Abnormality of nervous system morphology
Symptom Information:
| Symptom ID: | HPO:0012639 | ||||
| Synonyms: |
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| Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the nervous system(HPO:0000707) Abnormality of nervous system morphology(HPO:0012639) MedDRA: |
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| Database Frequency: | 25 / 7739 | ||||
| Resource: |
All diseases associated with this symptom:
| 15q24 microdeletion syndrome | (Orphanet:94065) |
| 5q14.3 microdeletion syndrome | (Orphanet:228384) |
| 6p22 microdeletion syndrome | (Orphanet:251046) |
| 6q25 microdeletion syndrome | (Orphanet:251056) |
| Aplasia cutis - myopia | (Orphanet:1117) |
| Arthrogryposis - hyperkeratosis, lethal form | (Orphanet:1485) |
| CHARGE syndrome | (Orphanet:138) |
| Carnitine palmitoyl transferase II deficiency | (Orphanet:157) |
| Carnitine palmitoyl transferase II deficiency, neonatal form | (Orphanet:228308) |
| Cerebro-oculo-nasal syndrome | (Orphanet:66625) |
| Chronic intestinal pseudo-obstruction | (Orphanet:2978) |
| Craniofacial conodysplasia | (Orphanet:85168) |
| Dermatoleukodystrophy | (Orphanet:1659) |
| Ehlers-Danlos syndrome with periventricular heterotopia | (Orphanet:82004) |
| Fanconi anemia | (Orphanet:84) |
| Glutaryl-CoA dehydrogenase deficiency | (Orphanet:25) |
| Holoprosencephaly | (Orphanet:2162) |
| Lethal multiple pterygium syndrome | (Orphanet:33108) |
| Megalencephaly-capillary malformation-polymicrogyria syndrome | (Orphanet:60040) |
| Mucolipidosis type 2 | (Orphanet:576) |
| Neu-Laxova syndrome | (Orphanet:2671) |
| Papilloma of choroid plexus | (Orphanet:2807) |
| Peroxisomal acyl-CoA oxidase deficiency | (Orphanet:2971) |
| Toriello-Lacassie-Droste syndrome | (Orphanet:3339) |
| Williams syndrome | (Orphanet:904) |