Upper limb involvement may occur later
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: | 10 / 7739 | |
Resource: |
All diseases associated with this symptom:
Autosomal dominant Charcot-Marie-Tooth disease type 2I | (Orphanet:99942) |
Autosomal dominant intermediate Charcot-Marie-Tooth disease type C | (Orphanet:100045) |
Autosomal dominant intermediate Charcot-Marie-Tooth disease type D | (Orphanet:100046) |
Charcot-Marie-Tooth disease type 1D | (Orphanet:101084) |
Charcot-Marie-Tooth disease type 2B1 | (Orphanet:98856) |
Charcot-Marie-Tooth disease type 4E | (Orphanet:99951) |
Charcot-Marie-Tooth disease type 4H | (Orphanet:99954) |
Distal hereditary motor neuropathy type 1 | (Orphanet:139518) |
X-linked Charcot-Marie-Tooth disease type 2 | (Orphanet:101076) |
X-linked Charcot-Marie-Tooth disease type 3 | (Orphanet:101077) |