SE-ATLAS

Dermatomyositis, neonatale Sarkoidose Neonatale autoimmune hämolytische Anämie Behçet-Syndrom Systemische Sklerose, diffuse kutane Lupus erythematodes, kutaner seltener Seckel-Syndrom Mischkollagenose STING-assoziierte Vaskulopathie mit Beginn in der Kindheit Lupus-Pannikulitis Vaskulitis, hypokomplementämische urtikarielle Castleman-Krankheit des Kindesalters Sklerodermie Neonatale Sklerodermie Lupus erythematosus, neonataler Lupus erythematodes, systemischer, des Kindesalters CREST-Syndrom Vaskulitis mit assoziierten antineutrophilen zytoplasmatischen Antikörpern Hajdu-Cheney-Syndrom Systemische Sklerodermie Hyperthyreose, seltene Polymyositis, juvenile DITRA Arthropathie, Progeria-assoziierte Fraser-Syndrom Autoimmune interstitielle Lungenerkrankung-Arthritis-Syndrom Marfan-Syndrom Kawasaki-Krankheit Adrenogenitales Syndrom Takayasu-Arteriitis Vaskulitis durch ADA2-Mangel Autoinflammatorisches Syndrom der Kindheit Vaskulitis, sekundäre Lupus erythematodes, systemischer, autosomal-rezessiver Arthritis, reaktive PLCG2-associated antibody deficiency and immune dysregulation Fasziitis, eosinophile Kryoglobulinämische Vaskulitis Zystische Fibrose Hydarthrose, intermittierende Hereditary periodic fever syndrome Mixed autoinflammatory and autoimmune syndrome Mitochondrial disease Autosomal dominant polycystic kidney disease Autosomal recessive polycystic kidney disease Blau syndrome Pyogenic autoinflammatory syndrome of childhood Rare systemic or rheumatological disease of childhood Transient neonatal myasthenia gravis Porphyria Autoinflammatory syndrome with pyogenic bacterial infection and amylopectinosis Periodic fever syndrome of childhood Autoinflammation-PLCG2-associated antibody deficiency-immune dysregulation Granulomatous autoinflammatory syndrome of childhood Turner syndrome Alport syndrome Genetic precocious puberty Unclassified autoinflammatory syndrome of childhood Sterile multifocal osteomyelitis with periostitis and pustulosis Unexplained periodic fever syndrome of childhood Gorham-Stout disease Infantile onset panniculitis with uveitis and systemic granulomatosis Renal agenesis, bilateral Bronchopulmonary dysplasia Refractory celiac disease STAT3-related early-onset multisystem autoimmune disease Idiopathic recurrent pericarditis Immunoglobulin A vasculitis Rare pediatric vasculitis Granulomatosis with polyangiitis Renal agenesis, unilateral Overlapping connective tissue disease Denys-Drash syndrome Chronic nonbacterial osteomyelitis/Chronic recurrent multifocal osteomyelitis Idiopathic juvenile osteoporosis Wilson disease Proteasome-associated autoinflammatory syndrome Mastocytosis Renal dysplasia Unclassified vasculitis Juvenile idiopathic arthritis Rare pediatric systemic disease Glycogen storage disease Secondary neonatal autoimmune disease Unexplained long-lasting fever/inflammatory syndrome Majeed syndrome Autoimmune hemolytic anemia-autoimmune thrombocytopenia-primary immunodeficiency syndrome Maple syrup urine disease Anti-glomerular basement membrane disease Noonan syndrome Cogan syndrome Sweet syndrome Juvenile dermatomyositis Bardet-Biedl syndrome Congenital isolated hyperinsulinism PAPA syndrome Neonatal antiphospholipid syndrome