OMOP Concept 4031805
Succinyl-CoA acetoacetate transferase deficiency
StandardConditionSNOMED238004006Disorder
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 Succinyl-CoA acetoacetate transferase deficiency via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C537527 | Succinyl-CoA:3-oxoacid CoA transferase deficiency | Non-standard |
| Nebraska Lexicon | 238004006 | Thioacyl transferase deficiency | Non-standard |
Synonyms
Alternative names recorded for Succinyl-CoA acetoacetate transferase deficiency across source vocabularies.
- 3-Ketoacid CoA transferase deficiency
- deficiencia de succinil-CoA acetoacetato transferasa
- deficiencia de succinil-CoA acetoacetato transferasa (trastorno)
- Succinyl-CoA 3-ketoacid transferase deficiency
- Succinyl-coenzyme A acetoacetate transferase deficiency
- Succinyl-coenzyme A acetoacetate transferase deficiency (disorder)
- Thioacyl transferase deficiency
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.
- 1Disorder of fatty acid metabolism
- 2Disorder of lipoprotein AND/OR lipid metabolism
- 2Disorder of organic acid metabolism
- 2Inborn error of metabolism
- 3Congenital disease
- 3Hereditary metabolic disease
- 3Metabolic disease
- 4Disease
- 4Disorder of fetus and/or newborn
- 4Hereditary disease
- 5Clinical finding
- 5Genetic disease
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