SE-ATLAS

AL amyloidosis Thrombotic microangiopathy Fabry disease Amyloidosis MiT family translocation renal cell carcinoma Primary systemic amyloidosis Karyomegalic interstitial nephritis Renal-hepatic-pancreatic dysplasia Congenital thrombotic thrombocytopenic purpura Neonatal diabetes-congenital hypothyroidism-congenital glaucoma-hepatic fibrosis-polycystic kidneys syndrome Immune-mediated thrombotic thrombocytopenic purpura Primary localized amyloidosis Genetic cystic renal disease Joubert syndrome with renal defect Ventriculomegaly-cystic kidney disease Atypical hemolytic uremic syndrome Primary membranous glomerulonephritis Autosomal dominant polycystic kidney disease Autosomal recessive polycystic kidney disease Familial juvenile hyperuricemic nephropathy type 1 Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis Primary hyperoxaluria type 1 Genetic glomerular disease Primary hyperoxaluria Tuberous sclerosis complex Renal or urinary tract malformation Thrombotic thrombocytopenic purpura Adult familial nephronophthisis-spastic quadriparesia syndrome Saldino-Mainzer syndrome Renal cell carcinoma Bardet-Biedl syndrome Bartter syndrome Meckel syndrome Cerebrorenodigital syndrome Birt-Hogg-Dubé syndrome Von Hippel-Lindau disease Alport syndrome