OMOP Concept 4239041
Crigler-Najjar syndrome, type II
StandardConditionSNOMED68067009Disorder
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 II via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 119764 | Crigler-Najjar syndrome, type II | Non-standard |
| MeSH | C536213 | Crigler Najjar syndrome, type 2 | Non-standard |
| Nebraska Lexicon | 68067009 | Arias syndrome | Non-standard |
Synonyms
Alternative names recorded for Crigler-Najjar syndrome, type II across source vocabularies.
- Arias syndrome
- Crigler-Najjar syndrome type II
- Crigler-Najjar syndrome, type II (disorder)
- Crigler - Najjar tipo 2
- Crigler-Najjar type 2
- síndrome de Arias
- síndrome de Crigler - Najjar, tipo II
- síndrome de Crigler - Najjar, tipo II (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(16)Roll up to these when you need a wider cohort.
- 1Crigler-Najjar syndrome
- 2Autosomal hereditary disorder
- 2Enzymopathy
- 2Hyperbilirubinemia
- 2Inherited disorder of bilirubin metabolism
- 3Disorder of bilirubin metabolism
- 3Hereditary disease
- 3Inborn error of metabolism
- 3Metabolic disease
- 4Congenital disease
- 4Disease
- 4Disorder of porphyrin metabolism
- 4Genetic disease
- 4Hereditary metabolic disease
- 5Clinical finding
- 5Disorder of fetus and/or newborn
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