SE-ATLAS

Acute promyelocytic leukemia Primary immunodeficiency Beckwith-Wiedemann syndrome Multiple intestinal atresia Short-limb skeletal dysplasia with severe combined immunodeficiency Schwartz-Jampel syndrome Moynahan syndrome Severe hemophilia B Glomerular disease Graft versus host disease Mild hemophilia B Genetic susceptibility to infections due to particular pathogens Severe hemophilia A Lupus erythematosus panniculitis Isolated osteopoikilosis Hemophilia B Hemophilia A Moderate hemophilia A Chronic cutaneous lupus erythematosus Autoimmune polyendocrinopathy type 2 Wolf-Hirschhorn syndrome Primary hyperoxaluria Dysosteosclerosis Oligoastrocytoma Dendritic cell sarcoma not otherwise specified T-B+ severe combined immunodeficiency due to IL-7Ralpha deficiency Hypophosphatasia Primary immunodeficiency with predisposition to severe viral infection Melorheostosis Other immunodeficiency syndromes due to defects in innate immunity Inverted duplicated chromosome 15 syndrome Isovaleric acidemia Astroblastoma Paroxysmal nocturnal hemoglobinuria Gray platelet syndrome Hemophilia Cystic fibrosis Severe combined immunodeficiency due to DNA-PKcs deficiency Osteomesopyknosis High-grade astrocytoma Osteopathia striata-cranial sclerosis syndrome Juvenile xanthogranuloma Dent disease type 1 Small cell lung cancer Adolescent-onset epilepsy syndrome Syndrome with combined immunodeficiency Alport syndrome Primary immunodeficiency due to a defect in adaptive immunity Familial hyperinsulinism Tetrasomy 12p Bleeding disorder in hemophilia A carriers Angelman syndrome Kimura disease Anhidrotic ectodermal dysplasia-immunodeficiency-osteopetrosis-lymphedema syndrome Reticular dysgenesis Giant cell glioblastoma W syndrome Bleeding disorder in hemophilia B carriers Buschke-Ollendorff syndrome Pycnodysostosis Chronic graft versus host disease Acute graft versus host disease Aromatase excess syndrome Anaplastic astrocytoma PHACE syndrome Dermatomyositis Von Willebrand disease Acute myeloid leukemia with 11q23 abnormalities Acute undifferentiated leukemia Combined T and B cell immunodeficiency Von Willebrand disease type 1 Acute biphenotypic leukemia Familial glucocorticoid deficiency Bilineal acute leukemia Low-grade astrocytoma Von Willebrand disease type 2 Protoplasmic astrocytoma Immunodeficiency predominantly affecting antibody production Astrocytoma Fibrillary astrocytoma Rhabdomyosarcoma Ependymoblastoma Simpson-Golabi-Behmel syndrome Atherosclerosis-deafness-diabetes-epilepsy-nephropathy syndrome Immune dysregulation disease with immunodeficiency Therapy related acute myeloid leukemia and myelodysplastic syndrome Gemistocytic astrocytoma Primary immunodeficiency due to a defect in innate immunity Acute leukemia of ambiguous lineage Medulloepithelioma of the central nervous system Melorheostosis with osteopoikilosis Rare pulmonary hypertension Left sided atrial isomerism Transposition of the great arteries Levocardia Patent arterial duct Hypoplastic left heart syndrome Tricuspid valve agenesis Congenital tricuspid stenosis Congenital mitral valve insufficiency and/or stenosis Congenital mitral stenosis Mitral valve agenesis Congenital coronary artery aneurysm Congenital anomaly of superior vena cava Atrial septal defect, coronary sinus type Congenital aortic valve atresia Tetralogy of Fallot Right sided atrial isomerism Cor triatriatum sinister Atrial septal defect, ostium primum type Persistent left superior vena cava connecting to the roof of left-sided atrium Agenesis of the superior vena cava Congenital total pulmonary venous return anomaly Truncus arteriosus Congenital renal artery stenosis Uhl anomaly Ebstein malformation of the tricuspid valve Congenitally uncorrected transposition of the great arteries Bockenheimer syndrome Congenital aortopulmonary window Dextrocardia Double outlet left ventricle Infective endocarditis Heart position anomaly Idiopathic recurrent pericarditis Aorta coarctation Eisenmenger syndrome Interatrial communication Pulmonary valve agenesis Pulmonary arteriovenous malformation Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency Glutaryl-CoA dehydrogenase deficiency Propionic acidemia Medium chain acyl-CoA dehydrogenase deficiency Supravalvular pulmonary stenosis Very long chain acyl-CoA dehydrogenase deficiency Phenylketonuria Valvular pulmonary stenosis Atrial septal defect, ostium secundum type Galactosemia Glycogen storage disease Disorder of purine or pyrimidine metabolism Disorder of carnitine cycle and carnitine transport Hereditary fructose intolerance Maple syrup urine disease Immunodeficiency due to a complement cascade protein anomaly Supravalvular aortic stenosis Congenital heart block Congenital aortic valve insufficiency Persistent left superior vena cava connecting through coronary sinus to left-sided atrium Glioblastoma Ventricular septal defect Unspecified juvenile idiopathic arthritis Vasculitis Marfan syndrome Juvenile idiopathic arthritis Polyarticular juvenile idiopathic arthritis Spondyloepiphyseal dysplasia tarda Periodic fever syndrome Von Willebrand disease type 3 Autosomal dominant polycystic kidney disease Autosomal recessive polycystic kidney disease Congenital anomaly of the inferior vena cava Azygos continuation of the inferior vena cava Congenital partial pulmonary venous return anomaly Moderate hemophilia B Mild hemophilia A Oligoarticular juvenile idiopathic arthritis Systemic-onset juvenile idiopathic arthritis Psoriasis-related juvenile idiopathic arthritis Enthesitis-related juvenile idiopathic arthritis Congenital pulmonary venous return anomaly Congenital aortic valve stenosis Aneurysm of sinus of Valsalva Coronary artery congenital malformation Quantitative and/or qualitative congenital phagocyte defect Scimitar syndrome Bicuspid aortic valve Atrial septal defect, sinus venosus type Double outlet right ventricle Hypoplastic right heart syndrome Pulmonary artery/pulmonary branch anomaly