Term Name: combined deficiency of vitamin K-dependent clotting factors 1
Synonyms: VKCFD1
Definition: A hereditary combined deficiency of vitamin K-dependent clotting factors that has_material_basis_in homozygous or compound heterozygous mutation in the GGCX gene on chromosome 2p11.2.
Ontology: Human Disease [DOID:0112173]   ( DOID:0112173 )

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