This table lists symptoms that people with this disease may have. For most diseases, symptoms will vary from person to person. People with the same disease may not have all the symptoms listed. This information comes from a database called the Human Phenotype Ontology (HPO) . The HPO collects information on symptoms that have been described in medical resources. The HPO is updated regularly. Use the HPO ID to access more in-depth information about a symptom.
|Medical Terms||Other Names||
|100% of people have these symptoms|
|80%-99% of people have these symptoms|
Pain in stomach
Stomach pain[ more ]
Chronic extreme exhaustion
|Exocrine pancreatic insufficiency||
Inability to properly digest food due to lack of pancreatic digestive enzymes
|30%-79% of people have these symptoms|
|Functional intestinal obstruction||0005249|
Yellowing of the skin[ more ]
Swollen lymph nodes
|5%-29% of people have these symptoms|
|Elevated hepatic transaminase||
High liver enzymes
Enlarged liver and spleen
|Nausea and vomiting||0002017|
Liver tumor[ more ]
Related diseases are conditions that have similar signs and symptoms. A health care provider may consider these conditions in the table below when making a diagnosis. Please note that the table may not include all the possible conditions related to this disease.
Conditions with similar signs and symptoms from Orphanet
Differential diagnoses include a wide variety of diseases such as acute and chronic pancreatitis, cholangitis, cholecystitis, cholelithiasis, bile duct tumors and strictures, and gastric cancer and ulcers.
Visit the Orphanet disease page for more information.
Research helps us better understand diseases and can lead to advances in diagnosis and treatment. This section provides resources to help you learn about medical research and ways to get involved.
Support and advocacy groups can help you connect with other patients and families, and they can provide valuable services. Many develop patient-centered information and are the driving force behind research for better treatments and possible cures. They can direct you to research, resources, and services. Many organizations also have experts who serve as medical advisors or provide lists of doctors/clinics. Visit the group’s website or contact them to learn about the services they offer. Inclusion on this list is not an endorsement by GARD.
Living with a genetic or rare disease can impact the daily lives of patients and families. These resources can help families navigate various aspects of living with a rare disease.
These resources provide more information about this condition or associated symptoms. The in-depth resources contain medical and scientific language that may be hard to understand. You may want to review these resources with a medical professional.
Questions sent to GARD may be posted here if the information could be helpful to others. We remove all identifying information when posting a question to protect your privacy. If you do not want your question posted, please let us know. Submit a new question
Both my mother and maternal aunt have been diagnosed with pancreatic adenocarcinoma. My question is: I have three siblings all in our late 40s, and three cousins the same. What are the recommendations for genetic testing and screening? My sister had an MRI, I'm not sure I will get it covered. Should we also be doing CA 19-9 blood tests (which were high in both my mother and aunt)? See answer