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

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

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