factor xii deficiency Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_2231)
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24 genes co-occuring with the disease factor xii deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
F12 coagulation factor XII (Hageman factor) 2.85062
F3 coagulation factor III (thromboplastin, tissue factor) 1.70406
KLKB1 kallikrein B, plasma (Fletcher factor) 1 1.39346
F11 coagulation factor XI 1.0324
F9 coagulation factor IX 1.0109
KNG1 kininogen 1 0.985585
PLG plasminogen 0.885979
PROS1 protein S (alpha) 0.86018
F2 coagulation factor II (thrombin) 0.838066
F8 coagulation factor VIII, procoagulant component 0.793361
VWF von Willebrand factor 0.782707
F7 coagulation factor VII (serum prothrombin conversion accelerator) 0.731381
F5 coagulation factor V (proaccelerin, labile factor) 0.613965
GP9 glycoprotein IX (platelet) 0.517265
SERPINC1 serpin peptidase inhibitor, clade C (antithrombin), member 1 0.495029
OR10R2 olfactory receptor, family 10, subfamily R, member 2 0.469576
PLAU plasminogen activator, urokinase 0.42664
PLAT plasminogen activator, tissue 0.396725
SERPINF2 serpin peptidase inhibitor, clade F (alpha-2 antiplasmin, pigment epithelium derived factor), member 2 0.364824
SERPINB6 serpin peptidase inhibitor, clade B (ovalbumin), member 6 0.338341
SERPIND1 serpin peptidase inhibitor, clade D (heparin cofactor), member 1 0.32009
KLK1 kallikrein 1 0.234225
IKBKAP inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase complex-associated protein 0.19582
CD46 CD46 molecule, complement regulatory protein 0.171036