:0018390 ovary decreased amount, abnormal ZP:0018399 female organism sterile, abnormal ZP:0018408 trunk absent, abnormal ZP:0018409 central nervous system decreased size, abnormal ZP:0018410 pericardium decreased size, abnormal ZP:0018411 trunk increased thickness, abnormal ZP:0018412 neuron central nervous system irregular spatial pattern, abnormal ZP:0018414 heart lacks all parts of type atrioventricular valve, abnormal ZP:0018415 pharyngeal arch 3 increased diameter, abnormal ZP:0018416 granulocyte intestinal bulb increased amount, abnormal ZP:0018417 goblet cell intestine increased amount, abnormal ZP:0018418 intestinal epithelial cell increased rate cell population proliferation, abnormal ZP:0018419 pectoral fin uncoordinated, abnormal ZP:0018420 pectoral fin movement quality, abnormal ZP:0018421 mandibular arch skeleton increased mobility, abnormal ZP:0018422 slit diaphragm assembly disrupted, abnormal ZP:0018423 renal glomerulus protruding into microvillus renal capsular space, abnormal ZP:0018424 podocyte foot glomerular basement membrane morphology, abnormal ZP:0018425 retinal pigmented epithelium detached from retina, abnormal ZP:0018426 neuron retina mislocalised, abnormal ZP:0018427 adherens junction outer limiting membrane absent, abnormal ZP:0018428 adherens junction outer limiting membrane malformed, abnormal ZP:0018429 eye photoreceptor cell immature, abnormal ZP:0018430 green sensitive photoreceptor cell absent, abnormal ZP:0018431 red sensitive photoreceptor cell absent, abnormal ZP:0018432 ventral region caudal vein decreased diameter, abnormal ZP:0018433 ventral region caudal vein plexus decreased diameter, abnormal ZP:0018434 hemangioblast cell differentiation process quality, abnormal ZP:0018435 photoreceptor inner segment photoreceptor cell absent, abnormal ZP:0018436 retinal inner nuclear layer apoptotic, abnormal ZP:0018437 female sex determination decreased process quality, abnormal ZP:0018441 retinal inner plexiform layer increased thickness, abnormal ZP:0018442 male organism decreased fecundity, abnormal ZP:0018447 glomerular basement membrane increased thickness, abnormal ZP:0018448 nucleate erythrocyte increased fluorescence, abnormal ZP:0018449 posterior cardinal vein malformed, abnormal ZP:0018450 blood cell low saturation, abnormal ZP:0018451 anatomical axis whole organism morphology, abnormal ZP:0018452 perichondrium edematous, abnormal ZP:0018453 distal region pronephros disorganized, abnormal ZP:0018454 cloaca increased width, abnormal ZP:0018455 epithelium cloaca disorganized, abnormal ZP:0018456 cell cloaca disconnected, abnormal ZP:0018457 posterior region caudal fin curled, abnormal ZP:0018458 posterior region caudal fin malformed, abnormal ZP:0018462 cilium assembly decreased process quality, abnormal ZP:0018463 intracellular cholesterol transport disrupted, abnormal ZP:0018464 cholesterol whole organism increased amount, abnormal ZP:0018465 spinal cord decreased amount, abnormal ZP:0018466 glial cell disrupted myelination, abnormal ZP:0018467 retinal inner plexiform layer circular, abnormal ZP:0018468 axon peripheral neuron morphology, abnormal ZP:0018469 Purkinje cell layer corpus cerebelli morphology, abnormal ZP:0018470 medial longitudinal fasciculus decreased amount, abnormal ZP:0018471 retinotectal tract morphology, abnormal ZP:0018472 glial cell central nervous system absent, abnormal ZP:0018473 axon peripheral neuron branchiness, abnormal ZP:0018474 peripheral neuron process quality axon guidance, abnormal ZP:0018475 myelinating Schwann cell posterior lateral line nerve decreased amount, abnormal ZP:0018476 axon peripheral neuron shape, abnormal ZP:0018477 retinal ganglion cell layer patchy, abnormal ZP:0018478 acetylcholine-gated channel complex myotome increased area, abnormal ZP:0018479 spinal cord decreased process quality motor neuron axon guidance, abnormal ZP:0018480 neuronal cell body motor neuron mislocalised, abnormal ZP:0018481 neuromuscular junction of skeletal muscle fiber myotome area, abnormal ZP:0018482 regulation of synaptic transmission, cholinergic decreased process quality, abnormal ZP:0018483 acetylcholine-gated channel complex myotome increased distribution, abnormal ZP:0018484 myotome decreased process quality regulation of synaptic transmission, cholinergic, abnormal ZP:0018485 pronephric distal late tubule spatial pattern, abnormal ZP:0018486 pronephros spatial pattern, abnormal ZP:0018487 pronephric proximal convoluted tubule spatial pattern, abnormal ZP:0018488 pronephric glomerulus spatial pattern, abnormal ZP:0018489 heart contraction increased frequency, abnormal ZP:0018490 vasodilation increased occurrence, abnormal ZP:0018491 artery increased diameter, abnormal ZP:0018492 blood circulation increased volume, abnormal ZP:0018495 mitochondrion skeletal muscle increased amount, abnormal ZP:0018496 sarcomere skeletal muscle increased thickness, abnormal ZP:0018497 cranial blood vessel process quality artery morphogenesis, abnormal ZP:0018498 dorsal aorta increased amount, abnormal ZP:0018499 optic artery increased amount, abnormal ZP:0018500 metencephalic artery increased amount, abnormal ZP:0018501 cell migration involved in heart development decreased occurrence, abnormal ZP:0018502 caudal division of the internal carotid artery increased width, abnormal ZP:0018503 endothelial cell caudal division of the internal carotid artery increased amount, abnormal ZP:0018504 internal carotid artery process quality blood vessel endothelial cell migration, abnormal ZP:0018505 aortic arch 1 process quality blood vessel development, abnormal ZP:0018506 endothelial cell internal carotid artery increased amount, abnormal ZP:0018507 internal carotid artery increased width, abnormal ZP:0018508 aortic arch 1 decreased occurrence cell migration involved in heart development, abnormal ZP:0018509 aortic arch 1 constricted, abnormal ZP:0018510 endothelial cell aortic arch 1 decreased amount, abnormal ZP:0018511 caudal division of the internal carotid artery process quality blood vessel endothelial cell migration, abnormal ZP:0018512 caudal division of the internal carotid artery process quality blood vessel development, abnormal ZP:0018513 aortic arch 1 morphology, abnormal ZP:0018514 aortic arch 1 process quality blood vessel endothelial cell migration, abnormal ZP:0018515 internal carotid artery process quality blood vessel development, abnormal ZP:0018516 caudal division of the internal carotid artery increased occurrence blood vessel endothelial cell migration, abnormal ZP:0018517 lateral dorsal aorta increased amount, abnormal ZP:0018518 aortic arch 1 decreased process quality blood vessel endothelial cell migration, abnormal ZP:0018519 aortic arch 1 increased amount, abnormal ZP:0018520 internal carotid artery increased amount, abnormal ZP:0018521 pancreatic B cell decreased area, abnormal ZP:0018522 endocrine pancreas decreased distribution, abnormal ZP:0018523 neuron trunk decreased distribution, abnormal ZP:0018524 melanophore stripe broken, abnormal ZP:0018525 anterior region spinal cord neural tube decreased distribution, abnormal ZP:0018526 anterior region spinal cord decreased distribution, abnormal ZP:0018527 dorsal root ganglion development disrupted, abnormal ZP:0018528 spinal cord has fewer parts of type ventral region myelin sheath spinal cord, abnormal ZP:0018529 oligodendrocyte development decreased process quality, abnormal ZP:0018530 spinal cord increased occurrence central nervous system myelination, abnormal ZP:0018531 spinal cord decreased occurrence central nervous system myelination, abnormal ZP:0018532 spinal cord premature central nervous system myelination, abnormal ZP:0018533 spinal cord premature axon ensheathment in central nervous system, abnormal ZP:0018534 spinal cord decreased occurrence oligodendrocyte development, abnormal ZP:0018535 oligodendrocyte progenitor proliferation decreased occurrence, abnormal ZP:0018536 spinal cord decreased occurrence axon ensheathment in central nervous system, abnormal ZP:0018537 posterior lateral line nerve decreased amount, abnormal ZP:0018538 muscle pioneer myotome absent, abnormal ZP:0018539 fast muscle cell myotome absent, abnormal ZP:0018540 swim bladder development decreased process quality, abnormal ZP:0018542 interneuron absent, abnormal ZP:0018543 neural tube decreased amount, abnormal ZP:0018544 skeletal muscle cell increased occurrence apoptotic process, abnormal ZP:0018545 skeletal muscle myofibril skeletal muscle morphology, abnormal ZP:0018546 whole organism increased amount, abnormal ZP:0018547 thymus decreased amount, abnormal ZP:0018548 retinal cone cell decreased process quality photoreceptor cell outer segment organization, abnormal ZP:0018549 dorsal region retinal outer nuclear layer decreased thickness, abnormal ZP:0018550 photoreceptor outer segment retinal cone cell irregular spatial pattern, abnormal ZP:0018551 posterior pronephric duct lacks all parts of type motile cilium posterior pronephric duct, abnormal ZP:0018552 pronephric duct decreased occurrence cilium assembly, abnormal ZP:0018553 retinal cone cell has fewer parts of type photoreceptor outer segment retinal cone cell, abnormal ZP:0018554 photoreceptor disc membrane retinal cone cell irregular spatial pattern, abnormal ZP:0018555 retinal outer nuclear layer mislocalised, abnormal ZP:0018556 photoreceptor connecting cilium eye photoreceptor cell decreased amount, abnormal ZP:0018557 dorsal region photoreceptor outer segment layer malformed, abnormal ZP:0018558 anterior lateral plate mesoderm increased distribution, abnormal ZP:0018559 heart primordium increased distribution, abnormal ZP:0018560 heart primordium decreased distribution, abnormal ZP:0018561 hematopoietic progenitor cell differentiation decreased process quality, abnormal ZP:0018562 hematopoietic system increased process quality apoptotic process, abnormal ZP:0018563 hematopoietic stem cell differentiation decreased process quality, abnormal ZP:0018564 blood island increased process quality apoptotic process, abnormal ZP:0018565 intermediate cell mass of mesoderm increased process quality apoptotic process, abnormal ZP:0018566 myeloid cell development decreased process quality, abnormal ZP:0018567 myeloid leukocyte differentiation decreased process quality, abnormal ZP:0018568 primitive hemopoiesis absent, abnormal ZP:0018569 myeloid cell development absent, abnormal ZP:0018570 cilium peripheral olfactory organ morphology, abnormal ZP:0018571 musculoskeletal movement, spinal reflex action decreased occurrence, abnormal ZP:0018572 nervous system wholly anterioralized, abnormal ZP:0018573 retina decreased amount, abnormal ZP:0018574 pancreatic B cell decreased mass, abnormal ZP:0018575 whole organism absent, abnormal ZP:0018576 whole organism decreased amount, abnormal ZP:0018577 posterior lateral line primordium has extra parts of type cell posterior lateral line primordium, abnormal ZP:0018578 posterior lateral line primordium has extra parts of type posterior region cell posterior lateral line primordium, abnormal ZP:0018579 posterior lateral line has extra parts of type posterior lateral line neuromast, abnormal ZP:0018580 posterior lateral line primordium decreased speed posterior lateral line neuromast primordium migration, abnormal ZP:0018581 trunk vasculature decreased occurrence blood circulation, abnormal ZP:0018582 posterior lateral line primordium increased occurrence cell population proliferation, abnormal ZP:0018583 posterior lateral line primordium increased distribution, abnormal ZP:0018584 dorsal aorta constricted, abnormal ZP:0018585 intersegmental vein closed, abnormal ZP:0018586 dorsal aorta morphogenesis decreased process quality, abnormal ZP:0018587 dorsal longitudinal anastomotic vessel closed, abnormal ZP:0018588 endothelial cell increased occurrence apoptotic process, abnormal ZP:0018589 endocrine pancreas increased distribution, abnormal ZP:0018590 motile cilium pronephric duct decreased functionality, abnormal ZP:0018591 pronephric duct decreased process quality epithelial cilium movement involved in extracellular fluid movement, abnormal ZP:0018592 ventral wall of dorsal aorta decreased amount, abnormal ZP:0018593 neuromast increased rate mitotic cell cycle, abnormal ZP:0018594 atrioventricular canal endocardium decreased amount, abnormal ZP:0018595 heart primordium decreased amount, abnormal ZP:0018596 establishment of epithelial cell polarity disrupted, abnormal ZP:0018597 endodermal cell decreased distribution, abnormal ZP:0018598 heart primordium hypoplastic, abnormal ZP:0018599 hindbrain decreased amount, abnormal ZP:0018600 rhombomere 4 morphogenesis process quality, abnormal ZP:0018601 hindbrain decreased occurrence cell proliferation in hindbrain, abnormal ZP:0018602 hindbrain increased amount, abnormal ZP:0018603 hindbrain decreased occurrence neuron differentiation, abnormal ZP:0018604 hindbrain lacks parts or has fewer parts of type Mauthner neuron, abnormal ZP:0018605 rhombomere 3 decreased length, abnormal ZP:0018606 rhombomere 4 decreased length, abnormal ZP:0018607 rhombomere 3 morphogenesis process quality, abnormal ZP:0018608 hindbrain increased occurrence Notch signaling pathway, abnormal ZP:0018609 leukocyte accumulation brain, abnormal ZP:0018610 brain vasculature increased fragility, abnormal ZP:0018611 nucleate erythrocyte accumulation brain, abnormal ZP:0018613 photoreceptor cell cilium photoreceptor cell decreased length, abnormal ZP:0018614 cilium renal system spatial pattern, abnormal ZP:0018615 preoptic area absent, abnormal ZP:0018616 cell body microglial cell increased size, abnormal ZP:0018617 microglial cell optic tectum morphology, abnormal ZP:0018618 cell body microglial cell increased volume, abnormal ZP:0018619 microglial cell increased frequency phagocytosis, abnormal ZP:0018620 cell projection microglial cell increased amount, abnormal ZP:0018621 ventral wall of dorsal aorta increased amount, abnormal ZP:0018622 somite atrophied, abnormal ZP:0018623 macrophage accumulation lysosome macrophage, abnormal ZP:0018624 macrophage decreased process quality myeloid leukocyte migration, abnormal ZP:0018625 macrophage process quality myeloid leukocyte migration, abnormal ZP:0018626 motor neuron fragile, abnormal ZP:0018627 neuromuscular junction motor neuron decreased amount, abnormal ZP:0018628 pancreatic D cell decreased amount, abnormal ZP:0018629 somatostatin secreting cell decreased distribution, abnormal ZP:0018630 retinal outer plexiform layer decreased occurrence synapse assembly, abnormal ZP:0018631 synapse retinal outer plexiform layer morphology, abnormal ZP:0018632 retina increased occurrence mitotic cell cycle, abnormal ZP:0018633 autophagosome assembly disrupted, abnormal ZP:0018634 autophagosome heart decreased amount, abnormal ZP:0018635 post-vent region increased occurrence cell death, abnormal ZP:0018636 atrioventricular canal increased distribution, abnormal ZP:0018637 atrioventricular canal mislocalised, abnormal ZP:0018638 cell decreased process quality autophagosome assembly, abnormal ZP:0018639 heart increased distribution, abnormal ZP:0018640 atrium increased distribution, abnormal ZP:0018641 cardiac ventricle increased distribution, abnormal ZP:0018642 epidermis increased occurrence cell death, abnormal ZP:0018643 basement membrane epidermis decreased distribution, abnormal ZP:0018644 epidermal cell mislocalised, abnormal ZP:0018645 peridermal cell aggregated, abnormal ZP:0018646 fin fold actinotrichium disassembled, abnormal ZP:0018647 keratinocyte epidermal basal stratum mislocalised, abnormal ZP:0018648 basement membrane epidermis broken, abnormal ZP:0018649 keratinocyte epidermal basal stratum increased amount, abnormal ZP:0018650 epidermal cell epidermis absent, abnormal ZP:0018651 peridermal cell circular, abnormal ZP:0018652 epidermis increased amount, abnormal ZP:0018653 epidermis increased distribution, abnormal ZP:0018654 thigmotaxis lacking processual parts regulation of twitch skeletal muscle contraction, abnormal ZP:0018656 thigmotaxis having decreased processual parts relaxation of skeletal muscle, abnormal ZP:0018657 cell ciliated cell decreased amount, abnormal ZP:0018658 forerunner cell group decreased occurrence cell population proliferation, abnormal ZP:0018660 plasma membrane EVL decreased amount, abnormal ZP:0018661 plasma membrane forerunner cell group decreased amount, abnormal ZP:0018662 mesoderm mislocalised, abnormal ZP:0018663 plasma membrane cell decreased amount, abnormal ZP:0018664 right side mesoderm mislocalised, abnormal ZP:0018665 determination of left/right asymmetry in lateral mesoderm decreased occurrence, abnormal ZP:0018667 cytoplasm forerunner cell group decreased acidity, abnormal ZP:0018668 basal region neuromast hair cell decreased amount, abnormal ZP:0018669 ciliated olfactory receptor neuron decreased occurrence olfactory bulb development, abnormal ZP:0018670 non-motile cilium neuromast hair cell absent, abnormal ZP:0018671 cranium increased amount, abnormal ZP:0018672 bone mineralization decreased occurrence, abnormal ZP:0018673 centrum hollow, abnormal ZP:0018674 determination of pancreatic left/right asymmetry decreased occurrence, abnormal ZP:0018675 right side lateral plate mesoderm mislocalised, abnormal ZP:0018676 mitotic cell cycle increased duration, abnormal ZP:0018677 centrosome duplication decreased occurrence, abnormal ZP:0018678 right side epithalamus mislocalised, abnormal ZP:0018679 cilium pronephric tubule decreased mobility, abnormal ZP:0018680 pancreatic bud decreased amount, abnormal ZP:0018681 cilium olfactory pit decreased mobility, abnormal ZP:0018682 cilium cloaca decreased mobility, abnormal ZP:0018683 pancreatic B cell increased area, abnormal ZP:0018684 exocrine pancreas decreased area, abnormal ZP:0018685 atrioventricular valve increased distribution, abnormal ZP:0018686 tectal ventricle distended, abnormal ZP:0018687 optic tectum decreased distribution, abnormal ZP:0018688 retina decreased distribution, abnormal ZP:0018689 trunk increased amount, abnormal ZP:0018690 lymphoid progenitor cell differentiation increased occurrence, abnormal ZP:0018691 myeloid progenitor cell differentiation decreased occurrence, abnormal ZP:0018692 lymphoid progenitor cell thymus increased amount, abnormal ZP:0018693 erythroid lineage cell decreased occurrence myeloid progenitor cell differentiation, abnormal ZP:0018694 female organism increased occurrence male gamete generation, abnormal ZP:0018695 female organism male, abnormal ZP:0018696 granulosa cell ovary absent, abnormal ZP:0018697 female organism has extra parts of type sperm, abnormal ZP:0018698 oocyte decreased amount, abnormal ZP:0018699 female organism has extra parts of type spermatogonium, abnormal ZP:0018700 oocyte maturation arrested, abnormal ZP:0018701 female organism has extra parts of type spermatocyte, abnormal ZP:0018702 oocyte degeneration, abnormal ZP:0018703 Melanin whole organism decreased amount, abnormal ZP:0018704 apical ectodermal ridge decreased amount, abnormal ZP:0018705 oocyte stage II spatial pattern, abnormal ZP:0018706 oocyte stage II increased distribution, abnormal ZP:0018707 oocyte stage I increased distribution, abnormal ZP:0018708 oocyte stage I spatial pattern, abnormal ZP:0018709 orbit constricted, abnormal ZP:0018710 supraorbital bone protruding out of orbit, abnormal ZP:0018711 ventral margin supraorbital bone rough, abnormal ZP:0018712 supraorbital bone distended, abnormal ZP:0018713 extracellular matrix skeletal muscle cell absent, abnormal ZP:0018714 muscle tendon junction skeletal muscle cell morphology, abnormal ZP:0018715 muscle post-vent region structure, abnormal ZP:0018716 plasma membrane trunk musculature decreased amount, abnormal ZP:0018717 skeletal muscle detached from muscle tendon junction skeletal muscle cell, abnormal ZP:0018718 trunk musculature pathological, abnormal ZP:0018719 cytoplasmic vesicle trunk musculature increased amount, abnormal ZP:0018720 pronephric duct lacks all parts of type motile cilium outer dynein arm pronephric duct, abnormal ZP:0018721 pronephric duct decreased occurrence outer dynein arm assembly, abnormal ZP:0018722 otolith organ absent, abnormal ZP:0018723 motor neuron activation quality, abnormal ZP:0018724 Mauthner neuron has fewer parts of type AMPA glutamate receptor complex Mauthner neuron, abnormal ZP:0018725 Mauthner neuron decreased rate AMPA selective glutamate receptor signaling pathway, abnormal ZP:0018726 hindbrain decreased occurrence AMPA glutamate receptor clustering, abnormal ZP:0018728 Mauthner neuron increased rate AMPA selective glutamate receptor signaling pathway, abnormal ZP:0018729 trigeminal motor nucleus mislocalised, abnormal ZP:0018730 branchiomotor neuron disorganized, abnormal ZP:0018731 motor nucleus of vagal nerve mislocalised, abnormal ZP:0018732 microtubule cytoskeleton brain disorganized, abnormal ZP:0018733 neuronal cell body facial nerve motor nucleus mislocalised, abnormal ZP:0018734 extension physical object quality, abnormal ZP:0018735 endosome skeletal muscle cell increased amount, abnormal ZP:0018736 membrane skeletal muscle cell convolute, abnormal ZP:0018737 caveola skeletal muscle cell decreased amount, abnormal ZP:0018738 caveola assembly disrupted, abnormal ZP:0018739 skeletal muscle decreased amount, abnormal ZP:0018740 skeletal muscle occurrence ERK1 and ERK2 cascade, abnormal ZP:0018741 cytoplasm skeletal muscle cell decreased amount, abnormal ZP:0018742 male organism decreased mass, abnormal ZP:0018743 sarcomere skeletal muscle cell spatial pattern, abnormal ZP:0018744 cytoplasm skeletal muscle cell mislocalised, abnormal ZP:0018745 cytoplasm skeletal muscle cell increased amount, abnormal ZP:0018746 skeletal muscle cell decreased process quality T-tubule organization, abnormal ZP:0018747 skeletal muscle increased amount, abnormal ZP:0018748 skeletal muscle cell has extra parts of type caveola skeletal muscle cell, abnormal ZP:0018749 skeletal muscle cell decreased diameter, abnormal ZP:0018750 female organism decreased length, abnormal ZP:0018751 male organism decreased length, abnormal ZP:0018752 skeletal muscle cell irregularly shaped, abnormal ZP:0018753 female organism decreased mass, abnormal ZP:0018754 definitive hemopoiesis decreased occurrence, abnormal ZP:0018755 cytoplasmic vesicle eye photoreceptor cell mislocalised, abnormal ZP:0018756 shield increased distribution, abnormal ZP:0018757 ventral region non neural ectoderm decreased distribution, abnormal ZP:0018758 ventral region whole organism decreased distribution, abnormal ZP:0018759 posterior region trunk absent, abnormal ZP:0018760 dorsal/ventral pattern formation decreased occurrence, abnormal ZP:0018761 dorsal region whole organism increased distribution, abnormal ZP:0018762 Wnt signaling pathway involved in dorsal/ventral axis specification increased occurrence, abnormal ZP:0018763 animal-vegetal axis whole organism elongated, abnormal ZP:0018764 anterior region neuroectoderm increased distribution, abnormal ZP:0018765 pronephros decreased process quality cilium movement, abnormal ZP:0018766 fourth ventricle decreased process quality cerebrospinal fluid circulation, abnormal ZP:0018767 ventral aorta increased diameter, abnormal ZP:0018768 thymus absent, abnormal ZP:0018769 pronephric glomerular capillary distended, abnormal ZP:0018770 protein poly-ADP-ribosylation increased occurrence, abnormal ZP:0018771 cilium posterior macula length, abnormal ZP:0018772 hindbrain neural tube increased distribution, abnormal ZP:0018773 posterior lateral line neuromast far from posterior lateral line neuromast, abnormal ZP:0018774 stereocilium bundle hair cell splayed, abnormal ZP:0018775 blood vessel endothelial cell common cardinal vein structure, cavities, abnormal ZP:0018776 intersegmental vessel disconnected, abnormal ZP:0018777 mitotic cell cycle decreased occurrence, abnormal ZP:0018778 cardiac muscle contraction process quality, abnormal ZP:0018779 cardiac muscle tissue regeneration decreased occurrence, abnormal ZP:0018780 hematopoietic progenitor cell differentiation decreased occurrence, abnormal ZP:0018781 granular vesicle neutrophil decreased amount, abnormal ZP:0018782 neutrophil differentiation decreased occurrence, abnormal ZP:0018783 neutrophil immature, abnormal ZP:0018784 liver increased occurrence cell population proliferation, abnormal ZP:0018785 liver decreased distribution, abnormal ZP:0018786 macrophage brain absent, abnormal ZP:0018787 myeloid lineage restricted progenitor cell arrested mitotic S phase, abnormal ZP:0018788 myeloid lineage restricted progenitor cell decreased occurrence myeloid leukocyte migration, abnormal ZP:0018789 myeloid lineage restricted progenitor cell rostral blood island decreased distribution, abnormal ZP:0018790 myeloid lineage restricted progenitor cell accumulation rostral blood island, abnormal ZP:0018791 DNA damage response, detection of DNA damage process quality, abnormal ZP:0018792 gut decreased process quality determination of digestive tract left/right asymmetry, abnormal ZP:0018793 right side posterior lateral plate mesoderm mislocalised, abnormal ZP:0018794 lateral plate mesoderm spatial pattern, abnormal ZP:0018795 right side heart rudiment mislocalised, abnormal ZP:0018796 heart tube decreased process quality heart jogging, abnormal ZP:0018797 habenula decreased process quality determination of left/right asymmetry in diencephalon, abnormal ZP:0018798 right side habenula mislocalised, abnormal ZP:0018799 heart decreased process quality heart looping, abnormal ZP:0018800 heart rudiment decreased process quality determination of heart left/right asymmetry, abnormal ZP:0018801 Kupffer's vesicle decreased process quality epithelial cilium movement involved in determination of left/right asymmetry, abnormal ZP:0018802 heart tube mislocalised medially, abnormal ZP:0018803 embryonic heart tube left/right pattern formation decreased occurrence, abnormal ZP:0018804 right side brain mislocalised, abnormal ZP:0018805 pancreatic centroacinar cell decreased amount, abnormal ZP:0018806 cell secondary islet decreased amount, abnormal ZP:0018807 trunk spatial pattern, abnormal ZP:0018808 migratory neural crest mislocalised, abnormal ZP:0018809 melanocyte whole organism shape, abnormal ZP:0018810 neural keel decreased amount, abnormal ZP:0018811 cranial motor neuron decreased amount, abnormal ZP:0018812 myelinating Schwann cell increased amount, abnormal ZP:0018813 myelinating Schwann cell decreased distribution, abnormal ZP:0018814 melanoblast neural crest increased amount, abnormal ZP:0018815 neural crest increased amount, abnormal ZP:0018816 glial cell (sensu Vertebrata) lateral line increased amount, abnormal ZP:0018817 glial cell (sensu Vertebrata) brain decreased amount, abnormal ZP:0018818 glial cell (sensu Vertebrata) cranium absent, abnormal ZP:0018819 iridophore trunk absent, abnormal ZP:0018820 somite increased amount, abnormal ZP:0018821 neuroblast epibranchial cartilage decreased amount, abnormal ZP:0018822 glial cell cranium absent, abnormal ZP:0018823 neural crest cell pharyngeal arch decreased amount, abnormal ZP:0018824 neuroblast head decreased amount, abnormal ZP:0018825 vagal neural crest decreased amount, abnormal ZP:0018826 glial cell (sensu Vertebrata) lateral line morphology, abnormal ZP:0018827 melanoblast head increased amount, abnormal ZP:0018828 neural crest spatial pattern, abnormal ZP:0018829 olfactory receptor cell decreased amount, abnormal ZP:0018830 perichondrium disorganized, abnormal ZP:0018831 neural plate border decreased amount, abnormal ZP:0018832 myelinating Schwann cell disrupted myelination, abnormal ZP:0018833 microvillous olfactory receptor neuron disorganized, abnormal ZP:0018834 chondrocyte pharyngeal arch absent, abnormal ZP:0018835 perichondrium decreased amount, abnormal ZP:0018836 esophageal epithelium decreased amount, abnormal ZP:0018837 detection of mechanical stimulus involved in sensory perception of sound disrupted, abnormal ZP:0018838 stereocilium neuromast hair cell decreased amount, abnormal ZP:0018839 neuromast hair cell lacks parts or has fewer parts of type stereocilium bundle neuromast hair cell, abnormal ZP:0018840 hair cell inner ear decreased amount, abnormal ZP:0018841 cell intestine apoptotic, abnormal ZP:0018842 retinal pigmented epithelium atrophied, abnormal ZP:0018843 intestine malformed, abnormal ZP:0018844 cytoplasm retina decreased amount, abnormal ZP:0018845 iridophore eye irregular spatial pattern, abnormal ZP:0018846 hair cell inner ear non-functional, abnormal ZP:0018847 retinal pigmented epithelium displaced to pigmented epithelial cell retinal outer nuclear layer, abnormal ZP:0018848 posterior surface lens degenerate, abnormal ZP:0018849 kinocilium neuromast hair cell decreased amount, abnormal ZP:0018850 inclusion body pigmented epithelial cell increased amount, abnormal ZP:0018851 primitive erythrocyte differentiation increased occurrence, abnormal ZP:0018852 mesoderm increased amount, abnormal ZP:0018853 myeloid cell increased distribution, abnormal ZP:0018854 positive regulation of receptor signaling pathway via JAK-STAT increased occurrence, abnormal ZP:0018855 lymphocyte thymus increased amount, abnormal ZP:0018856 common myeloid progenitor increased distribution, abnormal ZP:0018857 chloride transport process quality, abnormal ZP:0018858 stereocilium bundle hair cell shortened, abnormal ZP:0018859 neuromast hair cell decreased process quality action potential, abnormal ZP:0018860 neuromast hair cell decreased process quality membrane depolarization during action potential, abnormal ZP:0018861 stereocilium bundle hair cell absent, abnormal ZP:0018862 neuron increased occurrence cell death, abnormal ZP:0018863 central region retinal photoreceptor layer degenerate, abnormal ZP:0018864 photoreceptor cell lacks all parts of type cilium photoreceptor cell, abnormal ZP:0018865 retina lacks parts or has fewer parts of type central region retinal rod cell, abnormal ZP:0018866 photoreceptor cell disrupted cilium assembly, abnormal ZP:0018867 retinal rod cell decreased distribution, abnormal ZP:0018868 retina lacks parts or has fewer parts of type central region retinal cone cell, abnormal ZP:0018869 retinal cone cell decreased distribution, abnormal ZP:0018870 retina lacks all parts of type central region photoreceptor cell, abnormal ZP:0018871 cilium olfactory pit absent, abnormal ZP:0018872 retina lacks parts or has fewer parts of type central region photoreceptor cell, abnormal ZP:0018873 S-adenosyl-L-homocysteine liver decreased amount, abnormal ZP:0018874 cysteine liver decreased amount, abnormal ZP:0018876 common bile duct morphology, abnormal ZP:0018877 S-adenosyl-L-methionine liver decreased amount, abnormal ZP:0018879 liver and biliary system spatial pattern, abnormal ZP:0018880 homoserine liver decreased amount, abnormal ZP:0018882 bile accumulation liver, abnormal ZP:0018883 common bile duct decreased branchiness, abnormal ZP:0018884 protein methylation decreased occurrence, abnormal ZP:0018885 homocysteine liver decreased amount, abnormal ZP:0018886 serine liver decreased amount, abnormal ZP:0018887 common bile duct development process quality, abnormal ZP:0018888 methionine liver decreased amount, abnormal ZP:0018889 liver male organism decreased amount, abnormal ZP:0018890 lipid liver increased amount, abnormal ZP:0018891 triglyceride liver increased amount, abnormal ZP:0018892 muscle pioneer increased distribution, abnormal ZP:0018893 secondary motor neuron decreased process quality motor neuron axon guidance, abnormal ZP:0018894 primary motor neuron decreased process quality motor neuron axon guidance, abnormal ZP:0018895 medial side myotome absent, abnormal ZP:0018896 myotome process quality skeletal muscle cell differentiation, abnormal ZP:0018897 vertical myoseptum absent, abnormal ZP:0018898 vertical myoseptum decreased amount, abnormal ZP:0018899 extracellular matrix myotome absent, abnormal ZP:0018900 myotome decreased process quality skeletal muscle tissue development, abnormal ZP:0018901 medial side myotome decreased amount, abnormal ZP:0018902 myotome atrophied, abnormal ZP:0018903 myotome has extra parts of type muscle pioneer, abnormal ZP:0018904 slow muscle cell myotome shape, abnormal ZP:0018905 fast muscle cell myotome decreased area, abnormal ZP:0018906 fast muscle cell has fewer parts of type skeletal muscle myofibril fast muscle cell, abnormal ZP:0018907 dorsal aorta increased elasticity, abnormal ZP:0018908 basement membrane optic tectum spatial pattern, abnormal ZP:0018909 basement membrane hindbrain irregular spatial pattern, abnormal ZP:0018910 hindbrain decreased process quality basement membrane organization, abnormal ZP:0018911 retinal ganglion cell decreased process quality retinal ganglion cell axon guidance, abnormal ZP:0018912 cerebellar granule cell decreased process quality axon extension involved in axon guidance, abnormal ZP:0018913 optic tectum decreased process quality basement membrane organization, abnormal ZP:0018914 basement membrane hindbrain spatial pattern, abnormal ZP:0018915 basement membrane optic tectum irregular spatial pattern, abnormal ZP:0018916 basement membrane hindbrain bifurcated, abnormal ZP:0018917 axon cerebellar granule cell mislocalised, abnormal ZP:0018918 dorsal region hindbrain decreased amount, abnormal ZP:0018919 epidermal cell hindbrain decreased amount, abnormal ZP:0018920 basement membrane hindbrain truncated, abnormal ZP:0018921 basement membrane hindbrain branched, abnormal ZP:0018922 vertical myoseptum integument morphology, abnormal ZP:0018923 nucleus muscle cell increased size, abnormal ZP:0018924 T-tubule muscle increased size, abnormal ZP:0018925 sarcoplasm muscle cell undifferentiated, abnormal ZP:0018926 skeletal muscle myofibril skeletal muscle disorganized, abnormal ZP:0018927 Z disc muscle morphology, abnormal ZP:0018928 nucleolus muscle cell increased size, abnormal ZP:0018929 compartment boundary myotome morphology, abnormal ZP:0018930 muscle cell vacuolated, abnormal ZP:0018931 compartment boundary vertical myoseptum irregularly shaped, abnormal ZP:0018932 optic cup absent, abnormal ZP:0018933 intermediate cell mass of mesoderm decreased occurrence cell population proliferation, abnormal ZP:0018934 posterior region hematopoietic system increased amount, abnormal ZP:0018935 intermediate cell mass of mesoderm increased occurrence apoptotic process, abnormal ZP:0018936 posterior region trunk decreased amount, abnormal ZP:0018937 posterior region hematopoietic system decreased amount, abnormal ZP:0018938 hematopoietic multipotent progenitor cell thymus absent, abnormal ZP:0018939 somite decreased distribution, abnormal ZP:0018940 whole organism has fewer parts of type neural crest cell, abnormal ZP:0018941 pharyngeal arch 3-7 decreased occurrence cell population proliferation, abnormal ZP:0018942 lens eye opaque, abnormal ZP:0018943 lens decreased amount, abnormal ZP:0018944 lens eye decreased size, abnormal ZP:0018945 macrophage midbrain decreased amount, abnormal ZP:0018946 macrophage spleen decreased amount, abnormal ZP:0018947 macrophage liver decreased amount, abnormal ZP:0018948 macrophage decreased speed, abnormal ZP:0018949 macrophage pericardium decreased amount, abnormal ZP:0018950 macrophage caudal fin decreased amount, abnormal ZP:0018951 macrophage spherical, abnormal ZP:0018952 neutrophil trunk decreased amount, abnormal ZP:0018953 retinal inner plexiform layer decreased amount, abnormal ZP:0018954 portion of tissue broken, abnormal ZP:0018955 posterior region whole organism malformed, abnormal ZP:0018956 brain decreased amount, abnormal ZP:0018957 caudal fin decreased amount, abnormal ZP:0018958 yolk split, abnormal ZP:0018959 microtubule external yolk syncytial layer disorganized, abnormal ZP:0018960 microtubule external yolk syncytial layer absent, abnormal ZP:0018961 cell EVL elongated, abnormal ZP:0018962 actin cytoskeleton external yolk syncytial layer disorganized, abnormal ZP:0018963 cell EVL decreased amount, abnormal ZP:0018964 whole organism increased occurrence cytolysis, abnormal ZP:0018965 cell EVL increased size, abnormal ZP:0018966 convergent extension increased occurrence, abnormal ZP:0018967 actin cytoskeleton external yolk syncytial layer absent, abnormal ZP:0018968 microtubule external yolk syncytial layer decreased amount, abnormal ZP:0018969 actin cytoskeleton external yolk syncytial layer decreased amount, abnormal ZP:0018970 ventral region whole organism mislocalised, abnormal ZP:0018971 whole organism mislocalised, abnormal ZP:0018972 hindbrain neural keel decreased distribution, abnormal ZP:0018973 ventral region whole organism decreased amount, abnormal ZP:0018974 paraxial mesoderm spatial pattern, abnormal ZP:0018975 adaxial cell spatial pattern, abnormal ZP:0018976 neural plate spatial pattern, abnormal ZP:0018977 notochord spatial pattern, abnormal ZP:0018978 blastodisc decreased amount, abnormal ZP:0018979 segmental plate spatial pattern, abnormal ZP:0018980 yolk syncytial layer decreased amount, abnormal ZP:0018981 retinal pigmented epithelium absent, abnormal ZP:0018982 integument disrupted pigmentation, abnormal ZP:0018983 whole organism mottled, abnormal ZP:0018984 iridophore process quality pigmentation, abnormal ZP:0018985 preural vertebra decreased length, abnormal ZP:0018986 vertebra 8 decreased length, abnormal ZP:0018987 precaudal vertebra decreased length, abnormal ZP:0018988 centrum morphology, abnormal ZP:0018989 postcranial axial skeleton morphology, abnormal ZP:0018990 caudal vertebra decreased length, abnormal ZP:0018991 bone morphogenesis decreased process quality, abnormal ZP:0018992 bone growth decreased process quality, abnormal ZP:0018993 vertebra 7 decreased length, abnormal ZP:0018994 vertebra 9 decreased length, abnormal ZP:0018995 vertebra 11 decreased length, abnormal ZP:0018996 vertebra 10 decreased length, abnormal ZP:0018997 neuromast primordium migration arrested, abnormal ZP:0018998 cardiac ventricle decreased angle to atrium, abnormal ZP:0018999 male gamete generation premature, abnormal ZP:0019000 oocyte premature apoptotic process, abnormal ZP:0019001 germ line cell increased occurrence apoptotic process, abnormal ZP:0019002 swimming increased speed, abnormal ZP:0019003 pronephric proximal straight tubule increased distribution, abnormal ZP:0019004 pronephros wholly anterioralized, abnormal ZP:0019005 anterior/posterior pattern specification involved in pronephros development disrupted, abnormal ZP:0019006 pronephric distal late tubule decreased distribution, abnormal ZP:0019007 pronephric distal early tubule mislocalised, abnormal ZP:0019008 pronephric proximal convoluted tubule increased distribution, abnormal ZP:0019009 retinoic acid whole organism increased amount, abnormal ZP:0019010 pectoral fin decreased amount, abnormal ZP:0019011 dendrite morphogenesis disrupted, abnormal ZP:0019012 dendrite habenula truncated, abnormal ZP:0019013 neuron projection dorsal habenular nucleus decreased amount, abnormal ZP:0019014 interpeduncular nucleus tegmentum process quality innervation, abnormal ZP:0019015 neuron projection terminus dorsal habenular nucleus incomplete structure, abnormal ZP:0019016 neuron dorsal habenular nucleus morphology, abnormal ZP:0019017 lipoprotein lipase activity disrupted, abnormal ZP:0019018 cranial nerve X disorganized, abnormal ZP:0019019 axon retinal ganglion cell hypoplastic, abnormal ZP:0019020 cranial nerve X misrouted, abnormal ZP:0019021 cranial skeletal system development disrupted, abnormal ZP:0019022 CoPA decreased process quality axon extension involved in axon guidance, abnormal ZP:0019023 neuron projection CoPA misrouted, abnormal ZP:0019024 yolk displaced to blastodisc, abnormal ZP:0019025 cytoplasm organization process quality, abnormal ZP:0019026 microtubule oocyte stage I decreased amount, abnormal ZP:0019027 microtubule fertilized egg disoriented, abnormal ZP:0019028 cytoplasm yolk present, abnormal ZP:0019029 blastomere increased variability of size, abnormal ZP:0019030 embryonic cleavage variability, abnormal ZP:0019031 Spemann organizer formation at the embryonic shield process quality, abnormal ZP:0019032 cell division increased duration, abnormal ZP:0019033 medial-lateral axis notochord increased width, abnormal ZP:0019034 cortical granule exocytosis delayed, abnormal ZP:0019035 egg activation process quality, abnormal ZP:0019036 microtubule fertilized egg irregular spatial pattern, abnormal ZP:0019037 mesoderm formation process quality, abnormal ZP:0019038 heart disrupted blood circulation, abnormal ZP:0019039 yolk displaced to blastoderm, abnormal ZP:0019040 yolk amorphous, abnormal ZP:0019041 anterior-posterior axis notochord decreased length, abnormal ZP:0019042 synapse eye photoreceptor cell poorly differentiated, abnormal ZP:0019043 retina lacks parts or has fewer parts of type photoreceptor outer segment eye photoreceptor cell, abnormal ZP:0019044 peripheral region retina morphology, abnormal ZP:0019045 cell projection Muller cell decreased amount, abnormal ZP:0019046 cell projection Muller cell disorganized, abnormal ZP:0019047 nucleus photoreceptor cell disorganized, abnormal ZP:0019048 photoreceptor outer segment photoreceptor cell disorganized, abnormal ZP:0019049 retinal photoreceptor layer mislocalised, abnormal ZP:0019050 proliferative region brain decreased amount, abnormal ZP:0019051 ciliary marginal zone increased occurrence apoptotic process, abnormal ZP:0019052 optic tectum increased occurrence cell death, abnormal ZP:0019053 eye increased occurrence cell death, abnormal ZP:0019054 forebrain increased occurrence cell death, abnormal ZP:0019055 mouth decreased position, abnormal ZP:0019056 anterior region head increased length, abnormal ZP:0019057 regulation of transcription of nucleolar large rRNA by RNA polymerase I decreased process quality, abnormal ZP:0019058 nucleolar chromatin organization process quality, abnormal ZP:0019059 trunk curved caudal, abnormal ZP:0019060 hematopoietic stem cell intermediate cell mass of mesoderm decreased distribution, abnormal ZP:0019061 mRNA splicing, via spliceosome decreased occurrence, abnormal ZP:0019062 hematopoietic stem cell ventral wall of dorsal aorta decreased distribution, abnormal ZP:0019063 hematopoietic stem cell decreased distribution, abnormal ZP:0019065 skeletal muscle cell structure, abnormal ZP:0019066 T-tubule skeletal muscle cell bent, abnormal ZP:0019067 ventricular myocardium spatial pattern, abnormal ZP:0019068 skeletal muscle cell decreased size, abnormal ZP:0019069 sarcoplasmic reticulum skeletal muscle dilated, abnormal ZP:0019070 mitochondrion skeletal muscle cell dilated, abnormal ZP:0019071 endocrine pancreas decreased amount, abnormal ZP:0019072 pancreas decreased amount, abnormal ZP:0019073 anterior pancreatic bud disrupted type B pancreatic cell differentiation, abnormal ZP:0019074 primary islet has fewer parts of type pancreatic B cell, abnormal ZP:0019075 hypophysis increased amount, abnormal ZP:0019076 liver decreased amount, abnormal ZP:0019077 oviposition disrupted, abnormal ZP:0019078 swim bladder decreased functionality, abnormal ZP:0019079 thyroxine 5'-deiodinase activity disrupted, abnormal ZP:0019080 thyroxine 5'-deiodinase activity decreased process quality, abnormal ZP:0019081 retinal photoreceptor layer has fewer parts of type green sensitive photoreceptor cell retinal photoreceptor layer, abnormal ZP:0019082 retinal photoreceptor layer has fewer parts of type retinal cone cell, abnormal ZP:0019083 retinal photoreceptor layer has fewer parts of type blue sensitive photoreceptor cell retinal photoreceptor layer, abnormal ZP:0019084 response to light stimulus decreased occurrence, abnormal ZP:0019085 retinal photoreceptor layer has fewer parts of type red sensitive photoreceptor cell retinal photoreceptor layer, abnormal ZP:0019086 retinal photoreceptor layer has fewer parts of type UV sensitive photoreceptor cell retinal photoreceptor layer, abnormal ZP:0019087 neuron nervous system decreased distribution, abnormal ZP:0019088 neuron trigeminal ganglion decreased branchiness, abnormal ZP:0019089 trigeminal ganglion development disrupted, abnormal ZP:0019090 pigmentation increased amount, abnormal ZP:0019091 whole organism lethargic, abnormal ZP:0019092 cytoplasm endothelial cell spatial pattern, abnormal ZP:0019093 endothelial tip cell spatial pattern, abnormal ZP:0019094 membrane trunk musculature damage, abnormal ZP:0019095 myotome decreased process quality skeletal myofibril assembly, abnormal ZP:0019096 skeletal muscle structure, abnormal ZP:0019097 female organism increased amount, abnormal ZP:0019098 germ line cell testis decreased amount, abnormal ZP:0019099 male gonad development arrested, abnormal ZP:0019100 testis disorganized, abnormal ZP:0019101 gonad mislocalised, abnormal ZP:0019102 testis unlumenized, abnormal ZP:0019103 immature gonad decreased process quality apoptotic process, abnormal ZP:0019104 neural crest cell xanthoblast aggregated, abnormal ZP:0019105 neural crest cell melanoblast aggregated, abnormal ZP:0019106 Kupffer's vesicle decreased process quality epithelial cilium movement involved in extracellular fluid movement, abnormal ZP:0019107 nucleus lens apoptotic, abnormal ZP:0019108 cornea degenerate, abnormal ZP:0019109 nucleus lens present, abnormal ZP:0019110 lens elongated, abnormal ZP:0019111 male sex differentiation increased occurrence, abnormal ZP:0019113 testis aplastic/hypoplastic, abnormal ZP:0019114 gonad primordium lacks all parts of type germ line cell, abnormal ZP:0019115 germ line cell mislocalised, abnormal ZP:0019116 skeletal muscle cell increased diameter, abnormal ZP:0019117 somite hypoplastic, abnormal ZP:0019118 skeletal muscle cell decreased amount, abnormal ZP:0019119 podocyte foot pronephric glomerulus morphology, abnormal ZP:0019120 myeloid cell decreased distribution, abnormal ZP:0019121 nucleate erythrocyte decreased distribution, abnormal ZP:0019122 pancreas decreased distribution, abnormal ZP:0019123 lymphocyte thymus absent, abnormal ZP:0019124 bile ductule morphology, abnormal ZP:0019125 hepatocyte decreased distribution, abnormal ZP:0019126 posterior region hematopoietic system decreased distribution, abnormal ZP:0019127 nucleate erythrocyte malformed, abnormal ZP:0019128 blood cell decreased occurrence DNA methylation, abnormal ZP:0019129 hematopoietic cell head kidney decreased amount, abnormal ZP:0019130 pronephros decreased process quality cilium assembly, abnormal ZP:0019131 blood accumulation distal region caudal fin, abnormal ZP:0019132 caudal artery increased size, abnormal ZP:0019133 caudal artery fused with caudal vein, abnormal ZP:0019134 caudal vein increased size, abnormal ZP:0019135 membrane skeletal muscle damaged, abnormal ZP:0019136 nucleus whole organism apoptotic, abnormal ZP:0019137 histone H3-K4 methylation decreased process quality, abnormal ZP:0019138 blastodisc furrowed, abnormal ZP:0019140 mitotic spindle pole cell broken, abnormal ZP:0019141 mitotic spindle cell elongated, abnormal ZP:0019142 blastomere increased size, abnormal ZP:0019143 cell division arrested, abnormal ZP:0019144 blastomere deformed, abnormal ZP:0019145 nucleus whole organism decreased amount, abnormal ZP:0019146 mitotic spindle pole cell structure, abnormal ZP:0019147 non-motile cilium olfactory epithelium decreased length, abnormal ZP:0019148 Golgi stack eye photoreceptor cell distended, abnormal ZP:0019149 eye photoreceptor cell has extra parts of type photoreceptor inner segment lysosome eye photoreceptor cell, abnormal ZP:0019150 eye photoreceptor cell accumulation photoreceptor inner segment vacuole eye photoreceptor cell, abnormal ZP:0019151 eye photoreceptor cell has extra parts of type photoreceptor outer segment vesicle eye photoreceptor cell, abnormal ZP:0019152 photoreceptor disc membrane eye photoreceptor cell deformed, abnormal ZP:0019153 cell body eye photoreceptor cell mislocalised, abnormal ZP:0019154 eye photoreceptor cell vacuolated, abnormal ZP:0019155 eye photoreceptor cell accumulation photoreceptor inner segment vesicle eye photoreceptor cell, abnormal ZP:0019156 Golgi apparatus eye photoreceptor cell swollen, abnormal ZP:0019157 eye photoreceptor cell decreased distribution, abnormal ZP:0019158 floor plate has fewer parts of type motile cilium floor plate, abnormal ZP:0019159 cilium whole organism decreased amount, abnormal ZP:0019160 cilium whole organism absent, abnormal ZP:0019161 motile cilium whole organism absent, abnormal ZP:0019162 whole organism lacks parts or has fewer parts of type ceratobranchial 5 primary tooth, abnormal ZP:0019163 ventral region pharyngeal arch 1 decreased size, abnormal ZP:0019164 neural crest cell pharyngeal arch increased amount, abnormal ZP:0019165 ventral region pharyngeal arch 2 decreased amount, abnormal ZP:0019166 joint pharyngeal arch 2 absent, abnormal ZP:0019167 ventral region pharyngeal arch cartilage morphology, abnormal ZP:0019168 ventral region pharyngeal arch increased amount, abnormal ZP:0019169 ventral region pharyngeal arch 2 increased amount, abnormal ZP:0019170 ventral region pharyngeal arch 2 decreased size, abnormal ZP:0019171 ventral region pharyngeal arch cartilage decreased amount, abnormal ZP:0019172 pharyngeal arch 2 decreased amount, abnormal ZP:0019173 ventral region pharyngeal arch 1 decreased amount, abnormal ZP:0019174 nucleus somite morphology, abnormal ZP:0019175 filopodium hepatoblast decreased length, abnormal ZP:0019176 intestinal bulb primordium decreased curvature, abnormal ZP:0019177 hepatoblast shape, abnormal ZP:0019178 hepatoblast anterior orientation, abnormal ZP:0019179 liver primordium malformed, abnormal ZP:0019180 hepatoblast absent, abnormal ZP:0019181 apical junction complex mesoderm mislocalised, abnormal ZP:0019182 hepatocyte cell migration decreased occurrence, abnormal ZP:0019183 embryonic liver development process quality, abnormal ZP:0019184 embryonic digestive tract development decreased process quality, abnormal ZP:0019185 hepatoblast has fewer parts of type filopodium hepatoblast, abnormal ZP:0019186 lateral plate mesoderm decreased process quality establishment of epithelial cell apical/basal polarity, abnormal ZP:0019187 hepatoblast mislocalised medially, abnormal ZP:0019188 hepatoblast mislocalised, abnormal ZP:0019189 hepatoblast process quality regulation of filopodium assembly, abnormal ZP:0019190 hepatocyte cell migration process quality, abnormal ZP:0019191 hepatoblast mislocalised posteriorly, abnormal ZP:0019192 trabecular layer absent, abnormal ZP:0019193 heart decreased amount, abnormal ZP:0019194 commissure of the tract of the commissure of the caudal tuberculum has extra parts of type axon commissure of the tract of the commissure of the caudal tuberculum, abnormal ZP:0019195 forerunner cell group dispersed, abnormal ZP:0019196 heart decreased occurrence heart looping, abnormal ZP:0019197 spinal cord increased occurrence apoptotic process, abnormal ZP:0019198 spinal cord increased occurrence cell population proliferation, abnormal ZP:0019199 pharyngeal arch increased occurrence apoptotic process, abnormal ZP:0019200 brain increased occurrence cell population proliferation, abnormal ZP:0019201 neuroblast (sensu Vertebrata) increased occurrence apoptotic process, abnormal ZP:0019202 glial cell spinal cord deformed, abnormal ZP:0019203 neuroblast (sensu Vertebrata) spinal cord deformed, abnormal ZP:0019204 closure of optic fissure disrupted, abnormal ZP:0019205 dorsal-ventral axis head decreased height, abnormal ZP:0019206 ventral region retina decreased thickness, abnormal ZP:0019207 central nervous system increased occurrence apoptotic process, abnormal ZP:0019208 nuclear-transcribed mRNA catabolic process, nonsense-mediated decay increased process quality, abnormal ZP:0019209 retina increased amount, abnormal ZP:0019210 nucleus retina decreased amount, abnormal ZP:0019211 midbrain decreased amount, abnormal ZP:0019212 pronephric tubule decreased distribution, abnormal ZP:0019213 pronephric distal early tubule decreased distribution, abnormal ZP:0019214 pronephric proximal straight tubule decreased distribution, abnormal ZP:0019215 pronephric duct decreased distribution, abnormal ZP:0019216 pronephric glomerulus lacks parts or has fewer parts of type podocyte foot pronephric podocyte, abnormal ZP:0019217 renal glomerulus increased amount, abnormal ZP:0019218 macula utricle decreased process quality vestibular receptor cell stereocilium organization, abnormal ZP:0019219 lateral crista decreased process quality vestibular receptor cell stereocilium organization, abnormal ZP:0019220 lateral crista orientation stereocilium bundle lateral crista, abnormal ZP:0019221 neuromast hair cell orientation stereocilium bundle neuromast, abnormal ZP:0019222 macula utricle orientation stereocilium bundle macula utricle, abnormal ZP:0019223 stereocilium bundle neuromast unidirectional, abnormal ZP:0019224 posterior lateral line decreased process quality posterior lateral line neuromast development, abnormal ZP:0019225 posterior lateral line decreased process quality neuromast hair cell development, abnormal ZP:0019226 stereocilium bundle neuromast bilateral symmetry, abnormal ZP:0019227 chondrocyte ceratohyal cartilage increased variability of size, abnormal ZP:0019228 chondrocyte Meckel's cartilage increased variability of size, abnormal ZP:0019229 filopodium hepatoblast increased branchiness, abnormal ZP:0019230 pancreas decreased occurrence determination of pancreatic left/right asymmetry, abnormal ZP:0019231 Kupffer's vesicle loose, abnormal ZP:0019232 forerunner cell group mislocalised ventrally, abnormal ZP:0019235 forerunner cell group mislocalised anteriorly, abnormal ZP:0019236 Kupffer's vesicle irregularly shaped, abnormal ZP:0019237 liver decreased occurrence determination of liver left/right asymmetry, abnormal ZP:0019238 margin absent, abnormal ZP:0019239 heart tube decreased occurrence heart jogging, abnormal ZP:0019240 margin decreased amount, abnormal ZP:0019241 afferent neuron defasciculated, abnormal ZP:0019242 afferent neuron lacks all parts of type axon myelinating Schwann cell, abnormal ZP:0019243 myelinating Schwann cell posterior lateral line absent, abnormal ZP:0019244 glial cell (sensu Vertebrata) lateral line disorganized, abnormal ZP:0019245 photoreceptor inner segment retinal cone cell decreased amount, abnormal ZP:0019246 mitochondrion retinal cone cell decreased amount, abnormal ZP:0019247 mitochondrion retinal cone cell decreased size, abnormal ZP:0019248 retinal cone cell process quality mitochondrion morphogenesis, abnormal ZP:0019249 sister chromatid cohesion decreased process quality, abnormal ZP:0019250 mitotic spindle cell rotated, abnormal ZP:0019251 micronucleus cell increased amount, abnormal ZP:0019252 chromosome cell distributed, abnormal ZP:0019253 metaphase plate cell absent, abnormal ZP:0019254 cell separated from chromosome chromosome cell, abnormal ZP:0019255 chromosome organization decreased process quality, abnormal ZP:0019256 chromosome cell amount, abnormal ZP:0019257 mitotic chromosome decondensation premature, abnormal ZP:0019258 mitotic cytokinesis decreased occurrence, abnormal ZP:0019259 mitotic cell cycle increased occurrence, abnormal ZP:0019260 pharyngeal arch cartilage decreased process quality embryonic viscerocranium morphogenesis, abnormal ZP:0019261 pharyngeal arch 3-7 decreased process quality cartilage development, abnormal ZP:0019262 pharyngeal arch cartilage increased amount, abnormal ZP:0019263 myotome decreased occurrence striated muscle cell differentiation, abnormal ZP:0019264 pharyngeal arch cartilage decreased process quality cartilage development, abnormal ZP:0019265 myotome increased amount, abnormal ZP:0019266 pharyngeal musculature increased amount, abnormal ZP:0019267 myotome decreased amount, abnormal ZP:0019268 caudal vein plexus decreased amount, abnormal ZP:0019269 axial vasculature increased process quality apoptotic process, abnormal ZP:0019270 blood vasculature lacks parts or has fewer parts of type blood vessel, abnormal ZP:0019271 pronephros has fewer parts of type multi-ciliated epithelial cell pronephros, abnormal ZP:0019272 pronephric nephron tubule epithelial cell differentiation process quality, abnormal ZP:0019273 pronephros decreased occurrence multi-ciliated epithelial cell differentiation, abnormal ZP:0019274 pronephros decreased distribution, abnormal ZP:0019275 pronephric proximal straight tubule has fewer parts of type multi-ciliated epithelial cell pronephric proximal straight tubule, abnormal ZP:0019276 renal system process decreased occurrence, abnormal ZP:0019277 common lymphoid progenitor increased amount, abnormal ZP:0019278 intermediate cell mass of mesoderm decreased amount, abnormal ZP:0019279 whole organism has extra parts of type macrophage, abnormal ZP:0019280 kidney decreased amount, abnormal ZP:0019281 whole organism has extra parts of type monocyte, abnormal ZP:0019282 whole organism has extra parts of type neutrophil, abnormal ZP:0019283 whole organism has extra parts of type erythroblast, abnormal ZP:0019284 mitotic spindle midzone assembly process quality, abnormal ZP:0019285 cerebellar Purkinje cell layer structural organization disrupted, abnormal ZP:0019286 cranial nerve VII morphology, abnormal ZP:0019287 Purkinje cell cerebellum distributed, abnormal ZP:0019288 thymus decreased volume, abnormal ZP:0019289 thymus decreased distribution, abnormal ZP:0019290 myocardium decreased amount, abnormal ZP:0019292 posterior region whole organism increased distribution, abnormal ZP:0019293 heart jogging decreased occurrence, abnormal ZP:0019294 heart wholeness, abnormal ZP:0019295 rhombomere 3 decreased amount, abnormal ZP:0019296 blood accumulation extension, abnormal ZP:0019297 presumptive cardiac ventricle heart tube decreased amount, abnormal ZP:0019298 artery pharyngeal arch absent, abnormal ZP:0019299 cardiac muscle cell detached from atrium, abnormal ZP:0019300 gut straight, abnormal ZP:0019301 cardiac muscle cell detached from cardiac ventricle, abnormal ZP:0019302 endocardium decreased amount, abnormal ZP:0019304 rhombomere 5 decreased amount, abnormal ZP:0019308 heart decreased distribution, abnormal ZP:0019309 cardiac ventricle decreased amount, abnormal ZP:0019310 atrium decreased amount, abnormal ZP:0019311 ciliary basal body pronephric duct mislocalised, abnormal ZP:0019312 1-phosphatidyl-1D-myo-inositol 4,5-bisphosphate pronephric duct mislocalised, abnormal ZP:0019313 filamentous actin pronephric duct mislocalised, abnormal ZP:0019314 pronephric duct has fewer parts of type motile cilium pronephric duct, abnormal ZP:0019315 pronephric duct decreased process quality ciliary basal body-plasma membrane docking, abnormal ZP:0019316 pronephric duct decreased process quality actin filament bundle distribution, abnormal ZP:0019317 1-phosphatidyl-1D-myo-inositol 3,4,5-trisphosphate pronephric duct mislocalised, abnormal ZP:0019318 apical plasma membrane pronephric duct mislocalised, abnormal ZP:0019319 epiboly decreased process quality, abnormal ZP:0019320 blood coagulation, fibrin clot formation delayed, abnormal ZP:0019321 blood plasma decreased amount, abnormal ZP:0019322 whole organism has fewer parts of type eye, abnormal ZP:0019323 motor neuron process quality axon guidance, abnormal ZP:0019324 thymus increased distribution, abnormal ZP:0019325 anatomical structure increased distribution, abnormal ZP:0019326 myofilament skeletal muscle disorganized, abnormal ZP:0019327 mitochondrion cardiac muscle cell morphology, abnormal ZP:0019328 heart contraction decreased efficacy, abnormal ZP:0019329 autophagy disrupted, abnormal ZP:0019330 mitochondrion skeletal muscle morphology, abnormal ZP:0019331 skeletal muscle vacuolated, abnormal ZP:0019332 mitotic cell cycle lacking processual parts cytokinesis, abnormal ZP:0019333 cell polyploid, abnormal ZP:0019334 cell cycle lacking processual parts mitotic cell cycle, abnormal ZP:0019335 oligodendrocyte spinal cord increased amount, abnormal ZP:0019336 oligodendrocyte increased occurrence TOR signaling, abnormal ZP:0019337 whole organism increased occurrence TOR signaling, abnormal ZP:0019338 medial region spinal cord mislocalised, abnormal ZP:0019339 myelin sheath spinal cord increased thickness, abnormal ZP:0019340 myelin sheath spinal cord increased amount, abnormal ZP:0019341 whole organism increased occurrence cholesterol biosynthetic process, abnormal ZP:0019342 cell adhesion process quality, abnormal ZP:0019343 pharyngeal arch 4 has fewer parts of type cranial neural crest, abnormal ZP:0019344 digestive system duct increased distribution, abnormal ZP:0019345 liver development decreased occurrence, abnormal ZP:0019346 primary islet increased distribution, abnormal ZP:0019347 pancreas primordium increased distribution, abnormal ZP:0019348 insulin secreting cell increased distribution, abnormal ZP:0019349 insulin secreting cell increased amount, abnormal ZP:0019350 endoderm increased distribution, abnormal ZP:0019351 endocrine cell pancreas increased amount, abnormal ZP:0019352 lateral region endoderm mislocalised, abnormal ZP:0019353 posterior pancreatic bud increased distribution, abnormal ZP:0019354 endocrine pancreas increased occurrence pancreas induction, abnormal ZP:0019355 pancreas induction increased occurrence, abnormal ZP:0019356 intestine decreased distribution, abnormal ZP:0019357 somatostatin secreting cell increased amount, abnormal ZP:0019358 endocrine cell pancreatic bud increased distribution, abnormal ZP:0019359 endothelial cell medial facial lymph vessel decreased amount, abnormal ZP:0019360 endothelial cell lateral facial lymph vessel decreased amount, abnormal ZP:0019361 chondrocyte apoptotic, abnormal ZP:0019362 protein localization to peroxisome disrupted, abnormal ZP:0019363 ciliary basal body photoreceptor cell mislocalised, abnormal ZP:0019364 photoreceptor cell displaced to photoreceptor outer segment lateral surface photoreceptor cell, abnormal ZP:0019365 retinal cone cell absence due to degeneration, abnormal ZP:0019366 retinal rod cell absence due to degeneration, abnormal ZP:0019367 trunk vasculature has extra parts of type dorsal region blood vessel, abnormal ZP:0019368 vascular sprouts intersegmental vein increased amount, abnormal ZP:0019369 dorsal region intersegmental vessel increased branchiness, abnormal ZP:0019370 endothelial cell dorsal aorta increased amount, abnormal ZP:0019371 vascular sprouts intersegmental vessel increased amount, abnormal ZP:0019373 endothelial cell dorsal longitudinal anastomotic vessel increased amount, abnormal ZP:0019374 endothelial cell intersegmental vein increased amount, abnormal ZP:0019375 intersegmental vessel displaced to vascular sprouts neural tube, abnormal ZP:0019376 endothelial cell posterior cardinal vein increased amount, abnormal ZP:0019377 trunk vasculature has extra parts of type dorsal region vascular sprouts, abnormal ZP:0019378 thoracic duct decreased occurrence lymph vessel development, abnormal ZP:0019381 primordial hindbrain channel decreased occurrence vasculature development, abnormal ZP:0019382 swim bladder inflation decreased occurrence, abnormal ZP:0019383 endothelial cell posterior cardinal vein absent, abnormal ZP:0019384 anatomical structure decreased distribution, abnormal ZP:0019385 primordial hindbrain channel malformed, abnormal ZP:0019386 thoracic duct process quality lymph vessel development, abnormal ZP:0019387 vascular sprouts posterior caudal vein decreased amount, abnormal ZP:0019389 lateral