crigler-najjar syndrome Gene Set

Dataset DISEASES Curated Gene-Disease Association Evidence Scores
Category disease or phenotype associations
Type disease
Description A bilirubin metabolic disorder that involves a build up of bilirubin as bilirubin is not being broken down as a result of a lack or deficiency of the enzyme uridine diphosphate glycosyltransferase (UGT). (Human Disease Ontology, DOID_3803)
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Genes

1 genes involed in the disease crigler-najjar syndrome from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

Symbol Name
UGT1A1 UDP glucuronosyltransferase 1 family, polypeptide A1