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Hemochromatosis type 2B

MONDO:0013220

Any hemochromatosis type 2 in which the cause of the disease is a mutation in the HAMP gene.

Also known as: HAMP hemochromatosis type 2, HFE2B, hemochromatosis type 2 caused by mutation in HAMP, hemochromatosis, type 2B

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

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