Familial omphalocele syndrome with facial dysmorphism 770900000
SNOMED CT code
| SNOMED code | 770900000 |
|---|---|
| name | Familial omphalocele syndrome with facial dysmorphism |
| status | active |
| date introduced | 2019-01-31 |
| fully specified name(s) | Familial omphalocele syndrome with facial dysmorphism (disorder) |
| synonyms | Familial omphalocele syndrome with facial dysmorphism |
| attributes - group3 | |
| Pathological process | Pathological developmental process 308490002 |
| Occurrence | Congenital 255399007 |
| Finding site | Umbilical structure 78220002 |
| Associated morphology | Hernial opening 414402003 |
| attributes - group1 | |
| Pathological process | Pathological developmental process 308490002 |
| Associated morphology | Protrusion 112639008 |
| Occurrence | Congenital 255399007 |
| Finding site | Intestinal structure 113276009 |
| attributes - group2 | |
| Associated morphology | Morphologically abnormal structure 49755003 |
| Pathological process | Pathological developmental process 308490002 |
| Occurrence | Congenital 255399007 |
| Finding site | Face structure 89545001 |
| attributes - group4 | |
| Finding site | Intra-abdominopelvic structure 818986006 |
| Associated morphology | Hernia 414403008 |
| Occurrence | Congenital 255399007 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal dominant hereditary disorder 11164009 Familial omphalocele syndrome with facial dysmorphism 770900000 SNOMED CT Concept 138875005 Clinical finding 404684003 Viscus structure finding 406123005 Abdominal organ finding 249561001 Bowel finding 249562008 Disorder of intestine 85919009 Congenital anomaly of intestinal tract 126764002 Familial omphalocele syndrome with facial dysmorphism 770900000 SNOMED CT Concept 138875005 Clinical finding 404684003 General finding of soft tissue 248402002 Umbilicus finding 249537008 Disorder of umbilicus 397320006 Umbilical hernia 396347007 Congenital omphalocele 18735004 Familial omphalocele syndrome with facial dysmorphism 770900000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Familial omphalocele syndrome with facial dysmorphism 770900000 SNOMED CT Concept 138875005 Clinical finding 404684003 Digestive system finding 386617003 Disorder of digestive system 53619000 Digestive system hereditary disorder 363080007 Familial omphalocele syndrome with facial dysmorphism 770900000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of head 118934005 Disorder of face 118930001 Congenital anomaly of face 398302004 Multiple malformation syndrome with facial defects as major feature 65094009 Familial omphalocele syndrome with facial dysmorphism 770900000 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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