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 |
|---|
| 2003 | 1 | 0 | 1 |
| 2004 | 0 | 1 | 1 |
| 2008 | 1 | 1 | 2 |
| 2009 | 1 | 0 | 1 |
| 2010 | 1 | 0 | 1 |
| 2011 | 1 | 0 | 1 |
| 2012 | 1 | 0 | 1 |
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click here.
Below are the most recent publications written about "Cardiomyopathy, Hypertrophic, Familial" by people in Profiles.
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The diagnosis of hypertrophic cardiomyopathy by cardiovascular magnetic resonance. J Cardiovasc Magn Reson. 2012 Feb 20; 14:17.
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The mitral valve in hypertrophic cardiomyopathy: old versus new concepts. J Cardiovasc Transl Res. 2011 Dec; 4(6):757-66.
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Neonatal gene transfer of Serca2a delays onset of hypertrophic remodeling and improves function in familial hypertrophic cardiomyopathy. J Mol Cell Cardiol. 2010 Dec; 49(6):993-1002.
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Use of genetics in the clinical evaluation of cardiomyopathy. JAMA. 2009 Dec 09; 302(22):2471-6.
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Genetic evaluation of familial cardiomyopathy. J Cardiovasc Transl Res. 2008 Jun; 1(2):144-54.
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Familial hypertrophic cardiomyopathy associated with cardiac beta-myosin heavy chain and troponin I mutations. Pediatr Cardiol. 2008 Jul; 29(4):846-50.
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Predictors of outcome after alcohol septal ablation therapy in patients with hypertrophic obstructive cardiomyopathy. Circulation. 2004 Feb 24; 109(7):824-7.
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Familial hypertrophic cardiomyopathy-linked mutant troponin T causes stress-induced ventricular tachycardia and Ca2+-dependent action potential remodeling. Circ Res. 2003 Mar 07; 92(4):428-36.