OMOP Concept 4082810
Carbohydrate-deficient glycoprotein syndrome type II
StandardConditionSNOMED277894008Disorder
Maps from
2
Descendants
16
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
2 source codes normalize to Carbohydrate-deficient glycoprotein syndrome type II via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| HPO | HP_0003655 | Reduced level of N-acetylglucosaminyltransferase II | Non-standard |
| Nebraska Lexicon | 277894008 | CDG - Carbohydrate-deficient glycoprotein syndrome type II | Non-standard |
Synonyms
Alternative names recorded for Carbohydrate-deficient glycoprotein syndrome type II across source vocabularies.
- Carbohydrate-deficient glycoprotein syndrome type II (disorder)
- CDG - Carbohydrate-deficient glycoprotein syndrome type II
- N-Acetylglucosaminyl transferase II deficiency
- síndrome de glucoproteína deficiente en carbohidratos, tipo II
- síndrome de glucoproteína deficiente en carbohidratos, tipo II (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(11)Roll up to these when you need a wider cohort.
Narrower concepts
(16)Included automatically when you query with descendants.
- 1Carbohydrate deficient glycoprotein syndrome type 2a
- 1Carbohydrate deficient glycoprotein syndrome type 2d
- 1Carbohydrate deficient glycoprotein syndrome type 2k
- 1Carbohydrate deficient glycoprotein syndrome type II due to MAN1B1 deficiency
- 1CCDC115 congenital disorder of glycosylation
- 1COG1 congenital disorder of glycosylation
- 1COG2-related congenital disorder of glycosylation
- 1COG4 congenital disorder of glycosylation
- 1COG5 congenital disorder of glycosylation
- 1COG6-CGD - component of oligomeric golgi complex 6-congenital disorder of glycosylation
- 1COG7 congenital disorder of glycosylation
- 1COG8 congenital disorder of glycosylation
- 1Mannosyl-oligosaccharide glycosidase congenital disorder of glycosylation
- 1SLC39A8 congenital disorder of glycosylation
- 1Solute carrier family 35 member A2 congenital disorder of glycosylation
- 1TMEM199 congenital disorder of glycosylation
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