Autosomal dominant polycystic liver disease 890229002
SNOMED CT code
| SNOMED code | 890229002 |
|---|---|
| name | Autosomal dominant polycystic liver disease |
| status | active |
| date introduced | 2021-01-31 |
| fully specified name(s) | Autosomal dominant polycystic liver disease (disorder) |
| synonyms | Autosomal dominant polycystic liver disease |
| attributes - group1 | |
| Finding site | Liver structure 10200004 |
| Associated morphology | Polycystic change 3679006 |
| Occurrence | Congenital 255399007 |
| Pathological process | Pathological developmental process 308490002 |
| 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 Autosomal dominant polycystic liver disease 890229002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Autosomal dominant polycystic liver disease 890229002 SNOMED CT Concept 138875005 Clinical finding 404684003 Digestive system finding 386617003 Disorder of digestive system 53619000 Digestive system hereditary disorder 363080007 Autosomal dominant polycystic liver disease 890229002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Cyst 441457006 Cyst of abdomen 446064000 Liver cyst 85057007 Autosomal dominant polycystic liver disease 890229002 SNOMED CT Concept 138875005 Clinical finding 404684003 Digestive system finding 386617003 Liver finding 249565005 Disease of liver 235856003 Congenital anomaly of liver 89166001 Autosomal dominant polycystic liver disease 890229002 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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