SE-ATLAS

Azidose, renale tubuläre, primäre Nephrotisches Syndrom, kongenitales, finnischer Typ Nierenkrankheit, genetisch bedingte C3-Glomerulonephritis Nephronophthise Nephrotisches Syndrom, steroid-resistentes, genetisch bedingtes Vesicoureteraler Reflux, familiäre Form Hypophosphatämie, X-chromosomale Zystische Nierenerkrankung, genetisch bedingte Joubert-Syndrom mit Nierenstörung Digenisches Alport-Syndrom Senior-Loken-Syndrom Alport-Syndrom, X-chromosomales Hämolytisch-urämisches Syndrom mit DGKE-Mangel Okulo-zerebro-renales Syndrom Lowe Hämolytisch-urämisches Syndrom, atypische Form Autosomal recessive Alport syndrome Autosomal dominant Alport syndrome Renal tubular dysgenesis Autosomal dominant polycystic kidney disease Pauci-immune glomerulonephritis with ANCA Autosomal recessive polycystic kidney disease Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis Autosomal dominant primary hypomagnesemia with hypocalciuria Genetic glomerular disease Immunoglobulin A nephropathy Primary membranoproliferative glomerulonephritis Rare disorder potentially indicated for kidney transplant Fetal lower urinary tract obstruction Gitelman syndrome Renal or urinary tract malformation Congenital primary megaureter Genetic renal tubular disease Immunoglobulin-mediated membranoproliferative glomerulonephritis Non-syndromic renal or urinary tract malformation Renal hypoplasia Genetic hemolytic uremic syndrome Bardet-Biedl syndrome Hematological disorder with renal involvement Bartter syndrome Genetic renal or urinary tract malformation Idiopathic steroid-sensitive nephrotic syndrome with secondary steroid resistance Hypophosphatemic rickets Shiga toxin-associated hemolytic uremic syndrome X-linked Alport syndrome-diffuse leiomyomatosis Renal agenesis Multicystic dysplastic kidney Alport syndrome