OMOP Concept 4142467
Combined long chain hydroxyacyl-CoA dehydrogenase deficiency
StandardConditionSNOMED307128009Disorder
Maps from
1
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Combined long chain hydroxyacyl-CoA dehydrogenase deficiency via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 307128009 | Combined long chain hydroxyacyl-coenzyme A dehydrogenase deficiency | Non-standard |
Synonyms
Alternative names recorded for Combined long chain hydroxyacyl-CoA dehydrogenase deficiency across source vocabularies.
- Combined long chain hydroxyacyl-coenzyme A dehydrogenase deficiency
- Combined long chain hydroxyacyl-coenzyme A dehydrogenase deficiency (disorder)
- deficiencia combinada de hidroxiacil-CoA deshidrogenasa de cadena larga
- deficiencia combinada de hidroxiacil-CoA deshidrogenasa de cadena larga (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(16)Roll up to these when you need a wider cohort.
- 1Mitochondrial trifunctional protein deficiency
- 2Fatty acid oxidation defect
- 3Autosomal recessive hereditary disorder
- 3Disorder of fatty acid metabolism
- 4Autosomal hereditary disorder
- 4Disorder of lipoprotein AND/OR lipid metabolism
- 4Disorder of organic acid metabolism
- 4Inborn error of metabolism
- 5Congenital disease
- 5Hereditary disease
- 5Hereditary metabolic disease
- 5Metabolic disease
- 6Disease
- 6Disorder of fetus and/or newborn
- 6Genetic disease
- 7Clinical finding
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