hemochromatosis Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A metal metabolism disorder characterized by the accumulation of iron in various organs of the body. (Human Disease Ontology, DOID_2352)
External Link http://www.omim.org/entry/235200
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1 genes associated with the hemochromatosis phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
HFE hemochromatosis