Familial Hypertrophic Cardiomyopathy

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

Cardiovascular Diseases: 94258
- Heart Diseases: 26486
  - Cardiomyopathies: 19680
    - Hypertrophic Cardiomyopathy: 5086
      - Familial Hypertrophic Cardiomyopathy: 391
  - Heart Valve Diseases: 1907
    - Aortic Valve Disease: 828
      - Aortic Valve Stenosis: 8115
        Subvalvular Aortic Stenosis: 16
        Hypertrophic Cardiomyopathy: 5086
        Familial Hypertrophic Cardiomyopathy: 391
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 960
- Inborn Genetic Diseases: 12342
  - Familial Hypertrophic Cardiomyopathy: 391

Greg Boivin Selected Research

Greg Boivin Research Topics

Disease

Drug/Important Bio-Agent (IBA)