hyperbilirubinemia Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An inherited metabolic disorder that involves elevated levels of bilirubin resulting from disruption of bilirubin metabolism. (Human Disease Ontology, DOID_2741)
Similar Terms
Downloads & Tools

Genes

4 genes associated with the disease hyperbilirubinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
G6PD glucose-6-phosphate dehydrogenase
SLCO1B3 solute carrier organic anion transporter family, member 1B3
SLCO2A1 solute carrier organic anion transporter family, member 2A1
UGT1A1 UDP glucuronosyltransferase 1 family, polypeptide A1