Congenital factor V deficiency

Congenital factor V deficiency is an inherited bleeding disorder due to reduced plasma levels of factor V (FV) and characterized by mild to severe bleeding symptoms.

Also known as: Owren disease, Parahemophilia, Proaccelerin deficiency, congenital factor V deficiency, hereditary Factor V deficiency, hereditary factor V deficiency, labile factor deficiency, Owren Parahemophilia

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