Status: current, Primitive. Date: 31-Jul 2016. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3304081016 | Ependymoblastoma (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 3304082011 | Ependymoblastoma | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 3304083018 | A rare type of primitive neuroectodermal tumor (PNET) that usually occurs in young children under the age of 2 and is histologically distinguished by the production of ependymoblastic rosettes. It is associated with an aggressive course and a poor prognosis. | en | Definition | Active | Case sensitive | SNOMED CT core |
| 3304084012 | A rare type of primitive neuroectodermal tumour (PNET) that usually occurs in young children under the age of 2 and is histologically distinguished by the production of ependymoblastic rosettes. It is associated with an aggressive course and a poor prognosis. | en | Definition | Active | Case sensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Ependymoblastoma | Is a | Malignant neoplastic disease | true | Inferred relationship | Some | ||
| Ependymoblastoma | Associated morphology | Ependymoma, anaplastic | true | Inferred relationship | Some | 1 | |
| Ependymoblastoma | Is a | Primary malignant neoplasm | false | Inferred relationship | Some | ||
| Ependymoblastoma | Is a | Ependymoma | true | Inferred relationship | Some |
| 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
FHIR