Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers

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A rare, genetic muscular dystrophy affecting female carriers and characterized by variable degrees of muscle weakness due to progressive skeletal myopathy, sometimes associated with dilated cardiomyopathy or left ventricle dilation.

This is just here as a test because I lose it

Term information

database cross reference
  • ICD-10:G71.0 (NTBT (ORPHA code's Narrower Term maps to a Broader Term))
  • ICD-10:G71.0 (Attributed (The ICD10 code is attributed by Orphanet))
hasDbXref

ICD-10:G71.0

notation

ORPHA:206546