OMOP Concept 36717093
19q13.11 microdeletion syndrome
StandardConditionSNOMED719599008Disorder
Maps from
0
Descendants
0
Valid from
31 Jan 2017
Valid to
31 Dec 2099
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Synonyms
Alternative names recorded for 19q13.11 microdeletion syndrome across source vocabularies.
- 19q13.11 microdeletion syndrome (disorder)
- monosomía 19p13.11
- Monosomy 19q13.11
- síndrome de microdeleción 19p13.11
- síndrome de microdeleción 19p13.11 (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(23)Roll up to these when you need a wider cohort.
- 1Deletion of long arm of chromosome 19
- 1Intellectual disability
- 2Abnormal behavior
- 2Deletion of part of chromosome 19
- 2Impaired cognition
- 2Intellectual ability - finding
- 2Neurodevelopmental disorder
- 3Anomaly of chromosome pair 19
- 3Behavior finding
- 3Cognitive function finding
- 3Deletion of part of autosome
- 3Developmental disorder
- 3Intelligence finding
- 4Anomaly of chromosome pair
- 4Disease
- 4Functional finding
- 4Mental state, behavior and/or psychosocial function finding
- 4Monosomy and deletion from autosome
- 5Clinical finding
- 5Congenital chromosomal disease
- 6Chromosomal disorder
- 6Congenital disease
- 7Fetal and/or neonatal disorder
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