SE-ATLAS

Mapping of Health Care Providers
for People with Rare Diseases


In the following you will find the diseases that are treated in this facility:
Anti-neutrophil cytoplasmic antibody-associated vasculitis Autoimmune hemolytic anemia-autoimmune thrombocytopenia-primary immunodeficiency syndrome Autoimmune interstitial lung disease-arthritis syndrome Autoinflammatory syndrome of childhood Autosomal dominant polycystic kidney disease Bleeding disorder in hemophilia A carriers Bleeding disorder in hemophilia B carriers Cogan syndrome Cryoglobulinemic vasculitis Enthesitis-related juvenile idiopathic arthritis Eosinophilic fasciitis Gorham-Stout disease Granulomatous autoinflammatory syndrome of childhood Hajdu-Cheney syndrome Hemophilia Hemophilia A Hemophilia B Hypocomplementemic urticarial vasculitis Idiopathic juvenile osteoporosis Immunoglobulin A vasculitis Intermittent hydrarthrosis Juvenile dermatomyositis Juvenile idiopathic arthritis Juvenile polymyositis Kawasaki disease Mild hemophilia A Mild hemophilia B Mixed autoinflammatory and autoimmune syndrome Moderate hemophilia A Moderate hemophilia B Oligoarticular juvenile idiopathic arthritis Overlapping connective tissue disease PLCG2-associated antibody deficiency and immune dysregulation Pediatric Castleman disease Pediatric systemic lupus erythematosus Periodic fever syndrome of childhood Polyarticular juvenile idiopathic arthritis Progeria-associated arthropathy Psoriasis-related juvenile idiopathic arthritis Pyogenic autoinflammatory syndrome of childhood Rare pediatric systemic disease Rare pediatric vasculitis Rare systemic or rheumatological disease of childhood Reactive arthritis STAT3-related early-onset multisystem autoimmune disease STING-associated vasculopathy with onset in infancy Sarcoidosis Secondary neonatal autoimmune disease Secondary vasculitis Severe hemophilia A Severe hemophilia B Sweet syndrome Systemic sclerosis Systemic-onset juvenile idiopathic arthritis Takayasu arteritis Unclassified autoinflammatory syndrome of childhood Unclassified vasculitis Unexplained long-lasting fever/inflammatory syndrome Unspecified juvenile idiopathic arthritis Vasculitis due to ADA2 deficiency