facial lymph vessel truncated, abnormal ZP:0019390 otolithic lymph vessel absent, abnormal ZP:0019391 lymphangiogenic sprout lateral facial lymph vessel absent, abnormal ZP:0019392 parachordal vessel decreased occurrence vasculature development, abnormal ZP:0019393 lateral facial lymph vessel malformed, abnormal ZP:0019394 posterior cardinal vein decreased amount, abnormal ZP:0019395 lateral facial lymph vessel process quality lymph vessel development, abnormal ZP:0019396 otolithic lymph vessel delayed lymph vessel development, abnormal ZP:0019397 lateral facial lymph vessel closed, abnormal ZP:0019398 whole organism increased occurrence mRNA modification, abnormal ZP:0019399 hypocretin-secreting neuron increased occurrence synapse assembly, abnormal ZP:0019400 cholinergic neuron increased occurrence synapse assembly, abnormal ZP:0019401 motor neuron increased occurrence collateral sprouting, abnormal ZP:0019402 brain increased occurrence mRNA modification, abnormal ZP:0019403 motor neuron increased occurrence synapse assembly, abnormal ZP:0019404 atrioventricular valve morphogenesis decreased process quality, abnormal ZP:0019405 cell cardiac jelly decreased amount, abnormal ZP:0019406 cell atrioventricular canal spatial pattern, abnormal ZP:0019407 smooth muscle bulbus arteriosus absent, abnormal ZP:0019408 cardiac ventricle decreased rate cardiac muscle tissue growth, abnormal ZP:0019409 cardiac ventricle increased rate cardiac muscle tissue growth, abnormal ZP:0019410 cardiac ventricle hypotrophic growth cardiac muscle tissue growth, abnormal ZP:0019411 muscle precursor cell bulbus arteriosus increased amount, abnormal ZP:0019412 pharynx decreased amount, abnormal ZP:0019413 goblet cell disrupted cell maturation, abnormal ZP:0019414 aortic arch incomplete structure, abnormal ZP:0019415 pericyte brain vasculature decreased amount, abnormal ZP:0019416 vascular smooth muscle brain vasculature decreased amount, abnormal ZP:0019417 vascular smooth muscle brain vasculature decreased branchiness, abnormal ZP:0019418 pericyte decreased occurrence cell development, abnormal ZP:0019419 otic vesicle decreased distribution, abnormal ZP:0019420 dorsolateral placode decreased distribution, abnormal ZP:0019421 epibranchial field decreased distribution, abnormal ZP:0019422 posterior region neurogenic field decreased amount, abnormal ZP:0019423 otic placode decreased distribution, abnormal ZP:0019424 Kupffer's vesicle decreased distribution, abnormal ZP:0019425 posterior region whole organism decreased distribution, abnormal ZP:0019426 pharyngeal pouch 1 morphology, abnormal ZP:0019427 posterior pancreatic bud decreased amount, abnormal ZP:0019428 gut decreased amount, abnormal ZP:0019429 epiboly decreased rate, abnormal ZP:0019430 endoderm development decreased occurrence, abnormal ZP:0019431 embryonic liver development decreased occurrence, abnormal ZP:0019432 presumptive endoderm decreased amount, abnormal ZP:0019433 digestive tract development decreased occurrence, abnormal ZP:0019434 pharynx development decreased occurrence, abnormal ZP:0019435 liver primordium absent, abnormal ZP:0019436 pancreas development decreased occurrence, abnormal ZP:0019437 posterior pancreatic bud absent, abnormal ZP:0019438 female organism female semi-sterile, abnormal ZP:0019439 ovarian follicle stage III decreased amount, abnormal ZP:0019440 ovarian follicle stage IV decreased amount, abnormal ZP:0019441 ovarian follicle stage I decreased size, abnormal ZP:0019442 germ line cell decreased size, abnormal ZP:0019443 ovarian follicle development arrested, abnormal ZP:0019444 ovarian follicle stage IV absent, abnormal ZP:0019445 whole organism biological sex, abnormal ZP:0019446 testis decreased process quality growth, abnormal ZP:0019447 female organism decreased amount, abnormal ZP:0019448 testis decreased amount, abnormal ZP:0019449 testis immature, abnormal ZP:0019450 ovarian follicle stage II absent, abnormal ZP:0019451 ovarian follicle stage III absent, abnormal ZP:0019452 ovarian follicle stage I immature, abnormal ZP:0019453 male organism increased amount, abnormal ZP:0019454 brain absent, abnormal ZP:0019455 axon CoPA misrouted, abnormal ZP:0019456 CoPA process quality anterior/posterior axon guidance, abnormal ZP:0019457 axon CoPA mislocalised posteriorly, abnormal ZP:0019458 CoPA decreased process quality anterior/posterior axon guidance, abnormal ZP:0019459 planar cell polarity pathway involved in axon guidance decreased process quality, abnormal ZP:0019460 CoPA decreased process quality dorsal spinal cord interneuron anterior axon guidance, abnormal ZP:0019462 solid lens vesicle decreased amount, abnormal ZP:0019463 mesenchymal cell atrioventricular canal decreased amount, abnormal ZP:0019464 neuromuscular junction somite decreased area, abnormal ZP:0019465 neuromuscular junction muscle decreased amount, abnormal ZP:0019466 myofibril skeletal muscle decreased thickness, abnormal ZP:0019467 muscle disrupted axonogenesis, abnormal ZP:0019468 skeletal muscle myofibril skeletal muscle loose, abnormal ZP:0019469 muscle tendon junction myoseptum morphology, abnormal ZP:0019470 Z disc muscle decreased length, abnormal ZP:0019471 blood island mislocalised, abnormal ZP:0019472 intermediate cell mass of mesoderm mislocalised, abnormal ZP:0019473 atrioventricular canal increased amount, abnormal ZP:0019474 atrioventricular canal decreased amount, abnormal ZP:0019475 solid lens vesicle decreased distribution, abnormal ZP:0019476 olfactory placode decreased distribution, abnormal ZP:0019477 neurogenic field decreased amount, abnormal ZP:0019478 macrophage liver increased amount, abnormal ZP:0019479 macrophage brain morphology, abnormal ZP:0019480 microglial cell brain circular, abnormal ZP:0019482 dopaminergic neuron caudal periventricular hypothalamus decreased amount, abnormal ZP:0019483 macrophage decreased occurrence endocytic recycling, abnormal ZP:0019484 microglial cell increased accumulation brain, abnormal ZP:0019485 macrophage tectal ventricle increased size, abnormal ZP:0019486 glucosylceramidase activity decreased process quality, abnormal ZP:0019487 sphingolipid metabolic process disrupted, abnormal ZP:0019488 macrophage brain increased amount, abnormal ZP:0019490 glial cell projection brain retracted, abnormal ZP:0019491 vacuole microglial cell increased amount, abnormal ZP:0019492 inclusion body CNS neuron (sensu Vertebrata) increased amount, abnormal ZP:0019493 macrophage increased accumulation tectal ventricle, abnormal ZP:0019495 microglial cell spherical, abnormal ZP:0019496 macrophage thymus morphology, abnormal ZP:0019498 microglial cell activation increased occurrence, abnormal ZP:0019499 autophagosome brain increased amount, abnormal ZP:0019500 macrophage liver morphology, abnormal ZP:0019501 brain increased amount, abnormal ZP:0019502 mitochondrion brain decreased functionality, abnormal ZP:0019503 macrophage thymus increased amount, abnormal ZP:0019504 pancreatic A cell increased rate cell population proliferation, abnormal ZP:0019505 pancreatic A cell primary islet increased amount, abnormal ZP:0019506 glucagon secretion increased process quality, abnormal ZP:0019508 pancreatic A cell hyperplastic, abnormal ZP:0019509 axon peripheral neuron absent, abnormal ZP:0019510 ciliary marginal zone decreased amount, abnormal ZP:0019511 ciliary marginal zone decreased thickness, abnormal ZP:0019512 ciliary marginal zone decreased distribution, abnormal ZP:0019513 retinal inner nuclear layer increased distribution, abnormal ZP:0019514 lens mislocalised ventrally, abnormal ZP:0019515 retinal inner nuclear layer spatial pattern, abnormal ZP:0019516 T cell differentiation decreased occurrence, abnormal ZP:0019517 lymphoid progenitor cell thymus decreased amount, abnormal ZP:0019518 erythroid lineage cell posterior lateral mesoderm absent, abnormal ZP:0019519 head kidney decreased amount, abnormal ZP:0019520 synapse Mauthner neuron absent, abnormal ZP:0019521 spinal cord increased occurrence cell death, abnormal ZP:0019522 myelinating Schwann cell posterior lateral line decreased amount, abnormal ZP:0019523 Kupffer's vesicle decreased rate cilium movement, abnormal ZP:0019524 whole organism increased occurrence cell death, abnormal ZP:0019525 posterior lateral line nerve lacks parts or has fewer parts of type axon myelin sheath neuron, abnormal ZP:0019526 eurydendroid cell absent, abnormal ZP:0019527 myelinating Schwann cell anterior lateral line absent, abnormal ZP:0019528 axon posterior lateral line nerve decreased diameter, abnormal ZP:0019529 retinal pigmented epithelium increased occurrence cell death, abnormal ZP:0019530 poly(A)+ mRNA export from nucleus decreased occurrence, abnormal ZP:0019531 oligodendrocyte hindbrain spatial pattern, abnormal ZP:0019532 immature Schwann cell decreased occurrence cell population proliferation, abnormal ZP:0019533 anterior region posterior lateral line decreased distribution, abnormal ZP:0019534 cloaca decreased functionality, abnormal ZP:0019535 motor neuron spinal cord physical object quality, abnormal ZP:0019536 pronephric tubule lacks parts or has fewer parts of type multi-ciliated epithelial cell pronephric tubule, abnormal ZP:0019537 multi-ciliated epithelial cell pronephric duct absent, abnormal ZP:0019538 extracellular space chondrocyte mislocalised, abnormal ZP:0019539 chondrocyte ceratohyal cartilage increased amount, abnormal ZP:0019540 cranial cartilage increased amount, abnormal ZP:0019541 nucleus chondrocyte increased amount, abnormal ZP:0019542 nucleus chondrocyte mislocalised, abnormal ZP:0019543 Meckel's cartilage increased amount, abnormal ZP:0019545 chondrocyte Meckel's cartilage decreased amount, abnormal ZP:0019546 opercle decreased amount, abnormal ZP:0019547 palate increased amount, abnormal ZP:0019548 endochondral bone decreased occurrence ossification, abnormal ZP:0019549 cleithrum decreased amount, abnormal ZP:0019550 dermatocranium decreased amount, abnormal ZP:0019551 parasphenoid decreased amount, abnormal ZP:0019552 head decreased amount, abnormal ZP:0019553 dermatocranium decreased occurrence ossification, abnormal ZP:0019554 ceratohyal cartilage increased amount, abnormal ZP:0019555 Collagen Meckel's cartilage increased amount, abnormal ZP:0019556 cranial cartilage process quality chondrocyte development, abnormal ZP:0019557 chondrocyte cranial cartilage decreased amount, abnormal ZP:0019558 chondrocyte palatoquadrate cartilage increased amount, abnormal ZP:0019559 cranial skeletal system development process quality, abnormal ZP:0019560 dentary decreased amount, abnormal ZP:0019561 chondrocyte ceratohyal cartilage decreased amount, abnormal ZP:0019562 maxilla decreased amount, abnormal ZP:0019563 chondrocyte cranial cartilage increased amount, abnormal ZP:0019564 entopterygoid decreased amount, abnormal ZP:0019566 palatoquadrate cartilage increased amount, abnormal ZP:0019567 Collagen ceratohyal cartilage increased amount, abnormal ZP:0019568 transferase activity, transferring phosphorus-containing groups decreased process quality, abnormal ZP:0019569 head increased amount, abnormal ZP:0019570 gastrulation decreased speed, abnormal ZP:0019571 embryonic cleavage decreased occurrence, abnormal ZP:0019572 glucosidase activity decreased process quality, abnormal ZP:0019573 developmental process decreased speed, abnormal ZP:0019574 somite rostral/caudal axis specification process quality, abnormal ZP:0019575 site of double-strand break whole organism increased amount, abnormal ZP:0019576 posterior side somite absent, abnormal ZP:0019577 pronephros increased amount, abnormal ZP:0019578 posterior side trunk increased amount, abnormal ZP:0019579 anterior-most region segmental plate absent, abnormal ZP:0019580 post-vent region increased occurrence apoptotic process, abnormal ZP:0019581 DNA damage checkpoint increased process quality, abnormal ZP:0019582 horizontal myoseptum decreased amount, abnormal ZP:0019583 posterior lateral line primordium mislocalised dorsally, abnormal ZP:0019584 posterior lateral line primordium mislocalised anteriorly, abnormal ZP:0019585 posterior lateral line primordium decreased amount, abnormal ZP:0019586 posterior lateral line primordium increased thickness, abnormal ZP:0019587 ventral wall of dorsal aorta absent, abnormal ZP:0019588 ventral wall of dorsal aorta increased occurrence Notch signaling pathway, abnormal ZP:0019589 cell head kidney decreased amount, abnormal ZP:0019590 hemopoiesis increased occurrence, abnormal ZP:0019592 hair cell increased occurrence apoptotic process, abnormal ZP:0019593 desmosome neuromast hair cell disorganized, abnormal ZP:0019594 desmosome neuromast hair cell damaged, abnormal ZP:0019595 margin spatial pattern, abnormal ZP:0019596 yolk increased distribution, abnormal ZP:0019597 anterior region axis duplicated, abnormal ZP:0019598 cortical microtubule cytoskeleton fertilized egg spatial pattern, abnormal ZP:0019599 head aplastic/hypoplastic, abnormal ZP:0019600 animal-vegetal axis yolk decreased amount, abnormal ZP:0019601 fertilized egg has extra parts of type cortical microtubule cytoskeleton aster fertilized egg, abnormal ZP:0019602 basal region blastodisc mislocalised, abnormal ZP:0019603 pole plasm oocyte stage II increased distribution, abnormal ZP:0019604 pole plasm oocyte stage I increased distribution, abnormal ZP:0019605 motile cilium Kupffer's vesicle increased length, abnormal ZP:0019606 cone photoresponse recovery decreased efficacy, abnormal ZP:0019607 acetylcholine-gated channel complex myotome disorganized, abnormal ZP:0019608 acetylcholine-gated channel complex myotome mislocalised, abnormal ZP:0019609 otic vesicle decreased occurrence epithelial to mesenchymal transition, abnormal ZP:0019610 statoacoustic (VIII) ganglion has fewer parts of type neuroblast statoacoustic (VIII) ganglion, abnormal ZP:0019611 basal part of cell otic epithelium decreased amount, abnormal ZP:0019612 ventro-medial region otic vesicle increased distribution, abnormal ZP:0019613 ventro-medial region otic vesicle mislocalised, abnormal ZP:0019614 ventral region otic vesicle increased amount, abnormal ZP:0019615 otic vesicle decreased occurrence neuroblast delamination, abnormal ZP:0019616 neuron optic tectum increased amount, abnormal ZP:0019617 forebrain decreased amount, abnormal ZP:0019618 hypothalamus decreased amount, abnormal ZP:0019619 mitotic cell cycle asynchronous, abnormal ZP:0019620 embryonic morphogenesis arrested, abnormal ZP:0019621 iron ion homeostasis decreased occurrence, abnormal ZP:0019622 caudal fin decreased occurrence bone mineralization, abnormal ZP:0019623 vertebra decreased occurrence bone mineralization, abnormal ZP:0019625 pancreatic acinar gland absent, abnormal ZP:0019626 exocrine pancreas decreased occurrence growth, abnormal ZP:0019627 exocrine pancreas decreased distribution, abnormal ZP:0019628 epithelial cell of pancreas exocrine pancreas decreased amount, abnormal ZP:0019629 exocrine pancreas decreased occurrence cell population proliferation, abnormal ZP:0019630 protoneuromast decreased amount, abnormal ZP:0019631 posterior lateral line primordium decreased distribution, abnormal ZP:0019632 horizontal myoseptum decreased distribution, abnormal ZP:0019633 posterior lateral line primordium size, abnormal ZP:0019634 posterior lateral line neuromast decreased distribution, abnormal ZP:0019635 posterior lateral line primordium absent, abnormal ZP:0019636 protoneuromast decreased distribution, abnormal ZP:0019637 neuromast hair cell development disrupted, abnormal ZP:0019638 artery decreased amount, abnormal ZP:0019639 primitive hemopoiesis decreased occurrence, abnormal ZP:0019640 neuron hypothalamus decreased distribution, abnormal ZP:0019641 neuron hypothalamus absent, abnormal ZP:0019642 sleep behavioral quality of a process, abnormal ZP:0019643 histamine brain decreased amount, abnormal ZP:0019644 gliogenesis decreased process quality, abnormal ZP:0019645 exocrine pancreas development arrested, abnormal ZP:0019646 motor neuron decreased process quality axon guidance, abnormal ZP:0019647 motor neuron trunk increased amount, abnormal ZP:0019648 goblet cell intestine decreased amount, abnormal ZP:0019649 whole organism morbidity, abnormal ZP:0019650 head delayed neural crest cell migration, abnormal ZP:0019651 neural crest cell trunk decreased distribution, abnormal ZP:0019652 neural crest cell trunk decreased amount, abnormal ZP:0019653 neural crest cell head decreased amount, abnormal ZP:0019654 pharyngeal arch 3 decreased amount, abnormal ZP:0019655 ventral region brain decreased amount, abnormal ZP:0019656 neural crest cell head decreased distribution, abnormal ZP:0019657 pharyngeal arch 4 decreased amount, abnormal ZP:0019658 pharyngeal arch 1 decreased amount, abnormal ZP:0019659 oral ectoderm decreased distribution, abnormal ZP:0019660 ceratohyal cartilage increased angle to left side right side ceratohyal cartilage, abnormal ZP:0019661 trunk delayed neural crest cell migration, abnormal ZP:0019662 ethmoid cartilage decreased distribution, abnormal ZP:0019663 ethmoid cartilage decreased amount, abnormal ZP:0019664 endoderm pharynx decreased distribution, abnormal ZP:0019665 presumptive rhombomere 5 mislocalised, abnormal ZP:0019666 intestinal bulb primordium increased distribution, abnormal ZP:0019667 presumptive rhombomere 5 decreased distribution, abnormal ZP:0019668 hindbrain development process quality, abnormal ZP:0019669 pronephric tubule physical object quality, abnormal ZP:0019670 presumptive rhombomere 6 decreased distribution, abnormal ZP:0019671 endocrine pancreas absent, abnormal ZP:0019672 anterior region intestinal rod decreased distribution, abnormal ZP:0019673 posterior region intestinal bulb primordium mislocalised, abnormal ZP:0019674 pronephric glomerulus increased distribution, abnormal ZP:0019675 hepatocyte undifferentiated, abnormal ZP:0019676 terminal Schwann cell decreased amount, abnormal ZP:0019677 motor neuron disrupted axonogenesis, abnormal ZP:0019678 motor neuron disrupted axon development, abnormal ZP:0019679 eye decreased circumference, abnormal ZP:0019680 commissure of the tract of the commissure of the caudal tuberculum decreased process quality commissural neuron axon guidance, abnormal ZP:0019681 commissure of the tract of the commissure of the caudal tuberculum decreased occurrence axon extension involved in axon guidance, abnormal ZP:0019682 axon commissure of the tract of the commissure of the caudal tuberculum defasciculated, abnormal ZP:0019683 hindbrain dilated, abnormal ZP:0019684 forebrain dilated, abnormal ZP:0019685 midbrain dilated, abnormal ZP:0019686 dorsal region cranial vasculature increased branchiness, abnormal ZP:0019687 angiogenic sprout trunk vasculature increased amount, abnormal ZP:0019688 angiogenic sprout cranial vasculature increased amount, abnormal ZP:0019689 cranial vasculature increased branchiness, abnormal ZP:0019690 cranial vasculature increased occurrence angiogenesis, abnormal ZP:0019691 trunk vasculature increased occurrence angiogenesis, abnormal ZP:0019692 amacrine cell differentiation arrested, abnormal ZP:0019693 retina increased distribution, abnormal ZP:0019694 eye photoreceptor cell differentiation decreased process quality, abnormal ZP:0019695 retinal cone cell differentiation arrested, abnormal ZP:0019696 sinus venosus mislocalised, abnormal ZP:0019697 endocardial cushion increased distribution, abnormal ZP:0019698 cell atrioventricular canal endocardium increased distribution, abnormal ZP:0019699 bulbus arteriosus increased amount, abnormal ZP:0019700 cell body photoreceptor cell mislocalised, abnormal ZP:0019701 kinocilium hair cell disorganized, abnormal ZP:0019702 cilium olfactory pit swollen, abnormal ZP:0019703 kinocilium hair cell decreased length, abnormal ZP:0019704 kinocilium neuromast disorganized, abnormal ZP:0019705 cell body photoreceptor cell decreased size, abnormal ZP:0019707 cilium photoreceptor cell decreased length, abnormal ZP:0019708 ciliary tip photoreceptor cell increased amount, abnormal ZP:0019709 floor plate lacks all parts of type motile cilium floor plate, abnormal ZP:0019710 retinal photoreceptor layer increased occurrence apoptotic process, abnormal ZP:0019711 optic tectum has fewer parts of type axon terminus retinal ganglion cell, abnormal ZP:0019712 optic tectum decreased occurrence innervation, abnormal ZP:0019713 gonadotrophin-releasing hormone neuronal migration to the hypothalamus decreased occurrence, abnormal ZP:0019714 hypothalamus gonadotrophin-releasing hormone neuron development decreased occurrence, abnormal ZP:0019715 mature B cell decreased amount, abnormal ZP:0019716 pronephros decreased rate renal filtration, abnormal ZP:0019717 apical plasma membrane pronephric duct absent, abnormal ZP:0019718 pronephric duct decreased process quality establishment of epithelial cell apical/basal polarity, abnormal ZP:0019719 ciliary basal body pronephric duct absent, abnormal ZP:0019720 junctional membrane complex somite decreased size, abnormal ZP:0019721 muscle cell somite undulate, abnormal ZP:0019722 I band somite morphology, abnormal ZP:0019723 muscle cell somite sparse, abnormal ZP:0019724 A band somite morphology, abnormal ZP:0019725 eye oblique orientation, abnormal ZP:0019726 anterior region lens mislocalised, abnormal ZP:0019727 neuromuscular junction development, skeletal muscle fiber disrupted, abnormal ZP:0019728 lens has extra parts of type nucleus cell, abnormal ZP:0019729 somite attachment quality muscle cell myoseptum, abnormal ZP:0019730 nucleus lens mislocalised, abnormal ZP:0019731 pancreatic B cell increased distribution, abnormal ZP:0019732 pancreatic B cell primary islet decreased amount, abnormal ZP:0019733 caudal artery decreased distance caudal vein, abnormal ZP:0019734 blood island disorganized, abnormal ZP:0019735 common myeloid progenitor decreased amount, abnormal ZP:0019736 podocyte foot glomerular basement membrane increased width, abnormal ZP:0019738 leukocyte hematopoietic system increased amount, abnormal ZP:0019739 leukocyte thymus decreased amount, abnormal ZP:0019740 leukocyte thymus decreased distribution, abnormal ZP:0019741 macrophage increased distribution, abnormal ZP:0019742 intermediate cell mass of mesoderm decreased distribution, abnormal ZP:0019743 thymus decreased occurrence hematopoietic stem cell migration, abnormal ZP:0019744 leukocyte intermediate cell mass of mesoderm increased amount, abnormal ZP:0019745 neutrophil intermediate cell mass of mesoderm increased amount, abnormal ZP:0019746 neutrophil increased distribution, abnormal ZP:0019747 lymphoid lineage cell migration into thymus decreased process quality, abnormal ZP:0019748 hematopoietic system increased amount, abnormal ZP:0019749 thymus primordium absent, abnormal ZP:0019750 macrophage intermediate cell mass of mesoderm increased amount, abnormal ZP:0019751 optic tectum decreased occurrence apoptotic cell clearance, abnormal ZP:0019752 pharyngeal arch 2 skeleton decreased process quality embryonic skeletal joint development, abnormal ZP:0019753 interhyal-hyosymplectic joint increased process quality cartilage development, abnormal ZP:0019754 ceratohyal cartilage fused with interhyal cartilage, abnormal ZP:0019755 chondrocyte ceratohyal-interhyal joint increased amount, abnormal ZP:0019756 hyosymplectic cartilage fused with interhyal cartilage, abnormal ZP:0019757 ceratohyal-interhyal joint increased process quality cartilage development, abnormal ZP:0019758 joint pharyngeal arch 2 skeleton increased amount, abnormal ZP:0019759 ceratohyal-interhyal joint malformed, abnormal ZP:0019760 chondrocyte ceratohyal-interhyal joint increased size, abnormal ZP:0019761 chondrocyte interhyal-hyosymplectic joint increased amount, abnormal ZP:0019762 chondrocyte interhyal-hyosymplectic joint increased size, abnormal ZP:0019763 interhyal-hyosymplectic joint malformed, abnormal ZP:0019764 Z disc ventricular myocardium decreased amount, abnormal ZP:0019765 striated muscle thin filament ventricular myocardium decreased amount, abnormal ZP:0019766 Z disc cardiac muscle spatial pattern, abnormal ZP:0019767 Z disc cardiac muscle cell decreased amount, abnormal ZP:0019768 neuroectoderm decreased distribution, abnormal ZP:0019769 pharyngeal arch increased distribution, abnormal ZP:0019770 hyomandibula morphology, abnormal ZP:0019771 pharyngeal arch 1 increased distribution, abnormal ZP:0019772 pharyngeal arch 2 increased distribution, abnormal ZP:0019773 pronephros increased occurrence multi-ciliated epithelial cell differentiation, abnormal ZP:0019774 cilium assembly increased occurrence, abnormal ZP:0019775 pronephric tubule has extra parts of type multi-ciliated epithelial cell pronephric tubule, abnormal ZP:0019776 engulfment of apoptotic cell disrupted, abnormal ZP:0019777 apoptotic cell clearance arrested, abnormal ZP:0019778 anatomical structure spatial pattern, abnormal ZP:0019779 whole organism spatial pattern, abnormal ZP:0019780 somite increased occurrence apoptotic process, abnormal ZP:0019781 heart structure, cavities, abnormal ZP:0019782 lymph vessel development arrested, abnormal ZP:0019783 lymph vessel development delayed, abnormal ZP:0019784 primitive hemopoiesis increased occurrence, abnormal ZP:0019785 ventricular system brain decreased size, abnormal ZP:0019786 cell third ventricle mislocalised, abnormal ZP:0019787 neuroepithelial cell spatial pattern, abnormal ZP:0019788 neuroepithelial cell increased occurrence cell population proliferation, abnormal ZP:0019789 neuroepithelial cell third ventricle structure, abnormal ZP:0019790 neuroepithelial cell third ventricle wholeness, abnormal ZP:0019791 neuroepithelial cell third ventricle apical-basal polarity, abnormal ZP:0019792 ventricular system brain increased volume, abnormal ZP:0019793 neuroepithelial cell increased distribution, abnormal ZP:0019794 apical plasma membrane third ventricle spatial pattern, abnormal ZP:0019795 regulation of circadian sleep/wake cycle, sleep decreased process quality, abnormal ZP:0019796 cardiac muscle cell action potential involved in contraction decreased duration, abnormal ZP:0019797 atrium process quality cardiac muscle cell action potential, abnormal ZP:0019798 intersegmental vessel decreased occurrence sprouting angiogenesis, abnormal ZP:0019799 posterior lateral plate mesoderm decreased amount, abnormal ZP:0019800 posterior lateral plate mesoderm increased amount, abnormal ZP:0019801 neuroectoderm increased distribution, abnormal ZP:0019802 blood island decreased amount, abnormal ZP:0019803 angioblastic mesenchymal cell increased amount, abnormal ZP:0019804 hematopoietic system decreased amount, abnormal ZP:0019805 tegmentum decreased thickness, abnormal ZP:0019806 optic tectum decreased thickness, abnormal ZP:0019807 forebrain decreased process quality neuron differentiation, abnormal ZP:0019808 hypothalamus decreased thickness, abnormal ZP:0019809 nucleus forebrain elongated, abnormal ZP:0019810 midbrain decreased process quality neuron differentiation, abnormal ZP:0019811 medulla oblongata decreased thickness, abnormal ZP:0019812 nucleus midbrain elongated, abnormal ZP:0019813 axon neuron increased length, abnormal ZP:0019814 sensory neuron increased rate axon extension, abnormal ZP:0019815 motor neuron increased rate axon extension, abnormal ZP:0019816 filopodium neuron increased length, abnormal ZP:0019817 neuron decreased branchiness, abnormal ZP:0019818 efferent axon development in a lateral line nerve disrupted, abnormal ZP:0019819 photoreceptor connecting cilium photoreceptor cell absent, abnormal ZP:0019820 cilium hair cell anterior macula absent, abnormal ZP:0019821 retina has fewer parts of type central region retinal cone cell, abnormal ZP:0019822 cilium lateral crista decreased length, abnormal ZP:0019824 cilium posterior crista decreased amount, abnormal ZP:0019825 cilium lateral line absent, abnormal ZP:0019826 cilium anterior crista decreased amount, abnormal ZP:0019827 retinal rod cell structure, abnormal ZP:0019828 cilium lateral crista decreased amount, abnormal ZP:0019829 cilium photoreceptor cell absent, abnormal ZP:0019830 retinal cone cell non-functional, abnormal ZP:0019831 photoreceptor inner segment retinal rod cell mislocalised, abnormal ZP:0019832 cilium anterior crista decreased length, abnormal ZP:0019833 photoreceptor outer segment layer degenerate, abnormal ZP:0019834 central region retina degenerate, abnormal ZP:0019835 retinal outer nuclear layer absence due to degeneration, abnormal ZP:0019836 cilium posterior crista decreased length, abnormal ZP:0019837 cilium hair cell posterior macula absent, abnormal ZP:0019838 ciliary basal body photoreceptor cell absent, abnormal ZP:0019839 cilium central canal absent, abnormal ZP:0019840 optic tectum increased amount, abnormal ZP:0019841 optic tectum increased distribution, abnormal ZP:0019842 retinal ganglion cell layer decreased amount, abnormal ZP:0019843 melanosome melanocyte distended, abnormal ZP:0019844 axon terminus retinal ganglion cell increased branchiness, abnormal ZP:0019845 retinal ganglion cell decreased occurrence anterograde axonal transport of mitochondrion, abnormal ZP:0019846 cranial nerve II decreased occurrence anterograde axonal transport of mitochondrion, abnormal ZP:0019847 dendrite optic tectum decreased amount, abnormal ZP:0019848 retinal ganglion cell has fewer parts of type axon terminus mitochondrion retinal ganglion cell, abnormal ZP:0019849 axon retinal ganglion cell decreased amount, abnormal ZP:0019850 axon terminus retinal ganglion cell decreased branchiness, abnormal ZP:0019851 cranial nerve II decreased occurrence collateral sprouting, abnormal ZP:0019852 cranial nerve II delayed axonogenesis involved in innervation, abnormal ZP:0019853 cranial nerve II decreased occurrence anterograde trans-synaptic signaling, abnormal ZP:0019854 cranial nerve II increased occurrence collateral sprouting, abnormal ZP:0019855 optic tectum decreased occurrence anterograde trans-synaptic signaling, abnormal ZP:0019856 germ cell development decreased process quality, abnormal ZP:0019857 whole organism lacks all parts of type primordial germ cell, abnormal ZP:0019858 testis lacks all parts of type germ line cell, abnormal ZP:0019859 posterior region unfertilized egg increased amount, abnormal ZP:0019860 posterior region unfertilized egg increased distribution, abnormal ZP:0019861 egg activation decreased process quality, abnormal ZP:0019862 dorsal/ventral pattern formation decreased process quality, abnormal ZP:0019863 posterior region unfertilized egg mislocalised, abnormal ZP:0019864 unfertilized egg increased amount, abnormal ZP:0019865 unfertilized egg has extra parts of type posterior region cortical granule unfertilized egg, abnormal ZP:0019866 microtubule unfertilized egg disorganized, abnormal ZP:0019867 myotome increased distribution, abnormal ZP:0019868 regulation of protein processing process quality, abnormal ZP:0019869 cell cardiac jelly disorganized, abnormal ZP:0019870 podocyte foot podocyte morphology, abnormal ZP:0019871 myosin II filament chondrocyte position, abnormal ZP:0019872 filamentous actin chondrocyte position, abnormal ZP:0019873 ceratohyal cartilage increased width, abnormal ZP:0019874 MAP kinase kinase activity process quality, abnormal ZP:0019875 ceratohyal cartilage right angle to anterior-posterior axis whole organism, abnormal ZP:0019876 Meckel's cartilage distance ethmoid cartilage, abnormal ZP:0019877 Meckel's cartilage orientation anterior-posterior axis whole organism, abnormal ZP:0019878 Meckel's cartilage truncated, abnormal ZP:0019879 pharyngeal arch 1 disorganized, abnormal ZP:0019880 mouth atretic, abnormal ZP:0019881 lateral line has fewer parts of type neuromast, abnormal ZP:0019882 hair cell has extra parts of type neuromast, abnormal ZP:0019883 hematopoietic stem cell post-vent region decreased amount, abnormal ZP:0019884 hematopoietic stem cell thymus decreased amount, abnormal ZP:0019885 hematopoietic stem cell ventral wall of dorsal aorta normal amount, abnormal ZP:0019886 autophagosome blood island increased amount, abnormal ZP:0019887 hematopoietic stem cell kidney decreased amount, abnormal ZP:0019888 cytosolic large ribosomal subunit whole organism increased amount, abnormal ZP:0019890 presumptive retinal pigmented epithelium flattened, abnormal ZP:0019891 optic furrow malformed, abnormal ZP:0019892 lens ovate, abnormal ZP:0019893 cell presumptive neural retina decreased length, abnormal ZP:0019894 basal lamina optic cup spatial pattern, abnormal ZP:0019895 focal adhesion optic fissure decreased amount, abnormal ZP:0019897 presumptive neural retina flattened, abnormal ZP:0019898 cell motility involved in camera-type eye morphogenesis disrupted, abnormal ZP:0019899 basal lamina optic cup mislocalised, abnormal ZP:0019900 optic stalk increased diameter, abnormal ZP:0019901 establishment of epithelial cell apical/basal polarity involved in camera-type eye morphogenesis disrupted, abnormal ZP:0019902 somite detached from muscle cell somite, abnormal ZP:0019903 motile cilium Kupffer's vesicle decreased functionality, abnormal ZP:0019904 microglia development decreased process quality, abnormal ZP:0019905 ciliary marginal zone increased process quality cell population proliferation, abnormal ZP:0019906 pancreas has extra parts of type pancreatic B cell, abnormal ZP:0019908 glucose whole organism increased amount, abnormal ZP:0019909 nodal signaling pathway increased occurrence, abnormal ZP:0019910 ovulation process quality, abnormal ZP:0019911 testis decreased weight, abnormal ZP:0019912 postovulatory follicle absent, abnormal ZP:0019913 ovary increased size, abnormal ZP:0019914 ovary increased weight, abnormal ZP:0019915 ovarian follicle stage IV increased amount, abnormal ZP:0019916 postovulatory follicle increased amount, abnormal ZP:0019917 double-strand break repair via alternative nonhomologous end joining decreased process quality, abnormal ZP:0019918 double-strand break repair via alternative nonhomologous end joining increased process quality, abnormal ZP:0019919 hindbrain absent, abnormal ZP:0019920 midbrain absent, abnormal ZP:0019921 determination of left/right asymmetry in nervous system disrupted, abnormal ZP:0019922 atrioventricular valve functionality, abnormal ZP:0019923 atrioventricular valve closure, abnormal ZP:0019924 endothelial cell proliferation disrupted, abnormal ZP:0019925 glutamatergic neuron decreased distribution, abnormal ZP:0019927 spinal cord absent, abnormal ZP:0019928 anterior pancreatic bud decreased distribution, abnormal ZP:0019929 exocrine pancreas decreased amount, abnormal ZP:0019930 pancreas increased distribution, abnormal ZP:0019931 pancreatic bud increased distribution, abnormal ZP:0019932 anterior pancreatic bud decreased process quality cell population proliferation, abnormal ZP:0019933 supramolecular fiber ceratobranchial cartilage increased amount, abnormal ZP:0019934 supramolecular fiber ceratobranchial cartilage increased thickness, abnormal ZP:0019935 supramolecular fiber organization decreased process quality, abnormal ZP:0019936 establishment of synaptic specificity at neuromuscular junction decreased occurrence, abnormal ZP:0019937 acetylcholine-gated channel complex muscle decreased amount, abnormal ZP:0019938 midbrain hindbrain boundary decreased distribution, abnormal ZP:0019939 hindbrain increased distribution, abnormal ZP:0019940 cranium lacks parts or has fewer parts of type ceratobranchial cartilage, abnormal ZP:0019941 hindbrain decreased distribution, abnormal ZP:0019942 cranial neural crest cell decreased process quality neural crest cell migration, abnormal ZP:0019943 dorsal region hindbrain mislocalised, abnormal ZP:0019944 cranial neural crest cell decreased distribution, abnormal ZP:0019945 ceratobranchial 1 cartilage aplastic, abnormal ZP:0019946 rhombomere 6 mislocalised, abnormal ZP:0019947 hindbrain decreased process quality canonical Wnt signaling pathway, abnormal ZP:0019948 cranial neural crest cell decreased process quality canonical Wnt signaling pathway, abnormal ZP:0019949 tail bud decreased distribution, abnormal ZP:0019950 ceratobranchial 1 cartilage hypoplastic, abnormal ZP:0019951 volume-sensitive chloride channel activity decreased process quality, abnormal ZP:0019952 otic vesicle edematous, abnormal ZP:0019953 pronephric duct process quality kidney epithelium development, abnormal ZP:0019954 brain has fewer parts of type dopaminergic neuron, abnormal ZP:0019955 midbrain increased amount, abnormal ZP:0019956 apicolateral plasma membrane pronephric duct mislocalised, abnormal ZP:0019957 lens edematous, abnormal ZP:0019958 postoptic commissure increased amount, abnormal ZP:0019959 spinal cord has fewer parts of type neuron, abnormal ZP:0019960 diencephalon increased amount, abnormal ZP:0019961 mRNA processing decreased occurrence, abnormal ZP:0019962 iridophore scale increased amount, abnormal ZP:0019963 iridophore mislocalised, abnormal ZP:0019965 iridophore dorsal fin increased amount, abnormal ZP:0019966 iridophore displaced to dorsal root ganglion, abnormal ZP:0019967 iridophore displaced to pupil, abnormal ZP:0019968 iridophore caudal fin increased amount, abnormal ZP:0019969 iridophore displaced to trunk, abnormal ZP:0019971 iridophore anal fin increased amount, abnormal ZP:0019972 melanocyte scale increased amount, abnormal ZP:0019973 supramolecular fiber corneal stroma increased diameter, abnormal ZP:0019974 lymph vasculature hypoplastic, abnormal ZP:0019975 endothelial cell lymph vessel decreased amount, abnormal ZP:0019976 dorsal longitudinal lymphatic vessel absent, abnormal ZP:0019977 venous endothelial cell migration involved in lymph vessel development decreased process quality, abnormal ZP:0019978 venous endothelial cell migration involved in lymph vessel development process quality, abnormal ZP:0019979 lymphangioblast horizontal myoseptum morphology, abnormal ZP:0019980 intersegmental lymph vessel absent, abnormal ZP:0019981 endothelial cell lymphatic branchial arch 1 decreased amount, abnormal ZP:0019982 lymph vasculature aplastic, abnormal ZP:0019983 endothelial cell otolithic lymph vessel decreased amount, abnormal ZP:0019984 neural tube closure delayed, abnormal ZP:0019985 whole organism has extra parts of type neural tube, abnormal ZP:0019986 neural plate decreased rate cell migration, abnormal ZP:0019987 neural tube closure, abnormal ZP:0019988 cell neural keel morphology, abnormal ZP:0019989 microtubule cytoskeleton neural keel composition, abnormal ZP:0019990 ceratobranchial cartilage immature, abnormal ZP:0019991 hematopoietic progenitor cell differentiation increased occurrence, abnormal ZP:0019992 definitive hemopoiesis increased occurrence, abnormal ZP:0019993 ventral region whole organism increased distribution, abnormal ZP:0019994 neuroectoderm spatial pattern, abnormal ZP:0019995 dorsal region whole organism increased amount, abnormal ZP:0019996 prechordal plate spatial pattern, abnormal ZP:0019997 ventral region whole organism increased amount, abnormal ZP:0019998 cranial nerve VII decreased amount, abnormal ZP:0019999 facial nerve formation decreased process quality, abnormal ZP:0020000 cranial motor neuron trigeminal motor nucleus mislocalised, abnormal ZP:0020001 cranial nerve VII increased occurrence collateral sprouting in absence of injury, abnormal ZP:0020002 axon cranial nerve VII defasciculated, abnormal ZP:0020003 trigeminal motor nucleus development decreased process quality, abnormal ZP:0020004 trigeminal motor nucleus process quality motor neuron migration, abnormal ZP:0020005 posterior lateral line decreased amount, abnormal ZP:0020006 cranial nerve V absent, abnormal ZP:0020007 hair cell otic vesicle absent, abnormal ZP:0020008 cranial nerve V decreased amount, abnormal ZP:0020009 retina decreased occurrence mitotic cell cycle, abnormal ZP:0020010 head discolored, abnormal ZP:0020011 cysteine-type endopeptidase activity involved in apoptotic process increased process quality, abnormal ZP:0020012 epithelial cell pronephric tubule decreased amount, abnormal ZP:0020013 epithelial cell pronephric tubule apoptotic, abnormal ZP:0020015 atrioventricular ring morphology, abnormal ZP:0020016 atrium spatial pattern, abnormal ZP:0020017 atrioventricular canal absent, abnormal ZP:0020018 cardiac jelly decreased amount, abnormal ZP:0020019 endocardial cushion atrioventricular canal absent, abnormal ZP:0020020 cardiac ventricle spatial pattern, abnormal ZP:0020025 ventral telencephalon decreased distribution, abnormal ZP:0020026 hypothalamus decreased distribution, abnormal ZP:0020027 spinal cord increased amount, abnormal ZP:0020028 neuron mid intestine decreased amount, abnormal ZP:0020029 intestinal bulb has fewer parts of type enteric neuron, abnormal ZP:0020030 electrically responsive cell intestine increased distribution, abnormal ZP:0020031 neuron intestinal bulb decreased amount, abnormal ZP:0020032 neuron projection mid intestine decreased distribution, abnormal ZP:0020033 neuron projection mid intestine decreased amount, abnormal ZP:0020034 neuron mid intestine decreased distribution, abnormal ZP:0020035 neuron posterior intestine decreased amount, abnormal ZP:0020036 interstitial cell of Cajal differentiation delayed, abnormal ZP:0020037 phasic smooth muscle contraction occurrence, abnormal ZP:0020038 mid intestine has fewer parts of type enteric neuron, abnormal ZP:0020039 posterior intestine has fewer parts of type enteric neuron, abnormal ZP:0020040 neuron projection enteric neuron decreased distribution, abnormal ZP:0020041 serotonergic neuron mid intestine decreased distribution, abnormal ZP:0020042 neuron projection enteric neuron decreased amount, abnormal ZP:0020043 intestine smooth muscle contraction decreased frequency, abnormal ZP:0020044 phasic smooth muscle contraction frequency, abnormal ZP:0020045 posterior intestine lacks parts or has fewer parts of type enteric neuron, abnormal ZP:0020046 branchiostegal ray fused with opercle, abnormal ZP:0020047 head has extra parts of type bone tissue, abnormal ZP:0020048 branchiostegal ray increased size, abnormal ZP:0020049 mesenchyme increased distribution, abnormal ZP:0020050 fin bud absent, abnormal ZP:0020052 enteric neuron mid intestine decreased amount, abnormal ZP:0020053 enteric neuron intestinal bulb decreased amount, abnormal ZP:0020054 intestinal bulb primordium decreased amount, abnormal ZP:0020055 neural crest cell migration involved in autonomic nervous system development decreased process quality, abnormal ZP:0020059 anatomical region vagal ganglion mislocalised, abnormal ZP:0020060 neural crest cell migration involved in autonomic nervous system development decreased rate, abnormal ZP:0020061 enteric neuron gut decreased amount, abnormal ZP:0020064 fin bud decreased amount, abnormal ZP:0020065 neural crest cell decreased process quality cell population proliferation, abnormal ZP:0020066 gut endothelial cell absent, abnormal ZP:0020068 neural crest cell enteric nervous system decreased amount, abnormal ZP:0020070 right side heart primordium mislocalised, abnormal ZP:0020071 heart primordium absent, abnormal ZP:0020072 left/right pattern formation decreased efficacy, abnormal ZP:0020073 determination of heart left/right asymmetry decreased efficacy, abnormal ZP:0020074 pineal complex increased distribution, abnormal ZP:0020075 inner ear increased amount, abnormal ZP:0020076 pancreas primordium decreased amount, abnormal ZP:0020077 hematopoietic multipotent progenitor cell absent, abnormal ZP:0020078 nervous system decreased amount, abnormal ZP:0020079 nervous system increased amount, abnormal ZP:0020080 pancreas primordium absent, abnormal ZP:0020081 pancreas primordium increased amount, abnormal ZP:0020082 neuroblast increased amount, abnormal ZP:0020083 pronephric tubule increased distribution, abnormal ZP:0020084 post-vent region white, abnormal ZP:0020087 inner ear decreased amount, abnormal ZP:0020088 cleavage furrow blastomere morphology, abnormal ZP:0020089 early embryonic cell cellular adhesivity, abnormal ZP:0020090 blastomere has fewer parts of type actomyosin contractile ring filamentous actin blastomere, abnormal ZP:0020091 blastomere morphology, abnormal ZP:0020092 cleavage furrow blastomere decreased amount, abnormal ZP:0020093 early embryonic cell morphology, abnormal ZP:0020094 blastomere irregularly shaped, abnormal ZP:0020095 early embryonic cell multinucleate, abnormal ZP:0020096 vesicle blastomere increased amount, abnormal ZP:0020097 lymphangioblast cord broken, abnormal ZP:0020098 lymphangiogenic sprout posterior cardinal vein decreased amount, abnormal ZP:0020099 lymphatic endothelial cell migration disrupted, abnormal ZP:0020100 lymphangiogenic sprout absent, abnormal ZP:0020101 vascular sprouts posterior cardinal vein decreased distribution, abnormal ZP:0020102 lymphangiogenic sprout posterior cardinal vein absent, abnormal ZP:0020103 lymphangioblast cord hypoplastic, abnormal ZP:0020104 cardiac ventricle decreased magnitude cardiac muscle contraction, abnormal ZP:0020105 retina development in camera-type eye decreased process quality, abnormal ZP:0020106 cardiac ventricle increased duration ventricular cardiac muscle cell action potential, abnormal ZP:0020107 melanocyte melanophore stripe absent, abnormal ZP:0020108 melanocyte larval melanophore stripe absent, abnormal ZP:0020109 ventral region caudal fin decreased pigmentation, abnormal ZP:0020110 stereocilium inner ear decreased width, abnormal ZP:0020111 stereocilium inner ear decreased length, abnormal ZP:0020112 neuromast hair cell increased process quality apoptotic process, abnormal ZP:0020113 endothelial cell common cardinal vein decreased amount, abnormal ZP:0020114 primordial hindbrain channel decreased occurrence blood vessel development, abnormal ZP:0020115 primordial hindbrain channel decreased occurrence cell migration involved in sprouting angiogenesis, abnormal ZP:0020116 primordial hindbrain channel arrested angiogenesis, abnormal ZP:0020117 intersegmental vessel decreased occurrence blood vessel development, abnormal ZP:0020118 common cardinal vein decreased occurrence cell population proliferation, abnormal ZP:0020119 intersegmental vessel arrested angiogenesis, abnormal ZP:0020120 endothelial cell primordial hindbrain channel decreased amount, abnormal ZP:0020121 anatomical region primordial hindbrain channel absent, abnormal ZP:0020122 extension decreased amount, abnormal ZP:0020123 common cardinal vein decreased occurrence angiogenesis, abnormal ZP:0020124 common cardinal vein decreased occurrence blood vessel development, abnormal ZP:0020125 endothelial cell anterior cardinal vein decreased amount, abnormal ZP:0020126 primordial hindbrain channel arrested cell migration involved in sprouting angiogenesis, abnormal ZP:0020127 fat cell visceral fat decreased amount, abnormal ZP:0020128 fat cell differentiation disrupted, abnormal ZP:0020129 ventral fin fold absence due to degeneration, abnormal ZP:0020130 T-tubule skeletal muscle broken, abnormal ZP:0020131 ventral fin fold degenerate, abnormal ZP:0020132 skeletal muscle lacks all parts of type T-tubule sarcoplasmic reticulum skeletal muscle, abnormal ZP:0020133 vertical myoseptum increased amount, abnormal ZP:0020134 ciliary basal body pronephros disorganized, abnormal ZP:0020135 neutrophil progenitor cell decreased amount, abnormal ZP:0020136 skeletal muscle trunk increased amount, abnormal ZP:0020137 skeletal muscle cell decreased thickness, abnormal ZP:0020138 skeletal muscle increased process quality apoptotic process, abnormal ZP:0020139 skeletal muscle cell decondensed, abnormal ZP:0020140 skeletal muscle trunk decreased amount, abnormal ZP:0020141 actin filament skeletal muscle cell decreased length, abnormal ZP:0020142 head lacks parts or has fewer parts of type cephalic musculature, abnormal ZP:0020143 presumptive cephalic mesoderm disrupted gene expression, abnormal ZP:0020144 pharyngeal arch 6 has fewer parts of type cranial neural crest, abnormal ZP:0020145 pharyngeal arch 3 has fewer parts of type chondroblast, abnormal ZP:0020146 neural crest cell neuroectoderm decreased amount, abnormal ZP:0020147 pharyngeal arch 5 absent, abnormal ZP:0020148 copula absent, abnormal ZP:0020149 pharyngeal arch 5 has fewer parts of type cranial neural crest, abnormal ZP:0020150 chondroblast cranial neural crest decreased amount, abnormal ZP:0020151 pharyngeal arch 3 has fewer parts of type cranial neural crest, abnormal ZP:0020152 vasoconstriction increased occurrence, abnormal ZP:0020153 intestine decreased efficacy peristalsis, abnormal ZP:0020154 basement membrane intestinal epithelium spatial pattern, abnormal ZP:0020155 artery decreased diameter, abnormal ZP:0020157 mid intestine increased occurrence epithelial cell migration, abnormal ZP:0020158 posterior intestine increased occurrence epithelial cell migration, abnormal ZP:0020159 basement membrane intestine discontinuous, abnormal ZP:0020160 blood circulation decreased volume, abnormal ZP:0020161 invadopodium intestinal epithelium increased amount, abnormal ZP:0020162 nucleus fast muscle cell decreased amount, abnormal ZP:0020163 somite patchy, abnormal ZP:0020164 muscle cell detached from myotome, abnormal ZP:0020165 muscle cell misaligned with somite, abnormal ZP:0020166 muscle cell detached from somite border, abnormal ZP:0020167 interhyoideus spatial pattern, abnormal ZP:0020168 fast muscle cell spatial pattern, abnormal ZP:0020170 skeletal muscle myofibril cephalic musculature decreased amount, abnormal ZP:0020171 blood accumulation pericardial cavity, abnormal ZP:0020172 Z disc fast muscle cell irregular spatial pattern, abnormal ZP:0020173 Z disc myotome absent, abnormal ZP:0020174 somite border decreased distribution, abnormal ZP:0020175 striated muscle thin filament myotome disorganized, abnormal ZP:0020176 myofilament skeletal muscle cell decreased amount, abnormal ZP:0020177 sarcomere myotome absent, abnormal ZP:0020178 skeletal muscle myofibril cephalic musculature undulate, abnormal ZP:0020179 ventral intermandibularis posterior spatial pattern, abnormal ZP:0020180 fast muscle cell trunk musculature morphology, abnormal ZP:0020181 M band skeletal muscle cell absent, abnormal ZP:0020182 myofilament skeletal muscle cell disorganized, abnormal ZP:0020183 inferior hyohyoid spatial pattern, abnormal ZP:0020184 Z disc skeletal muscle cell absent, abnormal ZP:0020185 skeletal muscle myofibril cephalic musculature disorganized, abnormal ZP:0020186 fast muscle cell decreased distribution, abnormal ZP:0020187 sarcomere muscle cell absent, abnormal ZP:0020188 mitochondrion skeletal muscle cell increased size, abnormal ZP:0020189 microvillus intestine morphology, abnormal ZP:0020190 inclusion body enterocyte increased amount, abnormal ZP:0020191 enterocyte increased height, abnormal ZP:0020192 microvillus enterocyte mislocalised, abnormal ZP:0020193 enterocyte columnar, abnormal ZP:0020194 enterocyte morphology, abnormal ZP:0020195 enterocyte accumulation secretory granule apical side enterocyte, abnormal ZP:0020196 enterocyte gut decreased amount, abnormal ZP:0020197 anatomical axis whole organism bent, abnormal ZP:0020198 epiblast increased thickness, abnormal ZP:0020199 embryonic skeletal system development disrupted, abnormal ZP:0020200 CaP motoneuron increased occurrence collateral sprouting, abnormal ZP:0020201 ocular blood vessel decreased area, abnormal ZP:0020202 pineal complex split, abnormal ZP:0020203 pineal complex elongated, abnormal ZP:0020204 floor plate decreased amount, abnormal ZP:0020205 paraxial mesoderm head decreased amount, abnormal ZP:0020206 hypochord decreased amount, abnormal ZP:0020207 notochord decreased amount, abnormal ZP:0020208 paraxial mesoderm head aplastic/hypoplastic, abnormal ZP:0020209 hatching gland cell decreased amount, abnormal ZP:0020210 synaptic vesicle posterior lateral line nerve aggregated, abnormal ZP:0020211 axon posterior lateral line nerve decreased distribution, abnormal ZP:0020212 synaptic vesicle posterior lateral line nerve spatial pattern, abnormal ZP:0020213 neuron posterior lateral line ganglion decreased distribution, abnormal ZP:0020214 posterior lateral line ganglion decreased distribution, abnormal ZP:0020215 otolith non-functional, abnormal ZP:0020216 dorsal region whole organism decreased amount, abnormal ZP:0020217 shield decreased distribution, abnormal ZP:0020218 dorsal/ventral axis specification decreased process quality, abnormal ZP:0020219 dorsal region neuroectoderm decreased amount, abnormal ZP:0020220 ventro-lateral region presumptive mesoderm decreased amount, abnormal ZP:0020221 dorsal region whole organism decreased distribution, abnormal ZP:0020222 ventro-lateral region presumptive mesoderm decreased distribution, abnormal ZP:0020223 ventral region non neural ectoderm increased distribution, abnormal ZP:0020224 dorsal region neuroectoderm decreased distribution, abnormal ZP:0020225 efferent axon development in a lateral line nerve decreased process quality, abnormal ZP:0020226 synaptic ribbon neuromast hair cell increased amount, abnormal ZP:0020227 synaptic ribbon neuromast hair cell mislocalised, abnormal ZP:0020228 efferent neuron posterior lateral line nerve aplastic, abnormal ZP:0020229 neuromast hair cell increased distance synaptic ribbon synaptic ribbon neuromast hair cell, abnormal ZP:0020230 posterior lateral line neuromast has fewer parts of type synaptic ribbon neuromast hair cell, abnormal ZP:0020231 afferent neuron posterior lateral line nerve aplastic, abnormal ZP:0020232 afferent axon development in posterior lateral line nerve decreased process quality, abnormal ZP:0020233 synaptic ribbon neuromast hair cell decreased size, abnormal ZP:0020234 cell superior cervical ganglion increased amount, abnormal ZP:0020235 common bile duct cystic, abnormal ZP:0020236 gall bladder dilated, abnormal ZP:0020237 hepatocyte increased distance hepatocyte, abnormal ZP:0020238 swim bladder inflation delayed, abnormal ZP:0020239 photoreceptor outer segment eye photoreceptor cell structure, abnormal ZP:0020240 eye photoreceptor cell accumulation vesicle eye photoreceptor cell, abnormal ZP:0020241 eye photoreceptor cell disrupted protein localization, abnormal ZP:0020242 eye photoreceptor cell accumulation vacuole eye photoreceptor cell, abnormal ZP:0020243 neural tube increased occurrence apoptotic process, abnormal ZP:0020244 pharyngeal arch 2 decreased distribution, abnormal ZP:0020245 pharyngeal arch 1 decreased distribution, abnormal ZP:0020246 pharyngeal arch decreased distribution, abnormal ZP:0020247 aortic arch 6 decreased occurrence blood vessel lumenization, abnormal ZP:0020248 pharyngeal arch 2 absent, abnormal ZP:0020249 ventral region pharyngeal arch decreased distribution, abnormal ZP:0020250 pharyngeal arch 4 decreased distribution, abnormal ZP:0020251 aortic arch 3 decreased amount, abnormal ZP:0020252 pharyngeal arch 3 decreased distribution, abnormal ZP:0020253 aortic arch 5 decreased occurrence blood vessel lumenization, abnormal ZP:0020254 pancreatic bud absent, abnormal ZP:0020255 endothelial cell caudal vein swollen, abnormal ZP:0020257 zymogen granule exocrine pancreas decreased size, abnormal ZP:0020258 pancreatic duct absent, abnormal ZP:0020259 erythroid progenitor cell post-vent region decreased amount, abnormal ZP:0020261 hematopoietic multipotent progenitor cell post-vent region decreased amount, abnormal ZP:0020262 zymogen granule exocrine pancreas decreased amount, abnormal ZP:0020264 nucleate erythrocyte blood island decreased amount, abnormal ZP:0020265 nucleate erythrocyte hematopoietic system absent, abnormal ZP:0020266 rough endoplasmic reticulum exocrine pancreas absent, abnormal ZP:0020267 mitochondrion exocrine pancreas morphology, abnormal ZP:0020268 mitochondrion exocrine pancreas increased size, abnormal ZP:0020270 ribosomal small subunit biogenesis decreased occurrence, abnormal ZP:0020271 choroid plexus fourth ventricle shape, abnormal ZP:0020272 hindbrain has extra parts of type Mauthner neuron, abnormal ZP:0020273 Notch signaling involved in heart development decreased occurrence, abnormal ZP:0020274 parapineal organ has extra parts of type neuron parapineal organ, abnormal ZP:0020275 parapineal organ increased occurrence neuron fate specification, abnormal ZP:0020276 left side habenula decreased amount, abnormal ZP:0020277 pineal complex absent, abnormal ZP:0020278 habenula bilateral symmetry, abnormal ZP:0020279 right side habenula increased amount, abnormal ZP:0020280 epiphysis decreased amount, abnormal ZP:0020281 cardiovascular system decreased amount, abnormal ZP:0020282 posterior lateral plate mesoderm decreased distribution, abnormal ZP:0020283 basement membrane optic furrow present, abnormal ZP:0020284 heart spatial pattern, abnormal ZP:0020285 lateral plate mesoderm decreased size, abnormal ZP:0020286 posterior lateral mesoderm decreased amount, abnormal ZP:0020287 hematopoietic system absent, abnormal ZP:0020288 optic furrow delayed basement membrane disassembly, abnormal ZP:0020289 cardiovascular system decreased distribution, abnormal ZP:0020290 locomotor rhythm delayed, abnormal ZP:0020291 intestine decreased amount, abnormal ZP:0020292 autophagosome liver increased amount, abnormal ZP:0020293 eye increased amount, abnormal ZP:0020294 autolysosome hindbrain increased amount, abnormal ZP:0020295 pineal complex decreased amount, abnormal ZP:0020296 pineal complex has fewer parts of type photoreceptor cell pineal complex, abnormal ZP:0020297 pineal complex decreased occurrence photoreceptor cell fate specification, abnormal ZP:0020298 cell intersegmental vessel decreased amount, abnormal ZP:0020299 intersegmental vessel incomplete structure, abnormal ZP:0020300 vein decreased distribution, abnormal ZP:0020301 angioblast cell migration decreased process quality, abnormal ZP:0020302 cell vein decreased amount, abnormal ZP:0020303 ceratohyal cartilage disoriented, abnormal ZP:0020304 circadian behavior disrupted, abnormal ZP:0020305 sleep light phase, abnormal ZP:0020306 larval behavior decreased process quality, abnormal ZP:0020307 pancreatic bud decreased distribution, abnormal ZP:0020308 acinar cell absent, abnormal ZP:0020309 cell exocrine pancreas decreased amount, abnormal ZP:0020310 pancreas morphogenesis process quality, abnormal ZP:0020311 blood vessel endothelium common cardinal vein patchy, abnormal ZP:0020312 actin filament bundle common cardinal vein disoriented, abnormal ZP:0020313 venous blood vessel morphogenesis decreased process quality, abnormal ZP:0020314 cell-cell junction common cardinal vein decreased length, abnormal ZP:0020315 common cardinal vein decreased process quality actin filament bundle organization, abnormal ZP:0020316 mid cerebral vein absent, abnormal ZP:0020317 mid cerebral vein decreased length, abnormal ZP:0020318 retinal pigmented epithelium has fewer parts of type melanosome melanocyte, abnormal ZP:0020319 pronephric duct process quality epithelial cilium movement involved in extracellular fluid movement, abnormal ZP:0020320 anterior region pronephric duct dilated, abnormal ZP:0020321 cilium pronephric duct decreased coordination, abnormal ZP:0020322 podocyte foot renal glomerulus shape, abnormal ZP:0020323 glomerular capillary collapsed, abnormal ZP:0020324 renal glomerulus hypoplastic, abnormal ZP:0020325 intersegmental vessel decreased process quality angiogenesis, abnormal ZP:0020326 retina arrested mitotic cell cycle, abnormal ZP:0020327 retina increased duration mitotic cell cycle, abnormal ZP:0020328 peripheral olfactory organ increased size, abnormal ZP:0020329 peripheral olfactory organ increased distribution, abnormal ZP:0020330 synapse horizontal cell amount, abnormal ZP:0020331 optic tectum increased process quality mitotic cell cycle, abnormal ZP:0020332 brain increased process quality mitotic cell cycle, abnormal ZP:0020333 fourth ventricle increased process quality mitotic cell cycle, abnormal ZP:0020334 male mating behavior decreased occurrence, abnormal ZP:0020335 response to pheromone decreased occurrence, abnormal ZP:0020336 male courtship behavior decreased occurrence, abnormal ZP:0020337 pronephric glomerulus morphogenesis disrupted, abnormal ZP:0020338 glomerular visceral epithelial cell differentiation disrupted, abnormal ZP:0020339 pronephric proximal tubule development disrupted, abnormal ZP:0020340 pronephric podocyte mislocalised, abnormal ZP:0020341 pronephric podocyte absent, abnormal ZP:0020342 anterior region pronephric duct absent, abnormal ZP:0020343 anterior region intermediate mesoderm absent, abnormal ZP:0020344 neurosecretory neuron preoptic area increased distribution, abnormal ZP:0020345 caudal tuberculum decreased amount, abnormal ZP:0020346 social behavior process quality, abnormal ZP:0020347 response to stress behavioral quality of a process, abnormal ZP:0020348 caudal tuberculum decreased distribution, abnormal ZP:0020349 caudal tuberculum increased amount, abnormal ZP:0020350 neurosecretory neuron preoptic area increased amount, abnormal ZP:0020351 intersegmental vessel decreased distribution, abnormal ZP:0020352 nucleate erythrocyte spatial pattern, abnormal ZP:0020353 telencephalon decreased distribution, abnormal ZP:0020354 vasculature spatial pattern, abnormal ZP:0020355 caudal vein plexus irregularly shaped, abnormal ZP:0020356 tegmentum decreased distribution, abnormal ZP:0020357 hindbrain spatial pattern, abnormal ZP:0020358 diencephalon decreased distribution, abnormal ZP:0020359 tegmentum spatial pattern, abnormal ZP:0020360 caudal vein plexus hemorrhagic, abnormal ZP:0020361 posterior cardinal vein decreased distribution, abnormal ZP:0020362 central nervous system decreased distribution, abnormal ZP:0020363 dorsal aorta decreased distribution, abnormal ZP:0020364 ventro-lateral region otic vesicle increased distribution, abnormal ZP:0020365 otic vesicle decreased occurrence neuroblast proliferation, abnormal ZP:0020366 otic vesicle increased occurrence neuroblast delamination, abnormal ZP:0020367 cardioblast migration to the midline involved in heart rudiment formation decreased occurrence, abnormal ZP:0020368 anterior lateral plate mesoderm decreased amount, abnormal ZP:0020369 cardiac muscle cell anterior lateral plate mesoderm decreased amount, abnormal ZP:0020370 secondary heart field specification decreased occurrence, abnormal ZP:0020371 heart tube increased distribution, abnormal ZP:0020372 blood accumulation anatomical region atrium, abnormal ZP:0020373 lateral plate mesoderm increased distribution, abnormal ZP:0020374 proepicardium development decreased occurrence, abnormal ZP:0020375 heart tube decreased amount, abnormal ZP:0020376 smooth muscle bulbus arteriosus spatial pattern, abnormal ZP:0020377 neuron optic tectum morphology, abnormal ZP:0020378 optic tectum has extra parts of type neuron, abnormal ZP:0020380 embryonic viscerocranium morphogenesis delayed, abnormal ZP:0020381 head muscle delayed muscle fiber development, abnormal ZP:0020382 splanchnocranium delayed ossification, abnormal ZP:0020383 energy coupled proton transmembrane transport, against electrochemical gradient decreased process quality, abnormal ZP:0020384 retinal rod cell increased volume, abnormal ZP:0020385 chondrocranium cartilage decreased occurrence neural crest cell migration, abnormal ZP:0020386 cardiac muscle cell spatial pattern, abnormal ZP:0020387 cardioblast cell midline fusion decreased occurrence, abnormal ZP:0020388 cardiac muscle cell decreased speed, abnormal ZP:0020389 anterior lateral plate mesoderm far from