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FHIR Server FHIR Server 3.7.22-SNAPSHOT
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FHIR Version n/a
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FHIR
© HL7.org
|
Server Home |
FHIR Server FHIR Server 3.7.22-SNAPSHOT
|
FHIR Version n/a
User: [n/a]
Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 5403809014 | A rare non-hereditary condition characterized by gastrointestinal stromal tumors (GIST, intramural mesenchymal tumors of the gastrointestinal tract with neuronal or neural crest cell origin), pulmonary chondromas and extraadrenal paragangliomas. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5403810016 | A rare non-hereditary condition characterised by gastrointestinal stromal tumours (GIST, intramural mesenchymal tumours of the gastrointestinal tract with neuronal or neural crest cell origin), pulmonary chondromas and extraadrenal paragangliomas. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3499553019 | Carney triad | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3499554013 | Carney triad (disorder) | en | Fully specified name | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 962961000172119 | triade de Carney | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
| 173341000274113 | Carney-Trias | de | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| A rare non-hereditary condition characterised by gastrointestinal stromal tumours (GIST, intramural mesenchymal tumours of the gastrointestinal tract with neuronal or neural crest cell origin), pulmonary chondromas and extraadrenal paragangliomas. | Is a | Polyglandular dysfunction | true | Inferred relationship | Some | ||
| A rare non-hereditary condition characterised by gastrointestinal stromal tumours (GIST, intramural mesenchymal tumours of the gastrointestinal tract with neuronal or neural crest cell origin), pulmonary chondromas and extraadrenal paragangliomas. | Is a | Neoplasm of multiple endocrine glands | true | Inferred relationship | Some | ||
| A rare non-hereditary condition characterised by gastrointestinal stromal tumours (GIST, intramural mesenchymal tumours of the gastrointestinal tract with neuronal or neural crest cell origin), pulmonary chondromas and extraadrenal paragangliomas. | Is a | trouble multisytémique | false | Inferred relationship | Some | ||
| A rare non-hereditary condition characterised by gastrointestinal stromal tumours (GIST, intramural mesenchymal tumours of the gastrointestinal tract with neuronal or neural crest cell origin), pulmonary chondromas and extraadrenal paragangliomas. | Associated morphology | Neoplasm | true | Inferred relationship | Some | 1 | |
| A rare non-hereditary condition characterised by gastrointestinal stromal tumours (GIST, intramural mesenchymal tumours of the gastrointestinal tract with neuronal or neural crest cell origin), pulmonary chondromas and extraadrenal paragangliomas. | Finding site | Structure of multiple endocrine glands | 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)