SE-ATLAS

Autoimmune interstitial lung disease-arthritis syndrome Moderate hemophilia A Neonatal scleroderma Limited systemic sclerosis CREST syndrome Systemic sclerosis Mild hemophilia A Neonatal lupus erythematosus Hemophilia B Eosinophilic fasciitis Rheumatoid factor-negative polyarticular juvenile idiopathic arthritis Unspecified juvenile idiopathic arthritis Oligoarticular juvenile idiopathic arthritis with anti-nuclear antibodies Oligoarticular juvenile idiopathic arthritis without anti-nuclear antibodies Neuromuscular junction disease Juvenile polymyositis Cystic fibrosis Skeletal muscle disease Muscular channelopathy Motor neuron disease Neuromuscular disease 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 Unexplained long-lasting fever/inflammatory syndrome Osteochondrosis 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 Renal hypoplasia Idiopathic steroid-sensitive nephrotic syndrome C3 glomerulonephritis Cystinosis Autosomal dominant polycystic kidney disease Tubulointerstitial nephritis and uveitis syndrome Bardet-Biedl syndrome Bartter syndrome Waardenburg syndrome Idiopathic steroid-resistant nephrotic syndrome Dent disease Systemic lupus erythematosus Immunoglobulin A vasculitis Renal dysplasia Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency Biotinidase deficiency Genetic steroid-resistant nephrotic syndrome Carbamoyl-phosphate synthetase 1 deficiency Ornithine transcarbamylase deficiency Oligoarticular juvenile idiopathic arthritis Propionic acidemia Charcot-Marie-Tooth disease/Hereditary motor and sensory neuropathy Short chain acyl-CoA dehydrogenase deficiency Very long chain acyl-CoA dehydrogenase deficiency Medium chain acyl-CoA dehydrogenase deficiency Multicystic dysplastic kidney Citrullinemia PLCG2-associated antibody deficiency and immune dysregulation Fabry disease Phenylketonuria Jeune syndrome Autosomal recessive polycystic kidney disease Denys-Drash syndrome Galactosemia Glycogen storage disease Primary membranoproliferative glomerulonephritis Gaucher disease Renal or urinary tract malformation Mucopolysaccharidosis Mucolipidosis Rare hypercholesterolemia Maple syrup urine disease