Hereditary deficiency of other clotting factors

This code signifies a congenital or inherited disorder characterized by a deficiency in a clotting factor other than Factor VIII (hemophilia A) or Factor IX (hemophilia B). These deficiencies lead to impaired hemostasis, increasing the risk of bleeding episodes. The specific factor involved could include Factor I (fibrinogen), Factor II (prothrombin), Factor V, Factor VII, Factor X, Factor XI, or Factor XIII.

Use this code when documentation clearly indicates a hereditary deficiency of a specific clotting factor other than Factor VIII or IX, confirmed by laboratory testing. This applies to patients presenting with bleeding diatheses or identified through family screening for known hereditary coagulopathies. Documentation should specify the deficient factor if known, though this code is appropriate for "other" unspecified hereditary deficiencies.

• Do not use this code for acquired clotting factor deficiencies; those are coded elsewhere.
• If the specific hereditary factor deficiency is known (e.g., Factor VII deficiency), look for a more specific code within the D68.x category if available.
• Always review lab results and physician notes for confirmation of the hereditary nature and the specific factor involved to ensure accurate coding.