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Concept information

Preferred term

Cardiomyopathy, Hypertrophic, Familial  

Type

  • Topical Descriptor

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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