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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

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Tree Number(s): C14.280.238.100.500, C14.280.484.150.070.160.500, 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
  • 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
  • Obstructive Asymmetric Septal Hypertrophy
  • Hypertrophic Subaortic Stenosis, Idiopathic

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