Hypertrophic cardiomyopathy 13

Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the TNNC1 gene.

Also known as: CMH13, TNNC1 hypertrophic cardiomyopathy, cardiomyopathy, familial hypertrophic, type 13, cardiomyopathy, hypertrophic, 13, hypertrophic cardiomyopathy caused by mutation in TNNC1, hypertrophic cardiomyopathy type 13, cardiomyopathy, familial hypertrophic, 13

8 clinical trials for this condition and its sub-types, 0 tagged with Hypertrophic cardiomyopathy 13 itself.