SE-ATLAS

Overlapping connective tissue disease Rare pediatric systemic disease Juvenile dermatomyositis Pediatric systemic lupus erythematosus Mixed connective tissue disease PLCG2-associated antibody deficiency and immune dysregulation Cystic fibrosis Acute lymphoblastic leukemia Langerhans cell histiocytosis Classic galactosemia 3-methylcrotonyl-CoA carboxylase deficiency Acute myeloid leukemia Biotinidase deficiency Rhabdomyosarcoma 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 Hepatoblastoma Germ cell tumor Phenylketonuria Fanconi anemia Astrocytoma Mucopolysaccharidosis Chronic visceral acid sphingomyelinase deficiency Extragonadal germinoma Hodgkin lymphoma Neuroblastoma Diamond-Blackfan anemia Lesch-Nyhan syndrome Unexplained long-lasting fever/inflammatory syndrome Pediatric Castleman disease Juvenile polymyositis STAT3-related early-onset multisystem autoimmune disease Secondary neonatal autoimmune disease Oligoarticular juvenile idiopathic arthritis with anti-nuclear antibodies Oligoarticular juvenile idiopathic arthritis without anti-nuclear antibodies Autoimmune hemolytic anemia-autoimmune thrombocytopenia-primary immunodeficiency syndrome Systemic sclerosis Eosinophilic fasciitis