SE-ATLAS

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