A rare, genetic muscular dystrophy characterized by progressive muscle wasting and weakness due to degeneration of skeletal, smooth and cardiac muscle.

Synonyms: BMD Becker dystrophinopathy

This is just here as a test because I lose it

Term information

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UMLS:C0917713
OMIM:300376
MeSH:C537666
ICD-10:G71.0
OMIM:159050
MedDRA:10059117

notation

ORPHA:98895

Term relations

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