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||
|80%-99% of people have these symptoms|
|Decreased glomerular filtration rate||0012213|
|Elevated serum creatinine||
High blood creatinine level
Increased serum creatinine[ more ]
|30%-79% of people have these symptoms|
|Abnormal urinary electrolyte concentration||0012591|
Blood in urine
|Stage 5 chronic kidney disease||0003774|
|5%-29% of people have these symptoms|
|Aortic root aneurysm||
Bulge in wall of root of large artery that carries blood away from heart
Fluid-filled sac located in membrane surrounding brain or spinal cord
|Dilatation of the cerebral artery||0004944|
|Mitral valve prolapse||0001634|
|Polycystic liver disease||0006557|
|Recurrent urinary tract infections||
Frequent urinary tract infections
Repeated bladder infections
Repeated urinary tract infections
Urinary tract infections
Urinary tract infections, recurrent[ more ]
|Reduced sperm motility||0012207|
|1%-4% of people have these symptoms|
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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.
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I am curious if my fiance who has inherited polycystic disease from his mother will follow her patterns and symptoms that she has faced with this disease. In autosomal dominant polycystic kidney disease (ADPKD), do the symptoms and severity of symptoms tend to be the same among affected family members (e.g., would a mother and her son with ADPKD be similarly affected)? See answer