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 Transient neonatal myasthenia gravis Familial Mediterranean fever Immunoglobulin A vasculitis Overlapping connective tissue disease Granulomatosis with polyangiitis Rare pediatric vasculitis Juvenile dermatomyositis Neonatal autoimmune hemolytic anemia Behçet disease Mixed connective tissue disease Neonatal scleroderma Neonatal lupus erythematosus Systemic sclerosis Hajdu-Cheney syndrome Progeria-associated arthropathy Autoinflammatory syndrome of childhood Takayasu arteritis 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 Sweet syndrome Mucopolysaccharidosis type 4A Rheumatoid factor-positive polyarticular juvenile idiopathic arthritis Mucopolysaccharidosis type 4B Mixed autoinflammatory and autoimmune syndrome Mucopolysaccharidosis type 2 Mucopolysaccharidosis type 3 Mucopolysaccharidosis type 4 Mucopolysaccharidosis type 6 Mucopolysaccharidosis type 7 Autosomal dominant polycystic kidney disease Hyaluronidase deficiency Gaucher disease Glycogen storage disease due to acid maltase deficiency Mucopolysaccharidosis Pediatric systemic lupus erythematosus Mucopolysaccharidosis type 2, attenuated form Secondary neonatal autoimmune disease PFAPA syndrome Neonatal antiphospholipid syndrome Reactive arthritis Kawasaki disease Oligoarticular juvenile idiopathic arthritis with anti-nuclear antibodies Neonatal dermatomyositis CINCA syndrome Rare pediatric systemic disease Mucopolysaccharidosis type 1 Fieber-Syndrom, langanhaltendes unerklärbares Osteoporose, idiopathische juvenile Gorham-Stout-Krankheit Arthritis, idiopathische juvenile Autoinflammatorisches Syndrom, unklassifiziertes, der Kindheit Mukopolysaccharidose Typ 2, schwere Form