Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2021. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 4574216017 | Anaplastic oligoastrocytoma of central nervous system (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 4574217014 | Anaplastic oligoastrocytoma of central nervous system | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 4574218016 | A rare and aggressive glial neoplasm of the central nervous system that usually presents with seizures in adults. The neoplasm is most often located in the cerebral hemispheres and is associated with a very poor prognosis. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5080961000052118 | anaplastiskt oligoastrocytom i centrala nervsystemet | sv | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Sweden NRC maintained module (core metadata concept) |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Anaplastic oligoastrocytoma of central nervous system (disorder) | Is a | Mixed glioma (disorder) | true | Inferred relationship | Some | ||
| Anaplastic oligoastrocytoma of central nervous system (disorder) | Is a | Malignant glioma of central nervous system | true | Inferred relationship | Some | ||
| Anaplastic oligoastrocytoma of central nervous system (disorder) | Associated morphology | Anaplastic oligoastrocytoma | true | Inferred relationship | Some | 1 | |
| Anaplastic oligoastrocytoma of central nervous system (disorder) | Finding site | Structure of central nervous system (body structure) | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR