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Myopathy caused by variation in FKTN

MONDO:0700067

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

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

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

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Sub-types

Autosomal recessive limb-girdle muscular dystrophy type 2M (1) Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4 (0) Muscular dystrophy-dystroglycanopathy (congenital without intellectual disability), type B4 (0)

Broader categories

Disease (618) Nervous system disorder (217) 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)
Trials to join now! 33 Not yet recruiting 9 Not yet finished but already full! 7 Completed 13 Terminated 1
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