SE-ATLAS

Pyogenic autoinflammatory syndrome of childhood Rare systemic or rheumatological disease of childhood Psoriasis-related juvenile idiopathic arthritis Enthesitis-related juvenile idiopathic arthritis Periodic fever syndrome of childhood Granulomatous autoinflammatory syndrome of childhood Unclassified autoinflammatory syndrome of childhood Transient neonatal myasthenia gravis Familial Mediterranean fever Gorham-Stout disease Immunoglobulin A vasculitis Overlapping connective tissue disease Granulomatosis with polyangiitis Rare pediatric vasculitis Idiopathic juvenile osteoporosis PFAPA syndrome CINCA syndrome Juvenile idiopathic arthritis Secondary neonatal autoimmune disease Unexplained long-lasting fever/inflammatory syndrome Juvenile dermatomyositis Neonatal antiphospholipid syndrome Neonatal autoimmune hemolytic anemia Behçet disease Neonatal dermatomyositis Pediatric systemic lupus erythematosus Mixed connective tissue disease Neonatal scleroderma Neonatal lupus erythematosus Hajdu-Cheney syndrome Systemic sclerosis Progeria-associated arthropathy Kawasaki disease Autoinflammatory syndrome of childhood Takayasu arteritis Oligoarticular juvenile idiopathic arthritis with anti-nuclear antibodies Oligoarticular juvenile idiopathic arthritis without anti-nuclear antibodies Rheumatoid factor-negative polyarticular juvenile idiopathic arthritis Unspecified juvenile idiopathic arthritis Oligoarticular juvenile idiopathic arthritis Systemic-onset juvenile idiopathic arthritis Polyarticular juvenile idiopathic arthritis Intermittent hydrarthrosis Reactive arthritis Sweet syndrome Rare pediatric systemic disease Mucopolysaccharidosis type 4A Rheumatoid factor-positive polyarticular juvenile idiopathic arthritis Mucopolysaccharidosis type 4B Mixed autoinflammatory and autoimmune syndrome Mucopolysaccharidosis type 1 Mucopolysaccharidosis type 2 Mucopolysaccharidosis type 3 Mucopolysaccharidosis type 4 Mucopolysaccharidosis type 6 Mucopolysaccharidosis type 7 Autosomal dominant polycystic kidney disease Hyaluronidase deficiency Gaucher disease Mucopolysaccharidosis Glycogen storage disease due to acid maltase deficiency Mucopolysaccharidosis type 2, severe form Mucopolysaccharidosis type 2, attenuated form STXBP1-related encephalopathy