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DOID:0112173 - combined deficiency of vitamin K-dependent clotting factors 1
Disease Ontology 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.
Synonyms: VKCFD1,
Xenbase Genes : ggcx
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
autosomal recessive disease (is_a),
hereditary combined deficiency of vitamin K-dependent clotting factors (is_a)