anterior lateral plate mesoderm, abnormal ZP:0020390 anterior lateral plate mesoderm spatial pattern, abnormal ZP:0020391 roof of mouth development decreased process quality, abnormal ZP:0020392 heart primordium separated from heart primordium, abnormal ZP:0020393 cardiac muscle progenitor cell migration to the midline involved in heart field formation decreased efficacy, abnormal ZP:0020394 cardioblast migration to the midline involved in heart rudiment formation process quality, abnormal ZP:0020395 anterior lateral plate mesoderm separated from anterior lateral plate mesoderm, abnormal ZP:0020396 exocrine pancreas polarity, abnormal ZP:0020397 pancreatic acinar cell absent, abnormal ZP:0020398 secondary islet absent, abnormal ZP:0020399 secondary islet decreased amount, abnormal ZP:0020400 pancreatic B cell decreased distribution, abnormal ZP:0020401 dorsal aorta dilated, abnormal ZP:0020402 intersegmental vessel trunk disorganized, abnormal ZP:0020403 caudal artery dilated, abnormal ZP:0020404 hepatic portal vein disorganized, abnormal ZP:0020406 ceratobranchial 5 cartilage lacks parts or has fewer parts of type ceratobranchial 5 primary tooth, abnormal ZP:0020407 anterior segment eye malformed, abnormal ZP:0020408 odontogenesis disrupted, abnormal ZP:0020409 aqueous humor decreased volume, abnormal ZP:0020410 female sex determination disrupted, abnormal ZP:0020411 tooth 4V incomplete structure, abnormal ZP:0020412 cytoplasm Kupffer's vesicle decreased amount, abnormal ZP:0020413 Kolmer-Agduhr neuron decreased process quality response to muscle activity, abnormal ZP:0020414 Kolmer-Agduhr neuron decreased process quality response to mechanical stimulus, abnormal ZP:0020415 response to muscle activity decreased process quality, abnormal ZP:0020416 angiogenic sprout dorsal aorta decreased amount, abnormal ZP:0020417 cilium retinal photoreceptor layer decreased amount, abnormal ZP:0020418 mitotic spindle cell morphology, abnormal ZP:0020420 mitotic cell cycle process disrupted, abnormal ZP:0020421 centriole cell decreased amount, abnormal ZP:0020422 bone tissue surrounding notochord, abnormal ZP:0020423 hemal arch morphology, abnormal ZP:0020424 vertebra condensed, abnormal ZP:0020425 hypural curved, abnormal ZP:0020426 epithelium notochord deformed, abnormal ZP:0020427 bone tissue increased amount, abnormal ZP:0020428 centrum increased thickness, abnormal ZP:0020429 skeletal muscle cell horizontal myoseptum dense, abnormal ZP:0020430 parhypural curved, abnormal ZP:0020431 vertebra protruding, abnormal ZP:0020432 centrum decreased length, abnormal ZP:0020433 collagen fibril organization disrupted, abnormal ZP:0020434 rib curved, abnormal ZP:0020435 epithelium notochord proliferative, abnormal ZP:0020436 elastic fiber notochord morphology, abnormal ZP:0020437 neural arch morphology, abnormal ZP:0020438 epithelium notochord increased thickness, abnormal ZP:0020439 procollagen-lysine 5-dioxygenase activity disrupted, abnormal ZP:0020440 skeletal muscle cell horizontal myoseptum decreased diameter, abnormal ZP:0020441 collagen type I trimer notochord disorganized, abnormal ZP:0020442 rib kinked, abnormal ZP:0020443 trunk process quality motor neuron axon guidance, abnormal ZP:0020444 opercular flap mineralized, abnormal ZP:0020445 axon primary motor neuron spatial pattern, abnormal ZP:0020446 ventral root mislocalised, abnormal ZP:0020447 photoreceptor connecting cilium retina decreased length, abnormal ZP:0020448 photoreceptor connecting cilium retina decreased amount, abnormal ZP:0020449 neuron retina disorganized, abnormal ZP:0020450 photoreceptor outer segment retinal cone cell aplastic/hypoplastic, abnormal ZP:0020451 mitochondrial chromosome compound organ decreased amount, abnormal ZP:0020452 mitochondrial chromosome caudal fin decreased amount, abnormal ZP:0020453 mitochondrial DNA replication decreased occurrence, abnormal ZP:0020454 mitochondrial chromosome central nervous system decreased amount, abnormal ZP:0020455 central nervous system decreased process quality cellular respiration, abnormal ZP:0020456 ceratobranchial 5 tooth hypoplastic, abnormal ZP:0020457 rRNA transcription disrupted, abnormal ZP:0020458 ventral mandibular arch apoptotic, abnormal ZP:0020459 pharyngeal arch 1 decreased occurrence cell population proliferation, abnormal ZP:0020460 ceratohyal cartilage polarity, abnormal ZP:0020461 neural crest cell pharyngeal arch decreased distribution, abnormal ZP:0020462 neural crest cell pharyngeal arch spatial pattern, abnormal ZP:0020463 opercle hypoplastic, abnormal ZP:0020464 cranium increased occurrence apoptotic process, abnormal ZP:0020465 pharyngeal arch 2 decreased occurrence cell population proliferation, abnormal ZP:0020466 cranium necrotic, abnormal ZP:0020467 preoptic area decreased amount, abnormal ZP:0020468 fin decreased amount, abnormal ZP:0020469 trunk decreased distribution, abnormal ZP:0020470 anatomical margin dorsal aorta shape, abnormal ZP:0020471 anatomical margin posterior cardinal vein shape, abnormal ZP:0020472 cell body CaP motoneuron mislocalised anteriorly, abnormal ZP:0020473 motor neuron increased occurrence bleb assembly, abnormal ZP:0020474 CaP motoneuron process quality axonogenesis, abnormal ZP:0020475 axon CaP motoneuron morphology, abnormal ZP:0020476 membrane motor neuron decreased amount, abnormal ZP:0020477 retinal neural layer increased occurrence apoptotic process, abnormal ZP:0020478 negative regulation of hh target transcription factor activity disrupted, abnormal ZP:0020479 dendrite Purkinje cell decreased amount, abnormal ZP:0020480 dendrite Purkinje cell decreased branchiness, abnormal ZP:0020481 midbrain hindbrain boundary edematous, abnormal ZP:0020482 intracellular DEL mislocalised, abnormal ZP:0020483 endocytosis increased occurrence, abnormal ZP:0020484 cytosol DEL mislocalised, abnormal ZP:0020485 lateral plate mesoderm decreased distribution, abnormal ZP:0020486 lateral plate mesoderm decreased occurrence cell migration, abnormal ZP:0020487 caudal fin increased pigmentation, abnormal ZP:0020488 pronephric proximal convoluted tubule shape, abnormal ZP:0020489 ceratobranchial cartilage increased angle to anterior-posterior axis whole organism, abnormal ZP:0020490 mRNA destabilization decreased occurrence, abnormal ZP:0020491 Meckel's cartilage decreased distribution, abnormal ZP:0020492 integument has fewer parts of type NaK ionocyte, abnormal ZP:0020493 Meckel's cartilage decreased amount, abnormal ZP:0020494 branchiostegal ray decreased distribution, abnormal ZP:0020495 integument decreased amount, abnormal ZP:0020496 integument has fewer parts of type vH ionocyte, abnormal ZP:0020497 epidermis has fewer parts of type somatic stem cell, abnormal ZP:0020498 somatic stem cell epidermis decreased distribution, abnormal ZP:0020499 calcium ion import decreased rate, abnormal ZP:0020500 hindbrain has fewer parts of type ependymal cell motile cilium ependymal cell, abnormal ZP:0020501 vertebral column asymmetrically curved, abnormal ZP:0020502 ependymal cell decreased occurrence motile cilium assembly, abnormal ZP:0020503 vertebral column decreased process quality skeletal system morphogenesis, abnormal ZP:0020504 mitochondrial matrix skeletal muscle composition, abnormal ZP:0020505 mitochondrial membrane skeletal muscle broken, abnormal ZP:0020506 mitochondrial intermembrane space skeletal muscle increased size, abnormal ZP:0020507 mitochondrial crista skeletal muscle morphology, abnormal ZP:0020508 skeletal muscle accumulation mitochondrial matrix vesicle skeletal muscle, abnormal ZP:0020509 retina increased process quality mitotic cell cycle, abnormal ZP:0020510 locomotory behavior increased occurrence, abnormal ZP:0020511 sleep decreased occurrence, abnormal ZP:0020512 whole organism behavioural activity, abnormal ZP:0020513 neutrophil pericardium increased amount, abnormal ZP:0020514 fin broken, abnormal ZP:0020515 neutrophil otic vesicle decreased amount, abnormal ZP:0020516 neutrophil head decreased amount, abnormal ZP:0020517 cell binucleate, abnormal ZP:0020518 spinal cord motor neuron differentiation arrested, abnormal ZP:0020519 trunk increased distribution, abnormal ZP:0020520 mitotic cytokinesis checkpoint disrupted, abnormal ZP:0020521 proliferative region decreased amount, abnormal ZP:0020522 axon Rohon-Beard neuron disorganized, abnormal ZP:0020523 head increased distribution, abnormal ZP:0020524 axon sensory neuron spatial pattern, abnormal ZP:0020525 tail bud increased distribution, abnormal ZP:0020526 trigeminal sensory neuron disrupted spinal sensory neuron axon guidance, abnormal ZP:0020527 whole organism has extra parts of type nucleus embryonic structure, abnormal ZP:0020528 cytokinesis lacking processual parts membrane fission, abnormal ZP:0020529 blastoderm increased occurrence apoptotic process, abnormal ZP:0020530 axon microtubule bundle Rohon-Beard neuron disorganized, abnormal ZP:0020531 nucleus nucleate erythrocyte increased amount, abnormal ZP:0020532 cell decreased amount mitotic cell cycle, abnormal ZP:0020533 nucleate erythrocyte increased duration mitotic cell cycle, abnormal ZP:0020534 cell multinucleate, abnormal ZP:0020535 whole organism opacity, abnormal ZP:0020536 Rohon-Beard neuron disrupted spinal sensory neuron axon guidance, abnormal ZP:0020537 blood cell increased size, abnormal ZP:0020538 proliferative region decreased distribution, abnormal ZP:0020539 macrophage decreased distribution, abnormal ZP:0020540 primary motor neuron spatial pattern, abnormal ZP:0020541 CoSA spatial pattern, abnormal ZP:0020542 mitotic cell cycle has extra parts of type nuclear division, abnormal ZP:0020543 cell knobbled, abnormal ZP:0020544 spinal cord commissural neuron specification arrested, abnormal ZP:0020545 neutrophil decreased distribution, abnormal ZP:0020546 axon sensory neuron distended, abnormal ZP:0020547 intermediate cell mass of mesoderm spatial pattern, abnormal ZP:0020548 spinal cord interneuron spatial pattern, abnormal ZP:0020549 Rohon-Beard neuron spatial pattern, abnormal ZP:0020550 neuroblast decreased distribution, abnormal ZP:0020551 cardiac neural crest heart decreased amount, abnormal ZP:0020552 melanocyte epidermis position, abnormal ZP:0020553 cardiac neural crest accumulation posterior region otic vesicle, abnormal ZP:0020554 atrioventricular valve orientation ventriculo bulbo valve, abnormal ZP:0020555 blood cardiac ventricle decreased amount, abnormal ZP:0020556 cranial cartilage disrupted cartilage development, abnormal ZP:0020557 cardiac neural crest mislocalised, abnormal ZP:0020558 nucleate erythrocyte increased accumulation heart, abnormal ZP:0020559 atrioventricular valve decreased size, abnormal ZP:0020560 neural tube increased occurrence pigmentation, abnormal ZP:0020561 blood atrium decreased amount, abnormal ZP:0020562 developmental growth disrupted, abnormal ZP:0020563 ventriculo bulbo valve aplastic, abnormal ZP:0020564 ventriculo bulbo valve decreased size, abnormal ZP:0020565 kidney increased amount, abnormal ZP:0020566 eye decreased distribution, abnormal ZP:0020567 eye decreased occurrence cell population proliferation, abnormal ZP:0020568 ciliary marginal zone absent, abnormal ZP:0020569 acetylcholine-gated channel complex skeletal muscle distributed, abnormal ZP:0020570 CaP motoneuron decreased process quality synaptic vesicle exocytosis, abnormal ZP:0020571 CaP motoneuron decreased process quality action potential, abnormal ZP:0020572 CaP motoneuron process quality synaptic signaling, abnormal ZP:0020573 synapse CaP motoneuron decreased amount, abnormal ZP:0020574 CaP motoneuron decreased occurrence synaptic vesicle exocytosis, abnormal ZP:0020575 CaP motoneuron process quality regulation of synaptic plasticity, abnormal ZP:0020576 fast muscle cell process quality transmission of nerve impulse, abnormal ZP:0020577 muscle adaptation decreased process quality, abnormal ZP:0020578 heart process quality alternative mRNA splicing, via spliceosome, abnormal ZP:0020579 skeletal muscle contraction decreased efficacy, abnormal ZP:0020580 motor nucleus of vagal nerve shortened, abnormal ZP:0020581 nucleate erythrocyte intermediate cell mass of mesoderm decreased amount, abnormal ZP:0020582 ocular blood vessel disrupted blood vessel lumenization, abnormal ZP:0020583 eye disrupted vasculature development, abnormal ZP:0020584 ocular blood vessel decreased thickness, abnormal ZP:0020585 cone photoresponse recovery increased efficacy, abnormal ZP:0020586 brain vasculature lacks all parts of type central artery, abnormal ZP:0020587 primordial hindbrain channel decreased process quality establishment of endothelial blood-brain barrier, abnormal ZP:0020588 central artery decreased process quality vasculature development, abnormal ZP:0020589 primordial hindbrain channel has extra parts of type blood vessel endothelial cell, abnormal ZP:0020590 primordial hindbrain channel decreased process quality canonical Wnt signaling pathway, abnormal ZP:0020591 peripheral nervous system lacks all parts of type dorsal root ganglion, abnormal ZP:0020592 central artery decreased process quality canonical Wnt signaling pathway, abnormal ZP:0020593 dorsal root ganglion morphogenesis decreased process quality, abnormal ZP:0020594 brain vasculature lacks parts or has fewer parts of type central artery, abnormal ZP:0020595 brain vasculature has extra parts of type atrioventricular canal, abnormal ZP:0020596 primordial hindbrain channel mislocalised, abnormal ZP:0020597 hindbrain mislocalised, abnormal ZP:0020598 primary motor neuron increased amount, abnormal ZP:0020599 gut lacks all parts of type distal region enteric neuron, abnormal ZP:0020600 enteric nervous system absent, abnormal ZP:0020601 enteric nervous system development process quality, abnormal ZP:0020602 enteric nervous system decreased distribution, abnormal ZP:0020603 intestine decreased process quality peristalsis, abnormal ZP:0020604 enteric neuron absent, abnormal ZP:0020605 neuron neural crest derived gut absent, abnormal ZP:0020606 neuron neural crest derived gut decreased distribution, abnormal ZP:0020607 neural crest increased distribution, abnormal ZP:0020608 migratory neural crest increased amount, abnormal ZP:0020609 ectomesenchyme decreased amount, abnormal ZP:0020610 migratory neural crest increased occurrence cell population proliferation, abnormal ZP:0020611 migratory neural crest increased distribution, abnormal ZP:0020612 extension hypotrophic, abnormal ZP:0020613 whole organism bulbous, abnormal ZP:0020614 melanocyte larval melanophore stripe decreased amount, abnormal ZP:0020615 eye lacks all parts of type iridophore, abnormal ZP:0020616 convergent extension decreased process quality, abnormal ZP:0020617 photoreceptor outer segment photoreceptor outer segment layer shortened, abnormal ZP:0020618 retinal photoreceptor layer decreased amount, abnormal ZP:0020619 photoreceptor outer segment layer decreased distribution, abnormal ZP:0020621 nucleate erythrocyte irregularly shaped, abnormal ZP:0020622 central side anatomical structure mislocalised, abnormal ZP:0020623 erythrocyte maturation decreased occurrence, abnormal ZP:0020624 right side anatomical structure mislocalised, abnormal ZP:0020625 hindbrain inflated, abnormal ZP:0020626 microglial cell process quality lysosome organization, abnormal ZP:0020627 optic tectum has extra parts of type microglial cell phagolysosome microglial cell, abnormal ZP:0020628 microglial cell morphology, abnormal ZP:0020629 brain decreased occurrence apoptotic cell clearance, abnormal ZP:0020630 phagolysosome microglial cell increased size, abnormal ZP:0020631 microglial cell decreased occurrence lysosomal protein catabolic process, abnormal ZP:0020632 lysosome microglial cell increased size, abnormal ZP:0020633 retinal inner plexiform layer absent, abnormal ZP:0020634 intermediate cell mass of mesoderm absent, abnormal ZP:0020635 hypothalamus increased occurrence apoptotic process, abnormal ZP:0020636 hypothalamus spatial pattern, abnormal ZP:0020637 hypothalamus increased amount, abnormal ZP:0020638 hypothalamus increased occurrence mitotic cell cycle process, abnormal ZP:0020639 caudal hypothalamic zone absent, abnormal ZP:0020640 anterior region hypothalamus decreased amount, abnormal ZP:0020641 anterior region caudal hypothalamic zone mislocalised, abnormal ZP:0020643 hypothalamus decreased occurrence cell population proliferation, abnormal ZP:0020644 anterior region hypothalamus absent, abnormal ZP:0020645 anterior region caudal hypothalamic zone absent, abnormal ZP:0020646 telencephalon mislocalised, abnormal ZP:0020647 skeletal muscle myofibril skeletal muscle broken, abnormal ZP:0020648 sarcomere skeletal muscle structure, abnormal ZP:0020649 Z disc skeletal muscle broken, abnormal ZP:0020650 mitochondrion skeletal muscle infiltrative, abnormal ZP:0020651 splanchnocranium disrupted bone mineralization, abnormal ZP:0020652 epithelium post-vent region blistered, abnormal ZP:0020653 embryonic heart tube formation decreased occurrence, abnormal ZP:0020654 cell migration to the midline involved in heart development decreased occurrence, abnormal ZP:0020655 anterior-posterior axis ventral mandibular arch decreased length, abnormal ZP:0020656 heart contraction decreased efficiency, abnormal ZP:0020657 blood has fewer parts of type hemoglobin complex nucleate erythrocyte, abnormal ZP:0020658 granulocyte migration disrupted, abnormal ZP:0020659 medial region exocrine pancreas aplastic, abnormal ZP:0020660 basement membrane notochord malformed, abnormal ZP:0020661 vacuole notochord malformed, abnormal ZP:0020662 basement membrane notochord vacuolated, abnormal ZP:0020663 posterior region notochord absent, abnormal ZP:0020664 vacuole notochord position, abnormal ZP:0020665 vesicle chondrocyte mislocalised, abnormal ZP:0020666 goblet cell absent, abnormal ZP:0020667 chondrocyte mandibular arch skeleton decreased amount, abnormal ZP:0020668 forebrain process quality neuronal action potential, abnormal ZP:0020669 brain ictal synaptic signaling, abnormal ZP:0020670 posterior lateral plate mesoderm morphology, abnormal ZP:0020671 posterior lateral mesoderm decreased distribution, abnormal ZP:0020672 supramolecular fiber organization disrupted, abnormal ZP:0020673 pronephric glomerulus lacks parts or has fewer parts of type glomerular endothelium fenestra glomerular basement membrane, abnormal ZP:0020674 pronephric tubule atrophied, abnormal ZP:0020675 posterior lateral line primordium malformed, abnormal ZP:0020676 blood vessel endothelial cell common cardinal vein shape, abnormal ZP:0020677 common cardinal vein decreased process quality blood vessel endothelial cell migration, abnormal ZP:0020678 blood vessel endothelial cell common cardinal vein disorganized, abnormal ZP:0020679 cell-cell junction common cardinal vein irregular spatial pattern, abnormal ZP:0020680 cell-cell junction common cardinal vein spatial pattern, abnormal ZP:0020681 intestinal epithelial cell development disrupted, abnormal ZP:0020682 DNA damage response, signal transduction by p53 class mediator process quality, abnormal ZP:0020683 whole organism disrupted cell redox homeostasis, abnormal ZP:0020684 whole organism process quality cell cycle, abnormal ZP:0020685 neural tube process quality cilium assembly, abnormal ZP:0020686 fin regeneration decreased efficacy, abnormal ZP:0020687 regenerating fin decreased occurrence cell population proliferation, abnormal ZP:0020688 post-vent region decreased distribution, abnormal ZP:0020689 head decreased distribution, abnormal ZP:0020690 lateral line system development disrupted, abnormal ZP:0020691 trunk decreased occurrence cell population proliferation, abnormal ZP:0020692 head decreased occurrence cell population proliferation, abnormal ZP:0020693 hematopoietic progenitor cell differentiation disrupted, abnormal ZP:0020694 posterior lateral line neuromast deposition decreased occurrence, abnormal ZP:0020695 chondrocyte pectoral fin decreased amount, abnormal ZP:0020696 cerebellum shape, abnormal ZP:0020697 cilium neural tube absent, abnormal ZP:0020698 hepatocyte proliferation decreased rate, abnormal ZP:0020699 corpuscles of Stannius absent, abnormal ZP:0020700 pronephric proximal convoluted tubule mislocalised, abnormal ZP:0020701 pronephric proximal straight tubule absent, abnormal ZP:0020702 retinal outer nuclear layer temporally extended cell population proliferation, abnormal ZP:0020703 retinal outer nuclear layer increased occurrence apoptotic process, abnormal ZP:0020704 retinal rod cell increased occurrence cell population proliferation, abnormal ZP:0020705 retinal ganglion cell layer increased occurrence apoptotic process, abnormal ZP:0020706 retinal inner nuclear layer increased occurrence apoptotic process, abnormal ZP:0020707 oligodendrocyte brain decreased amount, abnormal ZP:0020708 oligodendrocyte midbrain decreased amount, abnormal ZP:0020709 cell projection oligodendrocyte decreased length, abnormal ZP:0020710 noradrenaline brain decreased amount, abnormal ZP:0020711 serotonin brain decreased amount, abnormal ZP:0020712 (5-hydroxyindol-3-yl)acetic acid brain increased amount, abnormal ZP:0020713 dopamine brain decreased amount, abnormal ZP:0020714 melanocyte caudal fin decreased pigmentation, abnormal ZP:0020715 mitochondrial inner membrane skeletal muscle broken, abnormal ZP:0020716 mitochondrial membrane skeletal muscle swollen, abnormal ZP:0020717 Mauthner neuron amplitude excitatory postsynaptic potential, abnormal ZP:0020718 neuromast hair cell disorganized, abnormal ZP:0020719 stereocilium auditory receptor cell decreased amount, abnormal ZP:0020720 neuromast hair cell posterior lateral line apoptotic, abnormal ZP:0020721 neuromast hair cell lateral line decreased amount, abnormal ZP:0020722 neuromast hair cell anterior lateral line apoptotic, abnormal ZP:0020723 whole organism decreased process quality manganese ion homeostasis, abnormal ZP:0020724 brain decreased process quality manganese ion homeostasis, abnormal ZP:0020725 hemoglobin biosynthetic process decreased occurrence, abnormal ZP:0020726 statoacoustic (VIII) ganglion decreased amount, abnormal ZP:0020727 dorsal region diencephalon decreased amount, abnormal ZP:0020728 anterior lateral line ganglion absent, abnormal ZP:0020729 interneuromast cell spatial pattern, abnormal ZP:0020730 midbrain hindbrain boundary decreased amount, abnormal ZP:0020731 telencephalon decreased amount, abnormal ZP:0020732 otic vesicle lacks parts or has fewer parts of type cilium otic epithelium, abnormal ZP:0020733 gall bladder hypoplastic, abnormal ZP:0020734 pharyngeal arch 3-7 delayed embryonic viscerocranium morphogenesis, abnormal ZP:0020735 heart tube decreased distribution, abnormal ZP:0020736 fast muscle cell increased distribution, abnormal ZP:0020737 slow muscle cell increased distribution, abnormal ZP:0020738 presumptive cardiac ventricle heart tube decreased distribution, abnormal ZP:0020739 embryonic cranial skeleton morphogenesis decreased process quality, abnormal ZP:0020740 terminal nerve decreased length, abnormal ZP:0020741 fast muscle cell decreased process quality neuromuscular synaptic transmission, abnormal ZP:0020742 synaptic cleft fast muscle cell decreased width, abnormal ZP:0020743 CaP motoneuron decreased process quality axon extension involved in axon guidance, abnormal ZP:0020744 neuromuscular junction fast muscle cell decreased width, abnormal ZP:0020745 fast muscle cell decreased process quality neuromuscular junction development, abnormal ZP:0020746 neural tube absent, abnormal ZP:0020747 dorso-lateral region hindbrain decreased distribution, abnormal ZP:0020748 ventral region diencephalon decreased amount, abnormal ZP:0020749 axial region hindbrain decreased amount, abnormal ZP:0020750 ventral region diencephalon decreased distribution, abnormal ZP:0020751 ventral region spinal cord absent, abnormal ZP:0020752 chondrocyte absent, abnormal ZP:0020753 spermine biosynthetic process decreased occurrence, abnormal ZP:0020754 skeletal muscle spatial pattern, abnormal ZP:0020755 common myeloid progenitor increased amount, abnormal ZP:0020756 lysosome macrophage increased size, abnormal ZP:0020757 macrophage increased size, abnormal ZP:0020758 lateral plate mesoderm increased amount, abnormal ZP:0020759 subcutaneous fat decreased amount, abnormal ZP:0020760 regulation of protein kinase B signaling disrupted, abnormal ZP:0020761 blood plasma increased amount, abnormal ZP:0020762 male organism has extra parts of type lipid droplet liver, abnormal ZP:0020763 whole organism increased rate growth, abnormal ZP:0020764 blood plasma decreased process quality response to insulin, abnormal ZP:0020765 liver decreased process quality cellular response to insulin stimulus, abnormal ZP:0020766 liver decreased process quality cellular response to glucagon stimulus, abnormal ZP:0020767 female organism has extra parts of type lipid droplet liver, abnormal ZP:0020768 whole organism decreased rate growth, abnormal ZP:0020769 liver disrupted regulation of tyrosine phosphorylation of STAT protein, abnormal ZP:0020770 chondrocyte pharyngeal arch decreased amount, abnormal ZP:0020771 blood vessel endothelium posterior cardinal vein decreased amount, abnormal ZP:0020772 blood vessel endothelium dorsal aorta decreased amount, abnormal ZP:0020773 left-right axis roof plate rhombomere region decreased width, abnormal ZP:0020774 adipose tissue development decreased process quality, abnormal ZP:0020775 nucleus fast muscle cell absent, abnormal ZP:0020776 lipid droplet pleuroperitoneal cavity decreased amount, abnormal ZP:0020777 fast muscle cell process quality calcium-mediated signaling, abnormal ZP:0020778 lipid droplet pleuroperitoneal cavity decreased size, abnormal ZP:0020779 rib broken, abnormal ZP:0020780 parasphenoid deformed, abnormal ZP:0020781 ossification involved in bone maturation process quality, abnormal ZP:0020782 cleithrum decreased distribution, abnormal ZP:0020783 skeletal system decreased process quality bone mineralization, abnormal ZP:0020784 nucleus osteoblast composition, abnormal ZP:0020785 cranium decreased process quality bone mineralization, abnormal ZP:0020786 ceratobranchial 5 primary tooth decreased process quality tooth mineralization, abnormal ZP:0020787 cranium has extra parts of type bone element, abnormal ZP:0020788 cranial suture morphogenesis disrupted, abnormal ZP:0020789 bone development delayed, abnormal ZP:0020790 vertebral column decreased process quality bone mineralization, abnormal ZP:0020791 cranial vault morphology, abnormal ZP:0020792 vertebra size, abnormal ZP:0020793 fibrous joint cranium increased amount, abnormal ZP:0020794 cranium domed, abnormal ZP:0020795 nucleus osteoblast circular, abnormal ZP:0020796 spinal cord disrupted microtubule cytoskeleton organization, abnormal ZP:0020797 primary motor neuron process quality axonogenesis, abnormal ZP:0020798 whole organism arched, abnormal ZP:0020799 axon microtubule bundle motor neuron decreased diameter, abnormal ZP:0020800 microtubule cytoskeleton spinal cord disorganized, abnormal ZP:0020801 lateral plate mesoderm absent, abnormal ZP:0020802 neural crest cell decreased occurrence cell population proliferation, abnormal ZP:0020803 palate shortened, abnormal ZP:0020804 anatomical structure apoptotic, abnormal ZP:0020805 DNA damage response, detection of DNA damage disrupted, abnormal ZP:0020806 xanthophore integument mislocalised, abnormal ZP:0020807 spermidine biosynthetic process decreased occurrence, abnormal ZP:0020808 tooth placode absent, abnormal ZP:0020809 tooth placode spatial pattern, abnormal ZP:0020810 tooth placode decreased amount, abnormal ZP:0020811 mitotic cell cycle, embryonic decreased occurrence, abnormal ZP:0020813 bone tissue decreased volume, abnormal ZP:0020814 anterior-posterior axis somite decreased length, abnormal ZP:0020815 cell whole organism decreased distribution, abnormal ZP:0020816 cell notochord increased area, abnormal ZP:0020817 cell notochord decreased length, abnormal ZP:0020818 cell notochord increased width, abnormal ZP:0020820 spinal cord increased occurrence mitotic cell cycle, abnormal ZP:0020821 lactate biosynthetic process increased occurrence, abnormal ZP:0020822 vasculature increased size, abnormal ZP:0020823 blood vessel dilated, abnormal ZP:0020824 anterior region head shortened, abnormal ZP:0020825 whole organism decreased process quality metabolic process, abnormal ZP:0020826 locomotor rhythm disrupted, abnormal ZP:0020827 forebrain electric potential, abnormal ZP:0020828 hematopoietic multipotent progenitor cell decreased occurrence cell population proliferation, abnormal ZP:0020829 thrombocyte intermediate cell mass of mesoderm decreased amount, abnormal ZP:0020830 late endosome retinal cone cell morphology, abnormal ZP:0020831 autophagosome retinal cone cell increased amount, abnormal ZP:0020832 late endosome retinal cone cell increased size, abnormal ZP:0020833 optic tectum decreased area, abnormal ZP:0020834 cranial neural crest cell disorganized, abnormal ZP:0020835 splanchnocranium immature, abnormal ZP:0020836 chondrocyte ceratobranchial cartilage absent, abnormal ZP:0020837 ceratobranchial cartilage disorganized, abnormal ZP:0020838 branching involved in blood vessel morphogenesis increased occurrence, abnormal ZP:0020839 brain vasculature increased branchiness, abnormal ZP:0020840 vasculature aortic arch dilated, abnormal ZP:0020841 whole organism lacks all parts of type heart, abnormal ZP:0020842 whole organism lacks all parts of type head, abnormal ZP:0020843 heart primordium anterior lateral plate mesoderm decreased amount, abnormal ZP:0020844 branchiomotor neuron decreased amount, abnormal ZP:0020845 heart tube decreased size, abnormal ZP:0020846 hypophysis decreased amount, abnormal ZP:0020847 corpuscles of Stannius increased distribution, abnormal ZP:0020848 cell corpuscles of Stannius increased amount, abnormal ZP:0020849 posterior region pronephros decreased distribution, abnormal ZP:0020850 blue sensitive photoreceptor cell retina decreased amount, abnormal ZP:0020851 parapineal organ has fewer parts of type neuron parapineal organ, abnormal ZP:0020852 foraging behavior decreased efficacy, abnormal ZP:0020853 UV sensitive photoreceptor cell retina increased amount, abnormal ZP:0020854 parapineal organ decreased occurrence neuron fate specification, abnormal ZP:0020855 embryonic pelvic fin morphogenesis arrested, abnormal ZP:0020856 pelvic fin bud arrested apical ectodermal ridge formation, abnormal ZP:0020857 hindlimb morphogenesis arrested, abnormal ZP:0020858 pelvic fin morphogenesis arrested, abnormal ZP:0020859 pelvic fin bud lacks all parts of type apical ectodermal ridge pelvic fin bud, abnormal ZP:0020860 embryonic hindlimb morphogenesis arrested, abnormal ZP:0020861 whole organism lacks all parts of type pelvic fin, abnormal ZP:0020862 mesenchyme pelvic fin bud absent, abnormal ZP:0020863 mesenchyme pelvic fin bud increased distribution, abnormal ZP:0020864 somite irregularly shaped, abnormal ZP:0020865 trunk has fewer parts of type central region dermomyotome, abnormal ZP:0020866 paraxial mesoderm decreased amount, abnormal ZP:0020867 head muscle aplastic/hypoplastic, abnormal ZP:0020868 hypobranchial artery detached from lateral dorsal aorta, abnormal ZP:0020869 hypobranchial artery shape, abnormal ZP:0020870 interhyoideus hypoplastic, abnormal ZP:0020871 intermandibularis hypoplastic, abnormal ZP:0020872 hypobranchial artery absent, abnormal ZP:0020873 aortic arch 4 decreased occurrence blood vessel lumenization, abnormal ZP:0020874 aortic arch 3 decreased occurrence blood vessel lumenization, abnormal ZP:0020875 pharyngeal vasculature absent, abnormal ZP:0020876 aortic arch 4 decreased amount, abnormal ZP:0020877 aortic arch 6 decreased amount, abnormal ZP:0020878 aortic arch 6 arrested blood vessel lumenization, abnormal ZP:0020879 aortic arch 5 decreased amount, abnormal ZP:0020880 nucleus thalamus absent, abnormal ZP:0020881 neuron thalamus absent, abnormal ZP:0020882 germ ring absent, abnormal ZP:0020883 dorsal region margin absent, abnormal ZP:0020884 larval heart development decreased process quality, abnormal ZP:0020885 neural tube closure decreased occurrence, abnormal ZP:0020886 lens fused with lens, abnormal ZP:0020887 pineal complex shape, abnormal ZP:0020888 pineal complex split bilaterally, abnormal ZP:0020889 neural plate process quality cell migration, abnormal ZP:0020890 axon notochord morphology, abnormal ZP:0020891 peripheral nervous system disrupted axonogenesis involved in innervation, abnormal ZP:0020892 muscle increased amount, abnormal ZP:0020893 head kidney increased amount, abnormal ZP:0020894 chromosome, telomeric region muscle decreased length, abnormal ZP:0020895 age-dependent general metabolic decline physiological state, abnormal ZP:0020896 chromosome, telomeric region gut decreased length, abnormal ZP:0020897 intestinal lamina propria mucosa increased occurrence leukocyte migration involved in inflammatory response, abnormal ZP:0020899 muscle cell atrophied, abnormal ZP:0020900 testis decreased occurrence cell population proliferation, abnormal ZP:0020901 chromosome, telomeric region testis decreased length, abnormal ZP:0020902 gut increased amount, abnormal ZP:0020903 neoplasm whole organism increased amount, abnormal ZP:0020904 muscle cell degeneration, abnormal ZP:0020905 whole organism degeneration, abnormal ZP:0020906 head kidney decreased occurrence cell population proliferation, abnormal ZP:0020907 gut decreased occurrence cell population proliferation, abnormal ZP:0020908 trunk decreased amount, abnormal ZP:0020909 circulating cell decreased amount, abnormal ZP:0020910 posterior lateral line neuromast irregular spatial pattern, abnormal ZP:0020911 endothelial cell trunk increased amount, abnormal ZP:0020912 caudal vein plexus increased occurrence apoptotic process, abnormal ZP:0020913 dorsal longitudinal anastomotic vessel decreased occurrence blood vessel development, abnormal ZP:0020914 ventral region somite absent, abnormal ZP:0020915 somite border blurry, abnormal ZP:0020916 proximal region pronephric duct absent, abnormal ZP:0020917 hypophysis increased distribution, abnormal ZP:0020918 pronephric duct decreased amount, abnormal ZP:0020919 cell hypophysis decreased volume, abnormal ZP:0020920 whole organism has fewer parts of type thyroid follicle, abnormal ZP:0020921 cell thyroid follicle decreased volume, abnormal ZP:0020922 thyroid follicle decreased distribution, abnormal ZP:0020923 mandibular arch skeleton has fewer parts of type cartilage element, abnormal ZP:0020924 thyroid follicle increased amount, abnormal ZP:0020925 cell thyroid follicle increased amount, abnormal ZP:0020926 thyroid follicle hyperplastic, abnormal ZP:0020927 thyroid follicle increased distribution, abnormal ZP:0020928 thyroid follicle increased size, abnormal ZP:0020929 cell hypophysis increased volume, abnormal ZP:0020930 UV sensitive photoreceptor cell increased amount, abnormal ZP:0020931 whole organism lacks parts or has fewer parts of type semicircular canal, abnormal ZP:0020932 synapse horizontal cell increased amount, abnormal ZP:0020933 cell thyroid follicle increased volume, abnormal ZP:0020934 whole organism has extra parts of type thyroid follicle, abnormal ZP:0020935 whole organism lacks parts or has fewer parts of type otolith, abnormal ZP:0020936 axon RoP motor neuron absent, abnormal ZP:0020937 RoP motor neuron decreased occurrence axon development, abnormal ZP:0020938 parachordal vessel decreased occurrence angiogenesis, abnormal ZP:0020939 cell projection endothelial tip cell morphology, abnormal ZP:0020940 MiP motor neuron process quality axon development, abnormal ZP:0020941 axon MiP motor neuron morphology, abnormal ZP:0020942 axon RoP motor neuron morphology, abnormal ZP:0020943 secondary motor neuron process quality axon development, abnormal ZP:0020944 xanthophore displaced to melanophore stripe, abnormal ZP:0020945 iridophore behavioral quality, abnormal ZP:0020946 iridophore displaced to melanophore stripe, abnormal ZP:0020947 iridophore structure, abnormal ZP:0020948 endocardium separated from myocardium, abnormal ZP:0020949 optic furrow disrupted basement membrane disassembly, abnormal ZP:0020951 filamentous actin vascular endothelium decreased amount, abnormal ZP:0020952 heart decreased volume, abnormal ZP:0020953 basement membrane optic furrow increased distribution, abnormal ZP:0020954 hyaloid vessel decreased distribution, abnormal ZP:0020955 hyaloid vessel hypotrophic, abnormal ZP:0020956 subintestinal vein disrupted blood vessel morphogenesis, abnormal ZP:0020957 muscle tendon junction skeletal muscle decreased amount, abnormal ZP:0020958 hyaluronic acid posterior cardinal vein increased amount, abnormal ZP:0020959 muscle tendon junction skeletal muscle disorganized, abnormal ZP:0020960 extracellular matrix skeletal muscle disorganized, abnormal ZP:0020961 fast muscle cell detached from muscle tendon junction trunk musculature, abnormal ZP:0020962 skeletal muscle cell detached from trunk musculature, abnormal ZP:0020963 muscle tendon junction skeletal muscle spatial pattern, abnormal ZP:0020964 protein complex involved in cell-matrix adhesion skeletal muscle disorganized, abnormal ZP:0020965 slow muscle cell detached from trunk musculature, abnormal ZP:0020966 endothelial cell dorsal aorta decreased distribution, abnormal ZP:0020967 hyaluronic acid dorsal aorta increased amount, abnormal ZP:0020968 extracellular matrix myocardium spatial pattern, abnormal ZP:0020969 skeletal muscle cell detached from muscle tendon junction trunk musculature, abnormal ZP:0020970 dystroglycan complex skeletal muscle disorganized, abnormal ZP:0020971 fast muscle cell detached from trunk musculature, abnormal ZP:0020972 myocardium spatial pattern, abnormal ZP:0020973 extracellular matrix myocardium disorganized, abnormal ZP:0020974 slow muscle cell detached from muscle tendon junction trunk musculature, abnormal ZP:0020975 endothelial cell posterior cardinal vein decreased distribution, abnormal ZP:0020976 cell pronephric glomerulus decreased amount, abnormal ZP:0020977 podocyte foot pronephric podocyte decreased amount, abnormal ZP:0020978 proximal convoluted tubule morphology, abnormal ZP:0020979 neuron intertectal commissure decreased amount, abnormal ZP:0020980 sarcolemma myotome broken, abnormal ZP:0020981 regulation of tyrosine phosphorylation of STAT protein disrupted, abnormal ZP:0020982 melanocyte stimulating hormone secreting cell pars intermedia decreased amount, abnormal ZP:0020983 trabecular layer cardiac ventricle absent, abnormal ZP:0020984 heart decreased process quality Notch signaling pathway, abnormal ZP:0020985 cardiac muscle cell decreased process quality Notch signaling pathway, abnormal ZP:0020986 endothelial cell decreased accumulation atrioventricular valve, abnormal ZP:0020987 hematopoietic stem cell homeostasis decreased process quality, abnormal ZP:0020988 double-strand break repair via nonhomologous end joining increased frequency, abnormal ZP:0020989 double-strand break repair via single-strand annealing increased frequency, abnormal ZP:0020990 eye ovate, abnormal ZP:0020991 anatomical surface retina decreased area, abnormal ZP:0020992 microtubule polymerization decreased rate, abnormal ZP:0020993 response to endoplasmic reticulum stress increased occurrence, abnormal ZP:0020994 N-glycan whole organism decreased amount, abnormal ZP:0020995 liver increased accumulation lipid droplet liver, abnormal ZP:0020996 cholesterol homeostasis disrupted, abnormal ZP:0020997 lipooligosaccharide whole organism decreased amount, abnormal ZP:0020998 endoplasmic reticulum hepatocyte distended, abnormal ZP:0020999 Golgi apparatus hepatocyte broken, abnormal ZP:0021000 tRNA processing disrupted, abnormal ZP:0021001 serotonergic neuron pretectum increased amount, abnormal ZP:0021002 sarcomere myotome spatial pattern, abnormal ZP:0021003 Z disc somite disorganized, abnormal ZP:0021004 sarcomere somite disorganized, abnormal ZP:0021005 sarcomere cardiac muscle disorganized, abnormal ZP:0021006 sarcomere somite decreased length, abnormal ZP:0021007 sarcomere somite spatial pattern, abnormal ZP:0021008 myofibril slow muscle cell damaged, abnormal ZP:0021009 Z disc somite spatial pattern, abnormal ZP:0021010 melanocyte whole organism absent, abnormal ZP:0021011 whole organism has extra parts of type Rohon-Beard neuron, abnormal ZP:0021012 epithelium optic vesicle disorganized, abnormal ZP:0021013 epithelium optic vesicle morphology, abnormal ZP:0021014 retinal cone cell photoreceptor outer segment layer decreased amount, abnormal ZP:0021015 artery trunk vasculature increased amount, abnormal ZP:0021016 trunk vasculature decreased amount, abnormal ZP:0021017 endothelial tip cell decreased rate blood vessel endothelial cell migration, abnormal ZP:0021018 hindbrain atrophied, abnormal ZP:0021019 motile cilium floor plate disoriented, abnormal ZP:0021020 pronephric podocyte decreased length, abnormal ZP:0021021 protein blood decreased amount, abnormal ZP:0021022 pronephric podocyte increased width, abnormal ZP:0021023 squamous epithelial cell epicardium morphology, abnormal ZP:0021024 cell epicardium decreased size, abnormal ZP:0021025 epicardium increased amount, abnormal ZP:0021026 pleuroperitoneal cavity fluid-filled, abnormal ZP:0021027 blood vessel heart vasculature disorganized, abnormal ZP:0021028 endothelial cell endocardium increased amount, abnormal ZP:0021029 endocardium increased amount, abnormal ZP:0021030 squamous epithelial cell epicardium ovate, abnormal ZP:0021031 heart vasculature increased amount, abnormal ZP:0021032 fibroblast accumulation epicardium, abnormal ZP:0021033 epicardium hemorrhagic, abnormal ZP:0021034 cardiac ventricle spherical, abnormal ZP:0021036 blood vessel heart vasculature increased amount, abnormal ZP:0021037 blood vessel heart vasculature disconnected, abnormal ZP:0021038 epicardium increased occurrence cell population proliferation, abnormal ZP:0021039 membrane epicardium smooth, abnormal ZP:0021040 endocardium increased occurrence cell population proliferation, abnormal ZP:0021041 myocardium increased occurrence cell population proliferation, abnormal ZP:0021042 motor behavior disrupted, abnormal ZP:0021043 vasculature decreased amount, abnormal ZP:0021044 whole organism lacks all parts of type anterior mesencephalic central artery, abnormal ZP:0021045 whole organism lacks all parts of type central artery, abnormal ZP:0021046 cardiac ventricle increased amount, abnormal ZP:0021047 dorsal aorta decreased amount, abnormal ZP:0021048 basilar artery morphology, abnormal ZP:0021049 whole organism lacks all parts of type cerebellar central artery, abnormal ZP:0021050 whole organism lacks all parts of type posterior mesencephalic central artery, abnormal ZP:0021051 heart decreased process quality regeneration, abnormal ZP:0021052 whole organism lacks all parts of type axial blood vessel, abnormal ZP:0021053 whole organism lacks all parts of type intersegmental vessel, abnormal ZP:0021054 whole organism lacks all parts of type middle mesencephalic central artery, abnormal ZP:0021055 whole organism lacks all parts of type basilar artery, abnormal ZP:0021056 nucleate erythrocyte brain aggregated, abnormal ZP:0021057 hindbrain disrupted vasculature development, abnormal ZP:0021058 midbrain disrupted vasculature development, abnormal ZP:0021059 thoracic duct decreased amount, abnormal ZP:0021060 facial lymphatic vessel decreased occurrence lymphangiogenesis, abnormal ZP:0021061 lymphangioblast cord decreased occurrence lymph vessel development, abnormal ZP:0021062 pronephric proximal straight tubule increased diameter, abnormal ZP:0021063 ciliated epithelial cell pronephric proximal straight tubule disorganized, abnormal ZP:0021064 epithelial cell pronephric proximal straight tubule decreased amount, abnormal ZP:0021065 pronephric proximal straight tubule increased occurrence cell population proliferation, abnormal ZP:0021066 pronephric duct curved, abnormal ZP:0021067 pronephric glomerulus swollen, abnormal ZP:0021068 subintestinal vein spatial pattern, abnormal ZP:0021069 pronephric proximal convoluted tubule increased occurrence cell population proliferation, abnormal ZP:0021070 pronephric tubule curved, abnormal ZP:0021071 cytoplasmic vesicle pronephric proximal straight tubule increased amount, abnormal ZP:0021072 ciliated epithelial cell pronephric proximal convoluted tubule disorganized, abnormal ZP:0021073 bicellular tight junction pronephric glomerulus decreased amount, abnormal ZP:0021074 pronephric proximal straight tubule apical-basal polarity, abnormal ZP:0021075 pronephric glomerulus atrophied, abnormal ZP:0021076 pronephric proximal straight tubule increased occurrence apoptotic process, abnormal ZP:0021077 podocyte increased amount, abnormal ZP:0021078 respiratory gaseous exchange by respiratory system increased occurrence, abnormal ZP:0021079 regulation of respiratory gaseous exchange increased occurrence, abnormal ZP:0021080 epithelial cell pronephric proximal convoluted tubule decreased amount, abnormal ZP:0021081 pronephric proximal convoluted tubule apical-basal polarity, abnormal ZP:0021082 cytoplasmic vesicle pronephric proximal convoluted tubule increased amount, abnormal ZP:0021083 pronephros shape, abnormal ZP:0021084 oligodendrocyte hindbrain decreased distribution, abnormal ZP:0021085 lysosome hepatocyte decreased amount, abnormal ZP:0021086 bile canaliculus distended, abnormal ZP:0021087 bile canaliculus obstructed, abnormal ZP:0021088 vacuole hepatocyte increased amount, abnormal ZP:0021089 microvillus bile canaliculus decreased length, abnormal ZP:0021090 pigment granule retina sparse, abnormal ZP:0021091 pigment granule integument sparse, abnormal ZP:0021092 microvillus bile canaliculus sparse, abnormal ZP:0021093 regulation of odontogenesis disrupted, abnormal ZP:0021094 telencephalon diencephalon boundary malformed, abnormal ZP:0021095 ventral thalamus decreased process quality forebrain morphogenesis, abnormal ZP:0021096 ventral telencephalon mislocalised, abnormal ZP:0021097 forebrain lacks all parts of type supraoptic tract, abnormal ZP:0021098 dorsal telencephalon decreased process quality forebrain morphogenesis, abnormal ZP:0021099 brain increased occurrence BMP signaling pathway, abnormal ZP:0021100 brain increased occurrence astrocyte development, abnormal ZP:0021101 brain decreased occurrence oligodendrocyte development, abnormal ZP:0021102 ventral thalamus decreased amount, abnormal ZP:0021103 ventral telencephalon decreased amount, abnormal ZP:0021104 dorsal region brain increased amount, abnormal ZP:0021105 ventral telencephalon decreased process quality forebrain morphogenesis, abnormal ZP:0021106 forebrain decreased process quality GABAergic neuron differentiation, abnormal ZP:0021107 postoptic commissure decreased occurrence central nervous system projection neuron axonogenesis, abnormal ZP:0021108 forebrain lacks all parts of type postoptic commissure, abnormal ZP:0021109 diencephalon decreased amount, abnormal ZP:0021110 anterior commissure decreased occurrence central nervous system projection neuron axonogenesis, abnormal ZP:0021111 supraoptic tract decreased occurrence central nervous system projection neuron axonogenesis, abnormal ZP:0021112 ventral thalamus increased amount, abnormal ZP:0021113 GABAergic neuron ventral telencephalon decreased amount, abnormal ZP:0021114 GABAergic neuron diencephalon decreased amount, abnormal ZP:0021115 telencephalon increased amount, abnormal ZP:0021116 GABAergic neuron nucleus of the tract of the postoptic commissure decreased amount, abnormal ZP:0021117 astrocyte brain increased amount, abnormal ZP:0021118 diencephalon absent, abnormal ZP:0021119 epithalamus decreased distribution, abnormal ZP:0021120 habenula decreased amount, abnormal ZP:0021121 pharyngeal pouch 2 decreased object quality, abnormal ZP:0021122 pharyngeal pouch 1 decreased object quality, abnormal ZP:0021123 ventral habenular nucleus absent, abnormal ZP:0021124 pharyngeal arch decreased process quality cartilage development, abnormal ZP:0021125 dorsal habenular nucleus decreased distribution, abnormal ZP:0021126 habenula decreased distribution, abnormal ZP:0021127 dorsal habenular nucleus decreased amount, abnormal ZP:0021128 dorsal region diencephalon absent, abnormal ZP:0021129 Meckel's cartilage dislocated, abnormal ZP:0021130 pharyngeal arch decreased occurrence Wnt protein secretion, abnormal ZP:0021131 ceratohyal cartilage dislocated, abnormal ZP:0021132 hematopoietic stem cell arrested mitotic G1 phase, abnormal ZP:0021133 response to mechanical stimulus decreased occurrence, abnormal ZP:0021134 hair cell has fewer parts of type cytoskeleton of presynaptic active zone synaptic vesicle hair cell, abnormal ZP:0021135 neuromast decreased distribution, abnormal ZP:0021136 hair cell decreased process quality presynaptic active zone organization, abnormal ZP:0021137 basolateral plasma membrane neuromast hair cell decreased amount, abnormal ZP:0021138 cytoskeleton of presynaptic active zone retinal cone cell decreased amount, abnormal ZP:0021139 cytoskeleton of presynaptic active zone retinal cone cell decreased size, abnormal ZP:0021140 ON-bipolar cell decreased process quality synaptic transmission, glutamatergic, abnormal ZP:0021141 detection of mechanical stimulus involved in sensory perception of sound decreased occurrence, abnormal ZP:0021142 retinal outer plexiform layer decreased process quality modulation of chemical synaptic transmission, abnormal ZP:0021143 macula saccule has fewer parts of type hair cell synaptic vesicle hair cell, abnormal ZP:0021144 response to auditory stimulus decreased occurrence, abnormal ZP:0021145 retinal cone cell decreased process quality synaptic transmission, glutamatergic, abnormal ZP:0021146 lateral crista has fewer parts of type hair cell ribbon synapse hair cell, abnormal ZP:0021147 detection of light stimulus involved in sensory perception decreased process quality, abnormal ZP:0021148 hair cell has fewer parts of type ribbon synapse synaptic vesicle hair cell, abnormal ZP:0021149 retinal outer plexiform layer decreased amount, abnormal ZP:0021150 retinal photoreceptor layer has fewer parts of type eye photoreceptor cell, abnormal ZP:0021151 hair cell inner ear decreased distribution, abnormal ZP:0021152 basolateral plasma membrane hair cell decreased amount, abnormal ZP:0021153 proepicardial cluster decreased amount, abnormal ZP:0021154 podocyte foot podocyte flattened, abnormal ZP:0021155 somite mislocalised, abnormal ZP:0021156 pronephric glomerulus decreased amount, abnormal ZP:0021157 cell atrioventricular canal morphology, abnormal ZP:0021158 determination of heart left/right asymmetry decreased occurrence, abnormal ZP:0021159 ciliary basal body proepicardial cluster absent, abnormal ZP:0021160 atrial myocardium separated from ventricular endocardium, abnormal ZP:0021161 atrioventricular valve development decreased occurrence, abnormal ZP:0021162 atrial myocardium decreased thickness, abnormal ZP:0021163 atrioventricular canal development decreased process quality, abnormal ZP:0021164 atrial myocardium separated from ventricular myocardium, abnormal ZP:0021165 posterior lateral line primordium has fewer parts of type cell posterior lateral line primordium, abnormal ZP:0021166 posterior pronephric duct morphology, abnormal ZP:0021167 dorsal longitudinal anastomotic vessel constricted, abnormal ZP:0021168 distal region pronephric tubule dilated, abnormal ZP:0021169 cerebellar central artery constricted, abnormal ZP:0021170 eye closure incomplete, abnormal ZP:0021171 single ciliated epithelial cell pronephric duct decreased amount, abnormal ZP:0021172 pronephric duct broken, abnormal ZP:0021173 angiogenic sprout lateral dorsal aorta increased amount, abnormal ZP:0021174 cloaca disorganized, abnormal ZP:0021175 proximal region pronephric tubule dilated, abnormal ZP:0021176 pronephric duct decreased process quality establishment or maintenance of cell polarity, abnormal ZP:0021177 cloaca atretic, abnormal ZP:0021178 embryo development increased duration, abnormal ZP:0021179 deoxyribonucleic acid whole organism increased amount, abnormal ZP:0021180 RNA catabolic process process quality, abnormal ZP:0021181 apoptotic cell clearance disrupted, abnormal ZP:0021182 heart increased length, abnormal ZP:0021183 whole organism decreased distribution, abnormal ZP:0021184 brain decreased distribution, abnormal ZP:0021185 atrium absent, abnormal ZP:0021186 cortical granule oocyte increased size, abnormal ZP:0021188 oocyte growth arrested, abnormal ZP:0021190 ovary increased process quality apoptotic process, abnormal ZP:0021191 cortical granule oocyte decreased amount, abnormal ZP:0021192 ventral fin fold decreased thickness, abnormal ZP:0021193 presumptive ventral mesoderm decreased distribution, abnormal ZP:0021194 somite distended, abnormal ZP:0021195 ventral region presumptive ectoderm decreased distribution, abnormal ZP:0021196 dorsal region mesoderm increased distribution, abnormal ZP:0021197 central nervous system decreased amount, abnormal ZP:0021198 oligodendrocyte decreased distribution, abnormal ZP:0021199 central region retina mislocalised, abnormal ZP:0021200 multi fate stem cell retina spatial pattern, abnormal ZP:0021201 retinal bipolar neuron increased distribution, abnormal ZP:0021202 nucleus retinal bipolar neuron absent, abnormal ZP:0021203 central region retina spatial pattern, abnormal ZP:0021204 midbrain mislocalised, abnormal ZP:0021205 neuron hindbrain spatial pattern, abnormal ZP:0021206 neuroblast retina spatial pattern, abnormal ZP:0021207 cell ciliary marginal zone spatial pattern, abnormal ZP:0021208 cell ciliary marginal zone increased distribution, abnormal ZP:0021209 neuroblast retina increased amount, abnormal ZP:0021210 multi fate stem cell retina increased amount, abnormal ZP:0021211 regulation of gene silencing disrupted, abnormal ZP:0021212 midbrain spatial pattern, abnormal ZP:0021213 retinal bipolar neuron spatial pattern, abnormal ZP:0021214 Kupffer's vesicle lacks all parts of type motile cilium Kupffer's vesicle, abnormal ZP:0021215 forerunner cell group decreased distribution, abnormal ZP:0021216 motile cilium pronephros decreased amount, abnormal ZP:0021217 pronephric glomerulus absent, abnormal ZP:0021221 skeletal muscle cell spatial pattern, abnormal ZP:0021269 otic vesicle decreased area, abnormal ZP:0021272 sagitta decreased area, abnormal ZP:0021278 swim bladder increased amount, abnormal ZP:0021301 male organism decreased life span, abnormal ZP:0021305 glucose blood increased amount, abnormal ZP:0021307 scale increased occurrence bone resorption, abnormal ZP:0021312 blood island decreased distribution, abnormal ZP:0021321 neutrophil chemotaxis decreased occurrence, abnormal ZP:0021328 otic vesicle increased distribution, abnormal ZP:0021329 solid lens vesicle absent, abnormal ZP:0021337 otic placode increased distribution, abnormal ZP:0021345 neurocranial trabecula decreased distribution, abnormal ZP:0021346 male organism decreased amount, abnormal ZP:0021358 otic vesicle process quality cilium assembly, abnormal ZP:0021359 whole organism decreased occurrence cholesterol biosynthetic process, abnormal ZP:0021360 whole organism decreased occurrence TOR signaling, abnormal ZP:0021361 myelin sheath spinal cord decreased thickness, abnormal ZP:0021363 segmental plate decreased amount, abnormal ZP:0021389 sleep occurrence, abnormal ZP:0021390 corpuscles of Stannius decreased distribution, abnormal ZP:0021393 hematopoietic stem cell intermediate cell mass of mesoderm increased amount, abnormal ZP:0021406 macrophage head increased amount, abnormal ZP:0021437 female organism female fertility, abnormal ZP:0021440 vertebral column curvature, abnormal ZP:0021443 posterior lateral line primordium increased amount, abnormal ZP:0021445 gill increased amount, abnormal ZP:0021446 intestine increased amount, abnormal ZP:0021478 neural crest cell aggregated, abnormal ZP:0021479 endosome neural crest cell immature, abnormal ZP:0021480 early endosome neural crest cell increased amount, abnormal ZP:0021481 early endosome neural crest cell increased size, abnormal ZP:0021482 early endosome neural crest cell aggregated, abnormal ZP:0021483 late endosome neural crest cell decreased size, abnormal ZP:0021484 late endosome neural crest cell decreased amount, abnormal ZP:0021485 neural crest cell process quality endocytosis, abnormal ZP:0021492 parasphenoid absent, abnormal ZP:0021496 calcium-mediated signaling decreased process quality, abnormal ZP:0021502 embryonic viscerocranium morphogenesis decreased occurrence, abnormal ZP:0021503 cranial skeletal system development decreased occurrence, abnormal ZP:0021514 liver spatial pattern, abnormal ZP:0021517 oligodendrocyte decreased occurrence TOR signaling, abnormal ZP:0021553 forebrain increased amount, abnormal ZP:0021573 microtubule yolk irregular spatial pattern, abnormal ZP:0021574 microtubule yolk disoriented, abnormal ZP:0021580 visual perception increased process quality, abnormal ZP:0021589 scale increased amount, abnormal ZP:0021601 thigmotaxis increased occurrence, abnormal ZP:0021629 DNA methylation increased occurrence, abnormal ZP:0021632 digestive system increased amount, abnormal ZP:0021651 glucose blood plasma increased amount, abnormal ZP:0021659 intermediate cell mass of mesoderm increased amount, abnormal ZP:0021663 myeloid cell increased occurrence cell population proliferation, abnormal ZP:0021666 lymphocyte head kidney decreased amount, abnormal ZP:0021671 myeloblast blood increased amount, abnormal ZP:0021672 myeloblast head kidney increased amount, abnormal ZP:0021674 granulocyte kidney increased amount, abnormal ZP:0021715 vasculature increased amount, abnormal ZP:0021716 female organism viability, abnormal ZP:0021725 adipose tissue increased amount, abnormal ZP:0021731 myocardium increased amount, abnormal ZP:0021740 muscle decreased amount, abnormal ZP:0021746 lateral dorsal aorta decreased amount, abnormal ZP:0021757 anterior neural plate decreased amount, abnormal ZP:0021768 spermatogonium decreased amount, abnormal ZP:0021795 notochord decreased distribution, abnormal ZP:0021800 swimming increased occurrence, abnormal ZP:0021815 gill decreased amount, abnormal ZP:0021835 brain female organism increased amount, abnormal ZP:0021836 ovary female organism increased amount, abnormal ZP:0021837 testis male organism increased amount, abnormal ZP:0021838 testis male organism decreased amount, abnormal ZP:0021841 optic tectum decreased amount, abnormal ZP:0021843 retinal inner nuclear layer increased amount, abnormal ZP:0021844 whole organism increased distribution, abnormal ZP:0021845 DNA methylation process quality, abnormal ZP:0021865 aggressive behavior decreased occurrence, abnormal ZP:0021892 ventricular endocardium mislocalised, abnormal ZP:0021893 ventricular myocardium mislocalised, abnormal ZP:0021900 ovarian follicle stage III increased amount, abnormal ZP:0021904 adult locomotory behavior process quality, abnormal ZP:0021916 response to absence of light decreased process quality, abnormal ZP:0021922 potassium(1+) whole organism decreased amount, abnormal ZP:0021939 triglyceride whole organism increased amount, abnormal ZP:0021941 lipid whole organism increased amount, abnormal ZP:0021992 blood vessel trunk vasculature decreased amount, abnormal ZP:0022023 presumptive atrium heart tube increased amount, abnormal ZP:0022029 atrium increased amount, abnormal ZP:0022049 photoreceptor outer segment retinal rod cell decreased amount, abnormal ZP:0022067 digestive system decreased amount, abnormal ZP:0022082 neurofibrosarcoma whole organism increased amount, abnormal ZP:0022083 atrioventricular valve shape, abnormal ZP:0022092 startle response increased occurrence, abnormal ZP:0022094 habenula increased amount, abnormal ZP:0022106 microglial cell optic tectum decreased amount, abnormal ZP:0022139 cardiac ventricle decreased velocity cardiac conduction, abnormal ZP:0022140 atrium decreased velocity cardiac conduction, abnormal ZP:0022141 atrial myocardium increased duration action potential, abnormal ZP:0022142 ventricular myocardium increased duration action potential, abnormal ZP:0022176 hematopoietic multipotent progenitor cell intermediate cell mass of mesoderm increased amount, abnormal ZP:0022179 pharyngeal arch 5 has fewer parts of type chondroblast, abnormal ZP:0022180 pharyngeal arch 6 has fewer parts of type chondroblast, abnormal ZP:0022183 retinal pigmented epithelium decreased amount, abnormal ZP:0022190 sperm cellular motility, abnormal ZP:0022206 whole organism has fewer parts of type swim bladder, abnormal ZP:0022207 ceratohyal bone mislocalised, abnormal ZP:0022233 muscle pioneer decreased distribution, abnormal ZP:0022272 exocrine pancreas spatial pattern, abnormal ZP:0022282 intramembranous ossification decreased process quality, abnormal ZP:0022283 perichondral ossification decreased process quality, abnormal ZP:0022284 opercle decreased process quality intramembranous ossification, abnormal ZP:0022285 branchiostegal ray decreased process quality intramembranous ossification, abnormal ZP:0022286 parasphenoid decreased process quality intramembranous ossification, abnormal ZP:0022287 ceratohyal bone decreased process quality perichondral ossification, abnormal ZP:0022288 hyomandibula decreased process quality perichondral ossification, abnormal ZP:0022289 ceratobranchial 5 bone decreased process quality perichondral ossification, abnormal ZP:0022290 osteoblast differentiation delayed, abnormal ZP:0022291 opercle decreased distribution, abnormal ZP:0022292 parasphenoid decreased distribution, abnormal ZP:0022293 osteoblast decreased distribution, abnormal ZP:0022294 osteoblast absent, abnormal ZP:0022297 developmental growth arrested, abnormal ZP:0022318 integument increased amount, abnormal ZP:0022319 intestinal epithelium increased amount, abnormal ZP:0022321 sleep increased occurrence, abnormal ZP:0022323 swimming behavior occurrence, abnormal ZP:0022324 response to light stimulus increased behavioural activity, abnormal ZP:0022325 sleep delayed, abnormal ZP:0022331 brain increased distribution, abnormal ZP:0022352 segmental plate absent, abnormal ZP:0022356 somite increased distribution, abnormal ZP:0022357 paraxial mesoderm increased amount, abnormal ZP:0022359 posterior region trunk increased distribution, abnormal ZP:0022360 posterior region trunk mislocalised, abnormal ZP:0022361 paraxial mesoderm increased distribution, abnormal ZP:0022362 segmental plate increased distribution, abnormal ZP:0022363 slow muscle myoblast increased amount, abnormal ZP:0022381 optic stalk increased amount, abnormal ZP:0022394 podocyte decreased amount, abnormal ZP:0022395 pronephric tubule increased amount, abnormal ZP:0022416 myotome mislocalised, abnormal ZP:0022434 hematopoietic multipotent progenitor cell increased occurrence apoptotic process, abnormal ZP:0022439 macrophage chemotaxis decreased occurrence, abnormal ZP:0022440 macrophage accumulation apoptotic body lysosome macrophage, abnormal ZP:0022464 pancreatic bud position, abnormal ZP:0022511 extension shape, abnormal ZP:0022512 spinal cord decreased distribution, abnormal ZP:0022534 endoderm decreased distribution, abnormal ZP:0022548 fin increased amount, abnormal ZP:0022572 regenerating tissue increased occurrence cell population proliferation, abnormal ZP:0022579 macrophage trunk decreased amount, abnormal ZP:0022581 