OMOP Concept 37110348
Coenzyme Q10 deficiency
StandardConditionSNOMED724575009Disorder
Maps from
1
Descendants
3
Valid from
31 Jul 2017
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Coenzyme Q10 deficiency via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C564403 | Coenzyme Q10 Deficiency | Non-standard |
Synonyms
Alternative names recorded for Coenzyme Q10 deficiency across source vocabularies.
- Coenzyme Q10 deficiency (disorder)
- deficiencia de coenzima Q10
- deficiencia de coenzima Q10 (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(14)Roll up to these when you need a wider cohort.
- 1Autosomal recessive hereditary disorder
- 1Disorder of mitochondrial respiratory chain complexes
- 1Mitochondrial cytopathy
- 2Autosomal hereditary disorder
- 2Disorder of pyruvate metabolism and mitochondrial respiratory chain
- 2Metabolic disease
- 3Disease
- 3Hereditary disease
- 3Inborn error of metabolism
- 4Clinical finding
- 4Congenital disease
- 4Genetic disease
- 4Hereditary metabolic disease
- 5Fetal and/or neonatal disorder
Narrower concepts
(3)Included automatically when you query with descendants.
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