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

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