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Disease Ontology Browser
hemochromatosis type 1 (DOID:0111029)
Alliance: disease page
Synonyms: HFE1; symptomatic form of classic hemochromatosis; symptomatic form of hemochromatosis type 1; symptomatic form of HFE-related hereditary hemochromatosis
Alt IDs: OMIM:235200, ICD10CM:E83.1, ORDO:465508
Definition: A hemochromatosis that has_material_basis_in homozygous or compound heterozygous mutation in the HFE gene on chromosome 6p22.

Disease References using Mouse Models (15)

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
MGI 6.23
The Jackson Laboratory