OMOP Concept 37161040
Multiple carboxylase deficiency
StandardConditionSNOMED1172966001Disorder
Maps from
2
Descendants
2
Valid from
30 Sept 2021
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
2 source codes normalize to Multiple carboxylase deficiency via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| ICD10CM | D81.818 | Other biotin-dependent carboxylase deficiency | Non-standard |
| MeSH | D009100 | Multiple Carboxylase Deficiency | Non-standard |
Synonyms
Alternative names recorded for Multiple carboxylase deficiency across source vocabularies.
- deficiencia múltiple de carboxilasa
- deficiencia múltiple de carboxilasa (trastorno)
- Multiple carboxylase deficiency (disorder)
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.
- 1Autosomal recessive hereditary disorder
- 1Disorder of amino acid and organic acid metabolism
- 1Inborn error of metabolism
- 1Specific enzyme deficiency
- 2Autosomal hereditary disorder
- 2Congenital disease
- 2Disorder of amino acid metabolism
- 2Enzymopathy
- 2Hereditary metabolic disease
- 3Disorder of organic acid metabolism
- 3Fetal and/or neonatal disorder
- 3Hereditary disease
- 3Metabolic disease
- 4Disease
- 4Genetic disease
- 5Clinical finding
Narrower concepts
(2)Included automatically when you query with descendants.
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