Congenital factor XIII deficiency

MONDO:0018029

Congenital factor XIII deficiency is an inherited bleeding disorder due to reduced levels and activity of factor XIII (FXIII) and characterized by hemorrhagic diathesis frequently associated with spontaneous abortions and defective wound healing. Factor XIII deficiency is one of the most rare coagulation factor deficiencies.

Also known as: fibrin-stabilizing factor deficiency, factor XIII deficiency, fibrin stabilising factor deficiency, fibrin stabilizing factor deficiency

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

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↑ Hemorrhagic disease (510) ↑ Congenital hematological disorder (101) ↑ Factor XIII deficiency (0)

Sub-types of Congenital factor XIII deficiency

Factor XIII, A subunit, deficiency of 0 trials
Factor XIII, b subunit, deficiency of 0 trials

Including sub-types (11) Tagged with Congenital factor XIII deficiency (0)

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