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Myopathy caused by variation in FKRP

MONDO:0700066

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

Also known as: FKRP myopathy, FKRP-related myopathy, myopathy caused by mutation in FKRP

67 clinical trials for this condition and its sub-types.

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Sub-types

Autosomal recessive limb-girdle muscular dystrophy type 2I (6) Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A5 (0) Muscular dystrophy-dystroglycanopathy type B5 (0)

Broader categories

Disease (618) Metabolic disease (215) Musculoskeletal system disorder (196) Hereditary disease (172) Muscle tissue disorder (53) Inborn errors of metabolism (42) Human disease (14) Myopathy (11) Skeletal muscle disorder (8) Congenital disorder of glycosylation (6)
Trials to join now! 33 Not yet recruiting 9 Not yet finished but already full! 10 Completed 14 Terminated 1
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