Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Jan 2025. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 5428951011 | Embryonal neoplasm with multilayered rosettes | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5428952016 | Embryonal neoplasm with multilayered rosettes (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5428957010 | ETMR - embryonal tumour with multilayered rosettes | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5428958017 | Embryonal tumor with multilayered rosettes | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5428959013 | ETMR - embryonal tumor with multilayered rosettes | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5428960015 | Embryonal tumour with multilayered rosettes | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5428961016 | A rare central nervous system embryonal tumour characterised by embryonal cells arranged in multilayered rosettes and displaying one of three morphological patterns: embryonal tumour with abundant neuropil and true rosettes, ependymoblastoma, or medulloepithelioma. The tumours typically have a C19MC alteration or (rarely) a DICER1 mutation and correspond to WHO grade IV. They are mostly localised intracranially, rarely in the spinal cord, and commonly cause signs and symptoms of elevated intracranial pressure, sometimes seizures and focal neurological signs. Most cases occur in children during the first two years of life. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5428962011 | A rare central nervous system embryonal tumor characterized by embryonal cells arranged in multilayered rosettes and displaying one of three morphological patterns: embryonal tumor with abundant neuropil and true rosettes, ependymoblastoma, or medulloepithelioma. The tumors typically have a C19MC alteration or (rarely) a DICER1 mutation and correspond to WHO grade IV. They are mostly localized intracranially, rarely in the spinal cord, and commonly cause signs and symptoms of elevated intracranial pressure, sometimes seizures and focal neurological signs. Most cases occur in children during the first two years of life. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Embryonal neoplasm with multilayered rosettes | Is a | Embryonal neuroepithelial neoplasm of central nervous system (disorder) | true | Inferred relationship | Some | ||
| Embryonal neoplasm with multilayered rosettes | Is a | Malignant glioma of central nervous system | true | Inferred relationship | Some | ||
| Embryonal neoplasm with multilayered rosettes | Finding site | Structure of central nervous system (body structure) | true | Inferred relationship | Some | 1 | |
| Embryonal neoplasm with multilayered rosettes | Associated morphology | Embryonal neoplasm with multilayered rosettes (morphologic abnormality) | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)
FHIR