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|
|Episodic abdominal pain||0002574|
Inflammation of the esophagus
|30%-79% of people have these symptoms|
|5%-29% of people have these symptoms|
|Elevated circulating parathyroid
|Growth hormone excess||0000845|
High blood calcium levels
Increased calcium in blood[ more ]
Elevated blood parathyroid hormone level
|Increased circulating cortisol level||0003118|
|Increased glucagon level||0030688|
|Increased urinary cortisol level||
High urine cortisol level
Intestinal blockage[ more ]
Yellowing of the skin[ more ]
Multiple fatty lumps
Enlarged parathyroid glands
|Pituitary growth hormone cell adenoma||0011760|
|Pituitary null cell adenoma||0011761|
|Pituitary prolactin cell adenoma||0006767|
|1%-4% of people have these symptoms|
|Percent of people who have these symptoms is not available through HPO|
|Abnormality of the thyroid gland||
|Confetti-like hypopigmented macules||0007449|
Low blood sugar
|Pancreatic islet cell adenoma||0008261|
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If you need medical advice, you can look for doctors or other healthcare professionals who have experience with this disease. You may find these specialists through advocacy organizations, clinical trials, or articles published in medical journals. You may also want to contact a university or tertiary medical center in your area, because these centers tend to see more complex cases and have the latest technology and treatments.
If you can’t find a specialist in your local area, try contacting national or international specialists. They may be able to refer you to someone they know through conferences or research efforts. Some specialists may be willing to consult with you or your local doctors over the phone or by email if you can't travel to them for care.
You can find more tips in our guide, How to Find a Disease Specialist. We also encourage you to explore the rest of this page to find resources that can help you find specialists.
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 other causes of increased acid output and elevated FSG levels: Helicobacter pylori infections, retained gastric antrum, gastric outlet obstruction, renal failure, antral G cell syndromes, idiopathic gastroesophageal reflux or peptic ulcer disease, and physiological causes of hypergastrinemia (atrophic gastritis, pernicious anemia, or use of potent antisecretory drugs).
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.
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
My dad had ZE syndrome and passed away at age 31. Are there genetic tests that could be done to see if my brother and I carry this gene? I have a gastro specialist and he tests my gastric levels every year for this reason. I have mixed feelings about knowing if I have the gene or not. See answer