Cardiomyopathy, Hypertrophic, Familial

**Definition:** 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.

**Tree numbers:** - C14.280.238.100.500 - C14.280.484.048.750.070.160.500 - C16.320.160

**Synonyms:** - Cardiomyopathy, Familial Hypertrophic - Familial Hypertrophic Cardiomyopathy - Asymmetric Septal Hypertrophy, Familial - Hereditary Ventricular Hypertrophy - Ventricular Hypertrophy, Hereditary - Ventricular Hypertrophy, Familial