SE-ATLAS

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