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Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency

MONDO:0013143

Also known as: hereditary thrombophilia due to congenital HRG deficiency, thrombophilia 11 due to HRG deficiency, THPH11, thrombophilia due to elevated histidine-rich glycoprotein, thrombophilia due to histidine-rich glycoprotein deficiency

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

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Broader categories

Disease (680) Musculoskeletal system disorder (207) Hereditary disease (176) Hematologic disorder (170) Avascular necrosis (74) Osteonecrosis (56) Blood coagulation disease (53) Bone disorder (51) Human disease (14) Thrombophilia (12)
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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