OMOP Concept 36717663
Carbohydrate deficient glycoprotein syndrome type 1m
StandardConditionSNOMED718712005Disorder
Maps from
2
Descendants
0
Valid from
31 Jan 2017
Valid to
31 Dec 2099
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Source codes that map to this concept
2 source codes normalize to Carbohydrate deficient glycoprotein syndrome type 1m via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C563666 | Congenital Disorder Of Glycosylation, Type Im | Non-standard |
| Nebraska Lexicon | 718712005 | Carbohydrate deficient glycoprotein syndrome type 1m | Non-standard |
Synonyms
Alternative names recorded for Carbohydrate deficient glycoprotein syndrome type 1m across source vocabularies.
- Carbohydrate deficient glycoprotein syndrome type 1m (disorder)
- Carbohydrate deficient glycoprotein syndrome type Im
- CDG1M - carbohydrate deficient glycoprotein syndrome type 1m
- síndrome de glicoproteínas deficientes en carbohidratos tipo 1m
- síndrome de glicoproteínas deficientes en carbohidratos tipo 1m (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
- 6Disorder of fetus and/or newborn
- 6Metabolic disease
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