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Chronic acquired pure red-cell aplasia (D60.000) 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 compi
Chronic idiopathic hemolytic anemia (D59.903) 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
Hemolytic jaundice is mainly due to intrinsic RBC defects or extrinsic injury causing massive RBC destruction and large hemoglobin release, raising plasma unconjugated bilirubin beyond hepatocellular processing capacity. Any hemolytic disease causes it.
血液科Acute hemolytic anemia (D59.901) 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.
Acquired hemolytic anemia (D59.900) 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.
Other acquired hemolytic anemia (D59.800) 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.
Hemoglobinuria with hemolytic anemia (D59.604) 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 compile
Paroxysmal cold hemoglobinuria (PCH) is a rare disease marked by sudden hemoglobinuria after systemic or local cold exposure. Hemolysis is usually triggered by cold; onset minutes-to-hours later with brief chills, fever.
血液科March hemoglobinuria is transient intravascular hemolysis and hemoglobinuria caused by mechanical RBC injury from repeated forceful impact of palms/soles or other body parts against hard surfaces.
血液科Exertional hemoglobinuria (D59.601) 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.
External-hemolysis hemoglobinuria (D59.600x004) 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 compil
Exercise hemoglobinuria (march hemoglobinuria) (D59.600x001) 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
Other hemoglobinuria from external hemolysis (D59.600) 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
Paroxysmal nocturnal hemoglobinuria with aplastic anemia (D59.501) 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 introduct
Paroxysmal nocturnal hemoglobinuria (PNH) is chronic intravascular hemolysis from acquired RBC-membrane defects, often worse during sleep, with episodic hemoglobinuria and pancytopenia. Rare but increasing; more common in northern China.
血液科Paroxysmal nocturnal hemoglobinuria (Marchiafava-Micheli) (D59.500) 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 introduc
Mechanical hemolytic anemia (D59.404) 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.
Microangiopathic hemolytic anemia is a severe diffuse thrombotic microangiopathy characterized by MAHA, thrombocytopenia from platelet consumption, and organ damage (kidney, CNS) from microthrombi. It is a hemolytic anemia syndrome caused by RBC fragmenta
血液科Infectious hemolytic anemia (D59.402) 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.
Secondary hemolytic anemia (D59.401) 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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