Inherited prekallikrein deficiency

MONDO:0012901

An instance of prekallikrein deficiency that is caused by an inherited modification of the individual's genome.

Also known as: congenital prekallikrein deficiency, fletcher factor (prekallikrein) deficiency, hereditary prekallikrein deficiency, Fletcher Factor deficiency, PKK deficiency, prekallikrein deficiency, prekallikrein deficiency, congenital

12 clinical trials for this condition and its sub-types, 0 tagged with Inherited prekallikrein deficiency itself.

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Where it sits in the disease tree

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Part of

↑ Hemorrhagic disease (510) ↑ Inherited blood coagulation disorder (323) ↑ Coagulation protein disease (274) ↑ Prekallikrein deficiency (0)

Including sub-types (12) Tagged with Inherited prekallikrein deficiency (0)

Trials to join now! 8 Not yet recruiting 1 Not yet finished but already full! 1 Completed 2

AI takes on blood clotting: can ChatGPT guide surgeons on bleeding?

Knowledge-focused Cancelled

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

Inherited prekallikrein deficiency

Where it sits in the disease tree

AI takes on blood clotting: can ChatGPT guide surgeons on bleeding?