SE-ATLAS

C3 glomerulopathy Glomerular disease Albright hereditary osteodystrophy Syndromic renal or urinary tract malformation Secondary glomerular disease Anti-neutrophil cytoplasmic antibody-associated vasculitis Basement membrane disease Drug-related renal tubular dysgenesis Methylcobalamin deficiency type cblG Sebastian syndrome HANAC syndrome Oculocerebrorenal syndrome of Lowe Familial steroid-resistant nephrotic syndrome with sensorineural deafness Osteofibrous dysplasia X-linked Alport syndrome Mixed connective tissue disease 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 Smith-Lemli-Opitz syndrome 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 Acromelic dysplasia Dense deposit disease Congenital hydronephrosis Spondylodysplastic dysplasia Nephrogenic diabetes insipidus-intracranial calcification-short stature-facial dysmorphism syndrome Mesomelic and rhizo-mesomelic dysplasia Tyrosinemia type 2 Transient pseudohypoaldosteronism Acromesomelic dysplasia Secondary vasculitis Pseudohypoaldosteronism type 2B Thrombotic microangiopathy Vasculitis due to ADA2 deficiency Atypical hemolytic uremic syndrome with MCP/CD46 anomaly Pseudohypoaldosteronism type 2A Campomelic dysplasia and related disorders 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 Primary bone dysplasia with multiple joint dislocations Pseudohypoaldosteronism type 2C Atypical hemolytic uremic syndrome with B factor anomaly 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 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 Renal dysplasia, unilateral Distal renal tubular acidosis Sporadic pheochromocytoma Reactive arthritis Immune-mediated thrombotic thrombocytopenic purpura Galloway-Mowat syndrome Unilateral congenital megacalycosis Carnitine palmitoyl transferase 1A deficiency Genetic primary hypomagnesemia Familial primary hypomagnesemia with normocalciuria and normocalcemia Congenital nephrotic syndrome, Finnish type Hereditary pheochromocytoma-paraganglioma Shiga toxin-associated hemolytic uremic syndrome Carnitine palmitoyltransferase II deficiency Renal pseudohypoaldosteronism type 1 Atypical hemolytic uremic syndrome with thrombomodulin anomaly Adenine phosphoribosyltransferase deficiency Genetic cystic renal disease Cleidocranial dysplasia and isolated cranial ossification defect Primary bone dysplasia with disorganized development of skeletal components Generalized pseudohypoaldosteronism type 1 2p21 microdeletion syndrome UMOD-related autosomal dominant tubulointerstitial kidney disease Autosomal dominant primary hypomagnesemia with hypocalciuria Systemic primary carnitine deficiency Primary osteolysis MUC1-related autosomal dominant tubulointerstitial kidney disease Congenital bilateral megacalycosis Nail-patella syndrome Oligoarticular juvenile idiopathic arthritis without anti-nuclear antibodies Rare hyperlipidemia Late-onset nephronophthisis Sporadic pheochromocytoma/secreting paraganglioma Idiopathic nephrotic syndrome Glutaryl-CoA dehydrogenase deficiency Rheumatoid factor-negative polyarticular juvenile idiopathic arthritis Methylmalonic acidemia with homocystinuria Dominant hypophosphatemia with nephrolithiasis or osteoporosis Tyrosinemia type 3 Infantile nephronophthisis Acquired monoclonal Ig light chain-associated Fanconi syndrome Primary renal tubular acidosis Oligoarticular juvenile idiopathic arthritis Interstitial lung disease-nephrotic syndrome-epidermolysis bullosa syndrome Immunotactoid or fibrillary glomerulopathy Juvenile nephronophthisis Action myoclonus-renal failure syndrome Unspecified juvenile idiopathic arthritis Bickerstaff brainstem encephalitis NPHP3-related Meckel-like syndrome Primary hyperoxaluria type 1 Renal tubular dysgenesis May-Hegglin thrombocytopenia Sporadic idiopathic steroid-resistant nephrotic syndrome with collapsing glomerulopathy Primary hyperoxaluria type 3 Phenylketonuria Rare inborn errors of metabolism Lysosomal disease Primary hyperoxaluria type 2 Catecholamine-producing tumor 