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non-functional pancreatic neuroendocrine tumor

The information provided on this page is for informational purposes only. The National Organization for Rare Disorders (NORD) does not endorse the information presented. The content has been gathered in partnership with the MONDO Disease Ontology. Please consult with a healthcare professional for medical advice and treatment.

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Disease Overview

A low or intermediate grade well differentiated tumor with neuroendocrine differentiation that arises from the pancreas. It is characterized by the absence of a hormone-related clinical syndrome.

Synonyms

  • inactive pancreatic endocrine tumor
  • inactive pancreatic endocrine tumour
  • non functioning pancreatic endocrine tumor
  • non functioning pancreatic endocrine tumour
  • non-functional pancreatic neuroendocrine tumor
  • non-functioning EPTs
  • non-functioning PNET
  • non-functioning endocrine pancreatic tumors
  • non-functioning endocrine pancreatic tumours
  • non-functioning neuroendocrine tumor of pancreas
  • non-functioning neuroendocrine tumour of pancreas
  • non-functioning pancreatic NET
  • non-functioning pancreatic endocrine tumor
  • non-functioning pancreatic endocrine tumour
  • non-functioning pancreatic neuroendocrine tumor
  • non-functioning pancreatic neuroendocrine tumour
  • non-functioning well differentiated pancreatic endocrine tumor
  • non-functioning well differentiated pancreatic endocrine tumour
  • non-functioning well-differentiated NEN of pancreas
  • non-functioning well-differentiated neuroendocrine neoplasm of pancreas
  • non-functioning well-differentiated pancreatic NEN
  • non-functioning well-differentiated pancreatic neuroendocrine neoplasm
  • non-syndromic pancreatic NET
  • non-syndromic pancreatic neuroendocrine tumor
  • non-syndromic pancreatic neuroendocrine tumour
  • nonfunctional pancreatic NET
  • nonfunctional pancreatic neuroendocrine tumor
  • nonfunctional pancreatic neuroendocrine tumour
  • nonsyndromic pancreatic endocrine tumor
  • nonsyndromic pancreatic endocrine tumour
  • nonsyndromic pancreatic neuroendocrine tumor
  • nonsyndromic pancreatic neuroendocrine tumour
GARD Disease Summary

The Genetic and Rare Diseases Information Center (GARD) has information and resources for patients, caregivers, and families that may be helpful before and after diagnosis of this condition. GARD is a program of the National Center for Advancing Translational Sciences (NCATS), part of the National Institutes of Health (NIH).

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Orphanet

Orphanet has a summary about this condition that may include information on the diagnosis, care, and treatment as well as other resources. Some of the information and resources are available in languages other than English. The summary may include medical terms, so we encourage you to share and discuss this information with your doctor. Orphanet is the French National Institute for Health and Medical Research and the Health Programme of the European Union.

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