Status: current, Primitive. Date: 31-May 2022. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
5048267015 | Hereditary malignant neuroendocrine tumor of small intestine | en | Synonym | Active | Case insensitive | SNOMED CT core |
5048268013 | Hereditary malignant neuroendocrine neoplasm of small intestine (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
5048269017 | Hereditary malignant neuroendocrine tumour of small intestine | en | Synonym | Active | Case insensitive | SNOMED CT core |
5048270016 | Hereditary malignant neuroendocrine tumour of small bowel | en | Synonym | Active | Case insensitive | SNOMED CT core |
5048271017 | Hereditary malignant neuroendocrine tumor of small bowel | en | Synonym | Active | Case insensitive | SNOMED CT core |
5048274013 | Hereditary malignant neuroendocrine neoplasm of small intestine | en | Synonym | Active | Case insensitive | SNOMED CT core |
5048272012 | A rare inherited cancer-predisposing syndrome characterized by occurrence of multiple synchronous primary carcinoids of the small intestine. Clinical presentation is otherwise indistinguishable from sporadic carcinoids and includes abdominal pain, flushing, and diarrhea, often becoming manifest only after a long asymptomatic period. Most patients present with low grade tumors. Occurrence of pulmonary carcinoids has also been reported. | en | Definition | Active | Case sensitive | SNOMED CT core |
5048273019 | A rare inherited cancer-predisposing syndrome characterised by occurrence of multiple synchronous primary carcinoids of the small intestine. Clinical presentation is otherwise indistinguishable from sporadic carcinoids and includes abdominal pain, flushing, and diarrhoea, often becoming manifest only after a long asymptomatic period. Most patients present with low grade tumours. Occurrence of pulmonary carcinoids has also been reported. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Hereditary malignant neuroendocrine neoplasm of small intestine | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Hereditary malignant neuroendocrine neoplasm of small intestine | Is a | Gastrointestinal hormone-secreting endocrine tumour | true | Inferred relationship | Some | ||
Hereditary malignant neuroendocrine neoplasm of small intestine | Is a | Carcinoid tumour of small intestine | true | Inferred relationship | Some | ||
Hereditary malignant neuroendocrine neoplasm of small intestine | Is a | Digestive system hereditary disorder | true | Inferred relationship | Some | ||
Hereditary malignant neuroendocrine neoplasm of small intestine | Is a | Malignant tumour of small intestine | true | Inferred relationship | Some | ||
Hereditary malignant neuroendocrine neoplasm of small intestine | Is a | Hereditary neoplastic syndrome | true | Inferred relationship | Some | ||
Hereditary malignant neuroendocrine neoplasm of small intestine | Finding site | Structure of small intestine | true | Inferred relationship | Some | 1 | |
Hereditary malignant neuroendocrine neoplasm of small intestine | Associated morphology | Malignant carcinoid tumour | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Clinical finding foundation reference set
Australian dialect reference set
Neoplasm and/or hamartoma reference set
Problem/Diagnosis reference set