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 Malformation du rein et des voies urinaires Purpura thrombotique thrombocytopénique Syndrome de néphronophtise familiale de l'adulte-quadriparésie spastique Syndrome de Saldino-Mainzer Carcinome rénal Syndrome de Bardet-Biedl Syndrome de Bartter Syndrome cérébrorénodigital Syndrome de Meckel Syndrome de Birt-Hogg-Dubé Maladie de von Hippel-Lindau Syndrome d'Alport Amylose AL Maladie de Fabry Microangiopathie thrombotique Cancer papillaire rénal héréditaire Amylose Carcinome rénal associé à une translocation de la famille MiT Amylose primitive systémique