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Erythropoietic protoporphyria is ferrochelatase deficiency causing protoporphyrin accumulation: acute photosensitivity (burning/itching) after sun exposure; beta-carotene, sun protection.
血液科Vitamin-K deficiency causes coagulopathy (elevated PT/INR, bleeding) in newborns (hemorrhagic disease) and in malabsorption/antibiotics/warfarin; treat by vitamin-K supplementation.
血液科Folate deficiency causes megaloblastic anemia, glossitis, neural-tube-defect risk in pregnancy; from poor diet/alcoholism/malabsorption/drugs; treat by folic-acid supplementation; important in pregnancy.
血液科Immune-mechanism disorder (D89.900) 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.
Kimura disease (D89.802) 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 light-chain-deposition disease (D89.800x011) 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
Koebner-Nobechi syndrome (D89.800x003) 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.
Gamma-globulin elevation (D89.800x002) 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 specified immune-mechanism disorders, unclassified elsewhere (D89.800) 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
Hypergammaglobulinemia (D89.200x001) 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.
Hypergammaglobulinemia (D89.200) 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.
Cryoglobulinemic glomerulonephritis () 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.
Spontaneous cryoglobulinemia (D89.100x007) 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.
Idiopathic cryoglobulinemia (D89.100x006) 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.
Mixed cryoglobulinemia (D89.100x005) 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.
Primary cryoglobulinemia (D89.100x004) 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.
Cryoglobulinemic purpura (D89.100x003) 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 compiled.
Secondary cryoglobulinemia (D89.100x002) 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.
Cryoglobulinemic vasculitis (D89.100x001) 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 compiled.
Polyclonal hypergammaglobulinemia (D89.002) 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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