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:0111031 - hemochromatosis type 5

Disease Ontology Definition:A hemochromatosis that has_material_basis_in heterozygous mutation in the FTH1 gene on chromosome 11q12.

Synonyms: FTH1-associated iron overload, FTH1-related iron overload, HFE5,

Xenbase Genes : bmp6, fth1.1, fth1.2

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014225 - hemochromatosis type 5


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)