Status: current, Defined. Date: 31-Mar 2022. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 4964793010 | Primary choriocarcinoma of central nervous system | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 4964794016 | Primary choriocarcinoma of central nervous system (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 4964791012 | A rare primary germ cell tumour of central nervous system characterised by a lesion typically in the region of the pineal gland and the suprasellar compartment, composed of cytotrophoblastic elements and multinucleated syncytiotrophoblastic giant cells. Ectatic stromal vascular channels, blood lakes, and extensive haemorrhagic necrosis are the rule. The tumour usually arises in the second decade of life and predominantly in males. Clinical presentation depends on location and size and includes signs of increased intracranial pressure, visual disturbances and endocrine abnormalities. Prognosis is generally poor. | en | Definition | Active | Case sensitive | SNOMED CT core |
| 4964792017 | A rare primary germ cell tumor of central nervous system characterized by a lesion typically in the region of the pineal gland and the suprasellar compartment, composed of cytotrophoblastic elements and multinucleated syncytiotrophoblastic giant cells. Ectatic stromal vascular channels, blood lakes, and extensive hemorrhagic necrosis are the rule. The tumor usually arises in the second decade of life and predominantly in males. Clinical presentation depends on location and size and includes signs of increased intracranial pressure, visual disturbances and endocrine abnormalities. Prognosis is generally poor. | en | Definition | Active | Case sensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Primary choriocarcinoma of central nervous system | Is a | Choriocarcinoma | true | Inferred relationship | Some | ||
| Primary choriocarcinoma of central nervous system | Finding site | Structure of central nervous system | true | Inferred relationship | Some | 1 | |
| Primary choriocarcinoma of central nervous system | Associated morphology | Choriocarcinoma | true | Inferred relationship | Some | 1 | |
| Primary choriocarcinoma of central nervous system | Is a | Primary malignant germ cell neoplasm | true | Inferred relationship | Some | ||
| Primary choriocarcinoma of central nervous system | Is a | Primary malignant neoplasm of central nervous system | true | Inferred relationship | Some | ||
| Primary choriocarcinoma of central nervous system | Finding site | Structure of central nervous system | false | Inferred relationship | Some | 2 | |
| Primary choriocarcinoma of central nervous system | Associated morphology | Neoplasm, malignant (primary) | false | Inferred relationship | Some | 2 | |
| Primary choriocarcinoma of central nervous system | Pathological process | Primary malignant neoplastic proliferation | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Clinical finding foundation reference set
Neoplasm and/or hamartoma reference set
Problem/Diagnosis reference set
FHIR