OMOP Concept 4238192
Anomaly of chromosome pair 5
StandardConditionSNOMED57361003Disorder
Maps from
2
Descendants
24
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 Anomaly of chromosome pair 5 via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 121588 | Anomaly of chromosome pair 5 | Non-standard |
| Nebraska Lexicon | 57361003 | Anomaly of chromosome pair 5 | Non-standard |
Synonyms
Alternative names recorded for Anomaly of chromosome pair 5 across source vocabularies.
- anomalía del par de cromosomas 5
- anomalía del par de cromosomas 5 (trastorno)
- Anomaly of chromosome pair 5 (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(7)Roll up to these when you need a wider cohort.
Narrower concepts
(24)Included automatically when you query with descendants.
- 1Deletion of part of chromosome 5
- 1Mosaic trisomy 5 syndrome
- 1Partial trisomy of chromosome 5
- 1Paternal uniparental disomy of chromosome 5
- 1Ring chromosome 5 syndrome
- 1Tetrasomy 5p mosaicism
- 1Tetrasomy 5p syndrome
- 25p partial trisomy
- 2Deletion of part of long arm of chromosome 5
- 2Partial deletion of short arm of chromosome 5
- 2Partial trisomy of long arm of chromosome 5
- 35p13 microduplication syndrome
- 35p partial monosomy syndrome
- 35q14.3 microdeletion syndrome
- 35q22.2 deletion syndrome
- 35q31.3 microdeletion syndrome
- 35q35 microduplication syndrome
- 3Deletion 5q35
- 3Distal trisomy 5q syndrome
- 3Joint contractures, developmental delay, Pierre Robin syndrome
- 3Medial deletion of long arm of chromosome 5
- 3Medial duplication of long arm of chromosome 5
- 3Proximal deletion of long arm of chromosome 5
- 3Proximal duplication of long arm of chromosome 5
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