SE-ATLAS

Glomérulopathie à dépôts de C3 Ostéodystrophie héréditaire d'Albright Anomalie syndromique du développement du rein et des voies urinaires Néphropathie glomérulaire secondaire Dysgénésie tubulaire rénale d'origine médicamenteuse Déficit en méthylcobalamine type cblG Syndrome HANAC Syndrome de Sebastian Syndrome oculo-cérébro-rénal de Lowe Dysplasie ostéofibreuse Syndrome néphrotique familial corticorésistant avec surdité neurosensorielle Syndrome d'Alport lié à l'X Connectivite mixte Amylose AApoAII Hyperaldostéronisme familial type I Syndrome d'épidermolyse bulleuse-syndrome néphrotique-surdité neurosensorielle Polykystose rénale autosomique dominante type 1 avec sclérose tubéreuse Vascularite urticarienne hypocomplémentémique Ciliopathies avec atteinte osseuse majeure AFib amyloidosis Smith-Lemli-Opitz syndrome C3 glomerulonephritis Hypertension due to gain-of-function mutations in the mineralocorticoid receptor Autosomal dominant progressive nephropathy with hypertension Dense deposit disease Nephrogenic diabetes insipidus-intracranial calcification-short stature-facial dysmorphism syndrome Congenital hydronephrosis Spondylodysplastic dysplasia Mesomelic and rhizo-mesomelic dysplasia Tyrosinemia type 2 Acromesomelic dysplasia Transient pseudohypoaldosteronism Vasculitis due to ADA2 deficiency Thrombotic microangiopathy Secondary vasculitis Pseudohypoaldosteronism type 2B Atypical hemolytic uremic syndrome with MCP/CD46 anomaly Pseudohypoaldosteronism type 2A Neonatal diabetes-congenital hypothyroidism-congenital glaucoma-hepatic fibrosis-polycystic kidneys syndrome Atypical hemolytic uremic syndrome with C3 anomaly Oligoarticular juvenile idiopathic arthritis with anti-nuclear antibodies Primary bone dysplasia with multiple joint dislocations Atypical hemolytic uremic syndrome with B factor anomaly Pseudohypoaldosteronism type 2C Idiopathic hypercalciuria Familial hyperthyroidism due to mutations in TSH receptor Dent disease Primary bone dysplasia with increased bone density Atypical hemolytic uremic syndrome with H factor anomaly Congenital thrombotic thrombocytopenic purpura Distal renal tubular acidosis Renal dysplasia, unilateral Sporadic pheochromocytoma Galloway-Mowat syndrome Reactive arthritis Unilateral congenital megacalycosis Carnitine palmitoyl transferase 1A deficiency Carnitine palmitoyltransferase II deficiency Hereditary pheochromocytoma-paraganglioma Genetic primary hypomagnesemia Congenital nephrotic syndrome, Finnish type Shiga toxin-associated hemolytic uremic syndrome Renal pseudohypoaldosteronism type 1 Genetic cystic renal disease Adenine phosphoribosyltransferase deficiency Primary bone dysplasia with disorganized development of skeletal components Generalized pseudohypoaldosteronism type 1 2p21 microdeletion syndrome UMOD-related autosomal dominant tubulointerstitial kidney disease Systemic primary carnitine deficiency Primary osteolysis MUC1-related autosomal dominant tubulointerstitial kidney disease Congenital bilateral megacalycosis Rare hyperlipidemia Rheumatoid factor-negative polyarticular juvenile idiopathic arthritis Acquired monoclonal Ig light chain-associated Fanconi syndrome Methylmalonic acidemia with homocystinuria Tyrosinemia type 3 Infantile nephronophthisis Dominant hypophosphatemia with nephrolithiasis or osteoporosis Primary renal tubular acidosis Interstitial lung disease-nephrotic syndrome-epidermolysis bullosa syndrome Juvenile nephronophthisis Unspecified juvenile idiopathic arthritis Primary hyperoxaluria type 1 May-Hegglin thrombocytopenia Renal tubular dysgenesis Primary hyperoxaluria type 3 Primary hyperoxaluria type 2 Lysosomal disease Short stature-advanced bone age-early-onset osteoarthritis syndrome Medium chain acyl-CoA dehydrogenase deficiency Bartter syndrome type 3 Autosomal dominant distal renal tubular acidosis Autosomal recessive proximal renal tubular acidosis Hypertrophic cardiomyopathy with kidney anomalies due to mitochondrial DNA mutation Apparent mineralocorticoid excess Brachydactyly-arterial hypertension syndrome Idiopathic steroid-sensitive nephrotic syndrome Primary hypomagnesemia with hypercalciuria and nephrocalcinosis Autosomal recessive polycystic kidney disease Exstrophy-epispadias complex Polyarticular juvenile idiopathic arthritis Cystinuria type B Idiopathic steroid-sensitive nephrotic syndrome with minimal change Pseudohypoaldosteronism type 2D Rheumatoid factor-positive polyarticular juvenile