factor v 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_2216)
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Genes

16 genes co-occuring with the disease factor v deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
F5 coagulation factor V (proaccelerin, labile factor) 2.52819
F2 coagulation factor II (thrombin) 1.41402
F3 coagulation factor III (thromboplastin, tissue factor) 1.28785
F8 coagulation factor VIII, procoagulant component 1.24515
F7 coagulation factor VII (serum prothrombin conversion accelerator) 1.10763
MCFD2 multiple coagulation factor deficiency 2 1.0168
MMRN1 multimerin 1 0.899924
SERPINA5 serpin peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 5 0.785984
COX5A cytochrome c oxidase subunit Va 0.768801
TFPI tissue factor pathway inhibitor (lipoprotein-associated coagulation inhibitor) 0.648928
LMAN1 lectin, mannose-binding, 1 0.608104
F9 coagulation factor IX 0.559062
PROS1 protein S (alpha) 0.43227
VWF von Willebrand factor 0.222822
F10 coagulation factor X 0.218715
CD52 CD52 molecule 0.1936