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Hemophilia is an X-linked recessive hereditary bleeding disorder: hemophilia A = factor VIII deficiency; hemophilia B = factor IX deficiency. Clinical: spontaneous bleeding, joint/muscle hematoma, prolonged bleeding after trauma.
血液科Hemophilia type A (D66.x01) is a disease entity listed in the National Clinical Version 2.0 of the Disease Classification and Codes standard issued by the National Health Commission; a detailed pathological introduction is being compiled.
Hereditary factor VIII deficiency (D66.x00) is a disease entity listed in the National Clinical Version 2.0 of the Disease Classification and Codes standard issued by the National Health Commission; a detailed pathological introduction is being compiled.
Purpura fulminans is a severe thrombotic syndrome of DIC with rapidly progressive skin purpura/necrosis, often following severe infection (meningococcal sepsis).
血液科Fibrinolytic purpura (D65.x03) is a disease entity listed in the National Clinical Version 2.0 of the Disease Classification and Codes standard issued by the National Health Commission; a detailed pathological introduction is being compiled.
Acquired fibrinolysis bleeding (D65.x02) is a disease entity listed in the National Clinical Version 2.0 of the Disease Classification and Codes standard issued by the National Health Commission; a detailed pathological introduction is being compiled.
Acquired afibrinogenemia (D65.x01) is a disease entity listed in the National Clinical Version 2.0 of the Disease Classification and Codes standard issued by the National Health Commission; a detailed pathological introduction is being compiled.
Consumption coagulopathy (D65.x00x005) is a disease entity listed in the National Clinical Version 2.0 of the Disease Classification and Codes standard issued by the National Health Commission; a detailed pathological introduction is being compiled.
Purpura fulminans (D65.x00x003) is a disease entity listed in the National Clinical Version 2.0 of the Disease Classification and Codes standard issued by the National Health Commission; a detailed pathological introduction is being compiled.
DIC is a syndrome of widespread intravascular clotting activation causing microthrombi, consumption of platelets/coagulation factors, and secondary bleeding. Triggered by severe infection, trauma, malignancy, obstetric complications.
血液科Disseminated intravascular coagulation (defibrination syndrome) (D65.x00) is a disease entity listed in the National Clinical Version 2.0 of the Disease Classification and Codes standard issued by the National Health Commission; a detailed pathological in
Secondary anemia (D64.904) is a disease entity listed in the National Clinical Version 2.0 of the Disease Classification and Codes standard issued by the National Health Commission; a detailed pathological introduction is being compiled.
Severe anemia (D64.903) is a disease entity listed in the National Clinical Version 2.0 of the Disease Classification and Codes standard issued by the National Health Commission; a detailed pathological introduction is being compiled.
Moderate anemia (D64.902) is a disease entity listed in the National Clinical Version 2.0 of the Disease Classification and Codes standard issued by the National Health Commission; a detailed pathological introduction is being compiled.
Mild anemia (D64.901) is a disease entity listed in the National Clinical Version 2.0 of the Disease Classification and Codes standard issued by the National Health Commission; a detailed pathological introduction is being compiled.
Infectious anemia (D64.900x007) is a disease entity listed in the National Clinical Version 2.0 of the Disease Classification and Codes standard issued by the National Health Commission; a detailed pathological introduction is being compiled.
Infantile anemia (D64.900x006) is a disease entity listed in the National Clinical Version 2.0 of the Disease Classification and Codes standard issued by the National Health Commission; a detailed pathological introduction is being compiled.
Renal anemia (D64.900x005) is a disease entity listed in the National Clinical Version 2.0 of the Disease Classification and Codes standard issued by the National Health Commission; a detailed pathological introduction is being compiled.
Anemia = hemoglobin/RBC count/hematocrit below lower normal limit. Adult male Hb<120 g/L, non-pregnant female <110 g/L, pregnant <100 g/L. Common; many causes: blood loss, impaired production, excessive destruction.
血液科Leukoerythroblastic anemia (D64.803) is a disease entity listed in the National Clinical Version 2.0 of the Disease Classification and Codes standard issued by the National Health Commission; a detailed pathological introduction is being compiled.
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