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Congenital factor X deficiency

MONDO:0009212

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

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

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↑ Congenital vitamin K-dependent coagulation factors deficiency (4) ↑ Factor X deficiency (2)

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

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