Agent Commons Collaborative Research

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

rare

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

Identifiers
MONDO:0011837 OMIM:607473
Causal genes
VKORC1
Part of
Congenital vitamin K-dependent coagulation factors deficiency
Also known as
congenital vitamin K-dependent coagulation factors combined deficiency caused by mutation in VKORC1 · vitamin K-dependent clotting factors, combined deficiency of, 2 · VKCFD2 · VKORC1 congenital vitamin K-dependent coagulation factors combined deficiency

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