OMOP Concept 4151846
Crigler-Najjar syndrome
StandardConditionSNOMED28259009Disorder
Maps from
11
Descendants
2
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
11 source codes normalize to Crigler-Najjar syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 143213 | Crigler-Najjar syndrome | Non-standard |
| CIM10 | E80.5 | Crigler-Najjar syndrome | Non-standard |
| ICD10 | E80.5 | Crigler-Najjar syndrome | Non-standard |
| ICD10CM | E80.5 | Crigler-Najjar syndrome | Non-standard |
| ICD10CN | E80.5 | Crigler-Najjar syndrome | Non-standard |
| ICD10CN | E80.500 | Crigler-Najjar syndrome | Non-standard |
| ICD10CN | E80.501 | Glucuronidase deficiency (machine translation) | Non-standard |
| ICD10GM | E80.5 | Crigler-Najjar syndrome | Non-standard |
| KCD7 | E80.5 | Crigler-Najjar syndrome | Non-standard |
| MeSH | D003414 | Crigler-Najjar Syndrome | Non-standard |
| Nebraska Lexicon | 28259009 | Crigler-Najjar syndrome | Non-standard |
Synonyms
Alternative names recorded for Crigler-Najjar syndrome across source vocabularies.
- Crigler-Najjar syndrome (disorder)
- síndrome de Crigler - Najjar
- síndrome de Crigler - Najjar (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(15)Roll up to these when you need a wider cohort.
- 1Autosomal hereditary disorder
- 1Enzymopathy
- 1Hyperbilirubinemia
- 1Inherited disorder of bilirubin metabolism
- 2Disorder of bilirubin metabolism
- 2Hereditary disease
- 2Inborn error of metabolism
- 2Metabolic disease
- 3Congenital disease
- 3Disease
- 3Disorder of porphyrin metabolism
- 3Genetic disease
- 3Hereditary metabolic disease
- 4Clinical finding
- 4Disorder of fetus and/or newborn
Narrower concepts
(2)Included automatically when you query with descendants.
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