U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

Links from MedGen

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:

Supplemental Content

Loading ...