Hypertrophic cardiomyopathy 14

Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the MYH6 gene.

Also known as: CMH14, MYH6 hypertrophic cardiomyopathy, cardiomyopathy, familial hypertrophic, type 14, cardiomyopathy, hypertrophic, 14, hypertrophic cardiomyopathy caused by mutation in MYH6, hypertrophic cardiomyopathy type 14, cardiomyopathy, familial hypertrophic, 14

8 clinical trials for this condition and its sub-types, 0 tagged with Hypertrophic cardiomyopathy 14 itself.