Status: current, Defined. Date: 31-Jul 2021. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 4574225011 | Gliomatosis cerebri (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 4574226012 | Gliomatosis cerebri | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 4574227015 | A rare glial neoplasm with characteristics of extensive infiltration of the brain, often extending to infratentorial structures and even the spinal cord. The neoplasm is composed of elongated glial cells typically resembling astrocytes. Cases in which the predominant cell type is oligodendroglial have also been described. Some neoplasms develop a circumscribed neoplastic mass in addition to the diffuse lesion, usually showing features of high-grade glioma. Clinical symptoms include dementia, headache, seizures, signs of increased intracranial pressure and a variety of neurological deficits. Prognosis is generally poor. | en | Definition | Active | Case sensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Gliomatosis cerebri | Associated morphology | Gliomatosis cerebri | true | Inferred relationship | Some | 1 | |
| Gliomatosis cerebri | Is a | Malignant glioma of brain | true | Inferred relationship | Some | ||
| Gliomatosis cerebri | Finding site | Brain tissue structure | 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