(Q28448698)

English

Hemochromatosis type 4

hemochromatosis that has material basis in heterozygous mutation in the SLC40A1 gene on chromosome 2q32

  • hemochromatosis type 4
  • hemochromatosis due to defect in ferroportin
  • HFE4
  • ferroportin disease
  • autosomal dominant hereditary hemochromatosis
  • HEMOCHROMATOSIS, TYPE 4; HFE4
  • HEMOCHROMATOSIS, TYPE 4
  • Hemochromatosis Due to Defect 1N Ferroportin
  • Hemochromatosis, Autosomal Dominant

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