OMOP Concept 45765423
Chromosome 2q37 deletion syndrome
StandardConditionSNOMED702357000Disorder
Maps from
2
Descendants
0
Valid from
31 Jul 2014
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 Chromosome 2q37 deletion syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C538317 | Chromosome 2q37 deletion syndrome | Non-standard |
| Nebraska Lexicon | 702357000 | Albright hereditary osteodystrophy-like syndrome | Non-standard |
Synonyms
Alternative names recorded for Chromosome 2q37 deletion syndrome across source vocabularies.
- 2q37 deletion syndrome
- Albright hereditary osteodystrophy-like syndrome
- Brachydactyly mental retardation syndrome
- Chromosome 2q37 deletion syndrome (disorder)
- síndrome de braquidactilia y retardo mental
- síndrome de deleción cromosómica 2q37
- síndrome de deleción cromosómica 2q37 (trastorno)
- síndrome similar a la osteodistrofia hereditaria de Albright
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.
- 1Congenital malformation
- 1Deletion of part of long arm of chromosome 2
- 2Congenital disease
- 2Deletion of part of chromosome 2
- 2Developmental disorder
- 3Anomaly of chromosome pair 2
- 3Deletion of part of autosome
- 3Disease
- 3Disorder of fetus and/or newborn
- 4Anomaly of chromosome pair
- 4Clinical finding
- 4Monosomy and deletion from autosome
- 5Congenital chromosomal disease
- 6Chromosomal disorder
Get this concept via the API
Resolve Chromosome 2q37 deletion syndrome - 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/45765423?include_relationships=true" \
-H "Authorization: Bearer $OMOPHUB_API_KEY"Get your free API key3,000 calls/month free · no credit card