neonatal hyperbilirubinemia Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A pigmentation disease characterized by a high level of bilirubin in the blood, causing a yellowing of the skin and other tissues of a newborn infant. (Human Disease Ontology, DOID_2383)
Similar Terms
Downloads & Tools

Genes

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

Symbol Name
UGT1A1 UDP glucuronosyltransferase 1 family, polypeptide A1