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Concept information

Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Cardiomyopathy, Hypertrophic, Familial
Cardiovascular Diseases > Heart Diseases > Cardiomyopathies > Cardiomyopathy, Hypertrophic > Cardiomyopathy, Hypertrophic, Familial
... > Cardiovascular Diseases > Heart Diseases > Heart Valve Diseases > Aortic Valve Disease > Aortic Valve Stenosis > Aortic Stenosis, Subvalvular > Cardiomyopathy, Hypertrophic > Cardiomyopathy, Hypertrophic, Familial
... > Cardiovascular Diseases > Heart Diseases > Ventricular Outflow Obstruction > Aortic Valve Stenosis > Aortic Stenosis, Subvalvular > Cardiomyopathy, Hypertrophic > Cardiomyopathy, Hypertrophic, Familial

Terme préférentiel

Cardiomyopathy, Hypertrophic, Familial  

Type

  • mesh:Descriptor

Définition

  • 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.

Concept générique

Concepts associés

Synonyme(s)

  • Asymmetric Septal Hypertrophy, Familial
  • Cardiomyopathy, Familial Hypertrophic
  • Familial Hypertrophic Cardiomyopathy
  • Hereditary Ventricular Hypertrophy
  • Ventricular Hypertrophy, Familial
  • Ventricular Hypertrophy, Hereditary

Qualificatif(s) autorisé(s)

Traductions

URI

http://data.loterre.fr/ark:/67375/JVR-LPK2347Q-R

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RDF/XML TURTLE JSON-LD Date de création 25/07/2001, dernière modification le 28/02/2020