OMOP Concept 4178536
Generalized uridine diphosphate galactose-4-epimerase deficiency
StandardConditionSNOMED297237003Disorder
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 Generalized uridine diphosphate galactose-4-epimerase deficiency via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 297237003 | Generalised uridine diphosphate galactose-4-epimerase deficiency | Non-standard |
Synonyms
Alternative names recorded for Generalized uridine diphosphate galactose-4-epimerase deficiency across source vocabularies.
- deficiencia generalizada de uridina difosfato galactosa-4-epimerasa
- deficiencia generalizada de uridina difosfato galactosa-4-epimerasa (trastorno)
- Generalised uridine diphosphate galactose-4-epimerase deficiency
- Generalized uridine diphosphate galactose-4-epimerase deficiency (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(13)Roll up to these when you need a wider cohort.
- 1Galactose epimerase deficiency
- 2Autosomal recessive hereditary disorder
- 2Galactosemia
- 2Specific enzyme deficiency
- 3Autosomal hereditary disorder
- 3Disorder of galactose metabolism
- 3Enzymopathy
- 4Disorder of carbohydrate metabolism
- 4Hereditary disease
- 4Metabolic disease
- 5Disease
- 5Genetic disease
- 6Clinical finding
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