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 Biotinidase deficiency Chronic visceral acid sphingomyelinase deficiency Classic galactosemia Cystic fibrosis Diamond-Blackfan anemia Extragonadal germinoma Fabry disease Fanconi anemia Germ cell tumor Glutaryl-CoA dehydrogenase deficiency Glycine encephalopathy Hepatoblastoma Hodgkin lymphoma Hypophosphatasia Langerhans cell histiocytosis Lesch-Nyhan syndrome Long chain acyl-CoA dehydrogenase deficiency Medium chain acyl-CoA dehydrogenase deficiency Mucopolysaccharidosis Neuroblastoma PLCG2-associated antibody deficiency and immune dysregulation Pediatric Castleman disease Phenylketonuria Rhabdomyosarcoma STAT3-related early-onset multisystem autoimmune disease Secondary neonatal autoimmune disease Smith-Lemli-Opitz syndrome Systemic primary carnitine deficiency Very long chain acyl-CoA dehydrogenase deficiency