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

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

Follow this condition — get notified about new trials

Broader categories

Sort by