SE-ATLAS

C3 glomerulopathy Glomerular disease Albright hereditary osteodystrophy Renal tubular dysgenesis due to twin-twin transfusion Syndromic renal or urinary tract malformation Secondary glomerular disease Anti-neutrophil cytoplasmic antibody-associated vasculitis Renal tubular dysgenesis of genetic origin Drug-related renal tubular dysgenesis Basement membrane disease Methylcobalamin deficiency type cblG Pediatric systemic lupus erythematosus Sebastian syndrome HANAC syndrome Oculocerebrorenal syndrome of Lowe Autosomal dominant Alport syndrome Familial steroid-resistant nephrotic syndrome with sensorineural deafness Osteofibrous dysplasia X-linked Alport syndrome Mixed connective tissue disease Autosomal recessive Alport syndrome AApoAII amyloidosis Familial hyperaldosteronism type I Nephrotic syndrome-epidermolysis bullosa-sensorineural deafness syndrome Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis ALys amyloidosis Hypocomplementemic urticarial vasculitis AApoAI amyloidosis Ciliopathies with major skeletal involvement AFib amyloidosis Joubert syndrome with oculorenal defect Smith-Lemli-Opitz syndrome Multiple epiphyseal dysplasia and pseudoachondroplasia Adrenocortical carcinoma Multiple metaphyseal dysplasia C3 glomerulonephritis Hypertension due to gain-of-function mutations in the mineralocorticoid receptor Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency Autosomal dominant progressive nephropathy with hypertension Primary hyperoxaluria Acromelic dysplasia Dense deposit disease Spondylodysplastic dysplasia Nephrogenic diabetes insipidus-intracranial calcification-short stature-facial dysmorphism syndrome Congenital hydronephrosis Mesomelic and rhizo-mesomelic dysplasia Tyrosinemia type 2 Transient pseudohypoaldosteronism Acromesomelic dysplasia Secondary vasculitis Thrombotic microangiopathy Pseudohypoaldosteronism type 2B Vasculitis due to ADA2 deficiency Slender bone dysplasia Atypical hemolytic uremic syndrome with MCP/CD46 anomaly Campomelic dysplasia and related disorders Pseudohypoaldosteronism type 2A Atypical hemolytic uremic syndrome with C3 anomaly Neonatal diabetes-congenital hypothyroidism-congenital glaucoma-hepatic fibrosis-polycystic kidneys syndrome Chondrodysplasia punctata Oligoarticular juvenile idiopathic arthritis with anti-nuclear antibodies Atypical hemolytic uremic syndrome with B factor anomaly Primary bone dysplasia with multiple joint dislocations Pseudohypoaldosteronism type 2C Primary hypomagnesemia with hypercalciuria and nephrocalcinosis with severe ocular involvement Familial hyperthyroidism due to mutations in TSH receptor Idiopathic hypercalciuria Atypical hemolytic uremic syndrome with anti-factor H antibodies Atypical hemolytic uremic syndrome with I factor anomaly Dent disease Primary bone dysplasia with increased bone density Rapidly progressive glomerulonephritis Atypical hemolytic uremic syndrome with H factor anomaly Renal dysplasia, bilateral Congenital thrombotic thrombocytopenic purpura Primary bone dysplasia with decreased bone density Hypotonia-cystinuria syndrome Distal renal tubular acidosis Renal dysplasia, unilateral Sporadic pheochromocytoma Senior-Loken syndrome Reactive arthritis Immune-mediated thrombotic thrombocytopenic purpura Galloway-Mowat syndrome Unilateral congenital megacalycosis Carnitine palmitoyl transferase 1A deficiency Genetic primary hypomagnesemia Carnitine palmitoyltransferase II deficiency Congenital nephrotic syndrome, Finnish type Familial primary hypomagnesemia with normocalciuria and normocalcemia Hereditary pheochromocytoma-paraganglioma Shiga toxin-associated hemolytic uremic syndrome Renal pseudohypoaldosteronism type 1 Primary bone dysplasia with defective bone mineralization Atypical hemolytic uremic syndrome with thrombomodulin anomaly Genetic cystic renal disease Adenine phosphoribosyltransferase deficiency Primary bone dysplasia with disorganized development of skeletal components Cleidocranial dysplasia and isolated cranial ossification defect UMOD-related autosomal dominant tubulointerstitial kidney disease Autosomal dominant primary hypomagnesemia with hypocalciuria Generalized pseudohypoaldosteronism type 1 2p21 microdeletion syndrome Nail-patella-like renal disease Systemic primary carnitine deficiency MUC1-related autosomal dominant tubulointerstitial kidney disease Congenital bilateral megacalycosis Primary osteolysis Nail-patella syndrome Carnitine-acylcarnitine translocase deficiency Oligoarticular juvenile idiopathic arthritis without anti-nuclear