OMOP Concept 4070569
Anomaly of chromosome pair 13
StandardConditionSNOMED17760001Disorder
Maps from
2
Descendants
25
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 13 via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 148678 | Anomaly of chromosome pair 13 | Non-standard |
| Nebraska Lexicon | 17760001 | Anomaly of chromosome pair 13 | Non-standard |
Synonyms
Alternative names recorded for Anomaly of chromosome pair 13 across source vocabularies.
- anomalía del par de cromosomas 13
- anomalía del par de cromosomas 13 (trastorno)
- Anomaly of chromosome pair 13 (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
(25)Included automatically when you query with descendants.
- 1Complete trisomy 13 syndrome
- 1Deletion of part of chromosome 13
- 1Maternal uniparental disomy of chromosome 13
- 1Partial trisomy 13 in Patau's syndrome
- 1Partial trisomy of chromosome 13
- 1Paternal uniparental disomy of chromosome 13
- 1Ring chromosome 13 syndrome
- 213p partial trisomy syndrome
- 213q partial trisomy syndrome
- 2Deletion of long arm of chromosome 13
- 2Distal deletion of chromosome 13
- 2Distal duplication of chromosome 13
- 2Medial deletion of chromosome 13
- 2Medial duplication of chromosome 13
- 2Proximal deletion of chromosome 13
- 2Proximal duplication of chromosome 13
- 2Trisomy 13, meiotic nondisjunction
- 2Trisomy 13 - mitotic nondisjunction mosaicism
- 313q12.3 microdeletion syndrome
- 313q partial monosomy syndrome
- 3Distal monosomy 13q syndrome
- 3Distal trisomy 13q
- 3Monosomy 13q14 syndrome
- 3Monosomy 13q34 syndrome
- 3Non-distal trisomy 13q
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