Crigler-Najjar syndrome, type I   8933000

SNOMED CT code


SNOMED code8933000
nameCrigler-Najjar syndrome, type I
statusactive
date introduced2002-01-31
fully specified name(s)Crigler-Najjar syndrome, type I (disorder)
synonyms
  • Crigler-Najjar syndrome, type I
  • Deficiency of glucuronosyltransferase
  • Glucuronyltransferase deficiency
  • UDP glucuronyl transferase deficiency
  • Crigler-Najjar type 1
  • Bilirubin UDP glucuronyl transferase deficiency
  • Bilirubin glucuronosyltransferase deficiency
  • Crigler-Najjar syndrome type I
attributes - group2
Finding siteLiver structure   10200004
attributes - group1
OccurrenceCongenital   255399007
parents
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Digestive system finding   386617003
      Liver finding   249565005
        Disease of liver   235856003
          Crigler-Najjar syndrome, type I   8933000

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Metabolic disease   75934005
        Enzymopathy   78548001
          Crigler-Najjar syndrome   28259009
            Crigler-Najjar syndrome, type I   8933000

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Digestive system finding   386617003
      Disorder of digestive system   53619000
        Digestive system hereditary disorder   363080007
          Crigler-Najjar syndrome, type I   8933000

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Autosomal hereditary disorder   1899006
            Autosomal recessive hereditary disorder   85995004
              Crigler-Najjar syndrome, type I   8933000

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