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

24 clinical trials for this condition and its sub-types.

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