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haemochromatosis

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  • [edit] Haemochromatosis or haemosiderosis. Historically, the term haemochromatosis (spelled hemochromatosis in American English) was initially used to refer to what is now more specifically called haemochromatosis type 1 (or HFE-related hereditary haemochromatosis). — “Iron overload - Wikipedia, the free encyclopedia”, en.wikipedia.org
  • Haemochromatosis type 3 is a type of Iron overload disorder associated with deficiencies in transferrin receptor 2. It exhibits an autosomal recessive inheritance "New insights into iron homeostasis through the study of non-HFE hereditary haemochromatosis". — “Haemochromatosis type 3 - Wikipedia, the free encyclopedia”, en.wikipedia.org
  • Hemochromatosis type 1[1] (or HFE hereditary hemochromatosis[2], or HFE-related hereditary haemochromatosis[3]) is a hereditary disease characterized by excessive absorption of dietary iron resulting in a pathological increase in total body iron stores. — “HFE hereditary hemochromatosis - Wikipedia, the free encyclopedia”, en.wikipedia.org

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