Duchenne muscular dystrophy (DMD) is a neuromuscular disease characterized by rapidly progressive muscle weakness and wasting due to degeneration of skeletal, smooth and cardiac muscle.

Synonyms: DMD Severe dystrophinopathy, Duchenne type

This is just here as a test because I lose it

Term information

database cross reference
  • MeSH:D020388 (E (exact mapping (the terms and the concepts are equivalent)))
  • ICD-10 (NTBT (narrower term maps to a broader term))
  • MedDRA (E (exact mapping (the terms and the concepts are equivalent)))
  • OMIM:310200 (E (exact mapping (the terms and the concepts are equivalent)))
  • ICD-10 (Inclusion term (The term is included under a ICD10 category and has not its own code))
  • UMLS (E (exact mapping (the terms and the concepts are equivalent)))
hasDbXref

MedDRA:10013801, UMLS:C0013264, ICD-10:G71.0, OMIM:310200, MeSH:D020388

notation

ORPHA:98896

Term relations

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