OMOP Concept 37164071
1p35.2 microdeletion syndrome
StandardConditionSNOMED1228844002Disorder
Maps from
0
Descendants
0
Valid from
31 May 2022
Valid to
31 Dec 2099
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Synonyms
Alternative names recorded for 1p35.2 microdeletion syndrome across source vocabularies.
- 1p35.2 microdeletion syndrome (disorder)
- deleción 1p35.2
- monosomía 1p35.2
- Monosomy 1p35.2
- síndrome de microdeleción 1p35.2
- síndrome de microdeleción 1p35.2 (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(33)Roll up to these when you need a wider cohort.
- 11p partial monosomy
- 1Developmental delay
- 1Multiple malformation syndrome with facial defects as major feature
- 1Short stature disorder
- 2Congenital anomaly of face
- 2Deletion of part of chromosome 1
- 2Developmental disorder
- 2Disorder of stature
- 2Multiple system malformation syndrome
- 2Short stature
- 3Anomaly of chromosome pair 1
- 3Body height below reference range
- 3Congenital anomaly of head
- 3Congenital malformation syndrome
- 3Deletion of part of autosome
- 3Disease
- 3Disorder of face
- 3Finding of general physiological development
- 3General finding of height
- 4Anomaly of chromosome pair
- 4Clinical finding
- 4Congenital malformation
- 4Disorder of head
- 4Finding of face
- 4Height / growth finding
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