(Q27674924)

English

hypertrophic cardiomyopathy 7

A hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the TNNI3 gene on chromosome 19q13.4.

  • CMH7
  • cardiomyopathy, familial hypertrophic 7
  • hypertrophic cardiomyopathy type 7
  • CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 7
  • CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 7; CMH7
  • Cardiomyopathy, Familial Hypertrophic, type 7

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