Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2019. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3743484018 | Desmoplastic infantile astrocytoma and ganglioglioma | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3743485017 | Desmoplastic infantile astrocytoma and ganglioglioma (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3743486016 | DIA/DIG - desmoplastic infantile astrocytoma/ganglioglioma | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 8254381000146112 | infantiel desmoplastisch astrocytoom/ganglioglioom | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 8254391000146114 | infantiel desmoplastisch astrocytoom/ganglioglioom (aandoening) | nl | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 3743487013 | A mixed neuronal-glial tumour representing a histological spectrum of the same tumour. They are usually supratentorially located, large, cystic masses with a peripheral solid component, characterised by prominent desmoplastic stroma and pleomorphic populations of neoplastic cells with either astrocytic or ganglionic differentiation and poorly differentiated cells in variable proportions. They usually present in the first 18 months of age with rapid head growth, bulging anterior fontanel and bone structures over the tumour, signs of raised intracranial pressure (headache, vomiting, papilloedema), focal neurological signs and sometimes seizures. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3743488015 | A mixed neuronal-glial tumor representing a histological spectrum of the same tumor. They are usually supratentorially located, large, cystic masses with a peripheral solid component, characterized by prominent desmoplastic stroma and pleomorphic populations of neoplastic cells with either astrocytic or ganglionic differentiation and poorly differentiated cells in variable proportions. They usually present in the first 18 months of age with rapid head growth, bulging anterior fontanel and bone structures over the tumor, signs of raised intracranial pressure (headache, vomiting, papilledema), focal neurological signs and sometimes seizures. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Desmoplastic infantile astrocytoma and ganglioglioma | Occurrence | Infancy | true | Inferred relationship | Some | 1 | |
| Desmoplastic infantile astrocytoma and ganglioglioma | Associated morphology | Desmoplastic infantile astrocytoma | true | Inferred relationship | Some | 1 | |
| Desmoplastic infantile astrocytoma and ganglioglioma | Finding site | Supratentorial brain | true | Inferred relationship | Some | 1 | |
| Desmoplastic infantile astrocytoma and ganglioglioma | Is a | Low grade glioma of cerebrum (disorder) | false | Inferred relationship | Some | ||
| Desmoplastic infantile astrocytoma and ganglioglioma | Is a | Neoplasm of uncertain or unknown behavior of brain, supratentorial | true | Inferred relationship | Some | ||
| Desmoplastic infantile astrocytoma and ganglioglioma | Is a | Glioma of central nervous system (disorder) | false | Inferred relationship | Some | ||
| Desmoplastic infantile astrocytoma and ganglioglioma | Is a | Low grade glioma of brain (disorder) | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR