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