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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Where it sits in the disease tree

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Part of

↑ Hemorrhagic disease (508) ↑ 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)

Trials to join now! 7 Not yet recruiting 1 Not yet finished but already full! 1 Completed 2

Ginger vs. heavy periods: a natural approach for women with bleeding disorders

Symptom relief Not yet recruiting

This study tests whether taking ginger powder for the first three days of each period can reduce heavy menstrual bleeding in women with coagulation disorders (bleeding problems). 74 women will be randomly assigned to receive either ginger or a placebo for six cycles. The goal is …

Early phase 1 • Sponsor: University of Valladolid • Aim: Symptom relief

Last updated Jun 27, 2026 12:35 UTC

Congenital factor XIII deficiency

Where it sits in the disease tree

Ginger vs. heavy periods: a natural approach for women with bleeding disorders