OMOP Concept 4188465
Ring chromosome 1 syndrome
StandardConditionSNOMED47017007Disorder
Maps from
2
Descendants
0
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 Ring chromosome 1 syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 127358 | Ring Chromosome 1 Syndrome | Non-standard |
| Nebraska Lexicon | 47017007 | Ring chromosome 1 syndrome | Non-standard |
Synonyms
Alternative names recorded for Ring chromosome 1 syndrome across source vocabularies.
- Ring chromosome 1 syndrome (disorder)
- síndrome de cromosoma en anillo 1
- síndrome de cromosoma en anillo 1 (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 1
- 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
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