idiopathic arthritis Rare systemic or rheumatological disease of childhood Enthesitis-related juvenile idiopathic arthritis Isolated autosomal dominant hypomagnesemia, Glaudemans type Bartter syndrome type 4 Psoriasis-related juvenile idiopathic arthritis Schimke immuno-osseous dysplasia Disorder of fatty acid oxidation and ketogenesis Hereditary xanthinuria Kosaki overgrowth syndrome Hereditary fructose intolerance Familial idiopathic steroid-resistant nephrotic syndrome with minimal changes Sporadic idiopathic steroid-resistant nephrotic syndrome with focal segmental hyalinosis Alport syndrome Rare renal disease X-linked Alport syndrome-diffuse leiomyomatosis Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis Primary Fanconi renotubular syndrome Pseudohypoaldosteronism type 2E Mitochondrial trifunctional protein deficiency Epstein syndrome Sporadic idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial proliferation Hereditary amyloidosis with primary renal involvement Hemolytic uremic syndrome with DGKE deficiency Pseudohypoaldosteronism type 1 Fechtner syndrome Adult familial nephronophthisis-spastic quadriparesia syndrome WAGR syndrome Pseudohypoaldosteronism type 2 Renal agenesis, bilateral Cystinosis Congenital renal artery stenosis Overlapping connective tissue disease Dent disease type 1 Multicystic dysplastic kidney Renal-hepatic-pancreatic dysplasia Primary glomerular disease Renal hypoplasia Primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement Renal agenesis, unilateral Megacystis-megaureter syndrome Congenital megacalycosis Posterior urethral valve Primary bone dysplasia Juvenile idiopathic arthritis Rare pediatric systemic disease Autosomal dominant intermediate Charcot-Marie-Tooth disease type E Unclassified vasculitis 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 Anti-glomerular basement membrane disease Hypotonia-cystinuria type 1 syndrome MYH9-related disease Immunoglobulin-mediated membranoproliferative glomerulonephritis Atresia of urethra Juvenile dermatomyositis Glutaric acidemia type 3 Nephronophthisis Hereditary renal hypouricemia Atypical hypotonia-cystinuria syndrome Pseudohypoparathyroidism type 2 Spondyloepiphyseal dysplasia and spondyloepimetaphyseal dysplasia Spondylometaphyseal dysplasia Tubulointerstitial nephritis and uveitis syndrome Liddle syndrome Disorder of purine or pyrimidine metabolism Familial juvenile hyperuricemic nephropathy type 1 Sporadic idiopathic steroid-resistant nephrotic syndrome Familial gestational hyperthyroidism Idiopathic steroid-sensitive nephrotic syndrome with focal segmental hyalinosis Isovaleric acidemia Propionic acidemia Sporadic idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis Rheumatoid factor-negative juvenile idiopathic arthritis with anti-nuclear antibodies Congenital primary megaureter, obstructed form Rheumatoid factor-negative juvenile idiopathic arthritis without anti-nuclear antibodies Proximal renal tubular acidosis Autosomal dominant proximal renal tubular acidosis Nail-patella-like renal disease Congenital primary megaureter, refluxing form Renal hypoplasia, unilateral Senior-Loken syndrome Renal tubular dysgenesis due to twin-twin transfusion Renal tubular dysgenesis of genetic origin Bartter syndrome Fibronectin glomerulopathy Sporadic secreting paraganglioma Carnitine-acylcarnitine translocase deficiency Megacystis-microcolon-intestinal hypoperistalsis syndrome Multiple epiphyseal dysplasia and pseudoachondroplasia Bartter syndrome with hypocalcemia Slender bone dysplasia Primary bone dysplasia with defective bone mineralization Joubert syndrome with oculorenal defect LAMB2-related infantile-onset nephrotic syndrome Atypical hemolytic uremic syndrome with anti-factor H antibodies Systemic-onset juvenile idiopathic arthritis Distal renal tubular acidosis with anemia Cystinuria type A Rare cause of hypertension Dent disease type 2 Renal coloboma syndrome Adrenocortical carcinoma Pseudohypoparathyroidism type 1A Ochoa syndrome Isolated epispadias Rare infectious disease Autosomal recessive Alport syndrome Autosomal dominant Alport syndrome Von Hippel-Lindau disease Pseudohypoparathyroidism type 1B Prune belly syndrome Renal dysplasia Pauci-immune glomerulonephritis Sporadic idiopathic steroid-resistant nephrotic syndrome with minimal changes Atypical hemolytic uremic syndrome Pediatric systemic lupus erythematosus Primary hyperoxaluria Lipoprotein glomerulopathy Tuberous sclerosis