Cardiomyopathy, Hypertrophic, Familial

MeSH code information

• Name
  Cardiomyopathy, Hypertrophic, Familial
• 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
  • C14.280.484.048.750.070.160.500
  • C16.320.160
• Qualifiers
  diagnosis, parasitology, immunology, microbiology, diagnostic imaging, physiopathology, rehabilitation, enzymology, etiology, mortality, epidemiology, blood, cerebrospinal fluid, chemically induced, diet therapy, drug therapy, therapy, psychology, urine, virology, veterinary, history, classification, economics, embryology, genetics, nursing, radiotherapy, ethnology, prevention & control, pathology, metabolism, complications, surgery