OMOP Concept 4035284
Succinate-coenzyme Q reductase deficiency
StandardConditionSNOMED237989003Disorder
Maps from
2
Descendants
2
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
2 source codes normalize to Succinate-coenzyme Q reductase deficiency via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C565375 | Mitochondrial Complex II Deficiency | Non-standard |
| Nebraska Lexicon | 237989003 | Succinate-coenzyme Q reductase deficiency | Non-standard |
Synonyms
Alternative names recorded for Succinate-coenzyme Q reductase deficiency across source vocabularies.
- Complex II deficiency
- deficiencia de la succinato-coenzima Q reductasa
- deficiencia de la succinato-coenzima Q reductasa (trastorno)
- Succinate-coenzyme Q reductase deficiency (disorder)
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.
- 1Deficiency in enzyme complexes of mitochondrial respiratory chain
- 2Disorder of mitochondrial respiratory chain complexes
- 2Enzymopathy
- 3Disorder of pyruvate metabolism and mitochondrial respiratory chain
- 3Metabolic disease
- 4Disease
- 4Inborn error of metabolism
- 5Clinical finding
- 5Congenital disease
- 5Hereditary metabolic disease
- 6Disorder of fetus and/or newborn
- 6Hereditary disease
- 7Genetic disease
Narrower concepts
(2)Included automatically when you query with descendants.
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