OMOP Concept 4148287
Citrullinemia, neonatal type
StandardConditionSNOMED30529005Disorder
Maps from
1
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Citrullinemia, neonatal type via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 145086 | Citrullinaemia, neonatal type | Non-standard |
Synonyms
Alternative names recorded for Citrullinemia, neonatal type across source vocabularies.
- citrulinemia, tipo neonatal
- citrulinemia, tipo neonatal (trastorno)
- Citrullinaemia, neonatal type
- Citrullinemia, neonatal type (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(21)Roll up to these when you need a wider cohort.
- 1Citrullinemia
- 1Neonatal metabolic disorder
- 2Aminoacidemia
- 2Autosomal recessive hereditary disorder
- 2Disorder of the urea cycle metabolism
- 2Enzymopathy
- 2Hereditary metabolic disease
- 2Metabolic disease
- 2Neonatal disorder
- 3Acidemia
- 3Autosomal hereditary disorder
- 3Disease
- 3Disorder of amino acid and organic acid metabolism
- 3Fetal and/or neonatal disorder
- 3Hereditary disease
- 3Neonatal finding
- 4Clinical finding
- 4Disorder of acid-base balance
- 4Disorder of amino acid metabolism
- 4Genetic disease
- 5Disorder of organic acid metabolism
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