OMOP Concept 37471173
COQ2-gene related coenzyme Q10 deficiency
StandardConditionSNOMED1366189009Disorder
Maps from
0
Descendants
0
Valid from
1 May 2025
Valid to
31 Dec 2099
OMOP concepts
Concept Lookup Tool
Search 11M+ concepts across SNOMED, RxNorm, ICD-10 & LOINC.
Synonyms
Alternative names recorded for COQ2-gene related coenzyme Q10 deficiency across source vocabularies.
- Coenzyme Q2, polyprenyltransferase gene related-coenzyme Q10 deficiency
- Coenzyme Q2, polyprenyltransferase gene related-coenzyme Q10 deficiency (disorder)
- COQ10D1- primary coenzyme Q10 deficiency-1
- deficiencia de coenzima Q10 relacionada con el gen COQ2
- deficiencia de coenzima Q10 relacionada con el gen de polipreniltransferasa de coenzima Q2
- deficiencia de coenzima Q10 relacionada con el gen de polipreniltransferasa de coenzima Q2 (trastorno)
- Primary coenzyme Q10 deficiency-1
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(15)Roll up to these when you need a wider cohort.
- 1Coenzyme Q10 deficiency
- 2Autosomal recessive hereditary disorder
- 2Disorder of mitochondrial respiratory chain complexes
- 2Mitochondrial cytopathy
- 3Autosomal hereditary disorder
- 3Disorder of pyruvate metabolism and mitochondrial respiratory chain
- 3Metabolic disease
- 4Disease
- 4Hereditary disease
- 4Inborn error of metabolism
- 5Clinical finding
- 5Congenital disease
- 5Genetic disease
- 5Hereditary metabolic disease
- 6Fetal and/or neonatal disorder
Get this concept via the API
Resolve COQ2-gene related coenzyme Q10 deficiency - and every code that maps to it - over HTTPS, against the current vocabulary release. No downloads, no local database.
curl "https://api.omophub.com/v1/concepts/37471173?include_relationships=true" \
-H "Authorization: Bearer $OMOPHUB_API_KEY"Get your free API key3,000 calls/month free · no credit card