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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, 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)