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Pyruvate-kinase-deficiency anemia (D55.204) 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.
Triose-phosphate-isomerase-deficiency anemia (D55.203) 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
Hexokinase-deficiency anemia (D55.202) 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 nonspherocytic hemolytic anemia type II (D55.201) 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
Hereditary nonspherocytic hemolytic anemia type II (D55.200x002) 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 introductio
Hexokinase-deficiency anemia (D55.200x001) 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.
Glycolytic-enzyme-disorder anemia (D55.200) 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 nonspherocytic hemolytic anemia type I (D55.101) 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
Hereditary nonspherocytic hemolytic anemia type I (D55.100x011) 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
Hexose-phosphatase-deficiency anemia (D55.100x003) 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 com
Glutathione-metabolism-disorder anemia (D55.100x001) 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 c
Other glutathione-metabolism-disorder anemia (D55.100) 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
Commonly called favism, it is hereditary G6PD deficiency - the most common hereditary enzyme-deficiency disease. ~200 million people worldwide. China is a high-prevalence area with south>north distribution, prevalence 0.2-44.8%. Cause: G6PD gene mutation
血液科Glucose-6-phosphate-dehydrogenase-deficiency anemia (D55.000x002) 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 introducti
G6PD-deficiency anemia (D55.000) 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 compiled.
Chronic simple anemia (D53.901) 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.
Nutritional chronic anemia (D53.900x002) 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.
Nutritional anemia = relative/absolute reduction in hematopoietic nutrients (iron, folate, vitamin D etc.) causing insufficient hemoglobin/RBC production and low hematopoietic function. Common in infants 6mo-2yr, pregnant/lactating women, and patients wit
血液科Vitamin D-deficiency anemia (D53.804) 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.
Molybdenum-deficiency anemia (D53.803) 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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