SE-ATLAS

STAT3-related early-onset multisystem autoimmune disease Bleeding disorder in hemophilia A carriers Bleeding disorder in hemophilia B carriers Overlapping connective tissue disease Von Willebrand disease Idiopathic juvenile osteoporosis Von Willebrand disease type 2 Neurofibromatosis type 1 Full NF2-related schwannomatosis Juvenile idiopathic arthritis Von Willebrand disease type 1 Rare pediatric systemic disease Von Willebrand disease type 2A Unclassified vasculitis Unexplained long-lasting fever/inflammatory syndrome Von Willebrand disease type 2B Autoimmune hemolytic anemia-autoimmune thrombocytopenia-primary immunodeficiency syndrome Von Willebrand disease type 2N Cogan syndrome Secondary neonatal autoimmune disease Von Willebrand disease type 2M Juvenile dermatomyositis Von Willebrand disease type 3 Sweet syndrome Gorham-Stout disease Full schwannomatosis Immunoglobulin A vasculitis Rare pediatric vasculitis Pediatric Castleman disease Mixed connective tissue disease Sarcoidosis Adrenogenital syndrome Moderate hemophilia B Diffuse cutaneous systemic sclerosis STING-associated vasculopathy with onset in infancy Severe hemophilia B Anti-neutrophil cytoplasmic antibody-associated vasculitis Pediatric systemic lupus erythematosus Hemophilia A Mild hemophilia B Autoimmune interstitial lung disease-arthritis syndrome Moderate hemophilia A Hypocomplementemic urticarial vasculitis Hemophilia B CREST syndrome Severe hemophilia A Systemic sclerosis Hajdu-Cheney syndrome Mild hemophilia A Progeria-associated arthropathy Juvenile polymyositis Autoimmune thrombocytopenia Oligoarticular juvenile idiopathic arthritis with anti-nuclear antibodies Kawasaki disease Takayasu arteritis Autoinflammatory syndrome of childhood Vasculitis due to ADA2 deficiency Secondary vasculitis Reactive arthritis PLCG2-associated antibody deficiency and immune dysregulation Oligoarticular juvenile idiopathic arthritis without anti-nuclear antibodies Cryoglobulinemic vasculitis Rheumatoid factor-negative polyarticular juvenile idiopathic arthritis Eosinophilic fasciitis Unspecified juvenile idiopathic arthritis Oligoarticular juvenile idiopathic arthritis Systemic-onset juvenile idiopathic arthritis Intermittent hydrarthrosis Hemophilia Polyarticular juvenile idiopathic arthritis Autosomal dominant polycystic kidney disease Autosomal recessive polycystic kidney disease Rheumatoid factor-positive polyarticular juvenile idiopathic arthritis Psoriasis-related juvenile idiopathic arthritis Enthesitis-related juvenile idiopathic arthritis Rare systemic or rheumatological disease of childhood Aicardi-Goutières syndrome