SE-ATLAS

Acquired idiopathic sideroblastic anemia Acquired neutropenia Acquired von Willebrand syndrome Acute myeloid leukemia and myelodysplastic syndromes related to radiation Acute myeloid leukemia and myelodysplastic syndromes related to topoisomerase type 2 inhibitor Acute panmyelosis with myelofibrosis Adult idiopathic neutropenia Alpha-thalassemia Angioosteohypertrophic syndrome Autoimmune hemolytic anemia Autoimmune hemolytic anemia, cold type Autoimmune hemolytic anemia, warm type Autosomal dominant aplasia and myelodysplasia Autosomal recessive sideroblastic anemia Bannayan-Riley-Ruvalcaba syndrome Bernard-Soulier syndrome Beta-thalassemia Beta-thalassemia intermedia Beta-thalassemia major Blue rubber bleb nevus CLOVES syndrome Capillary malformation-arteriovenous malformation Chronic eosinophilic leukemia Chronic myelomonocytic leukemia Class I glucose-6-phosphate dehydrogenase deficiency Cold agglutinin disease Congenital dyserythropoietic anemia Congenital dyserythropoietic anemia type I Congenital dyserythropoietic anemia type II Congenital dyserythropoietic anemia type III Congenital dyserythropoietic anemia type IV Congenital factor II deficiency Congenital factor V deficiency Congenital factor VII deficiency Congenital factor X deficiency Congenital factor XI deficiency Congenital factor XII deficiency Congenital factor XIII deficiency Congenital fibrinogen deficiency Congenital vitamin K-dependent coagulation factors deficiency Constitutional sideroblastic anemia Cowden syndrome Cutis marmorata telangiectatica congenita Cyclic neutropenia Deafness-lymphedema-leukemia syndrome Delta-beta-thalassemia Diamond-Blackfan anemia Diffuse lymphatic malformation Dominant beta-thalassemia Drug-induced autoimmune hemolytic anemia Dyskeratosis congenita Essential thrombocythemia Evans syndrome Familial afibrinogenemia Familial cerebral cavernous malformation Familial dysfibrinogenemia Familial platelet disorder with associated myeloid malignancy Felty syndrome Glanzmann thrombasthenia Glomuvenous malformation Glycogen storage disease due to aldolase A deficiency Glycogen storage disease due to muscle phosphofructokinase deficiency Glycogen storage disease due to phosphoglycerate kinase 1 deficiency Gorham-Stout disease Gray platelet syndrome Heinz body anemia Hemoglobin C disease Hemoglobin D disease Hemoglobin E disease Hemoglobinopathy Hemolytic anemia due to an erythrocyte nucleotide metabolism disorder Hemolytic anemia due to diphosphoglycerate mutase deficiency Hemolytic anemia due to glucophosphate isomerase deficiency Hemolytic anemia due to glyceraldehyde-3-phosphate dehydrogenase deficiency Hemolytic anemia due to hexose monophosphate shunt and glutathione metabolism anomalies Hemolytic anemia due to red cell pyruvate kinase deficiency Hemophilia A Heparin-induced thrombocytopenia Hereditary elliptocytosis Hereditary hemorrhagic telangiectasia Hereditary isolated aplastic anemia Hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome Hereditary spherocytosis Hereditary stomatocytosis Hereditary thrombophilia due to congenital antithrombin deficiency Hoyeraal-Hreidarsson syndrome Hypereosinophilic syndrome Idiopathic aplastic anemia Immune thrombocytopenia Immunoglobulin A vasculitis Inherited acute myeloid leukemia Intermittent neutropenia Juvenile myelomonocytic leukemia Kaposiform hemangioendothelioma Kostmann syndrome Lymphedema-distichiasis syndrome Maffucci syndrome Megalencephaly-capillary malformation-polymicrogyria syndrome Meige disease Milroy disease Mitochondrial myopathy and sideroblastic anemia Monocytopenia with susceptibility to infections Mucocutaneous venous malformations Myelodysplastic syndrome Myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality Neonatal alloimmune neutropenia Neonatal neutropenia Non-spherocytic hemolytic anemia due to hexokinase deficiency Noonan syndrome-like disorder with juvenile myelomonocytic leukemia PHACE syndrome PTEN hamartoma tumor syndrome Parkes Weber syndrome Paroxysmal nocturnal hemoglobinuria Pearson syndrome Primary acquired pure red cell aplasia Primary acquired red cell aplasia Primary lymphedema Primary myelofibrosis Proteus syndrome Rare acquired aplastic anemia Rare acquired hemolytic anemia Rare aplastic anemia Rare arteriovenous malformation Rare capillary malformation Rare constitutional aplastic anemia Rare hemolytic anemia Rare hereditary thrombophilia Rare lymphatic malformation Rare thrombotic disorder due to an acquired coagulation factors defect Rare venous malformation Refractory anemia Refractory anemia with excess blasts Refractory anemia with excess blasts in transformation Refractory anemia with excess blasts type 1 Refractory anemia with excess blasts type 2 Severe congenital hypochromic anemia with ringed sideroblasts Severe congenital neutropenia Severe hereditary thrombophilia due to congenital protein C deficiency Severe hereditary thrombophilia due to congenital protein S deficiency Sickle cell anemia Sickle cell-beta-thalassemia disease syndrome Sickle cell-hemoglobin C disease syndrome Sickle cell-hemoglobin D disease syndrome Sickle cell-hemoglobin E disease syndrome Sturge-Weber syndrome T-cell large granular lymphocyte leukemia Therapy related acute myeloid leukemia and myelodysplastic syndrome Thrombocytopenia with congenital dyserythropoietic anemia Thrombocytopenia-absent radius syndrome Transient erythroblastopenia of childhood Triose phosphate-isomerase deficiency Tufted angioma Unclassified myelodysplastic/myeloproliferative disease Unstable hemoglobin disease Vein of Galen aneurysmal malformation Von Willebrand disease X-linked dyserythropoietic anemia with abnormal platelets and neutropenia X-linked sideroblastic anemia X-linked sideroblastic anemia and spinocerebellar ataxia