Combined deficiency of vitamin K-dependent clotting factors type 2

The disease with the acronyme VKCFD2 is characterized by an autosomal recessive combined deficiency of vitamin-k dependent coagulation factors (I, VII, IX, and X) which is caused by a mutations of subunit 1 vitamin K epoxide reductase complex (VKORC1) gene.

Systematic

Disturbances of vitamin K metabolism
	Combined deficiency of vitamin K-dependent clotting factors type 1
	Combined deficiency of vitamin K-dependent clotting factors type 2
		VKORC1
	Coumarin resistance
	Pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency