Factor XIII deficiency
MONDO:0002241An acquired or inherited coagulation disorder due to reduced levels and activity of factor XIII.
Also known as: FXIIID
4 clinical trials for this condition and its sub-types, 0 tagged with Factor XIII deficiency itself.
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Browse by category →Sub-types of Factor XIII deficiency
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Acquired factor XIII deficiency 0 trials
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Congenital factor XIII deficiency 0 trials
2 sub-types
- Factor XIII, A subunit, deficiency of 0 trials
- Factor XIII, b subunit, deficiency of 0 trials