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Disease Ontology Browser
hemochromatosis type 3 (DOID:0111030)
Alliance: disease page
Synonyms: hemochromatosis due to defect in transferrin receptor 2; HFE3; TFR2-related hemochromatosis
Alt IDs: OMIM:604250, MESH:C537248, ORDO:225123, UMLS_CUI:C1858664
Definition: A hemochromatosis that has_material_basis_in homozygous or compound heterozygous mutation in the TFR2 gene on chromosome 7q22.

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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Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory