SE-ATLAS

Autoimmune interstitial lung disease-arthritis syndrome Neonatal scleroderma Moderate hemophilia A Limited systemic sclerosis CREST syndrome Systemic sclerosis Neonatal lupus erythematosus Mild hemophilia A Hemophilia B PLCG2-associated antibody deficiency and immune dysregulation Rheumatoid factor-negative polyarticular juvenile idiopathic arthritis Eosinophilic fasciitis Unspecified juvenile idiopathic arthritis Juvenile polymyositis Oligoarticular juvenile idiopathic arthritis with anti-nuclear antibodies Oligoarticular juvenile idiopathic arthritis without anti-nuclear antibodies Neuromuscular junction disease Cystic fibrosis Neuromuscular disease Skeletal muscle disease Muscular channelopathy Motor neuron disease Oligoarticular juvenile idiopathic arthritis Systemic-onset juvenile idiopathic arthritis Hemophilia Polyarticular juvenile idiopathic arthritis Rheumatoid factor-positive polyarticular juvenile idiopathic arthritis Psoriasis-related juvenile idiopathic arthritis Enthesitis-related juvenile idiopathic arthritis STAT3-related early-onset multisystem autoimmune disease Bleeding disorder in hemophilia B carriers Bleeding disorder in hemophilia A carriers Overlapping connective tissue disease Juvenile idiopathic arthritis Rare pediatric systemic disease Osteochondrosis Unexplained long-lasting fever/inflammatory syndrome Autoimmune hemolytic anemia-autoimmune thrombocytopenia-primary immunodeficiency syndrome Secondary neonatal autoimmune disease Juvenile dermatomyositis Sarcoidosis Pediatric Castleman disease Severe hemophilia B Diffuse cutaneous systemic sclerosis Moderate hemophilia B Pediatric systemic lupus erythematosus Neonatal dermatomyositis Mixed connective tissue disease Severe hemophilia A Hemophilia A Mild hemophilia B Genetic steroid-resistant nephrotic syndrome Systemic lupus erythematosus Charcot-Marie-Tooth disease/Hereditary motor and sensory neuropathy Renal hypoplasia Renal dysplasia Multicystic dysplastic kidney Idiopathic steroid-sensitive nephrotic syndrome C3 glomerulonephritis Cystinosis Autosomal dominant polycystic kidney disease Jeune syndrome Autosomal recessive polycystic kidney disease Denys-Drash syndrome Berger disease Primary membranoproliferative glomerulonephritis Renal or urinary tract malformation Tubulointerstitial nephritis and uveitis syndrome Bardet-Biedl syndrome Bartter syndrome Waardenburg syndrome Idiopathic steroid-resistant nephrotic syndrome Dent disease Immunoglobulin A vasculitis