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Hemochromatosis type 5

MONDO:0014225

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

Also known as: FTH1 hereditary hemochromatosis, FTH1-associated iron overload, FTH1-related iron overload, HFE5, hereditary hemochromatosis caused by mutation in FTH1, hemochromatosis, type 5, iron overload, autosomal dominant

1 clinical trial for this condition and its sub-types.

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Broader categories

Disease (680) Metabolic disease (233) Hereditary disease (176) Inborn errors of metabolism (45) Human disease (14) Hereditary hemochromatosis (8) Disease of genetic or genomic mechanism (2) Hemosiderosis (2) Iron metabolism disease (2) Mineral metabolism disease (2)
Trials to join now! 1
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  • NIH launches major study to unlock secrets of rare bone diseases

    Knowledge-focused Recruiting now

    This study aims to collect information and bone samples from up to 1,000 people with bone or mineral disorders, such as tumor-induced osteomalacia or familial tumoral calcinosis. Participants receive standard medical evaluations and may provide bone tissue from surgery or a biops…

    Sponsor: National Institute of Dental and Craniofacial Research (NIDCR) • Aim: Knowledge-focused

    Last updated Aug 18, 2026 04:00 UTC

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