SE-ATLAS

Bartter syndrome type 5 HANAC syndrome Liddle syndrome Enamel-renal syndrome Autosomal dominant proximal renal tubular acidosis Systemic lupus erythematosus Primary megaureter, adult-onset form Congenital primary megaureter, obstructed form Nail-patella syndrome Proximal renal tubular acidosis Congenital primary megaureter, refluxing form Renal agenesis Congenital primary megaureter, nonrefluxing and unobstructed form Alport syndrome Muckle-Wells syndrome Alström syndrome Familial vesicoureteral reflux Atypical hemolytic uremic syndrome Lipoprotein glomerulopathy Action myoclonus-renal failure syndrome Immunotactoid or fibrillary glomerulopathy Galloway-Mowat syndrome Distal renal tubular acidosis Oculocerebrorenal syndrome of Lowe Hereditary hypophosphatemic rickets with hypercalciuria De novo thrombotic microangiopathy after kidney transplantation Hypocomplementemic urticarial vasculitis Renal hypoplasia, unilateral Dominant hypophosphatemia with nephrolithiasis or osteoporosis Unilateral multicystic dysplastic kidney Renal hypoplasia, bilateral Bilateral multicystic dysplastic kidney Renal tubular dysgenesis due to twin-twin transfusion Drug-related renal tubular dysgenesis Hypotrichosis-lymphedema-telangiectasia-renal defect syndrome Atresia of urethra Pierson syndrome Senior-Boichis syndrome Bartter syndrome Behçet disease Collagen type III glomerulopathy Fibronectin glomerulopathy Autosomal recessive distal renal tubular acidosis LCAT deficiency Nephronophthisis Idiopathic hypercalciuria Hemolytic uremic syndrome with DGKE deficiency Phosphoribosylpyrophosphate synthetase superactivity Severe oculo-renal-cerebellar syndrome Isolated autosomal dominant hypomagnesemia, Glaudemans type Immunoglobulin-mediated membranoproliferative glomerulonephritis EAST syndrome Systemic sclerosis CREST syndrome Autoimmune interstitial lung disease-arthritis syndrome AApoAII amyloidosis Hemolytic uremic syndrome C3 glomerulonephritis Atypical hemolytic uremic syndrome with complement gene abnormality Cystinuria Takayasu arteritis Autosomal dominant polycystic kidney disease Denys-Drash syndrome Osteopetrosis with renal tubular acidosis Idiopathic steroid-sensitive nephrotic syndrome with secondary steroid resistance Idiopathic steroid-resistant nephrotic syndrome Idiopathic multidrug-resistant nephrotic syndrome Idiopathic steroid-resistant nephrotic syndrome with sensitivity to second-line immunosuppressive therapy Congenital and infantile nephrotic syndrome Primary membranous glomerulonephritis MYH9-related disease Schimke immuno-osseous dysplasia Nephrotic syndrome-epidermolysis bullosa-sensorineural deafness syndrome Apparent mineralocorticoid excess Primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement Congenital nephrotic syndrome, Finnish type Interstitial lung disease-nephrotic syndrome-epidermolysis bullosa syndrome Autosomal dominant hypophosphatemic rickets X-linked hypophosphatemia Familial steroid-resistant nephrotic syndrome with sensorineural deafness X-linked Alport syndrome Autosomal recessive Alport syndrome Autosomal dominant Alport syndrome Frasier syndrome Renal pseudohypoaldosteronism type 1 Autosomal dominant tubulointerstitial kidney disease Hypotonia-cystinuria syndrome Pediatric systemic lupus erythematosus MUC1-related autosomal dominant tubulointerstitial kidney disease IgG4-related kidney disease Anti-glomerular basement membrane disease AFib amyloidosis Juvenile polymyositis Dense deposit disease Familial hyperaldosteronism type III Atypical hemolytic uremic syndrome with anti-factor H antibodies Congenital thrombotic thrombocytopenic purpura Familial hyperaldosteronism type I Late-onset nephronophthisis Infantile nephronophthisis Prune belly syndrome Primary hyperoxaluria type 2 Methylmalonic acidemia with homocystinuria, type cblC Renal dysplasia HNF1B-related autosomal dominant tubulointerstitial kidney disease Shiga toxin-associated hemolytic uremic syndrome Autosomal dominant intermediate Charcot-Marie-Tooth disease type E Renal coloboma syndrome Idiopathic steroid-sensitive nephrotic syndrome Congenital membranous nephropathy due to fetomaternal anti-neutral endopeptidase alloimmunization Hereditary amyloidosis with primary renal involvement Familial renal glucosuria Familial steroid-resistant nephrotic syndrome with adrenal insufficiency Primary hypomagnesemia-refractory seizures-intellectual disability syndrome Juvenile dermatomyositis Renal dysplasia, unilateral Congenital primary megaureter Arthrogryposis-renal dysfunction-cholestasis syndrome Primary hypomagnesemia with hypercalciuria and nephrocalcinosis with severe ocular involvement Fetal lower urinary tract obstruction Anterior urethral valve Eosinophilic granulomatosis with polyangiitis AH amyloidosis Oligomeganephronia Microscopic polyangiitis Relapsing polychondritis Autosomal recessive polycystic kidney disease Polymyositis Dermatomyositis Autosomal dominant primary hypomagnesemia with hypocalciuria Hypohidrosis-electrolyte imbalance-lacrimal gland dysfunction-ichthyosis-xerostomia syndrome Streptococcus pneumoniae-associated hemolytic uremic syndrome Cloacal exstrophy Isolated epispadias Infection-related hemolytic uremic syndrome Diffuse cutaneous systemic sclerosis Bladder exstrophy Idiopathic non-lupus full-house nephropathy REN-related autosomal dominant tubulointerstitial kidney disease Pseudohypoaldosteronism type 1 Immunoglobulin A vasculitis Brachydactyly-arterial hypertension syndrome Polyarteritis nodosa Primary Fanconi renotubular syndrome Reynolds syndrome Joubert syndrome with oculorenal defect Oncogenic osteomalacia Pauci-immune glomerulonephritis with ANCA Medullary sponge kidney Pauci-immune glomerulonephritis without ANCA Sarcoidosis Immunotactoid glomerulopathy Mixed connective tissue disease Thrombotic thrombocytopenic purpura Renal agenesis, bilateral Multicystic dysplastic kidney Congenital renal artery stenosis Exstrophy-epispadias complex Primary systemic amyloidosis Non-amyloid monoclonal immunoglobulin deposition disease Primary localized amyloidosis Joubert syndrome with renal defect Familial Mediterranean fever Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis Generalized pseudohypoaldosteronism type 1 Gitelman syndrome Tubulointerstitial nephritis and uveitis syndrome Light and heavy chain deposition disease Heavy chain deposition disease Light chain deposition disease UMOD-related autosomal dominant tubulointerstitial kidney disease AApoAI amyloidosis Von Hippel-Lindau disease Granulomatosis with polyangiitis Hereditary renal hypouricemia Hereditary xanthinuria Immune-mediated thrombotic thrombocytopenic purpura Familial hyperaldosteronism type II Juvenile nephronophthisis Autosomal recessive hypophosphatemic rickets Hypophosphatemic rickets Dent disease type 2 Posterior urethral valve Dent disease type 1 AL amyloidosis AA amyloidosis AApoAIV amyloidosis Pauci-immune glomerulonephritis Adenine phosphoribosyltransferase deficiency Renal tubular dysgenesis Mitochondrial oxidative phosphorylation disorder Renal dysplasia, bilateral Acquired monoclonal Ig light chain-associated Fanconi syndrome Autosomal recessive infantile hypercalcemia Megacystis-megaureter syndrome Renal tubular dysgenesis of genetic origin Hypoxanthine-guanine phosphoribosyltransferase deficiency Dent disease Primary hypomagnesemia with secondary hypocalcemia Nephrogenic diabetes insipidus Non-amyloid fibrillary glomerulopathy ALys amyloidosis Primary hyperoxaluria type 1 Xanthinuria type I Buerger disease Familial hyperaldosteronism Cryoglobulinemic vasculitis Renal-hepatic-pancreatic dysplasia Primary membranoproliferative glomerulonephritis Primary hyperoxaluria type 3 Xanthinuria type II Genetic steroid-resistant nephrotic syndrome Pseudohypoaldosteronism type 2 Leigh syndrome with nephrotic syndrome Galactosemia Giant cell arteritis Primary hyperoxaluria Autosomal recessive proximal renal tubular acidosis Autosomal dominant distal renal tubular acidosis Cystinuria type B Cystinuria type A Nephrogenic syndrome of inappropriate antidiuresis Distal renal tubular acidosis with anemia Renal hypoplasia Renal agenesis, unilateral