DISEASES

Disease-gene associations mined from literature

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Human genes for Crigler-Najjar syndrome

Crigler-Najjar syndrome [DOID:3803]

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:  Crigler-Najjar syndrome,  CriglerNajjar syndrome,  Crigler-Najjar disease,  Crigler-Najjar disorder,  Crigler-Najjar syndromes ...

Linkouts:  OMIM #1 #2

The disease-gene associations are derived from automatic text mining of the biomedical literature, manually curated database annotations, cancer mutation data, and genome-wide association studies. The confidence of each association is signified by stars, where ★★★★★ is the highest confidence and ★☆☆☆☆ is the lowest.

Developed by Sune Frankild, Alexander Junge, Albert Pallejà, Dhouha Grissa, Kalliopi Tsafou, and Lars Juhl Jensen from the Novo Nordisk Foundation Center for Protein Research.