This document summarizes a study on hemophilia. Hemophilia is a genetic bleeding disorder caused by deficiencies in specific clotting factors, resulting in prolonged bleeding. There are two main types: hemophilia A caused by a lack of factor VIII (80% of cases) and hemophilia B caused by a lack of factor IX (20% of cases). A rare third type, hemophilia C, results from a deficiency in factor XI. Hemophilia is inherited and mainly affects males, as the gene is located on the X chromosome. The study examines the genetics and computational approaches to understanding the genes responsible for hemophilia.