SE-ATLAS

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