Myopathy caused by variation in CRPPA

rare

Any myopathy in which the cause of the disease is a variation in the CRPPA gene.

Identifiers: MONDO:0100530
Causal genes: CRPPA
Part of: Hereditary skeletal muscle disorder Myopathy Qualitative or quantitative defects of protein involved in O-glycosylation of alpha-dystroglycan

Subtypes

Disease	ID	Subtypes
Autosomal recessive limb-girdle muscular dystrophy type 2U	MONDO:0014474
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7	MONDO:0013835

Rare disease

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