Dilated cardiomyopathy 1S

Any familial isolated dilated cardiomyopathy in which the cause of the disease is a mutation in the MYH7 gene.

Also known as: CMD1S, MYH7 familial isolated dilated cardiomyopathy, cardiomyopathy, dilated, type 1S, dilated cardiomyopathy type 1S, familial isolated dilated cardiomyopathy caused by mutation in MYH7, cardiomyopathy, dilated, 1S, dilated cardiomyopathy-1S, left ventricular noncompaction 5

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