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Fibrinolytic defect

MONDO:0007605

Also known as: fibrinolytic defect

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

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Broader categories

Disease (618) Hereditary disease (172) Human disease (14) Disease of genetic or genomic mechanism (2) Disease by etiologic mechanism (0)

Trials to join now! 1 Completed 2

Could your genes raise your risk of a mystery stroke?

Knowledge-focused Recruiting now

This study is looking at whether certain gene changes (variants) in a protein called annexin A2 are linked to strokes that happen for no clear reason, especially in younger adults. Researchers will compare blood samples from 240 people who have had a stroke with no known cause. T…

Phase: NA • Sponsor: Centre Hospitalier Universitaire, Amiens • Aim: Knowledge-focused

Last updated Jun 27, 2026 08:11 UTC