Specific

Alder's syndrome; Alder-Reilly anomaly alpha-2 antiplasmin deficiency (alpha-2-plasmin inhibitor deficiency) antithrombin deficiency atransferrinemia bare lymphocyte syndrome blood group-Lutheran inhibitor (dominant Lu (a-b-) phenotype) coagulation factor deficiency congenital afibrinogenemia congenital amegakaryocytic thrombocytopenia Diamond-Blackfan syndrome (congenital erythroid hypoplasia) dysfibrinogenemia elliptocytosis type 1 elliptocytosis type 2 elliptocytosis type 3 elliptocytosis type 4 Epstein syndrome factor V Quebec factor XIII deficiency familial erythrocytosis familial histiocytic reticulosis; familial hemophagocytic reticulosis; familial hemophagocytic lymphohistiocytosis; familial erythrophagocytic lymphohistiocytosis familial neutropenia familial platelet disorder with associated myeloid malignancy Fechtner syndrome Ghosal hematodiaphyseal dysplasia hemoglobinopathy hemolytic anemia associated with ATPase deficiency heparin cofactor 2 deficiency hereditary bleeding disorder hereditary megaloblastic anemia 1; MGA1 Norwegian type; Imerslund-Grasbeck syndrome hereditary methemoglobinemia hereditary nonspherocytic hemolytic anemia hereditary pyropoikilocytosis hereditary spherocytosis hereditary stomatocytosis (cryohydrocytosis) macrothrombocytopenia with sensorineural deafness May-Hegglin anomaly methemoglobin reductase deficiency multiple coagulation factor deficiency 1 (MCFD1) multiple coagulation factor deficiency 3; combined deficiency of vitamin K-dependent clotting factors 1 (VKCFD1) myopathy with lactic acidosis & sideroblastic anemia; mitochondrial myopathy & sideroblastic anemia (MLASA) plasminogen activator inhibitor-1 deficiency plasminogen deficiency platelet glycoprotein IV deficiency (CD36 deficiency) protein C deficiency protein S deficiency prothrombin gene mutation PXE-like disorder with multiple coagulation factor deficiency; pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency pyrimidine 5' nucleotidase deficiency hemolytic anemia; P5N deficiency Quebec platelet disorder Sebastian syndrome thrombophilia due to factor IX defect thrombophilia due to histidine-rich glycoprotein deficiency thrombophilia due to thrombomodulin defect white blood cell count quantitative trait locus type 1 (WBCQ1) X-linked dyserythropoietic anemia & thrombocytopenia X-linked severe congenital neutropenia X-linked thrombocytopenia X-linked thrombocytopenia with beta-thalassemia; thrombocytopenia, platelet dysfunction, hemolysis, & imbalanced globin synthesis

General

chronic hematologic disease (chronic blood disorder) genetic disease