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.

Follow this condition — get notified about new trials

Sub-types

Broader categories

Sort by