Congenital Disorder

Factor XIII Deficiency

AMW:DIS:150051

A deficiency of blood coagulation FACTOR XIII or fibrin stabilizing factor (FSF) that prevents blood clot formation and results in a clinical hemorrhagic diathesis.

Pathology clinical

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Factor XIII Deficiency has parent Blood Coagulation Disorders, Inherited

Factor XIII Deficiency has parent Coagulation Protein Disorders

Factor XIII Deficiency has parent Hemorrhagic Disorders

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