hemochromatosis type 5

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Echinobase

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

Echinobase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: LOC100892337

MIM:

MIM:615517 - hemochromatosis, type 5; hfe5

MIM:615517 - hemochromatosis, type 5; hfe5

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): hemochromatosis (is_a)