Congenital factor V deficiency

MONDO:0009210

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

12 clinical trials for this condition and its sub-types, 0 tagged with Congenital factor V deficiency itself.

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↑ Hemorrhagic disease (510) ↑ Inherited blood coagulation disorder (323) ↑ Factor V deficiency (0)

Including sub-types (12) Tagged with Congenital factor V deficiency (0)

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