The association between UGT1A9 (UDP Glucuronosyltransferase Family 1 Member A9) and Bilirubin Metabolic Disorder is supported by expert-curated evidence, drawing on a single expert-curated source, which records pathogenic variants.
Sources1
Clinical variants16
Symptoms4
Compounds1
Trials0of 33 via UGT1A9 compounds
Publications0
01
At a glance
Association overview
A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.