Status: current, Defined. Date: 31-Jul 2016. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3307066018 | Embryonal sarcoma of liver (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3307067010 | Embryonal sarcoma of liver | en | Synonym | Active | Case insensitive | SNOMED CT core |
3307068017 | A rare primary malignant hepatic neoplasm of childhood that is mesenchymal in origin. It can rarely occur in adults. It has manifestations of abdominal mass, right upper quadrant or epigastric pain, nausea, anorexia, intermittent fever or headache. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Embryonal sarcoma of liver | Is a | Primary malignant neoplasm of liver | false | Inferred relationship | Some | ||
Embryonal sarcoma of liver | Is a | Sarcoma of liver | true | Inferred relationship | Some | ||
Embryonal sarcoma of liver | Associated morphology | Embryonal sarcoma | true | Inferred relationship | Some | 1 | |
Embryonal sarcoma of liver | Finding site | Liver structure | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Neoplasm and/or hamartoma reference set
Problem/Diagnosis reference set