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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

In OMIM:
OMIM:613313 - HEMOCHROMATOSIS, TYPE 2B; HFE2B

In Mondo Disease Ontology:
MONDO:0013220 - hemochromatosis type 2B

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : hamp

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): hemochromatosis type 2 (is_a)