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 Dysplasie rénale multikystique unilatérale Syndrome oculo-cérébro-rénal de Lowe Hypoplasie rénale bilatérale Microangiopathie thrombotique de novo après transplantation rénale Syndrome de Fanconi acquis associé à la chaine légère des Ig monoclonales Acidose tubulaire rénale distale Syndrome d'Alport autosomique récessif Syndrome d'Alport autosomique dominant Dysplasie rénale multikystique bilatérale Dysgénésie tubulaire rénale associée au syndrome de transfusion foeto-foetale Polymyosite juvénile Syndrome hémolytique et urémique atypique associé à des anticorps anti-facteur H Purpura thrombotique thrombocytopénique congénital Néphronophtise tardive Néphronophtise infantile Hyperoxalurie primitive type 2 Hyperoxalurie primitive type 3 Xanthinurie type II Acidose tubulaire rénale proximale autosomique récessive Acidose tubulaire rénale distale autosomique dominante Cystinurie type B Cystinurie type A Amylose héréditaire avec atteinte rénale primaire Glucosurie rénale familiale Dermatomyosite juvénile Syndrome hémolytique et urémique Syndrome hémolytique et urémique atypique lié à une anomalie d'un gène du complément Rachitisme hypophosphatémique autosomique dominant Hypophosphatémie liée à l'X Pseudohypoaldostéronisme type 1 rénal Syndrome d'hypotonie-cystinurie Syndrome hémolytique et urémique à Escherichia coli producteur de Shiga-toxines Atrésie de l'urètre Maladie de Behçet Syndrome CREST Cystinurie Excès apparent de minéralocorticoïdes Maladie des anticorps anti-membrane basale glomérulaire Hyperaldostéronisme familial type I Hyperoxalurie primitive Acidose tubulaire rénale distale autosomique récessive Déficit en LCAT Polykystose rénale autosomique dominante Syndrome de Williams Néphropathie tubulo-intersitielle autosomique dominante Hyperaldostéronisme familial type III Acidémie méthylmalonique avec homocystinurie type cblC Syndrome rein-colobome Syndrome autoimmun de pneumopathie interstitielle-arthrite Syndrome de Senior-Boichis Hypercalciurie idiopathique Hypomagnésémie primaire avec hypercalciurie et néphrocalcinose sans atteinte oculaire sévère Hypomagnésémie isolée autosomique dominante type Glaudemans Syndrome EAST Néphropathie tubulo-intersitielle autosomique dominante associée à MUC1 Maladie rénale associée à IgG4 Syndrome prune belly Dysplasie rénale Néphropathie tubulo-interstitielle autosomique dominante associée à HNF1B Syndrome d'hypomagnésémie primaire-épilepsie réfractaire-déficience intellectuelle Dysplasie rénale unilatérale Dysgénésie tubulaire rénale d'origine médicamenteuse Hyperactivité de la phosphoribosylpyrophosphate synthétase Artérite de Takayasu Hypomagnésémie primaire d'origine génétique avec hypocalciurie Hypomagnésémie primaire d'origine génétique avec normocalciurie Lupus érythémateux disséminé de l'enfant Amylose ALys 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