Autosomal dominant polycystic kidney disease

Orpha code: 730OMIM code: 600666

Definition

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).

Disease data
Classification

Disease

Synonyms
ADPKD
ADPKD
ORPHA code
730
OMIM code
600666
ICD10 code
Q61.2
ICD11 code
GB81

No additional description.

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