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DOID:2739 - Gilbert syndrome
Disease Ontology Definition:A bilirubin metabolic disorder that involves elevated levels of unconjugated bilirubin as bilirubin is not being conjugated as a result of reduced glucuronyltransferase activity.
Synonyms: Constitutional hyperbilirubinemia, Gilbert's disease, Gilbert's syndrome, Gilbert-Meulengracht syndrome, hereditary nonhemolytic jaundice,
Xenbase Genes
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
MONDO:0007745 - Gilbert syndrome |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
bilirubin metabolic disorder (is_a)