Dilated cardiomyopathy 1CC

MONDO:0013147

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

Also known as: CMD1CC, NEXN familial isolated dilated cardiomyopathy, cardiomyopathy, dilated, type 1Cc, dilated cardiomyopathy type 1CC, familial isolated dilated cardiomyopathy caused by mutation in NEXN, cardiomyopathy, dilated, 1CC

218 clinical trials for this condition and its sub-types.

Follow this condition — get notified about new trials

Broader categories

Sort by