OMOP Concept 37110735
Congenital disorder of glycosylation type 1e
StandardConditionSNOMED725078006Disorder
Maps from
1
Descendants
0
Valid from
31 Jul 2017
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Congenital disorder of glycosylation type 1e via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C535743 | Congenital disorder of glycosylation type 1E | Non-standard |
Synonyms
Alternative names recorded for Congenital disorder of glycosylation type 1e across source vocabularies.
- Carbohydrate deficient glycoprotein syndrome type Ie
- Congenital disorder of glycosylation type 1e (disorder)
- Dolichol-phosphate-mannose synthase 1 deficiency
- DPM1-CDG - dolichyl-phosphate mannosyltransferase 1 catalytic subunit congenital disorder of glycosylation
- trastorno congénito de la glicosilación tipo 1e
- trastorno congénito de la glicosilación tipo 1e (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(14)Roll up to these when you need a wider cohort.
- 1Autosomal recessive hereditary disorder
- 1Carbohydrate-deficient glycoprotein syndrome type I
- 2Autosomal hereditary disorder
- 2Carbohydrate-deficient glycoprotein syndrome
- 3Disorder of glycoprotein metabolism
- 3Hereditary disease
- 4Genetic disease
- 4Inborn error of metabolism
- 5Congenital disease
- 5Disease
- 5Hereditary metabolic disease
- 6Clinical finding
- 6Fetal and/or neonatal disorder
- 6Metabolic disease
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