OMOP Concept 36717745
2p15p16.1 microdeletion syndrome
StandardConditionSNOMED719651000Disorder
Maps from
0
Descendants
0
Valid from
31 Jan 2017
Valid to
31 Dec 2099
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Synonyms
Alternative names recorded for 2p15p16.1 microdeletion syndrome across source vocabularies.
- 2p15p16.1 microdeletion syndrome (disorder)
- monosomía 2p15p16.1
- Monosomy 2p15p16.1
- síndrome de microdeleción 2p15p16.1
- síndrome de microdeleción 2p15p16.1 (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(24)Roll up to these when you need a wider cohort.
- 1Deletion of part of short arm of chromosome 2
- 1Multiple malformation syndrome with facial defects as major feature
- 2Congenital anomaly of face
- 2Deletion of part of chromosome 2
- 2Multiple system malformation syndrome
- 3Anomaly of chromosome pair 2
- 3Congenital anomaly of head
- 3Congenital malformation syndrome
- 3Deletion of part of autosome
- 3Disorder of face
- 4Anomaly of chromosome pair
- 4Congenital malformation
- 4Disorder of head
- 4Finding of face
- 4Monosomy and deletion from autosome
- 5Congenital chromosomal disease
- 5Congenital disease
- 5Developmental disorder
- 5Disease
- 5Finding of head region
- 5Head finding
- 6Chromosomal disorder
- 6Clinical finding
- 6Fetal and/or neonatal disorder
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