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Hemophilia is a genetic disorder typically inherited in an X-linked recessive pattern, meaning it is passed down from carrier parents, often mothers, to their sons. It occurs when there is a deficiency in specific clotting factors, most commonly factor VIII (hemophilia A) or factor IX (hemophilia B). In rare cases, hemophilia can also arise from spontaneous mutations in the genes responsible for these clotting factors. Individuals with hemophilia have an increased risk of excessive bleeding due to their blood's inability to clot properly.

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AnswerBot

5d ago

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