hemochromatosis type 2B

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:0111032 - hemochromatosis type 2B

Disease Ontology Definition:A hemochromatosis type 2 that has_material_basis_in homozygous mutation in the HAMP gene on chromosome 19q13.

Synonyms: HFE2B

Xenbase 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

: hamp

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0013220 - hemochromatosis type 2B

MONDO:0013220 - hemochromatosis type 2B

MIM:

MIM:613313 - HEMOCHROMATOSIS, TYPE 2B; HFE2B

MIM:613313 - HEMOCHROMATOSIS, TYPE 2B; HFE2B

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

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

Parent(s): hemochromatosis type 2 (is_a)