Status: current, Primitive. Date: 31-Jul 2018. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3656012019 | Non-functioning paraganglioma | en | Synonym | Active | Case insensitive | SNOMED CT core |
3656013012 | Non-functioning paraganglioma (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3656014018 | Non-secreting paraganglioma | en | Synonym | Active | Case insensitive | SNOMED CT core |
3655801014 | A rare neuroendocrine neoplasm arising from neural crest-derived paraganglion cells (most often in the para-aortic region at the level of renal hilii, organ of Zuckerkandl, thoracic paraspinal region, bladder and carotid body) not associated with catecholamine secretion. These neoplasms are usually clinically silent and symptoms if present are nonspecific and depend on the location of the neoplasm. Association with certain hereditary cancer-predisposing syndromes, such as multiple endocrine neoplasia, neurofibromatosis type 1 or von Hippel lindau syndrome may be observed. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Non-functioning paraganglioma | Associated morphology | Paraganglioma | true | Inferred relationship | Some | 1 | |
Non-functioning paraganglioma | Is a | Paraganglioma | 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