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Duchenne muscular dystrophy
rareDuchenne muscular dystrophy (DMD) is a neuromuscular disease characterized by rapidly progressive muscle weakness and wasting due to degeneration of skeletal, smooth and cardiac muscle.
- Identifiers
- MONDO:0010679 OMIM:310200Orphanet:98896
- Part of
- DMD-related muscular dystrophy
- Also known as
- DMD · Duchenne muscular dystrophy, X-linked recessive · muscular dystrophy, Duchenne type · severe dystrophinopathy, Duchenne type
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