SE-ATLAS

Neonatal dermatomyositis Sarcoidosis Neonatal autoimmune hemolytic anemia Behçet disease Diffuse cutaneous systemic sclerosis Rare cutaneous lupus erythematosus Seckel syndrome Mixed connective tissue disease STING-associated vasculopathy with onset in infancy Lupus erythematosus panniculitis Hypocomplementemic urticarial vasculitis Pediatric Castleman disease Scleroderma Neonatal scleroderma Neonatal lupus erythematosus Pediatric systemic lupus erythematosus CREST syndrome Anti-neutrophil cytoplasmic antibody-associated vasculitis Hajdu-Cheney syndrome Systemic sclerosis Rare hyperthyroidism Juvenile polymyositis DITRA Progeria-associated arthropathy Fraser syndrome Autoimmune interstitial lung disease-arthritis syndrome Marfan syndrome Kawasaki disease Adrenogenital syndrome Takayasu arteritis Vasculitis due to ADA2 deficiency Autoinflammatory syndrome of childhood Secondary vasculitis Autosomal systemic lupus erythematosus Reactive arthritis PLCG2-associated antibody deficiency and immune dysregulation Eosinophilic fasciitis Cryoglobulinemic vasculitis Cystic fibrosis Intermittent hydrarthrosis 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 Refraktäre Zöliakie STAT3-assoziierte früh beginnende multisystemische Autoimmunkrankheit Perikarditis, idiopathische rekurrente Immunoglobulin A-Vaskulitis Seltene Vaskulitis des Kindes Granulomatose mit Polyangiitis Nierenagenesie, unilaterale Mischkollagenose, überlappende Denys-Drash-Syndrom Chronische nicht-bakterielle Osteomyelitis/rezidivierende multifokale Osteomyelitis Osteoporose, idiopathische juvenile Wilson-Krankheit Proteasom-assoziiertes autoinflammatorisches Syndrom Mastozytose Nierendysplasie Vaskulitis, unklassifizierte Arthritis, idiopathische juvenile Seltene systemische Krankheit des Kindes Glykogenose Sekundäre neonatale autoimmune Krankheit Fieber-Syndrom, langanhaltendes unerklärbares Majeed-Syndrom Evans-Syndrom mit assoziiertem primären Immundefekt Ahornsirup-Krankheit Antikörper vermittelte Krankheit der glomerulären Basalmembran Noonan-Syndrom Cogan-Syndrom Sweet-Syndrom Dermatomyositis, juvenile Bardet-Biedl-Syndrom Hyperinsulinismus, isolierter, kongenitaler PAPA-Syndrom Anti-Phospholipid-Syndrom, neonatales