OMOP Concept 35623151
Ring chromosome 19 syndrome
StandardConditionSNOMED765484001Disorder
Maps from
1
Descendants
0
Valid from
31 Jul 2018
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
1 source code normalizes to Ring chromosome 19 syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 765484001 | Ring chromosome 19 syndrome | Non-standard |
Synonyms
Alternative names recorded for Ring chromosome 19 syndrome across source vocabularies.
- Ring chromosome 19
- Ring chromosome 19 syndrome (disorder)
- síndrome de cromosoma 19 en anillo
- síndrome de cromosoma 19 en anillo (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(13)Roll up to these when you need a wider cohort.
- 1Anomaly of chromosome pair 19
- 1Multiple system malformation syndrome
- 1Ring chromosome
- 2Anomaly of chromosome pair
- 2Congenital chromosomal disease
- 2Congenital malformation syndrome
- 3Chromosomal disorder
- 3Congenital disease
- 3Congenital malformation
- 4Developmental disorder
- 4Disease
- 4Disorder of fetus and/or newborn
- 5Clinical finding
Get this concept via the API
Resolve Ring chromosome 19 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/35623151?include_relationships=true" \
-H "Authorization: Bearer $OMOPHUB_API_KEY"Get your free API key3,000 calls/month free · no credit card