Hemochromatosis type 4

MONDO:0011631

A form of rare hemochromatosis (HC) characterized by increased transferrin saturation and hepatocellular iron deposition with distribution patterns and clinical features indistinguishable from patients with other types of HC.

Also known as: Ferroportin Disease, HFE4, SLC40A1 hereditary hemochromatosis, ferroportin disease, hereditary hemochromatosis caused by mutation in SLC40A1, hemochromatosis, autosomal dominant, hemochromatosis, type 4

1 clinical trial for this condition and its sub-types, 0 tagged with Hemochromatosis type 4 itself.

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Where it sits in the disease tree

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↑ Hereditary hemochromatosis (8)

Including sub-types (1) Tagged with Hemochromatosis type 4 (0)

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 Sep 18, 2026 00:00 UTC

Hemochromatosis type 4

Where it sits in the disease tree

NIH launches major study to unlock secrets of rare bone diseases