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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,
Echinobase Genes :
MIM:613313 - hemochromatosis, type 2b; hfe2b |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
hemochromatosis type 2 (is_a)