Status: current, Defined. Date: 31-Mar 2022. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
4970740019 | Non-functioning neuroendocrine neoplasm of pancreas (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
4970741015 | Non-functioning PNET (pancreatic neuroendocrine tumor) | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
4970742010 | Non-functioning well-differentiated pancreatic NEN (neuroendocrine neoplasm) | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
4970743017 | Non-functioning PNET (pancreatic neuroendocrine tumour) | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
4970744011 | Non-functioning neuroendocrine neoplasm of pancreas | en | Synonym | Active | Case insensitive | SNOMED CT core |
4970745012 | Non-functioning well-differentiated neuroendocrine neoplasm of pancreas | en | Synonym | Active | Case insensitive | SNOMED CT core |
4970746013 | A rare neuroendocrine tumor of pancreas characterized by a well-differentiated epithelial pancreatic neuroendocrine neoplasm measuring at least 0.5 cm, without distinct hormonal syndrome. Tumors less than 0.5 cm are called microadenomas. Microadenomatosis is the multifocal occurrence of microadenomas. Histopathologic examination shows an organoid growth pattern and expression of synaptophysin and chromogranin A on immunohistochemistry. Tumors are often discovered incidentally, or patients may present with symptoms related to local or metastatic tumor spread. Microadenomas are considered benign, while larger tumors may behave in a malignant manner with extrapancreatic spread, metastasis, or recurrence. | en | Definition | Active | Case sensitive | SNOMED CT core |
4970747016 | A rare neuroendocrine tumour of pancreas characterised by a well-differentiated epithelial pancreatic neuroendocrine neoplasm measuring at least 0.5 cm, without distinct hormonal syndrome. Tumours less than 0.5 cm are called microadenomas. Microadenomatosis is the multifocal occurrence of microadenomas. Histopathologic examination shows an organoid growth pattern and expression of synaptophysin and chromogranin A on immunohistochemistry. Tumours are often discovered incidentally, or patients may present with symptoms related to local or metastatic tumour spread. Microadenomas are considered benign, while larger tumours may behave in a malignant manner with extrapancreatic spread, metastasis, or recurrence. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Non-functioning neuroendocrine neoplasm of pancreas | Finding site | Pancreatic structure | true | Inferred relationship | Some | 1 | |
Non-functioning neuroendocrine neoplasm of pancreas | Is a | Malignant neuroendocrine tumour | true | Inferred relationship | Some | ||
Non-functioning neuroendocrine neoplasm of pancreas | Is a | Malignant tumour of pancreas | true | Inferred relationship | Some | ||
Non-functioning neuroendocrine neoplasm of pancreas | Is a | Neuroendocrine tumour of pancreas | true | Inferred relationship | Some | ||
Non-functioning neuroendocrine neoplasm of pancreas | Associated morphology | Pancreatic endocrine tumour, nonfunctioning | 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