Autosomal dominant polycystic kidney disease
Synonyms: ADPKD
A rare genetic renal tubular disease characterized by progressive outgrowths of fluid-filled cysts from the renal epithelium which can manifest with hematuria urinary tract infections hypertension and abdominal or flank pain. The slowly progressive loss of kidney function may evolve to end stage kidney disease (ESKD).
Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview.
Reference: Access aggregated data from Orphanet at Orphadata.
Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http://www.orphadata.org. Data version April 2024
Newly diagnosed with
Autosomal dominant polycystic kidney disease?
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Advocacy Organizations
Help Hope Live
Help Hope Live assists individuals living with catastrophic injuries and illnesses to fundraise toward their medical expenses and related costs.
Syndromes Without A Name (SWAN) Australia
Provide information, support and advocacy to families caring for a child with an undiagnosed or rare genetic condition.
Clinical Trials
For a list of clinical trials in this disease area, please click here.