These are chiefly focused on the FSGS/Nephrotic syndrome spectrum and were strongly represented in the data set, covering about 60-65% of OMIM-mentioned FSGS-associated genes, followed by genes responsible for ciliopathies (nephronophthisis, Joubert, Bardet-Biedel Syndrome), and autosomal dominant polycystic kidney disease (ADPKD) and autosomal recessive polycystic kidney disease (ARPKD), namely GANAB3 and PKHD1 in addition to PKD1, PKD226,46. The gene discussed is PKHD1; the disease is nephronophthisis.