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| hematologic disease ： ウィキペディア英語版 |
hematologic disease
Hematologic diseases are disorders which primarily affect the blood. Hematology includes the study of these disorders.
==Myeloid==
*Hemoglobinopathies (congenital abnormality of the hemoglobin molecule or of the rate of hemoglobin synthesis)
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*Sickle-cell disease
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*Thalassemia
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*Methemoglobinemia
*Anemias (lack of red blood cells or hemoglobin)
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*Iron deficiency anemia
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*Megaloblastic anemia
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*Vitamin B12 deficiency
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*Pernicious anemia
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*Folate deficiency
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*Hemolytic anemias (destruction of red blood cells)
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*Genetic disorders of RBC membrane
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*Hereditary spherocytosis
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*Hereditary elliptocytosis
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*Congenital dyserythropoietic anemia
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*Genetic disorders of RBC metabolism
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*Glucose-6-phosphate dehydrogenase deficiency (G6PD)
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*Pyruvate kinase deficiency
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*Immune mediated hemolytic anemia (direct Coombs test is positive)
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*Autoimmune hemolytic anemia
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*Warm antibody autoimmune hemolytic anemia
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*Idiopathic
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*Systemic lupus erythematosus (SLE)
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*Evans' syndrome (antiplatelet antibodies and hemolytic antibodies)
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*Cold autoimmune hemolytic anemia
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*Cold agglutinin disease
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*Paroxysmal cold hemoglobinuria (rare)
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*Infectious mononucleosis
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*Alloimmune hemolytic anemia
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*Hemolytic disease of the newborn (HDN)
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*Rh disease (Rh D)
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*ABO hemolytic disease of the newborn
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*Anti-Kell hemolytic disease of the newborn
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*Rhesus c hemolytic disease of the newborn
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*Rhesus E hemolytic disease of the newborn
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*Other blood group incompatibility (RhC, Rhe, Kid, Duffy, MN, P and others)
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*Drug induced immune mediated hemolytic anemia
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*Penicillin (high dose)
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*Methyldopa
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*Hemoglobinopathies (where these is an unstable or crystalline hemoglobin)
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*Paroxysmal nocturnal hemoglobinuria (rare acquired clonal disorder of red blood cell surface proteins)
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*Direct physical damage to RBCs
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*Microangiopathic hemolytic anemia
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*Secondary to artificial heart valve(s)
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*Aplastic anemia
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*Fanconi anemia
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*Diamond-Blackfan anemia (inherited pure red cell aplasia)
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*Acquired pure red cell aplasia
*Decreased numbers of cells
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*Myelodysplastic syndrome
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*Myelofibrosis
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*Neutropenia (decrease in the number of neutrophils)
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*Agranulocytosis
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*Glanzmann's thrombasthenia
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*Thrombocytopenia (decrease in the number of platelets)
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*Idiopathic thrombocytopenic purpura (ITP)
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*Thrombotic thrombocytopenic purpura (TTP)
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*Heparin-induced thrombocytopenia (HIT)
*Myeloproliferative disorders (Increased numbers of cells)
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*Polycythemia vera (increase in the number of cells in general)
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*Erythrocytosis (increase in the number of red blood cells)
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*Leukocytosis (increase in the number of white blood cells)
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*Thrombocytosis (increase in the number of platelets)
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*Myeloproliferative disorder
*Coagulopathies (disorders of bleeding and coagulation)
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*Thrombocytosis
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*Recurrent thrombosis
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*Disseminated intravascular coagulation
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*Disorders of clotting proteins
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*Hemophilia
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*Hemophilia A
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*Hemophilia B (also known as Christmas disease)
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*Hemophilia C
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*Von Willebrand disease
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*Disseminated intravascular coagulation
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*Protein S deficiency
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*Antiphospholipid syndrome
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*Disorders of platelets
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*Thrombocytopenia
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*Glanzmann's thrombasthenia
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*Wiskott-Aldrich syndrome
抄文引用元・出典: フリー百科事典『 ウィキペディア（Wikipedia）』
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