Cardiomyopathy, Hypertrophic, Familial

MeSH code information
  • Name
  • Concept
    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.
  • Tree numbers
    • C14.280.238.100.500
    • C14.280.484.150.070.160.500
    • C16.320.160
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Cardiomyopathy, Hypertrophic, Familial - MeSH Info at Gentau
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