SE-ATLAS

6-phosphogluconate dehydrogenase deficiency Alpha-thalassemia Alpha-thalassemia and related disorders Alpha-thalassemia-X-linked intellectual disability syndrome Alpha-thalassemia-intellectual disability syndrome linked to chromosome 16 Alpha-thalassemia-myelodysplastic syndrome Bernard-Soulier syndrome Beta-thalassemia Beta-thalassemia and related diseases Beta-thalassemia associated with another hemoglobin anomaly Beta-thalassemia intermedia Beta-thalassemia major Beta-thalassemia with other manifestations Beta-thalassemia-X-linked thrombocytopenia syndrome Chédiak-Higashi syndrome Class I glucose-6-phosphate dehydrogenase deficiency Congenital amegakaryocytic thrombocytopenia Congenital dyserythropoietic anemia Congenital dyserythropoietic anemia type I Congenital dyserythropoietic anemia type II Congenital dyserythropoietic anemia type III Congenital dyserythropoietic anemia type IV Cyclic neutropenia Dehydrated hereditary stomatocytosis Delta-beta-thalassemia Diamond-Blackfan anemia Dominant beta-thalassemia Epstein syndrome Familial platelet disorder with associated myeloid malignancy Familial pseudohyperkalemia Familial thrombocytosis Fanconi anemia Fechtner syndrome Glanzmann thrombasthenia Glutathione synthetase deficiency Gray platelet syndrome Griscelli syndrome type 2 Hb Bart's hydrops fetalis Hemoglobin C disease Hemoglobin C-beta-thalassemia syndrome Hemoglobin D disease Hemoglobin E disease Hemoglobin E-beta-thalassemia syndrome Hemoglobin H disease Hemoglobin Lepore-beta-thalassemia syndrome Hemoglobin M disease Hemoglobinopathy Hemoglobinopathy Toms River Hemolytic anemia due to adenylate kinase deficiency Hemolytic anemia due to an erythrocyte nucleotide metabolism disorder Hemolytic anemia due to erythrocyte adenosine deaminase overproduction Hemolytic anemia due to glutathione reductase deficiency Hemolytic anemia due to hexose monophosphate shunt and glutathione metabolism anomalies Hemolytic anemia due to pyrimidine 5' nucleotidase deficiency Hemolytic anemia due to red cell pyruvate kinase deficiency Hereditary elliptocytosis Hereditary methemoglobinemia Hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome Hereditary persistence of fetal hemoglobin-sickle cell disease syndrome Hereditary spherocytosis Hereditary stomatocytosis Hermansky-Pudlak syndrome Hermansky-Pudlak syndrome due to AP-3 deficiency Hermansky-Pudlak syndrome due to BLOC-1 deficiency Hermansky-Pudlak syndrome due to BLOC-2 deficiency Hermansky-Pudlak syndrome due to BLOC-3 deficiency Hermansky-Pudlak syndrome type 8 Hermansky-Pudlak syndrome type 9 Isolated delta-storage pool disease Kostmann syndrome MYH9-related disease May-Hegglin thrombocytopenia Non-spherocytic hemolytic anemia due to hexokinase deficiency Overhydrated hereditary stomatocytosis Paris-Trousseau thrombocytopenia Primary familial polycythemia Pseudo-von Willebrand disease Quebec platelet disorder Radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome Sebastian syndrome Sickle cell anemia Sickle cell disease and related diseases Sickle cell disease associated with another hemoglobin anomaly Sickle cell-beta-thalassemia disease syndrome Sickle cell-hemoglobin C disease syndrome Sickle cell-hemoglobin D disease syndrome Sickle cell-hemoglobin E disease syndrome Southeast Asian ovalocytosis Stormorken-Sjaastad-Langslet syndrome Syndrome with alpha-thalassemia as a major feature Thrombocytopenia with congenital dyserythropoietic anemia Thrombocytopenia-absent radius syndrome Triose phosphate-isomerase deficiency Unstable hemoglobin disease Wiskott-Aldrich syndrome X-linked dyserythropoietic anemia with abnormal platelets and neutropenia