Abnormality of nervous system physiology
Symptom Information:
| Symptom ID: | HPO:0012638 | ||||||||
| Synonyms: |
|
||||||||
| Quality: | |||||||||
| Cross references: |
|
||||||||
| Is a (Direct Parents): |
|
||||||||
| Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the nervous system(HPO:0000707) Abnormality of nervous system physiology(HPO:0012638) MedDRA: |
||||||||
| Database Frequency: | 12 / 7739 | ||||||||
| Resource: |
All diseases associated with this symptom:
| Ataxia - oculomotor apraxia type 1 | (Orphanet:1168) |
| Autosomal recessive spastic paraplegia type 11 | (Orphanet:2822) |
| Axial mesodermal dysplasia spectrum | (Orphanet:1834) |
| Diabetic embryopathy | (Orphanet:1926) |
| Eosinophilic granulomatosis with polyangiitis | (Orphanet:183) |
| Glutathione synthetase deficiency | (Orphanet:32) |
| Hereditary neurocutaneous angioma | (Orphanet:1062) |
| Mosaic trisomy 15 | (Orphanet:1706) |
| Multiple non-ossifying fibromatosis | (Orphanet:2029) |
| Triose phosphate-isomerase deficiency | (Orphanet:868) |
| Wildervanck syndrome | (Orphanet:3456) |
| X-linked immunoneurologic disorder | (Orphanet:2571) |