Hyperuricemia Gene Set

Dataset DISEASES Experimental Gene-Disease Association Evidence Scores 2025
Category disease or phenotype associations
Type disease
Description An acquired metabolic disease that has_material_basis_in an abnormally high level of uric acid in the blood. (Human Disease Ontology, DOID_1920)
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Genes

9 genes associated with the disease Hyperuricemia in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.

Symbol Name Standardized Value
MAPKAPK5 mitogen-activated protein kinase-activated protein kinase 5 1.661
ACAD10 acyl-CoA dehydrogenase family, member 10 1.661
ALDH2 aldehyde dehydrogenase 2 family (mitochondrial) 1.661
WDR1 WD repeat domain 1 1.252
SLC2A9 solute carrier family 2 (facilitated glucose transporter), member 9 1.252
CNTN5 contactin 5 1.182
ABCG2 ATP-binding cassette, sub-family G (WHITE), member 2 (Junior blood group) 1.164
PKD2 polycystic kidney disease 2 (autosomal dominant) 1.164
SPP1 secreted phosphoprotein 1 1.164