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

Orpha code: 206546OMIM code:

Definition

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
Classification

Disease

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

No additional description.

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