Gardner syndrome 60876000
SNOMED CT code
| SNOMED code | 60876000 |
|---|---|
| name | Gardner syndrome |
| status | active |
| date introduced | 2002-01-31 |
| fully specified name(s) | Gardner syndrome (disorder) |
| synonyms |
|
| attributes - group1 | |
| Pathological process | Pathological developmental process 308490002 |
| Occurrence | Congenital 255399007 |
| Associated morphology | Multiple polyps 9499001 |
| Finding site | Large intestinal structure 14742008 |
| attributes - group2 | |
| Finding site | Large intestinal structure 14742008 |
| Occurrence | Congenital 255399007 |
| Associated morphology | Hamartoma 51398009 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Viscus structure finding 406123005 Abdominal organ finding 249561001 Bowel finding 249562008 Finding of large intestine 118436003 Disorder of large intestine 119523007 Congenital anomaly of large intestine 1492007 Gardner syndrome 60876000 SNOMED CT Concept 138875005 Clinical finding 404684003 Mass of body structure 300848003 Mass of digestive structure 300855001 Hamartoma of intestine 254594009 Gardner syndrome 60876000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Gardner syndrome 60876000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Congenital hamartoma 399960008 Gardner syndrome 60876000 SNOMED CT Concept 138875005 Clinical finding 404684003 Digestive system finding 386617003 Disorder of digestive system 53619000 Digestive system hereditary disorder 363080007 Familial multiple polyposis syndrome 72900001 Gardner syndrome 60876000 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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