Complete trisomy 13 syndrome 21111006
SNOMED CT code
SNOMED code | 21111006 |
---|---|
name | Complete trisomy 13 syndrome |
status | active |
date introduced | 2002-01-31 |
fully specified name(s) | Complete trisomy 13 syndrome (disorder) |
synonyms |
|
attributes - group2 | |
Associated morphology | Trisomy 78989007 |
attributes - group1 | |
Occurrence | Congenital 255399007 |
Finding site | Chromosome pair 13 55401003 |
Associated morphology | Cellular AND/OR subcellular abnormality 107673000 |
parents | |
children | |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Chromosomal disorder 409709004 Congenital chromosomal disease 74345006 Anomaly of chromosome pair 362984008 Anomaly of chromosome pair 13 17760001 Complete trisomy 13 syndrome 21111006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Chromosomal disorder 409709004 Congenital chromosomal disease 74345006 Trisomy and partial trisomy of autosome 270521004 Complete trisomy 13 syndrome 21111006 |
ancestors | sorted most to least specific
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cpt crosswalks |
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