combined deficiency of vitamin K-dependent clotting factors 1 Disease Ontology Browser

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Disease Ontology Browser

combined deficiency of vitamin K-dependent clotting factors 1 (DOID:0112173)
Alliance: disease page
Synonyms: VKCFD1
Alt IDs: OMIM:277450, MESH:C564741, UMLS_CUI:C1848534
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.

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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