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Disease Ontology Browser
hemochromatosis type 4 (DOID:0111028)
Alliance: disease page
Synonyms: autosomal dominant hereditary hemochromatosis; ferroportin disease; hemochromatosis due to defect in ferroportin; HFE4
Alt IDs: OMIM:606069, MESH:C537249, ORDO:139491, UMLS_CUI:C1853733
Definition: A hemochromatosis that has_material_basis_in heterozygous mutation in the SLC40A1 gene on chromosome 2q32.

Disease References using Mouse Models (2)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
11/30/2021
MGI 6.17
The Jackson Laboratory