SE-ATLAS

Acute basophilic leukemia Acute biphenotypic leukemia Acute graft versus host disease Acute leukemia of ambiguous lineage Acute monoblastic/monocytic leukemia Acute myeloid leukemia and myelodysplastic syndromes related to alkylating agent Acute myeloid leukemia and myelodysplastic syndromes related to radiation Acute myeloid leukemia and myelodysplastic syndromes related to topoisomerase type 2 inhibitor Acute myeloid leukemia with 11q23 abnormalities Acute myeloid leukemia with CEBPA somatic mutations Acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22) Acute myeloid leukemia with recurrent genetic anomaly Acute myeloid leukemia with t(8;16)(p11;p13) translocation Acute myeloid leukemia with t(8;21)(q22;q22) translocation Acute panmyelosis with myelofibrosis Acute promyelocytic leukemia Acute undifferentiated leukemia Adolescent-onset epilepsy syndrome Agenesis of the superior vena cava Alport syndrome Anaplastic astrocytoma Aneurysm of sinus of Valsalva Angelman syndrome Anhidrotic ectodermal dysplasia-immunodeficiency-osteopetrosis-lymphedema syndrome Aorta coarctation Aromatase excess syndrome Astroblastoma Astrocytoma Ataxia-telangiectasia Atherosclerosis-deafness-diabetes-epilepsy-nephropathy syndrome Atrial septal defect, coronary sinus type Atrial septal defect, ostium primum type Atrial septal defect, ostium secundum type Atrial septal defect, sinus venosus type Autoimmune polyendocrinopathy type 2 Autoinflammatory syndrome with immune deficiency Autosomal dominant polycystic kidney disease Autosomal recessive polycystic kidney disease Azygos continuation of the inferior vena cava Bartter syndrome Beckwith-Wiedemann syndrome Benign familial infantile epilepsy Benign familial neonatal-infantile seizures Bicuspid aortic valve Bilineal acute leukemia Bleeding disorder in hemophilia A carriers Bleeding disorder in hemophilia B carriers Bockenheimer syndrome Buschke-Ollendorff syndrome CNTNAP2-related developmental and epileptic encephalopathy Cerebral diseases of vascular origin with epilepsy Cerebral malformation with epilepsy Childhood-onset epilepsy syndrome Chromosomal anomaly with epilepsy as a major feature Chronic cutaneous lupus erythematosus Chronic graft versus host disease Chronic granulomatous disease Combined T and B cell immunodeficiency Congenital anomaly of superior vena cava Congenital anomaly of the inferior vena cava Congenital aortic valve atresia Congenital aortic valve insufficiency Congenital aortic valve stenosis Congenital aortopulmonary window Congenital coronary artery aneurysm Congenital heart block Congenital mitral stenosis Congenital mitral valve insufficiency and/or stenosis Congenital partial pulmonary venous return anomaly Congenital pulmonary venous return anomaly Congenital renal artery stenosis Congenital total pulmonary venous return anomaly Congenital tricuspid stenosis Congenitally uncorrected transposition of the great arteries Cor triatriatum sinister Coronary artery congenital malformation Cystic fibrosis DEND syndrome DITRA Dendritic cell sarcoma not otherwise specified Dent disease type 1 Dermatomyositis Dextrocardia Diffuse astrocytoma Disorder of carnitine cycle and carnitine transport Disorder of purine or pyrimidine metabolism Double outlet left ventricle Double outlet right ventricle Dysosteosclerosis Ebstein malformation of the tricuspid valve Eisenmenger syndrome Enthesitis-related juvenile idiopathic arthritis Ependymoblastoma Epilepsy syndrome Epilepsy-telangiectasia syndrome Familial glucocorticoid deficiency Familial hyperinsulinism Familial partial epilepsy Fibrillary astrocytoma Fragile X syndrome Galactosemia Gemistocytic astrocytoma Genetic susceptibility to infections due to particular pathogens Giant cell glioblastoma Gitelman syndrome Glioblastoma Glomerular disease Glutaryl-CoA dehydrogenase deficiency Glycogen storage disease Graft versus host disease Gray platelet syndrome Heart position anomaly Hemophilia Hemophilia A Hemophilia B Hereditary fructose intolerance High-grade astrocytoma Hypophosphatasia Hypoplastic left heart syndrome Hypoplastic right heart