Status: current. Date: 31-Jul 2022
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 5084136019 | Idiopathic peliosis hepatis | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5084138018 | Idiopathic peliosis hepatis (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5084141010 | A rare vascular liver disease characterized by widespread or focal cystic dilatation of sinusoidal blood-filled spaces of the liver without any known cause. Lesions can vary in diameter between few millimeters and several centimeters. The condition may remain asymptomatic or manifest with complications including rupture and intraperitoneal hemorrhage, hepatomegaly, portal hypertension, cholestasis and liver failure. | en | Definition | Inactive | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5084142015 | A rare vascular liver disease characterised by widespread or focal cystic dilatation of sinusoidal blood-filled spaces of the liver without any known cause. Lesions can vary in diameter between few millimetres and several centimetres. The condition may remain asymptomatic or manifest with complications including rupture and intraperitoneal haemorrhage, hepatomegaly, portal hypertension, cholestasis and liver failure. | en | Definition | Inactive | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5400221015 | A rare vascular liver disease characterized by widespread or focal cystic dilatation of sinusoidal blood-filled spaces of the liver without any known cause. Lesions can vary in diameter between few millimeters and several centimeters. The condition may remain asymptomatic or manifest with complications including rupture and intraperitoneal hemorrhage, hepatomegaly, portal hypertension, cholestasis, and liver failure. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5400222010 | A rare vascular liver disease characterised by widespread or focal cystic dilatation of sinusoidal blood-filled spaces of the liver without any known cause. Lesions can vary in diameter between few millimetres and several centimetres. The condition may remain asymptomatic or manifest with complications including rupture and intraperitoneal haemorrhage, hepatomegaly, portal hypertension, cholestasis, and liver failure. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Idiopathic peliosis hepatis | Is a | Idiopathic disease | true | Congenital syphilitic hepatomegaly | Congenital syphilitic hepatomegaly | ||
| Idiopathic peliosis hepatis | Is a | Peliosis hepatis | true | Congenital syphilitic hepatomegaly | Congenital syphilitic hepatomegaly | ||
| Idiopathic peliosis hepatis | Associated morphology | Hemorrhagic cyst | true | Congenital syphilitic hepatomegaly | Congenital syphilitic hepatomegaly | 1 | |
| Idiopathic peliosis hepatis | Finding site | Vascular structure of liver | true | Congenital syphilitic hepatomegaly | Congenital syphilitic hepatomegaly | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR