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Summary Literature (0)
DOID:0111028 - hemochromatosis type 4

Disease Ontology Definition:A hemochromatosis that has_material_basis_in heterozygous mutation in the SLC40A1 gene on chromosome 2q32.

Synonyms: HFE4, autosomal dominant hereditary hemochromatosis, ferroportin disease, hemochromatosis due to defect in ferroportin

Xenbase Genes : slc40a1

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011631 - hemochromatosis type 4

MIM:
MIM:606069 - HEMOCHROMATOSIS, TYPE 4; HFE4

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view
Parent(s): genetic disease (is_a), hemochromatosis (is_a)