OMOP Concept 4223372
Trehalase deficiency
StandardConditionSNOMED84193000Disorder
Maps from
3
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
3 source codes normalize to Trehalase deficiency via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 149052 | Alpha, alpha-trehalase deficiency | Non-standard |
| MeSH | C562603 | Trehalase Deficiency | Non-standard |
| Nebraska Lexicon | 84193000 | Alpha, alpha-trehalase deficiency | Non-standard |
Synonyms
Alternative names recorded for Trehalase deficiency across source vocabularies.
- Alpha, alpha-trehalase deficiency
- deficiencia de alfa, alfa - trehalasa
- deficiencia de trehalasa
- deficiencia de trehalasa (trastorno)
- intolerancia a la trehalosa
- Trehalase deficiency (disorder)
- Trehalose intolerance
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(15)Roll up to these when you need a wider cohort.
- 1Autosomal hereditary disorder
- 1Disorder of carbohydrate absorption
- 1Disorder of carbohydrate transport
- 1Inborn error of metabolism
- 1Specific enzyme deficiency
- 2Congenital disease
- 2Disorder of carbohydrate metabolism
- 2Enzymopathy
- 2Hereditary disease
- 2Hereditary metabolic disease
- 3Disorder of fetus and/or newborn
- 3Genetic disease
- 3Metabolic disease
- 4Disease
- 5Clinical finding
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