Peripheral axonal degeneration
Symptom Information:
| Symptom ID: | HPO:0000764 | ||||
| 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) Abnormal peripheral nervous system morphology(HPO:0000759) Peripheral axonal degeneration(HPO:0000764) MedDRA: |
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| Database Frequency: | 6 / 7739 | ||||
| Resource: |
All diseases associated with this symptom:
| Ataxia - oculomotor apraxia type 1 | (Orphanet:1168) |
| Autosomal dominant Charcot-Marie-Tooth disease type 2P | (Orphanet:300319) |
| Charcot-Marie-Tooth disease type 4A | (Orphanet:99948) |
| Charcot-Marie-Tooth disease type 4C | (Orphanet:99949) |
| Congenital cataracts - facial dysmorphism - neuropathy | (Orphanet:48431) |
| Spinal muscular atrophy with respiratory distress | (Orphanet:98920) |