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.

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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))