D68: Other coagulation defects
D68.2: Hereditary deficiency of other clotting factors
Hereditary deficiency of other clotting factors, as the name indicates, is a genetic condition in which the body doesn't produce enough clotting factor - proteins in the blood that control bleeding. They play a crucial role in the clotting process, which prevents excessive bleeding when you're injured. Without enough clotting factors, your body has a hard time stopping any bleeding that may occur, resulting in prolonged or spontaneous bleeding. Common symptoms often include frequent nosebleeds, heavy or prolonged menstrual bleeding, easy bruising, and bleeding into joints or muscles. The condition tends to manifest from birth or early childhood. The severity of the symptoms can vary and they can worsen over time if not properly managed. The blood and circulatory system are the central systems affected by this condition.
Patient Disclaimer
The information provided on this page is for general educational purposes only. It is not intended for self-diagnosis and does not replace professional medical advice. Always consult your doctor or a qualified healthcare provider with any questions or concerns about your health.
If you see an ICD diagnosis code (e.g., on a medical report), be aware that doctors may also include additional indicators to express diagnostic certainty. Only a healthcare professional can interpret these codes accurately in the context of your individual case.
For a complete understanding of your condition and what the diagnosis means for you, please speak directly with your doctor.