SE-ATLAS

Bartter syndrome type 5 Liddle syndrome Enamel-renal syndrome 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 Atypical hemolytic uremic syndrome Lipoprotein glomerulopathy Action myoclonus-renal failure syndrome Systemic lupus erythematosus Galloway-Mowat syndrome Distal renal tubular acidosis 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 Hypotonia-cystinuria syndrome Pediatric systemic lupus erythematosus IgG4-related kidney disease Anti-glomerular basement membrane disease AFib amyloidosis Juvenile polymyositis Immunotactoid or fibrillary glomerulopathy Dense deposit disease Familial hyperaldosteronism type III Oculocerebrorenal syndrome of Lowe 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 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 Hereditary hypophosphatemic rickets with hypercalciuria Familial renal glucosuria Familial steroid-resistant nephrotic syndrome with adrenal insufficiency Primary hypomagnesemia-refractory seizures-intellectual disability syndrome Juvenile dermatomyositis Renal dysplasia, unilateral De novo thrombotic microangiopathy after kidney transplantation Frasier syndrome Renal pseudohypoaldosteronism type 1 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 Pseudohypoaldosteronism type 1 Congenital primary megaureter 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 Exstrophy-epispadias complex Primary systemic amyloidosis 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 AApoAI amyloidosis Von Hippel-Lindau disease Granulomatosis with polyangiitis Congenital renal artery stenosis 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 Amylose AApoAIV Glomérulonéphrite pauci-immune Déficit en adénosine phosphoribosyltransférase Dysgénésie tubulaire rénale Anomalie de la phosphorylation oxydative mitochondriale Dysplasie rénale bilatérale Maladie des dépôts d'immunoglobuline monoclonale non-amyloïde Syndrome HANAC Méga-uretère primitif de l'adulte Syndrome d'Alström Reflux vésico-urétéral familial Syndrome de Fanconi acquis associé à la chaine légère des Ig monoclonales Hypercalcémie infantile autosomique récessive Syndrome mégavessie-méga-uretères Dysgénésie tubulaire rénale d'origine génétique Déficit en hypoxanthine-guanine phosphoryl transférase Maladie de Dent Hypomagnésémie primaire avec hypocalcémie secondaire Diabète insipide néphrogénique Glomérulonéphrite à dépôts fibrillaires pseudoamyloïdes Amylose ALys Hyperoxalurie primitive type 1 Xanthinurie type I Maladie de Buerger Hyperaldostéronisme familial Vascularite cryoglobulinémique Dysplasie réno-hépato-pancréatique Glomérulonéphrite membranoproliférative primaire Syndrome néphrotique corticorésistant d'origine génétique Pseudohypoaldostéronisme type 2 Syndrome de Leigh avec syndrome néphrotique Galactosémie Artérite à cellules géantes Hyperoxalurie primitive Hyperoxalurie primitive type 3 Xanthinurie type II Acidose tubulaire rénale proximale autosomique dominante Méga-uretère primitif obstructif congénital Acidose tubulaire rénale proximale autosomique récessive Acidose tubulaire rénale distale autosomique dominante Cystinurie type B Cystinurie type A Syndrome néphrogénique d'antidiurèse inappropriée Acidose tubulaire rénale distale avec anémie Hypoplasie rénale Agénésie rénale unilatérale