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DOID:3756 - protein C deficiency
Disease Ontology Definition:A thrombophilia that is characterized by recurrent venous thrombosis and that has_material_basis_in heterozygous mutation in the PROC gene on chromosome 2q14.
Synonyms:
Xenbase Genes : proc, proc.2
MONDO:0019145 - hereditary thrombophilia due to congenital protein C deficiency |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee