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

Orpha code: 206546OMIM code:

Definicja

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.

Disease data
Klasyfikacja

Disease

Kod ORPHA
206546
Kod OMIM
-
Kod ICD10
G71.0
Kod ICD11
-

No additional description.

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