SE-ATLAS

Dent disease Hereditary leiomyomatosis and renal cell cancer MYH9-related disease Karyomegalic interstitial nephritis Bartter syndrome type 4 X-linked Alport syndrome Autosomal recessive Alport syndrome Familial Mediterranean fever Autosomal dominant Alport syndrome Gitelman-like kidney tubulopathy due to mitochondrial DNA mutation Familial hyperaldosteronism type IV Bardet-Biedl syndrome Bartter syndrome UMOD-related autosomal dominant tubulointerstitial kidney disease Late-onset nephronophthisis Bartter syndrome type 3 Acute intermittent porphyria Bartter syndrome type 1 Hypophosphatemic rickets Bartter syndrome type 2 HNF1B-related autosomal dominant tubulointerstitial kidney disease Autosomal dominant intermediate Charcot-Marie-Tooth disease type E Atypical hemolytic uremic syndrome with complement gene abnormality Autosomal recessive polycystic kidney disease Congenital nephrotic syndrome, Finnish type Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis Gitelman syndrome MUC1-related autosomal dominant tubulointerstitial kidney disease Von Hippel-Lindau disease CHARGE syndrome Nephronophthisis PBX1-related congenital anomalies of kidney and urinary tract syndrome Medullary sponge kidney Birt-Hogg-Dubé syndrome Autosomal dominant polycystic kidney disease Alport syndrome Immunoglobulin A nephropathy Genetic steroid-resistant nephrotic syndrome Systemic lupus erythematosus Primary membranous glomerulonephritis Pauci-immune glomerulonephritis without ANCA Non-amyloid fibrillary glomerulopathy Tuberous sclerosis complex Primary membranoproliferative glomerulonephritis Tubulointerstitial nephritis and uveitis syndrome IgG4-related kidney disease Anti-glomerular basement membrane disease Light chain deposition disease Idiopathic nephrotic syndrome C3 glomerulopathy AL amyloidosis Anti-neutrophil cytoplasmic antibody-associated vasculitis