Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
DOID:0111902 - thrombophilia due to activated protein C resistance

Disease Ontology Definition:A thrombophilia characterized by resistance of F5 to cleavage and inactivation and increased tendency for thrombosis that has_material_basis_in heterozygous mutation in F5 on chromosome 1q24.2.

Synonyms: activated protein C resistance, APC resistance, PCCF deficiency, PROC cofactor deficiency, THPH2, thrombophilia due to deficiency of activated protein C cofactor, thrombophilia V

Xenbase Genes : f5


MIM:
MIM:188055 - THROMBOPHILIA DUE TO ACTIVATED PROTEIN C RESISTANCE; THPH2

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal dominant disease (is_a), thrombophilia (is_a)