Hemochromatosis Gene Set

Dataset CTD Gene-Disease Associations
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)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D006432
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12 genes/proteins associated with the disease Hemochromatosis from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
HFE hemochromatosis 2.88009
SLC11A2 solute carrier family 11 (proton-coupled divalent metal ion transporter), member 2 2.88009
AKR1D1 aldo-keto reductase family 1, member D1 2.88009
TFR2 transferrin receptor 2 2.88009
HFE2 hemochromatosis type 2 (juvenile) 2.88009
BMP2 bone morphogenetic protein 2 2.88009
BMP6 bone morphogenetic protein 6 2.88009
SLC40A1 solute carrier family 40 (iron-regulated transporter), member 1 2.88009
HP haptoglobin 2.88009
HAMP hepcidin antimicrobial peptide 2.88009
TNF tumor necrosis factor 2.88009
CP ceruloplasmin (ferroxidase) 2.88009