congenital afibrinogenemia 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_2236)
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28 genes co-occuring with the disease congenital afibrinogenemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
FGA fibrinogen alpha chain 2.59061
FGG fibrinogen gamma chain 2.57054
FGB fibrinogen beta chain 2.52547
CFI complement factor I 1.58448
CR1 complement component (3b/4b) receptor 1 (Knops blood group) 1.03493
VWF von Willebrand factor 1.01807
F2 coagulation factor II (thrombin) 0.958287
F3 coagulation factor III (thromboplastin, tissue factor) 0.797462
CD46 CD46 molecule, complement regulatory protein 0.764718
F8 coagulation factor VIII, procoagulant component 0.742735
PLG plasminogen 0.635921
CFB complement factor B 0.631991
CFP complement factor properdin 0.617486
ITGA2B integrin, alpha 2b (platelet glycoprotein IIb of IIb/IIIa complex, antigen CD41) 0.560227
FN1 fibronectin 1 0.545481
F7 coagulation factor VII (serum prothrombin conversion accelerator) 0.496175
CFHR1 complement factor H-related 1 0.487407
F12 coagulation factor XII (Hageman factor) 0.476014
C3 complement component 3 0.393374
SERPINC1 serpin peptidase inhibitor, clade C (antithrombin), member 1 0.389653
FBL fibrillarin 0.378514
F5 coagulation factor V (proaccelerin, labile factor) 0.354131
SRSF1 serine/arginine-rich splicing factor 1 0.339806
PML promyelocytic leukemia 0.32701
FBLL1 fibrillarin-like 1 0.324823
SERPINE1 serpin peptidase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1), member 1 0.173314
GRB2 growth factor receptor-bound protein 2 0.163729
ANGPT2 angiopoietin 2 0.162109