Conditions / Genetic
factor XII deficiency
info ยท Genetic
A blood coagulation disease that is characterized by prolonged PTT time without clinical symptoms, and has_material_basis_in a mutation in the F12 gene on chromosome 5q33.
Signs and symptoms
- Reduced factor XII activity
- Prolonged whole-blood clotting time
- Prolonged partial thromboplastin time
Also known as: Factor XII deficiency disease; Hageman Factor deficiency; deficiency, Hageman