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autosomal dominant polycystic kidney

ICD-10: Q61MeSH: D016891ORPHA: 730

Contents

  1. 1. Overview
  2. 2. Available Treatments
  3. 3. Clinical Presentation
  4. 4. Classification & Codes

Overview

human disease

Available Treatments (0)

No treatments linked yet

Clinical trials or compassionate use may be available — consult a specialist.

Clinical Presentation

Signs and symptoms associated with autosomal dominant polycystic kidney, sourced from HPO and Orphanet clinical annotations.

Renal insufficiencyRenal cystHepatic cystsElevated circulating creatinine concentrationDecreased glomerular filtration rateHematuriaHypertensionStage 5 chronic kidney diseaseAbnormal urinary electrolyte concentrationAlbuminuriaChronic kidney diseaseFlank painRecurrent urinary tract infectionsEnlarged kidneyUric acid nephrolithiasisMitral valve prolapsePancreatic cystsAortic root aneurysmDilatation of the cerebral arteryPolycystic liver diseaseCalcium oxalate nephrolithiasisAbnormal systemic arterial morphologyReduced sperm motilityPyelonephritisArachnoid cystPituitary growth hormone cell adenoma

Classification & Codes

ICD-10 Code

Q61

MeSH Code

D016891

Orphanet Code

ORPHA:730
autosomal dominant polycystic kidney
ICD-10Q61
MeSHD016891
OrphanetORPHA:730
Treatments0 drug(s)
Symptoms on record26 signs
Statuspublished
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO