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Factor XIII deficiency

MONDO:0002241

An acquired or inherited coagulation disorder due to reduced levels and activity of factor XIII.

Also known as: FXIIID

39 clinical trials for this condition and its sub-types.

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Sub-types

Acquired factor XIII deficiency (0) Congenital factor XIII deficiency (0) Factor XIII, A subunit, deficiency of (0) Factor XIII, b subunit, deficiency of (0)

Broader categories

Disease (618) Hematologic disorder (160) Blood coagulation disease (51) Human disease (14) Coagulation protein disease (12) Disease by body system or component (0)
Trials to join now! 17 Not yet recruiting 3 Not yet finished but already full! 5 Completed 13 Terminated 1
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