... crigler-najjar disease克-纳二氏病:先天性高胆红素血症,先天性家族性非溶血性黄疸 hemochromatosis血色素沉着(症),血色病 tyrosinemia 酪氨酸血症 ...
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新生儿血色素沉着症 Neonatal Hemoehromatosis
血色素沉着症 Hemochromatosis
血色素沉着病 [皮肤] hemochromatosis
遗传性血色素沉着症 hereditary hemochromatosis ; HH
围产期血色素沉着 perinatal hemochromatosis
围产期血色素沉着病 perinatal hemochromatosis
遗传性血色素沉着病 hereditaryhemochromatosis
新生儿血色素沉着病 perinatal hemochromatosis
特发性血色素沉着病 idiopathic hemochromatosis
例如，因为突变的基因可以提高铁的吸收效率，所以遗传性血色素沉着病突变可以保护带菌者不缺铁。
For example, the hereditary hemochromatosis mutation protects carriers from iron-deficiency because the mutated gene allows increased efficiency of iron absorption.
青铜色的色素沉着见于血色素沉着症和砷中毒。
Bronze hyperpigmentation is seen in hemochromatosis and arsenic intoxication.
当发生器官功能障碍时，则用“血色素沉着症”表示。
The term "hemochromatosis" is used when organ dysfunction occurs.
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