genetic disease of the blood/bone marrow
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More general terms
More specific terms
- 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