Hypertrophic cardiomyopathy 19

Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the CALR3 gene.

Also known as: CALR3 hypertrophic cardiomyopathy, CMH19, cardiomyopathy familial hypertrophic 19, cardiomyopathy, familial hypertrophic, type 19, hypertrophic cardiomyopathy caused by mutation in CALR3, hypertrophic cardiomyopathy type 19, cardiomyopathy, familial hypertrophic, 19

8 clinical trials for this condition and its sub-types, 0 tagged with Hypertrophic cardiomyopathy 19 itself.