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:
Adenylosuccinate lyase deficiency Anti-neutrophil cytoplasmic antibody-associated vasculitis Argininosuccinic aciduria Autoimmune hemolytic anemia-autoimmune thrombocytopenia-primary immunodeficiency syndrome Autoimmune interstitial lung disease-arthritis syndrome Autoinflammatory syndrome of childhood Behçet disease Bleeding disorder in hemophilia A carriers Bleeding disorder in hemophilia B carriers Carbamoyl-phosphate synthetase 1 deficiency Carnitine palmitoyl transferase 1A deficiency Citrullinemia type I 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 Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency Medium chain acyl-CoA dehydrogenase deficiency Mild hemophilia A Mild hemophilia B Mixed autoinflammatory and autoimmune syndrome Moderate hemophilia A Moderate hemophilia B Mucopolysaccharidosis type 1 Mucopolysaccharidosis type 2 Mucopolysaccharidosis type 3 Niemann-Pick disease type C Oligoarticular juvenile idiopathic arthritis Oligoarticular juvenile idiopathic arthritis with anti-nuclear antibodies Oligoarticular juvenile idiopathic arthritis without anti-nuclear antibodies Ornithine transcarbamylase deficiency Overlapping connective tissue disease PLCG2-associated antibody deficiency and immune dysregulation Pediatric Castleman disease Pediatric systemic lupus erythematosus Periodic fever syndrome of childhood Phenylketonuria Polyarticular juvenile idiopathic arthritis Progeria-associated arthropathy Psoriasis-related juvenile idiopathic arthritis Pyogenic autoinflammatory syndrome of childhood Rare coagulation disorder Rare hemorrhagic disorder Rare pediatric systemic disease Rare pediatric vasculitis Rare systemic or rheumatological disease of childhood Rare thrombotic disease of hematologic origin Reactive arthritis Rheumatoid factor-negative polyarticular juvenile idiopathic arthritis Rheumatoid factor-positive polyarticular juvenile idiopathic 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 Short chain acyl-CoA dehydrogenase deficiency 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 Very long chain acyl-CoA dehydrogenase deficiency