OMOP Concept 4197283
Anomaly of chromosome pair 9
StandardConditionSNOMED5051002Disorder
Maps from
1
Descendants
31
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Anomaly of chromosome pair 9 via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 148663 | Anomaly of chromosome pair 9 | Non-standard |
Synonyms
Alternative names recorded for Anomaly of chromosome pair 9 across source vocabularies.
- anomalía del par de cromosomas 9
- anomalía del par de cromosomas 9 (trastorno)
- Anomaly of chromosome pair 9 (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
(31)Included automatically when you query with descendants.
- 1Deletion of part of chromosome 9
- 1Maternal uniparental disomy of chromosome 9
- 1Partial tetrasomy of chromosome 9
- 1Ring chromosome 9 syndrome
- 1Trisomy 9
- 29p13 microdeletion syndrome
- 29q partial monosomy syndrome
- 2Complete trisomy 9 syndrome
- 2Distal monosomy 9p syndrome
- 2Monosomy 9p
- 2Mosaic trisomy 9 syndrome
- 2Partial trisomy of chromosome 9
- 2Proximal deletion of short arm of chromosome 9
- 2Tetrasomy of short arm of chromosome 9
- 39p24.3 deletion syndrome
- 39p partial trisomy syndrome
- 39q21.13 microdeletion syndrome
- 39q31.1q31.3 microdeletion syndrome
- 39q33.3q34.11 microdeletion syndrome
- 39q34 deletion syndrome
- 39q partial trisomy syndrome
- 3Distal deletion of long arm of chromosome 9
- 3Medial deletion of long arm of chromosome 9
- 3Monosomy 9q22.3 syndrome
- 3Proximal deletion of long arm of chromosome 9
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