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Crigler-Najjar Syndrome

Prevalence: 1/1000000

hepatic

Official·OMIM:218800 Official·ORPHA205

Bilirubin conjugation defect due to UGT1A1 gene mutations.

Associated Genes

UGT1A1UDP Glucuronosyltransferase Family 1 Member A1

Chromosome 2Autosomal Recessive