Dilated cardiomyopathy 1X

Any familial isolated dilated cardiomyopathy in which the cause of the disease is a mutation in the FKTN gene.

Also known as: CMD1X, FKTN familial isolated dilated cardiomyopathy, cardiomyopathy, dilated, type 1X, dilated cardiomyopathy type 1X, familial isolated dilated cardiomyopathy caused by mutation in FKTN, cardiomyopathy, dilated, 1X, cardiomyopathy, dilated, with mild or No proximal muscle weakness

8 clinical trials for this condition and its sub-types, 0 tagged with Dilated cardiomyopathy 1X itself.