Congenital factor XI deficiency

MONDO:0012897

Congenital factor XI deficiency is an inherited bleeding disorder characterized by reduced levels and activity of factor XI (FXI) resulting in moderate bleeding symptoms, usually occurring after trauma or surgery.

Also known as: PTA deficiency, Rosenthal factor deficiency, Rosenthal syndrome, Rosenthal's disease, congenital factor XI deficiency, factor XI deficiency, autosomal dominant, factor XI deficiency, autosomal recessive, haemophilia C

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

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Autosomal genetic disease (1666) ↑ Hemorrhagic disease (509) ↑ Inherited blood coagulation disorder (322) ↑ Congenital hematological disorder (101) ↑ Factor XI deficiency (0)

Including sub-types (13) Tagged with Congenital factor XI deficiency (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.