Congenital omphalocele, diaphragmatic hernia, cardiovascular anomalies, radial ray defect syndrome 1172589000
SNOMED CT code
| SNOMED code | 1172589000 |
|---|---|
| name | Congenital omphalocele, diaphragmatic hernia, cardiovascular anomalies, radial ray defect syndrome |
| status | active |
| date introduced | 2021-09-30 |
| fully specified name(s) | Congenital omphalocele, diaphragmatic hernia, cardiovascular anomalies, radial ray defect syndrome (disorder) |
| synonyms |
|
| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| Finding site | Umbilical structure 78220002 |
| Associated morphology | Hernial opening 414402003 |
| Pathological process | Pathological developmental process 308490002 |
| attributes - group2 | |
| Occurrence | Congenital 255399007 |
| Associated morphology | Hernia 414403008 |
| Finding site | Intra-abdominopelvic structure 818986006 |
| attributes - group3 | |
| Occurrence | Congenital 255399007 |
| Finding site | Limb structure 66019005 |
| Associated morphology | Morphologically abnormal structure 49755003 |
| Pathological process | Pathological developmental process 308490002 |
| attributes - group4 | |
| Occurrence | Congenital 255399007 |
| Finding site | Face structure 89545001 |
| Associated morphology | Morphologically abnormal structure 49755003 |
| Pathological process | Pathological developmental process 308490002 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 General finding of soft tissue 248402002 Umbilicus finding 249537008 Disorder of umbilicus 397320006 Umbilical hernia 396347007 Congenital omphalocele 18735004 Congenital omphalocele, diaphragmatic hernia, cardiovascular anomalies, radial ray defect syndrome 1172589000 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of limb structure 302293008 Disorder of limb 128605003 Congenital anomaly of limb 60475009 Multiple malformation syndrome with facial-limb defects as major feature 23359005 Congenital omphalocele, diaphragmatic hernia, cardiovascular anomalies, radial ray defect syndrome 1172589000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Congenital omphalocele, diaphragmatic hernia, cardiovascular anomalies, radial ray defect syndrome 1172589000 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
Thank you for choosing Find-A-Code, please Sign In to remove ads.
Quick, Current, Complete - www.findacode.com