unconjugated hyperbilirubinemia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An increased amount of unconjugated (indirect) bilurubin in the blood. (Human Phenotype Ontology, HP_0008282)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0008282
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Genes

4 genes associated with the unconjugated hyperbilirubinemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
G6PD glucose-6-phosphate dehydrogenase
PKLR pyruvate kinase, liver and RBC
RHAG Rh-associated glycoprotein
UGT1A1 UDP glucuronosyltransferase 1 family, polypeptide A1