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 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 (or HFE hereditary hemochromatosis, or HFE-related hereditary haemochromatosis) 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