Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Vasoactive intestinal peptide-secreting tumour |
Is a |
True |
Neuroendocrine tumor of pancreas (disorder) |
Inferred relationship |
Some |
|
tumeur carcinoide du pancréas |
Is a |
False |
Neuroendocrine tumor of pancreas (disorder) |
Inferred relationship |
Some |
|
néoplasme sécréteur de l'hormone de libération de l'hormone de croissance |
Is a |
False |
Neuroendocrine tumor of pancreas (disorder) |
Inferred relationship |
Some |
|
néoplasme neuroendocrine du pancréas sécrétant un peptide lié à la parathormone |
Is a |
False |
Neuroendocrine tumor of pancreas (disorder) |
Inferred relationship |
Some |
|
Human pancreatic polypeptide-secreting tumor |
Is a |
False |
Neuroendocrine tumor of pancreas (disorder) |
Inferred relationship |
Some |
|
néoplasme sécrétant du peptide inhibiteur gastrique |
Is a |
False |
Neuroendocrine tumor of pancreas (disorder) |
Inferred relationship |
Some |
|
glucagonome |
Is a |
False |
Neuroendocrine tumor of pancreas (disorder) |
Inferred relationship |
Some |
|
Gastrinoma |
Is a |
False |
Neuroendocrine tumor of pancreas (disorder) |
Inferred relationship |
Some |
|
tumeur carcinoïde de l'ampoule de Vater |
Is a |
False |
Neuroendocrine tumor of pancreas (disorder) |
Inferred relationship |
Some |
|
néoplasme neuroendocrine bénin du pancréas |
Is a |
False |
Neuroendocrine tumor of pancreas (disorder) |
Inferred relationship |
Some |
|
Pancreatic polypeptidoma |
Is a |
True |
Neuroendocrine tumor of pancreas (disorder) |
Inferred relationship |
Some |
|
Primary malignant neuroendocrine neoplasm of ampulla of Vater (disorder) |
Is a |
False |
Neuroendocrine tumor of pancreas (disorder) |
Inferred relationship |
Some |
|
Primary malignant neuroendocrine neoplasm of pancreas (disorder) |
Is a |
False |
Neuroendocrine tumor of pancreas (disorder) |
Inferred relationship |
Some |
|
gastrinome du pancréas |
Is a |
False |
Neuroendocrine tumor of pancreas (disorder) |
Inferred relationship |
Some |
|
Mixed ductal-neuroendocrine carcinoma of pancreas |
Is a |
False |
Neuroendocrine tumor of pancreas (disorder) |
Inferred relationship |
Some |
|
A rare neuroendocrine neoplasm of pancreas characterized by morphologically recognizable neuroendocrine and non-neuroendocrine components, each constituting at least 30% of the tumor volume. Based on histopathology, mixed ductal- and mixed acinar-neuroendocrine carcinomas are distinguished. Patients usually present with unspecific symptoms related to tumor growth and/or metastasis, although occurrence of Zollinger-Ellison syndrome has been reported. Resectability of the tumor is the most important prognostic factor. |
Is a |
False |
Neuroendocrine tumor of pancreas (disorder) |
Inferred relationship |
Some |
|
Neuroendocrine carcinoma of pancreas |
Is a |
False |
Neuroendocrine tumor of pancreas (disorder) |
Inferred relationship |
Some |
|
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 <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. |
Is a |
False |
Neuroendocrine tumor of pancreas (disorder) |
Inferred relationship |
Some |
|
insulinome |
Is a |
False |
Neuroendocrine tumor of pancreas (disorder) |
Inferred relationship |
Some |
|
Malignant glucagonoma of pancreas (disorder) |
Is a |
True |
Neuroendocrine tumor of pancreas (disorder) |
Inferred relationship |
Some |
|
Glucagonoma of uncertain behavior |
Is a |
False |
Neuroendocrine tumor of pancreas (disorder) |
Inferred relationship |
Some |
|
A rare functioning neuroendocrine tumour of pancreas characterised by a typically well-differentiated neoplasm composed of cells expressing serotonin. Patients may present with atypical carcinoid syndrome with abdominal pain, diarrhoea, weight loss, and/or flushing. Carcinoid syndrome is usually present only when there are liver metastases. The tumours tend to be larger than non-functioning tumours and are associated with a poorer prognosis because they are almost always metastatic. |
Is a |
True |
Neuroendocrine tumor of pancreas (disorder) |
Inferred relationship |
Some |
|
Malignant insulinoma |
Is a |
True |
Neuroendocrine tumor of pancreas (disorder) |
Inferred relationship |
Some |
|
Primary well-differentiated neuroendocrine tumor of pancreas (disorder) |
Is a |
True |
Neuroendocrine tumor of pancreas (disorder) |
Inferred relationship |
Some |
|
Well-differentiated neuroendocrine tumor of ampulla of Vater (disorder) |
Is a |
True |
Neuroendocrine tumor of pancreas (disorder) |
Inferred relationship |
Some |
|
Malignant gastrinoma of pancreas |
Is a |
True |
Neuroendocrine tumor of pancreas (disorder) |
Inferred relationship |
Some |
|
Growth hormone releasing factor-secreting tumor of pancreas |
Is a |
True |
Neuroendocrine tumor of pancreas (disorder) |
Inferred relationship |
Some |
|
Gastric inhibitory peptide-secreting tumor of pancreas (disorder) |
Is a |
True |
Neuroendocrine tumor of pancreas (disorder) |
Inferred relationship |
Some |
|
Parathyroid hormone-related peptide-secreting tumor of pancreas (disorder) |
Is a |
True |
Neuroendocrine tumor of pancreas (disorder) |
Inferred relationship |
Some |
|