factor viii deficiency Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description An X-linked disease that has_material_basis_in Factor VIII deficiency, which results in the formation of fibrin deficient clots which makes coagulation much more prolonged. The disease is inherited as an X-linked recessive trait. (Human Disease Ontology, DOID_12134)
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22 genes co-occuring with the disease factor viii deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
F8 coagulation factor VIII, procoagulant component 2.46949
F5 coagulation factor V (proaccelerin, labile factor) 1.83682
LMAN1 lectin, mannose-binding, 1 1.82368
MCFD2 multiple coagulation factor deficiency 2 1.63276
F9 coagulation factor IX 1.49833
F3 coagulation factor III (thromboplastin, tissue factor) 1.49394
F7 coagulation factor VII (serum prothrombin conversion accelerator) 1.22432
VWF von Willebrand factor 1.14687
SERPINA5 serpin peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 5 0.976323
F2 coagulation factor II (thrombin) 0.938704
F12 coagulation factor XII (Hageman factor) 0.767985
TFPI tissue factor pathway inhibitor (lipoprotein-associated coagulation inhibitor) 0.604981
COX5A cytochrome c oxidase subunit Va 0.60264
SSB Sjogren syndrome antigen B (autoantigen La) 0.548971
SERPINC1 serpin peptidase inhibitor, clade C (antithrombin), member 1 0.508424
ST14 suppression of tumorigenicity 14 (colon carcinoma) 0.335412
ITM2B integral membrane protein 2B 0.331391
MARK3 MAP/microtubule affinity-regulating kinase 3 0.330295
MARK2 MAP/microtubule affinity-regulating kinase 2 0.329565
FCER1A Fc fragment of IgE, high affinity I, receptor for; alpha polypeptide 0.321545
FCGR2B Fc fragment of IgG, low affinity IIb, receptor (CD32) 0.280796
MAPK1 mitogen-activated protein kinase 1 0.195183