Complete trisomy 16 syndrome 77269002
SNOMED CT code
| SNOMED code | 77269002 |
|---|---|
| name | Complete trisomy 16 syndrome |
| status | active |
| date introduced | 2002-01-31 |
| fully specified name(s) | Complete trisomy 16 syndrome (disorder) |
| synonyms | Complete trisomy 16 syndrome |
| attributes - group1 | |
| Associated morphology | Trisomy 78989007 |
| Pathological process | Pathological developmental process 308490002 |
| Occurrence | Congenital 255399007 |
| Finding site | Chromosome pair 16 39220001 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Chromosomal disorder 409709004 Congenital chromosomal disease 74345006 Trisomy and partial trisomy of autosome 270521004 Complete trisomy 16 syndrome 77269002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 Complete trisomy 16 syndrome 77269002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Chromosomal disorder 409709004 Congenital chromosomal disease 74345006 Anomaly of chromosome pair 362984008 Anomaly of chromosome pair 16 53392002 Complete trisomy 16 syndrome 77269002 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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