granulocyte monocyte progenitor cell decreased amount, abnormal ZP:0022641 stereocilium bundle neuromast hair cell decreased amount, abnormal ZP:0022649 proximal convoluted tubule decreased area, abnormal ZP:0022661 multi-ciliated epithelial cell pronephric tubule absent, abnormal ZP:0022691 segmental plate mislocalised, abnormal ZP:0022718 tail bud immature, abnormal ZP:0022719 epithelial to mesenchymal transition delayed, abnormal ZP:0022720 feeding behavior process quality, abnormal ZP:0022731 margin decreased distribution, abnormal ZP:0022747 whole organism has fewer parts of type dorsal region melanocyte, abnormal ZP:0022796 epidermis disrupted cell adhesion, abnormal ZP:0022800 cardiac ventricle truncated, abnormal ZP:0022801 cardiac muscle fiber development disrupted, abnormal ZP:0022802 cardiac muscle cell vacuolated, abnormal ZP:0022803 autophagosome cardiac muscle cell present, abnormal ZP:0022804 Z disc heart disorganized, abnormal ZP:0022841 spermatogenesis decreased occurrence, abnormal ZP:0022842 hypophysis absent, abnormal ZP:0022845 blood cell morphology, abnormal ZP:0022847 lens reflectivity, abnormal ZP:0022867 cardiac muscle cell increased occurrence cell population proliferation, abnormal ZP:0022876 eye photoreceptor cell mislocalised, abnormal ZP:0022893 axon primary motor neuron branchiness, abnormal ZP:0022920 neoplasm brain increased amount, abnormal ZP:0022969 brain process quality vasculature development, abnormal ZP:0022972 microglial cell hindbrain increased amount, abnormal ZP:0022974 retina mislocalised, abnormal ZP:0022977 striated muscle cell trunk musculature decreased amount, abnormal ZP:0022979 ceratohyal cartilage curved ventral, abnormal ZP:0022980 basihyal cartilage curved ventral, abnormal ZP:0022981 ceratobranchial 1 cartilage absent, abnormal ZP:0022983 cardiac muscle cell decreased occurrence cell population proliferation, abnormal ZP:0023050 endothelial cell dorsal aorta absent, abnormal ZP:0023061 cardiac ventricle decreased distribution, abnormal ZP:0100002 choroid plexus increased distribution, abnormal ZP:0100009 whole organism quality, abnormal ZP:0100010 anatomical system quality, abnormal ZP:0100013 cartilage element pharyngeal arch cartilage mislocalised, abnormal ZP:0100017 pronephric duct decreased occurrence autophagy, abnormal ZP:0100021 vent malformed, abnormal ZP:0100027 intermediate cell mass of mesoderm increased occurrence cell population proliferation, abnormal ZP:0100031 T cell thymus increased amount, abnormal ZP:0100037 optic vesicle decreased amount, abnormal ZP:0100038 anterior neural plate decreased distribution, abnormal ZP:0100039 posterior neural plate increased distribution, abnormal ZP:0100040 presumptive telencephalon decreased distribution, abnormal ZP:0100042 ventral wall of dorsal aorta has fewer parts of type hematopoietic multipotent progenitor cell, abnormal ZP:0100043 ventral wall of dorsal aorta has extra parts of type hematopoietic multipotent progenitor cell, abnormal ZP:0100044 hematopoietic multipotent progenitor cell ventral wall of dorsal aorta spatial pattern, abnormal ZP:0100045 neutrophil kidney decreased amount, abnormal ZP:0100047 cilium inner ear morphology, abnormal ZP:0100048 photoreceptor connecting cilium photoreceptor cell decreased amount, abnormal ZP:0100053 central region retina increased amount, abnormal ZP:0100058 Kupffer's vesicle decreased fluid flow, abnormal ZP:0100060 cell body Muller cell displaced, abnormal ZP:0100062 primordial germ cell aggregated, abnormal ZP:0100063 calcium carbonate caudal fin increased amount, abnormal ZP:0100065 axon retinal neural layer truncated, abnormal ZP:0100066 axon retinal neural layer decreased branchiness, abnormal ZP:0100067 heparan sulfate 6-O-sulfotransferase activity process quality, abnormal ZP:0100071 otolith development decreased process quality, abnormal ZP:0100075 hypochord spatial pattern, abnormal ZP:0100076 intermediate mesoderm spatial pattern, abnormal ZP:0100077 angioblastic mesenchymal cell spatial pattern, abnormal ZP:0100078 pronephric proximal convoluted tubule has extra parts of type cytoplasm vesicle pronephric proximal convoluted tubule, abnormal ZP:0100082 vesicle pronephric proximal convoluted tubule increased variability of size, abnormal ZP:0100083 cell pronephric proximal convoluted tubule botryoidal, abnormal ZP:0100084 cell pronephric proximal straight tubule botryoidal, abnormal ZP:0100085 pronephros development decreased process quality, abnormal ZP:0100086 pronephric podocyte increased amount, abnormal ZP:0100087 pronephric capsular space increased width, abnormal ZP:0100088 capillary loop nephron increased amount, abnormal ZP:0100089 capillary loop nephron dilated, abnormal ZP:0100095 trunk neural crest cell migration arrested, abnormal ZP:0100096 neural crest separated from dorsal aorta, abnormal ZP:0100097 midbrain lacks all parts of type lymph vessel endothelial cell, abnormal ZP:0100099 dorsal region spinal cord increased amount, abnormal ZP:0100100 ventral region spinal cord increased amount, abnormal ZP:0100101 ventricular zone hindbrain increased amount, abnormal ZP:0100102 ventricular zone forebrain increased amount, abnormal ZP:0100103 ventricular zone midbrain increased amount, abnormal ZP:0100104 neuronal stem cell increased amount, abnormal ZP:0100105 actin-based cell projection peridermal cell increased length, abnormal ZP:0100106 actin-based cell projection peridermal cell decreased length, abnormal ZP:0100107 posterior lateral line primordium spatial pattern, abnormal ZP:0100113 post-vent vasculature increased amount, abnormal ZP:0100115 paired fin morphology, abnormal ZP:0100116 paired fin absent, abnormal ZP:0100117 paired fin decreased size, abnormal ZP:0100118 thyroid follicle spatial pattern, abnormal ZP:0100119 aortic arch dysplastic, abnormal ZP:0100120 thyroid follicle decreased diameter, abnormal ZP:0100121 thyroid primordium increased amount, abnormal ZP:0100122 protein localization to plasma membrane disrupted, abnormal ZP:0100123 apical side peridermal cell increased amount, abnormal ZP:0100124 apical side peridermal cell decreased amount, abnormal ZP:0100126 actin-based cell projection peridermal cell increased amount, abnormal ZP:0100127 actin-based cell projection peridermal cell decreased amount, abnormal ZP:0100128 endothelial cell decreased distribution, abnormal ZP:0100129 skeletal muscle decreased occurrence skeletal myofibril assembly, abnormal ZP:0100130 skeletal muscle myofibril skeletal muscle cell decreased amount, abnormal ZP:0100131 myotome has fewer parts of type skeletal muscle cell skeletal muscle myofibril skeletal muscle cell, abnormal ZP:0100137 muscle tendon junction myotome spatial pattern, abnormal ZP:0100138 muscle tendon junction myotome increased amount, abnormal ZP:0100139 muscle tendon junction fast muscle cell increased amount, abnormal ZP:0100140 slow muscle cell degenerate, abnormal ZP:0100141 slow muscle cell detached from slow muscle cell, abnormal ZP:0100142 muscle tendon junction myotome decreased amount, abnormal ZP:0100143 olfactory pit arrested epithelial cilium movement involved in extracellular fluid movement, abnormal ZP:0100146 rhombomere 2 mislocalised, abnormal ZP:0100147 rhombomere 4 mislocalised, abnormal ZP:0100148 erythroblast premature mitophagy, abnormal ZP:0100149 erythroblast increased occurrence mitophagy, abnormal ZP:0100151 mitochondrion erythroblast decreased amount, abnormal ZP:0100152 erythroblast has extra parts of type lysosome mitochondrion erythroblast, abnormal ZP:0100154 nucleate erythrocyte decreased occurrence hemoglobin biosynthetic process, abnormal ZP:0100158 otolith amount, abnormal ZP:0100160 branchiomotor neuron rhombomere 4 mislocalised anteriorly, abnormal ZP:0100165 myofibril muscle patchy, abnormal ZP:0100166 trunk musculature increased duration relaxation of muscle, abnormal ZP:0100167 twitch skeletal muscle contraction increased duration, abnormal ZP:0100168 twitch skeletal muscle contraction decreased intensity, abnormal ZP:0100169 sarcomere trunk musculature increased diameter, abnormal ZP:0100170 sarcomere trunk musculature decreased length, abnormal ZP:0100171 tonic skeletal muscle contraction decreased intensity, abnormal ZP:0100172 skeletal muscle adaptation disrupted, abnormal ZP:0100173 sarcomere trunk musculature decreased diameter, abnormal ZP:0100174 sarcomere myotome malformed, abnormal ZP:0100175 skeletal muscle cell myotome spatial pattern, abnormal ZP:0100176 whole organism process quality respiratory gaseous exchange by respiratory system, abnormal ZP:0100178 mitochondrion fast muscle cell swollen, abnormal ZP:0100179 mitochondrial matrix muscle decreased mass density, abnormal ZP:0100181 skeletal muscle detached from myofibril muscle tendon junction skeletal muscle, abnormal ZP:0100183 mitochondrial crista muscle decreased amount, abnormal ZP:0100184 skeletal muscle cell damaged, abnormal ZP:0100199 skeletal muscle cell increased amount, abnormal ZP:0100201 chromosome, telomeric region cell decreased length, abnormal ZP:0100205 retina increased occurrence Notch signaling pathway, abnormal ZP:0100209 retinal outer nuclear layer increased amount, abnormal ZP:0100218 spinal cord spatial pattern, abnormal ZP:0100219 posterior cardinal vein increased amount, abnormal ZP:0100220 primordial hindbrain channel hypoplastic, abnormal ZP:0100222 basement membrane notochord absent, abnormal ZP:0100223 posterior region neuroectoderm increased distribution, abnormal ZP:0100229 sodium ion export across plasma membrane increased process quality, abnormal ZP:0100230 sodium ion import across plasma membrane increased process quality, abnormal ZP:0100231 integument decreased occurrence proton export across plasma membrane, abnormal ZP:0100232 proton export across plasma membrane decreased occurrence, abnormal ZP:0100234 vertebral artery absent, abnormal ZP:0100246 determination of digestive tract left/right asymmetry decreased occurrence, abnormal ZP:0100247 determination of liver left/right asymmetry decreased occurrence, abnormal ZP:0100248 digestive system spatial pattern, abnormal ZP:0100250 myofibril slow muscle cell increased length, abnormal ZP:0100251 myofibril slow muscle cell decreased width, abnormal ZP:0100252 anterior region whole organism decreased amount, abnormal ZP:0100253 neural crest increased occurrence apoptotic process, abnormal ZP:0100254 neural crest decreased occurrence cell population proliferation, abnormal ZP:0100255 neural crest cell development decreased occurrence, abnormal ZP:0100256 neural crest decreased amount, abnormal ZP:0100258 pronephric distal early tubule increased size, abnormal ZP:0100259 pronephric distal early tubule increased distribution, abnormal ZP:0100262 telencephalon increased occurrence apoptotic process, abnormal ZP:0100264 distal region pronephric tubule decreased distribution, abnormal ZP:0100265 distal region pronephric tubule decreased amount, abnormal ZP:0100266 pronephric tubule increased distance cell cell pronephric tubule, abnormal ZP:0100267 pronephric tubule has fewer parts of type proximal region cell, abnormal ZP:0100271 pronephric tubule decreased amount, abnormal ZP:0100272 lactate whole organism decreased amount, abnormal ZP:0100273 nucleate erythrocyte heart absent, abnormal ZP:0100276 cell cortex oocyte stage I absent, abnormal ZP:0100277 oocyte stage I decreased occurrence organelle disassembly, abnormal ZP:0100278 cortisol whole organism increased amount, abnormal ZP:0100282 anatomical region third ventricle absent, abnormal ZP:0100283 otic vesicle spatial pattern, abnormal ZP:0100284 otic vesicle increased amount, abnormal ZP:0100285 basement membrane retinal pigmented epithelium aplastic, abnormal ZP:0100286 pharyngeal arch 3-7 aplastic/hypoplastic, abnormal ZP:0100287 skeletal muscle myofibril fast muscle cell absent, abnormal ZP:0100288 vacuole slow muscle cell increased amount, abnormal ZP:0100289 vacuole fast muscle cell increased amount, abnormal ZP:0100290 sarcomere fast muscle cell absent, abnormal ZP:0100291 dorsal longitudinal vein morphology, abnormal ZP:0100292 dorsal longitudinal vein increased amount, abnormal ZP:0100293 mesencephalic vein absent, abnormal ZP:0100296 ciliary shaft lateral crista spatial pattern, abnormal ZP:0100297 ciliary shaft lateral crista increased amount, abnormal ZP:0100298 lateral crista has extra parts of type ciliary shaft intraciliary transport particle lateral crista, abnormal ZP:0100299 ciliary shaft olfactory epithelium spatial pattern, abnormal ZP:0100300 ciliary shaft olfactory epithelium increased amount, abnormal ZP:0100301 posterior region whole organism absent, abnormal ZP:0100302 neuroectoderm decreased amount, abnormal ZP:0100305 myocardium increased distribution, abnormal ZP:0100307 presumptive endoderm increased amount, abnormal ZP:0100308 presumptive ectoderm decreased distribution, abnormal ZP:0100309 presumptive ectoderm decreased amount, abnormal ZP:0100313 primordial germ cell decreased occurrence establishment of cell polarity, abnormal ZP:0100314 primordial germ cell process quality regulation of intracellular pH, abnormal ZP:0100319 liver increased occurrence cell death, abnormal ZP:0100321 retinal neural layer disrupted axon guidance, abnormal ZP:0100322 axon retinal neural layer mislocalised, abnormal ZP:0100328 anatomical region myoseptum increased distribution, abnormal ZP:0100329 posterior lateral line primordium has extra parts of type filopodium posterior lateral line primordium, abnormal ZP:0100330 secondary motor neuron amount, abnormal ZP:0100332 sperm increased cellular motility, abnormal ZP:0100333 sperm increased velocity, abnormal ZP:0100338 neuromast hair cell decreased process quality endocytosis, abnormal ZP:0100339 cuticular plate neuromast hair cell mislocalised, abnormal ZP:0100340 neuromast hair cell decreased process quality intraciliary transport, abnormal ZP:0100341 neuromast hair cell decreased process quality cilium assembly, abnormal ZP:0100342 kinociliary basal body neuromast hair cell spatial pattern, abnormal ZP:0100343 neuromast hair cell morphogenesis decreased process quality, abnormal ZP:0100346 Kupffer's vesicle spatial pattern, abnormal ZP:0100352 pronephric tubule decreased occurrence cell population proliferation, abnormal ZP:0100354 pronephros decreased amount, abnormal ZP:0100356 presumptive ventral mesoderm decreased amount, abnormal ZP:0100357 utricle arrested otolith formation, abnormal ZP:0100361 utricle lacks all parts of type lapillus, abnormal ZP:0100366 utricle delayed otolith formation, abnormal ZP:0100368 utricle has fewer parts of type lapillus, abnormal ZP:0100371 blood accumulation pharyngeal arch 3-7, abnormal ZP:0100374 margin increased distribution, abnormal ZP:0100376 whole organism dorsalized, abnormal ZP:0100380 inflammatory response to antigenic stimulus decreased efficacy, abnormal ZP:0100382 whole organism lacks parts or has fewer parts of type IgM immunoglobulin complex blood, abnormal ZP:0100383 whole organism lacks parts or has fewer parts of type thymus, abnormal ZP:0100384 mature B cell absent, abnormal ZP:0100385 lymphocyte absent, abnormal ZP:0100388 gut increased occurrence cell population proliferation, abnormal ZP:0100389 neutrophil gut increased amount, abnormal ZP:0100390 intestinal motility process quality, abnormal ZP:0100392 glutathione oxidoreductase activity increased occurrence, abnormal ZP:0100394 glutathione oxidoreductase activity decreased occurrence, abnormal ZP:0100397 gonad primordium decreased size, abnormal ZP:0100399 primary motor neuron disrupted axonogenesis, abnormal ZP:0100401 axon terminus primary motor neuron swollen, abnormal ZP:0100402 spinal cord lacks parts or has fewer parts of type postero-ventral region axon reticulospinal neuron, abnormal ZP:0100403 spinal cord lacks parts or has fewer parts of type posterior region axon reticulospinal neuron, abnormal ZP:0100404 spinal cord lacks parts or has fewer parts of type ventral region axon reticulospinal neuron, abnormal ZP:0100405 axon reticulospinal neuron decreased perimeter, abnormal ZP:0100406 epithalamus absent, abnormal ZP:0100407 habenula absent, abnormal ZP:0100408 optic furrow closure incomplete, abnormal ZP:0100410 central nervous system increased amount, abnormal ZP:0100412 cardiac conduction rate, abnormal ZP:0100413 cell-cell adhesion decreased process quality, abnormal ZP:0100414 anterior region neuroectoderm decreased amount, abnormal ZP:0100415 posterior region neuroectoderm decreased distribution, abnormal ZP:0100416 cranial nerve VIII process quality axon guidance, abnormal ZP:0100422 pupil irregularly shaped, abnormal ZP:0100424 nucleus brain increased amount, abnormal ZP:0100425 nucleus optic vesicle increased amount, abnormal ZP:0100426 sodium ion import across plasma membrane increased occurrence, abnormal ZP:0100428 caudal hematopoietic tissue increased amount, abnormal ZP:0100429 glutathione anatomical structure decreased amount, abnormal ZP:0100431 neuromuscular junction pectoral fin nerve decreased amount, abnormal ZP:0100432 axon terminus pectoral fin nerve decreased amount, abnormal ZP:0100433 pectoral fin decreased mobility, abnormal ZP:0100434 non neural ectoderm increased amount, abnormal ZP:0100435 endocardium unfused from endocardium, abnormal ZP:0100438 endothelial cell absent, abnormal ZP:0100439 cerebellum hemorrhagic, abnormal ZP:0100443 ventral wall of dorsal aorta lacks parts or has fewer parts of type hematopoietic multipotent progenitor cell, abnormal ZP:0100448 posterior region midbrain increased amount, abnormal ZP:0100449 axial hypoblast absent, abnormal ZP:0100465 hematopoietic stem cell caudal hematopoietic tissue decreased amount, abnormal ZP:0100470 slow muscle cell trunk disorganized, abnormal ZP:0100471 synaptic transmission, glycinergic process quality, abnormal ZP:0100473 filopodium intersegmental vessel decreased amount, abnormal ZP:0100478 antero-dorsal region whole organism absent, abnormal ZP:0100479 postero-dorsal region whole organism absent, abnormal ZP:0100480 posterior region neuroectoderm absent, abnormal ZP:0100481 lateral region shield absent, abnormal ZP:0100482 midbrain hindbrain boundary neural rod absent, abnormal ZP:0100484 anatomical region Kupffer's vesicle absent, abnormal ZP:0100485 skeletal muscle myofibril somite disorganized, abnormal ZP:0100486 water transport decreased process quality, abnormal ZP:0100487 carbon dioxide transport decreased process quality, abnormal ZP:0100488 oxygen transport decreased process quality, abnormal ZP:0100489 pectoral artery decreased amount, abnormal ZP:0100491 feeding behavior decreased occurrence, abnormal ZP:0100494 site of DNA damage whole organism increased amount, abnormal ZP:0100495 response to stress process quality, abnormal ZP:0100498 motor neuron disrupted axon extension, abnormal ZP:0100499 superior ocular sulcus morphology, abnormal ZP:0100500 superior ocular sulcus closure incomplete, abnormal ZP:0100502 heart functionality, abnormal ZP:0100503 dorsal aorta mislocalised, abnormal ZP:0100504 basal region peridermal cell decreased amount, abnormal ZP:0100505 peridermal cell has fewer parts of type basal region filamentous actin peridermal cell, abnormal ZP:0100506 aggressive behavior increased occurrence, abnormal ZP:0100508 pharyngeal arch 3-7 increased amount, abnormal ZP:0100510 basement membrane epidermis absent, abnormal ZP:0100511 basement membrane epidermis decreased thickness, abnormal ZP:0100513 pancreatic B cell decreased occurrence cell population proliferation, abnormal ZP:0100514 whole organism decreased process quality glucose homeostasis, abnormal ZP:0100515 striated muscle myosin thick filament heart disorganized, abnormal ZP:0100516 striated muscle thin filament heart disorganized, abnormal ZP:0100517 striated muscle thin filament heart decreased amount, abnormal ZP:0100518 muscle tendon junction muscle absent, abnormal ZP:0100519 Z disc heart structure, abnormal ZP:0100520 Z disc heart absent, abnormal ZP:0100522 cardiac ventricle absent, abnormal ZP:0100527 trunk vasculature increased amount, abnormal ZP:0100528 cell-cell junction dorsal aorta structure, abnormal ZP:0100529 cell-cell junction dorsal aorta decreased length, abnormal ZP:0100530 cell-cell junction dorsal aorta hypoplastic, abnormal ZP:0100531 dorsal region eye absent, abnormal ZP:0100534 facial nerve motor nucleus arrested motor neuron migration, abnormal ZP:0100535 motor neuron facial nerve motor nucleus increased amount, abnormal ZP:0100536 facial nerve motor nucleus displaced to motor neuron rhombomere 4, abnormal ZP:0100537 facial nerve motor nucleus decreased occurrence motor neuron migration, abnormal ZP:0100538 facial nerve motor nucleus displaced to motor neuron rhombomere 5, abnormal ZP:0100539 rhombomere 6 has fewer parts of type motor neuron facial nerve motor nucleus, abnormal ZP:0100541 chondrocyte ceratohyal cartilage circular, abnormal ZP:0100542 symplectic decreased volume, abnormal ZP:0100543 Meckel's cartilage condensed, abnormal ZP:0100544 Meckel's cartilage perpendicular to anterior-posterior axis whole organism, abnormal ZP:0100545 ceratohyal cartilage decreased volume, abnormal ZP:0100546 ceratohyal cartilage condensed, abnormal ZP:0100547 ceratohyal cartilage perpendicular to anterior-posterior axis whole organism, abnormal ZP:0100548 chondrocyte mandibular arch skeleton morphology, abnormal ZP:0100549 chondrocyte mandibular arch skeleton position, abnormal ZP:0100567 anatomical margin caudal fin increased distribution, abnormal ZP:0100573 caudal fin actinotrichium increased length, abnormal ZP:0100577 cholesterol blood plasma increased amount, abnormal ZP:0100580 lipid vasculature increased amount, abnormal ZP:0100589 nucleus intestinal epithelial cell pleomorphic, abnormal ZP:0100590 microvillus intestinal bulb decreased length, abnormal ZP:0100591 microvillus mid intestine decreased length, abnormal ZP:0100592 goblet cell mid intestine immature, abnormal ZP:0100593 enteroendocrine cell decreased amount, abnormal ZP:0100594 enterocyte cuboid, abnormal ZP:0100595 microvillus intestinal bulb decreased amount, abnormal ZP:0100596 microvillus mid intestine decreased amount, abnormal ZP:0100599 intestinal bulb increased process quality cell population proliferation, abnormal ZP:0100600 mid intestine increased process quality cell population proliferation, abnormal ZP:0100601 enterocyte intestinal bulb decreased height, abnormal ZP:0100602 enterocyte mid intestine decreased height, abnormal ZP:0100603 regenerating fin increased occurrence apoptotic process, abnormal ZP:0100616 spinal cord neural tube decreased distribution, abnormal ZP:0100617 glial cell morphology, abnormal ZP:0100618 glial cell disorganized, abnormal ZP:0100630 lateral plate mesoderm decreased occurrence tissue migration, abnormal ZP:0100631 lateral plate mesoderm decreased process quality tissue migration, abnormal ZP:0100633 slow muscle cell decreased process quality skeletal myofibril assembly, abnormal ZP:0100636 microtubule yolk structure, abnormal ZP:0100637 epiblast decreased amount, abnormal ZP:0100638 yolk process quality microtubule cytoskeleton organization, abnormal ZP:0100639 yolk process quality microtubule bundle formation, abnormal ZP:0100640 microtubule yolk area density, abnormal ZP:0100641 microtubule yolk syncytial layer area density, abnormal ZP:0100642 yolk process quality microtubule polymerization, abnormal ZP:0100643 pregnenolone whole organism increased amount, abnormal ZP:0100644 progesterone whole organism decreased amount, abnormal ZP:0100645 melanophore stripe decreased size, abnormal ZP:0100648 glycolytic process decreased process quality, abnormal ZP:0100649 heart has extra parts of type anatomical region muscle, abnormal ZP:0100650 atrioventricular canal morphogenesis decreased occurrence, abnormal ZP:0100651 sinus venosus absent, abnormal ZP:0100653 axis spatial pattern, abnormal ZP:0100654 axis decreased distribution, abnormal ZP:0100655 axis decreased amount, abnormal ZP:0100659 presumptive atrium heart tube spatial pattern, abnormal ZP:0100660 presumptive atrium heart tube increased distribution, abnormal ZP:0100661 pronephric proximal convoluted tubule increased amount, abnormal ZP:0100669 basement membrane caudal fin disorganized, abnormal ZP:0100670 basement membrane caudal fin distributed, abnormal ZP:0100679 dorsal aorta increased distribution, abnormal ZP:0100682 sclerotome decreased amount, abnormal ZP:0100686 chondrocyte palate irregular spatial pattern, abnormal ZP:0100687 palate increased width, abnormal ZP:0100689 chondrocyte interhyal cartilage decreased amount, abnormal ZP:0100690 retroarticular malformed, abnormal ZP:0100691 retroarticular shortened, abnormal ZP:0100692 quadrate-anguloarticular joint morphology, abnormal ZP:0100696 centrum delayed ossification, abnormal ZP:0100697 collagen type I trimer bone tissue physical quality, abnormal ZP:0100698 endoplasmic reticulum lumen osteoblast increased size, abnormal ZP:0100699 rib deformed, abnormal ZP:0100700 pelvic fin atrophied, abnormal ZP:0100701 pelvic fin kinked, abnormal ZP:0100702 neural spine sloped, abnormal ZP:0100704 optic cup decreased occurrence cell population proliferation, abnormal ZP:0100705 centrum increased process quality bone mineralization, abnormal ZP:0100706 hemal arch increased process quality bone mineralization, abnormal ZP:0100707 neural arch increased process quality bone mineralization, abnormal ZP:0100708 centrum increased mass density, abnormal ZP:0100709 hemal arch increased mass density, abnormal ZP:0100710 neural arch decreased volume, abnormal ZP:0100711 neural arch increased mass density, abnormal ZP:0100712 primordial germ cell absent, abnormal ZP:0100713 longitudinal sarcoplasmic reticulum skeletal muscle cell increased amount, abnormal ZP:0100714 T-tubule skeletal muscle cell decreased amount, abnormal ZP:0100718 forebrain spatial pattern, abnormal ZP:0100723 pretectum decreased amount, abnormal ZP:0100726 oligodendrocyte decreased occurrence MAPK cascade, abnormal ZP:0100728 heart trabecula formation decreased occurrence, abnormal ZP:0100732 triglyceride whole organism decreased amount, abnormal ZP:0100733 lactate whole organism increased amount, abnormal ZP:0100734 autophagy process quality, abnormal ZP:0100736 sarcomere cardiac muscle cell disassembled, abnormal ZP:0100739 cardiac muscle cell decreased length, abnormal ZP:0100740 rhombomere 5 has extra parts of type facial nerve motor nucleus neuron projection motor neuron, abnormal ZP:0100741 rhombomere 4 has extra parts of type facial nerve motor nucleus neuron projection motor neuron, abnormal ZP:0100742 response to absence of light decreased behavioural activity, abnormal ZP:0100743 response to absence of light behavioral quality of a process, abnormal ZP:0100744 regulation of action potential firing pattern disrupted, abnormal ZP:0100745 optic tectum spatial pattern, abnormal ZP:0100751 vasculature liver decreased branchiness, abnormal ZP:0100759 integument decreased process quality proton export across plasma membrane, abnormal ZP:0100774 pyridoxamine 5'-phosphate whole organism decreased amount, abnormal ZP:0100776 whole organism decreased fecundity, abnormal ZP:0100777 lipid caudal vein increased amount, abnormal ZP:0100780 male organism increased weight, abnormal ZP:0100782 female organism increased weight, abnormal ZP:0100789 glutathione whole organism decreased amount, abnormal ZP:0100796 visceral fat increased amount, abnormal ZP:0100797 triglyceride blood plasma increased amount, abnormal ZP:0100799 rhombomere 1 decreased amount, abnormal ZP:0100800 central nervous system increased occurrence cell death, abnormal ZP:0100809 glucose blood decreased amount, abnormal ZP:0100822 male organism decreased weight, abnormal ZP:0100823 oogenesis arrested, abnormal ZP:0100824 oocyte stage III decreased amount, abnormal ZP:0100825 oocyte stage I increased amount, abnormal ZP:0100826 oocyte stage IV decreased amount, abnormal ZP:0100829 whole organism increased mass, abnormal ZP:0100838 noradrenergic neuron locus coeruleus decreased amount, abnormal ZP:0100841 swim bladder immature, abnormal ZP:0100848 visual perception decreased sensitivity of a process response to light stimulus, abnormal ZP:0100849 retinal inner nuclear layer has fewer parts of type dopaminergic neuron, abnormal ZP:0100863 superoxide dismutase activity decreased efficacy, abnormal ZP:0100869 regenerating fin decreased area, abnormal ZP:0100872 reactive oxygen species whole organism increased amount, abnormal ZP:0100880 learning or memory disrupted, abnormal ZP:0100903 cholesterol liver increased amount, abnormal ZP:0100911 presumptive mesoderm increased distribution, abnormal ZP:0100912 endodermal cell increased amount, abnormal ZP:0100913 endoderm formation decreased occurrence, abnormal ZP:0100914 mesoderm formation decreased occurrence, abnormal ZP:0100916 presumptive rhombomere 3 decreased distribution, abnormal ZP:0100917 forebrain neural plate increased distribution, abnormal ZP:0100918 midbrain hindbrain boundary neural plate decreased distribution, abnormal ZP:0100919 rhombomere 5 decreased distribution, abnormal ZP:0100920 rhombomere 3 decreased distribution, abnormal ZP:0100921 midbrain hindbrain boundary neural keel absent, abnormal ZP:0100923 posterior region hindbrain spatial pattern, abnormal ZP:0100924 posterior region hindbrain increased distribution, abnormal ZP:0100925 posterior region mesoderm spatial pattern, abnormal ZP:0100926 posterior region mesoderm increased distribution, abnormal ZP:0100927 anterior margin paraxial mesoderm spatial pattern, abnormal ZP:0100928 anterior margin paraxial mesoderm decreased distribution, abnormal ZP:0100929 anterior margin spinal cord neural tube spatial pattern, abnormal ZP:0100930 anterior margin spinal cord neural tube decreased distribution, abnormal ZP:0100931 tail bud decreased amount, abnormal ZP:0100932 paraxial mesoderm decreased distribution, abnormal ZP:0100933 otic epithelium decreased distribution, abnormal ZP:0100935 presumptive rhombomere 5 decreased amount, abnormal ZP:0100936 presumptive rhombomere 3 decreased amount, abnormal ZP:0100939 joint Meckel's cartilage morphology, abnormal ZP:0100940 joint palatoquadrate cartilage morphology, abnormal ZP:0100941 joint decreased occurrence cell population proliferation, abnormal ZP:0100942 joint decreased occurrence cell migration, abnormal ZP:0100943 embryonic skeletal joint development decreased process quality, abnormal ZP:0100944 hematopoietic stem cell caudal hematopoietic tissue increased amount, abnormal ZP:0100945 myeloid lineage restricted progenitor cell caudal hematopoietic tissue increased amount, abnormal ZP:0100946 thymus epithelium morphogenesis disrupted, abnormal ZP:0100947 thymus decreased process quality cell population proliferation, abnormal ZP:0100948 thymus increased process quality apoptotic process, abnormal ZP:0100949 macrophage caudal hematopoietic tissue increased amount, abnormal ZP:0100950 neutrophil caudal hematopoietic tissue increased amount, abnormal ZP:0100952 pharynx decreased process quality cell population proliferation, abnormal ZP:0100953 pro-T cell caudal hematopoietic tissue increased amount, abnormal ZP:0100954 lymphoid progenitor cell thymus primordium decreased amount, abnormal ZP:0100955 pharynx hypotrophic, abnormal ZP:0100956 thymus primordium decreased amount, abnormal ZP:0100957 pharyngeal pouch 2 decreased amount, abnormal ZP:0100958 pharyngeal pouch 3 decreased amount, abnormal ZP:0100959 pharyngeal pouch 5 decreased amount, abnormal ZP:0100960 pharyngeal pouch 4 decreased amount, abnormal ZP:0100961 pharyngeal arch 5 decreased amount, abnormal ZP:0100962 cell liver fatty, abnormal ZP:0100971 hypothalamus increased distribution, abnormal ZP:0100973 forebrain increased occurrence action potential, abnormal ZP:0100974 optic tectum increased occurrence action potential, abnormal ZP:0100994 vertical myoseptum spatial pattern, abnormal ZP:0101011 glucose whole organism decreased amount, abnormal ZP:0101019 oocyte stage III increased amount, abnormal ZP:0101049 hemoglobin biosynthetic process increased occurrence, abnormal ZP:0101050 ovarian follicle increased amount, abnormal ZP:0101051 cysteine-type endopeptidase activity involved in apoptotic process increased occurrence, abnormal ZP:0101052 cysteine-type endopeptidase activity involved in apoptotic process decreased occurrence, abnormal ZP:0101070 primordial germ cell spatial pattern, abnormal ZP:0101081 blood vessel development decreased process quality, abnormal ZP:0101091 triglyceride liver decreased amount, abnormal ZP:0101097 liver male organism increased amount, abnormal ZP:0101100 midbrain hindbrain boundary increased amount, abnormal ZP:0101107 cerebellum increased amount, abnormal ZP:0101108 cerebellum decreased amount, abnormal ZP:0101115 photoreceptor outer segment retinal photoreceptor layer decreased amount, abnormal ZP:0101119 striated muscle cell increased length, abnormal ZP:0101120 striated muscle cell decreased width, abnormal ZP:0101125 hematopoietic stem cell migration decreased occurrence, abnormal ZP:0101130 dorsal telencephalon increased distribution, abnormal ZP:0101133 fatty acid blood plasma increased amount, abnormal ZP:0101135 dorsal longitudinal anastomotic vessel decreased amount, abnormal ZP:0101168 brain increased occurrence cell death, abnormal ZP:0101170 microglial cell brain increased amount, abnormal ZP:0101174 manganese(2+) brain increased amount, abnormal ZP:0101175 manganese(2+) liver increased amount, abnormal ZP:0101177 chondrocyte increased amount, abnormal ZP:0101183 hematopoietic multipotent progenitor cell decreased distribution, abnormal ZP:0101189 dentary absent, abnormal ZP:0101195 auditory receptor cell decreased amount, abnormal ZP:0101214 BMP signaling pathway decreased occurrence, abnormal ZP:0101215 margin increased amount, abnormal ZP:0101226 yolk hourglass-shaped, abnormal ZP:0101230 dopamine whole organism decreased amount, abnormal ZP:0101231 serotonin whole organism decreased amount, abnormal ZP:0101233 hematopoietic cell increased amount, abnormal ZP:0101238 glial cell projection oligodendrocyte decreased amount, abnormal ZP:0101239 neuromast trunk decreased amount, abnormal ZP:0101252 presumptive bulbus arteriosus absent, abnormal ZP:0101266 rhombomere 5 absent, abnormal ZP:0101280 skeletal tissue decreased area, abnormal ZP:0101289 neutrophil head kidney decreased amount, abnormal ZP:0101290 gut hemorrhagic, abnormal ZP:0101297 myocardial precursor anterior lateral plate mesoderm decreased amount, abnormal ZP:0101298 proton transmembrane transport disrupted, abnormal ZP:0101299 pharyngeal mesoderm decreased amount, abnormal ZP:0101302 dorsal region forebrain increased amount, abnormal ZP:0101303 ventral region forebrain increased amount, abnormal ZP:0101307 forebrain increased occurrence asymmetric stem cell division, abnormal ZP:0101308 response to chemical behavioral quality of a process, abnormal ZP:0101309 lysosome pronephric duct increased diameter, abnormal ZP:0101310 pectoral fin bud increased amount, abnormal ZP:0101314 diencephalon has fewer parts of type dopaminergic neuron diencephalon, abnormal ZP:0101317 endocardium increased distribution, abnormal ZP:0101318 ventricular endocardium increased occurrence Notch signaling involved in heart development, abnormal ZP:0101320 optic stalk decreased amount, abnormal ZP:0101321 prechordal plate decreased distribution, abnormal ZP:0101322 involuntary skeletal muscle contraction increased occurrence, abnormal ZP:0101325 posterior region whole organism decreased amount, abnormal ZP:0101329 retina layer formation decreased occurrence, abnormal ZP:0101333 medial longitudinal fasciculus decreased occurrence axonal fasciculation, abnormal ZP:0101334 neuron nucleus of the medial longitudinal fasciculus medulla oblongata loose, abnormal ZP:0101336 anterior margin neuroectoderm spatial pattern, abnormal ZP:0101337 anterior margin neuroectoderm decreased distribution, abnormal ZP:0101338 pancreatic D cell differentiation disrupted, abnormal ZP:0101339 pancreatic D cell absent, abnormal ZP:0101340 presumptive telencephalon increased distribution, abnormal ZP:0101343 estradiol whole organism decreased amount, abnormal ZP:0101345 intersegmental vessel trunk branchiness, abnormal ZP:0101348 vasculature increased permeability, abnormal ZP:0101350 lens fiber cell disorganized, abnormal ZP:0101351 nucleus lens swollen, abnormal ZP:0101352 posterior region whole organism increased amount, abnormal ZP:0101357 forebrain process quality transmission of nerve impulse, abnormal ZP:0101358 T cell receptor V(D)J recombination disrupted, abnormal ZP:0101359 T cell head kidney decreased amount, abnormal ZP:0101360 mature B cell head kidney decreased amount, abnormal ZP:0101361 photoreceptor outer segment layer decreased height, abnormal ZP:0101362 whole organism decreased efficacy ATP generation from ADP, abnormal ZP:0101363 whole organism decreased efficacy aerobic respiration, abnormal ZP:0101366 rhombomere 3 increased distribution, abnormal ZP:0101368 presumptive rhombomere 3 increased distribution, abnormal ZP:0101369 multi fate stem cell epidermis normal amount, abnormal ZP:0101370 skin development cellular spatiotemporal quality, abnormal ZP:0101371 NaK ionocyte increased amount, abnormal ZP:0101372 basement membrane pronephric tubule decreased width, abnormal ZP:0101373 convergent extension involved in gastrulation decreased occurrence, abnormal ZP:0101374 cell notochord position, abnormal ZP:0101378 glycolytic process decreased rate, abnormal ZP:0101380 oxidative phosphorylation decreased rate, abnormal ZP:0101383 swimming behavior increased magnitude, abnormal ZP:0101384 regulation of locomotor rhythm disrupted, abnormal ZP:0101386 atrium irregular rhythm heart contraction, abnormal ZP:0101387 cardiac conduction decreased process quality, abnormal ZP:0101388 cardiac muscle cell membrane repolarization decreased rate, abnormal ZP:0101391 nerve degeneration, abnormal ZP:0101392 blood spatial pattern, abnormal ZP:0101393 blood decreased distribution, abnormal ZP:0101394 endothelial cell atrioventricular canal mislocalised, abnormal ZP:0101395 pericardium decreased thickness, abnormal ZP:0101396 bulbus arteriosus shortened, abnormal ZP:0101397 atrioventricular canal spatial pattern, abnormal ZP:0101398 lateral plate mesoderm decreased amount, abnormal ZP:0101399 ventral region pharyngeal arch decreased amount, abnormal ZP:0101401 radical lens increased amount, abnormal ZP:0101402 lens disrupted cellular oxidant detoxification, abnormal ZP:0101403 retinal pigmented epithelium reflectivity, abnormal ZP:0101404 presumptive endoderm absent, abnormal ZP:0101405 mesendoderm development decreased process quality, abnormal ZP:0101406 hypoblast decreased amount, abnormal ZP:0101407 mitochondrial chromosome integument decreased amount, abnormal ZP:0101408 dorsal region midbrain decreased amount, abnormal ZP:0101411 liver decreased process quality intrahepatic bile duct development, abnormal ZP:0101413 bile ductule decreased occurrence morphogenesis of a branching epithelium, abnormal ZP:0101421 bile ductule decreased branchiness, abnormal ZP:0101422 mandibular arch skeleton increased amount, abnormal ZP:0101430 pronephric duct has extra parts of type anatomical region leukocyte, abnormal ZP:0101433 pronephric duct increased occurrence epithelial cell proliferation, abnormal ZP:0101434 atrioventricular canal functionality, abnormal ZP:0101435 posterior side midbrain increased distribution, abnormal ZP:0101436 posterior region midbrain absent, abnormal ZP:0101437 posterior region midbrain mislocalised, abnormal ZP:0101440 ventral telencephalon increased distribution, abnormal ZP:0101441 adenohypophyseal placode absent, abnormal ZP:0101442 optic fissure absent, abnormal ZP:0101444 pyruvate whole organism increased amount, abnormal ZP:0101447 cell-cell adhesion increased occurrence, abnormal ZP:0101453 ventral region forebrain decreased amount, abnormal ZP:0101454 brain decreased occurrence gamma-aminobutyric acid signaling pathway, abnormal ZP:0101455 interneuron hypothalamus decreased amount, abnormal ZP:0101456 interneuron telencephalon decreased amount, abnormal ZP:0101457 swimming behavior irregular duration, abnormal ZP:0101458 olfactory bulb decreased amount, abnormal ZP:0101459 locus coeruleus decreased amount, abnormal ZP:0101463 heart decreased occurrence cardiac muscle cell proliferation, abnormal ZP:0101464 basement membrane liver aplastic, abnormal ZP:0101472 blood vessel superior ocular sulcus morphology, abnormal ZP:0101474 blood vessel superior ocular sulcus mislocalised, abnormal ZP:0101475 circulating cell common cardinal vein decreased amount, abnormal ZP:0101481 dopamine head decreased amount, abnormal ZP:0101483 optic vesicle increased distribution, abnormal ZP:0101485 hematopoietic stem cell migration delayed, abnormal ZP:0101486 dorsal longitudinal anastomotic vessel increased size, abnormal ZP:0101489 cartilage element pharyngeal arch cartilage decreased length, abnormal ZP:0101490 cell symplectic decreased amount, abnormal ZP:0101492 whole organism process quality larval locomotory behavior, abnormal ZP:0101493 sarcoplasmic reticulum skeletal muscle increased size, abnormal ZP:0101494 contractile fiber skeletal muscle decreased amount, abnormal ZP:0101496 (R)-adrenaline head decreased amount, abnormal ZP:0101497 noradrenaline head decreased amount, abnormal ZP:0101498 histamine head increased amount, abnormal ZP:0101501 neuron caudal hypothalamic zone increased amount, abnormal ZP:0101502 neuron caudal hypothalamic zone increased distribution, abnormal ZP:0101518 cholesterol anatomical structure increased amount, abnormal ZP:0101519 triglyceride anatomical structure increased amount, abnormal ZP:0101520 high-density lipoprotein blood plasma decreased amount, abnormal ZP:0101521 low-density lipoprotein blood plasma increased amount, abnormal ZP:0101522 very-low-density lipoprotein blood plasma increased amount, abnormal ZP:0101523 lipid trunk vasculature increased amount, abnormal ZP:0101524 lipid macrophage increased amount, abnormal ZP:0101525 skeletal muscle cell skeletal muscle disorganized, abnormal ZP:0101527 sphingosine oocyte increased amount, abnormal ZP:0101529 sphingoid 1-phosphate oocyte absent, abnormal ZP:0101530 oocyte increased amount, abnormal ZP:0101531 sphingosine whole organism increased amount, abnormal ZP:0101532 sphingosine 1-phosphate whole organism decreased amount, abnormal ZP:0101536 yolk syncytial layer increased width, abnormal ZP:0101538 glutamic acid head increased amount, abnormal ZP:0101542 anatomical region intestinal bulb increased distribution, abnormal ZP:0101543 intestinal bulb lacks all parts of type anatomical region neural crest cell, abnormal ZP:0101544 anatomical region intestinal bulb primordium absent, abnormal ZP:0101545 gut has fewer parts of type anatomical region neural crest cell, abnormal ZP:0101546 determination of intestine left/right asymmetry decreased occurrence, abnormal ZP:0101547 right side lateral plate mesoderm spatial pattern, abnormal ZP:0101551 proximal region caudal fin increased amount, abnormal ZP:0101552 proximal region caudal fin decreased amount, abnormal ZP:0101553 distal region caudal fin increased amount, abnormal ZP:0101554 distal region caudal fin decreased amount, abnormal ZP:0101555 medial region caudal fin increased amount, abnormal ZP:0101556 medial region caudal fin decreased amount, abnormal ZP:0101558 anatomical region eye edematous, abnormal ZP:0101562 anatomical region heart tube mislocalised, abnormal ZP:0101563 anatomical region heart mislocalised, abnormal ZP:0101564 anatomical region atrioventricular canal mislocalised, abnormal ZP:0101565 anatomical region presumptive atrium heart tube mislocalised, abnormal ZP:0101566 anatomical region presumptive cardiac ventricle heart tube mislocalised, abnormal ZP:0101567 whole organism has extra parts of type iridophore, abnormal ZP:0101570 ectoderm increased amount, abnormal ZP:0101572 anatomical region heart edematous, abnormal ZP:0101573 anatomical region digestive system edematous, abnormal ZP:0101577 integument has extra parts of type NCC ionocyte, abnormal ZP:0101578 endothelial cell atrial endocardium increased amount, abnormal ZP:0101579 endothelial cell atrial endocardium decreased amount, abnormal ZP:0101580 endothelial cell atrioventricular canal endocardium decreased amount, abnormal ZP:0101582 retinal ganglion cell layer broken, abnormal ZP:0101583 retinal ganglion cell layer separated from retinal neural layer, abnormal ZP:0101587 hatching decreased process quality, abnormal ZP:0101590 spinal cord has fewer parts of type anatomical region angiogenic sprout, abnormal ZP:0101591 centrum increased volume, abnormal ZP:0101592 hemal arch decreased thickness, abnormal ZP:0101593 hemal arch decreased volume, abnormal ZP:0101594 neural arch decreased thickness, abnormal ZP:0101600 epicardium increased accumulation cell anatomical region heart vasculature, abnormal ZP:0101601 Meckel's cartilage increased distance ceratohyal cartilage, abnormal ZP:0101605 spinal cord has fewer parts of type glutamatergic neuron, abnormal ZP:0101606 spinal cord has extra parts of type glycinergic neuron, abnormal ZP:0101607 spinal cord interneuron absent, abnormal ZP:0101608 spinal cord interneuron decreased distribution, abnormal ZP:0101611 slow muscle cell spatial pattern, abnormal ZP:0101612 trigeminal ganglion disrupted axon arborization, abnormal ZP:0101613 gut discolored, abnormal ZP:0101615 pronephric proximal convoluted tubule increased occurrence blood vessel morphogenesis, abnormal ZP:0101617 pronephric proximal straight tubule increased occurrence blood vessel morphogenesis, abnormal ZP:0101619 pronephric proximal convoluted tubule increased occurrence renal system vasculature morphogenesis, abnormal ZP:0101621 pronephric proximal straight tubule increased occurrence renal system vasculature morphogenesis, abnormal ZP:0101622 pronephric proximal convoluted tubule increased occurrence endocytosis, abnormal ZP:0101623 pronephric proximal straight tubule increased occurrence endocytosis, abnormal ZP:0101624 midbrain has fewer parts of type lymph vessel endothelial cell, abnormal ZP:0101625 somite 1 has fewer parts of type lateral region cell notochord, abnormal ZP:0101626 somite 2 has fewer parts of type lateral region cell notochord, abnormal ZP:0101628 olfactory placode increased amount, abnormal ZP:0101633 osteoblast operculohyoid ligament mislocalised, abnormal ZP:0101634 ligamentous ossification increased occurrence, abnormal ZP:0101635 portion of connective tissue decreased amount, abnormal ZP:0101636 operculohyoid ligament ossified, abnormal ZP:0101641 vertebral column variability bone mineralization, abnormal ZP:0101642 apatite parietal bone decreased amount, abnormal ZP:0101643 extracellular matrix osteoblast composition, abnormal ZP:0101644 fibrous joint cranial vault morphology, abnormal ZP:0101645 osteoblast parietal bone morphology, abnormal ZP:0101646 orbitosphenoid poorly ossified, abnormal ZP:0101647 pterosphenoid poorly ossified, abnormal ZP:0101648 parasphenoid increased angle to frontal bone, abnormal ZP:0101649 anterior region cranial vault truncated, abnormal ZP:0101650 palatoquadrate arch truncated, abnormal ZP:0101651 bone element cranial vault irregularly shaped, abnormal ZP:0101652 cranial vault closure incomplete, abnormal ZP:0101653 osteoblast replacement bone mislocalised, abnormal ZP:0101661 epiphyseal bar increased width, abnormal ZP:0101662 inter-ventral hypohyal joint increased width, abnormal ZP:0101663 neural tube trunk decreased amount, abnormal ZP:0101664 neural tube post-vent region decreased amount, abnormal ZP:0101668 regulation of canonical Wnt signaling pathway involved in heart development disrupted, abnormal ZP:0101670 atrioventricular valve disorganized, abnormal ZP:0101671 hepaticobiliary system development decreased occurrence, abnormal ZP:0101672 liver has fewer parts of type intrahepatic bile duct, abnormal ZP:0101673 liver morphogenesis decreased occurrence, abnormal ZP:0101674 liver malformed, abnormal ZP:0101677 L-type voltage-gated calcium channel complex muscle cell decreased amount, abnormal ZP:0101678 muscle cell decreased process quality release of sequestered calcium ion into cytosol by sarcoplasmic reticulum, abnormal ZP:0101679 L-type voltage-gated calcium channel complex muscle cell structure, abnormal ZP:0101684 lateral recess decreased distribution, abnormal ZP:0101685 hypothalamus process quality neuron differentiation, abnormal ZP:0101686 neuron hypothalamus irregular spatial pattern, abnormal ZP:0101687 preoptic area decreased distribution, abnormal ZP:0101688 caudal hypothalamic zone decreased distribution, abnormal ZP:0101689 preoptic area increased distribution, abnormal ZP:0101690 caudal hypothalamic zone increased distribution, abnormal ZP:0101692 brain physical object quality, abnormal ZP:0101694 whole organism lacks parts or has fewer parts of type thoracic duct, abnormal ZP:0101696 vascular lymphangioblast position, abnormal ZP:0101697 anatomical region dorsal aorta absent, abnormal ZP:0101698 vascular associated smooth muscle cell dorsal aorta absent, abnormal ZP:0101699 vascular associated smooth muscle cell dorsal aorta decreased amount, abnormal ZP:0101702 gonad primordium decreased amount, abnormal ZP:0101703 immature gonad decreased occurrence germ cell development, abnormal ZP:0101704 immature gonad increased occurrence male gonad development, abnormal ZP:0101705 immature gonad decreased occurrence female gonad development, abnormal ZP:0101706 immature gonad decreased occurrence female somatic sex determination, abnormal ZP:0101707 immature gonad increased occurrence male somatic sex determination, abnormal ZP:0101708 somatic cell immature gonad increased amount, abnormal ZP:0101709 somatic cell immature gonad increased distribution, abnormal ZP:0101710 somatic cell immature gonad decreased distribution, abnormal ZP:0101711 somatic cell immature gonad decreased amount, abnormal ZP:0101712 immature gonad increased amount, abnormal ZP:0101713 immature gonad decreased amount, abnormal ZP:0101714 immature gonad has fewer parts of type germ line cell, abnormal ZP:0101715 gonad decreased occurrence cell population proliferation, abnormal ZP:0101716 germ line cell decreased occurrence cell population proliferation, abnormal ZP:0101717 somatic cell decreased occurrence cell population proliferation, abnormal ZP:0101720 smooth muscle intestine decreased amount, abnormal ZP:0101721 female sex determination decreased occurrence, abnormal ZP:0101723 female sex determination increased occurrence, abnormal ZP:0101725 male sex determination decreased occurrence, abnormal ZP:0101726 olfactory bulb process quality response to odorant, abnormal ZP:0101727 ciliated olfactory receptor neuron process quality response to odorant, abnormal ZP:0101728 blood vessel endothelial cell proliferation involved in sprouting angiogenesis decreased process quality, abnormal ZP:0101729 blood vessel endothelial cell migration decreased process quality, abnormal ZP:0101730 smooth muscle cell intestine decreased amount, abnormal ZP:0101731 gut decreased occurrence peristalsis, abnormal ZP:0101732 smooth muscle intestine increased amount, abnormal ZP:0101733 cardiac conduction system mislocalised, abnormal ZP:0101734 sinoatrial node increased distribution, abnormal ZP:0101735 sinoatrial node increased area, abnormal ZP:0101738 anatomical region gut spatial pattern, abnormal ZP:0101739 anatomical region gut decreased amount, abnormal ZP:0101740 lateral plate mesoderm decreased occurrence cell population proliferation, abnormal ZP:0101741 smooth muscle cell intestine disorganized, abnormal ZP:0101742 smooth muscle cell decreased occurrence cell maturation, abnormal ZP:0101743 smooth muscle cell intestine shape, abnormal ZP:0101744 brain aplastic/hypoplastic, abnormal ZP:0101747 reactive oxygen species metabolic process increased occurrence, abnormal ZP:0101748 myelinating Schwann cell lateral line decreased amount, abnormal ZP:0101749 myelinating Schwann cell lateral line absent, abnormal ZP:0101750 telencephalon decreased occurrence cell population proliferation, abnormal ZP:0101751 telencephalon decreased occurrence commitment of multipotent stem cells to neuronal lineage in forebrain, abnormal ZP:0101752 telencephalon aplastic/hypoplastic, abnormal ZP:0101754 ERK1 and ERK2 cascade decreased process quality, abnormal ZP:0101755 presumptive neural plate decreased distribution, abnormal ZP:0101756 presumptive neural plate decreased amount, abnormal ZP:0101757 anterior neural plate aplastic/hypoplastic, abnormal ZP:0101758 presumptive telencephalon aplastic/hypoplastic, abnormal ZP:0101759 presumptive telencephalon decreased amount, abnormal ZP:0101764 axon terminus posterior lateral line nerve swollen, abnormal ZP:0101765 axon terminus posterior lateral line neuromast swollen, abnormal ZP:0101766 posterior lateral line nerve decreased process quality anterograde axonal transport, abnormal ZP:0101767 axon terminus posterior lateral line nerve increased amount, abnormal ZP:0101768 axon terminus posterior lateral line neuromast increased amount, abnormal ZP:0101770 myoseptum spatial pattern, abnormal ZP:0101771 cell junction pronephric glomerulus decreased amount, abnormal ZP:0101772 podocyte foot pronephric podocyte decreased thickness, abnormal ZP:0101773 pronephric glomerular basement membrane decreased functionality, abnormal ZP:0101774 whole organism lacks all parts of type thoracic duct, abnormal ZP:0101776 leukocyte integument increased amount, abnormal ZP:0101777 leukocyte muscle increased amount, abnormal ZP:0101780 posterior lateral line nerve decreased occurrence retrograde axonal transport of mitochondrion, abnormal ZP:0101781 mitochondrion posterior lateral line nerve mislocalised, abnormal ZP:0101782 posterior lateral line nerve has extra parts of type axon terminus mitochondrion posterior lateral line nerve, abnormal ZP:0101783 posterior lateral line neuromast has extra parts of type axon terminus mitochondrion posterior lateral line neuromast, abnormal ZP:0101790 posterior lateral line nerve decreased diameter, abnormal ZP:0101798 spinal cord has fewer parts of type postero-dorsal region oligodendrocyte, abnormal ZP:0101799 spinal cord has fewer parts of type postero-ventral region oligodendrocyte, abnormal ZP:0101800 spinal cord has fewer parts of type posterior region oligodendrocyte, abnormal ZP:0101801 Mauthner neuron has fewer parts of type posterior region myelin sheath Mauthner neuron, abnormal ZP:0101802 oligodendrocyte increased occurrence cell death, abnormal ZP:0101803 oligodendrocyte decreased occurrence cell population proliferation, abnormal ZP:0101804 mesenchymal cell decreased amount, abnormal ZP:0101805 perineuronal satellite cell decreased amount, abnormal ZP:0101806 circadian regulation of gene expression rhythm quality, abnormal ZP:0101807 melanin biosynthetic process rhythm quality, abnormal ZP:0101808 presumptive mesoderm decreased amount, abnormal ZP:0101809 ventral mesoderm decreased amount, abnormal ZP:0101810 axial mesoderm decreased amount, abnormal ZP:0101811 cardiac neural crest increased amount, abnormal ZP:0101812 Meckel's cartilage dysplastic, abnormal ZP:0101813 palatoquadrate cartilage dysplastic, abnormal ZP:0101814 anterior segment eye edematous, abnormal ZP:0101816 neuromuscular junction ventral root structure, abnormal ZP:0101817 synapse ventral root decreased amount, abnormal ZP:0101818 presynapse assembly disrupted, abnormal ZP:0101819 swimming decreased duration, abnormal ZP:0101821 retina decreased occurrence Notch signaling pathway, abnormal ZP:0101822 myotome development decreased process quality, abnormal ZP:0101823 anterior side mesoderm decreased amount, abnormal ZP:0101824 erythroid lineage cell delayed cell cycle G1/S phase transition, abnormal ZP:0101855 pronephric tubule orientation anterior-posterior axis whole organism, abnormal ZP:0101858 retinal cone cell increased occurrence apoptotic process, abnormal ZP:0101859 retinal rod cell increased occurrence apoptotic process, abnormal ZP:0101860 retinal cone cell optical quality, abnormal ZP:0101866 Meckel's cartilage misaligned with palatoquadrate cartilage, abnormal ZP:0101867 oocyte increased occurrence reproductive senescence, abnormal ZP:0101868 oogenesis process quality, abnormal ZP:0101869 ovary senescent, abnormal ZP:0101870 gonad increased amount, abnormal ZP:0101871 ovary increased occurrence spermatogenesis, abnormal ZP:0101872 ovary disrupted maintenance of animal organ identity, abnormal ZP:0101874 photoreceptor outer segment layer has fewer parts of type photoreceptor disc membrane photoreceptor cell, abnormal ZP:0101875 photoreceptor outer segment layer has extra parts of type axoneme photoreceptor cell, abnormal ZP:0101877 pronephros decreased length, abnormal ZP:0101878 autophagosome trunk increased amount, abnormal ZP:0101881 3',5'-cyclic AMP whole organism decreased amount, abnormal ZP:0101882 pectoral fin motor nerve 3 process quality motor neuron axon guidance, abnormal ZP:0101883 axon pectoral fin motor nerve 4 decreased branchiness, abnormal ZP:0101884 sclerotome structure, abnormal ZP:0101885 gonadotrophin-releasing hormone neuronal migration to the hypothalamus disrupted, abnormal ZP:0101886 olfactory bulb spatial pattern, abnormal ZP:0101887 primary motor neuron process quality axon guidance, abnormal ZP:0101888 pectoral fin motor nerve 1 process quality motor neuron axon guidance, abnormal ZP:0101889 pectoral fin motor nerve 2 process quality motor neuron axon guidance, abnormal ZP:0101890 pectoral fin motor nerve 4 process quality motor neuron axon guidance, abnormal ZP:0101891 axon pectoral fin motor nerve 2 defasciculated, abnormal ZP:0101892 axon pectoral fin motor nerve 3 defasciculated, abnormal ZP:0101893 axon terminus pectoral fin motor nerve 2 mislocalised, abnormal ZP:0101894 axon terminus pectoral fin motor nerve 3 mislocalised, abnormal ZP:0101895 facial nerve motor nucleus premature neuron maturation, abnormal ZP:0101896 neuron projection facial nerve motor nucleus increased length, abnormal ZP:0101897 motor neuron facial nerve motor nucleus circular, abnormal ZP:0101898 facial nerve motor nucleus has extra parts of type neuron projection motor neuron, abnormal ZP:0101899 neuron projection facial nerve motor nucleus increased amount, abnormal ZP:0101900 motor neuron facial nerve motor nucleus increased volume, abnormal ZP:0101901 facial nerve motor nucleus rhombomere 6 increased volume, abnormal ZP:0101902 facial nerve motor nucleus rhombomere 5 increased volume, abnormal ZP:0101903 facial nerve motor nucleus rhombomere 4 increased volume, abnormal ZP:0101909 intestine lacks all parts of type distal region enteric neuron, abnormal ZP:0101910 hematopoietic multipotent progenitor cell ventral wall of dorsal aorta decreased distribution, abnormal ZP:0101911 germ cell migration decreased occurrence, abnormal ZP:0101912 primordial germ cell increased occurrence bleb assembly, abnormal ZP:0101913 primordial germ cell decreased occurrence actin filament polymerization, abnormal ZP:0101916 retina decreased occurrence cell proliferation involved in compound eye morphogenesis, abnormal ZP:0101917 intersegmental vein decreased branchiness, abnormal ZP:0101924 dorsal longitudinal anastomotic vessel aplastic/hypoplastic, abnormal ZP:0101925 cell projection oligodendrocyte absent, abnormal ZP:0101926 lamellipodium intersegmental vessel decreased amount, abnormal ZP:0101928 forebrain neural keel increased size, abnormal ZP:0101929 spinal cord neural keel decreased size, abnormal ZP:0101930 spinal cord neural keel decreased distribution, abnormal ZP:0101931 posterior region neuroectoderm decreased size, abnormal ZP:0101932 nucleosome positioning process quality, abnormal ZP:0101935 ventro-lateral region mesoderm decreased amount, abnormal ZP:0101936 dorsal region diencephalon increased amount, abnormal ZP:0101937 trunk increased occurrence cell death, abnormal ZP:0101938 ionocyte decreased process quality proton export across plasma membrane, abnormal ZP:0101939 vH ionocyte decreased process quality proton export across plasma membrane, abnormal ZP:0101940 dendrite habenula decreased branchiness, abnormal ZP:0101941 habenula process quality dendrite arborization, abnormal ZP:0101942 whole organism disrupted thigmotaxis, abnormal ZP:0101943 mitochondrion eye morphology, abnormal ZP:0101944 lysosome brain hypertrophic, abnormal ZP:0101945 lysosome whole organism increased size, abnormal ZP:0101946 axon brain disorganized, abnormal ZP:0101947 axon brain aggregated, abnormal ZP:0101948 axon optic tectum absent, abnormal ZP:0101949 apoptotic body forebrain increased amount, abnormal ZP:0101950 optic tectum disrupted regulation of neuronal action potential, abnormal ZP:0101951 astrocyte spinal cord increased amount, abnormal ZP:0101952 regulation of mitochondrial membrane potential disrupted, abnormal ZP:0101953 sleep decreased process quality, abnormal ZP:0101954 neuromast hair cell decreased process quality response to mechanical stimulus, abnormal ZP:0101955 stereocilium neuromast hair cell decreased functionality, abnormal ZP:0101956 hair cell lateral crista decreased functionality, abnormal ZP:0101961 anterior region pronephros increased amount, abnormal ZP:0101962 posterior region vasculature increased amount, abnormal ZP:0101963 post-vent vasculature decreased process quality vasculature development, abnormal ZP:0101964 primordial germ cell increased amount, abnormal ZP:0101965 cardiac ventricle decreased process quality regulation of cardiac muscle contraction by calcium ion signaling, abnormal ZP:0101966 cilium ventricular zone decreased amount, abnormal ZP:0101967 retina broken, abnormal ZP:0101968 ventricular zone ciliatedness, abnormal ZP:0101970 neuron morphology, abnormal ZP:0101974 nucleus fast muscle cell undistributed, abnormal ZP:0101978 lateral crista decreased process quality inner ear receptor cell stereocilium organization, abnormal ZP:0101992 cranial vasculature decreased amount, abnormal ZP:0101993 motile cilium multi-ciliated epithelial cell decreased amount, abnormal ZP:0101996 fast muscle cell disrupted myoblast fusion, abnormal ZP:0101997 fast muscle myoblast nucleate quality, abnormal ZP:0101998 fast muscle cell decreased size, abnormal ZP:0102000 pharyngeal arch 3-7 skeleton lacks parts or has fewer parts of type ceratobranchial cartilage, abnormal ZP:0102001 ceratohyal cartilage posterior orientation, abnormal ZP:0102002 Meckel's cartilage physical object quality, abnormal ZP:0102003 ceratobranchial cartilage agenesis, abnormal ZP:0102004 photoreceptor outer segment photoreceptor cell degenerate, abnormal ZP:0102005 eye photoreceptor cell detached from photoreceptor outer segment photoreceptor inner segment eye photoreceptor cell, abnormal ZP:0102006 photoreceptor outer segment retinal cone cell degenerate, abnormal ZP:0102007 retinal photoreceptor layer has extra parts of type vesicle retinal photoreceptor layer, abnormal ZP:0102008 retina process quality regulation of apoptotic cell clearance, abnormal ZP:0102011 photoreceptor outer segment retinal rod cell disorganized, abnormal ZP:0102014 posterior region midbrain hindbrain boundary decreased distribution, abnormal ZP:0102015 mesoderm disorganized, abnormal ZP:0102016 gut decreased distribution, abnormal ZP:0102017 