Hemophilia is classified as what type of disorder?

Hemophilia is classified as a genetic disorder. It specifically results from mutations in genes involved in the production of clotting factors, which are essential for normal blood clotting. Individuals with hemophilia have a hereditary deficiency of these factors, predominantly factor VIII or factor IX, leading to an increased tendency to bleed.

While bleeding is a significant clinical manifestation of hemophilia and can be referenced in the context of the condition, the underlying cause and classification rest squarely on its genetic basis. This distinction is crucial as it underlines the nature of the disorder, emphasizing genetic inheritance and the specific mutations that lead to the symptoms observed in patients. Understanding that hemophilia is fundamentally a genetic disorder can aid in recognizing how it might be inherited and the implications for family members of affected individuals.