OMOP Concept 4174285
Carbohydrate-deficient glycoprotein syndrome type I
StandardConditionSNOMED277893002Disorder
Maps from
1
Descendants
27
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 Carbohydrate-deficient glycoprotein syndrome type I via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C535739 | Congenital disorder of glycosylation type 1A | Non-standard |
Synonyms
Alternative names recorded for Carbohydrate-deficient glycoprotein syndrome type I across source vocabularies.
- Carbohydrate-deficient glycoprotein syndrome type I (disorder)
- CDG - Carbohydrate-deficient glycoprotein syndrome type I
- síndrome de glucoproteína deficiente en carbohidratos, tipo I
- síndrome de glucoproteína deficiente en carbohidratos, tipo I (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
(27)Included automatically when you query with descendants.
- 1ALG12-congenital disorder of glycosylation
- 1ALG1 congenital disorder of glycosylation
- 1ALG3 congenital disorder of glycosylation
- 1ALG8 congenital disorder of glycosylation
- 1ALG9 congenital disorder of glycosylation
- 1CAD-CDG - carbamoyl-phosphate synthetase 2, aspartate transcarbamylase, and dihydroorotase congenital disorder of glycosylation
- 1Carbohydrate deficient glycoprotein syndrome type 1m
- 1Carbohydrate deficient glycoprotein syndrome type 1o
- 1Congenital disorder of glycosylation type 1c
- 1Congenital disorder of glycosylation type 1cc
- 1Congenital disorder of glycosylation type 1e
- 1Congenital disorder of glycosylation type 1f
- 1Congenital disorder of glycosylation type 1i
- 1Congenital disorder of glycosylation type 1j
- 1Congenital disorder of glycosylation type 1n
- 1Congenital disorder of glycosylation type 1p
- 1Congenital disorder of glycosylation type 1q
- 1Congenital disorder of glycosylation type 1r
- 1Congenital disorder of glycosylation type 1s
- 1Congenital disorder of glycosylation type 1w
- 1Congenital disorder of glycosylation type 1x
- 1Congenital disorder of glycosylation type 1y
- 1Congenital disorder of glycosylation type Ia
- 1Congenital muscular dystrophy with intellectual disability and severe epilepsy
- 1Congenital myasthenic syndrome with glycosylation defect due to ALG14 UDP-N-acetylglucosaminyltransferase subunit gene mutation
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