Proximal muscle involvement may occur
Symptom Information:
Symptom ID: | OMIM : No Id available | |
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Database Frequency: | 3 / 7739 | |
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All diseases associated with this symptom:
Autosomal dominant Charcot-Marie-Tooth disease type 2K | (Orphanet:99944) |
Charcot-Marie-Tooth disease type 2B1 | (Orphanet:98856) |
Myotilin-related myofibrillar myopathy without spheroid body | (Orphanet:98911) |