syndrome Idiopathic or cryptogenic familial epilepsy syndrome with identified loci/genes Idiopathic recurrent pericarditis Immune dysregulation disease with immunodeficiency Immunodeficiency due to a complement cascade protein anomaly Immunodeficiency predominantly affecting antibody production Infantile epilepsy syndrome Infantile spasms-broad thumbs syndrome Infectious disease with epilepsy Infective endocarditis Inflammatory and autoimmune disease with epilepsy Inherited acute myeloid leukemia Interatrial communication Inverted duplicated chromosome 15 syndrome Isolated osteopoikilosis Isovaleric acidemia Juvenile idiopathic arthritis Juvenile xanthogranuloma Kimura disease Kleefstra syndrome due to 9q34 microdeletion Left sided atrial isomerism Levocardia Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency Low-grade astrocytoma Lupus erythematosus panniculitis Maple syrup urine disease Medium chain acyl-CoA dehydrogenase deficiency Medulloepithelioma of the central nervous system Melnick-Needles syndrome Melorheostosis Melorheostosis with osteopoikilosis Metabolic diseases with epilepsy Mild hemophilia A Mild hemophilia B Miller-Dieker syndrome Mitral valve agenesis Moderate hemophilia A Moderate hemophilia B Monogenic disease with epilepsy Moynahan syndrome Multiple intestinal atresia NLRP3-associated autoinflammatory disease Neonatal epilepsy syndrome Neonatal inflammatory skin and bowel disease Neonatal lupus erythematosus Neurocutaneous syndrome with epilepsy Oculocerebrocutaneous syndrome Oculocerebrorenal syndrome of Lowe Oligoarticular juvenile idiopathic arthritis Oligoastrocytoma Osteomesopyknosis Osteopathia striata-cranial sclerosis syndrome Other immunodeficiency syndromes due to defects in innate immunity PAPA syndrome PEHO syndrome PEHO-like syndrome PHACE syndrome PLCG2-associated antibody deficiency and immune dysregulation Paroxysmal nocturnal hemoglobinuria Patent arterial duct Persistent left superior vena cava connecting through coronary sinus to left-sided atrium Persistent left superior vena cava connecting to the roof of left-sided atrium Phenylketonuria Pilocytic astrocytoma Polyarticular juvenile idiopathic arthritis Precursor T-cell acute lymphoblastic leukemia Primary hyperoxaluria Primary immunodeficiency Primary immunodeficiency due to a defect in adaptive immunity Primary immunodeficiency due to a defect in innate immunity Primary immunodeficiency with predisposition to severe viral infection Propionic acidemia Protoplasmic astrocytoma Psoriasis-related juvenile idiopathic arthritis Pulmonary arteriovenous malformation Pulmonary artery/pulmonary branch anomaly Pulmonary valve agenesis Pycnodysostosis Quantitative and/or qualitative congenital phagocyte defect Rare epilepsy Rare gastroenterologic disease Rare hematologic disease Rare pulmonary hypertension Rasmussen subacute encephalitis Reticular dysgenesis Rhabdomyosarcoma Rheumatic fever Right sided atrial isomerism Ring chromosome 14 syndrome Ring chromosome 20 syndrome Schwartz-Jampel syndrome Scimitar syndrome Severe combined immunodeficiency due to DNA-PKcs deficiency Severe hemophilia A Severe hemophilia B Short-limb skeletal dysplasia with severe combined immunodeficiency Simpson-Golabi-Behmel syndrome Small cell lung cancer Spondyloepiphyseal dysplasia tarda Subependymal giant cell astrocytoma Supravalvular aortic stenosis Supravalvular pulmonary stenosis Syndrome with combined immunodeficiency Systemic-onset juvenile idiopathic arthritis T-B+ severe combined immunodeficiency due to IL-7Ralpha deficiency Tetralogy of Fallot Tetrasomy 12p Therapy related acute myeloid leukemia and myelodysplastic syndrome Tick-borne encephalitis Transposition of the great arteries Tricuspid valve agenesis Truncus arteriosus Uhl anomaly Unclassified acute myeloid leukemia Unspecified juvenile idiopathic arthritis Valvular pulmonary stenosis Ventricular septal defect Very long chain acyl-CoA dehydrogenase deficiency Von Willebrand disease Von Willebrand disease type 1 Von Willebrand disease type 2 Von Willebrand disease type 3 W syndrome Wolf-Hirschhorn syndrome