OnlineIMD

Crigler-Najjar syndrome

  • Synonym(s)
    • UDP-glucuronosyltransferase A1 deficiency
  • Type
    Disease
  • External link(s)
    • Orphanet
    • IEMbase
  • Gene
    • UGT1A1 / UDP Glucuronosyltransferase Family 1 Member A1
      • 2q37.1
      • OMIM
      • GnomAD
      • Ensembl
      • HGNC
      • VMH
      • LOVD
  • Gene product
    • UDP-glucuronosyltransferase 1A1
  • Disease group(s)
    • 17.2    Disorders of heme degradation and bilirubin metabolism
  • Child entries
    • Crigler-Najjar syndrome type 1
    • Crigler-Najjar syndrome type 2
    • Transient familial neonatal hyperbilirubinemia
    • Gilbert syndrome