OMOP Concept 4174285
Carbohydrate-deficient glycoprotein syndrome type I
StandardConditionSNOMED277893002Disorder
Maps from
2
Descendants
25
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
Concept Lookup Tool
Search 11M+ concepts across SNOMED, RxNorm, ICD-10 & LOINC.
Source codes that map to this concept
2 source codes normalize 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 |
| Nebraska Lexicon | 277893002 | CDG - Carbohydrate-deficient glycoprotein syndrome type I | 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
(25)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 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
- 1Mannosephosphate isomerase congenital disorder of glycosylation
- 1PGM1-related congenital disorder of glycosylation
Get this concept via the API
Resolve Carbohydrate-deficient glycoprotein syndrome type I - and every code that maps to it - over HTTPS, against the current vocabulary release. No downloads, no local database.
curl "https://api.omophub.com/v1/concepts/4174285?include_relationships=true" \
-H "Authorization: Bearer $OMOPHUB_API_KEY"Get your free API key3,000 calls/month free · no credit card