OMOP Concept 4241701
Hyperlysinemia
StandardConditionSNOMED58558003Disorder
Maps from
5
Descendants
3
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
5 source codes normalize to Hyperlysinemia via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 138265 | Hyperlysinaemia | Non-standard |
| HPO | HP_0002161 | Hyperlysinemia | Non-standard |
| MeSH | D020167 | Hyperlysinemias | Non-standard |
| Nebraska Lexicon | 58558003 | Alpha-aminoadipic semialdehyde deficiency | Non-standard |
| Read | C307400 | Hyperlysinaemia | Non-standard |
Synonyms
Alternative names recorded for Hyperlysinemia across source vocabularies.
- Alpha-aminoadipic semialdehyde deficiency
- hiperlisinemia
- hiperlisinemia (trastorno)
- Hyperlysinaemia
- Hyperlysinemia (disorder)
- Saccharopine dehydrogenase deficiency
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(11)Roll up to these when you need a wider cohort.
- 1Aminoacidemia
- 1Disorder of lysine and hydroxylysine metabolism
- 2Acidemia
- 2Disorder of amino acid and organic acid metabolism
- 2Disorder of lysine AND/OR hydroxylysine metabolism
- 3Disorder of acid-base balance
- 3Disorder of amino acid metabolism
- 4Disorder of organic acid metabolism
- 4Metabolic disease
- 5Disease
- 6Clinical finding
Narrower concepts
(3)Included automatically when you query with descendants.
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