Term Name: combined deficiency of vitamin K-dependent clotting factors 2
Synonyms: VKCFD2
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.
Ontology: Human Disease [DOID:0112174]   ( DOID:0112174 )

Relationships
is a type of: autosomal recessive disease hereditary combined deficiency of vitamin K-dependent clotting factors