Concept information
Preferred term
Cardiomyopathy, Hypertrophic, Familial
Type
-
Topical Descriptor
Broader concept
Entry terms
- Asymmetric Septal Hypertrophy, Familial
- Cardiomyopathies, Familial Hypertrophic
- Cardiomyopathy, Familial Hypertrophic
- Familial Hypertrophic Cardiomyopathies
- Familial Hypertrophic Cardiomyopathy
- Familial Ventricular Hypertrophies
- Familial Ventricular Hypertrophy
- Hereditary Ventricular Hypertrophies
- Hereditary Ventricular Hypertrophy
- Hypertrophic Cardiomyopathies, Familial
- Hypertrophic Cardiomyopathy, Familial
- Hypertrophies, Hereditary Ventricular
- Hypertrophy, Familial Ventricular
- Hypertrophy, Hereditary Ventricular
- Ventricular Hypertrophies, Familial
- Ventricular Hypertrophies, Hereditary
- Ventricular Hypertrophy, Familial
- Ventricular Hypertrophy, Hereditary
Scope note
- 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.
History note
- 2002
In other languages
-
Finnish
-
familiaalinen HCM
-
familiaalinen hypertrofinen sydänlihassairaus
-
familiaarinen hypertrofinen kardiomyopatia
-
familiaarinen hypertrofinen sydänlihassairaus
-
suvuittain esiintyvä HCM
-
suvuittain esiintyvä hypertrofinen kardiomyopatia
-
suvuittain esiintyvä hypertrofinen sydänlihassairaus
-
Swedish
-
Familjär ventrikulär hypertrofi
-
Obstruktiv asymmetrisk septal hypertrofi
-
Ärftlig ventrikulär hypertrofi
URI
http://www.yso.fi/onto/mesh/D024741
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