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Hemochromatosis type 5

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Description

Any hereditary hemochromatosis in which the cause of the disease is a mutation in the FTH1 gene.

MONDO

  • Mode of Inheritance

  • Autosomal dominant inheritance

VARIANTS

19

SEE THE VARIANTS →

Genes

  • FTH1

External Links

  • OMIM

    615517

  • Orphanet
  • HPO
  • Medgen

    C1851316

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