Status: current, Defined. Date: 31-Jul 2021. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 4574210011 | Anaplastic ependymoma of central nervous system | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 4574211010 | Anaplastic ependymoma of central nervous system (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 4574212015 | A rare malignant type of ependymoma that most often arises in the supratentorial region of the brain of children and young adults and that manifests with variable symptoms including headaches, nausea, vision impairment, memory loss and difficulty walking. | en | Definition | Active | Case sensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Anaplastic ependymoma of central nervous system | Is a | Malignant glioma of central nervous system | true | Inferred relationship | Some | ||
| Anaplastic ependymoma of central nervous system | Associated morphology | Ependymoma, anaplastic | true | Inferred relationship | Some | 1 | |
| Anaplastic ependymoma of central nervous system | Is a | Ependymoma of central nervous system | true | Inferred relationship | Some | ||
| Anaplastic ependymoma of central nervous system | Finding site | Structure of central nervous system | true | Inferred relationship | Some | 1 | |
| Anaplastic ependymoma of central nervous system | Is a | Embryonal neuroepithelial neoplasm of central nervous system | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Clinical finding foundation reference set
Australian dialect reference set
Neoplasm and/or hamartoma reference set
Problem/Diagnosis reference set
Description inactivation indicator reference set
FHIR