cholesterol embolism Gene Set

Dataset	DISEASES Text-mining Gene-Disease Association 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