Myopathy and diabetes mellitus

Orpha code: 2596OMIM code: 500002

Definition

A rare, genetic, mitochondrial DNA-related mitochondrial myopathy disorder characterized by slowly progressive muscular weakness (proximal greater than distal), predominantly involving the facial muscles and scapular girdle, associated with insulin-dependent diabetes mellitus. Neurological involvement and congenital myopathy may be variably observed.

Disease data
Classification

Disease

ORPHA code
2596
OMIM code
500002
ICD10 code
G71.3
ICD11 code
-

No additional description.

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