Cardiomyopathy, Hypertrophic, Familial
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.
Year introduced: 2002
PubMed search builder options
Subheadings:
Tree Number(s): C14.280.238.100.500, C14.280.484.048.750.070.160.500, C16.320.160
MeSH Unique ID: D024741
Entry Terms:
- Cardiomyopathy, Familial Hypertrophic
- Cardiomyopathies, Familial Hypertrophic
- Familial Hypertrophic Cardiomyopathies
- Hypertrophic Cardiomyopathies, Familial
- Hypertrophic Cardiomyopathy, Familial
- Familial Hypertrophic Cardiomyopathy
- Asymmetric Septal Hypertrophy, Familial
- Hereditary Ventricular Hypertrophy
- Hereditary Ventricular Hypertrophies
- Hypertrophies, Hereditary Ventricular
- Hypertrophy, Hereditary Ventricular
- Ventricular Hypertrophies, Hereditary
- Ventricular Hypertrophy, Hereditary
- Ventricular Hypertrophy, Familial
- Familial Ventricular Hypertrophies
- Familial Ventricular Hypertrophy
- Hypertrophy, Familial Ventricular
- Ventricular Hypertrophies, Familial
- Obstructive Asymmetric Septal Hypertrophy
- Hypertrophic Subaortic Stenosis, Idiopathic
Previous Indexing:
See Also: