SE-ATLAS

Glomerular disease Nephrogenic diabetes insipidus-intracranial calcification-short stature-facial dysmorphism syndrome Primary Fanconi renotubular syndrome Nephrogenic syndrome of inappropriate antidiuresis Renal or urinary tract malformation Hyperuricemia-pulmonary hypertension-renal failure-alkalosis syndrome Tubulointerstitial nephritis and uveitis syndrome Transient pseudohypoaldosteronism Bardet-Biedl syndrome Bartter syndrome REN-related autosomal dominant tubulointerstitial kidney disease Rare cause of hypertension Dent disease Pseudohypoaldosteronism type 1 Hypotonia-cystinuria type 1 syndrome Acquired monoclonal Ig light chain-associated Fanconi syndrome Thrombotic microangiopathy Primary renal tubular acidosis Hereditary renal hypouricemia Nephronophthisis Genetic cystic renal disease Dominant hypophosphatemia with nephrolithiasis or osteoporosis Idiopathic hypercalciuria Oculocerebrorenal syndrome of Lowe Cystinuria Atypical hemolytic uremic syndrome Primary membranous glomerulonephritis Autosomal dominant polycystic kidney disease Nephrogenic diabetes insipidus Primary hyperoxaluria Rare renal tubular disease Rare primary hyperaldosteronism Gitelman syndrome Pseudohypoparathyroidism Anti-neutrophil cytoplasmic antibody-associated vasculitis