hemochromatosis Gene Set

Dataset DISEASES Curated Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A metal metabolism disorder characterized by the accumulation of iron in various organs of the body. (Human Disease Ontology, DOID_2352)
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Genes

5 genes involed in the disease hemochromatosis from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

Symbol Name
HAMP hepcidin antimicrobial peptide
HFE hemochromatosis
HFE2 hemochromatosis type 2 (juvenile)
SLC40A1 solute carrier family 40 (iron-regulated transporter), member 1
TFR2 transferrin receptor 2