OMOP Concept 436802
Complete trisomy 13 syndrome
StandardConditionSNOMED21111006Disorder
Maps from
23
Descendants
2
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
23 source codes normalize to Complete trisomy 13 syndrome via the OMOP "Maps to" relationship.
Synonyms
Alternative names recorded for Complete trisomy 13 syndrome across source vocabularies.
- Complete trisomy 13 syndrome (disorder)
- D>1< trisomy syndrome
- D1 trisomy syndrome
- D<sub>1</sub> trisomy syndrome
- Patau syndrome
- síndrome de Patau
- síndrome de trisomía 13 completa
- síndrome de trisomía 13 completa (trastorno)
- síndrome de trisomía D1
- síndrome de trisomía D>1<
- síndrome de trisomía D<sub>1</sub>
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(12)Roll up to these when you need a wider cohort.
- 1Anomaly of chromosome pair 13
- 1Trisomy and partial trisomy of autosome
- 2Anomaly of chromosome pair
- 2Autosomal duplication
- 2Congenital chromosomal disease
- 3Autosomal chromosomal disorder
- 3Chromosomal disorder
- 3Congenital disease
- 3Duplication of chromosome
- 4Disease
- 4Disorder of fetus and/or newborn
- 5Clinical finding
Narrower concepts
(2)Included automatically when you query with descendants.
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