Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
DOID:3803 - Crigler-Najjar syndrome


Disease Ontology Definition: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).

Synonyms: Bilirubin UDP glucuronyl transferase deficiency, Crigler Najjar syndrome, Crigler-Najjar syndrome, type I, Crigler-Najjar syndrome, type I (disorder)

In OMIM:
OMIM:218800 - CRIGLER-NAJJAR SYNDROME, TYPE I

In Mondo Disease Ontology:
MONDO:0009044 - Crigler-Najjar syndrome

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : ugt1a1

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): bilirubin metabolic disorder (is_a)