CMD1XFKTN familial isolated dilated cardiomyopathycardiomyopathy, dilated, type 1Xdilated cardiomyopathy type 1Xdilated cardiomyopathy with mild or no proximal muscle weaknessfamilial isolated dilated cardiomyopathy caused by mutation in FKTNcardiomyopathy, dilated, 1Xcardiomyopathy, dilated, with mild or No proximal muscle weakness
Definition
Any familial isolated dilated cardiomyopathy in which the cause of the disease is a mutation in the FKTN gene.
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