hemochromatosis type 3 (Q3144936)

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hemochromatosis that has material basis in homozygous or compound heterozygous mutation in the TFR2 gene on chromosome 7q22
  • TFR2-related hemochromatosis
  • HFE3
  • hemochromatosis due to defect in transferrin receptor 2
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Language Label Description Also known as
English
hemochromatosis type 3
hemochromatosis that has material basis in homozygous or compound heterozygous mutation in the TFR2 gene on chromosome 7q22
  • TFR2-related hemochromatosis
  • HFE3
  • hemochromatosis due to defect in transferrin receptor 2

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