combined deficiency of vitamin K-dependent clotting factors 2 (DOID:0112174)
Alliance: disease page
Synonyms: VKCFD2
Alt IDs: OMIM:607473, MESH:C564393
Definition: A hereditary combined deficiency of vitamin K-dependent clotting factors that has_material_basis_in homozygous or compound heterozygous mutation in the VKORC1 gene on chromosome 16p11.2.