Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the TCAP gene. The disease is hypertrophic cardiomyopathy 25 (MONDO_0011843). Also known as: CMH25, TCAP hypertrophic cardiomyopathy, Tcap hypertrophic cardiomyopathy, cardiomyopathy familial hypertrophic 25, cardiomyopathy, familial hypertrophic, type 25, cardiomyopathy, hypertrophic, 25, hypertrophic cardiomyopathy caused by mutation in TCAP, hypertrophic cardiomyopathy type 25.