OMOP Concept 4278079
Persistent hyperlysinemia
StandardConditionSNOMED66002008Disorder
Maps from
2
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
2 source codes normalize to Persistent hyperlysinemia via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 130360 | Persistent Hyperlysinemia | Non-standard |
| Nebraska Lexicon | 66002008 | Persistent hyperlysinaemia without hyperammonaemia | Non-standard |
Synonyms
Alternative names recorded for Persistent hyperlysinemia across source vocabularies.
- hiperlisinemia persistente
- hiperlisinemia persistente sin hiperamonemia
- hiperlisinemia persistente (trastorno)
- Persistent hyperlysinaemia
- Persistent hyperlysinaemia without hyperammonaemia
- Persistent hyperlysinemia (disorder)
- Persistent hyperlysinemia without hyperammonemia
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(12)Roll up to these when you need a wider cohort.
- 1Hyperlysinemia
- 2Aminoacidemia
- 2Disorder of lysine and hydroxylysine metabolism
- 3Acidemia
- 3Disorder of amino acid and organic acid metabolism
- 3Disorder of lysine AND/OR hydroxylysine metabolism
- 4Disorder of acid-base balance
- 4Disorder of amino acid metabolism
- 5Disorder of organic acid metabolism
- 5Metabolic disease
- 6Disease
- 7Clinical finding
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