combined deficiency of vitamin K-dependent clotting factors 2 Disease Ontology Browser

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Disease Ontology Browser

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.

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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