hypertrophic cardiomyopathy 18 (Q27674937)

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A hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the gene encoding phospholamban (PLN) on chromosome 6q22.1.
  • CMH18
  • cardiomyopathy familial hypertrophic 18
  • Cardiomyopathy, Familial Hypertrophic, type 18
  • CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 18; CMH18
  • CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 18
  • hypertrophic cardiomyopathy type 18
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English
hypertrophic cardiomyopathy 18
A hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the gene encoding phospholamban (PLN) on chromosome 6q22.1.
  • CMH18
  • cardiomyopathy familial hypertrophic 18
  • Cardiomyopathy, Familial Hypertrophic, type 18
  • CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 18; CMH18
  • CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 18
  • hypertrophic cardiomyopathy type 18

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