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 Primary membranous glomerulonephritis Bartter syndrome type 3 Medium chain acyl-CoA dehydrogenase deficiency Peroxisomal disease Autosomal dominant distal renal tubular acidosis Autosomal recessive proximal renal tubular acidosis Genetic primary hypomagnesemia with hypocalciuria Thrombotic thrombocytopenic purpura Hypertrophic cardiomyopathy with kidney anomalies due to mitochondrial DNA mutation Autosomal recessive distal renal tubular acidosis without deafness Apparent mineralocorticoid excess Autosomal recessive distal renal tubular acidosis with deafness Idiopathic steroid-sensitive nephrotic syndrome Brachydactyly-arterial hypertension syndrome Primary hypomagnesemia with hypercalciuria and nephrocalcinosis Autosomal recessive polycystic kidney disease Exstrophy-epispadias complex Congenital membranous nephropathy due to fetomaternal anti-neutral endopeptidase alloimmunization Polyarticular juvenile idiopathic arthritis Cystinuria type B Autosomal dominant tubulointerstitial kidney disease Pseudohypoaldosteronism type 2D Idiopathic steroid-sensitive nephrotic syndrome with minimal change Rheumatoid factor-positive polyarticular juvenile idiopathic arthritis Rare systemic or rheumatological disease of childhood Rare genetic cause of hypertension Idiopathic steroid-sensitive nephrotic syndrome with diffuse mesangial proliferation Isolated autosomal dominant hypomagnesemia, Glaudemans type Bartter syndrome type 4 Enthesitis-related juvenile idiopathic arthritis REN-related autosomal dominant tubulointerstitial kidney disease Genetic primary hypomagnesemia with normocalciuria Disorder of fatty acid oxidation and ketogenesis Psoriasis-related juvenile idiopathic arthritis Schimke immuno-osseous dysplasia Hereditary xanthinuria Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial proliferation Osteopetrosis with renal tubular acidosis Kosaki overgrowth syndrome Familial idiopathic steroid-resistant nephrotic syndrome with focal segmental hyalinosis Multiple acyl-CoA dehydrogenase deficiency Very long chain acyl-CoA dehydrogenase deficiency Hereditary fructose intolerance Familial idiopathic steroid-resistant nephrotic syndrome with minimal changes Disorder of urea cycle metabolism and ammonia detoxification Sporadic idiopathic steroid-resistant nephrotic syndrome with focal segmental hyalinosis Disorder of carnitine cycle and carnitine transport Rare renal disease X-linked Alport syndrome-diffuse leiomyomatosis Alport syndrome Mitochondrial trifunctional protein deficiency Primary Fanconi renotubular syndrome Pseudohypoaldosteronism type 2E Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis Tyrosinemia type 1 Epstein syndrome Pseudopseudohypoparathyroidism Senior-Boichis syndrome Pseudohypoparathyroidism type 1C Sporadic idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial proliferation Hereditary amyloidosis with primary renal involvement Hemolytic uremic syndrome with DGKE deficiency Congenital primary megaureter Collagen type III glomerulopathy Hyperuricemia-pulmonary hypertension-renal failure-alkalosis syndrome Pseudohypoparathyroidism Fechtner syndrome Pseudohypoaldosteronism type 1 Frasier syndrome WAGR syndrome Adult familial nephronophthisis-spastic quadriparesia syndrome Pseudohypoaldosteronism type 2 Renal agenesis, bilateral Pseudoxanthoma elasticum Cystinosis Congenital renal artery stenosis Overlapping connective tissue disease Cystinuria Dent disease type 1 Oligomeganephronia Multicystic dysplastic kidney Pierson syndrome Urachal cyst Renal-hepatic-pancreatic dysplasia Primary glomerular disease Galactosemia Renal hypoplasia Medullary sponge kidney Primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement Renal agenesis, unilateral RHYNS syndrome Denys-Drash syndrome Primary membranoproliferative glomerulonephritis Megacystis-megaureter syndrome Gitelman syndrome Williams syndrome Nephrogenic diabetes insipidus Congenital megacalycosis Posterior