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Summary Literature (0)
DOID:0080701 - prothrombin thrombophilia

Disease Ontology Definition:A thrombophilia that is characterized by increases the risk of blood clots including deep vein thrombosis and pulmonary embolism and that has_material_basis_in heterozygous mutation in the thrombin gene (F2 gene) on chromosome 11p11.

Synonyms:

Xenbase Genes : f2, habp2, f13a1, mthfr



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)