Hypertrophic cardiomyopathy 16

Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the MYOZ2 gene.

Also known as: CMH16, MYOZ2 hypertrophic cardiomyopathy, cardiomyopathy, familial hypertrophic, type 16, cardiomyopathy, hypertrophic, 16, hypertrophic cardiomyopathy caused by mutation in MYOZ2, hypertrophic cardiomyopathy type 16, cardiomyopathy, familial hypertrophic, 16

8 clinical trials for this condition and its sub-types, 0 tagged with Hypertrophic cardiomyopathy 16 itself.