spinal cord interneuron mislocalised, abnormal ZP:0102018 hindbrain interneuron spatial pattern, abnormal ZP:0102019 retinal ganglion cell decreased distribution, abnormal ZP:0102020 whole organism decreased occurrence apoptotic process, abnormal ZP:0102021 endothelial cell intersegmental vessel increased amount, abnormal ZP:0102022 hematopoietic stem cell proliferation disrupted, abnormal ZP:0102024 proliferative region retina increased amount, abnormal ZP:0102025 proliferative region retina mislocalised, abnormal ZP:0102026 dorsal longitudinal anastomotic vessel arrested angiogenic sprout fusion, abnormal ZP:0102036 neuromast hair cell process quality innervation, abnormal ZP:0102042 anterior region whole organism decreased size, abnormal ZP:0102043 endoderm increased amount, abnormal ZP:0102048 type B pancreatic cell differentiation premature, abnormal ZP:0102049 pancreatic A cell differentiation decreased occurrence, abnormal ZP:0102050 myelin sheath oligodendrocyte increased length, abnormal ZP:0102055 cell projection xanthophore decreased amount, abnormal ZP:0102059 thrombocyte decreased occurrence cell population proliferation, abnormal ZP:0102060 thrombocyte blood decreased amount, abnormal ZP:0102061 thrombocyte head kidney decreased amount, abnormal ZP:0102062 hematopoietic multipotent progenitor cell head kidney decreased amount, abnormal ZP:0102063 thromboblast decreased occurrence cell population proliferation, abnormal ZP:0102066 hemin whole organism decreased amount, abnormal ZP:0102067 axon hindbrain commissure decreased amount, abnormal ZP:0102068 neuron cerebellum spatial pattern, abnormal ZP:0102069 midbrain hindbrain boundary increased thickness, abnormal ZP:0102070 midbrain structure, abnormal ZP:0102071 supraoptic commissure absent, abnormal ZP:0102072 compartment boundary rhombomere absent, abnormal ZP:0102073 hindbrain lacks all parts of type compartment boundary rhombomere, abnormal ZP:0102074 post-vent region immobile, abnormal ZP:0102075 hindbrain increased process quality neurogenesis, abnormal ZP:0102078 neuroblast (sensu Vertebrata) decreased amount, abnormal ZP:0102079 dopaminergic neuron differentiation disrupted, abnormal ZP:0102080 endocardium process quality cardioblast cell midline fusion, abnormal ZP:0102081 medial region whole organism absent, abnormal ZP:0102082 anterior lateral plate mesoderm absent, abnormal ZP:0102083 cardioblast cell midline fusion arrested, abnormal ZP:0102084 cardioblast cell midline fusion process quality, abnormal ZP:0102085 presumptive atrium heart tube increased width, abnormal ZP:0102086 presumptive atrium heart tube distended, abnormal ZP:0102087 presumptive cardiac ventricle heart tube increased width, abnormal ZP:0102088 anterior-posterior axis whole organism decreased size, abnormal ZP:0102089 swim bladder inflation process quality, abnormal ZP:0102090 heart collapsed, abnormal ZP:0102091 oral region process quality neural crest cell migration, abnormal ZP:0102092 dopaminergic neuron midbrain decreased amount, abnormal ZP:0102093 ATP whole organism decreased amount, abnormal ZP:0102094 slow muscle cell process quality calcium-mediated signaling, abnormal ZP:0102099 blood cell accumulation heart, abnormal ZP:0102104 axon cranial motor neuron decreased amount, abnormal ZP:0102106 motor neuron migration decreased process quality, abnormal ZP:0102110 notochord increased fragility, abnormal ZP:0102111 notochord inner cell collapsed, abnormal ZP:0102118 notochord outer sheath cell displaced to central region notochord, abnormal ZP:0102120 notochord outer sheath cell metaplastic, abnormal ZP:0102121 notochord inner cell metaplastic, abnormal ZP:0102122 notochord outer sheath cell increased amount, abnormal ZP:0102123 chondrocyte palatoquadrate cartilage decreased area, abnormal ZP:0102124 cleithrum length, abnormal ZP:0102125 branchiostegal ray length, abnormal ZP:0102126 entopterygoid length, abnormal ZP:0102127 palatoquadrate cartilage decreased area, abnormal ZP:0102128 brain decreased occurrence endothelial cell development, abnormal ZP:0102129 brain vasculature decreased amount, abnormal ZP:0102131 blood vessel brain morphology, abnormal ZP:0102132 endothelial cell brain decreased amount, abnormal ZP:0102133 endothelial cell brain absent, abnormal ZP:0102136 hematopoietic cell decreased amount, abnormal ZP:0102139 epicardium increased size, abnormal ZP:0102140 blood accumulation yolk syncytial layer, abnormal ZP:0102141 erythroid progenitor cell dysplastic, abnormal ZP:0102142 plasma membrane notochord inner cell broken, abnormal ZP:0102144 notochord development decreased process quality, abnormal ZP:0102145 caveola notochord inner cell malformed, abnormal ZP:0102146 notochord inner cell malformed, abnormal ZP:0102147 notochord inner cell has fewer parts of type plasma membrane caveola notochord inner cell, abnormal ZP:0102148 caveola neck notochord inner cell increased width, abnormal ZP:0102149 caveola bulb notochord inner cell decreased depth, abnormal ZP:0102153 thymus development decreased process quality, abnormal ZP:0102154 immune response decreased process quality, abnormal ZP:0102155 T cell receptor V(D)J recombination arrested, abnormal ZP:0102156 T cell activation arrested, abnormal ZP:0102157 B cell activation arrested, abnormal ZP:0102158 immunoglobulin heavy chain V-D-J recombination arrested, abnormal ZP:0102159 spleen absent, abnormal ZP:0102160 kidney absent, abnormal ZP:0102161 kidney decreased thickness, abnormal ZP:0102162 kidney decreased mass density, abnormal ZP:0102171 anal fin development process quality, abnormal ZP:0102172 caudal fin development process quality, abnormal ZP:0102173 dorsal fin development process quality, abnormal ZP:0102174 dorsal fin morphogenesis process quality, abnormal ZP:0102175 caudal fin morphogenesis process quality, abnormal ZP:0102176 anal fin morphogenesis process quality, abnormal ZP:0102181 autophagy decreased occurrence, abnormal ZP:0102184 dorsal aorta has extra parts of type circulating cell neutrophil, abnormal ZP:0102186 hypobranchial artery increased variability of size, abnormal ZP:0102187 hematopoietic multipotent progenitor cell thymus increased amount, abnormal ZP:0102192 post-vent region decreased amount, abnormal ZP:0102195 filopodium intersegmental vessel variability of count, abnormal ZP:0102198 cytoskeleton muscle cell disorganized, abnormal ZP:0102199 defense response to Gram-positive bacterium decreased process quality, abnormal ZP:0102200 somite amount, abnormal ZP:0102201 endothelial cell trabecular layer decreased amount, abnormal ZP:0102202 angiogenesis involved in coronary vascular morphogenesis disrupted, abnormal ZP:0102203 cell-cell junction DEL decreased amount, abnormal ZP:0102204 DEL delayed cell migration involved in gastrulation, abnormal ZP:0102205 DEL process quality cell migration involved in gastrulation, abnormal ZP:0102206 blastomere organization quality, abnormal ZP:0102210 CaP motoneuron disrupted axonogenesis, abnormal ZP:0102211 axon secondary motor neuron decreased branchiness, abnormal ZP:0102212 neuromuscular junction myotome increased distribution, abnormal ZP:0102213 presynaptic density myotome increased amount, abnormal ZP:0102215 peripheral nervous system has fewer parts of type myelinating Schwann cell, abnormal ZP:0102216 motor neuron has fewer parts of type myelinating Schwann cell, abnormal ZP:0102218 glial cell decreased thickness, abnormal ZP:0102220 manganese(2+) whole organism increased amount, abnormal ZP:0102222 manganese atom whole organism increased amount, abnormal ZP:0102224 manganese atom whole organism decreased amount, abnormal ZP:0102226 vertebra process quality bone mineralization, abnormal ZP:0102227 neural arch increased area, abnormal ZP:0102228 neural arch decreased angle to vertebra, abnormal ZP:0102229 vertebra increased size, abnormal ZP:0102230 fourth ventricle absent, abnormal ZP:0102231 fourth ventricle decreased amount, abnormal ZP:0102232 tegmentum decreased amount, abnormal ZP:0102234 blood vessel lumenization decreased occurrence, abnormal ZP:0102235 artery malformed, abnormal ZP:0102236 vein malformed, abnormal ZP:0102239 whole organism decreased mass, abnormal ZP:0102246 orbital region edematous, abnormal ZP:0102247 pronephric duct kinked, abnormal ZP:0102250 vasculature hematopoietic system increased amount, abnormal ZP:0102251 endoderm spatial pattern, abnormal ZP:0102252 cilium ependymal cell increased length, abnormal ZP:0102254 skeletal tissue disrupted tissue homeostasis, abnormal ZP:0102255 vertebra decreased distance vertebra, abnormal ZP:0102256 ventral mandibular arch decreased width, abnormal ZP:0102257 skeletal tissue decreased amount, abnormal ZP:0102258 pericardial cavity process quality bone mineralization, abnormal ZP:0102259 cilium neural tube increased length, abnormal ZP:0102260 neural tube has fewer parts of type cilium neural tube, abnormal ZP:0102261 olfactory pit process quality cilium assembly, abnormal ZP:0102262 9+2 non-motile cilium ciliated olfactory receptor neuron malformed, abnormal ZP:0102263 myotome process quality cilium assembly, abnormal ZP:0102264 non-motile cilium myotome increased length, abnormal ZP:0102265 brainstem decreased size, abnormal ZP:0102266 brainstem morphology, abnormal ZP:0102267 vascular associated smooth muscle cell cerebellar central artery decreased amount, abnormal ZP:0102268 actin filament bundle keratinocyte decreased amount, abnormal ZP:0102269 epidermal superficial stratum morphology, abnormal ZP:0102270 keratinocyte increased size, abnormal ZP:0102271 spinal cord interneuron arrested synapse assembly, abnormal ZP:0102272 Mauthner neuron arrested synapse assembly, abnormal ZP:0102273 afferent neuron arrested synapse assembly, abnormal ZP:0102274 synapse cranial nerve VIII absent, abnormal ZP:0102275 synapse spinal cord interneuron absent, abnormal ZP:0102276 synapse Mauthner neuron non-functional, abnormal ZP:0102277 synapse afferent neuron absent, abnormal ZP:0102278 startle response latency, abnormal ZP:0102279 Meckel's cartilage immature, abnormal ZP:0102280 ceratohyal cartilage immature, abnormal ZP:0102281 hypothalamus disrupted axon extension, abnormal ZP:0102282 cerebellum disrupted axon extension, abnormal ZP:0102283 neuroblast differentiation disrupted, abnormal ZP:0102284 regulation of neuroblast proliferation disrupted, abnormal ZP:0102285 posterior side whole organism absent, abnormal ZP:0102286 iridophore eye disorganized, abnormal ZP:0102287 ventral mandibular arch immature, abnormal ZP:0102289 hematopoietic system increased occurrence cell death, abnormal ZP:0102290 stromal cell caudal vein plexus apoptotic, abnormal ZP:0102291 granulocyte differentiation decreased process quality, abnormal ZP:0102292 thymus lacks all parts of type lymphoid progenitor cell, abnormal ZP:0102293 caudal vein plexus has fewer parts of type hematopoietic stem cell, abnormal ZP:0102294 neuronal stem cell disrupted cell population proliferation, abnormal ZP:0102295 afferent neuron decreased occurrence synapse assembly, abnormal ZP:0102296 synapse cranial nerve VIII decreased amount, abnormal ZP:0102297 synapse afferent neuron decreased amount, abnormal ZP:0102298 maturation of SSU-rRNA from tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA) disrupted, abnormal ZP:0102299 sympathetic nervous system development disrupted, abnormal ZP:0102300 superior cervical ganglion decreased size, abnormal ZP:0102301 superior cervical ganglion hypoplastic, abnormal ZP:0102302 superior cervical ganglion decreased distribution, abnormal ZP:0102303 sarcomere somite absent, abnormal ZP:0102304 superior cervical ganglion decreased amount, abnormal ZP:0102317 pharynx inflamed, abnormal ZP:0102318 gill inflamed, abnormal ZP:0102319 integument inflamed, abnormal ZP:0102320 olfactory epithelium inflamed, abnormal ZP:0102321 gill filament swollen, abnormal ZP:0102322 intestine swollen, abnormal ZP:0102323 T cell pharynx increased amount, abnormal ZP:0102324 T cell integument increased amount, abnormal ZP:0102325 T cell olfactory epithelium increased amount, abnormal ZP:0102326 T cell gill filament increased amount, abnormal ZP:0102327 T cell intestine increased amount, abnormal ZP:0102328 pharynx has extra parts of type T cell, abnormal ZP:0102329 gill has extra parts of type T cell, abnormal ZP:0102330 integument has extra parts of type T cell, abnormal ZP:0102331 olfactory epithelium has extra parts of type T cell, abnormal ZP:0102332 intestine has extra parts of type T cell, abnormal ZP:0102334 intestine lumen decreased volume, abnormal ZP:0102336 intestinal epithelium decreased amount, abnormal ZP:0102351 calcium ion import increased occurrence, abnormal ZP:0102353 epidermis rough, abnormal ZP:0102354 keratinocyte morphology, abnormal ZP:0102355 Wnt signaling pathway, calcium modulating pathway decreased occurrence, abnormal ZP:0102357 blood vessel endothelial cell intersegmental vessel apoptotic, abnormal ZP:0102358 blood vessel endothelial cell trunk vasculature apoptotic, abnormal ZP:0102360 whole organism decreased velocity, abnormal ZP:0102361 intersegmental vessel hemorrhagic, abnormal ZP:0102362 basal side cardiac muscle cell absent, abnormal ZP:0102366 caudal fin lepidotrichium spatial pattern, abnormal ZP:0102367 caudal fin lepidotrichium broken, abnormal ZP:0102368 caudal fin lepidotrichium lacks parts or has fewer parts of type lepidotrichium joint, abnormal ZP:0102369 trigeminal ganglion absent, abnormal ZP:0102370 trigeminal ganglion increased amount, abnormal ZP:0102371 posterior lateral line neuromast hair cell morphogenesis disrupted, abnormal ZP:0102372 neuromast spatial pattern, abnormal ZP:0102374 posterior lateral line primordium disrupted cell population proliferation, abnormal ZP:0102375 myoseptum decreased amount, abnormal ZP:0102382 cell pancreas apoptotic, abnormal ZP:0102383 intestinal bulb epithelium morphology, abnormal ZP:0102384 histone H3-K27 methylation disrupted, abnormal ZP:0102386 posterior lateral line neuromast deposition decreased rate, abnormal ZP:0102396 growth decreased efficacy, abnormal ZP:0102397 carotenoid integument decreased amount, abnormal ZP:0102398 carotenoid vesicle xanthophore aggregated, abnormal ZP:0102401 intersegmental vessel trunk increased branchiness, abnormal ZP:0102407 intersegmental vessel detached from dorsal longitudinal anastomotic vessel, abnormal ZP:0102410 mesodermal cell tail bud increased distribution, abnormal ZP:0102413 myofilament cardiac muscle cell disorganized, abnormal ZP:0102414 myofilament cardiac muscle cell decreased thickness, abnormal ZP:0102415 cardiac muscle cell misaligned with myofilament myofilament cardiac muscle cell, abnormal ZP:0102416 cardiac muscle cell separated from myofilament myofilament cardiac muscle cell, abnormal ZP:0102417 cardiac muscle cell has extra parts of type plasma membrane cell projection cardiac muscle cell, abnormal ZP:0102421 yolk syncytial layer mislocalised, abnormal ZP:0102422 muscle pioneer disorganized, abnormal ZP:0102423 pharyngeal arch 3-7 decreased distribution, abnormal ZP:0102424 somite border incomplete structure, abnormal ZP:0102428 cell migration involved in heart development process quality, abnormal ZP:0102429 melanoma eye present, abnormal ZP:0102430 melanoma trunk present, abnormal ZP:0102431 melanoma in situ whole organism increased amount, abnormal ZP:0102432 sex determination disrupted, abnormal ZP:0102433 fertilization disrupted, abnormal ZP:0102434 oogenesis disrupted, abnormal ZP:0102435 oocyte female organism viability, abnormal ZP:0102436 cell division asynchronous, abnormal ZP:0102437 blastomere asymmetrical, abnormal ZP:0102438 pharyngeal arch decreased process quality embryonic viscerocranium morphogenesis, abnormal ZP:0102439 pharyngeal arch cartilage decreased occurrence chondrocyte differentiation, abnormal ZP:0102440 pectoral fin decreased process quality cartilage development, abnormal ZP:0102442 pectoral girdle lacks all parts of type cleithrum, abnormal ZP:0102443 pectoral girdle lacks all parts of type scapulocoracoid, abnormal ZP:0102446 erythroblast decreased occurrence mitophagy, abnormal ZP:0102447 blood cell increased accumulation ventricular system, abnormal ZP:0102448 cell-cell junction blood vessel decreased amount, abnormal ZP:0102449 blood vasculature brain decreased amount, abnormal ZP:0102450 blood vessel brain broken, abnormal ZP:0102451 brain separated from blood vessel endothelial cell blood vessel endothelial cell, abnormal ZP:0102452 aerobic respiration decreased process quality, abnormal ZP:0102454 cholangiocyte increased amount, abnormal ZP:0102455 liver increased occurrence Wnt signaling pathway, abnormal ZP:0102456 cholangiocyte increased occurrence Wnt signaling pathway, abnormal ZP:0102468 epithelial cell regenerating fin apoptotic, abnormal ZP:0102469 epithelial cell protruding out of regenerating fin, abnormal ZP:0102471 actin-based cell projection peridermal cell decreased size, abnormal ZP:0102472 photoreceptor outer segment photoreceptor outer segment layer disorganized, abnormal ZP:0102473 cilium retina absent, abnormal ZP:0102474 regulation of hippo signaling disrupted, abnormal ZP:0102475 angioblastic mesenchymal cell posterior lateral mesoderm spatial pattern, abnormal ZP:0102476 angioblastic mesenchymal cell irregular spatial pattern, abnormal ZP:0102477 medial region pharyngeal arch 2 decreased amount, abnormal ZP:0102478 medial region pharyngeal arch 1 decreased amount, abnormal ZP:0102479 ventral region pharyngeal arch 2 absent, abnormal ZP:0102480 ventral region pharyngeal arch 1 absent, abnormal ZP:0102481 ventral hyoid arch mislocalised, abnormal ZP:0102482 intersegmental artery decreased process quality sprouting angiogenesis, abnormal ZP:0102492 atrioventricular canal process quality blood circulation, abnormal ZP:0102495 notochord post-vent region bent, abnormal ZP:0102498 nucleus optic vesicle decreased amount, abnormal ZP:0102499 brain decreased process quality regulation of cell cycle, abnormal ZP:0102500 retina decreased process quality regulation of cell cycle, abnormal ZP:0102503 locomotory exploration behavior decreased process quality, abnormal ZP:0102504 optic tectum process quality microglial cell migration, abnormal ZP:0102509 midbrain increased distribution, abnormal ZP:0102512 axoneme anterior neural tube structure, abnormal ZP:0102513 axoneme spinal cord neural tube structure, abnormal ZP:0102514 motile cilium assembly process quality, abnormal ZP:0102515 9+2 motile cilium olfactory epithelium absent, abnormal ZP:0102516 9+2 motile cilium olfactory epithelium decreased mobility, abnormal ZP:0102517 epithelial cilium movement involved in extracellular fluid movement decreased process quality, abnormal ZP:0102520 spinal cord process quality cilium movement, abnormal ZP:0102521 hindbrain arrested mitotic cell cycle, abnormal ZP:0102522 centrosome hindbrain size, abnormal ZP:0102523 hindbrain adjacent to centrosome centrosome hindbrain, abnormal ZP:0102524 spindle hindbrain spatial pattern, abnormal ZP:0102525 spindle hindbrain decreased amount, abnormal ZP:0102526 centrosome cycle process quality, abnormal ZP:0102527 mitotic centrosome separation decreased occurrence, abnormal ZP:0102528 monocyte ventral wall of dorsal aorta decreased amount, abnormal ZP:0102529 nucleate erythrocyte ventral wall of dorsal aorta decreased amount, abnormal ZP:0102535 pronephric podocyte decreased process quality glomerular visceral epithelial cell development, abnormal ZP:0102536 pronephros decreased occurrence renal filtration, abnormal ZP:0102537 podocyte foot pronephric podocyte malformed, abnormal ZP:0102538 podocyte foot pronephric podocyte dystrophic, abnormal ZP:0102539 pronephric glomerulus increased width, abnormal ZP:0102540 pronephric tubule decreased length, abnormal ZP:0102541 centrosome somite border spatial pattern, abnormal ZP:0102542 somite border decreased occurrence mesenchymal to epithelial transition, abnormal ZP:0102543 epithelial cell somite border morphology, abnormal ZP:0102544 actin filament somite border morphology, abnormal ZP:0102545 actin filament somite border malformed, abnormal ZP:0102546 cardiac ventricle decreased process quality cardiac muscle cell proliferation, abnormal ZP:0102548 pronephros increased occurrence apoptotic process, abnormal ZP:0102549 podocyte foot pronephric podocyte immature, abnormal ZP:0102552 neuron spinal cord decreased distribution, abnormal ZP:0102553 tail bud spatial pattern, abnormal ZP:0102554 post-vent region increased process quality cell death, abnormal ZP:0102555 midbrain hindbrain boundary spatial pattern, abnormal ZP:0102557 lateral line ganglion decreased distribution, abnormal ZP:0102558 midbrain hindbrain boundary neural rod decreased distribution, abnormal ZP:0102561 posterior region caudal fin absent, abnormal ZP:0102562 ventral region caudal fin absent, abnormal ZP:0102563 ventral region trunk absent, abnormal ZP:0102564 ventral region margin decreased distribution, abnormal ZP:0102565 ventral region margin decreased amount, abnormal ZP:0102566 ventral mesoderm mislocalised, abnormal ZP:0102567 axial mesoderm increased amount, abnormal ZP:0102568 axial mesoderm increased distribution, abnormal ZP:0102569 nucleus presumptive mesoderm absent, abnormal ZP:0102570 nucleus ectodermal cell absent, abnormal ZP:0102571 male courtship behavior decreased process quality, abnormal ZP:0102574 pancreas decreased occurrence pancreatic A cell differentiation, abnormal ZP:0102575 endocrine pancreas has fewer parts of type pancreatic A cell, abnormal ZP:0102576 islet decreased process quality cell differentiation, abnormal ZP:0102577 exocrine pancreas malformed, abnormal ZP:0102585 gut epithelium mislocalised, abnormal ZP:0102586 intrapancreatic duct mislocalised, abnormal ZP:0102587 axon cranial motor neuron decreased length, abnormal ZP:0102588 otic vesicle decreased occurrence cell population proliferation, abnormal ZP:0102589 stereocilium neuromast hair cell decreased length, abnormal ZP:0102590 stereocilium neuromast hair cell decreased thickness, abnormal ZP:0102591 autophagosome skeletal muscle increased amount, abnormal ZP:0102592 glycogen granule heart increased amount, abnormal ZP:0102593 glycogen granule liver increased amount, abnormal ZP:0102594 glycogen granule skeletal muscle increased amount, abnormal ZP:0102595 alpha-glucosidase activity decreased efficacy, abnormal ZP:0102597 heart increased occurrence apoptotic process, abnormal ZP:0102598 vasculature aortic arch hypoplastic, abnormal ZP:0102603 ceratohyal cartilage process quality cartilage morphogenesis, abnormal ZP:0102614 retroarticular decreased occurrence cell population proliferation, abnormal ZP:0102616 axon cranial nerve VIII mislocalised, abnormal ZP:0102617 cranial nerve VIII defasciculated, abnormal ZP:0102622 cholesteryl ester blood plasma increased amount, abnormal ZP:0102623 cardiac ventricle process quality action potential, abnormal ZP:0102624 mitochondrion chondrocyte position, abnormal ZP:0102625 endoplasmic reticulum chondrocyte position, abnormal ZP:0102626 extracellular matrix chondrocyte spatial pattern, abnormal ZP:0102627 chondrocyte decreased occurrence secretion, abnormal ZP:0102647 dentary morphology, abnormal ZP:0102650 ceratobranchial 5 bone absent, abnormal ZP:0102651 endochondral bone absent, abnormal ZP:0102652 head muscle decreased length, abnormal ZP:0102653 microtubule organizing center chondrocyte disorganized, abnormal ZP:0102654 Meckel's cartilage process quality cartilage morphogenesis, abnormal ZP:0102655 chondrocyte Meckel's cartilage morphology, abnormal ZP:0102656 chondrocyte Meckel's cartilage positional polarity, abnormal ZP:0102657 chondrocyte palate decreased size, abnormal ZP:0102659 maxilla absent, abnormal ZP:0102660 quadrate absent, abnormal ZP:0102662 branchiostegal ray absent, abnormal ZP:0102664 chondrocyte proliferation disrupted, abnormal ZP:0102665 epidermis decreased rate mitotic cell cycle, abnormal ZP:0102676 muscle pioneer process quality skeletal muscle cell differentiation, abnormal ZP:0102677 Z disc fast muscle cell increased thickness, abnormal ZP:0102678 fast muscle cell decreased process quality skeletal muscle fiber development, abnormal ZP:0102679 MiP motor neuron decreased process quality axon extension involved in axon guidance, abnormal ZP:0102680 RoP motor neuron decreased process quality axon extension involved in axon guidance, abnormal ZP:0102681 fast muscle cell myotome loose, abnormal ZP:0102682 anatomical region Kupffer's vesicle decreased volume, abnormal ZP:0102683 Kupffer's vesicle decreased occurrence tube formation, abnormal ZP:0102684 anatomical space Kupffer's vesicle decreased volume, abnormal ZP:0102685 Kupffer's vesicle shape, abnormal ZP:0102686 right side diencephalon spatial pattern, abnormal ZP:0102696 taurine whole organism decreased amount, abnormal ZP:0102699 methionine whole organism decreased amount, abnormal ZP:0102700 gamma-aminobutyric acid whole organism decreased amount, abnormal ZP:0102702 L-saccharopine whole organism increased amount, abnormal ZP:0102703 beta-alanine whole organism increased amount, abnormal ZP:0102704 allysine whole organism increased amount, abnormal ZP:0102705 pyridoxal whole organism decreased amount, abnormal ZP:0102706 serine whole organism increased amount, abnormal ZP:0102707 tyrosine whole organism increased amount, abnormal ZP:0102708 alpha-aminobutyric acid whole organism decreased amount, abnormal ZP:0102709 pipecolate whole organism increased amount, abnormal ZP:0102710 1-piperideine-6-carboxylic acid whole organism increased amount, abnormal ZP:0102715 optic tectum electric potential, abnormal ZP:0102716 segmental plate increased amount, abnormal ZP:0102717 neuron projection terminal nerve disorganized, abnormal ZP:0102718 neuron projection terminal nerve decreased branchiness, abnormal ZP:0102719 cell retinal inner nuclear layer swollen, abnormal ZP:0102720 retinal inner nuclear layer hollow, abnormal ZP:0102723 axoneme neural tube structure, abnormal ZP:0102728 lateral dorsal aorta absent, abnormal ZP:0102731 trunk vasculature absent, abnormal ZP:0102737 lens decreased frequency autophagy, abnormal ZP:0102738 spinal cord decreased frequency autophagy, abnormal ZP:0102739 myotome decreased frequency autophagy, abnormal ZP:0102740 optic cup decreased frequency autophagy, abnormal ZP:0102741 lymphocyte thymus decreased amount, abnormal ZP:0102742 cranial neural crest process quality neural crest cell differentiation, abnormal ZP:0102743 ceratohyal cartilage decreased amount, abnormal ZP:0102744 posterior region intermediate cell mass of mesoderm decreased amount, abnormal ZP:0102745 caudal hematopoietic tissue decreased occurrence hematopoietic stem cell proliferation, abnormal ZP:0102750 caudal vein plexus decreased volume, abnormal ZP:0102751 blood island decreased rate hematopoietic stem cell proliferation, abnormal ZP:0102752 head kidney increased rate hematopoietic stem cell proliferation, abnormal ZP:0102753 sex differentiation process quality, abnormal ZP:0102754 blood island increased occurrence hepatoblast apoptotic process, abnormal ZP:0102755 pronephric distal late tubule decreased amount, abnormal ZP:0102756 hematopoietic multipotent progenitor cell caudal hematopoietic tissue decreased amount, abnormal ZP:0102771 thromboblast head kidney increased amount, abnormal ZP:0102782 cranial neural crest cell increased occurrence cell death, abnormal ZP:0102783 migratory cranial neural crest cell pharyngeal arch decreased amount, abnormal ZP:0102784 raphe nucleus process quality neuronal action potential, abnormal ZP:0102786 filopodium cranial neural crest cell decreased length, abnormal ZP:0102787 filopodium cranial neural crest cell decreased amount, abnormal ZP:0102788 pharyngeal pouch process quality neural crest cell migration, abnormal ZP:0102789 pharyngeal pouch decreased occurrence neural crest cell migration, abnormal ZP:0102790 macrophage migration decreased process quality, abnormal ZP:0102791 blood island lacks all parts of type erythroid progenitor cell, abnormal ZP:0102792 heart lacks all parts of type nucleate erythrocyte, abnormal ZP:0102793 common cardinal vein lacks all parts of type nucleate erythrocyte, abnormal ZP:0102794 optic tectum lacks parts or has fewer parts of type microglial cell, abnormal ZP:0102795 macrophage retina decreased amount, abnormal ZP:0102796 macrophage migration decreased rate, abnormal ZP:0102797 macrophage retina mislocalised, abnormal ZP:0102803 macrophage yolk increased amount, abnormal ZP:0102806 neutrophil aggregated, abnormal ZP:0102807 macrophage eye decreased amount, abnormal ZP:0102808 macrophage vitreous decreased amount, abnormal ZP:0102812 otic vesicle absent, abnormal ZP:0102829 CaP motoneuron distance CaP motoneuron, abnormal ZP:0102830 neuron undifferentiated, abnormal ZP:0102831 trabecular layer of ventricle decreased object quality, abnormal ZP:0102832 subcutaneous fat increased amount, abnormal ZP:0102836 neutrophil caudal hematopoietic tissue decreased amount, abnormal ZP:0102838 hematopoietic stem cell increased occurrence cell population proliferation, abnormal ZP:0102840 cell-cell junction epidermis decreased amount, abnormal ZP:0102841 nucleate erythrocyte increased accumulation pericardium, abnormal ZP:0102842 actin cytoskeleton epidermis structure, abnormal ZP:0102843 epidermal cell integument decreased area, abnormal ZP:0102844 dorsal aorta disrupted blood vessel lumenization, abnormal ZP:0102845 telomerase activity decreased process quality, abnormal ZP:0102846 nucleate erythrocyte radius, abnormal ZP:0102847 lipid male organism increased amount, abnormal ZP:0102848 lipid female organism increased amount, abnormal ZP:0102851 D3 vitamins liver decreased amount, abnormal ZP:0102852 D3 vitamins blood plasma decreased amount, abnormal ZP:0102853 D3 vitamins visceral fat decreased amount, abnormal ZP:0102856 mitochondrion visceral fat membrane potential, abnormal ZP:0102857 mitochondrion visceral fat decreased functionality, abnormal ZP:0102858 mitochondrion visceral fat decreased amount, abnormal ZP:0102861 visceral fat decreased amount, abnormal ZP:0102863 swimming behavior increased rate, abnormal ZP:0102864 eye increased height, abnormal ZP:0102866 whole organism increased velocity, abnormal ZP:0102867 head increased height, abnormal ZP:0102871 eye increased width, abnormal ZP:0102872 head increased length, abnormal ZP:0102875 left side Kupffer's vesicle mislocalised, abnormal ZP:0102878 very-low-density lipoprotein blood plasma decreased amount, abnormal ZP:0102881 lipid blood plasma increased amount, abnormal ZP:0102883 myeloid cell head kidney decreased amount, abnormal ZP:0102884 optic primordium decreased distribution, abnormal ZP:0102885 forebrain neural plate decreased distribution, abnormal ZP:0102886 forebrain neural rod decreased distribution, abnormal ZP:0102891 heart process rhythm quality, abnormal ZP:0102893 photoreceptor outer segment blue sensitive photoreceptor cell decreased amount, abnormal ZP:0102894 photoreceptor outer segment green sensitive photoreceptor cell decreased thickness, abnormal ZP:0102896 photoreceptor outer segment red sensitive photoreceptor cell decreased amount, abnormal ZP:0102897 photoreceptor outer segment retinal rod cell decreased thickness, abnormal ZP:0102898 photoreceptor inner segment retina mislocalised, abnormal ZP:0102899 filamentous actin retina disorganized, abnormal ZP:0102902 axon trigeminal ganglion branchiness, abnormal ZP:0102905 olfactory receptor cell absent, abnormal ZP:0102906 germ line cell seminiferous tubule absent, abnormal ZP:0102907 lymphocyte testis increased amount, abnormal ZP:0102910 gonad decreased amount, abnormal ZP:0102911 vacuole primordial germ cell increased amount, abnormal ZP:0102912 primordial germ cell gonad decreased amount, abnormal ZP:0102913 meiosis I arrested, abnormal ZP:0102914 germ cell development arrested, abnormal ZP:0102915 meiotic cell cycle arrested, abnormal ZP:0102916 gonad spatial pattern, abnormal ZP:0102919 melatonin whole organism decreased amount, abnormal ZP:0102921 triglyceride skeletal muscle increased amount, abnormal ZP:0102922 lipid skeletal muscle increased amount, abnormal ZP:0102923 regulation of lipid metabolic process process quality, abnormal ZP:0102924 muscle hyperplastic, abnormal ZP:0102925 adipose tissue decreased amount, abnormal ZP:0102926 muscle cell hyperplastic, abnormal ZP:0102929 retinal pigmented epithelium has extra parts of type inclusion body retinal pigmented epithelium, abnormal ZP:0102931 ciliary marginal zone increased occurrence apoptotic chromosome condensation, abnormal ZP:0102932 cell ciliary marginal zone apoptotic, abnormal ZP:0102933 digestion decreased rate, abnormal ZP:0102935 digestive system delayed G1/S transition of mitotic cell cycle, abnormal ZP:0102937 digestive system disrupted cell population proliferation, abnormal ZP:0102938 whole organism decreased duration swimming, abnormal ZP:0102939 spinal cord process quality ossification, abnormal ZP:0102940 anatomical region Kupffer's vesicle spatial pattern, abnormal ZP:0102941 Kupffer's vesicle structure, cavities, abnormal ZP:0102942 Kupffer's vesicle uninflated, abnormal ZP:0102945 pharyngeal arch 3 absent, abnormal ZP:0102946 pharyngeal arch 4 absent, abnormal ZP:0102948 lens increased occurrence cell death, abnormal ZP:0102949 lens development in camera-type eye arrested, abnormal ZP:0102952 lens epithelium mislocalised, abnormal ZP:0102964 swim bladder flattened, abnormal ZP:0102970 pronephric glomerular capillary collapsed, abnormal ZP:0102971 blood plasma blood vasculature decreased amount, abnormal ZP:0102972 glomerular filtration decreased occurrence, abnormal ZP:0102974 anterior margin ethmoid cartilage emarginate, abnormal ZP:0102975 pharyngeal arch 3-7 has fewer parts of type ectomesenchyme, abnormal ZP:0102981 neuron projection cranial nerve II physical object quality, abnormal ZP:0102982 cranial nerve II optic chiasm malformed, abnormal ZP:0102983 NCC ionocyte gill decreased amount, abnormal ZP:0102984 corpuscles of Stannius decreased amount, abnormal ZP:0102986 chloride whole organism decreased amount, abnormal ZP:0102987 sodium(1+) gill decreased amount, abnormal ZP:0102988 sodium(1+) whole organism decreased amount, abnormal ZP:0102991 vH ionocyte pronephric duct decreased amount, abnormal ZP:0102992 vH ionocyte pronephric proximal convoluted tubule decreased amount, abnormal ZP:0102993 vH ionocyte pronephric proximal straight tubule decreased amount, abnormal ZP:0102999 glycosaminoglycan cornea increased amount, abnormal ZP:0103020 nucleus lens fiber cell present, abnormal ZP:0103021 early endosome lens fiber cell present, abnormal ZP:0103022 late endosome lens fiber cell present, abnormal ZP:0103023 late endosome lens fiber cell mislocalised, abnormal ZP:0103024 organelle lens fiber cell present, abnormal ZP:0103025 epithelial cell lens epithelium increased amount, abnormal ZP:0103026 activation of cysteine-type endopeptidase activity involved in apoptotic process decreased process quality, abnormal ZP:0103027 lens fiber cell increased amount, abnormal ZP:0103028 estradiol blood decreased amount, abnormal ZP:0103029 11-oxotestosterone blood decreased amount, abnormal ZP:0103030 oocyte stage IV disrupted oocyte maturation, abnormal ZP:0103036 female organism decreased rate ovulation, abnormal ZP:0103037 oocyte stage IV disrupted meiosis II nuclear envelope disassembly, abnormal ZP:0103038 hypophysis male organism decreased amount, abnormal ZP:0103039 hypophysis female organism decreased amount, abnormal ZP:0103040 flagellated sperm motility decreased process quality, abnormal ZP:0103041 female organism proportionality to male organism, abnormal ZP:0103042 female organism decreased female fertility, abnormal ZP:0103043 female organism has fewer parts of type oocyte stage V, abnormal ZP:0103044 ovary has fewer parts of type ovarian follicle stage IV, abnormal ZP:0103045 testis lacks parts or has fewer parts of type sperm, abnormal ZP:0103046 testis has extra parts of type spermatocyte, abnormal ZP:0103047 testis has extra parts of type spermatogonium, abnormal ZP:0103049 atrioventricular canal arrested endocardial cushion formation, abnormal ZP:0103050 atrioventricular canal lacks all parts of type endocardial cushion atrioventricular canal, abnormal ZP:0103051 atrioventricular canal endocardium absent, abnormal ZP:0103052 whole organism ventralized, abnormal ZP:0103053 anterior region neuroectoderm decreased distribution, abnormal ZP:0103054 optic vesicle decreased distribution, abnormal ZP:0103055 cilium lateral crista increased length, abnormal ZP:0103056 cilium olfactory epithelium increased length, abnormal ZP:0103057 ciliary base macula absent, abnormal ZP:0103059 ciliary base macula decreased amount, abnormal ZP:0103060 head decreased diameter, abnormal ZP:0103064 atrioventricular canal endocardium increased occurrence Notch signaling involved in heart development, abnormal ZP:0103065 ventricular endocardium increased distribution, abnormal ZP:0103066 atrioventricular canal endocardium increased distribution, abnormal ZP:0103068 germ line cell gonad absent, abnormal ZP:0103069 germ line cell testis absent, abnormal ZP:0103071 oogonia absent, abnormal ZP:0103072 testis increased occurrence apoptotic process, abnormal ZP:0103073 spermatogonium apoptotic, abnormal ZP:0103074 spermatogonium deformed, abnormal ZP:0103077 male organism proportionality to female organism, abnormal ZP:0103078 estradiol blood absent, abnormal ZP:0103079 immature gonad absent, abnormal ZP:0103080 testosterone male organism increased amount, abnormal ZP:0103082 estradiol female organism decreased amount, abnormal ZP:0103083 11-oxotestosterone male organism increased amount, abnormal ZP:0103088 bulbus arteriosus decreased amount, abnormal ZP:0103089 cleithrum decreased process quality bone mineralization, abnormal ZP:0103090 mouth shape, abnormal ZP:0103092 chondrocyte palate circular, abnormal ZP:0103093 chondrocyte palate size, abnormal ZP:0103094 palate increased length, abnormal ZP:0103095 palate decreased width, abnormal ZP:0103096 palate process quality cell migration, abnormal ZP:0103097 vertebra split, abnormal ZP:0103098 vertebra curved, abnormal ZP:0103099 mouth position, abnormal ZP:0103100 caudal fin principal ray morphology, abnormal ZP:0103101 caudal fin principal ray deformed, abnormal ZP:0103102 caudal fin principal ray decreased amount, abnormal ZP:0103103 nasal bone morphology, abnormal ZP:0103104 caudal fin principal ray shortened, abnormal ZP:0103105 vertebra caudal peduncle deformed, abnormal ZP:0103106 caudal peduncle deformed, abnormal ZP:0103107 horizontal plane cranium morphology, abnormal ZP:0103108 dermis fin absent, abnormal ZP:0103109 pelvic fin deformed, abnormal ZP:0103110 lepidotrichium shortened, abnormal ZP:0103111 paired fin shortened, abnormal ZP:0103112 median fin shortened, abnormal ZP:0103113 lepidotrichium segment shortened, abnormal ZP:0103114 melanophore stripe increased distance melanophore stripe, abnormal ZP:0103115 vertebra composition, abnormal ZP:0103116 germ line cell gonad primordium decreased amount, abnormal ZP:0103117 somatic cell gonad primordium morphology, abnormal ZP:0103118 somatic cell gonad primordium absent, abnormal ZP:0103119 somatic cell gonad primordium decreased amount, abnormal ZP:0103120 gonad primordium absent, abnormal ZP:0103121 germ line cell immature gonad decreased amount, abnormal ZP:0103122 gonad primordium decreased process quality cell population proliferation, abnormal ZP:0103123 germ line cell gonad decreased amount, abnormal ZP:0103124 gonad disorganized, abnormal ZP:0103125 Sertoli cell absent, abnormal ZP:0103126 pericardium increased area, abnormal ZP:0103127 atrium increased area, abnormal ZP:0103128 17alpha-hydroxyprogesterone whole organism present, abnormal ZP:0103129 cortisol whole organism decreased amount, abnormal ZP:0103130 21-deoxycortisol whole organism present, abnormal ZP:0103132 steroid biosynthetic process process quality, abnormal ZP:0103134 neurohypophysis increased distribution, abnormal ZP:0103135 adenohypophysis increased distribution, abnormal ZP:0103136 interrenal gland increased size, abnormal ZP:0103137 interrenal gland increased distribution, abnormal ZP:0103139 thromboblast caudal hematopoietic tissue decreased amount, abnormal ZP:0103140 chondrocyte neurocranial trabecula morphology, abnormal ZP:0103141 mouth decreased width, abnormal ZP:0103142 mesenchyme pharyngeal arch 1 decreased amount, abnormal ZP:0103144 retinal rod cell decreased process quality photoreceptor cell outer segment organization, abnormal ZP:0103145 cell body retinal rod cell mislocalised, abnormal ZP:0103146 photoreceptor cell cilium retinal rod cell decreased length, abnormal ZP:0103148 retinal rod cell lacks all parts of type photoreceptor outer segment retinal rod cell, abnormal ZP:0103149 melanosome melanocyte mislocalised, abnormal ZP:0103150 photoreceptor inner segment retinal cone cell mislocalised, abnormal ZP:0103151 cell body retinal cone cell mislocalised, abnormal ZP:0103152 synapse retinal cone cell mislocalised, abnormal ZP:0103153 retinal cone cell decreased process quality retinal cone cell development, abnormal ZP:0103154 ciliary base eye photoreceptor cell decreased amount, abnormal ZP:0103156 yolk color, abnormal ZP:0103161 fertilization increased occurrence, abnormal ZP:0103162 whole organism increased fertility, abnormal ZP:0103165 ethmoid cartilage cleft, abnormal ZP:0103166 ethmoid cartilage circular, abnormal ZP:0103167 axon spinal cord swollen, abnormal ZP:0103168 axon posterior lateral line swollen, abnormal ZP:0103174 axis elongation decreased occurrence, abnormal ZP:0103175 embryonic structure decreased amount, abnormal ZP:0103176 intersegmental vessel has fewer parts of type endothelial tip cell filopodium endothelial tip cell, abnormal ZP:0103177 dorsal longitudinal anastomotic vessel decreased occurrence blood vessel morphogenesis, abnormal ZP:0103178 photoreceptor outer segment retina decreased amount, abnormal ZP:0103179 photoreceptor outer segment photoreceptor outer segment layer disoriented, abnormal ZP:0103180 photoreceptor outer segment retinal cone cell mislocalised, abnormal ZP:0103181 photoreceptor outer segment retinal rod cell mislocalised, abnormal ZP:0103182 retinal inner nuclear layer incomplete structure, abnormal ZP:0103183 retinal outer nuclear layer incomplete structure, abnormal ZP:0103184 endothelial tip cell decreased rate cell migration involved in sprouting angiogenesis, abnormal ZP:0103185 endothelial tip cell decreased occurrence cell division, abnormal ZP:0103186 filamentous actin epidermal cell increased distribution, abnormal ZP:0103187 spinal cord has fewer parts of type glioblast spinal cord, abnormal ZP:0103190 spinal cord decreased rate mitotic cell cycle, abnormal ZP:0103191 spinal cord decreased rate oligodendrocyte progenitor proliferation, abnormal ZP:0103192 epidermal cell decreased size, abnormal ZP:0103195 neuron projection terminus afferent neuron decreased amount, abnormal ZP:0103196 posterior lateral line neuromast decreased occurrence innervation, abnormal ZP:0103201 heart decreased process quality heart morphogenesis, abnormal ZP:0103202 otic vesicle decreased process quality otolith development, abnormal ZP:0103203 Kupffer's vesicle decreased occurrence motile cilium assembly, abnormal ZP:0103204 pronephros decreased process quality epithelial cilium movement involved in extracellular fluid movement, abnormal ZP:0103205 pancreatic A cell differentiation process quality, abnormal ZP:0103210 left side lateral plate mesoderm absent, abnormal ZP:0103212 left side lateral plate mesoderm decreased amount, abnormal ZP:0103213 determination of intestine left/right asymmetry arrested, abnormal ZP:0103214 pancreas bilateral, abnormal ZP:0103217 pronephric proximal convoluted tubule decreased distribution, abnormal ZP:0103218 pronephric proximal convoluted tubule decreased area, abnormal ZP:0103219 endocrine pancreas spatial pattern, abnormal ZP:0103220 whole organism has fewer parts of type forerunner cell group, abnormal ZP:0103221 muscle cell structure, abnormal ZP:0103222 skeletal muscle myofibril muscle cell structure, abnormal ZP:0103223 myotome increased occurrence apoptotic process, abnormal ZP:0103224 skeletal muscle fiber development decreased process quality, abnormal ZP:0103225 muscle cell detached from myoseptum, abnormal ZP:0103227 rhombomere decreased size, abnormal ZP:0103228 presumptive neural retina increased amount, abnormal ZP:0103229 presumptive neural retina decreased amount, abnormal ZP:0103230 posterior lateral line ganglion decreased amount, abnormal ZP:0103231 dopamine retina decreased amount, abnormal ZP:0103232 dopaminergic neuron retinal inner nuclear layer decreased distribution, abnormal ZP:0103235 pronephric tubule has fewer parts of type motile cilium inner dynein arm pronephric tubule, abnormal ZP:0103236 pronephric tubule has fewer parts of type motile cilium outer dynein arm pronephric tubule, abnormal ZP:0103237 motile cilium peripheral olfactory organ immobile, abnormal ZP:0103238 motile cilium pronephric tubule immobile, abnormal ZP:0103239 cytoplasm pronephric tubule decreased amount, abnormal ZP:0103246 cardiac ventricle decreased process quality trabecula formation, abnormal ZP:0103247 ventricular trabecula myocardium morphogenesis decreased process quality, abnormal ZP:0103248 trabecular layer of ventricle malformed, abnormal ZP:0103249 trabecular layer of ventricle lacks parts or has fewer parts of type cardiac muscle cell, abnormal ZP:0103258 cell surface whole organism shape, abnormal ZP:0103259 cranial motor neuron absent, abnormal ZP:0103260 cortical actin cytoskeleton compact layer of ventricle spatial pattern, abnormal ZP:0103261 cortical actin cytoskeleton compact layer of ventricle malformed, abnormal ZP:0103263 focal adhesion heart absent, abnormal ZP:0103265 liver decreased occurrence canonical Wnt signaling pathway, abnormal ZP:0103266 exocrine pancreas decreased occurrence canonical Wnt signaling pathway, abnormal ZP:0103272 endodermal cell liver decreased amount, abnormal ZP:0103273 endodermal cell exocrine pancreas decreased amount, abnormal ZP:0103279 anterior-posterior axis whole organism size, abnormal ZP:0103280 angiogenic sprout intersegmental vessel morphology, abnormal ZP:0103281 endothelial cell angiogenic sprout morphology, abnormal ZP:0103282 cerebellar central artery process quality angiogenesis, abnormal ZP:0103283 middle mesencephalic central artery process quality angiogenesis, abnormal ZP:0103284 intersegmental vessel disrupted blood circulation, abnormal ZP:0103285 nasal ciliary artery separated from angiogenic sprout dorsal ciliary vein, abnormal ZP:0103286 angiogenic sprout mesencephalic vein morphology, abnormal ZP:0103288 nucleate erythrocyte dorsal aorta decreased velocity, abnormal ZP:0103296 parachordal vessel intersegmental vessel decreased amount, abnormal ZP:0103301 notochord development process quality, abnormal ZP:0103302 photoreceptor outer segment retinal cone cell decreased volume, abnormal ZP:0103303 RoP motor neuron decreased amount, abnormal ZP:0103304 CaP motoneuron increased branchiness, abnormal ZP:0103305 primary motor neuron shape, abnormal ZP:0103309 hemal arch increased thickness, abnormal ZP:0103310 hemal arch increased volume, abnormal ZP:0103311 neural arch increased thickness, abnormal ZP:0103315 circadian sleep/wake cycle, wakefulness increased duration, abnormal ZP:0103325 neuroectoderm increased amount, abnormal ZP:0103327 presumptive rhombomere 4 decreased amount, abnormal ZP:0103334 cranium decreased amount, abnormal ZP:0103346 retinal ganglion cell axon guidance decreased process quality, abnormal ZP:0103367 pronephric glomerulus increased occurrence apoptotic process, abnormal ZP:0103383 central nervous system absent, abnormal ZP:0103390 migratory neural crest cell increased amount, abnormal ZP:0103414 pectoral fin bud decreased amount, abnormal ZP:0103424 autophagosome heart increased amount, abnormal ZP:0103425 eye photoreceptor cell increased occurrence apoptotic process, abnormal ZP:0103426 ciliary basal body eye photoreceptor cell mislocalised, abnormal ZP:0103427 perikaryon eye photoreceptor cell mislocalised, abnormal ZP:0103428 ciliary basal body eye photoreceptor cell decreased amount, abnormal ZP:0103429 retinal photoreceptor layer has fewer parts of type photoreceptor outer segment eye photoreceptor cell, abnormal ZP:0103438 11-oxotestosterone whole organism increased amount, abnormal ZP:0103439 lipid droplet muscle increased amount, abnormal ZP:0103440 brain female organism decreased amount, abnormal ZP:0103441 liver female organism decreased amount, abnormal ZP:0103442 testis male organism increased size, abnormal ZP:0103444 oocyte stage II increased amount, abnormal ZP:0103445 unfertilized egg decreased amount, abnormal ZP:0103446 Sertoli cell increased amount, abnormal ZP:0103447 granulosa cell absent, abnormal ZP:0103448 breeding tubercle male organism deformed, abnormal ZP:0103449 breeding tubercle male organism decreased amount, abnormal ZP:0103450 wound healing decreased occurrence, abnormal ZP:0103451 angiogenic sprout central artery complexity, abnormal ZP:0103452 angiogenic sprout central artery decreased amount, abnormal ZP:0103453 angiogenic sprout central artery decreased branchiness, abnormal ZP:0103454 nucleus cell increased amount, abnormal ZP:0103455 EVL fused with nucleus nucleus EVL, abnormal ZP:0103456 cell detached from cell, abnormal ZP:0103457 cleavage furrow blastomere blurry, abnormal ZP:0103458 cleavage furrow cell decreased amount, abnormal ZP:0103460 acetylcholine-gated channel complex skeletal muscle decreased size, abnormal ZP:0103461 neuromuscular junction skeletal muscle morphology, abnormal ZP:0103462 skeletal muscle myofibril skeletal muscle structure, abnormal ZP:0103463 liver primordium decreased amount, abnormal ZP:0103464 posterior side neural plate T-shaped, abnormal ZP:0103465 cell brain mislocalised, abnormal ZP:0103466 neural tube duplicated, abnormal ZP:0103467 retinal ganglion cell aplastic/hypoplastic, abnormal ZP:0103468 myotome decreased magnitude skeletal muscle contraction, abnormal ZP:0103469 sarcoplasm skeletal muscle cell increased size, abnormal ZP:0103474 Z disc skeletal muscle cell malformed, abnormal ZP:0103475 optic tectum decreased occurrence neuron projection development, abnormal ZP:0103476 skeletal muscle cell decreased process quality sarcomere organization, abnormal ZP:0103477 optic tectum has fewer parts of type neuron projection optic tectum, abnormal ZP:0103478 oocyte stage I decreased occurrence establishment of cell polarity, abnormal ZP:0103479 mitochondrial cloud oocyte stage I increased life span, abnormal ZP:0103480 oocyte stage I polarity, abnormal ZP:0103485 hematopoietic cell anterior lateral mesoderm decreased amount, abnormal ZP:0103486 hematopoietic cell posterior lateral mesoderm decreased amount, abnormal ZP:0103487 capillary endocrine pancreas decreased diameter, abnormal ZP:0103488 capillary endocrine pancreas decreased amount, abnormal ZP:0103492 dorsal telencephalon increased amount, abnormal ZP:0103493 medial region ventral thalamus absent, abnormal ZP:0103494 neuron projection ventral thalamus spatial pattern, abnormal ZP:0103495 neuron projection ventral thalamus disorganized, abnormal ZP:0103496 lateral region ventral thalamus increased amount, abnormal ZP:0103498 pancreatic acinar cell exocrine pancreas disorganized, abnormal ZP:0103499 pancreatic acinar cell exocrine pancreas dispersed, abnormal ZP:0103501 macrophage head increased distribution, abnormal ZP:0103503 intestine male organism increased amount, abnormal ZP:0103504 intestine male organism decreased amount, abnormal ZP:0103505 intestine female organism increased amount, abnormal ZP:0103511 liver female organism increased amount, abnormal ZP:0103512 caudal vein plexus increased permeability, abnormal ZP:0103513 cranial vasculature decreased size, abnormal ZP:0103514 neutrophil head increased distribution, abnormal ZP:0103515 macrophage head decreased distribution, abnormal ZP:0103516 neutrophil head decreased distribution, abnormal ZP:0103518 nucleate erythrocyte caudal hematopoietic tissue increased amount, abnormal ZP:0103519 monocyte pronephros increased amount, abnormal ZP:0103520 myeloid cell caudal hematopoietic tissue increased amount, abnormal ZP:0103521 basophilic erythroblast increased amount, abnormal ZP:0103529 caudal hematopoietic tissue decreased amount, abnormal ZP:0103530 myosin filament skeletal muscle disorganized, abnormal ZP:0103531 pineal complex decreased distribution, abnormal ZP:0103532 pineal complex decreased process quality animal organ formation, abnormal ZP:0103533 left side habenula absent, abnormal ZP:0103534 left side habenula increased amount, abnormal ZP:0103535 pinealocyte decreased process quality pineal gland development, abnormal ZP:0103536 pineal complex decreased occurrence cell differentiation, abnormal ZP:0103537 pinealocyte decreased occurrence cell differentiation, abnormal ZP:0103538 epiphysis process quality photoreceptor cell differentiation, abnormal ZP:0103539 parapineal organ decreased process quality animal organ formation, abnormal ZP:0103540 photoreceptor cell epiphysis absent, abnormal ZP:0103541 photoreceptor cell epiphysis decreased amount, abnormal ZP:0103542 pineal complex lacks all parts of type parapineal organ, abnormal ZP:0103543 pineal complex lacks all parts of type pinealocyte, abnormal ZP:0103544 parapineal organ absent, abnormal ZP:0103545 pinealocyte absent, abnormal ZP:0103546 whole organism decreased process quality DNA methylation, abnormal ZP:0103547 estrogen female organism decreased amount, abnormal ZP:0103548 3,3',5-triiodo-L-thyronine whole organism decreased amount, abnormal ZP:0103549 epiphysis decreased distribution, abnormal ZP:0103550 epiphysis increased occurrence neuron projection development, abnormal ZP:0103551 visible light photoreceptor cell epiphysis absent, abnormal ZP:0103552 median fin decreased size, abnormal ZP:0103561 cell roof plate amount, abnormal ZP:0103562 cell roof plate disorganized, abnormal ZP:0103563 floor plate spatial pattern, abnormal ZP:0103564 floor plate spinal cord region decreased amount, abnormal ZP:0103565 dorsal side spinal cord increased amount, abnormal ZP:0103585 gut cystic, abnormal ZP:0103586 microvillus pronephros decreased amount, abnormal ZP:0103589 ciliary basal body pronephros mislocalised, abnormal ZP:0103591 ciliary membrane pronephros absent, abnormal ZP:0103592 ciliary basal body-plasma membrane docking disrupted, abnormal ZP:0103593 microvillus brush border epithelial cell absent, abnormal ZP:0103594 peptidylglycine monooxygenase activity disrupted, abnormal ZP:0103595 swim bladder arrested surfactant homeostasis, abnormal ZP:0103596 swim bladder decreased occurrence surfactant homeostasis, abnormal ZP:0103597 swim bladder decreased amount, abnormal ZP:0103598 Melanin melanocyte decreased amount, abnormal ZP:0103599 retinal pigmented epithelium decreased process quality melanosome organization, abnormal ZP:0103600 melanocyte decreased occurrence cellular pigmentation, abnormal ZP:0103601 eye decreased occurrence iridophore differentiation, abnormal ZP:0103603 optic tectum has extra parts of type posterior region lysosome optic tectum, abnormal ZP:0103604 optic tectum decreased process quality lysosome localization, abnormal ZP:0103605 iridophore decreased process quality pigment granule organization, abnormal ZP:0103606 iridophore differentiation decreased process quality, abnormal ZP:0103607 iridophore lacks all parts of type iridosome iridophore, abnormal ZP:0103608 integument decreased occurrence melanocyte differentiation, abnormal ZP:0103609 integument decreased occurrence iridophore differentiation, abnormal ZP:0103610 mesenchyme swim bladder decreased amount, abnormal ZP:0103611 epithelium swim bladder decreased amount, abnormal ZP:0103612 neuroblast brain decreased amount, abnormal ZP:0103613 neuroblast hindbrain decreased amount, abnormal ZP:0103614 neuroblast spinal cord decreased amount, abnormal ZP:0103615 neuroblast forebrain decreased amount, abnormal ZP:0103616 glioblast decreased amount, abnormal ZP:0103617 homocysteine brain increased amount, abnormal ZP:0103618 B cell head kidney decreased amount, abnormal ZP:0103620 cell projection posterior lateral line neuromast direction, abnormal ZP:0103630 central artery hindbrain increased branchiness, abnormal ZP:0103631 transverse plane eye decreased length, abnormal ZP:0103632 retinal neural layer folded, abnormal ZP:0103633 retinal pigmented epithelium folded, abnormal ZP:0103634 optic furrow increased amount, abnormal ZP:0103635 closure of optic fissure decreased occurrence, abnormal ZP:0103636 enteric nervous system decreased amount, abnormal ZP:0103637 neuron projection intestine increased thickness, abnormal ZP:0103638 neuron projection intestine disorganized, abnormal ZP:0103639 neuron projection intestine shortened, abnormal ZP:0103641 hatching behavior decreased rate, abnormal ZP:0103643 presumptive rhombomere 4 increased amount, abnormal ZP:0103644 presumptive rhombomere 3 increased amount, abnormal ZP:0103645 hindbrain hemorrhagic, abnormal ZP:0103646 muscle hemorrhagic, abnormal ZP:0103647 gill filament hemorrhagic, abnormal ZP:0103648 hemostasis disrupted, abnormal ZP:0103651 presumptive rhombomere 4 mislocalised, abnormal ZP:0103652 striated muscle myosin thick filament slow muscle cell decreased length, abnormal ZP:0103653 striated muscle thin filament slow muscle cell decreased length, abnormal ZP:0103664 intersegmental vein process quality sprouting angiogenesis, abnormal ZP:0103665 angiogenic sprout intersegmental vein decreased length, abnormal ZP:0103666 vascular lymphangioblast morphology, abnormal ZP:0103671 cysteine-type endopeptidase activity involved in apoptotic process decreased process quality, abnormal ZP:0103672 slow muscle cell somite 7 spatial pattern, abnormal ZP:0103676 post-vent vasculature hemorrhagic, abnormal ZP:0103677 startle response increased sensitivity of a process sensory perception of sound, abnormal ZP:0103678 xanthophore disrupted pigment biosynthetic process, abnormal ZP:0103685 testis increased occurrence cell population proliferation, abnormal ZP:0103686 caudal fin decreased process quality male pigmentation, abnormal ZP:0103687 pleuroperitoneal cavity male organism increased size, abnormal ZP:0103688 pleuroperitoneal cavity female organism increased size, abnormal ZP:0103689 developmental process involved in reproduction process quality, abnormal ZP:0103690 male gonad development increased duration, abnormal ZP:0103691 male gonad development peramorphic growth, abnormal ZP:0103692 development of primary sexual characteristics process quality, abnormal ZP:0103693 development of primary male sexual characteristics process quality, abnormal ZP:0103694 oocyte development process quality, abnormal ZP:0103695 ovary hypertrophic, abnormal ZP:0103696 spermatid decreased amount, abnormal ZP:0103697 oogonia increased amount, abnormal ZP:0103698 testis spatial pattern, abnormal ZP:0103699 testis increased distribution, abnormal ZP:0103700 actin filament forerunner cell group structure, abnormal ZP:0103701 somatic cell testis disorganized, abnormal ZP:0103702 testis vacuolated, abnormal ZP:0103703 oocyte stage I present, abnormal ZP:0103704 Leydig cell testis increased amount, abnormal ZP:0103705 heart tube spatial pattern, abnormal ZP:0103706 axis increased amount, abnormal ZP:0103707 axis increased distribution, abnormal ZP:0103708 anatomical margin blastodisc increased amount, abnormal ZP:0103709 cilium inner ear absent, abnormal ZP:0103710 membrane photoreceptor cell irregularly shaped, abnormal ZP:0103711 optic cup decreased rate cell population proliferation, abnormal ZP:0103712 basement membrane optic cup morphology, abnormal ZP:0103713 basement membrane disassembly disrupted, abnormal ZP:0103715 brain decreased process quality cell population proliferation, abnormal ZP:0103716 plasma membrane retinal rod cell mislocalised, abnormal ZP:0103717 retinal photoreceptor layer retinal rod cell decreased thickness, abnormal ZP:0103718 apical region photoreceptor cell mislocalised, abnormal ZP:0103719 copper-63 liver decreased amount, abnormal ZP:0103720 copper-63 midbrain decreased amount, abnormal ZP:0103721 copper-63 retina absent, abnormal ZP:0103722 copper-63 nervous system decreased amount, abnormal ZP:0103723 copper-63 kidney increased amount, abnormal ZP:0103724 copper-63 retinal outer nuclear layer decreased amount, abnormal ZP:0103740 mRNA cis splicing, via spliceosome process quality, abnormal ZP:0103748 convergent extension involved in axis elongation decreased occurrence, abnormal ZP:0103751 photoreceptor outer segment layer spatial pattern, abnormal ZP:0103752 cell midbrain degenerate, abnormal ZP:0103753 cell midbrain vacuolated, abnormal ZP:0103754 dorsal region midbrain increased amount, abnormal ZP:0103755 dorsal region midbrain mislocalised, abnormal ZP:0103756 epiboly increased duration, abnormal ZP:0103757 mitotic G2 phase increased duration, abnormal ZP:0103758 scale disrupted growth, abnormal ZP:0103759 scale fin decreased size, abnormal ZP:0103763 pronephric duct process quality regulation of autophagy, abnormal ZP:0103765 endoplasmic reticulum lumen liver increased width, abnormal ZP:0103766 endoplasmic reticulum lumen liver dilated, abnormal ZP:0103767 endoplasmic reticulum lumen enterocyte increased width, abnormal ZP:0103768 lipid droplet enterocyte increased amount, abnormal ZP:0103769 low-density lipoprotein particle whole organism decreased amount, abnormal ZP:0103771 retina decreased process quality transmission of nerve impulse, abnormal ZP:0103772 retinal bipolar neuron decreased process quality transmission of nerve impulse, abnormal ZP:0103773 cell hindbrain apoptotic, abnormal ZP:0103774 ventricular zone spatial pattern, abnormal ZP:0103775 dorso-lateral region hindbrain increased amount, abnormal ZP:0103776 cell forebrain apoptotic, abnormal ZP:0103777 cell third ventricle apoptotic, abnormal ZP:0103778 tegmentum increased amount, abnormal ZP:0103779 medulla oblongata decreased amount, abnormal ZP:0103780 hindbrain nucleus decreased amount, abnormal ZP:0103783 female organism decreased fecundity, abnormal ZP:0103784 frontal bone morphology, abnormal ZP:0103785 opercular flap morphology, abnormal ZP:0103786 anal fin morphology, abnormal ZP:0103787 dorsal fin morphology, abnormal ZP:0103788 ovarian follicle stage IV degenerate, abnormal ZP:0103791 exploration behavior decreased process quality, abnormal ZP:0103803 musculoskeletal movement decreased frequency, abnormal ZP:0103804 cell yolk syncytial layer position, abnormal ZP:0103805 yolk syncytial layer absent, abnormal ZP:0103806 DEL increased amount, abnormal ZP:0103807 actin filament yolk syncytial layer structure, abnormal ZP:0103808 blastoderm detached from yolk, abnormal ZP:0103809 epiblast absent, abnormal ZP:0103810 centrosome cell absent, abnormal ZP:0103811 olfactory bulb absent, abnormal ZP:0103814 shield spatial pattern, abnormal ZP:0103828 mesodermal cell migration decreased process quality, abnormal ZP:0103829 blastoderm spatial pattern, abnormal ZP:0103830 caudal fin decreased occurrence blood circulation, abnormal ZP:0103831 mesenchyme caudal fin morphology, abnormal ZP:0103832 mesenchyme ventral fin fold morphology, abnormal