SE-ATLAS

Promyelozytenleukämie, akute Immundefekt, primärer Beckwith-Wiedemann-Syndrom Isolierte multiple intestinale Atresie Skelettdysplasie mit verkürzten Extremitäten und schwerem kombinierten Immundefekt Schwartz-Jampel-Syndrom Moynahan-Syndrom Hämophilie B, schwere Glomerulopathie Graft versus host-Krankheit Hämophilie B, milde Genetische Prädisposition für Infektionen durch spezifische Pathogene Hämophilie A, schwere Lupus erythematodes Pannikulitis Osteopoikilose, isolierte Hämophilie B Hämophilie A Hämophilie A, mittelschwere Lupus erythematodes, kutaner, chronischer Autoimmun-Polyendokrinopathie Typ 2 Wolf-Hirschhorn-Syndrom Hyperoxalurie, primäre Dysosteosklerose Oligoastrozytom mit dualem Genotyp Dendritisches Zell-Sarkom, andernorts nicht klassifiziert Immundefekt, kombinierter schwerer, T-B+NK+, durch IL-7Ralpha-Mangel Hypophosphatasie Immundefekt, primärer, mit Prädisposition zur schweren Virusinfektion Melorheostose Sonstiges Immundefekt-Syndrom durch Störung der adaptiven Immunität Inversion/Duplikation Chromosom 15 Isovalerianazidämie Astroblastom Hämoglobinurie, nächtliche paroxysmale Gray-platelet-Syndrom Hämophilie Zystische Fibrose Immundefekt, kombinierter schwerer, T-B-NK+, durch DNA-PKcs-Mangel Osteomesopyknose Astrozytom, hochgradiges Osteopathia striata - kraniale Sklerose Xanthogranulom, juveniles Dent-Krankheit Typ 1 Bronchialkarzinom, kleinzelliges Epilepsie-Syndrom, im Erwachsenenalter beginnend Syndrome mit kombiniertem Immundefekt Alport-Syndrom Primärer Immundefekt durch Störung der adaptiven Immunität Hyperinsulinismus, familiärer Pallister-Killian-Syndrom Symptomatische Form der Hämophilie A bei weiblichen Anlageträgerinnen Angelman-Syndrom Kimura-Krankheit Hypohidrotische ektodermale Dysplasie-Immundefekt-Osteopetrose-Lymphödem-Syndrom Retikuläre Dysgenesie Riesenzell-Glioblastom W-Syndrom Symptomatische Form der Hämophilie B bei weiblichen Anlageträgerinnen Buschke-Ollendorff-Syndrom Pyknodysostose Graft versus host-Krankheit, chronische Graft versus host-Krankheit, akute Aromatase-Exzess-Syndrom Astrozytom Grad 3 PHACE-Syndrom Dermatomyositis Von-Willebrand-Erkrankung AML mit 11q23-Anomalien Leukämie, akute undifferenzierte T- und B-Zell-Immundefekt, kombinierter Von-Willebrand-Erkrankung Typ 1 Leukämie, akute biphänotypische 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