Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
DOID:0111030 - hemochromatosis type 3

Disease Ontology Definition:A hemochromatosis that has_material_basis_in homozygous or compound heterozygous mutation in the TFR2 gene on chromosome 7q22.

Synonyms: hemochromatosis due to defect in transferrin receptor 2, HFE3, TFR2-related hemochromatosis

Xenbase Genes : tfr2

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011417 - hemochromatosis type 3


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

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