Congenital factor X deficiency

Congenital factor X deficiency is an inherited bleeding disorder with a decreased antigen and/or activity of factor X (FX) and characterized by mild to severe bleeding symptoms.

Also known as: Stuart-Prower factor deficiency, congenital Stuart factor deficiency, congenital factor X deficiency, hereditary Factor X deficiency, F10 deficiency, Stuart factor deficiency, congenital, Stuart-Prower Factor deficiency, factor 10 deficiency

46 clinical trials for this condition and its sub-types.