Axonal atrophy on nerve biopsy
Symptom Information:
Symptom ID: | OMIM : No Id available | |
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Is a (Whole tree): |
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MedDRA: |
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Database Frequency: | 5 / 7739 | |
Resource: |
All diseases associated with this symptom:
Autosomal dominant Charcot-Marie-Tooth disease type 2A1 | (Orphanet:99946) |
Autosomal dominant Charcot-Marie-Tooth disease type 2A2 | (Orphanet:99947) |
Autosomal dominant Charcot-Marie-Tooth disease type 2B | (Orphanet:99936) |
Autosomal dominant Charcot-Marie-Tooth disease type 2G | (Orphanet:99941) |
Charcot-Marie-Tooth disease type 2B1 | (Orphanet:98856) |