OMOP Concept 37164180
9q21.13 microdeletion syndrome
StandardConditionSNOMED1229875002Disorder
Maps from
0
Descendants
0
Valid from
31 May 2022
Valid to
31 Dec 2099
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Synonyms
Alternative names recorded for 9q21.13 microdeletion syndrome across source vocabularies.
- 9q21.13 microdeletion syndrome (disorder)
- síndrome de microdeleción 9q21.13
- síndrome de microdeleción 9q21.13 (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(39)Roll up to these when you need a wider cohort.
- 19q partial monosomy syndrome
- 1Genetic intellectual disability
- 1Global developmental delay
- 1Multiple malformation syndrome with facial defects as major feature
- 1Neurodevelopmental delay
- 2Congenital anomaly of face
- 2Deletion of part of chromosome 9
- 2Developmental delay
- 2Genetic disease
- 2Intellectual disability
- 2Multiple system malformation syndrome
- 2Neurodevelopmental disorder
- 3Abnormal behavior
- 3Anomaly of chromosome pair 9
- 3Congenital anomaly of head
- 3Congenital malformation syndrome
- 3Deletion of part of autosome
- 3Developmental disorder
- 3Disease
- 3Disorder of face
- 3Impaired cognition
- 3Intellectual ability - finding
- 4Anomaly of chromosome pair
- 4Behavior finding
- 4Clinical finding
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