Cardiomyopathy, Hypertrophic, Familial
"Cardiomyopathy, Hypertrophic, Familial" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
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.
| Descriptor ID |
D024741
|
| MeSH Number(s) |
C14.280.238.100.500 C14.280.484.150.070.160.500 C16.320.160
|
| Concept/Terms |
Cardiomyopathy, Hypertrophic, Familial- Cardiomyopathy, Hypertrophic, Familial
- Cardiomyopathy, Familial Hypertrophic
- Cardiomyopathies, Familial Hypertrophic
- Familial Hypertrophic Cardiomyopathies
- Hypertrophic Cardiomyopathies, Familial
- Hypertrophic Cardiomyopathy, Familial
- Familial Hypertrophic Cardiomyopathy
- Ventricular Hypertrophy, Familial
- Familial Ventricular Hypertrophies
- Familial Ventricular Hypertrophy
- Hypertrophy, Familial Ventricular
- Ventricular Hypertrophies, Familial
- Ventricular Hypertrophy, Hereditary
- Asymmetric Septal Hypertrophy, Familial
- Hereditary Ventricular Hypertrophy
- Hereditary Ventricular Hypertrophies
- Hypertrophies, Hereditary Ventricular
- Hypertrophy, Hereditary Ventricular
- Ventricular Hypertrophies, Hereditary
|
Below are MeSH descriptors whose meaning is more general than "Cardiomyopathy, Hypertrophic, Familial".
- Diseases [C]
- Cardiovascular Diseases [C14]
- Heart Diseases [C14.280]
- Cardiomyopathies [C14.280.238]
- Cardiomyopathy, Hypertrophic [C14.280.238.100]
- Cardiomyopathy, Hypertrophic, Familial [C14.280.238.100.500]
- Heart Valve Diseases [C14.280.484]
- Aortic Valve Stenosis [C14.280.484.150]
- Aortic Stenosis, Subvalvular [C14.280.484.150.070]
- Cardiomyopathy, Hypertrophic [C14.280.484.150.070.160]
- Cardiomyopathy, Hypertrophic, Familial [C14.280.484.150.070.160.500]
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
- Genetic Diseases, Inborn [C16.320]
- Cardiomyopathy, Hypertrophic, Familial [C16.320.160]
Below are MeSH descriptors whose meaning is more specific than "Cardiomyopathy, Hypertrophic, Familial".
This graph shows the total number of publications written about "Cardiomyopathy, Hypertrophic, Familial" by people in this website by year, and whether "Cardiomyopathy, Hypertrophic, Familial" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2008 | 1 | 0 | 1 |
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Below are the most recent publications written about "Cardiomyopathy, Hypertrophic, Familial" by people in Profiles.
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Two strikes and you're out: gene-gene mutation interactions in HCM. Circ Res. 2014 Jul 07; 115(2):208-10.
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Ventricular fibrillation following autologous intramyocardial cell therapy for inherited cardiomyopathy. Cardiovasc Pathol. 2010 Mar-Apr; 19(2):e33-6.
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Beta-myosin heavy chain gene mutations in familial hypertrophic cardiomyopathy: the usual suspect? Circ Res. 2002 Feb 22; 90(3):246-7.