Mesh term Cardiomyopathy, Hypertrophic, Familial
Browse to parent terms:Cardiomyopathy, Hypertrophic
Genetic Diseases, Inborn
Description
An autosomal dominant inherited form of HYPERTROPHIC CARDIOMYOPATHY. It results from any of more than 50 mutations involving genes encoding contractile proteins such as VENTRICULAR MYOSINS; cardiac TROPONIN T; ALPHA-TROPOMYOSIN.Search for this term in our Faculty Database
View this term at the NCBI website
