OMOP Concept 435233
Disorder of fatty acid metabolism
StandardConditionSNOMED39929009Disorder
Maps from
17
Descendants
39
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
17 source codes normalize to Disorder of fatty acid metabolism via the OMOP "Maps to" relationship.
Synonyms
Alternative names recorded for Disorder of fatty acid metabolism across source vocabularies.
- Disorder of fat oxidation
- Disorder of fatty acid metabolism (disorder)
- Disorders of fatty-acid metabolism
- trastorno del metabolismo de los ácidos grasos
- trastorno del metabolismo de los ácidos grasos (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(11)Roll up to these when you need a wider cohort.
Narrower concepts
(39)Included automatically when you query with descendants.
- 13-hydroxy-3-methylglutaryl-coenzyme A synthase deficiency
- 1Carnitine deficiency due to inborn error of metabolism
- 1Carnitine palmitoyltransferase deficiency
- 1Combined deficiency of long chain 3-hydroxyacyl-CoA dehydrogenase and enoyl-CoA hydratase
- 1Combined malonic and methylmalonic aciduria
- 1Deficiency of 2,4-dienoyl-CoA reductase
- 1Deficiency of carnitine acetyltransferase
- 1Fatty acid oxidation defect
- 1Glutaric aciduria, type 2
- 1HSMN IV
- 1Long-chain fatty acid transport deficiency
- 1Malonic aciduria
- 1Succinyl-CoA acetoacetate transferase deficiency
- 2Acyl-CoA dehydrogenase deficiency
- 2Alpha chain electron transfer flavoprotein deficiency
- 2Ataxia co-occurrent and due to phytanic acid storage disease
- 2Beta chain electron transfer flavoprotein deficiency
- 2Carnitine acylcarnitine translocase deficiency
- 2Carnitine palmitoyltransferase I deficiency
- 2Carnitine palmitoyltransferase II deficiency
- 2Deficiency of 3-hydroxyacyl-CoA dehydrogenase
- 2Electron transfer flavoprotein-ubiquinone oxidoreductase deficiency
- 2Epsilon-N-trimethyllysine hydroxylase carnitine deficiency disorder
- 2Hydroxymethylglutaric aciduria
- 2Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency
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