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Frontal encephalocele (Q01.000) is a disease included in the National Health Commission's 'Disease Classification and Codes, National Clinical Version 2.0' standard; a detailed pathological introduction is being compiled.
Closed iniencephaly (Q00.200x201) is a disease included in the National Health Commission's 'Disease Classification and Codes, National Clinical Version 2.0' standard; a detailed pathological introduction is being compiled.
Open iniencephaly (Q00.200x101) is a disease included in the National Health Commission's 'Disease Classification and Codes, National Clinical Version 2.0' standard; a detailed pathological introduction is being compiled.
Iniencephaly (Q00.200) is a disease included in the National Health Commission's 'Disease Classification and Codes, National Clinical Version 2.0' standard; a detailed pathological introduction is being compiled.
Craniorachischisis (Q00.100) is a disease included in the National Health Commission's 'Disease Classification and Codes, National Clinical Version 2.0' standard; a detailed pathological introduction is being compiled.
Hemochromatosis is iron overload (HFE C282Y) causing cirrhosis, diabetes, skin pigmentation, cardiomyopathy, arthropathy; treat by phlebotomy.
遗传病科Porphyrias are heme-pathway enzyme defects: acute (neurovisceral: AIP/variegate/hereditary coproporphyria) vs cutaneous (photosensitivity/blistering); avoid triggers, treat acutely with hemin.
遗传病科Congenital adrenal hyperplasia (CAH) is a group of diseases caused by congenital defects of one or more enzymes in the enzyme system for the biosynthesis of adrenocortical hormones, resulting in altered levels of hormones such as cortisol. It usually foll
遗传病科
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