Crigler-Najjar syndrome type 2

MONDO:0011725

Type 2 Crigler-Najjar syndrome (CNS2) is a hereditary disorder of bilirubin metabolism characterized by unconjugated hyperbilirubinemia due to reduced and inducible activity of hepatic bilirubin glucuronosyltransferase (GT). CNS2 is a milder form of CNS than CNS1.

Also known as: Arias syndrome, UGT deficiency type 2, bilirubin uridinediphosphate glucuronosyltransferase deficiency type 2, bilirubin-UGT deficiency type 2, hereditary unconjugated hyperbilirubinemia type 2, Crigler Najjar syndrome, type 2, Crigler-Najjar syndrome, type 2, Crigler-Najjar syndrome, type II

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