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, 0 tagged with Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Osteonecrosis of genetic origin (102) ↑ Secondary avascular necrosis (38) ↑ Inherited thrombophilia (28)

Including sub-types (4) Tagged with Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency (0)

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

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

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

Where it sits in the disease tree

Scientists dig into genetic roots of rare bleeding disorders