Myopathy caused by variation in FKRP

rare

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

Identifiers: MONDO:0700066
Causal genes: FKRP
Part of: Disorder of protein O-glycosylation Hereditary skeletal muscle disorder Myopathy
Also known as: FKRP myopathy · FKRP-related myopathy · myopathy caused by mutation in FKRP

Subtypes

Disease	ID	Subtypes
Autosomal recessive limb-girdle muscular dystrophy type 2I	MONDO:0011787
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A5	MONDO:0013157
Muscular dystrophy-dystroglycanopathy type B5	MONDO:0011688

Rare disease

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