OMOP Concept 45763567
Carnitine deficiency due to inborn error of metabolism
StandardConditionSNOMED55341000119107Disorder
Maps from
4
Descendants
0
Valid from
31 Jan 2015
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
4 source codes normalize to Carnitine deficiency due to inborn error of metabolism via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 113343 | Carnitine Deficiency due to Inborn Errors of Metabolism | Non-standard |
| ICD10CM | E71.42 | Carnitine deficiency due to inborn errors of metabolism | Non-standard |
| ICD9CM | 277.82 | Carnitine deficiency due to inborn errors of metabolism | Non-standard |
| Nebraska Lexicon | 55341000119107 | Carnitine deficiency due to inborn error of metabolism | Non-standard |
Synonyms
Alternative names recorded for Carnitine deficiency due to inborn error of metabolism across source vocabularies.
- Carnitine deficiency due to inborn error of metabolism (disorder)
- deficiencia de carnitina debida a error innato del metabolismo
- deficiencia de carnitina debida a error innato del metabolismo (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(19)Roll up to these when you need a wider cohort.
- 1Carnitine deficiency
- 1Disorder of fatty acid metabolism
- 2Amino acid deficiency
- 2Disorder of lipoprotein AND/OR lipid metabolism
- 2Disorder of organic acid metabolism
- 2Inborn error of metabolism
- 3Congenital disease
- 3Deficiency of micronutrients
- 3Disorder of amino acid metabolism
- 3Hereditary metabolic disease
- 3Metabolic disease
- 4Disease
- 4Disorder of fetus and/or newborn
- 4Hereditary disease
- 4Undernutrition
- 5Clinical finding
- 5Genetic disease
- 5Nutritional deficiency disorder
- 6Nutritional disorder
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