SE-ATLAS

Autosomal dominant polycystic kidney disease Von Hippel-Lindau disease Gitelman syndrome Nephronophthisis Dent disease Alport syndrome Birt-Hogg-Dubé syndrome Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis Atypical hemolytic uremic syndrome with complement gene abnormality X-linked Alport syndrome Hypophosphatemic rickets Autosomal recessive Alport syndrome Autosomal dominant Alport syndrome Gitelman-like kidney tubulopathy due to mitochondrial DNA mutation Fabry disease Congenital nephrotic syndrome, Finnish type PBX1-related congenital anomalies of kidney and urinary tract syndrome CHARGE syndrome Karyomegalic interstitial nephritis Hereditary leiomyomatosis and renal cell cancer Genetic steroid-resistant nephrotic syndrome Bartter syndrome type 4 Late-onset nephronophthisis Familial Mediterranean fever Autosomal recessive polycystic kidney disease Medullary sponge kidney MYH9-related disease Bartter syndrome type 3 Familial hyperaldosteronism type IV Acute intermittent porphyria Bardet-Biedl syndrome Bartter syndrome Bartter syndrome type 1 MUC1-related autosomal dominant tubulointerstitial kidney disease Bartter syndrome type 2 HNF1B-related autosomal dominant tubulointerstitial kidney disease UMOD-related autosomal dominant tubulointerstitial kidney disease Autosomal dominant intermediate Charcot-Marie-Tooth disease type E