OMOP Concept 4229773
Crigler-Najjar syndrome, type I
StandardConditionSNOMED8933000Disorder
Maps from
3
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
3 source codes normalize to Crigler-Najjar syndrome, type I via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 143212 | Crigler-Najjar syndrome, type I | Non-standard |
| Nebraska Lexicon | 8933000 | Bilirubin glucuronosyltransferase deficiency | Non-standard |
| Read | C374000 | Crigler - Najjar syndrome | Non-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.
Broader concepts
(38)Roll up to these when you need a wider cohort.
- 1Autosomal recessive hereditary disorder
- 1Crigler-Najjar syndrome
- 1Digestive system hereditary disorder
- 1Disease of liver
- 1Disorder of digestive system specific to fetus OR newborn
- 2Autosomal hereditary disorder
- 2Disorder of digestive system
- 2Disorder of fetus and/or newborn
- 2Disorder of liver and/or biliary tract
- 2Enzymopathy
- 2Hereditary disorder by system
- 2Hyperbilirubinemia
- 2Inherited disorder of bilirubin metabolism
- 2Liver finding
- 2OMOP Acute Liver Failure 1
- 2OMOP Acute Liver Failure 2
- 2OMOP Acute Liver Failure 8
- 3Abdominal organ finding
- 3Digestive system finding
- 3Disease
- 3Disorder of abdomen
- 3Disorder of bilirubin metabolism
- 3Disorder of body system
- 3Disorder of digestive organ
- 3Hereditary disease
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