SE-ATLAS

Glomerular disease Undifferentiated connective tissue syndrome Secondary glomerular disease Basement membrane disease IgG4-related kidney disease Giant cell arteritis Pediatric systemic lupus erythematosus Oculocerebrorenal syndrome of Lowe Mixed connective tissue disease Satoyoshi syndrome Sjögren-Larsson syndrome Joubert syndrome with oculorenal defect Adrenocortical carcinoma Systemic sclerosis Juvenile polymyositis Pseudohypoaldosteronism Autoimmune interstitial lung disease-arthritis syndrome Anaplastic thyroid carcinoma Nephrogenic diabetes insipidus-intracranial calcification-short stature-facial dysmorphism syndrome Neonatal severe primary hyperparathyroidism Differentiated thyroid carcinoma Secondary vasculitis Thrombotic microangiopathy Systemic autoimmune disease Atypical hemolytic uremic syndrome with MCP/CD46 anomaly Atypical hemolytic uremic syndrome with C3 anomaly Genetic renal tubular disease Atypical hemolytic uremic syndrome with H factor anomaly Takayasu arteritis Atypical hemolytic uremic syndrome with B factor anomaly Idiopathic hypercalciuria Atypical hemolytic uremic syndrome with anti-factor H antibodies Cranioectodermal dysplasia Autosomal systemic lupus erythematosus Dent disease Atypical hemolytic uremic syndrome with I factor anomaly Senior-Loken syndrome Susac syndrome Genetic primary hypomagnesemia IgG4-related disease Shiga toxin-associated hemolytic uremic syndrome Atypical hemolytic uremic syndrome with thrombomodulin anomaly Genetic cystic renal disease Nail-patella syndrome Familial primary hyperparathyroidism Dominant hypophosphatemia with nephrolithiasis or osteoporosis Primary renal tubular acidosis Hypophosphatemic rickets Nephropathy secondary to a storage or other metabolic disease PLCG2-associated antibody deficiency and immune dysregulation Simple cryoglobulinemia VIPoma Rare renal tubular disease Nephrogenic syndrome of inappropriate antidiuresis Familial papillary thyroid carcinoma with renal papillary neoplasia Microscopic polyangiitis Relapsing polychondritis Cystinuria type B Cystinuria type A Polymyositis Fabry disease Genetic hyperparathyroidism Rare genetic cause of hypertension Rare cause of hypertension REN-related autosomal dominant tubulointerstitial kidney disease Mitochondrial DNA depletion syndrome, hepatocerebrorenal form Familial nonmedullary thyroid carcinoma Primary Fanconi renotubular syndrome Alström syndrome Multiple endocrine neoplasia type 4 Jeune syndrome Multiple endocrine neoplasia Senior-Boichis syndrome Multiple endocrine neoplasia type 2A Multiple endocrine neoplasia type 2B Hyperuricemia-pulmonary hypertension-renal failure-alkalosis syndrome STAT3-related early-onset multisystem autoimmune disease Pseudohypoparathyroidism EAST syndrome Syndrome hémolytique et urémique par déficit en DGKE Sténose congénitale de l'artère rénale Fibrose rétropéritonéale associée à IgG4 Maladie de chevauchement du tissu conjonctif Cystinurie Syndrome de Saldino-Mainzer Néphropathie glomérulaire primitive Syndrome des antisynthétases Granulomatose avec polyangéite Syndrome RHYNS Syndrome de Gitelman Syndrome de Cushing indépendant de l'ACTH Diabète insipide néphrogénique Syndrome hémolytique et urémique atypique Maladie rare avec un syndrome de Cushing surrénalien comme manifestation majeure Syndrome de Cushing par sécrétion ectopique d'ACTH Syndrome de Cushing dépendant de l'ACTH Syndrome de Cushing endogène Syndrome de Cushing dû à une maladie macronodulaire bilatérale des surrénales Dermatomyosite Syndrome de Cushing surrénalien Néphropathie tubulo-interstitielle autosomique dominante associée à HNF1B Syndrome d'anémie hémolytique autoimmune-thrombocytopénie autoimmune-déficit immunitaire primaire Vascularite non classifiée Maladie auto-immune néonatale secondaire Maladie de Cushing Syndrome de Reynolds Prolactinome Syndrome d'hypotonie-cystinurie type 1 Cancer médullaire de la thyroïde Néoplasie endocrinienne multiple type 1 Dermatomyosite juvénile Néoplasie endocrinienne multiple type 2 Néphronophtise Vascularite des vaisseaux de gros calibre Maladie auto-immune multisystémique syndromique par déficit en Itch Syndrome de Bartter Vascularite des vaisseaux de petit calibre Vascularite Hypo-uricémie rénale héréditaire Vascularite des vaisseaux de moyen calibre Carcinome rare de la thyroïde Sarcoïdose Maladie de Behçet Néphrite tubulo-interstitielle et uvéite