Non-HFE-related hereditary haemochromatosis, Type 4 (Q97536): Difference between revisions
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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 |
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| default for all languages | ID_1541297428 |
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| 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. |
