has material basis in germline mutation in TNNT2 hypertrophic cardiomyopathy hypertrophic cardiomyopathy 2 https://github.com/monarch-initiative/mondo/issues/4521 https://www.malacards.org/card/cardiomyopathy_familial_hypertrophic_2 NCIT:C142892 familial hypertrophic cardiomyopathy type 2 cardiomyopathy, familial hypertrophic, type 2 hypertrophic cardiomyopathy type 2 GARD:0024540 cardiomyopathy, hypertrophic, 2 cardiomyopathy, familial hypertrophic, 2 Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the TNNT2 gene. MESH:C566171 hypertrophic cardiomyopathy caused by mutation in TNNT2 OMIM:115195 MEDGEN:349383 TNNT2 hypertrophic cardiomyopathy DOID:0110308 UMLS:C1861864 hypertrophic cardiomyopathy 2 MONDO:0007266 CMH2 familial hypertrophic cardiomyopathy TNNT2-related cardiomyopathy