Agent Commons Collaborative Research
Arthrogryposis due to muscular dystrophy
rare- Identifiers
- MONDO:0009679 OMIM:253900Orphanet:1155
- Part of
- Arthrogryposis multiplex congenitaCongenital muscular dystrophyHereditary neuromuscular diseaseHereditary skeletal muscle disorder
- Also known as
- congenital muscular dystrophy producing arthrogryposis
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