OMOP Concept 36714441
6q25 microdeletion syndrome
StandardConditionSNOMED719663005Disorder
Maps from
1
Descendants
0
Valid from
31 Jan 2017
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to 6q25 microdeletion syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 719663005 | 6q25 microdeletion syndrome | Non-standard |
Synonyms
Alternative names recorded for 6q25 microdeletion syndrome across source vocabularies.
- 6q25 microdeletion syndrome (disorder)
- monosomía 6q25
- Monosomy 6q25
- síndrome de microdeleción 6q25
- síndrome de microdeleción 6q25 (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(12)Roll up to these when you need a wider cohort.
- 1Deletion of part of long arm of chromosome 6
- 2Deletion of part of chromosome 6
- 3Anomaly of chromosome pair 6
- 3Deletion of part of autosome
- 4Anomaly of chromosome pair
- 4Monosomy and deletion from autosome
- 5Congenital chromosomal disease
- 6Chromosomal disorder
- 6Congenital disease
- 7Disease
- 7Disorder of fetus and/or newborn
- 8Clinical finding
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