prothrombin 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_2235)
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Genes

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

Symbol Name Standardized Value
F2 coagulation factor II (thrombin) 1.9769
F3 coagulation factor III (thromboplastin, tissue factor) 1.16778
F9 coagulation factor IX 0.961216
F7 coagulation factor VII (serum prothrombin conversion accelerator) 0.508808
PROS1 protein S (alpha) 0.435651
F8 coagulation factor VIII, procoagulant component 0.27153
SERPINC1 serpin peptidase inhibitor, clade C (antithrombin), member 1 0.24715
TNFSF13B tumor necrosis factor (ligand) superfamily, member 13b 0.23492