OMOP Concept 37165247
16p12.1p12.3 triplication syndrome
StandardConditionSNOMED1251450006Disorder
Maps from
0
Descendants
0
Valid from
30 Sept 2022
Valid to
31 Dec 2099
OMOP concepts
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Synonyms
Alternative names recorded for 16p12.1p12.3 triplication syndrome across source vocabularies.
- 16p12.1p12.3 triplication syndrome (disorder)
- síndrome de triplicación 16p12.1p12.3
- síndrome de triplicación 16p12.1p12.3 (trastorno)
- tetrasomía 16p12.1p12.3
- Tetrasomy 16p12.1p12.3
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(40)Roll up to these when you need a wider cohort.
- 1Anomaly of chromosome pair 16
- 1Congenital anomaly of finger
- 1Global developmental delay
- 1Multiple malformation syndrome with facial-limb defects as major feature
- 2Anomaly of chromosome pair
- 2Congenital anomaly of digit
- 2Congenital anomaly of hand
- 2Congenital anomaly of limb
- 2Developmental delay
- 2Disorder of finger
- 2Multiple malformation syndrome with facial defects as major feature
- 2Multiple malformation syndrome with limb defect as major feature
- 3Congenital anomaly of face
- 3Congenital anomaly of upper limb
- 3Congenital chromosomal disease
- 3Congenital malformation
- 3Developmental disorder
- 3Disorder of digit
- 3Disorder of hand
- 3Disorder of limb
- 3Finding of finger
- 3Multiple system malformation syndrome
- 3Structural abnormality of hand
- 4Chromosomal disorder
- 4Congenital anomaly of head
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