SE-ATLAS

Neonatal dermatomyositis Sarcoidosis Neonatal autoimmune hemolytic anemia Behçet disease Diffuse cutaneous systemic sclerosis Rare cutaneous lupus erythematosus Seckel syndrome STING-associated vasculopathy with onset in infancy Mixed connective tissue disease Lupus erythematosus panniculitis Hypocomplementemic urticarial vasculitis Pediatric Castleman disease Neonatal scleroderma Neonatal lupus erythematosus Pediatric systemic lupus erythematosus CREST syndrome Scleroderma 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 Takayasu arteritis Adrenogenital syndrome 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 Prader-Willi syndrome Autoinflammation-PLCG2-associated antibody deficiency-immune dysregulation Periodic fever syndrome of childhood 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 Infantile onset panniculitis with uveitis and systemic granulomatosis Gorham-Stout disease Renal agenesis, bilateral Bronchopulmonary dysplasia Refractory celiac disease STAT3-related early-onset multisystem autoimmune disease Idiopathic recurrent pericarditis Immunoglobulin A vasculitis Rare pediatric vasculitis Renal agenesis, unilateral Overlapping connective tissue disease Granulomatosis with polyangiitis 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 Unexplained long-lasting fever/inflammatory syndrome Secondary neonatal autoimmune disease 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