hypertrophic cardiomyopathy 10 (MONDO_0012112) is 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 caused by mutation in MYL2, hypertrophic cardiomyopathy type 10.