Cardiomyopathy, Hypertrophic, Familial |
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| Asymmetric Septal Hypertrophy, Familial; Cardiomyopathy, Familial Hypertrophic; Ventricular Hypertrophy, Familial; Cardiomyopathies, Familial Hypertrophic; Familial Hypertrophic Cardiomyopathies; Familial Ventricular Hypertrophy | |
| 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. | |