urethral valve Rare pediatric vasculitis Primary bone dysplasia Bladder exstrophy Juvenile idiopathic arthritis Cloacal exstrophy Rare pediatric systemic disease Autosomal dominant intermediate Charcot-Marie-Tooth disease type E Unclassified vasculitis Primary bone dysplasia with micromelia Glycogen storage disease Primary megaureter, adult-onset form Primary bone dysplasia with progressive ossification of skin, skeletal muscle, fascia, tendons and ligaments Primary hypomagnesemia with secondary hypocalcemia Duplication of urethra Maple syrup urine disease Multiple paragangliomas associated with polycythemia Anti-glomerular basement membrane disease Congenital primary megaureter, nonrefluxing and unobstructed form Hypotonia-cystinuria type 1 syndrome MYH9-related disease Early-onset progressive leukoencephalopathy-central nervous system calcification-deafness-visual impairment syndrome Immunoglobulin-mediated membranoproliferative glomerulonephritis Atresia of urethra Otopalatodigital syndrome spectrum disorder Juvenile dermatomyositis Glutaric acidemia type 3 Nephronophthisis Syndrome néphrotique corticorésistant d'origine génétique Hypo-uricémie rénale héréditaire Syndrome d'hypotonie-cystinurie atypique Pseudohypoparathyroïdie type 2 Dysplasie rénale multikystique unilatérale Dysplasie spondylo-épiphysaire et dysplasie spondylo-épimétaphysaire Hypoplasie rénale bilatérale Dysplasie spondylo-métaphysaire Néphrite tubulo-interstitielle et uvéite Syndrome de Liddle Trouble du métabolisme des purines ou pyrimidines Nephropathie hyperuricémique juvénile familiale type 1 Anomalie non syndromique du développement du rein et des voies urinaires Syndrome néphrotique idiopathique sporadique corticorésistant Malformation du rein et des voies urinaires Hyperthyroïdie gestationnelle Acidémie méthylmalonique sans homocystinurie Dysplasie rénale multikystique bilatérale Acidose tubulaire rénale proximale autosomique dominante Syndrome néphrotique idiopathique corticosensible avec hyalinose segmentaire focale Acidémie isovalérique Acidémie propionique Syndrome néphrotique idiopathique sporadique corticorésistant avec sclérose mésangiale diffuse Arthrite juvénile idiopathique sans facteur rhumatoïde avec anticorps anti-nucléaire Maladie rénale nail-patella-like Méga-uretère primitif obstructif congénital Arthrite juvénile idiopathique sans facteur rhumatoïde sans anticorps anti-nucléaire Acidose tubulaire rénale proximale Méga-uretère primitif congénital avec reflux Hypoplasie rénale unilatérale Pseudohypoparathyroïdie type 1A Syndrome de Senior-Loken Dysgénésie tubulaire rénale associée au syndrome de transfusion foeto-foetale Dysgénésie tubulaire rénale d'origine génétique Syndrome de Bartter Glomérulopathie à dépôts de fibronectine Syndrome d'Ochoa Paragangliome sécrétant sporadique Déficit en carnitine-acylcarnitine translocase Syndrome d'hypopéristaltisme intestinal-microcôlon-mégavessie Epispadias isolé Dysplasie multi-épiphysaire et pseudoachondroplasie Syndrome de Bartter avec hypocalcémie Dysplasie avec gracilité osseuse Dysplasie osseuse primaire par défaut de minéralisation Syndrome de Joubert avec atteinte oculo-rénale Maladie infectieuse rare Syndrome néphrotique infantile lié à LAMB2 Syndrome d'Alport autosomique récessif Syndrome d'Alport autosomique dominant Maladie de von Hippel-Lindau Pseudohypoparathyroïdie type 1B Syndrome hémolytique et urémique atypique associé à des anticorps anti-facteur H Syndrome prune belly Arthrite juvénile idiopathique systémique Acidose tubulaire rénale distale avec anémie Cystinurie type A Hypertension artérielle de cause rare Dysplasie rénale Maladie de Dent type 2 Syndrome rein-colobome Glomérulonéphrite pauci-immune Corticosurrénalome Syndrome néphrotique idiopathique sporadique corticorésistant à lésions glomérulaires minimes Syndrome hémolytique et urémique atypique Glomérulopathie lipoprotéinique Sclérose tubéreuse de Bourneville Hyperoxalurie primitive Lupus érythémateux disséminé de l'enfant