Dilated cardiomyopathy 1M

MONDO:0011840

Any familial isolated dilated cardiomyopathy in which the cause of the disease is a mutation in the CSRP3 gene.

Also known as: CMD1M, CSRP3 familial isolated dilated cardiomyopathy, cardiomyopathy, dilated, type 1M, dilated cardiomyopathy type 1M, familial isolated dilated cardiomyopathy caused by mutation in CSRP3, cardiomyopathy, dilated, 1M

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

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