OMOP Concept 4229773

Crigler-Najjar syndrome, type I

StandardConditionSNOMED8933000Disorder
Maps from
3
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts

Concept Lookup Tool

Search 11M+ concepts across SNOMED, RxNorm, ICD-10 & LOINC.

Source codes that map to this concept

3 source codes normalize to Crigler-Najjar syndrome, type I via the OMOP "Maps to" relationship.

VocabularyCodeNameType
CIEL143212Crigler-Najjar syndrome, type INon-standard
Nebraska Lexicon8933000Bilirubin glucuronosyltransferase deficiencyNon-standard
ReadC374000Crigler - Najjar syndromeNon-standard

Synonyms

Alternative names recorded for Crigler-Najjar syndrome, type I across source vocabularies.

  • Bilirubin glucuronosyltransferase deficiency
  • Bilirubin UDP glucuronyl transferase deficiency
  • Crigler-Najjar syndrome type I
  • Crigler-Najjar syndrome, type I (disorder)
  • Crigler-Najjar type 1
  • deficiencia de glucoroniltransferasa
  • deficiencia de glucuronosiltransferasa
  • deficiencia de UDP glucuronil transferasa
  • Deficiency of glucuronosyltransferase
  • Glucuronyltransferase deficiency
  • síndrome de Crigler - Najjar, tipo I
  • síndrome de Crigler - Najjar, tipo I (trastorno)
  • UDP glucuronyl transferase deficiency

Where it sits in the hierarchy

Ordered by distance - 1 is a direct parent or child.

Get this concept via the API

Resolve Crigler-Najjar syndrome, type I - and every code that maps to it - over HTTPS, against the current vocabulary release. No downloads, no local database.

curl "https://api.omophub.com/v1/concepts/4229773?include_relationships=true" \
  -H "Authorization: Bearer $OMOPHUB_API_KEY"
Get your free API key3,000 calls/month free · no credit card