Genetic Kidney Disease

Polycystic Kidney Disease (PKD) is result from hereditary factors. In polycystic kidney disease number of cysts develops in the kidney, these cysts gradually replace the mass of kidney. Impairing kidney function and leading to renal failure.

  • Polycystic Kidney Disease
  • Autosomal Dominant Polycystic Kidney Disease
  • Cystic Diseases of the Kidney
  • Autosomal Recessive Polycystic Kidney Disease
  • Alport Syndrome
  • Medullary Cystic Kidney Disease
  • Nephronophthisis
  • Bartter Syndrome
  • Congenital Nephrotic Syndrome
  • Ciliopathy
  • Von Hippel–Lindau Disease
  • Tuberous Sclerosis
  • Renal Agenesis
  • Atypical Hemolytic Uremic Syndrome
  • Cystinuria
  • Hypercalciuria
  • Fabry Disease
  • Gitelman Syndrome
  • Cystinosis
  • Branchiootorenal Syndrome
  • Papillorenal Syndrome
  • Oculocerebrorenal Syndrome
  • Senior-Løken Syndrome
  • Meckel-Gruber Syndrome
  • Tubulopathy
  • Fraser Syndrome
  • Primary Hyperoxaluria
  • Bardet-Biedl Syndrome
  • Mineral and Bone Disorder in Chronic Kidney Disease

Related Conference of Genetic Kidney Disease

August 28-29, 2025

10th World Kidney Congress

London, UK
November 03-04, 2025

29th European Nephrology Conference

Rome, Italy
December 10-11, 2025

12th World Congress on Epidemiology & Public Health

Amsterdam, Netherlands
March 09-10, 2026

17th Nephrology,Renal Medicine & Renal Care

Dubai, UAE
March 26-27, 2026

22nd World Nephrology Conference

Amsterdam, Netherlands
June 29-30, 2026

18th World Nephrology Summit

Aix-en-Provence, France

Genetic Kidney Disease Conference Speakers

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