Any congenital vitamin K-dependent coagulation factors combined deficiency in which the cause of the disease is a mutation in the VKORC1 gene.
Comprehensive, easy-to-understand information about this condition
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Gene data from MyGene.info • Click to view on NCBI Gene
congenital factor VII deficiency
MONDO:0009211
congenital factor X deficiency
MONDO:0009212
vitamin K-dependent clotting factors, combined deficiency of, type 1
MONDO:0010187
congenital prothrombin deficiency
MONDO:0013361