OMOP Concept 4029255
Glutaryl-CoA oxidase deficiency
StandardConditionSNOMED238070003Disorder
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 Glutaryl-CoA oxidase deficiency via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C562818 | Glutaric Aciduria III | Non-standard |
| Nebraska Lexicon | 238070003 | Glutaryl-coenzyme A oxidase deficiency | Non-standard |
Synonyms
Alternative names recorded for Glutaryl-CoA oxidase deficiency across source vocabularies.
- acidemia glutárica tipo 3
- aciduria glutárica tipo 3
- deficiencia de glutaril-CoA oxidasa
- deficiencia de glutaril coenzima A oxidasa
- deficiencia de glutaril coenzima A oxidasa asociada al gen SUGCT
- deficiencia de glutaril coenzima A oxidasa (trastorno)
- Glutaric acidaemia type 3
- Glutaric acidemia type 3
- Glutaric aciduria type 3
- Glutaryl-coenzyme A oxidase deficiency
- Glutaryl-coenzyme A oxidase deficiency (disorder)
- SUGCT-gene related glutaryl-coenzyme A oxidase deficiency
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(13)Roll up to these when you need a wider cohort.
- 1Autosomal recessive hereditary disorder
- 1Loss of single peroxisomal function
- 2Autosomal hereditary disorder
- 2Disorder of peroxisomal function
- 3Hereditary disease
- 3Inborn error of metabolism
- 4Congenital disease
- 4Genetic disease
- 4Hereditary metabolic disease
- 5Disease
- 5Disorder of fetus and/or newborn
- 5Metabolic disease
- 6Clinical finding
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