OMOP Concept 36714440
6p22 microdeletion syndrome
StandardConditionSNOMED719662000Disorder
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 6p22 microdeletion syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 719662000 | 6p22 microdeletion syndrome | Non-standard |
Synonyms
Alternative names recorded for 6p22 microdeletion syndrome across source vocabularies.
- 6p22 microdeletion syndrome (disorder)
- monosomía 6p22
- Monosomy 6p22
- síndrome de microdeleción 6p22
- síndrome de microdeleción 6p22 (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(16)Roll up to these when you need a wider cohort.
- 1Deletion of part of short arm of chromosome 6
- 1Multiple system malformation syndrome
- 2Congenital malformation syndrome
- 2Deletion of part of chromosome 6
- 3Anomaly of chromosome pair 6
- 3Congenital malformation
- 3Deletion of part of autosome
- 4Anomaly of chromosome pair
- 4Congenital disease
- 4Developmental disorder
- 4Monosomy and deletion from autosome
- 5Congenital chromosomal disease
- 5Disease
- 5Disorder of fetus and/or newborn
- 6Chromosomal disorder
- 6Clinical finding
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