ZP:0103833 blood increased accumulation caudal fin, abnormal ZP:0103834 endodermal cell apoptotic, abnormal ZP:0103835 central artery increased branchiness, abnormal ZP:0103836 endothelial cell cranial blood vessel spatial pattern, abnormal ZP:0103838 optic tectum process quality neuronal action potential, abnormal ZP:0103839 endoderm process quality cell migration involved in gastrulation, abnormal ZP:0103840 blood accumulation blood vessel, abnormal ZP:0103842 cardiac atrium morphogenesis decreased process quality, abnormal ZP:0103843 atrial myocardium increased occurrence cell population proliferation, abnormal ZP:0103844 atrium decreased process quality cardiac conduction, abnormal ZP:0103848 retinal cone cell retinal outer nuclear layer decreased amount, abnormal ZP:0103850 ciliary marginal zone mislocalised, abnormal ZP:0103852 nucleus nucleate erythrocyte size, abnormal ZP:0103856 hyoid muscle decreased process quality tendon formation, abnormal ZP:0103857 skeletal muscle cell interhyoideus mislocalised, abnormal ZP:0103858 ventral intermandibularis posterior decreased process quality determination of muscle attachment site, abnormal ZP:0103859 interhyoideus decreased process quality determination of muscle attachment site, abnormal ZP:0103860 skeletal muscle cell sternohyoid mislocalised medially, abnormal ZP:0103861 skeletal muscle cell ventral intermandibularis anterior mislocalised, abnormal ZP:0103862 skeletal muscle cell ventral intermandibularis posterior mislocalised, abnormal ZP:0103863 skeletal muscle cell hyohyoideus mislocalised, abnormal ZP:0103864 ventral intermandibularis posterior increased length, abnormal ZP:0103865 anterior region basihyal cartilage hypoplastic, abnormal ZP:0103866 medial region Meckel's cartilage malformed, abnormal ZP:0103867 medial region ceratohyal cartilage malformed, abnormal ZP:0103869 mandibular muscle decreased process quality tendon development, abnormal ZP:0103870 hyoid muscle decreased process quality tendon development, abnormal ZP:0103871 anterior region basihyal cartilage decreased width, abnormal ZP:0103872 parasphenoid decreased width, abnormal ZP:0103873 adenohypophyseal placode decreased amount, abnormal ZP:0103874 thymus primordium has fewer parts of type lymphocyte, abnormal ZP:0103880 paired fin decreased amount, abnormal ZP:0103881 ventral region iris morphology, abnormal ZP:0103882 ethmoid cartilage size, abnormal ZP:0103883 anterior chamber eye decreased size, abnormal ZP:0103884 integument anterior segment eye mislocalised, abnormal ZP:0103885 cartilage tissue eye mislocalised, abnormal ZP:0103886 cartilage tissue anterior segment eye mislocalised, abnormal ZP:0103887 eye opacity, abnormal ZP:0103888 iris absent, abnormal ZP:0103889 iris hypoplastic, abnormal ZP:0103890 corneal epithelium mislocalised, abnormal ZP:0103891 corneal epithelium vacuolated, abnormal ZP:0103892 corneal epithelium decreased amount, abnormal ZP:0103893 corneal stroma morphology, abnormal ZP:0103894 corneal stroma spatial pattern, abnormal ZP:0103895 corneal stroma position, abnormal ZP:0103896 corneal stroma increased thickness, abnormal ZP:0103897 corneal stroma decreased thickness, abnormal ZP:0103898 corneal stroma undulate, abnormal ZP:0103899 corneal endothelium morphology, abnormal ZP:0103900 corneal endothelium increased thickness, abnormal ZP:0103901 corneal endothelium disorganized, abnormal ZP:0103902 iris stroma morphology, abnormal ZP:0103903 lens capsule morphology, abnormal ZP:0103904 anterior chamber eye morphology, abnormal ZP:0103905 anterior chamber eye absent, abnormal ZP:0103906 cornea abutting lens capsule, abnormal ZP:0103907 annular ligament morphology, abnormal ZP:0103908 corneal epithelium irregular thickness, abnormal ZP:0103909 corneal stroma irregular thickness, abnormal ZP:0103911 vasculature decreased functionality, abnormal ZP:0103912 dorsal region whole organism absent, abnormal ZP:0103913 axial mesoderm decreased process quality mediolateral intercalation, abnormal ZP:0103914 lateral margin notochord irregularly shaped, abnormal ZP:0103915 whole organism decreased occurrence cell population proliferation, abnormal ZP:0103916 notochord process quality cell-cell adhesion, abnormal ZP:0103917 cell Kupffer's vesicle morphology, abnormal ZP:0103918 left/right pattern formation decreased occurrence, abnormal ZP:0103919 palate disrupted cell population proliferation, abnormal ZP:0103920 cranial neural crest cell disrupted cell population proliferation, abnormal ZP:0103921 splanchnocranium process quality skeletal muscle tissue development, abnormal ZP:0103922 sarcomere interhyoideus disorganized, abnormal ZP:0103923 Z disc interhyoideus absent, abnormal ZP:0103924 A band interhyoideus absent, abnormal ZP:0103925 I band interhyoideus absent, abnormal ZP:0103926 anterior region central nervous system malformed, abnormal ZP:0103927 ventro-medial region brain absent, abnormal ZP:0103928 neuron spinal cord absent, abnormal ZP:0103929 floor plate spinal cord region absent, abnormal ZP:0103930 pharyngeal endoderm absent, abnormal ZP:0103931 pharyngeal mesoderm absent, abnormal ZP:0103932 dorsal region germ ring decreased amount, abnormal ZP:0103933 germ ring spatial pattern, abnormal ZP:0103934 anterior region axial mesoderm absent, abnormal ZP:0103935 posterior region axial mesoderm absent, abnormal ZP:0103936 axial chorda mesoderm absent, abnormal ZP:0103937 hypoblast absent, abnormal ZP:0103938 neuroectoderm absent, abnormal ZP:0103947 glycogen hepatocyte decreased amount, abnormal ZP:0103948 cytoplasm hepatocyte mislocalised, abnormal ZP:0103949 mitochondrion hepatocyte malformed, abnormal ZP:0103950 hepatocyte increased occurrence autophagy, abnormal ZP:0103951 intracellular canaliculus hepatocyte spatial pattern, abnormal ZP:0103953 bile acid secretion decreased occurrence, abnormal ZP:0103954 bile canaliculus spatial pattern, abnormal ZP:0103955 hepatocyte has extra parts of type autophagosome hepatocyte, abnormal ZP:0103956 bile canaliculus malformed, abnormal ZP:0103957 mitochondrion hepatocyte swollen, abnormal ZP:0103958 plasma membrane hepatocyte degenerate, abnormal ZP:0103959 mitochondrial crista hepatocyte degenerate, abnormal ZP:0103960 posterior region gut epithelium absent, abnormal ZP:0103961 intracellular canaliculus hepatocyte absent, abnormal ZP:0103962 bile canaliculus absent, abnormal ZP:0103965 EVL broken, abnormal ZP:0103967 midbrain hindbrain boundary neural tube morphology, abnormal ZP:0103970 cell periderm increased size, abnormal ZP:0103972 neuron projection cranial nerve X decreased amount, abnormal ZP:0103973 intestinal motility disrupted, abnormal ZP:0103977 ventricular epicardium absent, abnormal ZP:0103978 hindbrain decreased height, abnormal ZP:0103980 head kidney decreased volume, abnormal ZP:0103981 microglial cell retina increased amount, abnormal ZP:0103983 lymph vessel trunk absent, abnormal ZP:0103984 facial lymphatic vessel decreased amount, abnormal ZP:0103985 posterior cardinal vein disrupted sprouting angiogenesis, abnormal ZP:0103986 primordial hindbrain channel immature, abnormal ZP:0103988 intersegmental vein somite decreased amount, abnormal ZP:0103989 intersegmental vessel thoracic duct absent, abnormal ZP:0103990 primordial germ cell morphology, abnormal ZP:0103991 primordial germ cell decreased occurrence cell migration, abnormal ZP:0103993 cardiac muscle cell bulbus arteriosus decreased amount, abnormal ZP:0103994 closure of optic fissure delayed, abnormal ZP:0103995 optic cup mislocalised, abnormal ZP:0103996 optic cup increased distribution, abnormal ZP:0103997 retina delayed cell cycle arrest, abnormal ZP:0103999 retina decreased occurrence cell division, abnormal ZP:0104000 retinal cell apoptotic process increased occurrence, abnormal ZP:0104001 retina degree of pigmentation, abnormal ZP:0104002 retinal ganglion cell layer increased width, abnormal ZP:0104003 retinal inner nuclear layer increased width, abnormal ZP:0104004 cardiac muscle myoblast disrupted cell population proliferation, abnormal ZP:0104005 MAP kinase kinase activity increased rate, abnormal ZP:0104007 lens morphogenesis in camera-type eye decreased process quality, abnormal ZP:0104008 lens fiber cell differentiation increased occurrence, abnormal ZP:0104021 cysteine whole organism increased amount, abnormal ZP:0104022 cystine whole organism increased amount, abnormal ZP:0104023 glutathione disulfide whole organism increased amount, abnormal ZP:0104027 cystine brain increased amount, abnormal ZP:0104028 cystine heart increased amount, abnormal ZP:0104029 cystine liver increased amount, abnormal ZP:0104030 cystine kidney increased amount, abnormal ZP:0104031 neutrophilic myelocyte blood increased amount, abnormal ZP:0104032 neutrophilic metamyelocyte blood increased amount, abnormal ZP:0104033 memory process quality, abnormal ZP:0104035 response to misfolded protein increased occurrence, abnormal ZP:0104036 female organism process quality oocyte maturation, abnormal ZP:0104038 male organism arrested sperm ejaculation, abnormal ZP:0104039 male organism increased occurrence development of secondary female sexual characteristics, abnormal ZP:0104041 male organism decreased occurrence development of secondary male sexual characteristics, abnormal ZP:0104043 ovary female organism decreased amount, abnormal ZP:0104044 female organism has fewer parts of type ovary oocyte stage III, abnormal ZP:0104045 female organism has extra parts of type ovary oocyte stage I, abnormal ZP:0104046 trunk male organism obtuse, abnormal ZP:0104050 anal fin male organism white, abnormal ZP:0104052 seminiferous tubule male organism malformed, abnormal ZP:0104053 seminiferous tubule male organism disorganized, abnormal ZP:0104054 spermatogenic cyst male organism malformed, abnormal ZP:0104055 spermatogenic cyst male organism disorganized, abnormal ZP:0104057 ovary delayed oocyte maturation, abnormal ZP:0104058 testis delayed spermatid development, abnormal ZP:0104060 female organism lacks all parts of type ovary oocyte stage III, abnormal ZP:0104061 testis lacks all parts of type spermatid, abnormal ZP:0104063 retina decreased process quality detection of light stimulus involved in visual perception, abnormal ZP:0104065 synapse eye photoreceptor cell mislocalised, abnormal ZP:0104066 photoreceptor inner segment layer mislocalised, abnormal ZP:0104068 positive regulation of NIK/NF-kappaB signaling disrupted, abnormal ZP:0104073 atrial cardiac muscle cell action potential decreased duration, abnormal ZP:0104074 whole organism has fewer parts of type pectoral fin, abnormal ZP:0104075 lymphoid progenitor cell caudal hematopoietic tissue increased amount, abnormal ZP:0104076 T cell migration decreased process quality, abnormal ZP:0104077 cartilage tissue decreased amount, abnormal ZP:0104078 pectoral fin cartilage decreased amount, abnormal ZP:0104079 pharyngeal pouch 1 decreased amount, abnormal ZP:0104083 anatomical region thymus increased amount, abnormal ZP:0104084 anatomical region thymus decreased amount, abnormal ZP:0104085 T cell increased occurrence apoptotic process, abnormal ZP:0104086 T cell decreased occurrence cell maturation, abnormal ZP:0104088 ventral telencephalon increased amount, abnormal ZP:0104089 facial ganglion decreased distribution, abnormal ZP:0104090 facial ganglion decreased amount, abnormal ZP:0104091 glossopharyngeal ganglion decreased amount, abnormal ZP:0104092 vagal ganglion 1 decreased distribution, abnormal ZP:0104093 vagal ganglion 1 decreased amount, abnormal ZP:0104094 vagal ganglion 2 decreased distribution, abnormal ZP:0104095 vagal ganglion 2 decreased amount, abnormal ZP:0104096 vagal ganglion 1 spatial pattern, abnormal ZP:0104097 vagal ganglion 2 spatial pattern, abnormal ZP:0104098 otic placode increased amount, abnormal ZP:0104106 ectoderm absent, abnormal ZP:0104107 yolk syncytial layer decreased thickness, abnormal ZP:0104116 notochord decreased distance prechordal plate, abnormal ZP:0104117 forerunner cell group process quality cell migration, abnormal ZP:0104118 presumptive paraxial mesoderm spatial pattern, abnormal ZP:0104119 presumptive ventral mesoderm increased distribution, abnormal ZP:0104121 mediolateral intercalation decreased process quality, abnormal ZP:0104122 anterior-posterior axis somite decreased width, abnormal ZP:0104128 trabecular layer of ventricle increased thickness, abnormal ZP:0104131 cell migration involved in mesendoderm migration process quality, abnormal ZP:0104132 extracellular matrix endoderm decreased amount, abnormal ZP:0104133 extracellular matrix organization process quality, abnormal ZP:0104134 fibronectin fibril organization decreased process quality, abnormal ZP:0104135 antero-dorsal region rhombomere 1 absent, abnormal ZP:0104136 antero-dorsal region rhombomere 1 increased amount, abnormal ZP:0104137 anterior margin hindbrain increased amount, abnormal ZP:0104138 anterior margin hindbrain mislocalised, abnormal ZP:0104139 cerebellar granule cell differentiation decreased process quality, abnormal ZP:0104140 corpus cerebelli has fewer parts of type parallel fiber, abnormal ZP:0104141 cerebellar granule cell precursor tangential migration decreased process quality, abnormal ZP:0104146 cardioblast migration to the midline involved in heart field formation decreased occurrence, abnormal ZP:0104149 compact layer of ventricle increased occurrence cardiac muscle cell proliferation, abnormal ZP:0104150 compact layer of ventricle increased thickness, abnormal ZP:0104151 corpus cerebelli decreased occurrence cerebellar granule cell differentiation, abnormal ZP:0104152 granular eminence decreased occurrence cerebellar granule cell differentiation, abnormal ZP:0104153 medial caudal lobe decreased occurrence cerebellar granule cell differentiation, abnormal ZP:0104154 cerebellar granule cell corpus cerebelli decreased amount, abnormal ZP:0104155 cerebellar granule cell granular eminence decreased amount, abnormal ZP:0104156 cerebellar granule cell medial caudal lobe decreased amount, abnormal ZP:0104157 glutamatergic neuron cerebellum decreased amount, abnormal ZP:0104158 corpus cerebelli has fewer parts of type cerebellar granule cell, abnormal ZP:0104159 granular eminence has fewer parts of type cerebellar granule cell, abnormal ZP:0104160 medial caudal lobe increased amount, abnormal ZP:0104161 medial caudal lobe mislocalised, abnormal ZP:0104162 medial caudal lobe has fewer parts of type cerebellar granule cell, abnormal ZP:0104165 mitochondrion whole organism decreased amount, abnormal ZP:0104166 mandibular arch skeleton disrupted bone mineralization, abnormal ZP:0104167 ceratobranchial 5 tooth detached from mandibular arch skeleton, abnormal ZP:0104168 palatoquadrate arch decreased thickness, abnormal ZP:0104170 ceratobranchial 5 tooth disrupted tooth mineralization, abnormal ZP:0104172 dentinogenesis disrupted, abnormal ZP:0104174 tooth placode disoriented, abnormal ZP:0104175 tooth pulp disorganized, abnormal ZP:0104176 tooth pulp increased mass density, abnormal ZP:0104177 odontoblast shape, abnormal ZP:0104179 iron(3+) whole organism increased amount, abnormal ZP:0104181 iron(3+) brain increased amount, abnormal ZP:0104183 iron(3+) gut increased amount, abnormal ZP:0104184 iron(3+) liver increased amount, abnormal ZP:0104187 iron(3+) muscle increased amount, abnormal ZP:0104188 cartilage tissue palate shortened, abnormal ZP:0104189 ceratobranchial 5 cartilage morphology, abnormal ZP:0104190 ventral region hypothalamus increased amount, abnormal ZP:0104191 ventral region hypothalamus increased distribution, abnormal ZP:0104192 hypocretin-secreting neuron hypothalamus increased amount, abnormal ZP:0104193 insulin-like growth factor receptor signaling pathway increased occurrence, abnormal ZP:0104194 superior raphe nucleus increased amount, abnormal ZP:0104195 locus coeruleus increased amount, abnormal ZP:0104196 vertebra decreased occurrence ossification, abnormal ZP:0104197 Melanin eye decreased amount, abnormal ZP:0104199 neuron development disrupted, abnormal ZP:0104201 magnesium(2+) whole organism decreased amount, abnormal ZP:0104202 post-vent region disrupted blood circulation, abnormal ZP:0104203 yolk disrupted metabolic process, abnormal ZP:0104206 axon Mauthner neuron absent, abnormal ZP:0104208 posterior lateral line delayed myelination in peripheral nervous system, abnormal ZP:0104209 posterior lateral line delayed myelination of posterior lateral line nerve axons, abnormal ZP:0104210 myelinating Schwann cell posterior lateral line decreased distribution, abnormal ZP:0104212 immature Schwann cell posterior lateral line decreased distribution, abnormal ZP:0104213 immature Schwann cell posterior lateral line decreased amount, abnormal ZP:0104215 caudal fin increased process quality I-kappaB kinase/NF-kappaB signaling, abnormal ZP:0104216 ceratohyal cartilage decreased distance Meckel's cartilage, abnormal ZP:0104217 post-vent vasculature fused with post-vent vasculature, abnormal ZP:0104221 dorsal region eye decreased distribution, abnormal ZP:0104222 dorsal region eye decreased amount, abnormal ZP:0104227 blood vessel compact layer of ventricle increased amount, abnormal ZP:0104230 blood vessel superior ocular sulcus decreased size, abnormal ZP:0104231 blood vessel superior ocular sulcus decreased branchiness, abnormal ZP:0104233 blood vessel superior ocular sulcus degenerate, abnormal ZP:0104235 statoacoustic (VIII) ganglion absent, abnormal ZP:0104236 anterior lateral line ganglion decreased amount, abnormal ZP:0104237 caudal vein plexus decreased occurrence sprouting angiogenesis, abnormal ZP:0104238 blood increased accumulation caudal vein plexus, abnormal ZP:0104240 epidermis increased occurrence apoptotic process, abnormal ZP:0104243 trunk decreased occurrence startle response, abnormal ZP:0104245 trunk decreased occurrence thigmotaxis, abnormal ZP:0104246 corpus cerebelli decreased size, abnormal ZP:0104247 diffuse nucleus inferior lobe increased amount, abnormal ZP:0104248 ventral hypothalamic zone decreased amount, abnormal ZP:0104249 nucleate erythrocyte vasculature absent, abnormal ZP:0104251 cell dorsal aorta increased area, abnormal ZP:0104252 iridophore opercular flap decreased amount, abnormal ZP:0104253 opercular flap has fewer parts of type iridophore, abnormal ZP:0104256 regenerating fin process quality blood circulation, abnormal ZP:0104257 artery regenerating fin increased diameter, abnormal ZP:0104258 artery regenerating fin increased area, abnormal ZP:0104259 vein regenerating fin increased diameter, abnormal ZP:0104260 vein regenerating fin increased area, abnormal ZP:0104261 blood vessel brain irregular spatial pattern, abnormal ZP:0104262 blood vessel brain dilated, abnormal ZP:0104263 blood vessel brain kinked, abnormal ZP:0104264 endothelial cell artery decreased mass density, abnormal ZP:0104265 endothelial cell vein increased amount, abnormal ZP:0104266 blood accumulation vasculature regenerating fin, abnormal ZP:0104267 intersegmental vein decreased process quality blood circulation, abnormal ZP:0104268 vein intersegmental vein decreased diameter, abnormal ZP:0104270 arteriole intersegmental vein dilated, abnormal ZP:0104271 blood cell dorsal aorta increased velocity, abnormal ZP:0104272 blood cell posterior cardinal vein increased velocity, abnormal ZP:0104273 nucleate erythrocyte intersegmental vein absent, abnormal ZP:0104277 gap junction spinal cord interneuron absent, abnormal ZP:0104278 gap junction Mauthner neuron absent, abnormal ZP:0104279 spinal cord interneuron decreased occurrence gap junction assembly, abnormal ZP:0104280 Mauthner neuron decreased occurrence gap junction assembly, abnormal ZP:0104281 spinal cord interneuron arrested gap junction-mediated intercellular transport, abnormal ZP:0104282 Mauthner neuron arrested gap junction-mediated intercellular transport, abnormal ZP:0104286 rhombomere 4 decreased amount, abnormal ZP:0104287 rhombomere 3 spatial pattern, abnormal ZP:0104288 rhombomere 4 absent, abnormal ZP:0104289 rhombomere 4 decreased distribution, abnormal ZP:0104290 anterior/posterior compartment boundary rhombomere 2 morphology, abnormal ZP:0104291 anterior/posterior compartment boundary rhombomere 2 absent, abnormal ZP:0104292 anterior/posterior compartment boundary rhombomere 5 spatial pattern, abnormal ZP:0104293 anterior/posterior compartment boundary rhombomere 5 decreased distribution, abnormal ZP:0104294 anterior/posterior compartment boundary rhombomere 3 morphology, abnormal ZP:0104295 anterior/posterior compartment boundary rhombomere 3 spatial pattern, abnormal ZP:0104296 anterior/posterior compartment boundary rhombomere 3 absent, abnormal ZP:0104297 anterior/posterior compartment boundary rhombomere 3 decreased distribution, abnormal ZP:0104298 anterior/posterior compartment boundary rhombomere 4 morphology, abnormal ZP:0104299 anterior/posterior compartment boundary rhombomere 4 spatial pattern, abnormal ZP:0104300 anterior/posterior compartment boundary rhombomere 4 absent, abnormal ZP:0104301 anterior/posterior compartment boundary rhombomere 4 decreased distribution, abnormal ZP:0104302 migratory cranial neural crest rhombomere 2 morphology, abnormal ZP:0104303 migratory cranial neural crest rhombomere 2 spatial pattern, abnormal ZP:0104304 rhombomere 2 fused with migratory cranial neural crest migratory cranial neural crest rhombomere 4, abnormal ZP:0104305 migratory cranial neural crest rhombomere 4 morphology, abnormal ZP:0104306 migratory cranial neural crest rhombomere 4 spatial pattern, abnormal ZP:0104307 MiD3cm absent, abnormal ZP:0104317 hemoglobin whole organism decreased amount, abnormal ZP:0104318 retina process quality transmission of nerve impulse, abnormal ZP:0104319 periciliary membrane compartment photoreceptor cell absent, abnormal ZP:0104320 periciliary membrane compartment photoreceptor cell decreased amount, abnormal ZP:0104321 cranial division of the internal carotid artery dysplastic, abnormal ZP:0104322 basal communicating artery fused with primordial midbrain channel, abnormal ZP:0104323 basal communicating artery dilated, abnormal ZP:0104324 basal communicating artery deformed, abnormal ZP:0104325 posterior communicating artery dilated, abnormal ZP:0104326 posterior communicating artery deformed, abnormal ZP:0104327 basilar artery fused with primordial hindbrain channel, abnormal ZP:0104329 central canal decreased occurrence detection of mechanical stimulus, abnormal ZP:0104331 olfactory receptor cell process quality axon guidance, abnormal ZP:0104332 olfactory receptor cell displaced to neuron projection central zone olfactory bulb, abnormal ZP:0104333 dorsal zone olfactory bulb has fewer parts of type neuron projection olfactory receptor cell, abnormal ZP:0104334 olfactory receptor cell displaced to neuron projection dorsal zone olfactory bulb, abnormal ZP:0104335 central zone olfactory bulb has fewer parts of type neuron projection olfactory receptor cell, abnormal ZP:0104336 maG1 has extra parts of type neuron projection olfactory receptor cell, abnormal ZP:0104337 spinal cord decreased occurrence epithelial cilium movement involved in extracellular fluid movement, abnormal ZP:0104338 spinal cord decreased occurrence cerebrospinal fluid circulation, abnormal ZP:0104339 mechanoreceptor cell central canal decreased functionality, abnormal ZP:0104340 mechanoreceptor cell central canal absent, abnormal ZP:0104341 vertebral column decreased process quality skeletal system development, abnormal ZP:0104342 vertebral column convex, abnormal ZP:0104343 glucagon blood plasma decreased amount, abnormal ZP:0104344 branchiomotor neuron rhombomere 6 absent, abnormal ZP:0104345 motor neuron migration decreased occurrence, abnormal ZP:0104346 branchiomotor neuron rhombomere 6 decreased amount, abnormal ZP:0104348 whole organism decreased occurrence double-strand break repair, abnormal ZP:0104351 pronephric glomerulus development decreased occurrence, abnormal ZP:0104352 interrenal primordium increased amount, abnormal ZP:0104353 interrenal primordium increased distribution, abnormal ZP:0104355 cardiac muscle cell polyploid, abnormal ZP:0104356 pancreatic A cell primary islet decreased amount, abnormal ZP:0104360 neuromuscular junction trunk musculature malformed, abnormal ZP:0104361 skeletal muscle cell trunk musculature irregular spatial pattern, abnormal ZP:0104362 skeletal muscle cell trunk musculature sparse, abnormal ZP:0104363 motor neuron malformed, abnormal ZP:0104367 anatomical space Kupffer's vesicle increased permeability, abnormal ZP:0104368 tight junction Kupffer's vesicle structure, abnormal ZP:0104369 blood cell accumulation anatomical region caudal fin, abnormal ZP:0104370 blood cell accumulation yolk, abnormal ZP:0104382 dorsal aorta decreased efficacy blood circulation, abnormal ZP:0104383 caudal vein decreased efficacy blood circulation, abnormal ZP:0104384 intersegmental vessel decreased efficacy blood circulation, abnormal ZP:0104386 caudal artery increased distribution, abnormal ZP:0104387 caudal vein plexus increased amount, abnormal ZP:0104388 caudal vein plexus mislocalised, abnormal ZP:0104389 caudal vein plexus increased distribution, abnormal ZP:0104395 caudal artery decreased distribution, abnormal ZP:0104396 caudal artery decreased amount, abnormal ZP:0104411 pronephros lacks parts or has fewer parts of type pronephric podocyte, abnormal ZP:0104412 pancreatic B cell exocrine pancreas increased amount, abnormal ZP:0104418 dark adaptation increased process quality, abnormal ZP:0104422 head lacks parts or has fewer parts of type eye, abnormal ZP:0104424 GABAergic neuron decreased occurrence axon arborization, abnormal ZP:0104425 optic tectum increased occurrence neuronal action potential, abnormal ZP:0104426 optic tectum decreased occurrence negative regulation of neuronal action potential, abnormal ZP:0104436 vertebral column curved dorsal, abnormal ZP:0104441 filamentous actin lens disorganized, abnormal ZP:0104442 pharyngeal arch 2 spatial pattern, abnormal ZP:0104455 dorsal region VeLD absent, abnormal ZP:0104456 dorsal region VeLD decreased amount, abnormal ZP:0104457 medial region Kolmer-Agduhr neuron absent, abnormal ZP:0104458 medial region Kolmer-Agduhr neuron decreased amount, abnormal ZP:0104459 Kolmer-Agduhr neuron lacks parts or has fewer parts of type medial region GABAergic neuron, abnormal ZP:0104460 ventral region VeLD absent, abnormal ZP:0104461 ventral region VeLD decreased amount, abnormal ZP:0104462 ventro-medial region Kolmer-Agduhr neuron absent, abnormal ZP:0104463 ventro-medial region Kolmer-Agduhr neuron decreased amount, abnormal ZP:0104464 Kolmer-Agduhr neuron lacks parts or has fewer parts of type ventro-medial region GABAergic neuron, abnormal ZP:0104465 primary motor neuron increased occurrence cell division, abnormal ZP:0104466 VeLD has fewer parts of type GABAergic neuron, abnormal ZP:0104468 ventral-most region Kolmer-Agduhr neuron absent, abnormal ZP:0104469 epiphysis absent, abnormal ZP:0104470 somite development decreased occurrence, abnormal ZP:0104471 auditory behavior process quality, abnormal ZP:0104472 iridoblast absent, abnormal ZP:0104473 whole organism has fewer parts of type iridophore, abnormal ZP:0104474 basement membrane eye spatial pattern, abnormal ZP:0104479 ribonucleoprotein complex blastomere mislocalised, abnormal ZP:0104480 blastomere displaced to ribonucleoprotein complex peripheral region blastodisc, abnormal ZP:0104487 proximal pars anterior decreased amount, abnormal ZP:0104491 copper-63 brain decreased amount, abnormal ZP:0104496 skeletal muscle myotome malformed, abnormal ZP:0104497 proteasome-mediated ubiquitin-dependent protein catabolic process decreased occurrence, abnormal ZP:0104498 anterior lateral plate mesoderm decreased distribution, abnormal ZP:0104508 anterior region lens increased amount, abnormal ZP:0104509 anterior region lens increased distribution, abnormal ZP:0104513 lens fiber cell absent, abnormal ZP:0104514 angioblastic mesenchymal cell pharyngeal arch absent, abnormal ZP:0104515 pharyngeal arch has fewer parts of type angioblastic mesenchymal cell, abnormal ZP:0104516 levator arcus palatini absent, abnormal ZP:0104517 adductor operculi absent, abnormal ZP:0104518 dilatator operculi absent, abnormal ZP:0104519 levator operculi absent, abnormal ZP:0104520 ventral intermandibularis anterior absent, abnormal ZP:0104521 ventral intermandibularis posterior absent, abnormal ZP:0104522 adductor mandibulae absent, abnormal ZP:0104523 interhyoideus absent, abnormal ZP:0104524 adductor hyomandibulae absent, abnormal ZP:0104527 cilium Kupffer's vesicle anterior orientation, abnormal ZP:0104528 ciliary basal body Kupffer's vesicle mislocalised anteriorly, abnormal ZP:0104529 Kupffer's vesicle process quality epithelial cilium movement involved in determination of left/right asymmetry, abnormal ZP:0104530 endodermal cell displaced, abnormal ZP:0104532 enteric smooth muscle cell differentiation process quality, abnormal ZP:0104533 pharynx development process quality, abnormal ZP:0104538 ventral-most region Kolmer-Agduhr neuron increased amount, abnormal ZP:0104539 ventral-most region Kolmer-Agduhr neuron decreased amount, abnormal ZP:0104540 Kolmer-Agduhr neuron has fewer parts of type ventral-most region GABAergic neuron, abnormal ZP:0104542 Kolmer-Agduhr neuron has extra parts of type medial region GABAergic neuron, abnormal ZP:0104543 Kolmer-Agduhr neuron has fewer parts of type ventro-medial region GABAergic neuron, abnormal ZP:0104544 glutamatergic neuron differentiation increased occurrence, abnormal ZP:0104546 radial glial cell process quality cell quiescence, abnormal ZP:0104548 ceratohyal-interhyal joint absent, abnormal ZP:0104549 interhyal-hyosymplectic joint absent, abnormal ZP:0104551 posterior lateral line neuromast decreased occurrence synapse assembly, abnormal ZP:0104552 posterior lateral line neuromast orientation stereocilium bundle posterior lateral line neuromast, abnormal ZP:0104553 symplectic articulated with hyomandibula, abnormal ZP:0104554 hyosymplectic cartilage has extra parts of type joint, abnormal ZP:0104555 presumptive rhombomere 2 spatial pattern, abnormal ZP:0104556 midbrain hindbrain boundary neural keel spatial pattern, abnormal ZP:0104557 rhombomere 2 morphology, abnormal ZP:0104558 presumptive rhombomere 4 morphology, abnormal ZP:0104559 presumptive rhombomere 4 spatial pattern, abnormal ZP:0104560 presumptive rhombomere 4 decreased size, abnormal ZP:0104561 presumptive rhombomere 4 decreased distribution, abnormal ZP:0104562 presumptive rhombomere 3 spatial pattern, abnormal ZP:0104563 presumptive rhombomere 3 mislocalised, abnormal ZP:0104564 hindbrain neural plate spatial pattern, abnormal ZP:0104565 rhombomere 6 decreased distribution, abnormal ZP:0104571 chorion deformed, abnormal ZP:0104573 ovarian follicle degenerate, abnormal ZP:0104574 thyroid follicle aplastic/hypoplastic, abnormal ZP:0104577 Kolmer-Agduhr neuron lacks all parts of type medial region GABAergic neuron, abnormal ZP:0104578 Kolmer-Agduhr neuron has fewer parts of type medial region GABAergic neuron, abnormal ZP:0104588 otic vesicle increased occurrence otolith formation, abnormal ZP:0104589 sagitta increased size, abnormal ZP:0104590 sagitta ovate, abnormal ZP:0104591 otic vesicle decreased frequency epithelial cilium movement involved in extracellular fluid movement, abnormal ZP:0104592 otic vesicle process quality otolith formation, abnormal ZP:0104595 anatomical region dorsal aorta disorganized, abnormal ZP:0104596 dorsal aorta decreased occurrence sprouting angiogenesis, abnormal ZP:0104607 whole organism lacks parts or has fewer parts of type anterior region nucleate erythrocyte, abnormal ZP:0104608 nucleate erythrocyte trunk increased amount, abnormal ZP:0104609 blood island increased distribution, abnormal ZP:0104610 nucleate erythrocyte increased accumulation posterior region intermediate cell mass of mesoderm, abnormal ZP:0104611 whole organism lacks parts or has fewer parts of type posterior region nucleate erythrocyte, abnormal ZP:0104612 anatomical region posterior cardinal vein disorganized, abnormal ZP:0104613 hematopoietic cell decreased occurrence blood circulation, abnormal ZP:0104614 axoneme sperm decreased amount, abnormal ZP:0104615 inner dynein arm sperm decreased amount, abnormal ZP:0104616 axoneme sperm absent, abnormal ZP:0104617 sperm flagellum sperm absent, abnormal ZP:0104618 outer dynein arm sperm absent, abnormal ZP:0104619 flagellated sperm motility process quality, abnormal ZP:0104620 anatomical region midbrain necrotic, abnormal ZP:0104621 retina arrested neurogenesis, abnormal ZP:0104622 optic tectum arrested neurogenesis, abnormal ZP:0104623 mitotic S phase process quality, abnormal ZP:0104624 central nervous system decreased volume, abnormal ZP:0104625 hypothalamus disorganized, abnormal ZP:0104626 eye decreased volume, abnormal ZP:0104627 ventral telencephalon disorganized, abnormal ZP:0104628 nucleus optic tectum increased diameter, abnormal ZP:0104629 central zone of the optic tectum arrested neurogenesis, abnormal ZP:0104630 proliferative region optic tectum increased thickness, abnormal ZP:0104631 ball shape, abnormal ZP:0104634 artery pharyngeal arch morphology, abnormal ZP:0104635 CaP motoneuron occurrence release of sequestered calcium ion into cytosol, abnormal ZP:0104636 CaP motoneuron asynchronous release of sequestered calcium ion into cytosol, abnormal ZP:0104637 involuntary skeletal muscle contraction decreased occurrence, abnormal ZP:0104639 myotome has extra parts of type skeletal muscle cell vesicle skeletal muscle cell, abnormal ZP:0104640 mitochondrion skeletal muscle malformed, abnormal ZP:0104641 skeletal muscle decreased process quality skeletal myofibril assembly, abnormal ZP:0104643 skeletal muscle decreased process quality sarcomere organization, abnormal ZP:0104646 skeletal muscle cell has fewer parts of type skeletal muscle myofibril skeletal muscle cell, abnormal ZP:0104651 Kupffer's vesicle physical quality of a process epithelial cilium movement involved in determination of left/right asymmetry, abnormal ZP:0104652 Kupffer's vesicle elliptic, abnormal ZP:0104653 gut decreased occurrence determination of digestive tract left/right asymmetry, abnormal ZP:0104654 nucleus Kupffer's vesicle broken, abnormal ZP:0104655 vacuole Kupffer's vesicle increased volume, abnormal ZP:0104656 Kupffer's vesicle decreased rate vacuolar transport, abnormal ZP:0104658 Kupffer's vesicle has extra parts of type posterior region vacuole Kupffer's vesicle, abnormal ZP:0104659 Kupffer's vesicle process quality epithelial cell morphogenesis, abnormal ZP:0104660 epithelial cell Kupffer's vesicle columnar, abnormal ZP:0104666 leukocyte spatial pattern, abnormal ZP:0104667 sphingolipid liver increased amount, abnormal ZP:0104668 skeletal muscle satellite cell decreased amount, abnormal ZP:0104669 skeletal muscle decreased distribution, abnormal ZP:0104671 very long-chain fatty acid whole organism increased amount, abnormal ZP:0104672 very long-chain fatty acid metabolic process disrupted, abnormal ZP:0104673 oligodendrocyte brain spatial pattern, abnormal ZP:0104674 oligodendrocyte spinal cord spatial pattern, abnormal ZP:0104675 optic tectum increased occurrence cellular response to light stimulus, abnormal ZP:0104676 optic tectum increased occurrence membrane depolarization during action potential, abnormal ZP:0104677 cephalic mesoderm absent, abnormal ZP:0104678 axial blood vessel absent, abnormal ZP:0104679 axial blood vessel increased distribution, abnormal ZP:0104683 blood vessel endothelial cell posterior cardinal vein increased amount, abnormal ZP:0104684 angiogenic sprout cerebellar central artery decreased amount, abnormal ZP:0104685 mesencephalic artery absent, abnormal ZP:0104688 cerebellar central artery decreased amount, abnormal ZP:0104691 metencephalic artery absent, abnormal ZP:0104692 GABAergic neuron decreased occurrence inhibitory synapse assembly, abnormal ZP:0104693 hindbrain has fewer parts of type inhibitory synapse hindbrain, abnormal ZP:0104694 spinal cord has fewer parts of type inhibitory synapse spinal cord, abnormal ZP:0104695 telencephalon has fewer parts of type inhibitory synapse telencephalon, abnormal ZP:0104697 optic tectum has fewer parts of type inhibitory synapse optic tectum, abnormal ZP:0104699 response to light stimulus increased magnitude, abnormal ZP:0104700 postsynaptic density hindbrain decreased distribution, abnormal ZP:0104701 postsynaptic density hindbrain decreased amount, abnormal ZP:0104702 GABA-ergic synapse hindbrain decreased distribution, abnormal ZP:0104703 GABA-ergic synapse hindbrain decreased amount, abnormal ZP:0104704 GABAergic neuron hindbrain decreased distribution, abnormal ZP:0104705 GABAergic neuron spinal cord decreased distribution, abnormal ZP:0104706 GABAergic neuron telencephalon decreased distribution, abnormal ZP:0104707 GABAergic neuron telencephalon decreased amount, abnormal ZP:0104708 GABAergic neuron optic tectum decreased distribution, abnormal ZP:0104709 GABAergic neuron optic tectum decreased amount, abnormal ZP:0104716 lens fiber cell differentiation decreased occurrence, abnormal ZP:0104719 lens epithelium increased amount, abnormal ZP:0104721 lens epithelium increased distribution, abnormal ZP:0104722 lens epithelium decreased amount, abnormal ZP:0104723 lens epithelium decreased occurrence early endosome to late endosome transport, abnormal ZP:0104724 lens epithelium decreased occurrence early endosome to recycling endosome transport, abnormal ZP:0104725 heart decreased occurrence tube formation, abnormal ZP:0104726 endocardium accumulation endothelial cell anatomical space heart, abnormal ZP:0104727 atrium hypotrophic, abnormal ZP:0104728 heart valve malformed, abnormal ZP:0104729 heart hypotrophic, abnormal ZP:0104730 heart valve trabecular, abnormal ZP:0104731 presumptive cardiac ventricle primitive heart tube delayed cardioblast migration to the midline involved in heart field formation, abnormal ZP:0104732 cardioblast migration to the midline involved in heart field formation delayed, abnormal ZP:0104734 determination of left/right asymmetry in nervous system process quality, abnormal ZP:0104735 cilium Kupffer's vesicle posterior orientation, abnormal ZP:0104736 gut process quality determination of digestive tract left/right asymmetry, abnormal ZP:0104740 cilium Kupffer's vesicle decreased size, abnormal ZP:0104748 female mating behavior process quality, abnormal ZP:0104750 ovarian follicle stage I increased amount, abnormal ZP:0104751 ovarian follicle stage II decreased amount, abnormal ZP:0104752 peripheral region blastodisc mislocalised, abnormal ZP:0104753 blastomere has fewer parts of type cleavage furrow ribonucleoprotein complex blastodisc, abnormal ZP:0104754 filamentous actin blastomere spatial pattern, abnormal ZP:0104755 paraxial mesoderm irregular spatial pattern, abnormal ZP:0104756 myoblast disorganized, abnormal ZP:0104768 serotonin hindbrain increased amount, abnormal ZP:0104769 noradrenaline hindbrain decreased amount, abnormal ZP:0104770 (3,4-dihydroxyphenyl)acetic acid hindbrain decreased amount, abnormal ZP:0104771 (3,4-dihydroxyphenyl)acetic acid telencephalon decreased amount, abnormal ZP:0104772 (3,4-dihydroxyphenyl)acetic acid diencephalon decreased amount, abnormal ZP:0104773 (3,4-dihydroxyphenyl)acetic acid optic tectum decreased amount, abnormal ZP:0104774 brain decreased occurrence nitric oxide mediated signal transduction, abnormal ZP:0104776 response to environmental enrichment occurrence, abnormal ZP:0104777 radial glial cell increased occurrence neuron differentiation, abnormal ZP:0104779 neuronal stem cell radial glial cell decreased amount, abnormal ZP:0104780 cell body Mauthner neuron increased area, abnormal ZP:0104781 establishment of left/right asymmetry disrupted, abnormal ZP:0104784 thigmotaxis delayed, abnormal ZP:0104788 CaP motoneuron has fewer parts of type neuronal cell body membrane glutamatergic synapse CaP motoneuron, abnormal ZP:0104791 CaP motoneuron decreased occurrence excitatory synapse assembly, abnormal ZP:0104794 vertical myoseptum skeletal muscle mislocalised, abnormal ZP:0104795 skeletal muscle mislocalised, abnormal ZP:0104796 primitive heart tube increased distribution, abnormal ZP:0104797 skeletal muscle cell accumulation actin cytoskeleton vertical myoseptum, abnormal ZP:0105640 neutrophil decreased process quality peroxidase activity, abnormal ZP:0105641 corpuscles of Stannius increased occurrence specification of animal organ identity, abnormal ZP:0105642 corpuscles of Stannius decreased occurrence specification of animal organ identity, abnormal ZP:0105643 pronephric distal early tubule decreased amount, abnormal ZP:0105644 corpuscles of Stannius decreased process quality embryonic organ development, abnormal ZP:0105645 podocyte foot pronephric podocyte flattened, abnormal ZP:0105646 lamina rara interna structure, cavities, abnormal ZP:0105647 ependymal cell decreased occurrence epithelial cilium movement involved in extracellular fluid movement, abnormal ZP:0105648 motile cilium ependymal cell inactive, abnormal ZP:0105649 central canal decreased occurrence cerebrospinal fluid circulation, abnormal ZP:0105651 midsagittal plane brain absent, abnormal ZP:0105652 polster decreased amount, abnormal ZP:0105653 intermediate mesoderm decreased amount, abnormal ZP:0105657 retinal ganglion cell decreased occurrence cysteine-type endopeptidase activity, abnormal ZP:0105659 melanocyte decreased process quality catechol oxidase activity, abnormal ZP:0105660 midsagittal plane neural tube absent, abnormal ZP:0105662 neural rod spatial pattern, abnormal ZP:0105663 neural rod mislocalised, abnormal ZP:0105664 neural tube decreased occurrence specification of symmetry, abnormal ZP:0105665 plasma membrane region neural tube mislocalised, abnormal ZP:0105666 ciliary basal body Kupffer's vesicle position, abnormal ZP:0105667 determination of left/right asymmetry in lateral mesoderm occurrence, abnormal ZP:0105668 determination of heart left/right asymmetry occurrence, abnormal ZP:0105669 determination of digestive tract left/right asymmetry occurrence, abnormal ZP:0105671 myocardium mislocalised medially, abnormal ZP:0105674 microtubule blastomere spatial pattern, abnormal ZP:0105675 microtubule blastomere mislocalised, abnormal ZP:0105682 hypophysis male organism increased amount, abnormal ZP:0105699 presumptive rhombomere 5 absent, abnormal ZP:0105700 presumptive rhombomere 4 absent, abnormal ZP:0105701 presumptive rhombomere 3 absent, abnormal ZP:0105702 forebrain neural keel decreased amount, abnormal ZP:0105703 negative regulation of convergent extension involved in axis elongation delayed, abnormal ZP:0105706 Reissner's fiber spatial pattern, abnormal ZP:0105707 Reissner's fiber malformed, abnormal ZP:0105708 Reissner's fiber decreased amount, abnormal ZP:0105709 brain increased process quality acetylcholinesterase activity, abnormal ZP:0105711 anterior region posterior lateral line primordium mislocalised, abnormal ZP:0105713 central region posterior lateral line primordium mislocalised, abnormal ZP:0105714 posterior lateral line primordium decreased process quality posterior lateral line development, abnormal ZP:0105715 central region posterior lateral line primordium increased amount, abnormal ZP:0105716 posterior lateral line primordium decreased rate posterior lateral line neuromast primordium migration, abnormal ZP:0105717 posterior lateral line ganglion fused with posterior lateral line placode, abnormal ZP:0105728 neuromast hair cell decreased occurrence detection of mechanical stimulus involved in sensory perception of sound, abnormal ZP:0105733 opercle absent, abnormal ZP:0105735 intrahepatic bile duct epithelial cell decreased amount, abnormal ZP:0105739 dorsal aorta decreased occurrence alkaline phosphatase activity, abnormal ZP:0105740 oligodendrocyte abutting myelin sheath cell body neuron, abnormal ZP:0105742 basolateral plasma membrane posterior lateral line neuromast decreased amount, abnormal ZP:0105745 chromatin organization process quality, abnormal ZP:0105746 rhombomere 6 absent, abnormal ZP:0105747 centrum decreased process quality bone mineralization, abnormal ZP:0105748 hemal arch decreased process quality bone mineralization, abnormal ZP:0105749 neural arch decreased process quality bone mineralization, abnormal ZP:0105750 centrum decreased volume, abnormal ZP:0105751 osteoblast increased accumulation rib, abnormal ZP:0105752 hematopoietic stem cell dorsal aorta absent, abnormal ZP:0105753 vascular cord decreased amount, abnormal ZP:0105754 mesoderm trunk decreased amount, abnormal ZP:0105755 vH ionocyte rate proton transmembrane transport, abnormal ZP:0105756 vH ionocyte decreased rate proton transmembrane transport, abnormal ZP:0105758 posterior lateral line neuromast decreased process quality detection of mechanical stimulus involved in sensory perception of sound, abnormal ZP:0105760 motile cilium ependymal cell decreased length, abnormal ZP:0105761 spinal cord decreased occurrence motile cilium assembly, abnormal ZP:0105762 spinal cord has fewer parts of type ependymal cell motile cilium ependymal cell, abnormal ZP:0105767 optic vesicle process quality cell migration, abnormal ZP:0105768 optic stalk process quality cell migration, abnormal ZP:0105769 optic cup process quality cell migration, abnormal ZP:0105770 optic fissure process quality cell migration, abnormal ZP:0105771 optic fissure increased amount, abnormal ZP:0105772 optic fissure increased distribution, abnormal ZP:0105773 optic vesicle increased amount, abnormal ZP:0105777 pronephric duct increased distribution, abnormal ZP:0105779 posterior caudal vein decreased amount, abnormal ZP:0105781 Mauthner neuron decreased duration NMDA glutamate receptor activity, abnormal ZP:0105782 Mauthner neuron decreased process quality NMDA glutamate receptor activity, abnormal ZP:0105783 whole organism decreased occurrence phosphodiesterase I activity, abnormal ZP:0105785 cardiac muscle cell process quality establishment of animal organ orientation, abnormal ZP:0105786 cardiac muscle cell orientation heart tube, abnormal ZP:0105790 neutrophil intestine decreased amount, abnormal ZP:0105791 photoreceptor cell accumulation vesicle apical region photoreceptor cell, abnormal ZP:0105792 photoreceptor outer segment eye photoreceptor cell mislocalised, abnormal ZP:0105793 vesicle eye photoreceptor cell mislocalised, abnormal ZP:0105795 tectal neuropile decreased amount, abnormal ZP:0105796 intestine lumen decreased occurrence chitin synthase activity, abnormal ZP:0105801 rhombomere 4 increased distribution, abnormal ZP:0105802 heme whole organism increased amount, abnormal ZP:0105803 secretory granule neutrophil absent, abnormal ZP:0105804 rhombomere 3 mislocalised, abnormal ZP:0105805 rhombomere 1 mislocalised, abnormal ZP:0105806 Mauthner neuron rhombomere 4 decreased amount, abnormal ZP:0105809 anterior region central nervous system decreased amount, abnormal ZP:0105810 pronephric duct opening decreased amount, abnormal ZP:0105812 central artery decreased process quality blood vessel lumenization, abnormal ZP:0105813 pharyngeal arch 2 increased amount, abnormal ZP:0105814 pharyngeal arch 1 increased amount, abnormal ZP:0105821 ribonucleoprotein granule blastomere position, abnormal ZP:0105822 blastomere decreased accumulation ribonucleoprotein granule cleavage furrow blastomere, abnormal ZP:0105827 pericardial region edematous, abnormal ZP:0105835 lipid intestine increased amount, abnormal ZP:0105837 lipid hepatocyte increased amount, abnormal ZP:0105838 thyroxine thyroid follicle absent, abnormal ZP:0105839 melanophore stripe has extra parts of type melanocyte, abnormal ZP:0105840 anterior region posterior lateral line primordium increased amount, abnormal ZP:0105865 locomotory exploration behavior decreased occurrence, abnormal ZP:0105866 telencephalon has fewer parts of type dopaminergic neuron, abnormal ZP:0105880 brain decreased occurrence monoamine oxidase activity, abnormal ZP:0105881 regulation of neuronal action potential disrupted, abnormal ZP:0105892 oocyte stage IV increased amount, abnormal ZP:0105901 swimming behavior frequency, abnormal ZP:0105902 circadian behavior process quality, abnormal ZP:0105903 regulation of locomotor rhythm process quality, abnormal ZP:0105911 retinal outer plexiform layer increased thickness, abnormal ZP:0105913 oocyte stage V decreased amount, abnormal ZP:0105920 multi-ciliated epithelial cell pronephros decreased distribution, abnormal ZP:0105921 corpuscles of Stannius spatial pattern, abnormal ZP:0105922 corpuscles of Stannius mislocalised, abnormal ZP:0105925 hemoglobin blood decreased amount, abnormal ZP:0105931 vertebral column decreased length, abnormal ZP:0105932 ovarian follicle stage III has extra parts of type micropylar cell, abnormal ZP:0105933 micropylar cell mislocalised, abnormal ZP:0105934 brain increased occurrence protein serine/threonine kinase activity, abnormal ZP:0105935 spinal cord increased occurrence protein serine/threonine kinase activity, abnormal ZP:0105936 eye increased occurrence protein serine/threonine kinase activity, abnormal ZP:0105937 liver increased occurrence protein serine/threonine kinase activity, abnormal ZP:0105938 kidney increased occurrence protein serine/threonine kinase activity, abnormal ZP:0105939 intestine increased occurrence protein serine/threonine kinase activity, abnormal ZP:0105940 whole organism decreased occurrence NADH dehydrogenase (ubiquinone) activity, abnormal ZP:0105941 adipose tissue decreased size, abnormal ZP:0105945 floor plate increased distribution, abnormal ZP:0105953 macrophage trunk absent, abnormal ZP:0105967 sterol trunk spatial pattern, abnormal ZP:0105968 cholesterol transport process quality, abnormal ZP:0105986 optic tectum has fewer parts of type dorso-lateral region microglial cell, abnormal ZP:0105989 eye disrupted catechol oxidase activity, abnormal ZP:0105990 melanocyte disrupted catechol oxidase activity, abnormal ZP:0105992 medial region trunk absent, abnormal ZP:0105996 central artery decreased occurrence angiogenesis, abnormal ZP:0106000 central artery decreased occurrence blood vessel morphogenesis, abnormal ZP:0106003 neuronal stem cell brain decreased amount, abnormal ZP:0106004 neuronal stem cell spinal cord decreased amount, abnormal ZP:0106005 spinal cord neural tube increased amount, abnormal ZP:0106006 melanocyte hypodermal cell decreased amount, abnormal ZP:0106007 iridophore peritoneum absent, abnormal ZP:0106008 iridophore hypodermal cell decreased amount, abnormal ZP:0106010 optic choroid vascular plexus decreased amount, abnormal ZP:0106013 central nervous system decreased process quality central nervous system myelination, abnormal ZP:0106014 peripheral nervous system decreased process quality myelination in peripheral nervous system, abnormal ZP:0106015 oligodendrocyte central nervous system decreased amount, abnormal ZP:0106016 myelinating Schwann cell peripheral nervous system decreased amount, abnormal ZP:0106017 dorsal region trunk increased distribution, abnormal ZP:0106018 neural crest cell trunk absent, abnormal ZP:0106019 dorsal region trunk absent, abnormal ZP:0106022 midbrain hindbrain boundary notched, abnormal ZP:0106023 neural crest cell pharyngeal arch disorganized, abnormal ZP:0106024 Rohon-Beard neuron decreased process quality voltage-gated sodium channel activity, abnormal ZP:0106025 brain decreased process quality cytochrome-c oxidase activity, abnormal ZP:0106026 brain increased process quality chitinase activity, abnormal ZP:0106027 brain decreased process quality ubiquinol-cytochrome-c reductase activity, abnormal ZP:0106028 brain increased process quality hexosaminidase activity, abnormal ZP:0106029 alanine whole organism decreased amount, abnormal ZP:0106030 ADP whole organism increased amount, abnormal ZP:0106031 guanosine 5'-monophosphate whole organism increased amount, abnormal ZP:0106032 histidine whole organism decreased amount, abnormal ZP:0106033 glutamine whole organism increased amount, abnormal ZP:0106034 glutathione metabolic process process quality, abnormal ZP:0106038 macrophage increased occurrence phagocytosis, abnormal ZP:0106039 renal albumin absorption decreased occurrence, abnormal ZP:0106040 peritoneum edematous, abnormal ZP:0106041 lateral side peripheral olfactory organ absent, abnormal ZP:0106042 posterior lateral mesoderm increased distribution, abnormal ZP:0106043 vascular endothelium increased distribution, abnormal ZP:0106045 brain vasculature process quality angiogenic sprout fusion, abnormal ZP:0106048 gall bladder absent lipase activity, abnormal ZP:0106049 intestine decreased occurrence lipase activity, abnormal ZP:0106052 myotome decreased occurrence neuromuscular junction development, abnormal ZP:0106057 dorsal region pharyngeal arch 2 absent, abnormal ZP:0106058 dorsal region pharyngeal arch 2 decreased amount, abnormal ZP:0106059 dorsal region pharyngeal arch 1 absent, abnormal ZP:0106060 dorsal region pharyngeal arch 1 decreased amount, abnormal ZP:0106061 ventral-most region pharyngeal arch 1 absent, abnormal ZP:0106062 medial region pharyngeal arch 2 spatial pattern, abnormal ZP:0106063 medial region pharyngeal arch 2 increased distribution, abnormal ZP:0106064 medial region pharyngeal arch 1 spatial pattern, abnormal ZP:0106065 medial region pharyngeal arch 1 increased distribution, abnormal ZP:0106066 ventral region pharyngeal arch 2 increased distribution, abnormal ZP:0106067 ventral region pharyngeal arch 1 increased distribution, abnormal ZP:0106070 opercle aplastic/hypoplastic, abnormal ZP:0106073 brain decreased occurrence mRNA (2'-O-methyladenosine-N6-)-methyltransferase activity, abnormal ZP:0106074 liver decreased occurrence mRNA (2'-O-methyladenosine-N6-)-methyltransferase activity, abnormal ZP:0106075 ovary decreased occurrence mRNA (2'-O-methyladenosine-N6-)-methyltransferase activity, abnormal ZP:0106076 testis decreased occurrence mRNA (2'-O-methyladenosine-N6-)-methyltransferase activity, abnormal ZP:0106077 muscle decreased occurrence mRNA (2'-O-methyladenosine-N6-)-methyltransferase activity, abnormal ZP:0106078 anterior-most region cranium decreased size, abnormal ZP:0106079 vertebral column condensed, abnormal ZP:0106080 cranial vault decreased thickness, abnormal ZP:0106089 optic furrow morphology, abnormal ZP:0106090 whole organism decreased process quality glutathione transferase activity, abnormal ZP:0106092 cerebellum atrophied, abnormal ZP:0106093 trabecular layer increased occurrence cardiac muscle cell proliferation, abnormal ZP:0106094 whole organism decreased process quality protein N-linked glycosylation, abnormal ZP:0106095 podocyte absent, abnormal ZP:0106096 anterior crista process quality innervation, abnormal ZP:0106097 occipital lateral line neuromast process quality innervation, abnormal ZP:0106098 nerve anterior crista absent, abnormal ZP:0106099 basal region cardiac muscle cell deformed, abnormal ZP:0106100 cardiac muscle cell smooth, abnormal ZP:0106101 noradrenaline whole organism decreased amount, abnormal ZP:0106102 norepinephrine biosynthetic process process quality, abnormal ZP:0106104 heart rudiment increased distribution, abnormal ZP:0106107 anterior lateral plate mesoderm increased amount, abnormal ZP:0106108 spinal cord has fewer parts of type ventral region myelin sheath oligodendrocyte, abnormal ZP:0106113 Z disc atrium blurry, abnormal ZP:0106114 sarcomere cardiac ventricle decreased length, abnormal ZP:0106115 sarcomere cardiac ventricle increased width, abnormal ZP:0106116 sarcomere atrium decreased length, abnormal ZP:0106117 sarcomere atrium increased width, abnormal ZP:0106118 sarcomere atrium disorganized, abnormal ZP:0106119 Z disc cardiac ventricle increased thickness, abnormal ZP:0106120 M band cardiac ventricle absent, abnormal ZP:0106121 I band cardiac ventricle absent, abnormal ZP:0106122 I band atrium absent, abnormal ZP:0106123 cardiac conduction irregular rhythm, abnormal ZP:0106124 cardiac muscle cell presumptive sinus venosus absent, abnormal ZP:0106125 posterior lateral line neuromast has fewer parts of type hair cell, abnormal ZP:0106126 blood absent, abnormal ZP:0106128 fusion of sperm to egg plasma membrane involved in single fertilization disrupted, abnormal ZP:0106130 sperm-egg recognition disrupted, abnormal ZP:0106131 unfertilized egg absent, abnormal ZP:0106132 heart tube heterotaxic, abnormal ZP:0106133 post-vent vasculature swollen, abnormal ZP:0106134 oligodendrocyte central nervous system increased amount, abnormal ZP:0106138 posterior lateral line primordium has fewer parts of type cell, abnormal ZP:0106139 whole organism has fewer parts of type posterior lateral line neuromast, abnormal ZP:0106140 peripheral region heart rudiment absent, abnormal ZP:0106142 whole organism decreased process quality galactose metabolic process, abnormal ZP:0106143 brain arrested UDP-glucose:hexose-1-phosphate uridylyltransferase activity, abnormal ZP:0106144 ovary arrested UDP-glucose:hexose-1-phosphate uridylyltransferase activity, abnormal ZP:0106145 skeletal muscle arrested UDP-glucose:hexose-1-phosphate uridylyltransferase activity, abnormal ZP:0106146 raphe nucleus decreased distribution, abnormal ZP:0106148 specification of pronephric distal tubule identity process quality, abnormal ZP:0106152 anal fin male organism decreased pigmentation, abnormal ZP:0106153 pectoral fin breeding tubercle male organism absent, abnormal ZP:0106154 fertilization decreased rate, abnormal ZP:0106155 germ cell proliferation decreased occurrence, abnormal ZP:0106156 female organism has fewer parts of type oocyte, abnormal ZP:0106157 ovary transparent, abnormal ZP:0106158 ovary lacks all parts of type oocyte, abnormal ZP:0106159 ovary has fewer parts of type oocyte, abnormal ZP:0106160 testis transparent, abnormal ZP:0106161 testis has fewer parts of type sperm, abnormal ZP:0106162 testis has extra parts of type Sertoli cell, abnormal ZP:0106163 ovarian follicle atretic, abnormal ZP:0106164 spermatogenic cyst decreased size, abnormal ZP:0106165 spermatogonium increased size, abnormal ZP:0106166 caudal fin has number of regenerating fin regeneration epithelium, abnormal ZP:0106167 rhombomere 6 increased distribution, abnormal ZP:0106168 rhombomere 2 increased distribution, abnormal ZP:0106169 paraxial mesoderm condensed, abnormal ZP:0106170 centriole notochord mislocalised, abnormal ZP:0106171 centriole neuroectoderm mislocalised, abnormal ZP:0106172 microtubule organizing center localization disrupted, abnormal ZP:0106173 convergent extension involved in notochord morphogenesis process quality, abnormal ZP:0106174 spinal cord has extra parts of type dorsal region myelin sheath oligodendrocyte, abnormal ZP:0106176 cell body oligodendrocyte mislocalised, abnormal ZP:0106177 cell body oligodendrocyte increased distribution, abnormal ZP:0106181 dorsal longitudinal vein truncated, abnormal ZP:0106182 mesencephalic vein truncated, abnormal ZP:0106183 lysosome neuromast increased amount, abnormal ZP:0106184 cholesterol neuromast increased amount, abnormal ZP:0106185 liver opaque, abnormal ZP:0106186 axon hindbrain structure, abnormal ZP:0106187 Purkinje cell disorganized, abnormal ZP:0106188 cholesterol trunk increased amount, abnormal ZP:0106189 lysosome peripheral olfactory organ increased amount, abnormal ZP:0106190 cholesterol yolk syncytial layer increased amount, abnormal ZP:0106191 cholesterol extension increased amount, abnormal ZP:0106192 microglial cell brain absent, abnormal ZP:0106193 trunk lacks all parts of type iridophore, abnormal ZP:0106194 caudal fin lacks all parts of type iridophore, abnormal ZP:0106197 central canal lacks all parts of type Reissner's fiber, abnormal ZP:0106198 ventricular system lacks all parts of type Reissner's fiber, abnormal ZP:0106199 Reissner's fiber absent, abnormal ZP:0106201 third ventricle lacks all parts of type Reissner's fiber, abnormal ZP:0106202 subcommissural organ absent, abnormal ZP:0106203 neural tube spinal cord duplicated, abnormal ZP:0106204 neural tube split bilaterally, abnormal ZP:0106211 retinal cone cell structure, abnormal ZP:0106212 retinal cone cell decreased functionality, abnormal ZP:0106213 cilium pronephros dispersed, abnormal ZP:0106214 pronephros decreased rate cilium movement, abnormal ZP:0106215 pronephros decreased occurrence cilium movement, abnormal ZP:0106221 tail bud lacks all parts of type Kupffer's vesicle, abnormal ZP:0106222 photoreceptor cell decreased occurrence synaptic vesicle docking, abnormal ZP:0106223 synaptic ribbon photoreceptor cell position, abnormal ZP:0106224 OFF-bipolar cell process quality synaptic signaling, abnormal ZP:0106225 retinal outer plexiform layer spatial pattern, abnormal ZP:0106228 centrum decreased thickness, abnormal ZP:0106229 ligament vertebral column composition, abnormal ZP:0106230 bone tissue vertebra morphology, abnormal ZP:0106231 dermis decreased thickness, abnormal ZP:0106232 notochord inner cell morphology, abnormal ZP:0106233 notochord inner cell has fewer parts of type vacuole notochord inner cell, abnormal ZP:0106234 neuromuscular junction skeletal muscle cell spatial pattern, abnormal ZP:0106237 pleuroperitoneal region increased process quality cell population proliferation, abnormal ZP:0106238 neoplasm pleuroperitoneal cavity increased amount, abnormal ZP:0106239 cardiac muscle decreased amount, abnormal ZP:0106240 pleuroperitoneal region neoplastic, abnormal ZP:0106241 whole organism decreased process quality histone H3-K36 trimethylation, abnormal ZP:0106242 whole organism decreased process quality histone H3-K36 dimethylation, abnormal ZP:0106243 medial side somite increased distribution, abnormal ZP:0106244 somite trunk decreased amount, abnormal ZP:0106245 yolk mislocalised, abnormal ZP:0106246 immature eye decreased distribution, abnormal ZP:0106247 primordial vasculature spatial pattern, abnormal ZP:0106248 primordial vasculature decreased amount, abnormal ZP:0106249 anterior side whole organism decreased amount, abnormal ZP:0106250 ventral side somite mislocalised, abnormal ZP:0106252 anatomical region pronephros mislocalised, abnormal ZP:0106253 periderm decreased amount, abnormal ZP:0106256 yolk syncytial layer increased amount, abnormal ZP:0106257 brain decreased occurrence MAPK cascade, abnormal ZP:0106258 whole organism decreased occurrence MAPK cascade, abnormal ZP:0106259 central artery decreased occurrence MAPK cascade, abnormal ZP:0106260 whole organism decreased occurrence protein kinase B signaling, abnormal ZP:0106264 central artery decreased occurrence vasculature development, abnormal ZP:0106265 central artery hindbrain malformed, abnormal ZP:0106270 central artery decreased rate blood vessel endothelial cell migration, abnormal ZP:0106272 central artery decreased occurrence vascular endothelial cell proliferation, abnormal ZP:0106273 prechordal plate process quality cell migration involved in gastrulation, abnormal ZP:0106275 chorion attached to fertilized egg, abnormal ZP:0106276 blastodisc hypoplastic, abnormal ZP:0106277 midbrain neoplastic, abnormal ZP:0106278 nucleus optic tectum increased size, abnormal ZP:0106279 nucleus optic tectum broken, abnormal ZP:0106280 retinal inner nuclear layer mislocalised, abnormal ZP:0106281 optic tectum mislocalised, abnormal ZP:0106282 thalamus mislocalised, abnormal ZP:0106283 thalamus increased distribution, abnormal ZP:0106284 retinal outer nuclear layer increased