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Heparin cofactor 2 deficiency

MONDO:0012876

Also known as: heparin cofactor 2 deficiency, thrombophilia 10 due to heparin cofactor II deficiency, Hcf 2 deficiency, Hcf2 deficiency, heparin cofactor II deficiency, thrombophilia due to heparin cofactor 2 deficiency

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

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Broader categories

Disease (680) Hereditary disease (176) Hematologic disorder (170) Blood coagulation disease (53) Human disease (14) Thrombophilia (12) Inherited blood coagulation disorder (8) Disease of genetic or genomic mechanism (2) Disease by body system or component (0) Disease by etiologic mechanism (0)
Trials to join now! 1 Not yet recruiting 1 Not yet finished but already full! 1 Completed 1
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  • Scientists dig into genetic roots of rare bleeding disorders

    Knowledge-focused Recruiting now

    This study looks at how blood cells interact and what goes wrong in inherited bleeding disorders like Glanzmann thrombasthenia. Researchers will analyze blood samples from up to 60 healthy volunteers and patients to find genetic defects. The goal is to better understand these con…

    Sponsor: Rockefeller University • Aim: Knowledge-focused

    Last updated Jun 27, 2026 07:55 UTC

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