antibodies Late-onset nephronophthisis Rare hyperlipidemia Sporadic pheochromocytoma/secreting paraganglioma Idiopathic nephrotic syndrome Glutaryl-CoA dehydrogenase deficiency Rheumatoid factor-negative polyarticular juvenile idiopathic arthritis Tyrosinemia type 3 Methylmalonic acidemia with homocystinuria Infantile nephronophthisis Acquired monoclonal Ig light chain-associated Fanconi syndrome Dominant hypophosphatemia with nephrolithiasis or osteoporosis Primary renal tubular acidosis Oligoarticular juvenile idiopathic arthritis Interstitial lung disease-nephrotic syndrome-epidermolysis bullosa syndrome Immunotactoid or fibrillary glomerulopathy Action myoclonus-renal failure syndrome Juvenile nephronophthisis Sporadic secreting paraganglioma Unspecified juvenile idiopathic arthritis Bickerstaff brainstem encephalitis NPHP3-related Meckel-like syndrome Systemic-onset juvenile idiopathic arthritis May-Hegglin thrombocytopenia Primary hyperoxaluria type 1 Renal tubular dysgenesis Rheumatoid factor-negative juvenile idiopathic arthritis with anti-nuclear antibodies Isovaleric acidemia Phenylketonuria Primary hyperoxaluria type 3 Sporadic idiopathic steroid-resistant nephrotic syndrome with collapsing glomerulopathy Rare inborn errors of metabolism Catecholamine-producing tumor Lysosomal disease Primary hyperoxaluria type 2 Propionic acidemia Xanthinuria type II Lethal chondrodysplasia Xanthinuria type I Antenatal Bartter syndrome Congenital and infantile nephrotic syndrome Rare renal tubular disease Short stature-advanced bone age-early-onset osteoarthritis syndrome Cystic fibrosis Nephrogenic syndrome of inappropriate antidiuresis LAMB2-related infantile-onset nephrotic syndrome Bartter syndrome type 3 Primary membranous glomerulonephritis Medium chain acyl-CoA dehydrogenase deficiency Peroxisomal disease Rheumatoid factor-negative juvenile idiopathic arthritis without anti-nuclear antibodies Autosomal dominant distal renal tubular acidosis Autosomal recessive proximal renal tubular acidosis Genetic primary hypomagnesemia with hypocalciuria Thrombotic thrombocytopenic purpura Distal renal tubular acidosis with anemia Hypertrophic cardiomyopathy with kidney anomalies due to mitochondrial DNA mutation Autosomal recessive distal renal tubular acidosis without deafness Cystinuria type A Apparent mineralocorticoid excess Brachydactyly-arterial hypertension syndrome Autosomal recessive distal renal tubular acidosis with deafness Idiopathic steroid-sensitive nephrotic syndrome Primary hypomagnesemia with hypercalciuria and nephrocalcinosis Autosomal recessive polycystic kidney disease Exstrophy-epispadias complex Bartter syndrome with hypocalcemia Polyarticular juvenile idiopathic arthritis Congenital membranous nephropathy due to fetomaternal anti-neutral endopeptidase alloimmunization Cystinuria type B Pseudohypoaldosteronism type 2D Autosomal dominant tubulointerstitial kidney disease Idiopathic steroid-sensitive nephrotic syndrome with minimal change Idiopathic steroid-sensitive nephrotic syndrome with focal segmental hyalinosis Rheumatoid factor-positive polyarticular juvenile idiopathic arthritis Rare systemic or rheumatological disease of childhood Rare cause of hypertension Rare genetic cause of hypertension Idiopathic steroid-sensitive nephrotic syndrome with diffuse mesangial proliferation Isolated autosomal dominant hypomagnesemia, Glaudemans type Enthesitis-related juvenile idiopathic arthritis REN-related autosomal dominant tubulointerstitial kidney disease Bartter syndrome type 4 Psoriasis-related juvenile idiopathic arthritis Disorder of fatty acid oxidation and ketogenesis Schimke immuno-osseous dysplasia Genetic primary hypomagnesemia with normocalciuria Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial proliferation Hereditary xanthinuria Osteopetrosis with renal tubular acidosis Kosaki overgrowth syndrome Familial idiopathic steroid-resistant nephrotic syndrome with focal segmental hyalinosis Multiple acyl-CoA dehydrogenase deficiency Megacystis-microcolon-intestinal hypoperistalsis syndrome Maladie de Dent type 2 Déficit en acyl-CoA déshydrogénase des acides gras à chaîne très longue Intolérance au fructose héréditaire Syndrome néphrotique idiopathique familial corticorésistant à lésions glomérulaires minimes Trouble du métabolisme du cycle de l'urée et de la détoxification de l'ammoniac Pseudohypoparathyroïdie type 1A Syndrome néphrotique idiopathique sporadique corticorésistant avec hyalinose segmentaire focale Trouble du cycle de la carnitine et