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Hemochromatosis type 4

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Description

Hemochromatosis type 4 (HFE4) is a dominantly inherited iron overload disorder with heterogeneous phenotypic manifestations that can be classified into 2 groups. One group is characterized by an early rise in ferritin (see 134790) levels with low to normal transferrin (190000) saturation and iron accumulation predominantly in macrophages. The other group is similar to classical hemochromatosis, with high transferrin saturation and prominent parenchymal iron loading (summary by De Domenico et al., 2005). For general background information and a discussion of genetic heterogeneity of hereditary hemochromatosis, see 235200.

OMIM

  • Mode of Inheritance

  • Autosomal dominant inheritance

VARIANTS

89

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Genes

External Links

  • OMIM

    606069

  • Orphanet

    139491

  • HPO
  • Medgen

    C1853733

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