hypertrophic cardiomyopathy 15 (MONDO_0013200, a Monarch Disease Ontology id) is any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the VCL gene. Also known as: CMH15, VCL hypertrophic cardiomyopathy, cardiomyopathy familial hypertrophic 15, cardiomyopathy, familial hypertrophic, type 15, cardiomyopathy, hypertrophic, 15, hypertrophic cardiomyopathy caused by mutation in VCL, hypertrophic cardiomyopathy type 15.