SE-ATLAS

Buerger disease Hereditary renal hypouricemia Renal or urinary tract malformation Liddle syndrome Glomerular disease Tubulointerstitial nephritis and uveitis syndrome Familial hyperaldosteronism type I Adrenocortical carcinoma Autosomal dominant progressive nephropathy with hypertension Hypertension due to gain-of-function mutations in the mineralocorticoid receptor Thrombotic microangiopathy Transient pseudohypoaldosteronism Nephrogenic diabetes insipidus-intracranial calcification-short stature-facial dysmorphism syndrome Familial hyperthyroidism due to mutations in TSH receptor Idiopathic hypercalciuria Dent disease Genetic primary hypomagnesemia Genetic cystic renal disease Dominant hypophosphatemia with nephrolithiasis or osteoporosis Primary renal tubular acidosis Catecholamine-producing tumor Rare renal tubular disease Nephrogenic syndrome of inappropriate antidiuresis Apparent mineralocorticoid excess Brachydactyly-arterial hypertension syndrome Rare genetic cause of hypertension Rare cause of hypertension REN-related autosomal dominant tubulointerstitial kidney disease Primary Fanconi renotubular syndrome Pseudohypoaldosteronism type 1 Pseudohypoparathyreoidismus Pseudohypoaldosteronismus Typ 2 Pseudoxanthoma elasticum Zystinurie Hyperurikämie-pulmonale Hypertension- Nierenversagen-Alkalose-Syndrom Nierenarterienstenose, kongenitale Gitelman-Syndrom Williams-Syndrom Diabetes insipidus, nephrogener Hypotonie-Cystinurie-Syndrom Typ 1 Bartter-Syndrom