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Hemochromatosis type 2

MONDO:0019257

Hemochromatosis type 2 (juvenile) is the early-onset and most severe form of rare hereditary hemochromatosis (HH), a group of diseases characterized by excessive tissue iron deposition of genetic origin.

Also known as: Juvenile Hemochromatosis, juvenile hemochromatosis, hemochromatosis juvenile, iron overload disease juvenile

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

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Sub-types

Hemochromatosis type 2A (0) Hemochromatosis type 2B (0)

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 05:00 UTC

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