distribution, abnormal ZP:0106285 brain increased occurrence mitotic cell cycle, abnormal ZP:0106286 ceratohyal cartilage increased distance Meckel's cartilage, abnormal ZP:0106287 ceratohyal cartilage angle palatoquadrate cartilage, abnormal ZP:0106288 ceratohyal cartilage angle ceratohyal cartilage, abnormal ZP:0106289 ceratohyal cartilage increased angle to palatoquadrate cartilage, abnormal ZP:0106290 precaudal vertebra fused with hemal arch hemal arch precaudal vertebra, abnormal ZP:0106291 caudal vertebra fused with neural arch neural arch caudal vertebra, abnormal ZP:0106292 Weberian vertebra fused with neural arch centrum Weberian vertebra, abnormal ZP:0106293 pectoral girdle asymmetrical, abnormal ZP:0106294 postcleithrum anterior orientation, abnormal ZP:0106295 hemal arch unfused from hemal arch, abnormal ZP:0106296 exoccipital decreased size, abnormal ZP:0106297 neural arch asymmetrical, abnormal ZP:0106298 neural arch unfused from neural arch, abnormal ZP:0106299 Weberian vertebra fused with Weberian vertebra, abnormal ZP:0106300 oocyte stage II arrested chorion micropyle formation, abnormal ZP:0106301 oocyte stage III arrested chorion micropyle formation, abnormal ZP:0106304 oocyte development decreased occurrence, abnormal ZP:0106305 ovarian follicle stage II lacks all parts of type micropylar cell, abnormal ZP:0106306 ovarian follicle stage III lacks all parts of type micropylar cell, abnormal ZP:0106307 unfertilized egg arrested chorion micropyle formation, abnormal ZP:0106308 unfertilized egg lacks all parts of type micropyle unfertilized egg, abnormal ZP:0106309 median fin fold ruffled, abnormal ZP:0106310 pelvic fin musculature absent, abnormal ZP:0106311 abdominal musculature absent, abnormal ZP:0106312 microtubule cytoskeleton yolk increased amount, abnormal ZP:0106313 cleavage furrow blastomere mislocalised radially, abnormal ZP:0106314 calcium-mediated signaling cellular spatiotemporal quality, abnormal ZP:0106315 embryonic cleavage process efficacy, abnormal ZP:0106316 chromosome movement towards spindle pole disrupted, abnormal ZP:0106328 ventral mandibular arch decreased amount, abnormal ZP:0106329 interopercular-mandibular ligament mislocalised, abnormal ZP:0106335 brain opaque, abnormal ZP:0106336 1-piperideine-6-carboxylate whole organism increased amount, abnormal ZP:0106337 pipecolic acid whole organism increased amount, abnormal ZP:0106338 aortic arch 3 decreased length, abnormal ZP:0106339 aortic arch 3 constricted, abnormal ZP:0106340 aortic arch 4 decreased length, abnormal ZP:0106341 aortic arch 4 constricted, abnormal ZP:0106342 aortic arch 5 decreased length, abnormal ZP:0106343 aortic arch 5 constricted, abnormal ZP:0106344 aortic arch 6 decreased length, abnormal ZP:0106345 aortic arch 6 constricted, abnormal ZP:0106346 embryonic blood vessel endothelial progenitor cell aortic arch decreased amount, abnormal ZP:0106347 aortic arch 3 decreased occurrence angioblast cell differentiation, abnormal ZP:0106348 aortic arch 4 decreased occurrence angioblast cell differentiation, abnormal ZP:0106349 aortic arch 5 decreased occurrence angioblast cell differentiation, abnormal ZP:0106350 aortic arch 6 decreased occurrence angioblast cell differentiation, abnormal ZP:0106351 angioblastic mesenchymal cell aortic arch 3 decreased amount, abnormal ZP:0106352 angioblastic mesenchymal cell aortic arch 4 decreased amount, abnormal ZP:0106353 angioblastic mesenchymal cell aortic arch 5 decreased amount, abnormal ZP:0106354 angioblastic mesenchymal cell aortic arch 6 decreased amount, abnormal ZP:0106355 aortic arch 3 decreased occurrence vasculogenesis, abnormal ZP:0106356 aortic arch 4 decreased occurrence vasculogenesis, abnormal ZP:0106357 aortic arch 5 decreased occurrence vasculogenesis, abnormal ZP:0106358 aortic arch 6 decreased occurrence vasculogenesis, abnormal ZP:0106359 angioblastic mesenchymal cell aortic arch decreased amount, abnormal ZP:0106361 pharynx atrophied, abnormal ZP:0106362 aortic arch 3 arrested blood circulation, abnormal ZP:0106363 aortic arch 4 arrested blood circulation, abnormal ZP:0106364 aortic arch 5 arrested blood circulation, abnormal ZP:0106365 aortic arch 6 arrested blood circulation, abnormal ZP:0106366 aortic arch 3 has fewer parts of type blood vessel endothelial cell aortic arch 3, abnormal ZP:0106367 aortic arch 4 has fewer parts of type blood vessel endothelial cell aortic arch 4, abnormal ZP:0106368 aortic arch 5 lacks all parts of type blood vessel endothelium aortic arch 5, abnormal ZP:0106369 aortic arch 6 has fewer parts of type blood vessel endothelial cell aortic arch 6, abnormal ZP:0106370 migratory cranial neural crest decreased amount, abnormal ZP:0106371 migratory cranial neural crest pharyngeal arch decreased amount, abnormal ZP:0106372 dorsal region neurocranium absent, abnormal ZP:0106376 aortic arch 3 decreased occurrence cell population proliferation, abnormal ZP:0106377 aortic arch 4 decreased occurrence cell population proliferation, abnormal ZP:0106378 aortic arch 5 decreased occurrence cell population proliferation, abnormal ZP:0106379 aortic arch 6 decreased occurrence cell population proliferation, abnormal ZP:0106381 stereocilium otic sensory epithelium decreased length, abnormal ZP:0106382 stereocilium otic sensory epithelium decreased amount, abnormal ZP:0106383 photoreceptor outer segment eye photoreceptor cell degenerate, abnormal ZP:0106384 photoreceptor disc membrane eye photoreceptor cell disorganized, abnormal ZP:0106385 auditory behavior decreased occurrence, abnormal ZP:0106386 retinal rod cell position, abnormal ZP:0106387 macula position, abnormal ZP:0106388 statoacoustic (VIII) ganglion position, abnormal ZP:0106390 neurocranial trabecula deformed, abnormal ZP:0106391 pterygoid process decreased size, abnormal ZP:0106392 dentary increased amount, abnormal ZP:0106393 ceratobranchial 2 cartilage decreased amount, abnormal ZP:0106394 ceratobranchial 3 cartilage decreased amount, abnormal ZP:0106395 ceratobranchial 4 cartilage decreased amount, abnormal ZP:0106396 ceratobranchial 1 cartilage decreased amount, abnormal ZP:0106397 ceratobranchial 5 cartilage decreased amount, abnormal ZP:0106398 neurocranium decreased amount, abnormal ZP:0106405 optic tectum has fewer parts of type ventral region microglial cell, abnormal ZP:0106416 microglial cell optic tectum absent, abnormal ZP:0106420 adipose tissue increased size, abnormal ZP:0106422 cleavage furrow ingression process quality, abnormal ZP:0106423 cleavage furrow ingression decreased occurrence, abnormal ZP:0106424 calcium(2+) blastomere amount, abnormal ZP:0106425 blastomere process quality actin filament-based process, abnormal ZP:0106426 blastomere increased frequency release of sequestered calcium ion into cytosol, abnormal ZP:0106427 blastomere process quality release of sequestered calcium ion into cytosol, abnormal ZP:0106428 blastomere decreased accumulation mitochondrion cleavage furrow blastomere, abnormal ZP:0106429 blastomere decreased accumulation lysosome cleavage furrow blastomere, abnormal ZP:0106430 blastomere decreased accumulation endoplasmic reticulum cleavage furrow blastomere, abnormal ZP:0106431 cerebellum morphogenesis decreased process quality, abnormal ZP:0106432 cerebellum decreased area, abnormal ZP:0106433 cerebellum has fewer parts of type cerebellar granule cell, abnormal ZP:0106434 cerebellum has fewer parts of type Purkinje cell, abnormal ZP:0106435 unfertilized egg decreased occurrence pseudocleavage, abnormal ZP:0106436 blastomere process quality microtubule cytoskeleton organization, abnormal ZP:0106437 lateral rectus absent, abnormal ZP:0106438 ventral transverse absent, abnormal ZP:0106439 dorsal oblique extraocular muscle absent, abnormal ZP:0106440 hypaxial myotome region absent, abnormal ZP:0106441 brain segmentation decreased process quality, abnormal ZP:0106443 parachordal vessel decreased occurrence lymph vessel development, abnormal ZP:0106444 lymphangiogenic sprout process quality lymphangiogenesis, abnormal ZP:0106445 fatty acid beta-oxidation decreased process quality, abnormal ZP:0106446 docosahexaenoic acid whole organism decreased amount, abnormal ZP:0106449 blood cell caudal vein decreased amount, abnormal ZP:0106450 hemoglobin blood cell decreased amount, abnormal ZP:0106451 erythroblast caudal hematopoietic tissue decreased amount, abnormal ZP:0106454 rhombomere 6 vestigial, abnormal ZP:0106455 rhombomere 5 vestigial, abnormal ZP:0106456 abducens motor nucleus rhombomere 6 absent, abnormal ZP:0106457 abducens motor nucleus rhombomere 5 absent, abnormal ZP:0106458 abducens motor nucleus process quality axon guidance, abnormal ZP:0106459 abducens motor nucleus decreased occurrence axon extension, abnormal ZP:0106460 neuronal cell body abducens motor nucleus mislocalised dorsally, abnormal ZP:0106465 primordial germ cell decreased process quality microtubule organizing center organization, abnormal ZP:0106466 primordial germ cell has extra parts of type microtubule organizing center primordial germ cell, abnormal ZP:0106467 primordial germ cell decreased rate cell division, abnormal ZP:0106468 pharyngeal arch 2 decreased occurrence cartilage development, abnormal ZP:0106469 pharyngeal arch 1 decreased occurrence cartilage development, abnormal ZP:0106472 palatoquadrate cartilage decreased amount, abnormal ZP:0106477 ventral wall of dorsal aorta decreased distribution, abnormal ZP:0106478 endothelial cell decreased occurrence cell population proliferation, abnormal ZP:0106479 mitochondrion endothelial cell decreased amount, abnormal ZP:0106480 endothelial cell increased process quality mitochondrial ATP synthesis coupled electron transport, abnormal ZP:0106490 right side lateral mesoderm mislocalised, abnormal ZP:0106497 grey matter hindbrain physical object quality, abnormal ZP:0106498 response to external stimulus process quality, abnormal ZP:0106499 axoneme sperm malformed, abnormal ZP:0106500 sperm decreased process quality sperm axoneme assembly, abnormal ZP:0106501 sperm flagellum sperm decreased length, abnormal ZP:0106502 sperm head sperm increased size, abnormal ZP:0106503 sperm head sperm vacuolated, abnormal ZP:0106504 spermatocyte decreased occurrence regulation of meiotic cell cycle phase transition, abnormal ZP:0106505 sperm head plasma membrane sperm dislocated, abnormal ZP:0106509 neuromast hair cell process quality establishment of planar polarity, abnormal ZP:0106510 neuromast hair cell process quality establishment of animal organ orientation, abnormal ZP:0106513 3',5'-cyclic AMP thrombocyte increased amount, abnormal ZP:0106514 cardiac muscle cell cardiac ventricle disorganized, abnormal ZP:0106515 cardiac muscle cell cardiac ventricle condensed, abnormal ZP:0106516 cardiac muscle cell atrium disorganized, abnormal ZP:0106517 cardiac muscle cell atrium condensed, abnormal ZP:0106518 anatomical region atrioventricular canal cellular quality, abnormal ZP:0106519 filamentous actin endothelial cell spatial pattern, abnormal ZP:0106520 cell endocardium 3-D shape, abnormal ZP:0106521 endocardial cushion formation decreased occurrence, abnormal ZP:0106523 cell presumptive atrioventricular canal 3-D shape, abnormal ZP:0106524 atrioventricular canal aplastic/hypoplastic, abnormal ZP:0106525 heart process quality determination of heart left/right asymmetry, abnormal ZP:0106526 intersegmental vessel decreased efficacy cell migration involved in sprouting angiogenesis, abnormal ZP:0106527 intersegmental vessel process quality blood vessel development, abnormal ZP:0106528 trunk vasculature decreased process quality blood circulation, abnormal ZP:0106529 endothelial cell endocardium mislocalised, abnormal ZP:0106530 endocardium morphogenesis decreased occurrence, abnormal ZP:0106531 endocardium formation decreased occurrence, abnormal ZP:0106532 heart arrested heart looping, abnormal ZP:0106533 ventral mandibular arch mislocalised posteriorly, abnormal ZP:0106534 photoreceptor inner segment layer decreased thickness, abnormal ZP:0106535 anterior region posterior lateral line primordium decreased amount, abnormal ZP:0106536 central region posterior lateral line primordium decreased amount, abnormal ZP:0106537 posterior lateral line primordium arrested posterior lateral line neuromast primordium migration, abnormal ZP:0106538 anterior region posterior lateral line primordium decreased distribution, abnormal ZP:0106539 posterior region posterior lateral line primordium increased amount, abnormal ZP:0106540 posterior region posterior lateral line primordium increased distribution, abnormal ZP:0106541 posterior region posterior lateral line primordium decreased amount, abnormal ZP:0106542 posterior region posterior lateral line primordium mislocalised, abnormal ZP:0106543 posterior lateral line primordium delayed posterior lateral line neuromast deposition, abnormal ZP:0106545 protein blood plasma increased amount, abnormal ZP:0106546 high-density lipoprotein cholesterol blood plasma increased amount, abnormal ZP:0106549 regulation of appetite decreased process quality, abnormal ZP:0106550 eating behavior increased occurrence, abnormal ZP:0106551 nucleus of the medial longitudinal fasciculus synencephalon absent, abnormal ZP:0106553 ocular blood vessel hemorrhagic, abnormal ZP:0106556 lateral dorsal aorta increased diameter, abnormal ZP:0106559 myelinating Schwann cell scale absent, abnormal ZP:0106560 axon scale decreased amount, abnormal ZP:0106565 integument orientation axon integument, abnormal ZP:0106566 integument process quality innervation, abnormal ZP:0106567 integument orientation blood vessel integument, abnormal ZP:0106568 blood vessel integument decreased amount, abnormal ZP:0106569 trunk lacks all parts of type epidermis axon sensory neuron, abnormal ZP:0106570 trunk has fewer parts of type epidermis axon sensory neuron, abnormal ZP:0106571 scale decreased occurrence innervation, abnormal ZP:0106573 ependymal cell absent, abnormal ZP:0106574 ependymal cell decreased amount, abnormal ZP:0106581 mandibular lateral line neuromast decreased occurrence detection of mechanical stimulus involved in sensory perception of sound, abnormal ZP:0106582 otic lateral line neuromast decreased occurrence detection of mechanical stimulus involved in sensory perception of sound, abnormal ZP:0106584 opercular lateral line neuromast decreased occurrence detection of mechanical stimulus involved in sensory perception of sound, abnormal ZP:0106585 middle lateral line neuromast decreased occurrence detection of mechanical stimulus involved in sensory perception of sound, abnormal ZP:0106586 posterior lateral line neuromast decreased occurrence detection of mechanical stimulus involved in sensory perception of sound, abnormal ZP:0106588 epiboly involved in gastrulation with mouth forming second onset quality, abnormal ZP:0106589 epiboly involved in gastrulation with mouth forming second increased duration, abnormal ZP:0106590 external yolk syncytial layer decreased occurrence actomyosin structure organization, abnormal ZP:0106591 actomyosin external yolk syncytial layer decreased width, abnormal ZP:0106592 marginal blastomere external yolk syncytial layer shape, abnormal ZP:0106593 EVL shape, abnormal ZP:0106601 blastomere absent, abnormal ZP:0106603 multi-ciliated epithelial cell olfactory placode decreased amount, abnormal ZP:0106604 glucose-6-phosphate dehydrogenase activity decreased occurrence, abnormal ZP:0106606 ceratohyal cartilage rotated, abnormal ZP:0106608 mitochondrial cloud oocyte morphology, abnormal ZP:0106609 mitochondrial cloud oocyte decreased size, abnormal ZP:0106624 cardiac ventricle arrested cardiac muscle contraction, abnormal ZP:0106625 atrium arrested cardiac muscle contraction, abnormal ZP:0106626 endothelial cell pronephric glomerulus swollen, abnormal ZP:0106630 macrophage optic tectum decreased amount, abnormal ZP:0106647 microglial cell optic tectum increased amount, abnormal ZP:0106652 pronephros hypoplastic, abnormal ZP:0106653 proximal convoluted tubule increased size, abnormal ZP:0106654 proximal straight tubule increased diameter, abnormal ZP:0106655 forebrain midbrain boundary increased occurrence apoptotic process, abnormal ZP:0106656 brain disrupted mitotic cell cycle process, abnormal ZP:0106661 compartment boundary myotome broken, abnormal ZP:0106662 muscle cell myotome position, abnormal ZP:0106663 muscle cell spatial pattern, abnormal ZP:0106667 endoderm increased width, abnormal ZP:0106668 endoderm decreased efficacy cell migration involved in gastrulation, abnormal ZP:0106669 endoderm process quality convergent extension involved in gastrulation, abnormal ZP:0106670 endoderm decreased efficacy convergent extension involved in gastrulation, abnormal ZP:0106671 granulocyte ventral wall of dorsal aorta decreased amount, abnormal ZP:0106672 granulocyte rostral blood island decreased amount, abnormal ZP:0106673 granulocyte blood island decreased amount, abnormal ZP:0106674 hypermethylation of CpG island increased occurrence, abnormal ZP:0106676 lateral plate mesoderm decreased occurrence determination of left/right asymmetry in lateral mesoderm, abnormal ZP:0106677 endocrine pancreas decreased occurrence determination of pancreatic left/right asymmetry, abnormal ZP:0106678 whole organism decreased occurrence smoothened signaling pathway, abnormal ZP:0106685 melanocyte melanophore stripe decreased pigmentation, abnormal ZP:0106686 whole organism color pattern, abnormal ZP:0106690 cytosol myocardium mislocalised, abnormal ZP:0106691 cytosol myocardium increased distribution, abnormal ZP:0106692 Z disc myocardium disorganized, abnormal ZP:0106693 myocardium decreased process quality sarcomere organization, abnormal ZP:0106697 cardiac ventricle decreased occurrence heart contraction, abnormal ZP:0106698 male organism decreased process quality heart contraction, abnormal ZP:0106699 female organism decreased process quality heart contraction, abnormal ZP:0106701 atrium female organism increased area, abnormal ZP:0106703 female organism decreased weight, abnormal ZP:0106704 atrial myocardium has fewer parts of type sarcomere atrial myocardium, abnormal ZP:0106705 ventricular myocardium has fewer parts of type sarcomere ventricular myocardium, abnormal ZP:0106706 melanocyte caudal fin increased amount, abnormal ZP:0106707 melanocyte caudal fin increased area, abnormal ZP:0106708 pigment cell increased amount, abnormal ZP:0106712 retinal cone cell delayed cone photoresponse recovery, abnormal ZP:0106713 retinal cone cell decreased occurrence cone photoresponse recovery, abnormal ZP:0106717 blood dorsal aorta decreased velocity, abnormal ZP:0106718 blood posterior cardinal vein decreased velocity, abnormal ZP:0106719 skeletal muscle myofibril myotome bent, abnormal ZP:0106720 myoseptum irregularly shaped, abnormal ZP:0106721 sarcoplasmic reticulum skeletal muscle disorganized, abnormal ZP:0106722 A band skeletal muscle disorganized, abnormal ZP:0106723 I band skeletal muscle disorganized, abnormal ZP:0106724 heart valve formation delayed, abnormal ZP:0106725 skeletal muscle malformed, abnormal ZP:0106726 glucose blood molecular quality, abnormal ZP:0106727 ionocyte yolk increased amount, abnormal ZP:0106729 double-stranded DNA fragment whole organism decreased amount, abnormal ZP:0106730 translation increased occurrence, abnormal ZP:0106731 nucleus blastomere broken, abnormal ZP:0106732 plasma membrane blastomere structure, abnormal ZP:0106733 tubulin complex assembly decreased occurrence, abnormal ZP:0106734 cleavage furrow formation decreased occurrence, abnormal ZP:0106735 oocyte stage V decreased occurrence proteolysis, abnormal ZP:0106736 blastomere shape, abnormal ZP:0106737 blastomere position, abnormal ZP:0106738 cortical granule fertilized egg increased amount, abnormal ZP:0106739 cortical granule exocytosis decreased occurrence, abnormal ZP:0106740 chorion decreased elevation, abnormal ZP:0106741 chorion decreased diameter, abnormal ZP:0106742 nuclear pore blastomere absent, abnormal ZP:0106743 oocyte stage V opaque, abnormal ZP:0106744 oocyte stage V immature, abnormal ZP:0106745 cytoplasm pronephric distal early tubule mislocalised, abnormal ZP:0106746 epithelial cell pronephric proximal straight tubule increased length, abnormal ZP:0106747 epithelial cell pronephric distal late tubule increased length, abnormal ZP:0106748 pronephric proximal straight tubule decreased width, abnormal ZP:0106749 pronephric distal late tubule increased width, abnormal ZP:0106752 caudal commissure has fewer parts of type axon caudal commissure, abnormal ZP:0106753 rhombomere disorganized, abnormal ZP:0106754 supraoptic tract has fewer parts of type axon supraoptic tract, abnormal ZP:0106755 white matter morphology, abnormal ZP:0106756 whole organism process quality social behavior, abnormal ZP:0106757 cranial neural crest cell delayed cell migration, abnormal ZP:0106758 cranial neural crest cell decreased process quality cell migration, abnormal ZP:0106759 migratory cranial neural crest cell hindbrain mislocalised, abnormal ZP:0106760 migratory cranial neural crest increased distribution, abnormal ZP:0106761 basal communicating artery increased curvature, abnormal ZP:0106762 basal communicating artery kinked, abnormal ZP:0106763 posterior communicating artery increased curvature, abnormal ZP:0106764 posterior communicating artery kinked, abnormal ZP:0106767 ventral region eye increased amount, abnormal ZP:0106768 ventral region eye increased distribution, abnormal ZP:0106769 optic furrow increased distribution, abnormal ZP:0106770 retinal cone cell process quality cellular response to light stimulus, abnormal ZP:0106771 retinal cone cell decreased process quality regulation of calcium ion transmembrane transport, abnormal ZP:0106774 primordial midbrain channel increased amount, abnormal ZP:0106775 ventricular zone decreased size, abnormal ZP:0106776 endothelial cell primordial midbrain channel increased amount, abnormal ZP:0106784 dorsal region trunk decreased distribution, abnormal ZP:0106785 dorsal region trunk decreased amount, abnormal ZP:0106786 medial region trunk decreased amount, abnormal ZP:0106787 ventral region trunk decreased amount, abnormal ZP:0106788 melanocyte ball decreased amount, abnormal ZP:0106800 ovulation arrested, abnormal ZP:0106801 opercular flap protruding, abnormal ZP:0106802 cranium decreased height, abnormal ZP:0106803 caudal fin broken, abnormal ZP:0106804 head has fewer parts of type barbel, abnormal ZP:0106805 anal fin broken, abnormal ZP:0106806 dorsal fin broken, abnormal ZP:0106807 head lacks all parts of type barbel, abnormal ZP:0106817 epidermal cell head morphology, abnormal ZP:0106818 epidermal cell trunk morphology, abnormal ZP:0106819 lysosome peridermal cell increased amount, abnormal ZP:0106820 peridermal cell increased occurrence endocytosis, abnormal ZP:0106821 epidermis increased occurrence cell population proliferation, abnormal ZP:0106822 peridermal cell increased occurrence cell population proliferation, abnormal ZP:0106823 perinucleolar compartment peridermal cell increased amount, abnormal ZP:0106827 heme neutrophil decreased amount, abnormal ZP:0106829 neutrophil arrested peroxidase activity, abnormal ZP:0106830 desmosome heart disorganized, abnormal ZP:0106831 desmosome integument disorganized, abnormal ZP:0106832 heme nucleate erythrocyte increased amount, abnormal ZP:0106833 floor plate increased amount, abnormal ZP:0106839 caudal hematopoietic tissue absent, abnormal ZP:0106840 heme whole organism absent, abnormal ZP:0106843 blood island edematous, abnormal ZP:0106844 nucleate erythrocyte circulating cell decreased amount, abnormal ZP:0106845 central region lens refractivity, abnormal ZP:0106846 lens decreased process quality lens development in camera-type eye, abnormal ZP:0106847 anterior region lens opaque, abnormal ZP:0106848 lens decreased process quality lens morphogenesis in camera-type eye, abnormal ZP:0106849 lens fiber cell decreased process quality lens fiber cell morphogenesis, abnormal ZP:0106850 lens refractivity, abnormal ZP:0106851 central region lens opaque, abnormal ZP:0106854 epiboly involved in gastrulation with mouth forming second decreased occurrence, abnormal ZP:0106855 embryonic structure detached from yolk, abnormal ZP:0106856 periderm broken, abnormal ZP:0106857 melanin biosynthetic process decreased occurrence, abnormal ZP:0106861 myofilament muscle disorganized, abnormal ZP:0106862 lens fiber cell shape, abnormal ZP:0106863 lens fiber cell convex 3-D shape, abnormal ZP:0106864 sarcomere heart tube disorganized, abnormal ZP:0106865 immature eye increased distribution, abnormal ZP:0106866 diencephalon has fewer parts of type ventral region dopaminergic neuron diencephalon, abnormal ZP:0106867 caudal periventricular hypothalamus has fewer parts of type serotonergic neuron caudal periventricular hypothalamus, abnormal ZP:0106868 paraventricular organ has fewer parts of type serotonergic neuron paraventricular organ, abnormal ZP:0106869 ventral region caudal tuberculum absent, abnormal ZP:0106870 raphe nucleus decreased amount, abnormal ZP:0106871 vasculature decreased distribution, abnormal ZP:0106875 fear response increased process quality, abnormal ZP:0106879 hyaluronic acid heart decreased amount, abnormal ZP:0106880 cardiac jelly atrioventricular canal absent, abnormal ZP:0106881 endocardial cushion development decreased occurrence, abnormal ZP:0106882 cardiac jelly development decreased occurrence, abnormal ZP:0106888 scale primordium absent, abnormal ZP:0106890 dermis absent, abnormal ZP:0106891 pronephric tubule decreased occurrence lysosomal protein catabolic process, abnormal ZP:0106897 autophagosome pronephric tubule increased size, abnormal ZP:0106898 pronephric tubule has extra parts of type autophagosome pronephric tubule, abnormal ZP:0106899 renal tubule occurrence autophagy, abnormal ZP:0106900 cortical granule oocyte stage II increased amount, abnormal ZP:0106901 cortical granule oocyte stage II decreased size, abnormal ZP:0106902 skeletal muscle has extra parts of type mitochondrion inclusion body skeletal muscle, abnormal ZP:0106905 swim bladder increased variability of size, abnormal ZP:0106907 Kupffer's vesicle orientation cilium Kupffer's vesicle, abnormal ZP:0106908 stereocilium bundle posterior lateral line neuromast decreased functionality, abnormal ZP:0106909 inner ear arrested detection of mechanical stimulus involved in sensory perception of sound, abnormal ZP:0106912 neutrophil decreased occurrence cell maturation, abnormal ZP:0106916 stereocilium bundle hair cell anterior macula decreased amount, abnormal ZP:0106918 axon midbrain mislocalised, abnormal ZP:0106919 axon spinal cord defasciculated, abnormal ZP:0106920 post-vent region lacks all parts of type posterior lateral line neuromast, abnormal ZP:0106922 hematopoietic stem cell decreased occurrence maintenance of location, abnormal ZP:0106923 granulocyte caudal hematopoietic tissue decreased amount, abnormal ZP:0106924 macrophage caudal hematopoietic tissue decreased amount, abnormal ZP:0106925 erythroid lineage cell caudal hematopoietic tissue decreased amount, abnormal ZP:0106926 macrophage caudal hematopoietic tissue absent, abnormal ZP:0106928 dorsal convergence decreased occurrence, abnormal ZP:0106929 endodermal cell decreased occurrence dorsal convergence, abnormal ZP:0106932 anterior region trunk musculature decreased amount, abnormal ZP:0106933 anterior region trunk decreased amount, abnormal ZP:0106934 nucleus blastomere absent, abnormal ZP:0106935 plasma membrane blastomere absent, abnormal ZP:0106936 ectoderm increased distribution, abnormal ZP:0106937 axis increased thickness, abnormal ZP:0106938 medial region whole organism increased amount, abnormal ZP:0106939 medial region whole organism increased distribution, abnormal ZP:0106940 left side lateral plate mesoderm mislocalised, abnormal ZP:0106941 notochord increased distribution, abnormal ZP:0106942 anatomical region Kupffer's vesicle decreased amount, abnormal ZP:0106950 apical side cardiac muscle cell constricted, abnormal ZP:0106951 cardiac muscle cell has extra parts of type basal region cell projection cardiac muscle cell, abnormal ZP:0106952 actomyosin cardiac ventricle spatial pattern, abnormal ZP:0106953 actomyosin cardiac ventricle polarity, abnormal ZP:0106954 actomyosin heart spatial pattern, abnormal ZP:0106955 actomyosin myocardium increased distribution, abnormal ZP:0106956 cytoplasm whole organism decreased amount, abnormal ZP:0106957 blastomere increased occurrence apoptotic process, abnormal ZP:0106958 blastomere arrested cell population proliferation, abnormal ZP:0106959 microtubule cytoskeleton organization process quality, abnormal ZP:0106960 cytoplasm blastomere mislocalised, abnormal ZP:0106961 gamma-tubulin small complex blastomere absent, abnormal ZP:0106962 perinuclear region of cytoplasm blastomere mislocalised, abnormal ZP:0106965 thrombocyte activation process quality, abnormal ZP:0106966 thromboblast head kidney decreased amount, abnormal ZP:0106967 axon extension accelerated growth, abnormal ZP:0106968 neuron projection CaP motoneuron increased length, abnormal ZP:0106969 vein caudal fin tangled, abnormal ZP:0106970 intersegmental vein caudal fin morphology, abnormal ZP:0106971 intersegmental vein caudal fin dilated, abnormal ZP:0106972 subintestinal vein caudal fin morphology, abnormal ZP:0106973 subintestinal vein caudal fin dilated, abnormal ZP:0106974 vein protruding out of intersegmental vein caudal fin, abnormal ZP:0106975 vein protruding out of subintestinal vein caudal fin, abnormal ZP:0106976 aggressive behavior process quality, abnormal ZP:0106977 forebrain decreased occurrence axonal fasciculation, abnormal ZP:0106978 midbrain decreased occurrence axonal fasciculation, abnormal ZP:0106979 axon forebrain defasciculated, abnormal ZP:0106980 axon midbrain defasciculated, abnormal ZP:0106981 peripheral nervous system has fewer parts of type peripheral neuron, abnormal ZP:0106982 trigeminal ganglion increased length, abnormal ZP:0106983 trigeminal ganglion increased width, abnormal ZP:0106984 trigeminal ganglion decondensed, abnormal ZP:0106985 posterior region hypothalamus decreased amount, abnormal ZP:0106986 hindbrain has fewer parts of type dopaminergic neuron, abnormal ZP:0106987 midbrain has fewer parts of type dopaminergic neuron, abnormal ZP:0106988 endohypothalamic tract decreased amount, abnormal ZP:0106989 statoacoustic (VIII) ganglion increased amount, abnormal ZP:0106990 posterior lateral line ganglion increased amount, abnormal ZP:0106991 anterior region trunk apoptotic, abnormal ZP:0106992 neuromuscular junction of skeletal muscle fiber fast muscle cell morphology, abnormal ZP:0106993 cholinergic synapse fast muscle cell spatial pattern, abnormal ZP:0106994 hindbrain has fewer parts of type cranial motor neuron, abnormal ZP:0106995 midbrain has fewer parts of type cranial motor neuron, abnormal ZP:0106996 cholesterol caudal vein increased amount, abnormal ZP:0106997 low-density lipoprotein cholesterol whole organism increased amount, abnormal ZP:0106998 intestine lumen distended, abnormal ZP:0107000 mitochondrion retinal pigmented epithelium increased amount, abnormal ZP:0107001 mitochondrion retinal pigmented epithelium increased area, abnormal ZP:0107002 mitochondrion retinal cone cell morphology, abnormal ZP:0107003 mitochondrion retinal cone cell circular, abnormal ZP:0107004 mitochondrion retinal cone cell increased size, abnormal ZP:0107006 cell projection Muller cell increased distribution, abnormal ZP:0107007 phagocytic vesicle retinal pigmented epithelium increased amount, abnormal ZP:0107008 cranial neural crest pharyngeal arch decreased amount, abnormal ZP:0107009 neural crest pharyngeal arch decreased amount, abnormal ZP:0107010 ceratobranchial 2 cartilage morphology, abnormal ZP:0107011 ceratobranchial 2 cartilage decreased size, abnormal ZP:0107012 ceratobranchial 3 cartilage morphology, abnormal ZP:0107013 ceratobranchial 3 cartilage decreased size, abnormal ZP:0107014 ceratobranchial 4 cartilage morphology, abnormal ZP:0107015 ceratobranchial 1 cartilage morphology, abnormal ZP:0107016 ceratobranchial 1 cartilage decreased size, abnormal ZP:0107017 ceratobranchial 5 cartilage decreased size, abnormal ZP:0107018 pharyngeal pouch increased amount, abnormal ZP:0107019 Non-Lymphoid leukaemias whole organism increased amount, abnormal ZP:0107020 sarcoma whole organism increased amount, abnormal ZP:0107021 vasculature neoplastic, abnormal ZP:0107022 germ line cell neoplastic, abnormal ZP:0107023 B cell spleen decreased amount, abnormal ZP:0107026 spinal cord has extra parts of type anterior region axon Mauthner neuron, abnormal ZP:0107028 neural crest pharyngeal arch 3 decreased amount, abnormal ZP:0107029 neural crest pharyngeal arch 4 decreased amount, abnormal ZP:0107030 neural crest pharyngeal arch 5 decreased amount, abnormal ZP:0107031 neural crest pharyngeal arch 6 decreased amount, abnormal ZP:0107032 neural crest pharyngeal arch 2 decreased amount, abnormal ZP:0107033 neural crest pharyngeal arch 1 decreased amount, abnormal ZP:0107034 (R)-lactate blood plasma increased amount, abnormal ZP:0107036 B cell increased occurrence apoptotic process, abnormal ZP:0107037 T cell head kidney increased amount, abnormal ZP:0107041 spinal cord has fewer parts of type anterior region axon reticulospinal neuron, abnormal ZP:0107042 spinal cord has fewer parts of type posterior region axon reticulospinal neuron, abnormal ZP:0107043 reticulospinal neuron decreased occurrence axon extension, abnormal ZP:0107044 cranial neural crest ceratohyal cartilage decreased amount, abnormal ZP:0107045 ATP cell decreased amount, abnormal ZP:0107046 subcutaneous fat dorsal fin increased amount, abnormal ZP:0107047 calcium import into the mitochondrion disrupted, abnormal ZP:0107049 caudal fin fat increased amount, abnormal ZP:0107051 proctodeum decreased amount, abnormal ZP:0107052 skeletal element head morphology, abnormal ZP:0107053 pectoral fin increased amount, abnormal ZP:0107054 cell pharyngeal arch 2 decreased amount, abnormal ZP:0107055 cell pharyngeal arch 1 decreased amount, abnormal ZP:0107056 anatomical margin median fin fold irregularly shaped, abnormal ZP:0107057 anatomical margin pectoral fin irregularly shaped, abnormal ZP:0107058 proximal region fin fold pectoral fin bud absent, abnormal ZP:0107059 renal system development process quality, abnormal ZP:0107060 renal system morphology, abnormal ZP:0107061 pectoral fin blistered, abnormal ZP:0107062 nephron morphology, abnormal ZP:0107063 blood vasculature misrouted, abnormal ZP:0107064 intersegmental vessel has extra parts of type angiogenic sprout, abnormal ZP:0107065 dorsal longitudinal vein attached to mesencephalic artery, abnormal ZP:0107066 dorsal longitudinal vein attached to mesencephalic vein, abnormal ZP:0107067 lateral dorsal aorta shape, abnormal ZP:0107068 neural crest cell pharyngeal arch 2 shape, abnormal ZP:0107069 germ line cell testis spatial pattern, abnormal ZP:0107070 testis translucent, abnormal ZP:0107071 condensed nuclear chromosome ovary spatial pattern, abnormal ZP:0107072 condensed nuclear chromosome testis spatial pattern, abnormal ZP:0107073 synaptonemal structure spermatocyte absent, abnormal ZP:0107074 meiotic sister chromatid cohesion process quality, abnormal ZP:0107075 chromosome organization involved in meiotic cell cycle process quality, abnormal ZP:0107076 synaptonemal complex organization process quality, abnormal ZP:0107077 anterior-posterior axis vertebral column increased curvature, abnormal ZP:0107081 cone photoreceptor disc membrane retinal cone cell broken, abnormal ZP:0107082 vertebral column deformed, abnormal ZP:0107083 nuclear chromosome segregation disrupted, abnormal ZP:0107084 hindbrain decreased magnitude axonogenesis, abnormal ZP:0107086 cranial nerve X decreased occurrence axon arborization, abnormal ZP:0107087 cranial nerve IX decreased occurrence axon arborization, abnormal ZP:0107088 cranial nerve X decreased amount, abnormal ZP:0107089 cranial nerve VII misrouted, abnormal ZP:0107090 cranial nerve VII defasciculated, abnormal ZP:0107091 cranial nerve IX decreased amount, abnormal ZP:0107093 vestibular reflex decreased process quality, abnormal ZP:0107097 cranial nerve IX misrouted, abnormal ZP:0107098 pronephric glomerulus increased diameter, abnormal ZP:0107099 cytoskeleton intestinal epithelium mislocalised, abnormal ZP:0107102 pharyngeal arch 3 increased amount, abnormal ZP:0107103 pharyngeal arch 4 increased amount, abnormal ZP:0107104 pharyngeal arch 5 increased amount, abnormal ZP:0107105 pharyngeal arch 6 increased amount, abnormal ZP:0107106 pharyngeal arch 7 increased amount, abnormal ZP:0107107 periocular mesenchyme decreased amount, abnormal ZP:0107110 central region oocyte stage II mislocalised, abnormal ZP:0107111 cytoplasm oocyte stage II mislocalised, abnormal ZP:0107112 basement membrane epidermis morphology, abnormal ZP:0107114 dorsal aorta decreased occurrence Notch signaling pathway, abnormal ZP:0107115 posterior region whole organism curved ventral, abnormal ZP:0107124 pillar of the semicircular canal malformed, abnormal ZP:0107128 dorsal region spinal cord neural keel decreased amount, abnormal ZP:0107130 dorsal longitudinal anastomotic vessel decreased occurrence sprouting angiogenesis, abnormal ZP:0107131 dorsal longitudinal anastomotic vessel split, abnormal ZP:0107133 neural crest cell spatial pattern, abnormal ZP:0107140 photoreceptor ribbon synapse eye morphology, abnormal ZP:0107141 extraocular musculature morphology, abnormal ZP:0107142 extraocular musculature increased amount, abnormal ZP:0107143 extraocular musculature increased distribution, abnormal ZP:0107144 muscle pharyngeal arch morphology, abnormal ZP:0107145 medial rectus morphology, abnormal ZP:0107146 medial rectus decreased amount, abnormal ZP:0107147 dorsal rectus decreased amount, abnormal ZP:0107148 lateral rectus morphology, abnormal ZP:0107149 lateral rectus decreased amount, abnormal ZP:0107150 ventral rectus decreased amount, abnormal ZP:0107151 dorsal oblique extraocular muscle decreased amount, abnormal ZP:0107152 ventral oblique extraocular muscle decreased amount, abnormal ZP:0107153 ventral region retina absent, abnormal ZP:0107154 pharyngeal arch 6 decreased amount, abnormal ZP:0107155 pharyngeal arch 7 decreased amount, abnormal ZP:0107156 periocular mesenchyme absent, abnormal ZP:0107158 neural keel spatial pattern, abnormal ZP:0107159 neural keel increased distribution, abnormal ZP:0107160 optic primordium decreased amount, abnormal ZP:0107161 anterior neural keel decreased amount, abnormal ZP:0107162 optic vesicle delayed neurogenesis, abnormal ZP:0107163 neural plate increased distribution, abnormal ZP:0107164 cellular anatomical entity myoseptum aggregated, abnormal ZP:0107165 cellular anatomical entity skeletal muscle aggregated, abnormal ZP:0107166 intersegmental vessel decreased occurrence cell migration involved in sprouting angiogenesis, abnormal ZP:0107167 blood vessel endothelial cell accumulation intersegmental vessel, abnormal ZP:0107169 xanthophore disrupted cell migration, abnormal ZP:0107170 head decreased occurrence macrophage migration, abnormal ZP:0107171 head decreased duration macrophage migration, abnormal ZP:0107172 cell projection melanocyte increased amount, abnormal ZP:0107173 mRNA splicing, via spliceosome process efficacy, abnormal ZP:0107174 mRNA splice site selection disrupted, abnormal ZP:0107175 cornea edematous, abnormal ZP:0107177 anterior region spinal cord decreased size, abnormal ZP:0107178 dorsal region neural keel decreased amount, abnormal ZP:0107179 anatomical region common cardinal vein increased amount, abnormal ZP:0107180 metallopeptidase activity increased occurrence, abnormal ZP:0107183 pronephric distal early tubule increased volume, abnormal ZP:0107184 pronephric distal late tubule decreased volume, abnormal ZP:0107185 male organism decreased size, abnormal ZP:0107188 pronephric duct increased area, abnormal ZP:0107189 melanocyte migration process quality, abnormal ZP:0107190 myeloid cell decreased process quality cell migration, abnormal ZP:0107191 neutrophil circulating cell decreased amount, abnormal ZP:0107193 myeloid cell kidney decreased amount, abnormal ZP:0107194 dihydroceramide whole organism increased amount, abnormal ZP:0107195 Collagen semicircular canal present, abnormal ZP:0107199 semicircular canal aplastic/hypoplastic, abnormal ZP:0107202 otic vesicle ventral protrusion present, abnormal ZP:0107203 pillar of the lateral semicircular canal absent, abnormal ZP:0107204 inner ear lacks parts or has fewer parts of type semicircular canal, abnormal ZP:0107205 proteoglycan otic vesicle protrusion decreased amount, abnormal ZP:0107206 Collagen otic vesicle protrusion decreased amount, abnormal ZP:0107207 otic vesicle lacks parts or has fewer parts of type otic vesicle protrusion, abnormal ZP:0107209 heart decreased process quality cardiac muscle tissue growth involved in heart morphogenesis, abnormal ZP:0107210 cell cortex cardiac muscle cell spatial pattern, abnormal ZP:0107211 cell cortex cardiac muscle cell increased amount, abnormal ZP:0107212 cell cortex cardiac muscle cell mislocalised, abnormal ZP:0107213 cardiac muscle cell decreased process quality actin filament organization, abnormal ZP:0107214 filamentous actin cardiac muscle cell mislocalised radially, abnormal ZP:0107215 cardiac muscle cell decreased occurrence endocytic recycling, abnormal ZP:0107216 cardiac muscle cell has extra parts of type recycling endosome cardiac muscle cell, abnormal ZP:0107218 cardiac ventricle decreased occurrence cardiac chamber ballooning, abnormal ZP:0107219 atrium decreased occurrence cardiac chamber ballooning, abnormal ZP:0107220 cardiac muscle cell process quality regulation of embryonic cell shape, abnormal ZP:0107221 dorsal fin fold decreased process quality embryonic dorsal fin morphogenesis, abnormal ZP:0107222 ventral fin fold decreased process quality embryonic anal fin morphogenesis, abnormal ZP:0107223 recycling endosome cardiac muscle cell increased amount, abnormal ZP:0107224 recycling endosome cardiac muscle cell increased size, abnormal ZP:0107225 epithelial cell dorsal fin fold protruding, abnormal ZP:0107226 epithelial cell ventral fin fold protruding, abnormal ZP:0107227 dorsal fin fold malformed, abnormal ZP:0107228 cardiac muscle cell obtuse, abnormal ZP:0107229 cardiac muscle cell protruding out of myocardium, abnormal ZP:0107230 anterior neural plate absent, abnormal ZP:0107232 postero-medial margin ceratohyal cartilage increased amount, abnormal ZP:0107233 ceratohyal cartilage premature ossification, abnormal ZP:0107235 ceratohyal bone irregularly shaped, abnormal ZP:0107236 anterior region palatoquadrate cartilage decreased size, abnormal ZP:0107237 ventral hypohyal bone premature ossification, abnormal ZP:0107238 anguloarticular premature ossification, abnormal ZP:0107239 quadrate premature ossification, abnormal ZP:0107240 symplectic premature ossification, abnormal ZP:0107241 ceratobranchial 2 cartilage premature ossification, abnormal ZP:0107242 ceratobranchial 1 cartilage premature ossification, abnormal ZP:0107245 ventral mandibular arch lacks parts or has fewer parts of type Meckel's cartilage, abnormal ZP:0107248 neurocranium hypertrophic, abnormal ZP:0107249 endothelial tip cell intersegmental vessel spade-shaped, abnormal ZP:0107250 lymph vessel development decreased occurrence, abnormal ZP:0107251 cardiovascular system lacks all parts of type thoracic duct, abnormal ZP:0107252 cardiovascular system lacks all parts of type vascular lymphangioblast, abnormal ZP:0107253 endothelial tip cell decreased occurrence calcium-mediated signaling, abnormal ZP:0107254 endothelial tip cell decreased occurrence regulation of cytosolic calcium ion concentration, abnormal ZP:0107255 endothelial tip cell decreased occurrence regulation of store-operated calcium channel activity, abnormal ZP:0107256 endothelial tip cell intersegmental vessel decreased amount, abnormal ZP:0107257 intersegmental vessel decreased occurrence Notch signaling pathway, abnormal ZP:0107258 intersegmental vessel decreased occurrence endothelial tip cell filopodium assembly, abnormal ZP:0107259 intersegmental vessel decreased occurrence MAPK cascade, abnormal ZP:0107261 dorsal longitudinal anastomotic vessel increased diameter, abnormal ZP:0107269 eye growth quality of occurrent organ growth, abnormal ZP:0107270 eye circular, abnormal ZP:0107271 ciliary marginal zone decreased occurrence cell population proliferation, abnormal ZP:0107272 retinal ganglion cell layer decreased distribution, abnormal ZP:0107275 progesterone blood plasma increased amount, abnormal ZP:0107276 estradiol blood plasma decreased amount, abnormal ZP:0107277 (20R)-17,20-dihydroxypregn-4-en-3-one testis increased amount, abnormal ZP:0107278 blood male organism increased amount, abnormal ZP:0107279 sperm increased amount, abnormal ZP:0107281 chorion micropyle formation decreased occurrence, abnormal ZP:0107283 micropylar cell absent, abnormal ZP:0107284 pronucleus fertilized egg decreased amount, abnormal ZP:0107285 micropyle fertilized egg absent, abnormal ZP:0107286 pronephric proximal straight tubule increased occurrence pronephric nephron tubule epithelial cell differentiation, abnormal ZP:0107287 pronephric distal late tubule decreased occurrence pronephric nephron tubule epithelial cell differentiation, abnormal ZP:0107288 pronephric tubule decreased occurrence multi-ciliated epithelial cell differentiation, abnormal ZP:0107289 pronephric tubule has fewer parts of type multi-ciliated epithelial cell pronephric tubule, abnormal ZP:0107290 neurohypophysis absent, abnormal ZP:0107291 intrahepatic bile duct aggregated, abnormal ZP:0107292 intrahepatic bile duct epithelial cell spatial pattern, abnormal ZP:0110336 pronephric tubule mislocalised, abnormal ZP:0110337 mitochondrion neuromast hair cell functionality, abnormal ZP:0110338 neuromast hair cell process quality regulation of mitochondrial membrane potential, abnormal ZP:0110340 multi-ciliated epithelial cell malformed, abnormal ZP:0110341 mitochondrion neuromast hair cell spatial pattern, abnormal ZP:0110348 apical region pronephric duct decreased amount, abnormal ZP:0110349 apical side pronephric glomerular capsule epithelium mislocalised, abnormal ZP:0110350 cilium pronephric tubule malformed, abnormal ZP:0110351 filamentous actin pronephric tubule malformed, abnormal ZP:0110352 pronephric tubule decreased occurrence ciliary basal body-plasma membrane docking, abnormal ZP:0110353 pronephric glomerular capsule epithelium apical-basal polarity, abnormal ZP:0130672 ventral region diencephalon increased amount, abnormal ZP:0130673 ventral region spinal cord decreased size, abnormal ZP:0130675 adherens junction EVL structure, abnormal ZP:0130677 trunk has extra parts of type ventral region melanocyte, abnormal ZP:0130678 trunk has extra parts of type ventral region iridophore, abnormal ZP:0130679 adherens junction neural tube morphology, abnormal ZP:0130682 hypochord absent, abnormal ZP:0130683 dorsoventral diencephalic tract process quality axon guidance, abnormal ZP:0130684 Rohon-Beard neuron process quality axon guidance, abnormal ZP:0130685 roof plate spinal cord region absent, abnormal ZP:0130688 atrioventricular canal endocardium process quality tissue morphogenesis, abnormal ZP:0130689 atrioventricular valve process quality tissue morphogenesis, abnormal ZP:0130690 atrioventricular valve morphogenesis decreased occurrence, abnormal ZP:0130701 cytosolic large ribosomal subunit whole organism decreased amount, abnormal ZP:0130702 anatomical region whole organism absent, abnormal ZP:0130704 cilium ependymal cell decreased amount, abnormal ZP:0130705 fourth ventricle increased area, abnormal ZP:0130706 tectal ventricle increased area, abnormal ZP:0130707 telencephalic ventricle dilated, abnormal ZP:0130708 intestinal epithelium detached from cell intestinal epithelium, abnormal ZP:0130709 neuromast increased occurrence cell population proliferation, abnormal ZP:0130712 rhombomere 6 increased distance somite 1, abnormal ZP:0130713 basement membrane pronephric glomerulus increased thickness, abnormal ZP:0130714 basement membrane pronephric glomerulus disorganized, abnormal ZP:0130715 pronephric glomerulus collapsed, abnormal ZP:0130716 adherens junction median fin fold composition, abnormal ZP:0130717 adherens junction Meckel's cartilage increased amount, abnormal ZP:0130718 adherens junction chondrocyte increased amount, abnormal ZP:0130719 melanocyte accumulation posterior-most region otic vesicle, abnormal ZP:0130720 melanocyte accumulation lateral margin pharyngeal arch, abnormal ZP:0130725 axon anterior commissure mislocalised, abnormal ZP:0130726 postoptic commissure decreased amount, abnormal ZP:0130727 anterior commissure decreased amount, abnormal ZP:0130728 axon postoptic commissure mislocalised, abnormal ZP:0130729 neuron projection eye absent, abnormal ZP:0130730 neuron projection eye disorganized, abnormal ZP:0130731 neuron projection eye decreased amount, abnormal ZP:0130732 neuron projection optic tectum absent, abnormal ZP:0130733 neuron eye decreased amount, abnormal ZP:0130734 caudal commissure decreased amount, abnormal ZP:0130735 tectal neuropile decreased size, abnormal ZP:0130736 posterior side midbrain hindbrain boundary irregularly shaped, abnormal ZP:0130738 blastoderm decreased occurrence cell-cell adhesion, abnormal ZP:0130739 blastoderm decreased viscosity, abnormal ZP:0130740 cilium cloaca decreased length, abnormal ZP:0130741 cilium cloaca decreased amount, abnormal ZP:0130744 posterior region inner ear anterioralized, abnormal ZP:0130745 inner ear lacks all parts of type posterior macula, abnormal ZP:0130746 inner ear has extra parts of type lateral crista, abnormal ZP:0130747 sagitta mislocalised ventrally, abnormal ZP:0130750 forebrain increased occurrence transmission of nerve impulse, abnormal ZP:0130752 cardiac ventricle increased occurrence cell population proliferation, abnormal ZP:0130755 ceratohyal cartilage angle basihyal cartilage, abnormal ZP:0130757 reactive oxygen species biosynthetic process increased occurrence, abnormal ZP:0130767 cell forerunner cell group decreased amount, abnormal ZP:0130768 cilium cloaca increased length, abnormal ZP:0130770 muscle cell decreased diameter, abnormal ZP:0130783 intestine increased occurrence apoptotic process, abnormal ZP:0130790 intestinal motility decreased process quality, abnormal ZP:0130795 brain decreased occurrence phagocytosis, abnormal ZP:0130801 vasculature increased distribution, abnormal ZP:0130802 basement membrane pronephric glomerulus morphology, abnormal ZP:0130803 adherens junction posterior lateral line primordium decreased object quality, abnormal ZP:0130807 left side intestinal bulb mislocalised, abnormal ZP:0130808 left side mid intestine absent, abnormal ZP:0130809 right side intestinal bulb mislocalised, abnormal ZP:0130810 right side mid intestine absent, abnormal ZP:0130812 stereocilium bundle lateral crista malformed, abnormal ZP:0130818 brain vasculature hindbrain decreased amount, abnormal ZP:0130819 neural crest patchy, abnormal ZP:0130821 neural crest cell cellular adhesivity, abnormal ZP:0130822 cleavage furrow blastomere incomplete structure, abnormal ZP:0130823 cortical granule blastomere mislocalised, abnormal ZP:0130824 cortical granule early embryonic cell mislocalised, abnormal ZP:0130825 cortical actin cytoskeleton organization process quality, abnormal ZP:0130826 cortical actin cytoskeleton organization decreased occurrence, abnormal ZP:0130827 cortical granule exocytosis process quality, abnormal ZP:0130828 chorion decreased size, abnormal ZP:0130829 chorion increased fragility, abnormal ZP:0130830 blastodisc decreased height, abnormal ZP:0130831 left side diencephalon absent, abnormal ZP:0130836 cell notochord cuboid, abnormal ZP:0130837 mouth movement quality, abnormal ZP:0130838 Meckel's cartilage-palatoquadrate cartilage joint morphology, abnormal ZP:0130839 Meckel's cartilage-palatoquadrate cartilage joint decreased size, abnormal ZP:0130840 Meckel's cartilage-palatoquadrate cartilage joint movement quality, abnormal ZP:0130841 opercle inflexible, abnormal ZP:0130842 mandibular arch skeleton inflexible, abnormal ZP:0130843 chondrocyte Meckel's cartilage hypertrophic, abnormal ZP:0130844 chondrocyte mandibular arch skeleton immature, abnormal ZP:0130845 Meckel's cartilage-palatoquadrate cartilage joint decreased amount, abnormal ZP:0130846 post-vent vasculature decreased occurrence blood circulation, abnormal ZP:0130847 caudal fin accumulation blood caudal fin, abnormal ZP:0130848 blood vessel retina decreased amount, abnormal ZP:0130849 blood plasma retina decreased amount, abnormal ZP:0130850 neurosecretory neuron hypothalamus absent, abnormal ZP:0130851 anatomical region pronephric glomerulus cystic, abnormal ZP:0130852 axon lateral line increased amount, abnormal ZP:0130858 podocyte foot pronephric podocyte morphology, abnormal ZP:0130860 pronephric glomerulus increased volume, abnormal ZP:0130862 bulbus arteriosus decreased functionality, abnormal ZP:0130863 blood vasculature increased permeability, abnormal ZP:0130864 blood brain mislocalised, abnormal ZP:0130866 thigmotaxis decreased duration, abnormal ZP:0130867 caudal vertebra fused with caudal vertebra, abnormal ZP:0130868 caudal vertebra malformed, abnormal ZP:0130869 non-Weberian precaudal vertebra malformed, abnormal ZP:0130870 non-Weberian precaudal vertebra increased curvature, abnormal ZP:0130872 axon spinal cord decreased thickness, abnormal ZP:0130873 axon spinal cord truncated, abnormal ZP:0130876 atrioventricular canal morphogenesis decreased process quality, abnormal ZP:0130877 atrioventricular canal decreased process quality cardiac muscle cell development, abnormal ZP:0130878 myocardium atrioventricular canal decreased amount, abnormal ZP:0130879 hematopoietic cell increased distribution, abnormal ZP:0130880 thrombocyte thymus absent, abnormal ZP:0130881 lymphoid lineage cell migration into thymus decreased occurrence, abnormal ZP:0130882 spinal cord curved dorsal, abnormal ZP:0130883 spinal cord kinked, abnormal ZP:0130884 axis curved dorsal, abnormal ZP:0130885 axis kinked, abnormal ZP:0130887 slit diaphragm pronephros decreased amount, abnormal ZP:0130888 pronephric glomerulus retracted, abnormal ZP:0130890 olfactory placode process quality cilium assembly, abnormal ZP:0130892 ceratobranchial 5 tooth decreased efficacy tooth mineralization, abnormal ZP:0130893 ceratobranchial 5 tooth composition, abnormal ZP:0130894 ceratobranchial 5 tooth rough, abnormal ZP:0130895 ceratobranchial 5 tooth porous, abnormal ZP:0130896 ceratobranchial 5 bone lacks parts or has fewer parts of type tooth 5V, abnormal ZP:0130897 ceratobranchial 5 bone lacks parts or has fewer parts of type tooth 4V, abnormal ZP:0130898 ceratobranchial 5 bone lacks parts or has fewer parts of type tooth 3V, abnormal ZP:0130899 ceratohyal cartilage decreased distance palatoquadrate cartilage, abnormal ZP:0130900 ceratohyal cartilage increased variability of size, abnormal ZP:0130901 basihyal cartilage oblique orientation, abnormal ZP:0130902 brain disrupted cellular macromolecule catabolic process, abnormal ZP:0130903 pharyngeal arch 1 disrupted cellular macromolecule catabolic process, abnormal ZP:0130904 dental epithelium absent, abnormal ZP:0130905 dental mesenchyme absent, abnormal ZP:0130906 ameloblast absent, abnormal ZP:0130907 ameloblast decreased amount, abnormal ZP:0130908 odontoblast decreased amount, abnormal ZP:0130910 centrum increased amount, abnormal ZP:0130911 neutrophil gut decreased amount, abnormal ZP:0130913 lipid heart increased amount, abnormal ZP:0130914 blood vessel liver and biliary system fatty, abnormal ZP:0130915 glutathione disulfide whole organism decreased amount, abnormal ZP:0130916 organosulfur compound whole organism decreased amount, abnormal ZP:0130917 mitochondrion hepatocyte distended, abnormal ZP:0130918 mitochondrial crista hepatocyte damaged, abnormal ZP:0130919 mitochondrial crista hepatocyte swollen, abnormal ZP:0130920 postero-medial region otic vesicle mislocalised, abnormal ZP:0130921 anterior region otic vesicle decreased amount, abnormal ZP:0130922 neuroblast statoacoustic (VIII) ganglion decreased amount, abnormal ZP:0130925 posterior macula fused with anterior macula, abnormal ZP:0130938 collagen trimer Meckel's cartilage-palatoquadrate cartilage joint irregular spatial pattern, abnormal ZP:0130939 collagen trimer Meckel's cartilage-palatoquadrate cartilage joint increased thickness, abnormal ZP:0130940 branchiomotor neuron morphology, abnormal ZP:0130942 L-alanine:2-oxoglutarate aminotransferase activity increased occurrence, abnormal ZP:0130943 nucleus germ line cell physical object quality, abnormal ZP:0130945 axoneme ependymal cell decreased amount, abnormal ZP:0130946 scale has extra parts of type ventral region melanocyte, abnormal ZP:0130947 scale has extra parts of type ventral region xanthophore, abnormal ZP:0130948 scale has extra parts of type ventral region iridophore, abnormal ZP:0130949 ventral region scale dorsalized, abnormal ZP:0130950 head has extra parts of type ventral surface melanocyte, abnormal ZP:0130951 trunk has fewer parts of type ventral surface iridophore, abnormal ZP:0130952 trunk has extra parts of type ventral surface melanocyte, abnormal ZP:0130953 trunk has extra parts of type ventral surface xanthophore, abnormal ZP:0130954 ventral mandibular arch has extra parts of type melanocyte, abnormal ZP:0130955 melanophore stripe dorsalized, abnormal ZP:0130967 whole organism symmetry, abnormal ZP:0130968 myofibril skeletal muscle degenerate, abnormal ZP:0130970 blood accumulation coelom, abnormal ZP:0130971 cranial cartilage immature, abnormal ZP:0130972 cartilage tissue decreased size, abnormal ZP:0130973 lateral dorsal aorta disconnected, abnormal ZP:0130974 lateral dorsal aorta structurally discontinuous, abnormal ZP:0130975 angiogenic sprout intersegmental vessel mislocalised, abnormal ZP:0130976 intersegmental vessel misrouted, abnormal ZP:0130977 late endosome microglial cell increased size, abnormal ZP:0130978 late endosome to lysosome transport decreased occurrence, abnormal ZP:0130979 microglial cell has extra parts of type late endosome microglial cell, abnormal ZP:0130985 microglial cell decreased process quality vacuolar calcium ion homeostasis, abnormal ZP:0130986 lysosome microglial cell decreased functionality, abnormal ZP:0130987 microglial cell optic tectum circular, abnormal ZP:0130988 optic tectum has extra parts of type microglial cell vacuole microglial cell, abnormal ZP:0130990 microglial cell has extra parts of type vacuole microglial cell, abnormal ZP:0130991 optic tectum separated from neuron microglial cell optic tectum, abnormal ZP:0130994 Meckel's cartilage increased angle to ceratohyal cartilage, abnormal ZP:0130996 neuron decreased occurrence chromosome organization, abnormal ZP:0130999 muscle physical object quality, abnormal ZP:0131001 caudal vein plexus decreased occurrence cell population proliferation, abnormal ZP:0131002 caudal vein plexus decreased efficacy developmental growth, abnormal ZP:0131003 myelin sheath dorsal funiculus increased amount, abnormal ZP:0131004 myelin sheath ventral funiculus increased amount, abnormal ZP:0131005 myelin sheath oligodendrocyte increased amount, abnormal ZP:0131006 dorsal funiculus increased width, abnormal ZP:0131007 ventral funiculus increased width, abnormal ZP:0131008 cholesterol blood plasma decreased amount, abnormal ZP:0131009 phospholipid blood plasma decreased amount, abnormal ZP:0131010 triglyceride blood plasma decreased amount, abnormal ZP:0131011 lipid liver decreased amount, abnormal ZP:0131012 fatty acid blood plasma decreased amount, abnormal ZP:0131013 feeding behavior increased rate, abnormal ZP:0131014 phospholipid blood plasma increased amount, abnormal ZP:0131015 lipid biosynthetic process increased occurrence, abnormal ZP:0131017 phagocytic vesicle microglial cell increased diameter, abnormal ZP:0131018 6-phospho-D-gluconate head increased amount, abnormal ZP:0131019 microglial cell increased duration phagocytosis, engulfment, abnormal ZP:0131020 microglial cell decreased occurrence microglial cell migration, abnormal ZP:0131021 microglial cell increased size, abnormal ZP:0131027 trunk has extra parts of type ventral region pigment cell, abnormal ZP:0131029 angiogenic sprout central artery increased amount, abnormal ZP:0131030 nucleus skeletal muscle cell decreased amount, abnormal ZP:0131031 skeletal muscle has extra parts of type adipose tissue, abnormal ZP:0131032 fat cell mislocalised, abnormal ZP:0131033 skeletal muscle cell decreased length, abnormal ZP:0131034 neural crest cell increased occurrence cell population proliferation, abnormal ZP:0131037 pectoral fin lepidotrichium decreased length, abnormal ZP:0131042 pronephros lacks all parts of type multi-ciliated epithelial cell cilium multi-ciliated epithelial cell, abnormal ZP:0131043 Meckel's cartilage decreased distance pharyngeal arch 2, abnormal ZP:0131044 intersegmental vein increased occurrence endothelial cell proliferation, abnormal ZP:0131045 intersegmental vein increased occurrence cell population proliferation, abnormal ZP:0131050 intestinal bulb decreased distribution, abnormal ZP:0131051 axon retinal ganglion cell decreased length, abnormal ZP:0131052 retinal ganglion cell process quality axon extension, abnormal ZP:0131054 digestive system decreased process quality cell population proliferation, abnormal ZP:0131057 podocyte foot pronephric podocyte irregularly shaped, abnormal ZP:0131058 pronephric podocyte pronephric capsular space morphology, abnormal ZP:0131059 JNK cascade decreased occurrence, abnormal ZP:0131060 myeloid cell differentiation decreased occurrence, abnormal ZP:0131061 lymphoid progenitor cell differentiation decreased occurrence, abnormal ZP:0131062 caudal hematopoietic tissue decreased distribution, abnormal ZP:0131063 cloacal chamber increased occurrence inflammatory response, abnormal ZP:0131064 posterior intestine decreased amount, abnormal ZP:0131065 lymphocyte spleen increased amount, abnormal ZP:0131067 11-oxotestosterone whole organism decreased amount, abnormal ZP:0131068 blood plasma male organism decreased amount, abnormal ZP:0131070 hematopoietic stem cell decreased occurrence cell population proliferation, abnormal ZP:0131071 intersegmental vessel post-vent vasculature morphology, abnormal ZP:0131072 blood plasma post-vent vasculature decreased amount, abnormal ZP:0131073 sperm process quality DNA methylation, abnormal ZP:0131075 epithelial cell protruding out of epidermal superficial stratum, abnormal ZP:0131076 epidermal basal stratum increased occurrence cell motility, abnormal ZP:0131077 epidermal basal stratum decreased process quality cell-cell adhesion, abnormal ZP:0131079 epidermal superficial stratum increased occurrence cell population proliferation, abnormal ZP:0131081 cytoplasm epidermal basal stratum mislocalised, abnormal ZP:0131082 axon habenula decreased amount, abnormal ZP:0131083 axon telencephalon decreased amount, abnormal ZP:0131084 skeletal muscle myofibril skeletal muscle undulate, abnormal ZP:0131086 myoseptum increased distribution, abnormal ZP:0131089 atrioventricular canal endocardium decreased occurrence cell migration, abnormal ZP:0131100 microglial cell decreased occurrence phagosome