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.
Also Known As:
Cardiomyopathy, Familial Hypertrophic; Cardiomyopathy, Hypertrophic, Familial; Asymmetric Septal Hypertrophy, Familial; Hereditary Ventricular Hypertrophy; Hypertrophic Subaortic Stenosis, Idiopathic; Obstructive Asymmetric Septal Hypertrophy; Ventricular Hypertrophy, Familial; Ventricular Hypertrophy, Hereditary; Cardiomyopathies, Familial Hypertrophic; Familial Hypertrophic Cardiomyopathies; Familial Ventricular Hypertrophies; Familial Ventricular Hypertrophy; Hereditary Ventricular Hypertrophies; Hypertrophic Cardiomyopathies, Familial; Hypertrophic Cardiomyopathy, Familial; Hypertrophies, Hereditary Ventricular; Hypertrophy, Familial Ventricular; Hypertrophy, Hereditary Ventricular; Ventricular Hypertrophies, Familial; Ventricular Hypertrophies, Hereditary