du transport de la carnitine Syndrome d'Alport Maladie rénale rare Syndrome d'Alport lié à l'X-léiomyomatose diffuse Syndrome néphrotique idiopathique familial corticorésistant avec sclérose mésangiale diffuse Déficit en protéine trifonctionnelle mitochondriale Pseudohypoaldostéronisme type 2E Syndrome de Fanconi primitif rénotubulaire Tyrosinémie type 1 Syndrome néphrotique idiopathique sporadique corticorésistant avec sclérose mésangiale diffuse Syndrome d'Epstein Pseudopseudohypoparathyroïdie Syndrome de Senior-Boichis Pseudohypoparathyroïdie type 1C Syndrome néphrotique idiopathique sporadique corticorésistant avec prolifération mésangiale diffuse Syndrome néphrotique idiopathique sporadique corticorésistant à lésions glomérulaires minimes Amylose héréditaire avec atteinte rénale primaire Syndrome hémolytique et urémique par déficit en DGKE Méga-uretère primitif congénital Glomérulopathie à dépôts de collagène de type III Syndrome d'hyperuricémie-hypertension artérielle pulmonaire-insuffisance rénale-alcalose Pseudo-hypoparathyroïdie Maladie de von Hippel-Lindau Pseudohypoaldostéronisme type 1 Glomérulopathie à dépôts de fibronectine Syndrome de Fechtner Syndrome de Frasier Syndrome WAGR Syndrome de néphronophtise familiale de l'adulte-quadriparésie spastique Pseudohypoaldostéronisme type 2 Agénésie rénale bilatérale Pseudoxanthome élastique Cystinose Sténose congénitale de l'artère rénale Maladie de chevauchement du tissu conjonctif Cystinurie Oligoméganéphronie Maladie de Dent type 1 Dysplasie rénale multikystique Syndrome de Pierson Dysplasie réno-hépato-pancréatique Kyste de l'ouraque Néphropathie glomérulaire primitive Galactosémie Hypoplasie rénale Ectasie canaliculaire précalicielle Agénésie rénale unilatérale Hypomagnésémie primaire avec hypercalciurie et néphrocalcinose sans atteinte oculaire sévère Syndrome RHYNS Maladie infectieuse rare Syndrome de Denys-Drash Syndrome mégavessie-méga-uretères Glomérulonéphrite membranoproliférative primaire Syndrome de Gitelman Syndrome de Williams Diabète insipide néphrogénique Syndrome hémolytique et urémique atypique Epispadias isolé Valve de l'urètre postérieur Vascularite rare de l'enfant Mégacalicose congénitale Dysplasie rénale Dysplasie osseuse primaire Exstrophie de la vessie Arthrite juvénile idiopathique Séquence d'omphalocèle-exstrophie cloacale-anus imperforé-anomalie spinale Maladie systémique rare de l'enfant Maladie de Charcot-Marie-Tooth intermédiaire autosomique dominante E Acidose tubulaire rénale proximale autosomique dominante Dysplasie osseuse primaire avec micromélie Maladie de stockage du glycogène Vascularite non classifiée Méga-uretère primitif de l'adulte Méga-uretère primitif congénital avec reflux Dysplasie osseuse primaire avec ossification progressive de la peau, des muscles squelettiques, fascias, tendons et ligaments Hypomagnésémie primaire avec hypocalcémie secondaire Glomérulopathie lipoprotéinique Duplication de l'urètre Paragangliomes multiples avec polycythémie Maladie des urines sirop d'érable Méga-uretère primitif obstructif congénital Maladie des anticorps anti-membrane basale glomérulaire Méga-uretère primitif congénital nonobstructif sans reflux Syndrome d'hypotonie-cystinurie type 1 Syndrome MYH9 Syndrome de leucoencéphalopathie progressive à début précoce-calcification du système nerveux central-surdité-cécité Glomérulonéphrite membranoproliférative médiée par les immunoglobulines Atrésie de l'urètre Acidose tubulaire rénale proximale Syndrome prune belly Dermatomyosite juvénile Spectre phénotypique des ostéodysplasies oto-palato-digitales Glomérulonéphrite pauci-immune Acidémie glutarique type 3 Néphronophtise Syndrome néphrotique corticorésistant d'origine génétique Renal coloboma syndrome Bartter syndrome Hereditary renal hypouricemia Ochoa syndrome Renal hypoplasia, unilateral Atypical hypotonia-cystinuria syndrome Pseudohypoparathyroidism type 2 Unilateral multicystic dysplastic kidney Pseudohypoparathyroidism type 1B Spondyloepiphyseal dysplasia and spondyloepimetaphyseal dysplasia Renal hypoplasia, bilateral Spondylometaphyseal dysplasia Tubulointerstitial nephritis and uveitis syndrome Liddle syndrome Familial juvenile hyperuricemic nephropathy type 1 Non-syndromic renal or urinary tract malformation Disorder of purine or pyrimidine metabolism Methylmalonic acidemia without homocystinuria Renal or urinary tract malformation Sporadic idiopathic steroid-resistant nephrotic syndrome Familial gestational hyperthyroidism Bilateral multicystic dysplastic kidney Fabry disease