Hypertrophic cardiomyopathy 10

Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the MYL2 gene.

Also known as: CMH10, MYL2 hypertrophic cardiomyopathy, cardiomyopathy, familial hypertrophic, 10, cardiomyopathy, familial hypertrophic, type 10, cardiomyopathy, hypertrophic, 10, hypertrophic cardiomyopathy 10, hypertrophic cardiomyopathy caused by mutation in MYL2, hypertrophic cardiomyopathy type 10

8 clinical trials for this condition and its sub-types, 0 tagged with Hypertrophic cardiomyopathy 10 itself.