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Hemophilia is a genetic bleeding disorder caused by mutations that prevent blood from clotting properly. There are several types of hemophilia based on which clotting factor is deficient: hemophilia A is caused by a lack of factor VIII, hemophilia B by a lack of factor IX, and hemophilia C by a lack of factor XI. The genes for hemophilia A and B are located on the X chromosome and are usually inherited from a carrier mother. Symptoms include prolonged bleeding from cuts or wounds and bleeding into joints or

Author

Yoga Angga Trinanda

Language

EN