Hemosiderosis Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An iron metabolism disease that has_material_basis_in an accumulation of hemosiderin, an iron-storage complex, resulting in iron overload. (Human Disease Ontology, DOID_12119)
External Link https://www.disgenet.org/browser/0/1/0/C0019114
Similar Terms
Downloads & Tools

Genes

8 genes associated with the disease Hemosiderosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ACSM3 acyl-CoA synthetase medium-chain family member 3
CP ceruloplasmin (ferroxidase)
GDF15 growth differentiation factor 15
HAMP hepcidin antimicrobial peptide
HFE hemochromatosis
HP haptoglobin
TNFRSF1A tumor necrosis factor receptor superfamily, member 1A
TTR transthyretin