SE-ATLAS

Primary renal tubular acidosis Congenital nephrotic syndrome, Finnish type Rare genetic renal disease C3 glomerulonephritis Nephronophthisis Genetic steroid-resistant nephrotic syndrome Familial vesicoureteral reflux X-linked hypophosphatemia Genetic cystic renal disease Joubert syndrome with renal defect Digenic Alport syndrome Senior-Loken syndrome X-linked Alport syndrome Hemolytic uremic syndrome with DGKE deficiency Oculocerebrorenal syndrome of Lowe Atypical hemolytic uremic syndrome 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