(Q27674923)

English

hypertrophic cardiomyopathy 6

hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the gene encoding the gamma-2 regulatory subunit of AMP-activated protein kinase (PRKAG2)

  • CMH6
  • cardiomyopathy, familial hypertrophic 6
  • hypertrophic cardiomyopathy type 6
  • CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 6; CMH6
  • CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 6
  • Cardiomyopathy, Familial Hypertrophic, type 6
  • familial hypertrophic cardiomyopathy type 6

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