OMOP Concept 4262793
Aminoacidemia
StandardConditionSNOMED46556004Disorder
Maps from
1
Descendants
55
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
1 source code normalizes to Aminoacidemia via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 121661 | Aminoacidaemia | Non-standard |
Synonyms
Alternative names recorded for Aminoacidemia across source vocabularies.
- Aminoacidaemia
- aminoacidemia
- Aminoacidemia (disorder)
- aminoacidemia (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(8)Roll up to these when you need a wider cohort.
Narrower concepts
(55)Included automatically when you query with descendants.
- 1Citrullinemia
- 1Glutathionemia
- 1Hyperglycinemia
- 1Hyperhydroxyprolinemia
- 1Hyperleucine-isoleucinemia
- 1Hyperleucinemia
- 1Hyperlysinemia
- 1Hyperornithinemia
- 1Hyperphenylalaninemia
- 1Hyperprolinemia
- 1Hypertyrosinemia
- 1Hypervalinemia
- 1Pipecolic acidemia
- 2Citrin deficiency
- 2Citrullinemia, neonatal type
- 2Citrullinemia, subacute type
- 2Citrullinemia type I
- 2Hereditary hypertyrosinemia
- 2Hyperdicarboxylicaminoaciduria AND hyperprolinemia
- 2Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
- 2Hyperphenylalaninemia due to DNAJC12 deficiency
- 2Hyperprolinemia type 2
- 2Non-ketotic hyperglycinemia
- 2Periodic hyperlysinemia
- 2Periodic hyperlysinemia with hyperammonemia
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