OMOP Concept 608006
Fatty acid oxidation defect
StandardConditionSNOMED1156591005Disorder
Maps from
1
Descendants
21
Valid from
31 Jul 2021
Valid to
31 Dec 2099
OMOP concepts
Concept Lookup Tool
Search 11M+ concepts across SNOMED, RxNorm, ICD-10 & LOINC.
Source codes that map to this concept
1 source code normalizes to Fatty acid oxidation defect via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| ICD10CM | E71.318 | Other disorders of fatty-acid oxidation | Non-standard |
Synonyms
Alternative names recorded for Fatty acid oxidation defect across source vocabularies.
- defecto de oxidación de ácidos grasos
- defecto de oxidación de ácidos grasos (trastorno)
- FAOD - fatty acid oxidation defect
- Fatty acid oxidation defect (disorder)
- Fatty acid oxidation disorder
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 fatty acid metabolism
- 2Autosomal hereditary disorder
- 2Disorder of lipoprotein AND/OR lipid metabolism
- 2Disorder of organic acid metabolism
- 2Inborn error of metabolism
- 3Congenital disease
- 3Hereditary disease
- 3Hereditary metabolic disease
- 3Metabolic disease
- 4Disease
- 4Fetal and/or neonatal disorder
- 4Genetic disease
- 5Clinical finding
Narrower concepts
(21)Included automatically when you query with descendants.
- 1Acyl-CoA dehydrogenase deficiency
- 1Carnitine acylcarnitine translocase deficiency
- 1Carnitine palmitoyltransferase I deficiency
- 1Carnitine palmitoyltransferase II deficiency
- 1Deficiency of 3-hydroxyacyl-CoA dehydrogenase
- 1Hydroxymethylglutaric aciduria
- 1Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency
- 1Mitochondrial trifunctional protein deficiency
- 23-Ketoacyl-CoA triolase deficiency
- 2Combined long chain hydroxyacyl-CoA dehydrogenase deficiency
- 2Deficiency of enoyl-CoA hydratase
- 2Isolated long chain hydroxyacyl-CoA dehydrogenase deficiency
- 2Long chain acyl-CoA dehydrogenase deficiency
- 2Medium-chain acyl-coenzyme A dehydrogenase deficiency
- 2Myopathic form of carnitine palmitoyltransferase II deficiency
- 2Neonatal form of carnitine palmitoyltransferase II deficiency
- 2Severe infantile form of carnitine palmitoyltransferase II deficiency
- 2Short chain 3-hydroxyacyl-CoA dehydrogenase deficiency
- 2Short chain acyl-coenzyme A dehydrogenase deficiency
- 2Transient neonatal multiple acyl-coenzyme A dehydrogenase deficiency
- 2Very long chain acyl-CoA dehydrogenase deficiency
Get this concept via the API
Resolve Fatty acid oxidation defect - 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/608006?include_relationships=true" \
-H "Authorization: Bearer $OMOPHUB_API_KEY"Get your free API key3,000 calls/month free · no credit card