OMOP Concept 4263859
Anomaly of chromosome pair 11
StandardConditionSNOMED60891003Disorder
Maps from
1
Descendants
21
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
1 source code normalizes to Anomaly of chromosome pair 11 via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 148680 | Anomaly of chromosome pair 11 | Non-standard |
Synonyms
Alternative names recorded for Anomaly of chromosome pair 11 across source vocabularies.
- anomalía del par de cromosomas 11
- anomalía del par de cromosomas 11 (trastorno)
- Anomaly of chromosome pair 11 (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
(21)Included automatically when you query with descendants.
- 1Deletion of part of chromosome 11
- 1Maternal uniparental disomy of chromosome 11
- 1Partial trisomy of chromosome 11
- 1Paternal uniparental disomy of chromosome 11
- 1Ring chromosome 11 syndrome
- 1Tetrasomy 11q24.1
- 211p15.4 microduplication syndrome
- 211p partial monosomy syndrome
- 211p partial trisomy syndrome
- 211q partial monosomy syndrome
- 211q partial trisomy syndrome
- 2Jacobsen syndrome
- 2Oculootodental syndrome
- 311p15 deletion syndrome
- 311p15 duplication syndrome
- 311q22.2q22.3 microdeletion syndrome
- 3Distal trisomy 11q
- 3Potocki-Shaffer syndrome
- 3Proximal deletion of long arm of chromosome 11
- 3Proximal duplication of long arm of chromosome 11
- 3WAGR syndrome
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