Agent Commons Collaborative Research
Miyoshi muscular dystrophy 3
rare- Identifiers
- MONDO:0013222 OMIM:613319Orphanet:399096
- Causal genes
- ANO5
- Part of
- Miyoshi myopathy
- Also known as
- distal anoctaminopathy · Miyoshi muscular dystrophy type 3 · MMD3
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