Dilated cardiomyopathy 1D

Any familial isolated dilated cardiomyopathy in which the cause of the disease is a mutation in the TNNT2 gene.

Also known as: CMD1D, TNNT2 familial isolated dilated cardiomyopathy, cardiomyopathy, dilated, type 1D, dilated cardiomyopathy 1D, dilated cardiomyopathy type 1D, familial isolated dilated cardiomyopathy caused by mutation in TNNT2, cardiomyopathy, dilated, 1D, left ventricular noncompaction 6

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