Vitamin K-dependent clotting factors, combined deficiency of, type 2

Any congenital vitamin K-dependent coagulation factors combined deficiency in which the cause of the disease is a mutation in the VKORC1 gene.

Also known as: VKORC1 congenital vitamin K-dependent coagulation factors combined deficiency, congenital vitamin K-dependent coagulation factors combined deficiency caused by mutation in VKORC1, vitamin K-dependent clotting factors, combined deficiency of, 2, vitamin K-dependent clotting factors, combined deficiency of, type 2, VKCFD2

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