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10 Familial Hypertrophic Cardiomyopathy

mutation in MYL2

Also Known As:

Cardiomyopathy, Familial Hypertrophic, 10; Cardiomyopathy, Hypertrophic, Mid-Left Ventricular Chamber Type, 2

Networked: 0 relevant articles (0 outcomes, 0 trials/studies)

Disease Context: Research Results

Cardiovascular Diseases: 91362
- Heart Diseases: 26014
  - Cardiomyopathies: 19128
    - Hypertrophic Cardiomyopathy: 4931
      - Familial Hypertrophic Cardiomyopathy: 388
        10 Familial Hypertrophic Cardiomyopathy
  - Heart Valve Diseases: 1865
    - Aortic Valve Disease: 802
      - Aortic Valve Stenosis: 7844
        Subvalvular Aortic Stenosis: 16
        Hypertrophic Cardiomyopathy: 4931
        Familial Hypertrophic Cardiomyopathy: 388
        10 Familial Hypertrophic Cardiomyopathy
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
- Inborn Genetic Diseases: 11939
  - Familial Hypertrophic Cardiomyopathy: 388
    - 10 Familial Hypertrophic Cardiomyopathy