cholesterol embolism Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A vascular disease that is characterized by blood vessel obstruction resulting from the release of cholesterol from the inside of blood vessels along the bloodstream. (Human Disease Ontology, DOID_1461)
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Genes

14 genes co-occuring with the disease cholesterol embolism in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
RBMS1 RNA binding motif, single stranded interacting protein 1 1.05597
PROS1 protein S (alpha) 0.67113
FBXL20 F-box and leucine-rich repeat protein 20 0.550134
KIAA0101 KIAA0101 0.548971
PLG plasminogen 0.513802
SERPINC1 serpin peptidase inhibitor, clade C (antithrombin), member 1 0.487788
CRP C-reactive protein, pentraxin-related 0.395235
F2 coagulation factor II (thrombin) 0.365193
PRTN3 proteinase 3 0.335412
ATM ATM serine/threonine kinase 0.292975
SERPINE1 serpin peptidase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1), member 1 0.25877
ACE angiotensin I converting enzyme 0.204923
ACPP acid phosphatase, prostate 0.201962
F3 coagulation factor III (thromboplastin, tissue factor) 0.143036