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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, ICD10CM:E83.1, 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 Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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MGI 6.11
The Jackson Laboratory