SE-ATLAS

Karyomegalic interstitial nephritis Hereditary leiomyomatosis and renal cell cancer Renal-hepatic-pancreatic dysplasia Congenital thrombotic thrombocytopenic purpura Neonatal diabetes-congenital hypothyroidism-congenital glaucoma-hepatic fibrosis-polycystic kidneys syndrome Immune-mediated thrombotic thrombocytopenic purpura Hereditary pheochromocytoma-paraganglioma Primary localized amyloidosis Joubert syndrome with renal defect Ventriculomegaly-cystic kidney disease Genetic cystic renal 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 Primary hyperoxaluria Genetic glomerular disease Tuberous sclerosis complex Autosomal dominant tubulointerstitial kidney disease 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 Cerebrorenodigital syndrome Meckel syndrome Birt-Hogg-Dubé syndrome Von Hippel-Lindau disease Alport syndrome AL amyloidosis Fabry disease Thrombotic microangiopathy Hereditary papillary renal cell carcinoma Amyloidosis MiT family translocation renal cell carcinoma Primary systemic amyloidosis