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 Rare epilepsy Neonatal autoimmune hemolytic anemia Behçet disease Neonatal dermatomyositis Pediatric systemic lupus erythematosus Mixed connective tissue disease Neonatal scleroderma Neonatal lupus erythematosus Systemic sclerosis Hajdu-Cheney syndrome 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 Mucopolysaccharidosis type 2, attenuated form 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 Fabry disease 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 STXBP1-related encephalopathy