SE-ATLAS

Adrenogenital syndrome Alport syndrome Anti-glomerular basement membrane disease Anti-neutrophil cytoplasmic antibody-associated vasculitis Autoimmune hemolytic anemia-autoimmune thrombocytopenia-primary immunodeficiency syndrome Autoimmune interstitial lung disease-arthritis syndrome Autoinflammation-PLCG2-associated antibody deficiency-immune dysregulation Autoinflammatory syndrome of childhood Autoinflammatory syndrome with pyogenic bacterial infection and amylopectinosis Autosomal dominant polycystic kidney disease Autosomal recessive polycystic kidney disease Autosomal systemic lupus erythematosus Bardet-Biedl syndrome Behçet disease Blau syndrome Bronchopulmonary dysplasia CREST syndrome Chronic nonbacterial osteomyelitis/Chronic recurrent multifocal osteomyelitis Cogan syndrome Congenital isolated hyperinsulinism Cryoglobulinemic vasculitis Cystic fibrosis DITRA Denys-Drash syndrome Diffuse cutaneous systemic sclerosis Eosinophilic fasciitis Fraser syndrome Genetic precocious puberty Glycogen storage disease Gorham-Stout disease Granulomatosis with polyangiitis Granulomatous autoinflammatory syndrome of childhood Hajdu-Cheney syndrome Hereditary periodic fever syndrome Hypocomplementemic urticarial vasculitis Idiopathic juvenile osteoporosis Idiopathic recurrent pericarditis Immunoglobulin A vasculitis Infantile onset panniculitis with uveitis and systemic granulomatosis Intermittent hydrarthrosis Juvenile dermatomyositis Juvenile idiopathic arthritis Juvenile polymyositis Kawasaki disease Lupus erythematosus panniculitis Majeed syndrome Maple syrup urine disease Marfan syndrome Mastocytosis Mitochondrial disease Mixed autoinflammatory and autoimmune syndrome Mixed connective tissue disease Neonatal antiphospholipid syndrome Neonatal autoimmune hemolytic anemia Neonatal dermatomyositis Neonatal lupus erythematosus Neonatal scleroderma Noonan syndrome Overlapping connective tissue disease PAPA syndrome PLCG2-associated antibody deficiency and immune dysregulation Pediatric Castleman disease Pediatric systemic lupus erythematosus Periodic fever syndrome of childhood Porphyria Prader-Willi syndrome Progeria-associated arthropathy Proteasome-associated autoinflammatory syndrome Pyogenic autoinflammatory syndrome of childhood Rare cutaneous lupus erythematosus Rare hyperthyroidism Rare pediatric systemic disease Rare pediatric vasculitis Rare systemic or rheumatological disease of childhood Reactive arthritis Refractory celiac disease Renal agenesis, bilateral Renal agenesis, unilateral Renal dysplasia STAT3-related early-onset multisystem autoimmune disease STING-associated vasculopathy with onset in infancy Sarcoidosis Scleroderma Seckel syndrome Secondary neonatal autoimmune disease Secondary vasculitis Sterile multifocal osteomyelitis with periostitis and pustulosis Sweet syndrome Systemic sclerosis Takayasu arteritis Transient neonatal myasthenia gravis Turner syndrome Unclassified autoinflammatory syndrome of childhood Unclassified vasculitis Unexplained long-lasting fever/inflammatory syndrome Unexplained periodic fever syndrome of childhood Vasculitis due to ADA2 deficiency Wilson disease