has material basis in germline mutation in TCAP hypertrophic cardiomyopathy hypertrophic cardiomyopathy 25 https://github.com/monarch-initiative/mondo/issues/4521 https://www.malacards.org/card/cardiomyopathy_familial_hypertrophic_25 MESH:C564388 cardiomyopathy, familial hypertrophic, type 25 hypertrophic cardiomyopathy caused by mutation in TCAP OMIM:607487 MEDGEN:895360 Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the TCAP gene. Tcap hypertrophic cardiomyopathy GARD:0024827 DOID:0110328 TCAP hypertrophic cardiomyopathy hypertrophic cardiomyopathy type 25 cardiomyopathy, familial hypertrophic, 25 MONDO:0011843 cardiomyopathy, hypertrophic, 25 CMH25 UMLS:C4225408 neuromuscular disease caused by qualitative or quantitative defects of telethonin familial dilated cardiomyopathy familial hypertrophic cardiomyopathy