SE-ATLAS

3-methylcrotonyl-CoA carboxylase deficiency Acute lymphoblastic leukemia Acute myeloid leukemia Alpha-1-antitrypsin deficiency Astrocytoma Autoimmune hemolytic anemia-autoimmune thrombocytopenia-primary immunodeficiency syndrome Autoimmune interstitial lung disease-arthritis syndrome Biotinidase deficiency Chronic visceral acid sphingomyelinase deficiency Classic galactosemia Cystic fibrosis Cystinosis Diamond-Blackfan anemia Enthesitis-related juvenile idiopathic arthritis Eosinophilic fasciitis Extragonadal germinoma Fabry disease Fanconi anemia Germ cell tumor Glutaryl-CoA dehydrogenase deficiency Glycine encephalopathy Hepatoblastoma Hodgkin lymphoma Homocystinuria due to cystathionine beta-synthase deficiency Hypophosphatasia Juvenile dermatomyositis Juvenile idiopathic arthritis Juvenile polymyositis Langerhans cell histiocytosis Lesch-Nyhan syndrome Long chain acyl-CoA dehydrogenase deficiency Medium chain acyl-CoA dehydrogenase deficiency Mixed connective tissue disease Mucolipidosis Mucolipidosis type II Mucopolysaccharidosis Mucopolysaccharidosis type 1 Mucopolysaccharidosis type 2 Mucopolysaccharidosis type 3 Mucopolysaccharidosis type 4 Mucopolysaccharidosis type 6 Mucopolysaccharidosis type 7 Neuroblastoma Oligoarticular juvenile idiopathic arthritis Oligoarticular juvenile idiopathic arthritis with anti-nuclear antibodies Oligoarticular juvenile idiopathic arthritis without anti-nuclear antibodies Overlapping connective tissue disease PLCG2-associated antibody deficiency and immune dysregulation Pediatric Castleman disease Pediatric systemic lupus erythematosus Phenylketonuria Polyarticular juvenile idiopathic arthritis Psoriasis-related juvenile idiopathic arthritis Rare anemia Rare coagulation disorder Rare pediatric systemic disease Rhabdomyosarcoma Rheumatoid factor-negative polyarticular juvenile idiopathic arthritis Rheumatoid factor-positive polyarticular juvenile idiopathic arthritis STAT3-related early-onset multisystem autoimmune disease Sarcoidosis Secondary neonatal autoimmune disease Smith-Lemli-Opitz syndrome Systemic primary carnitine deficiency Systemic sclerosis Systemic-onset juvenile idiopathic arthritis Unexplained long-lasting fever/inflammatory syndrome Unspecified juvenile idiopathic arthritis Very long chain acyl-CoA dehydrogenase deficiency