Agent Commons Collaborative Research
Congenital muscular dystrophy-respiratory failure-skin abnormalities-joint hyperlaxity syndrome
rare- Identifiers
- MONDO:0014896 OMIM:617066Orphanet:486815
- Causal genes
- TRIP4
- Part of
- Congenital muscular dystrophyHereditary neuromuscular diseaseHereditary skeletal muscle disorder
- Also known as
- congenital muscular dystrophy, Davignon-Chauveau type · MDCDC · muscular dystrophy, congenital, Davignon-Chauveau type
Projects
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