complex Immunotactoid or fibrillary glomerulopathy Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency Idiopathic steroid-sensitive nephrotic syndrome with diffuse mesangial proliferation Glutaryl-CoA dehydrogenase deficiency Familial idiopathic steroid-resistant nephrotic syndrome with focal segmental hyalinosis Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial proliferation Oligoarticular juvenile idiopathic arthritis without anti-nuclear antibodies Congenital primary megaureter, nonrefluxing and unobstructed form Unilateral multicystic dysplastic kidney Genetic steroid-resistant nephrotic syndrome RHYNS syndrome Phenylketonuria Multiple paragangliomas associated with polycythemia Rare pediatric vasculitis Renal hypoplasia, bilateral Bilateral multicystic dysplastic kidney Primary membranoproliferative glomerulonephritis Senior-Boichis syndrome Collagen type III glomerulopathy Idiopathic nephrotic syndrome Sporadic pheochromocytoma/secreting paraganglioma Primary hypomagnesemia with hypercalciuria and nephrocalcinosis with severe ocular involvement Multiple acyl-CoA dehydrogenase deficiency Very long chain acyl-CoA dehydrogenase deficiency Hyperuricemia-pulmonary hypertension-renal failure-alkalosis syndrome Oligomeganephronia Cystinuria Nephrogenic diabetes insipidus Multiple metaphyseal dysplasia Acromelic dysplasia Campomelic dysplasia and related disorders Chondrodysplasia punctata Primary bone dysplasia with decreased bone density Cleidocranial dysplasia and isolated cranial ossification defect Sporadic idiopathic steroid-resistant nephrotic syndrome with collapsing glomerulopathy Congenital and infantile nephrotic syndrome Chondrodysplasie létale Glomérulonéphrite extra membraneuse primitive Ectasie canaliculaire précalicielle Rhombencéphalite de Bickerstaff Pseudo-hypoparathyroïdie Trouble du métabolisme du cycle de l'urée et de la détoxification de l'ammoniac Hypomagnésémie primaire d'origine génétique avec hypocalciurie Syndrome de Frasier Hypomagnésémie primaire d'origine génétique avec normocalciurie Galactosémie Maladie de stockage du glycogène Néphropathie tubulo-intersitielle autosomique dominante Syndrome de Gitelman Malformation du rein et des voies urinaires Anomalie non syndromique du développement du rein et des voies urinaires Néphropathie glomérulaire Basalopathie Amylose ALys Amylose AApoAI Syndrome hémolytique et urémique atypique associé à une anomalie du facteur I Purpura thrombotique thrombocytopénique d'origine immunitaire Néphronophtise tardive Xanthinurie type I Néphropathie tubulaire rare Arthrite juvénile idiopathique oligoarticulaire Xanthinurie type II Syndrome de Bartter anténatal Syndrome néphrogénique d'antidiurèse inappropriée Acidose tubulaire rénale distale autosomique récessive sans surdité Acidose tubulaire rénale distale autosomique récessive avec surdité Glomérulopathie extra-membraneuse congénitale par allo-immunisation foetomaternelle anti-endopeptidase neutre Kyste de l'ouraque Acidémie méthylmalonique sans homocystinurie Vascularite associée aux anticorps antineutrophiles cytoplasmiques Hypomagnésémie primaire familiale avec normocalciurie et normocalcémie Ostéopétrose avec acidose tubulaire rénale Exstrophie de la vessie Pseudoxanthome élastique Syndrome de leucoencéphalopathie progressive à début précoce-calcification du système nerveux central-surdité-cécité Syndrome de Denys-Drash Néphropathie tubulo-intersitielle autosomique dominante associée à REN Hypoplasie pontocérébelleuse type 2 Syndrome nail-patella Mucoviscidose Pseudopseudohypoparathyroïdie Pseudohypoparathyroïdie type 1C Méga-uretère primitif congénital Syndrome de Pierson Tumeur sécrétrice de catécholamines Hypomagnésémie primaire autosomique dominante avec hypocalciurie Erreurs innées du métabolisme rares Séquence d'omphalocèle-exstrophie cloacale-anus imperforé-anomalie spinale Maladie péroxysomale Purpura thrombotique thrombocytopénique Syndrome d'hypotonie-cystinurie Syndrome de myoclonus d'action-insuffisance rénale Tyrosinémie type 1 Syndrome de Williams Trouble du cycle de la carnitine et du transport de la carnitine Syndrome hémolytique et urémique atypique associé à une anomalie de la thrombomoduline Hypertension artérielle de cause génétique rare Syndrome Meckel-like associé à NPHP3 Dysplasie rénale bilatérale Spectre phénotypique des ostéodysplasies oto-palato-digitales Glomérulonéphrite rapidement progressive Dysplasie osseuse primaire avec micromélie