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Congenital factor VII deficiency

MONDO:0009211

Factor VII (FVII) deficiency is a rare hereditary hemorrhagic disease caused by the diminution or absence of this coagulation factor.

Also known as: congenital factor VII deficiency, congenital proconvertin deficiency, hypoproconvertinemia, F7 deficiency, factor 7 deficiency, factor VII deficiency

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

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Broader categories

Disease (680) Hereditary disease (176) Hematologic disorder (170) Hemorrhagic disease (103) Blood coagulation disease (53) Human disease (14) Coagulation protein disease (13) Inherited blood coagulation disorder (8) Factor VII deficiency (6) Disease of genetic or genomic mechanism (2)
Trials to join now! 10 Not yet recruiting 2 Not yet finished but already full! 1 Completed 2
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  • AI takes on blood clotting: can ChatGPT guide surgeons on bleeding?

    Knowledge-focused Terminated

    This study evaluates whether artificial intelligence models can accurately interpret ROTEM blood clotting tests and recommend treatments for coagulopathy. Researchers will compare AI decisions to those of a panel of clinical experts using data from adults undergoing elective card…

    Sponsor: Ondokuz Mayıs University • Aim: Knowledge-focused

    Last updated Jul 04, 2026 00:00 UTC

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