maturation, abnormal ZP:0131106 insulin (human) blood plasma increased amount, abnormal ZP:0131107 liver increased occurrence glucose-6-phosphatase activity, abnormal ZP:0131108 liver decreased occurrence glucose-6-phosphatase activity, abnormal ZP:0131109 liver increased occurrence phosphoenolpyruvate carboxykinase activity, abnormal ZP:0131110 liver increased occurrence pyruvate kinase activity, abnormal ZP:0131111 liver decreased occurrence pyruvate kinase activity, abnormal ZP:0131112 muscle decreased occurrence pyruvate kinase activity, abnormal ZP:0131113 glucose-6-phosphatase activity increased occurrence, abnormal ZP:0131114 phosphoenolpyruvate carboxykinase activity increased occurrence, abnormal ZP:0131115 liver decreased occurrence phosphoenolpyruvate carboxykinase activity, abnormal ZP:0131118 reactive oxygen species skeletal muscle increased amount, abnormal ZP:0131122 muscle cell morphology, abnormal ZP:0131124 G1 to G0 transition involved in cell differentiation decreased occurrence, abnormal ZP:0131125 microglial cell head decreased amount, abnormal ZP:0131129 macrophage spinal cord increased amount, abnormal ZP:0131131 migratory cranial neural crest disrupted establishment of cell polarity, abnormal ZP:0131132 migratory neural crest irregular spatial pattern, abnormal ZP:0131134 migratory neural crest patchy, abnormal ZP:0131135 migratory neural crest positional polarity, abnormal ZP:0131136 migratory neural crest ovate, abnormal ZP:0131137 migratory neural crest mislocalised dorsally, abnormal ZP:0131138 migratory neural crest mislocalised anteriorly, abnormal ZP:0131139 migratory neural crest mislocalized adaxially, abnormal ZP:0131141 CaP motoneuron arrested neuron projection extension, abnormal ZP:0131144 iridophore eye decreased area, abnormal ZP:0131145 iridophore trunk decreased area, abnormal ZP:0131159 female organism size, abnormal ZP:0131160 ovarian follicle absence due to degeneration, abnormal ZP:0131162 cardiac ventricle increased occurrence cardiac muscle cell proliferation, abnormal ZP:0131164 skeletal muscle myofibril skeletal muscle spatial pattern, abnormal ZP:0131167 primary neuron forebrain decreased amount, abnormal ZP:0131169 head increased frequency apoptotic process, abnormal ZP:0131170 Meckel's cartilage increased angle to Meckel's cartilage, abnormal ZP:0131171 lamellipodium migratory neural crest cell absent, abnormal ZP:0131172 filopodium migratory neural crest cell absent, abnormal ZP:0131173 bleb migratory neural crest cell increased amount, abnormal ZP:0131174 migratory neural crest lobed, abnormal ZP:0131175 male organism increased duration swimming, abnormal ZP:0131176 muscle cell decreased amount, abnormal ZP:0131177 cranial nerve IX disrupted axon guidance, abnormal ZP:0131180 compartment boundary rhombomere decreased amount, abnormal ZP:0131181 retinal ganglion cell layer process quality neuron differentiation, abnormal ZP:0131183 sleep latency, abnormal ZP:0131192 cilium neural tube decreased amount, abnormal ZP:0131193 whole organism decreased occurrence developmental process, abnormal ZP:0131194 neural tube decreased occurrence cilium assembly, abnormal ZP:0131195 lens development in camera-type eye decreased process quality, abnormal ZP:0131196 cilium retina decreased amount, abnormal ZP:0131199 cerebellar white matter cerebellum decreased amount, abnormal ZP:0131200 corpus cerebelli morphology, abnormal ZP:0131201 corpus cerebelli hypoplastic, abnormal ZP:0131203 skeletal muscle myofibril skeletal muscle decreased width, abnormal ZP:0131204 heart primordium mislocalised, abnormal ZP:0131207 Golgi apparatus hair cell anterior macula functionality, abnormal ZP:0131208 locomotory behavior decreased spatial extent of a process, abnormal ZP:0131209 hair cell anterior macula morphology, abnormal ZP:0131210 hair cell anterior macula increased height, abnormal ZP:0131211 hair cell anterior macula decreased width, abnormal ZP:0131212 hair cell anterior macula splayed, abnormal ZP:0131213 premigratory neural crest cell increased amount, abnormal ZP:0131214 migratory neural crest cell decreased amount, abnormal ZP:0131225 head decreased occurrence mitophagy, abnormal ZP:0131226 dorsal region neural tube absent, abnormal ZP:0131227 dorsal region neural tube decreased amount, abnormal ZP:0131232 neural crest cell increased occurrence apoptotic process, abnormal ZP:0131233 nucleus skeletal muscle cell absent, abnormal ZP:0131234 skeletal muscle cell myotome absent, abnormal ZP:0131240 myotome decreased height, abnormal ZP:0131241 migratory neural crest cell mislocalised, abnormal ZP:0131242 migratory neural crest cell aggregated, abnormal ZP:0131243 neural crest cell trunk increased distribution, abnormal ZP:0131244 cranial ganglion increased distribution, abnormal ZP:0131245 intestinal villus hypoplastic, abnormal ZP:0131246 ovarian follicle development disrupted, abnormal ZP:0131247 female organism decreased size, abnormal ZP:0131250 estradiol female organism increased amount, abnormal ZP:0131251 11-oxotestosterone female organism decreased amount, abnormal ZP:0131252 ovarian follicle decreased occurrence vitellogenesis, abnormal ZP:0131253 ovary degenerate, abnormal ZP:0131254 ovarian follicle stage IV absence due to degeneration, abnormal ZP:0131256 seminiferous tubule development delayed, abnormal ZP:0131257 seminiferous tubule lumen hypoplastic, abnormal ZP:0131258 male organism occurrence social behavior, abnormal ZP:0131259 male organism disrupted interspecies interaction between organisms, abnormal ZP:0131262 bile alcohol whole organism decreased amount, abnormal ZP:0131265 forebrain decreased occurrence cell population proliferation, abnormal ZP:0131267 myotome has extra parts of type fast muscle cell, abnormal ZP:0131270 cerebellum formation disrupted, abnormal ZP:0131271 motor neuron notochord morphology, abnormal ZP:0131272 3-dehydrosphinganine whole organism increased amount, abnormal ZP:0131273 thrombocyte post-vent region decreased amount, abnormal ZP:0131277 microvillus intestinal epithelium absent, abnormal ZP:0131278 adherens junction intestinal epithelium incomplete structure, abnormal ZP:0131279 digestion decreased efficacy, abnormal ZP:0131280 mid intestine lacks parts or has fewer parts of type intestinal villus, abnormal ZP:0131283 cell rhombomere mislocalised, abnormal ZP:0137210 caudal vein plexus fused with caudal vein plexus, abnormal ZP:0137211 nucleolus cell increased amount, abnormal ZP:0137214 posterior lateral plate mesoderm absent, abnormal ZP:0137225 CaP motoneuron amplitude neuromuscular synaptic transmission, abnormal ZP:0137226 neuron projection CaP motoneuron decreased size, abnormal ZP:0137227 neuron projection CaP motoneuron decreased amount, abnormal ZP:0137228 synapse CaP motoneuron morphology, abnormal ZP:0137229 synapse CaP motoneuron decreased size, abnormal ZP:0137231 neuromuscular junction of skeletal muscle fiber CaP motoneuron increased width, abnormal ZP:0137233 filopodium CaP motoneuron decreased length, abnormal ZP:0137235 caudal vein plexus decreased distribution, abnormal ZP:0137237 Collagen chondrocyte spatial pattern, abnormal ZP:0137238 chondrocyte process quality protein targeting, abnormal ZP:0137239 vacuole notochord inner cell obtuse, abnormal ZP:0137240 notochord inner cell irregular spatial pattern, abnormal ZP:0137241 floor plate decreased occurrence establishment or maintenance of cell polarity, abnormal ZP:0137242 trunk vasculature increased occurrence sprouting angiogenesis, abnormal ZP:0137243 myoseptum absent, abnormal ZP:0137244 primitive heart tube spatial pattern, abnormal ZP:0137252 axon collateral Mauthner neuron decreased amount, abnormal ZP:0137260 posterior region trunk shortened, abnormal ZP:0137261 ventral region caudal fin aplastic/hypoplastic, abnormal ZP:0137262 multi-ciliated epithelial cell pronephric duct decreased amount, abnormal ZP:0137263 ionocyte progenitor cell spatial pattern, abnormal ZP:0137264 ionocyte progenitor cell irregular spatial pattern, abnormal ZP:0137265 ionocyte progenitor cell aggregated, abnormal ZP:0137267 angiogenic sprout intersegmental vessel spatial pattern, abnormal ZP:0137268 circulatory system development disrupted, abnormal ZP:0137275 cytoskeleton organization decreased process quality, abnormal ZP:0137276 pronephric glomerular basement membrane structure, abnormal ZP:0137277 poly(ethylene imine) cranial cartilage spatial pattern, abnormal ZP:0137288 compartment boundary brain amorphous, abnormal ZP:0137289 lateral longitudinal fasciculus decreased process quality axonal fasciculation, abnormal ZP:0137290 medial longitudinal fasciculus decreased process quality axonal fasciculation, abnormal ZP:0137291 white matter disorganized, abnormal ZP:0137292 integument pectoral fin fold increased amount, abnormal ZP:0137293 neural plate process quality dorsal convergence, abnormal ZP:0137294 neural plate decreased occurrence dorsal convergence, abnormal ZP:0137295 neural keel formation process quality, abnormal ZP:0137296 NaK ionocyte absent, abnormal ZP:0137297 vH ionocyte absent, abnormal ZP:0137298 cell yolk syncytial layer absent, abnormal ZP:0137299 ionocyte progenitor cell decreased amount, abnormal ZP:0137300 epidermal cell absent, abnormal ZP:0137302 nitric oxide yolk syncytial layer increased amount, abnormal ZP:0137303 caudal fin neoplastic, abnormal ZP:0137306 chondroitin sulfate whole organism amount, abnormal ZP:0137311 epibranchial field absent, abnormal ZP:0137312 peptide hormone secreting cell intestinal bulb decreased amount, abnormal ZP:0137315 peripheral region heart rudiment increased distribution, abnormal ZP:0137316 midbrain hindbrain boundary constriction process quality epithelial cell morphogenesis, abnormal ZP:0137317 midbrain hindbrain boundary constriction process quality midbrain-hindbrain boundary morphogenesis, abnormal ZP:0137322 inferior raphe nucleus absent, abnormal ZP:0137323 pretectum absent, abnormal ZP:0137324 superior raphe nucleus absent, abnormal ZP:0137325 medulla oblongata absent, abnormal ZP:0137326 raphe nucleus absent, abnormal ZP:0137327 primitive neurectodermal tumor whole organism increased amount, abnormal ZP:0137336 epiphysis increased amount, abnormal ZP:0137355 endoplasmic reticulum calcium ion homeostasis process quality, abnormal ZP:0137369 epibranchial field decreased amount, abnormal ZP:0137372 cell midbrain hindbrain boundary constriction increased length, abnormal ZP:0137373 cell midbrain hindbrain boundary constriction decreased length, abnormal ZP:0137375 midbrain hindbrain boundary constriction increased angle to midbrain hindbrain boundary constriction, abnormal ZP:0137405 intermediate cell mass of mesoderm increased distribution, abnormal ZP:0137411 lymph vessel decreased distribution, abnormal ZP:0137414 ciliary marginal zone increased occurrence cell population proliferation, abnormal ZP:0137415 retinal outer nuclear layer decreased amount, abnormal ZP:0137422 swimming decreased linear velocity, abnormal ZP:0137423 blastoderm increased amount, abnormal ZP:0137424 anatomical compartment boundary rhombomere decreased amount, abnormal ZP:0137427 blood viscosity, abnormal ZP:0137428 ventriculo bulbo valve malformed, abnormal ZP:0137430 ventral region optic cup increased distribution, abnormal ZP:0137431 optic stalk increased distribution, abnormal ZP:0137432 optic cup unfused from optic cup, abnormal ZP:0137433 posterior region optic vesicle mislocalised, abnormal ZP:0137434 posterior segment eye lacks parts or has fewer parts of type proximal side retinal pigmented epithelium, abnormal ZP:0137435 proximal side posterior segment eye irregularly shaped, abnormal ZP:0137436 photoreceptor inner segment photoreceptor cell malformed, abnormal ZP:0137437 retinal neural layer protruding into brain, abnormal ZP:0137438 retinal pigmented epithelium decreased area, abnormal ZP:0137439 histone modification disrupted, abnormal ZP:0137440 retina spatial pattern, abnormal ZP:0137441 endothelial cell lateral dorsal aorta elongated, abnormal ZP:0137442 endothelial cell lateral dorsal aorta increased area, abnormal ZP:0137444 trunk vasculature decreased occurrence sprouting angiogenesis, abnormal ZP:0137445 dorsal longitudinal anastomotic vessel truncated, abnormal ZP:0137446 vascular lymphangioblast spatial pattern, abnormal ZP:0137447 vascular lymphangioblast decreased distribution, abnormal ZP:0137448 vascular lymphangioblast aplastic/hypoplastic, abnormal ZP:0137455 semicircular canal fusion disrupted, abnormal ZP:0137456 peripheral nervous system decreased distribution, abnormal ZP:0137457 pillar of the anterior semicircular canal increased amount, abnormal ZP:0137458 pillar of the anterior semicircular canal swollen, abnormal ZP:0137459 pillar of the lateral semicircular canal increased amount, abnormal ZP:0137460 pillar of the lateral semicircular canal swollen, abnormal ZP:0137461 pillar of the posterior semicircular canal increased amount, abnormal ZP:0137462 pillar of the posterior semicircular canal swollen, abnormal ZP:0137463 caudal fin increased distribution, abnormal ZP:0137464 axon cranial nerve II decreased branchiness, abnormal ZP:0137465 cranial nerve II decreased occurrence axon extension, abnormal ZP:0137466 cranial nerve II decreased occurrence axon arborization, abnormal ZP:0137469 ventral side somite spatial pattern, abnormal ZP:0137474 atrioventricular valve spatial pattern, abnormal ZP:0137478 goblet cell posterior intestine increased amount, abnormal ZP:0137483 cytoskeleton organization increased process quality, abnormal ZP:0137485 heart decreased process quality blood circulation, abnormal ZP:0137486 head arrested blood circulation, abnormal ZP:0137487 post-vent region arrested blood circulation, abnormal ZP:0137488 blood accumulation vasculature, abnormal ZP:0137489 snout circular, abnormal ZP:0137490 snout shortened, abnormal ZP:0137491 eye increased distance otic vesicle, abnormal ZP:0137495 germ ring mislocalised, abnormal ZP:0137496 germ ring increased distribution, abnormal ZP:0137497 anatomical margin blastodisc spatial pattern, abnormal ZP:0137498 anatomical margin blastodisc increased distribution, abnormal ZP:0137505 glycogen liver decreased amount, abnormal ZP:0137506 secondary motor neuron process quality axon guidance, abnormal ZP:0137509 erythroid progenitor cell arrested mitotic cell cycle, abnormal ZP:0137510 ventriculo bulbo valve morphogenesis delayed, abnormal ZP:0137512 apical region endolymphatic sac closed, abnormal ZP:0137513 endolymphatic sac lacks parts or has fewer parts of type basal region cell projection endolymphatic sac, abnormal ZP:0137514 cell projection endolymphatic sac decreased amount, abnormal ZP:0137515 endolymphatic sac increased size, abnormal ZP:0137518 nucleus liver decreased amount, abnormal ZP:0137519 endocardial cushion bulbus arteriosus decreased amount, abnormal ZP:0137520 ventriculo bulbo valve development decreased process quality, abnormal ZP:0137522 cell endocardium increased amount, abnormal ZP:0137524 cell junction compact layer of ventricle oblique orientation, abnormal ZP:0137526 pronephric duct has fewer parts of type multi-ciliated epithelial cell cilium multi-ciliated epithelial cell, abnormal ZP:0137527 multi-ciliated epithelial cell pronephric proximal convoluted tubule decreased amount, abnormal ZP:0137528 multi-ciliated epithelial cell pronephric proximal straight tubule decreased distribution, abnormal ZP:0137530 common myeloid progenitor cell proliferation process quality, abnormal ZP:0137531 myeloid cell increased occurrence apoptotic process, abnormal ZP:0137532 common myeloid progenitor cell proliferation disrupted, abnormal ZP:0137534 cell projection tendon cell decreased length, abnormal ZP:0137536 otolithic lymph vessel decreased amount, abnormal ZP:0137537 vasculature hindbrain decreased amount, abnormal ZP:0137539 retina hemorrhagic, abnormal ZP:0137541 ovulation from ovarian follicle decreased occurrence, abnormal ZP:0137545 NADPH whole organism decreased amount, abnormal ZP:0137547 ventricular myocardium decreased occurrence ATP-activated inward rectifier potassium channel activity, abnormal ZP:0137548 cardiac muscle cell decreased occurrence ATP-activated inward rectifier potassium channel activity, abnormal ZP:0137549 cardiac ventricle increased occurrence apoptotic process, abnormal ZP:0137550 atrium increased occurrence apoptotic process, abnormal ZP:0137553 histone H3-K27 methylation decreased occurrence, abnormal ZP:0137554 histone H3-K27 trimethylation decreased occurrence, abnormal ZP:0137555 glycosphingolipid whole organism decreased amount, abnormal ZP:0137556 Golgi apparatus anterior macula structure, abnormal ZP:0137559 water whole organism decreased amount, abnormal ZP:0137561 L-tyrosine muscle decreased amount, abnormal ZP:0137562 L-lysine muscle increased amount, abnormal ZP:0137563 protein whole organism increased amount, abnormal ZP:0137564 hexokinase activity increased occurrence, abnormal ZP:0137565 adult feeding behavior decreased occurrence, abnormal ZP:0137566 fat cell skeletal muscle increased amount, abnormal ZP:0137568 skeletal muscle cell somite decreased amount, abnormal ZP:0137572 intestinal epithelial cell spatial pattern, abnormal ZP:0137573 intestinal epithelium has extra parts of type neutrophil, abnormal ZP:0137574 vesicle intestinal epithelium decreased amount, abnormal ZP:0137575 vesicle myotome decreased amount, abnormal ZP:0137576 sternohyoid decreased thickness, abnormal ZP:0137577 sternohyoid decreased area, abnormal ZP:0137582 contractile fiber primitive pectoral fin adductor decreased amount, abnormal ZP:0137583 contractile fiber primitive pectoral fin abductor decreased amount, abnormal ZP:0137584 pelvic fin musculature decreased amount, abnormal ZP:0137585 pectoral fin musculature structure, abnormal ZP:0137586 pectoral fin musculature asymmetrical, abnormal ZP:0137587 adductor muscle decreased amount, abnormal ZP:0137588 abductor muscle decreased amount, abnormal ZP:0137589 adductor muscle pectoral fin decreased amount, abnormal ZP:0137590 abductor muscle pectoral fin decreased amount, abnormal ZP:0137591 whole organism lacks parts or has fewer parts of type primitive pectoral fin abductor, abnormal ZP:0137592 primitive pectoral fin adductor decreased amount, abnormal ZP:0137593 primitive pectoral fin abductor decreased amount, abnormal ZP:0137599 pectoral fin decreased functionality, abnormal ZP:0137600 pectoral fin bud decreased process quality cell population proliferation, abnormal ZP:0137602 pectoral fin clavate, abnormal ZP:0137603 cardiac ventricle inverted, abnormal ZP:0137604 regulation of termination of RNA polymerase II transcription disrupted, abnormal ZP:0137605 neural crest cell migration involved in heart formation disrupted, abnormal ZP:0137606 cardiac neural crest spatial pattern, abnormal ZP:0137607 cardiac muscle cell decondensed, abnormal ZP:0137608 skeletal muscle myofibril trunk musculature increased length, abnormal ZP:0137609 muscle cell trunk musculature morphology, abnormal ZP:0137610 muscle cell trunk musculature decondensed, abnormal ZP:0137611 larval feeding behavior disrupted, abnormal ZP:0137612 neuromuscular process decreased efficacy, abnormal ZP:0137613 adherens junction epidermal cell malformed, abnormal ZP:0137614 periderm decreased thickness, abnormal ZP:0137615 scale primordium morphology, abnormal ZP:0137616 peridermal cell elongated, abnormal ZP:0137617 nucleus chondrocyte decreased amount, abnormal ZP:0137618 sarcomere fast muscle cell morphology, abnormal ZP:0137619 myosin filament fast muscle cell decreased amount, abnormal ZP:0137620 Z disc fast muscle cell decreased amount, abnormal ZP:0137621 M band fast muscle cell decreased amount, abnormal ZP:0137622 neuron projection motor neuron branchiness, abnormal ZP:0137623 cell trigeminal motor nucleus decreased amount, abnormal ZP:0137624 motor neuron trunk musculature branchiness, abnormal ZP:0137625 neuron projection motor neuron increased amount, abnormal ZP:0137626 neuron projection motor neuron truncated, abnormal ZP:0137627 angiogenic sprout disorganized, abnormal ZP:0137628 dorsal longitudinal anastomotic vessel agenesis, abnormal ZP:0137631 sinoatrial ring absent, abnormal ZP:0137632 blood vessel endothelial cell disrupted endothelial cell migration, abnormal ZP:0137633 gonad male organism distended, abnormal ZP:0137634 male organism has fewer parts of type gonad spermatogenic cyst, abnormal ZP:0137635 male organism has extra parts of type gonad ovarian follicle, abnormal ZP:0137636 male organism color pattern, abnormal ZP:0137637 ovary has fewer parts of type ovarian follicle stage III, abnormal ZP:0137638 ovary has extra parts of type ovarian follicle stage I, abnormal ZP:0137639 ovary has extra parts of type anatomical space, abnormal ZP:0137640 hindbrain granular, abnormal ZP:0137641 midbrain granular, abnormal ZP:0137644 distal region pronephros decreased distribution, abnormal ZP:0137645 distal region pronephros decreased amount, abnormal ZP:0137646 nucleus pronephric distal early tubule absent, abnormal ZP:0137649 pronephric distal early tubule decreased occurrence pronephric nephron tubule epithelial cell differentiation, abnormal ZP:0137650 apical part of cell pronephric distal early tubule absent, abnormal ZP:0137651 pronephric distal early tubule decreased occurrence early distal convoluted tubule development, abnormal ZP:0137652 nucleus pronephric distal early tubule decreased size, abnormal ZP:0137653 notochord increased occurrence apoptotic process, abnormal ZP:0137656 kidney epithelial cell pronephric distal early tubule decreased size, abnormal ZP:0137672 centrosome branchiomotor neuron position, abnormal ZP:0137673 neuron projection branchiomotor neuron amount, abnormal ZP:0137674 neuron projection branchiomotor neuron length, abnormal ZP:0137675 branchiomotor neuron orientation neuron projection rhombomere 4, abnormal ZP:0137676 cell body branchiomotor neuron shape, abnormal ZP:0137677 branchiomotor neuron orientation cell body axon branchiomotor neuron, abnormal ZP:0137678 branchiomotor neuron process quality motor neuron migration, abnormal ZP:0137679 rhombomere 6 branchiomotor neuron absent, abnormal ZP:0137680 rhombomere 5 branchiomotor neuron absent, abnormal ZP:0137681 branchiomotor neuron accumulation rhombomere 4, abnormal ZP:0137682 branchiomotor neuron decreased speed, abnormal ZP:0137684 eye photoreceptor cell alignment eye photoreceptor cell, abnormal ZP:0137687 pathway-restricted SMAD protein phosphorylation decreased occurrence, abnormal ZP:0137688 ventral region ventral fin fold decreased distribution, abnormal ZP:0137689 pathway-restricted SMAD protein phosphorylation increased occurrence, abnormal ZP:0137690 ventral region ventral fin fold increased distribution, abnormal ZP:0137691 cell retinal inner nuclear layer mislocalised, abnormal ZP:0137692 outer limiting membrane morphology, abnormal ZP:0137693 pronephric proximal straight tubule occurrence pronephric nephron tubule epithelial cell differentiation, abnormal ZP:0137694 pronephric distal late tubule occurrence pronephric nephron tubule epithelial cell differentiation, abnormal ZP:0137697 lens capsule increased thickness, abnormal ZP:0137700 anterior side segmental plate absent, abnormal ZP:0137703 posterior region postcranial axial skeleton morphology, abnormal ZP:0137704 keratinocyte decreased amount, abnormal ZP:0137705 ionocyte decreased amount, abnormal ZP:0137706 NaK ionocyte extension decreased amount, abnormal ZP:0137707 vH ionocyte extension decreased amount, abnormal ZP:0137708 ectoderm decreased occurrence stem cell proliferation, abnormal ZP:0137709 NaK ionocyte ball decreased amount, abnormal ZP:0137710 vH ionocyte ball decreased amount, abnormal ZP:0137711 axon MiP motor neuron bifurcated, abnormal ZP:0137712 axon CaP motoneuron bifurcated, abnormal ZP:0137714 trunk neural crest cell migration disrupted, abnormal ZP:0137715 VaP motor neuron increased amount, abnormal ZP:0137716 CaP motoneuron increased amount, abnormal ZP:0137718 neuron dorsal root ganglion increased amount, abnormal ZP:0137719 MiD3cm increased amount, abnormal ZP:0137724 glutamate(1-) whole organism decreased amount, abnormal ZP:0137725 glycine whole organism increased amount, abnormal ZP:0137726 sarcosine whole organism increased amount, abnormal ZP:0137727 cystathionine whole organism increased amount, abnormal ZP:0137729 leucine whole organism increased amount, abnormal ZP:0137730 proline whole organism increased amount, abnormal ZP:0137731 valine whole organism increased amount, abnormal ZP:0137733 arginine whole organism increased amount, abnormal ZP:0137747 primary ovarian follicle growth non-progressive, abnormal ZP:0137748 ovarian follicle stage I disrupted ovarian follicle development, abnormal ZP:0137749 cell gonad decreased size, abnormal ZP:0137751 gonad has fewer parts of type ovarian follicle stage II, abnormal ZP:0137757 CaP motoneuron arrested axon extension, abnormal ZP:0137758 Rohon-Beard neuron decreased occurrence innervation, abnormal ZP:0137759 axon secondary motor neuron defasciculated, abnormal ZP:0137760 secondary motor neuron arrested axon extension, abnormal ZP:0137761 growth cone secondary motor neuron increased size, abnormal ZP:0137763 hematopoietic system physical object quality, abnormal ZP:0137764 adaxial-abaxial axis whole organism decreased size, abnormal ZP:0137765 anatomical boundary hepatocyte amorphous, abnormal ZP:0137766 nucleus intestine irregular spatial pattern, abnormal ZP:0137767 nucleus muscle circular, abnormal ZP:0137768 intestinal villus truncated, abnormal ZP:0137769 muscle atrophied, abnormal ZP:0137770 hepatocyte crowded, abnormal ZP:0137772 erythroid lineage cell blood decreased amount, abnormal ZP:0137774 thigmotaxis latency, abnormal ZP:0137780 basement membrane vertical myoseptum increased amount, abnormal ZP:0137781 myotome decreased occurrence cell adhesion, abnormal ZP:0137782 muscle cell myotome morphology, abnormal ZP:0137783 myotome detached from muscle cell myotome, abnormal ZP:0137784 muscle cell myotome sinuous, abnormal ZP:0137785 muscle cell myotome decreased amount, abnormal ZP:0137786 myotome extends beyond muscle cell vertical myoseptum, abnormal ZP:0137787 connective tissue cell myotome increased amount, abnormal ZP:0137788 pericardium increased amount, abnormal ZP:0137789 caudal vein increased amount, abnormal ZP:0137790 myotome spatial pattern, abnormal ZP:0137791 multicellular organismal movement decreased occurrence, abnormal ZP:0137792 muscle cell inflexible, abnormal ZP:0137793 banded collagen fibril vertical myoseptum decreased amount, abnormal ZP:0137794 myotome detached from muscle cell basement membrane myotome, abnormal ZP:0137795 myotome structurally discontinuous, abnormal ZP:0137796 liver decreased occurrence fatty acid beta-oxidation, abnormal ZP:0137797 muscle decreased occurrence fatty acid beta-oxidation, abnormal ZP:0137799 intersegmental vessel decreased occurrence angiogenesis, abnormal ZP:0137800 trunk vasculature process quality vasculature development, abnormal ZP:0137801 blood vessel trunk vasculature decreased length, abnormal ZP:0137802 blastomere detached from yolk, abnormal ZP:0137803 primitive heart tube shape, abnormal ZP:0137804 cardiac muscle cell bulbus arteriosus increased amount, abnormal ZP:0137805 blood cell accumulation trunk vasculature, abnormal ZP:0137806 bulbus arteriosus increased occurrence cell population proliferation, abnormal ZP:0137807 atrium increased occurrence cell population proliferation, abnormal ZP:0137808 pharyngeal mesoderm increased amount, abnormal ZP:0137809 pharyngeal mesoderm increased distribution, abnormal ZP:0137814 pronephros asynchronous epithelial cilium movement involved in extracellular fluid movement, abnormal ZP:0137815 Kupffer's vesicle asynchronous epithelial cilium movement involved in determination of left/right asymmetry, abnormal ZP:0137816 spinal cord asynchronous epithelial cilium movement involved in extracellular fluid movement, abnormal ZP:0137817 cilium spinal cord movement quality, abnormal ZP:0137822 hematopoietic cell thymus decreased amount, abnormal ZP:0137823 hematopoietic cell caudal hematopoietic tissue decreased amount, abnormal ZP:0137824 hematopoietic cell caudal hematopoietic tissue increased amount, abnormal ZP:0137825 caudal hematopoietic tissue increased distribution, abnormal ZP:0137826 insulin whole organism increased amount, abnormal ZP:0137828 detection of light stimulus involved in sensory perception process quality, abnormal ZP:0137830 kidney interstitial cell morphology, abnormal ZP:0137831 pronephric duct increased width, abnormal ZP:0137832 pronephric duct opening obstructed, abnormal ZP:0137833 pronephric proximal convoluted tubule cystic, abnormal ZP:0137834 neural tube increased occurrence cell population proliferation, abnormal ZP:0137835 pronephric duct increased occurrence apoptotic process, abnormal ZP:0137836 cloaca increased occurrence apoptotic process, abnormal ZP:0137839 epithelium endolymphatic sac increased thickness, abnormal ZP:0137840 epithelium endolymphatic sac thickness, abnormal ZP:0137841 basal region midbrain hindbrain boundary constriction structure, abnormal ZP:0137842 basal region midbrain hindbrain boundary constriction increased width, abnormal ZP:0137843 pharyngeal arch cartilage decreased occurrence canonical Wnt signaling pathway, abnormal ZP:0137844 bulbus arteriosus decreased occurrence canonical Wnt signaling pathway involved in heart development, abnormal ZP:0137845 atrioventricular valve process quality canonical Wnt signaling pathway involved in heart development, abnormal ZP:0137846 pharyngeal arch cartilage decreased amount, abnormal ZP:0137847 endothelial cell lymphatic system increased distribution, abnormal ZP:0137848 vascular lymphangioblast horizontal myoseptum immature, abnormal ZP:0137849 nucleus posterior cardinal vein elliptic, abnormal ZP:0137850 vascular lymphangioblast horizontal myoseptum increased cellular motility, abnormal ZP:0137851 endothelial cell normal amount, abnormal ZP:0137857 cerebrospinal fluid contacting neuron process quality cell morphogenesis, abnormal ZP:0137858 cell projection cerebrospinal fluid contacting neuron decreased size, abnormal ZP:0137859 cerebrospinal fluid contacting neuron process quality cellular response to mechanical stimulus, abnormal ZP:0137861 cone telodendria UV sensitive photoreceptor cell morphology, abnormal ZP:0137862 cone telodendria UV sensitive photoreceptor cell branched, abnormal ZP:0137863 cone telodendria UV sensitive photoreceptor cell decreased amount, abnormal ZP:0137864 heart trabecula morphogenesis disrupted, abnormal ZP:0137865 H3K4Me3 whole organism decreased amount, abnormal ZP:0137867 histone modification process quality, abnormal ZP:0137868 blood accumulation ventral aorta, abnormal ZP:0137869 endothelial cell somite decreased amount, abnormal ZP:0137871 endoderm development arrested, abnormal ZP:0137872 cell body Muller cell spatial pattern, abnormal ZP:0137873 cell body Muller cell position, abnormal ZP:0137874 cell body Muller cell mislocalised, abnormal ZP:0137875 glial cell projection Muller cell mislocalised, abnormal ZP:0137876 glial cell projection Muller cell decreased amount, abnormal ZP:0137877 inner limiting membrane morphology, abnormal ZP:0137878 outer limiting membrane broken, abnormal ZP:0137879 Muller cell physical object quality, abnormal ZP:0137880 Muller cell irregularly shaped, abnormal ZP:0137881 glial cell projection Muller cell increased thickness, abnormal ZP:0137882 outer limiting membrane irregular thickness, abnormal ZP:0137883 glial cell projection Muller cell morphology, abnormal ZP:0137884 retinal inner plexiform layer irregular thickness, abnormal ZP:0137885 Muller cell overlap with glial cell projection glial cell projection Muller cell, abnormal ZP:0137886 glial limiting end-foot Muller cell absent, abnormal ZP:0137887 retinal neural layer lacks parts or has fewer parts of type inner limiting membrane, abnormal ZP:0137888 glial cell projection Muller cell position, abnormal ZP:0137889 glial limiting end-foot Muller cell decreased amount, abnormal ZP:0137890 glial cell projection Muller cell spatial pattern, abnormal ZP:0137891 glial cell projection Muller cell structure, abnormal ZP:0137893 dermatan sulfate whole organism decreased amount, abnormal ZP:0137894 hydroxyproline whole organism decreased amount, abnormal ZP:0137896 neurotransmitter trunk decreased amount, abnormal ZP:0137897 proline whole organism decreased amount, abnormal ZP:0137898 heparan sulfate whole organism decreased amount, abnormal ZP:0137899 chondroitin sulfate whole organism decreased amount, abnormal ZP:0137901 coenzyme Q10 whole organism decreased amount, abnormal ZP:0137902 keratan sulfate whole organism decreased amount, abnormal ZP:0137903 behavioral defense response disrupted, abnormal ZP:0137904 telomerase activity decreased efficacy, abnormal ZP:0137905 catalase activity decreased efficacy, abnormal ZP:0137908 social behavior disrupted, abnormal ZP:0137909 exploration behavior decreased occurrence, abnormal ZP:0137910 creatininase activity decreased efficacy, abnormal ZP:0137911 retinal inner nuclear layer has fewer parts of type interneuron, abnormal ZP:0137912 whole organism senescent, abnormal ZP:0137913 intestine increased permeability, abnormal ZP:0137914 retinal outer nuclear layer has fewer parts of type eye photoreceptor cell, abnormal ZP:0137915 pleuroperitoneal region decreased size, abnormal ZP:0137916 muscle tendon junction vertical myoseptum decreased amount, abnormal ZP:0137917 vertical myoseptum increased distribution, abnormal ZP:0137918 tendon cell decondensed, abnormal ZP:0137922 Kupffer's vesicle process quality epithelial cilium movement involved in extracellular fluid movement, abnormal ZP:0137923 forerunner cell group arrested cell cycle G1/S phase transition, abnormal ZP:0137924 forerunner cell group increased distribution, abnormal ZP:0137927 head misaligned with condensed chromosome mitotic spindle microtubule head, abnormal ZP:0137928 mitotic spindle head disorganized, abnormal ZP:0137934 endothelial cell ventral wall of dorsal aorta decreased amount, abnormal ZP:0137935 cilium blood vessel decreased length, abnormal ZP:0137936 cilium blood vessel decreased amount, abnormal ZP:0137937 splanchnocranium decreased process quality skeletal muscle tissue development, abnormal ZP:0137938 splanchnocranium decreased process quality tendon development, abnormal ZP:0137939 tendon ceratohyal cartilage malformed, abnormal ZP:0137940 tendon ventral intermandibularis posterior malformed, abnormal ZP:0137941 tendon interhyoideus malformed, abnormal ZP:0137942 skeletal muscle cell adductor mandibulae mislocalised, abnormal ZP:0137945 rib decreased process quality bone mineralization, abnormal ZP:0137947 rib decreased process quality bone morphogenesis, abnormal ZP:0137950 dentary composition, abnormal ZP:0137951 dentary decreased mass density, abnormal ZP:0137954 skeletal system lacks all parts of type rib, abnormal ZP:0137956 intervertebral ligament malformed, abnormal ZP:0137958 rib of vertebra 5 absent, abnormal ZP:0137959 rib of vertebra 6 absent, abnormal ZP:0137960 skeletal system lacks parts or has fewer parts of type rib, abnormal ZP:0137961 ligament Meckel's cartilage decreased amount, abnormal ZP:0137962 ligament palatoquadrate cartilage decreased amount, abnormal ZP:0137963 tendon sternohyoid decreased amount, abnormal ZP:0137967 Mauthner neuron process quality axon regeneration, abnormal ZP:0137969 Mauthner neuron process quality axon extension involved in regeneration, abnormal ZP:0137980 blood cardinal system absent, abnormal ZP:0137991 dorsal aorta decreased occurrence endothelial tube lumen extension, abnormal ZP:0137992 posterior cardinal vein decreased occurrence endothelial tube lumen extension, abnormal ZP:0137993 endothelial tube lumen extension decreased occurrence, abnormal ZP:0137994 dorsal aorta attached to posterior cardinal vein, abnormal ZP:0137995 dorsal aorta decreased length, abnormal ZP:0137996 posterior cardinal vein decreased length, abnormal ZP:0137997 blood vessel endothelium artery decreased amount, abnormal ZP:0137998 epiphysis disrupted cellular response to UV, abnormal ZP:0137999 epiphysis disrupted cellular response to blue light, abnormal ZP:0138000 epiphysis disrupted cellular response to red light, abnormal ZP:0138003 blastoderm segmentation delayed, abnormal ZP:0138004 blastoderm cell decreased adhesivity, abnormal ZP:0138005 vascular cord decreased occurrence Notch signaling pathway, abnormal ZP:0138006 posterior lateral plate mesoderm process quality cell migration involved in vasculogenesis, abnormal ZP:0138007 cell posterior lateral plate mesoderm morphology, abnormal ZP:0138008 cell posterior lateral plate mesoderm decreased adhesivity, abnormal ZP:0138009 angiogenic sprout vascular cord decreased amount, abnormal ZP:0138010 angioblast cell migration from lateral mesoderm to midline decreased occurrence, abnormal ZP:0138016 central region centrum calcified, abnormal ZP:0138017 phosphate vertebral body end plate decreased amount, abnormal ZP:0138018 carbonate vertebral body end plate increased amount, abnormal ZP:0138019 apatite vertebral body end plate crystal configuration, abnormal ZP:0138020 collagen network vertebral body end plate immature, abnormal ZP:0138021 centrum dysplastic, abnormal ZP:0138022 rib fragile, abnormal ZP:0138023 rib scarred, abnormal ZP:0138024 vertebra collapsed, abnormal ZP:0138025 lepidotrichium deformed, abnormal ZP:0138026 lacunocanalicular system decreased volume, abnormal ZP:0138028 vertebral body end plate decreased elasticity, abnormal ZP:0138029 osteocyte proportionality to bone tissue, abnormal ZP:0138030 bone mineralization involved in bone maturation decreased rate, abnormal ZP:0138031 centrum poorly ossified, abnormal ZP:0138041 neuron mislocalised, abnormal ZP:0138042 hypothalamus shape, abnormal ZP:0138043 serotonergic neuron hypothalamus decreased amount, abnormal ZP:0138044 hypothalamus increased occurrence cell death, abnormal ZP:0138045 lateral mesoderm disrupted determination of heart left/right asymmetry, abnormal ZP:0138049 response to absence of light increased process quality, abnormal ZP:0138050 swimming decreased frequency, abnormal ZP:0138051 swimming increased linear velocity, abnormal ZP:0138052 swimming increased spatial extent of a process, abnormal ZP:0138053 habituation decreased rate, abnormal ZP:0138054 prepulse inhibition decreased magnitude, abnormal ZP:0138061 prepulse inhibition increased magnitude, abnormal ZP:0138062 swimming decreased spatial extent of a process, abnormal ZP:0138063 habituation increased rate, abnormal ZP:0138065 tendon decreased process quality collagen fibril organization, abnormal ZP:0138066 tendon sternohyoid composition, abnormal ZP:0138067 nucleus fast muscle cell disorganized, abnormal ZP:0138068 actin filament fast muscle cell decreased thickness, abnormal ZP:0138069 myotome fast muscle cell morphology, abnormal ZP:0138070 optic tectum has fewer parts of type axon retinal ganglion cell, abnormal ZP:0138071 retinal ganglion cell delayed axon extension, abnormal ZP:0138074 cell body MiD3cl position, abnormal ZP:0138075 MiD2cm decreased occurrence commissural neuron axon guidance, abnormal ZP:0138076 MiD3cl decreased occurrence commissural neuron axon guidance, abnormal ZP:0138077 MiD3cm decreased occurrence commissural neuron axon guidance, abnormal ZP:0138078 RoL2 decreased occurrence commissural neuron axon guidance, abnormal ZP:0138079 hindbrain interneuron decreased occurrence commissural neuron axon guidance, abnormal ZP:0138094 spermatocyte decreased occurrence meiosis II, abnormal ZP:0138095 mitochondrion myocardium swollen, abnormal ZP:0138096 intercalated disc myocardium morphology, abnormal ZP:0138097 Z disc myocardium irregular thickness, abnormal ZP:0138098 desmosome myocardium morphology, abnormal ZP:0138099 I band cardiac muscle absent, abnormal ZP:0138100 myocardium edematous, abnormal ZP:0138102 vertebra increased process quality bone mineralization, abnormal ZP:0138103 vacuole notochord inner cell broken, abnormal ZP:0138104 notochord inner cell decreased process quality notochord cell vacuolation, abnormal ZP:0138106 notochord inner cell decreased volume, abnormal ZP:0138107 notochord inner cell irregularly shaped, abnormal ZP:0138108 notochord inner cell decreased occurrence vesicle fusion with vacuole, abnormal ZP:0138113 cardiac chamber development disrupted, abnormal ZP:0138115 nucleus notochord inner cell spheroid, abnormal ZP:0138116 nucleus notochord inner cell mislocalised medially, abnormal ZP:0138125 sprouting angiogenesis increased process quality, abnormal ZP:0138130 atrium process quality cardiac conduction system development, abnormal ZP:0138131 cardiac muscle process quality macroautophagy, abnormal ZP:0138132 skeletal muscle increased process quality TOR signaling, abnormal ZP:0138134 cardiac ventricle increased process quality cardiac muscle cell contraction, abnormal ZP:0138135 cardiac myofibril cardiac ventricle increased contractility, abnormal ZP:0138136 regulation of heart contraction decreased process quality, abnormal ZP:0138137 heart obtuse, abnormal ZP:0138138 trabecular layer has extra parts of type cardiac muscle cell, abnormal ZP:0138139 trabecular layer of the atrium increased thickness, abnormal ZP:0138140 cardiac muscle cell has extra parts of type autophagosome cardiac muscle cell, abnormal ZP:0138141 apical side pronephric tubule absent, abnormal ZP:0138145 omega-9 fatty acid whole organism increased amount, abnormal ZP:0138146 methylglyoxal whole organism increased amount, abnormal ZP:0138147 omega-3 fatty acid whole organism increased amount, abnormal ZP:0138148 saturated fatty acid whole organism increased amount, abnormal ZP:0138149 whole organism arrested lactoylglutathione lyase activity, abnormal ZP:0138162 otolith formation arrested, abnormal ZP:0138163 rod photoreceptor outer segment retinal rod cell increased length, abnormal ZP:0138164 retinal photoreceptor layer has fewer parts of type UV sensitive photoreceptor cell, abnormal ZP:0138165 retinal photoreceptor layer has fewer parts of type blue sensitive photoreceptor cell, abnormal ZP:0138166 retinal photoreceptor layer has fewer parts of type green sensitive photoreceptor cell, abnormal ZP:0138167 retinal photoreceptor layer has fewer parts of type red sensitive photoreceptor cell, abnormal ZP:0138168 eye photoreceptor cell decreased process quality photoreceptor cell outer segment organization, abnormal ZP:0138169 photoreceptor disc membrane eye photoreceptor cell malformed, abnormal ZP:0138172 eye photoreceptor cell retinal outer nuclear layer sparse, abnormal ZP:0138174 cone photoreceptor outer segment red sensitive photoreceptor cell spatial pattern, abnormal ZP:0138175 cone photoreceptor outer segment red sensitive photoreceptor cell mislocalised, abnormal ZP:0138176 rod photoreceptor outer segment retinal rod cell spatial pattern, abnormal ZP:0138187 reactive oxygen species neutrophil decreased amount, abnormal ZP:0138188 neutrophil disrupted calcium-mediated signaling, abnormal ZP:0138197 cerebellar Purkinje cell layer morphogenesis decreased occurrence, abnormal ZP:0138200 granular layer corpus cerebelli has extra parts of type Purkinje cell, abnormal ZP:0138201 Purkinje cell layer corpus cerebelli has fewer parts of type Purkinje cell, abnormal ZP:0138202 Purkinje cell inserted into granular layer corpus cerebelli, abnormal ZP:0138203 granule cell torus longitudinalis absent, abnormal ZP:0138204 neuron optic tectum mislocalised radially, abnormal ZP:0138205 molecular layer corpus cerebelli absent, abnormal ZP:0138206 cerebellar crest absent, abnormal ZP:0138207 stratum marginale absent, abnormal ZP:0138208 stratum opticum absent, abnormal ZP:0138209 cerebellar granule cell absent, abnormal ZP:0138210 neuron projection Purkinje cell disoriented, abnormal ZP:0138213 granular layer corpus cerebelli has extra parts of type eurydendroid cell, abnormal ZP:0138214 Purkinje cell layer corpus cerebelli has fewer parts of type eurydendroid cell, abnormal ZP:0138215 eurydendroid cell inserted into granular layer corpus cerebelli, abnormal ZP:0138216 granular layer corpus cerebelli has extra parts of type Bergmann glial cell, abnormal ZP:0138217 Bergmann glial cell inserted into granular layer corpus cerebelli, abnormal ZP:0138219 calcium import into the mitochondrion decreased occurrence, abnormal ZP:0138223 ventral aorta decreased length, abnormal ZP:0138224 pericyte decreased amount, abnormal ZP:0138225 vascular associated smooth muscle cell decreased amount, abnormal ZP:0138226 regulation of mitochondrial membrane potential decreased process quality, abnormal ZP:0138227 mitochondrion dopaminergic neuron decreased area, abnormal ZP:0138233 posterior lateral line primordium decreased rate cell migration, abnormal ZP:0138235 cell posterior lateral line primordium normal amount, abnormal ZP:0138237 mitochondrion skeletal muscle cell decreased volume, abnormal ZP:0138238 mitochondrion skeletal muscle cell deformed, abnormal ZP:0138239 cell-cell junction blood vessel endothelial cell decreased distribution, abnormal ZP:0138241 intersegmental vessel process quality cell-cell junction organization, abnormal ZP:0138242 intersegmental vessel process quality blood vessel morphogenesis, abnormal ZP:0138244 somatic stem cell intestine decreased amount, abnormal ZP:0138245 intestinal stem cell homeostasis disrupted, abnormal ZP:0138246 goblet cell decreased area, abnormal ZP:0138247 chordoma intestine increased amount, abnormal ZP:0138248 testis fibrotic, abnormal ZP:0138249 oocyte atretic, abnormal ZP:0138250 myocardium condensed, abnormal ZP:0138251 oocyte stage II decreased amount, abnormal ZP:0138252 intestinal mucosa morphology, abnormal ZP:0138253 seminiferous tubule morphology, abnormal ZP:0138254 mitochondrion intestine swollen, abnormal ZP:0138255 mitochondrial outer membrane skeletal muscle dilated, abnormal ZP:0138256 mucin granule goblet cell dense, abnormal ZP:0138257 mitotic cell cycle phase transition disrupted, abnormal ZP:0138258 cortical actin cytoskeleton blastoderm cell increased thickness, abnormal ZP:0138259 cell projection blastoderm increased amount, abnormal ZP:0138260 basal surface ceratobranchial 5 tooth osseous, abnormal ZP:0138261 centrum increased diameter, abnormal ZP:0138262 integument lacks all parts of type xanthophore, abnormal ZP:0138263 integument has fewer parts of type melanocyte, abnormal ZP:0138264 neural arch dorsal orientation, abnormal ZP:0138267 scale decreased occurrence bone resorption, abnormal ZP:0138285 autophagosome-lysosome fusion disrupted, abnormal ZP:0138286 lysosome whole organism increased amount, abnormal ZP:0138287 endosome whole organism increased amount, abnormal ZP:0138288 caudal hematopoietic tissue increased occurrence cell death, abnormal ZP:0138289 podocyte foot pronephric glomerulus absent, abnormal ZP:0138290 dorsal aorta decreased linear velocity blood circulation, abnormal ZP:0138291 intercalated disc heart structure, abnormal ZP:0138292 cardiac myofibril heart structure, abnormal ZP:0138294 otic epithelium decreased size, abnormal ZP:0138295 skeletal muscle myoblast decreased occurrence cell population proliferation, abnormal ZP:0138296 ribosomal RNA skeletal muscle myoblast decreased amount, abnormal ZP:0138297 fibrillar center skeletal muscle cell spatial pattern, abnormal ZP:0138298 nucleolus skeletal muscle cell spatial pattern, abnormal ZP:0138299 nucleolus skeletal muscle cell increased size, abnormal ZP:0138300 skeletal muscle myoblast decreased occurrence rRNA processing, abnormal ZP:0138301 skeletal muscle myoblast decreased occurrence rRNA transcription, abnormal ZP:0138302 sarcomere skeletal muscle decreased amount, abnormal ZP:0138303 skeletal muscle myoblast decreased occurrence ribosome biogenesis, abnormal ZP:0138304 skeletal muscle contraction process quality, abnormal ZP:0138306 primitive pectoral fin adductor decreased size, abnormal ZP:0138314 axis elongation delayed, abnormal ZP:0138316 male courtship behavior behavioral quality of a process, abnormal ZP:0138317 convergent extension involved in neural plate elongation delayed, abnormal ZP:0138320 yolk extension decreased length, abnormal ZP:0138331 pharyngeal arch protruding, abnormal ZP:0138336 nucleus yolk syncytial layer distributed, abnormal ZP:0138337 yolk syncytial layer decreased width, abnormal ZP:0138338 yolk syncytial layer decreased occurrence actin filament organization, abnormal ZP:0138339 filamentous actin yolk syncytial layer mislocalised, abnormal ZP:0138340 actin cytoskeleton organization decreased occurrence, abnormal ZP:0138341 EVL increased distance DEL, abnormal ZP:0138342 optic stalk increased occurrence cell death, abnormal ZP:0138343 lens decreased occurrence cell population proliferation, abnormal ZP:0138344 lens epithelium absent, abnormal ZP:0138345 lens fiber cell decreased amount, abnormal ZP:0138346 vascular lymphangioblast cranial vasculature decreased amount, abnormal ZP:0138348 lateral facial lymph vessel lacks parts or has fewer parts of type endothelial cell, abnormal ZP:0138349 lateral facial lymph vessel has fewer parts of type endothelial cell, abnormal ZP:0138350 otolithic lymph vessel lacks parts or has fewer parts of type endothelial cell, abnormal ZP:0138351 otolithic lymph vessel has fewer parts of type endothelial cell, abnormal ZP:0138352 medial facial lymph vessel lacks parts or has fewer parts of type endothelial cell, abnormal ZP:0138353 medial facial lymph vessel has fewer parts of type endothelial cell, abnormal ZP:0138357 left side dorsal habenular nucleus increased amount, abnormal ZP:0138358 left side dorsal habenular nucleus decreased amount, abnormal ZP:0138359 dorsal habenular nucleus decreased process quality neurogenesis, abnormal ZP:0138362 neuron projection parapineal organ decreased length, abnormal ZP:0138363 neuron projection parapineal organ decreased amount, abnormal ZP:0138364 neuron projection parapineal organ decreased branchiness, abnormal ZP:0138365 efferent neuron parapineal organ morphology, abnormal ZP:0138366 motor neuron process quality neuron projection development, abnormal ZP:0138368 lateral facial lymph vessel absent, abnormal ZP:0138369 medial facial lymph vessel absent, abnormal ZP:0138370 optic vesicle decreased occurrence cell population proliferation, abnormal ZP:0138371 axon sensory neuron branchiness, abnormal ZP:0138372 hypochord increased amount, abnormal ZP:0138373 hypochord increased distribution, abnormal ZP:0138375 pronephric tubule decreased occurrence endocytosis, abnormal ZP:0138384 lysosome microglial cell morphology, abnormal ZP:0138385 head decreased process quality hexosaminidase activity, abnormal ZP:0138387 oligosaccharide brain increased amount, abnormal ZP:0138388 oligosaccharide liver increased amount, abnormal ZP:0138389 oligosaccharide pancreas increased amount, abnormal ZP:0138390 oligosaccharide gonad increased amount, abnormal ZP:0138391 oligosaccharide spleen increased amount, abnormal ZP:0138392 oligosaccharide intestine increased amount, abnormal ZP:0138393 brain decreased process quality hexosaminidase activity, abnormal ZP:0138394 liver decreased process quality hexosaminidase activity, abnormal ZP:0138395 pancreas decreased process quality hexosaminidase activity, abnormal ZP:0138396 gonad decreased process quality hexosaminidase activity, abnormal ZP:0138397 spleen decreased process quality hexosaminidase activity, abnormal ZP:0138398 intestine decreased process quality hexosaminidase activity, abnormal ZP:0138400 caudal hematopoietic tissue has fewer parts of type neutrophil, abnormal ZP:0138401 macrophage decreased occurrence phagocytosis, abnormal ZP:0138402 pronephric podocyte retracted, abnormal ZP:0138403 hexosaminidase activity decreased process quality, abnormal ZP:0138404 parasphenoid decreased occurrence ossification, abnormal ZP:0138405 splanchnocranium disrupted ossification, abnormal ZP:0138406 branchiostegal ray 1 decreased occurrence ossification, abnormal ZP:0138407 branchiostegal ray 2 decreased occurrence ossification, abnormal ZP:0138408 nucleus nucleate erythrocyte decreased size, abnormal ZP:0138409 blood has fewer parts of type cell, abnormal ZP:0138410 pupil increased distance pupil, abnormal ZP:0138411 vertebral column decreased width, abnormal ZP:0138412 nucleate erythrocyte decreased volume, abnormal ZP:0138413 ceratobranchial 5 bone poorly ossified, abnormal ZP:0138414 lateral larval melanophore stripe increased pigmentation, abnormal ZP:0138415 scale increased occurrence tissue remodeling, abnormal ZP:0138416 scale increased occurrence bone remodeling, abnormal ZP:0138417 scale increased occurrence bone development, abnormal ZP:0138418 infraorbital increased occurrence bone development, abnormal ZP:0138419 neural arch angle centrum, abnormal ZP:0138420 aerobic respiration decreased occurrence, abnormal ZP:0138425 ventral region cranial vault decreased width, abnormal ZP:0138426 cranial vault male organism decreased width, abnormal ZP:0138427 cranial vault female organism decreased width, abnormal ZP:0138428 subintestinal vein has extra parts of type vascular sprouts, abnormal ZP:0138429 nerve sheath tumor muscle increased amount, abnormal ZP:0138430 nerve sheath tumor bone tissue increased amount, abnormal ZP:0138431 retinal pigmented epithelium incomplete structure, abnormal ZP:0138432 vagal ganglion decreased amount, abnormal ZP:0138433 pigment cell organization quality, abnormal ZP:0138434 cranial nerve II disrupted axon guidance, abnormal ZP:0138435 cranial nerve II disrupted axonal fasciculation, abnormal ZP:0138436 optic nerve head fasciculation, abnormal ZP:0138439 posterior lateral line nerve absent, abnormal ZP:0138452 synapse neurohypophysis decreased amount, abnormal ZP:0138455 actin filament neurohypophysis increased stability, abnormal ZP:0138457 hypophyseal capillary process quality pore complex assembly, abnormal ZP:0138458 hypophyseal capillary decreased process quality pore complex assembly, abnormal ZP:0138460 hypophyseal capillary decreased process quality regulation of vascular permeability, abnormal ZP:0138462 CaP motoneuron frequency calcium-mediated signaling, abnormal ZP:0138463 CaP motoneuron spatial pattern, abnormal ZP:0138464 neuromast lacks all parts of type neuromast hair cell, abnormal ZP:0138465 muscle cell myotome disorganized, abnormal ZP:0138468 CaP motoneuron decreased occurrence axon guidance, abnormal ZP:0138469 CaP motoneuron arrested axon extension involved in axon guidance, abnormal ZP:0138470 growth cone filopodium CaP motoneuron decreased amount, abnormal ZP:0138471 optic vesicle increased variability of size, abnormal ZP:0138472 head bilateral symmetry, abnormal ZP:0138473 apical surface optic vesicle spatial pattern, abnormal ZP:0138474 basal surface optic vesicle spatial pattern, abnormal ZP:0138475 epithelium disrupted adherens junction organization, abnormal ZP:0138476 optic vesicle disrupted establishment of apical/basal cell polarity, abnormal ZP:0138477 optic vesicle displaced to neuroepithelial cell anatomical space posterior segment eye, abnormal ZP:0138478 pronephric tubule malformed, abnormal ZP:0138479 optic vesicle elongation disrupted, abnormal ZP:0138480 optic vesicle asymmetrical, abnormal ZP:0138485 yolk agenesis, abnormal ZP:0138486 cell body secondary motor neuron mislocalised, abnormal ZP:0138495 central nervous system increased process quality apoptotic process, abnormal ZP:0138496 optic cup increased process quality apoptotic process, abnormal ZP:0138498 fourth ventricle lacks parts or has fewer parts of type apical side cilium fourth ventricle, abnormal ZP:0138499 apical side ventricular system absent, abnormal ZP:0138500 ventricular system lacks parts or has fewer parts of type apical side gamma-tubulin complex ventricular system, abnormal ZP:0138501 ventricular system has fewer parts of type apical side microtubule organizing center ventricular system, abnormal ZP:0138502 ventricular system has fewer parts of type apical side microtubule ventricular system, abnormal ZP:0138503 gamma-tubulin complex ventricular system absent, abnormal ZP:0138504 cilium fourth ventricle mislocalised, abnormal ZP:0138505 cilium fourth ventricle decreased amount, abnormal ZP:0138506 fourth ventricle decreased occurrence epithelial tube formation, abnormal ZP:0138507 tectal ventricle decreased occurrence epithelial tube formation, abnormal ZP:0138508 pronephric duct decreased occurrence nephric duct formation, abnormal ZP:0138509 apical side gut absent, abnormal ZP:0138510 gut lacks parts or has fewer parts of type apical side gamma-tubulin complex gut, abnormal ZP:0138511 gamma-tubulin complex gut absent, abnormal ZP:0138512 gut has fewer parts of type apical side microtubule gut, abnormal ZP:0138513 pancreatic duct decreased occurrence epithelial tube formation, abnormal ZP:0138514 gut decreased occurrence epithelial tube formation, abnormal ZP:0138515 gut spatial pattern, abnormal ZP:0138516 gut shortened, abnormal ZP:0138517 exocrine pancreas position, abnormal ZP:0138518 brain decreased occurrence DNA methylation, abnormal ZP:0138519 fin decreased occurrence DNA methylation, abnormal ZP:0138520 integument decreased occurrence DNA methylation, abnormal ZP:0138521 muscle decreased occurrence DNA methylation, abnormal ZP:0138522 IgD immunoglobulin complex whole organism decreased amount, abnormal ZP:0138523 IgM immunoglobulin complex whole organism decreased amount, abnormal ZP:0138524 IgZ immunoglobulin complex whole organism decreased amount, abnormal ZP:0138525 filopodium intersegmental vessel absent, abnormal ZP:0138526 slit diaphragm pronephric podocyte morphology, abnormal ZP:0138527 ventriculo bulbo valve morphogenesis decreased process quality, abnormal ZP:0138532 posterior macula decreased occurrence succinate dehydrogenase activity, abnormal ZP:0138536 posterior macula decreased occurrence cytochrome-c oxidase activity, abnormal ZP:0138538 swimming behavioral quality of a process, abnormal ZP:0138539 posterior macula has fewer parts of type mitochondrion hair cell posterior macula, abnormal ZP:0138540 neuromast hair cell anterior lateral line neuromast decreased amount, abnormal ZP:0138541 aerobic respiration disrupted, abnormal ZP:0138542 mitochondrial tRNA thio-modification disrupted, abnormal ZP:0138543 tRNA-specific 2-thiouridylase activity disrupted, abnormal ZP:0138544 macula lagena has fewer parts of type hair cell, abnormal ZP:0138545 cerebral spinal fluid fourth ventricle increased amount, abnormal ZP:0138546 cerebral spinal fluid ventricular system increased amount, abnormal ZP:0138547 dorsal spinal nerve decreased occurrence myelination, abnormal ZP:0138548 ventral spinal nerve decreased occurrence myelination, abnormal ZP:0138555 dorsal spinal nerve morphology, abnormal ZP:0138558 ventral aorta decreased amount, abnormal ZP:0138559 migrasome whole organism decreased amount, abnormal ZP:0138560 determination of left/right symmetry decreased occurrence, abnormal ZP:0138561 forerunner cell group irregular spatial pattern, abnormal ZP:0138562 migrasome shield decreased amount, abnormal ZP:0138563 endocardial cushion bulbus arteriosus spatial pattern, abnormal ZP:0138564 bulbus arteriosus lacks all parts of type ventriculo bulbo valve, abnormal ZP:0138565 bulbus arteriosus decreased process quality smooth muscle tissue development, abnormal ZP:0138566 vascular smooth muscle bulbus arteriosus decreased amount, abnormal ZP:0138567 bulbus arteriosus decreased diameter, abnormal ZP:0138568 ventriculo bulbo valve decreased process quality Notch signaling involved in heart development, abnormal ZP:0138569 posterior region ventriculo bulbo valve decreased amount, abnormal ZP:0138570 intersegmental vessel decreased efficacy angiogenesis, abnormal ZP:0138571 liver increased occurrence cellular response to DNA damage stimulus, abnormal ZP:0138573 pronephric tubule decreased occurrence determination of left/right symmetry, abnormal ZP:0138574 pronephric tubule decreased size, abnormal ZP:0138575 brain disrupted cell communication by electrical coupling, abnormal ZP:0138576 endocardial cushion bulbus arteriosus increased amount, abnormal ZP:0138577 nucleus pronephric duct increased amount, abnormal ZP:0138578 cytoplasm pronephric duct decreased amount, abnormal ZP:0138579 caudal fin increased frequency striated muscle contraction, abnormal ZP:0138580 VeLD decreased process quality action potential, abnormal ZP:0138584 lipid yolk increased amount, abnormal ZP:0138590 phenylalanine whole organism increased amount, abnormal ZP:0138591 spinal cord has fewer parts of type axon myelin sheath spinal cord, abnormal ZP:0138592 spinal cord process quality central nervous system myelin formation, abnormal ZP:0138593 myelin sheath spinal cord decreased length, abnormal ZP:0138594 spinal cord surrounding myelin sheath neuronal cell body spinal cord, abnormal ZP:0138599 spinal cord decreased rate central nervous system myelin formation, abnormal ZP:0138600 17beta-estradiol ovary decreased amount, abnormal ZP:0138601 17beta-estradiol testis decreased amount, abnormal ZP:0138602 oocyte stage III increased occurrence apoptotic process, abnormal ZP:0138603 oocyte stage IV increased occurrence apoptotic process, abnormal ZP:0138604 granulosa cell increased occurrence apoptotic process, abnormal ZP:0138605 theca cell increased occurrence apoptotic process, abnormal ZP:0138606 http://purl.obolibrary.org/obo/ZFA_0005926 decreased length, abnormal ZP:0138609 muscle absent, abnormal ZP:0138615 http://purl.obolibrary.org/obo/ZFA_0005921 delayed cell migration, abnormal ZP:0138622 http://purl.obolibrary.org/obo/ZFA_0005926 decreased size, abnormal ZP:0138623 http://purl.obolibrary.org/obo/ZFA_0005922 hypoplastic, abnormal ZP:0138624 xanthophore head discolored, abnormal ZP:0138625 xanthophore caudal fin decreased amount, abnormal ZP:0138627 xanthophore trunk discolored, abnormal ZP:0138637 http://purl.obolibrary.org/obo/ZFA_0005923 hypoplastic, abnormal ZP:0138638 http://purl.obolibrary.org/obo/ZFA_0005925 hypoplastic, abnormal ZP:0138639 primitive pectoral fin adductor absent, abnormal ZP:0138640 primitive pectoral fin abductor absent, abnormal ZP:0138651 immature neutrophil increased amount, abnormal ZP:0138654 sarcomere slow muscle cell increased size, abnormal ZP:0138655 slow muscle cell somite increased length, abnormal ZP:0138663 eye increased process quality cell population proliferation, abnormal ZP:0138667 pronephric duct deformed, abnormal ZP:0138668 pronephric duct irregularly shaped, abnormal ZP:0138669 pronephric duct structurally discontinuous, abnormal ZP:0138670 pronephric duct opening structure, abnormal ZP:0138671 locomotion involved in locomotory behavior rhythm quality, abnormal ZP:0138672 reproduction decreased efficacy, abnormal ZP:0138673 oocyte maturation decreased process quality, abnormal ZP:0138674 oviposition decreased frequency, abnormal ZP:0138676 hindbrain shortened, abnormal ZP:0138686 liver primordium mislocalised, abnormal ZP:0138687 intestinal bulb primordium spatial pattern, abnormal ZP:0138688 intestinal bulb primordium absent, abnormal ZP:0138689 duct gall bladder absent, abnormal ZP:0138690 intestine lumen intrahepatic bile duct mislocalised, abnormal ZP:0138691 left side intestine mislocalised, abnormal ZP:0138692 intestinal bulb spatial pattern, abnormal ZP:0138693 hepatic duct absent, abnormal