Non-HFE-related hereditary haemochromatosis, Type 4 (Q97536): Difference between revisions

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Latest revision as of 13:39, 16 August 2026

Hemochromatosis type 4 (also called ferroportin disease) is a rare form of hereditary hemochromatosis, a group of diseases characterised by excessive tissue iron deposition of genetic origin. It is phenotypically heterogeneous with two sub-types. Ferroportin disease form A is the usual form and is generally asymptomatic with no tissue damage and further complications. Ferroportin disease form B is rarer and resembles hemochromatosis type 1, but can affect children.

Language	Label	Description	Also known as
default for all languages	ID_1541297428
English	Non-HFE-related hereditary haemochromatosis, Type 4	Hemochromatosis type 4 (also called ferroportin disease) is a rare form of hereditary hemochromatosis, a group of diseases characterised by excessive tissue iron deposition of genetic origin. It is phenotypically heterogeneous with two sub-types. Ferroportin disease form A is the usual form and is generally asymptomatic with no tissue damage and further complications. Ferroportin disease form B is rarer and resembles hemochromatosis type 1, but can affect children.