branch retinal artery occlusion Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
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Genes

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

Symbol Name Standardized Value
PSD pleckstrin and Sec7 domain containing 1.7623
F5 coagulation factor V (proaccelerin, labile factor) 1.15325
PROS1 protein S (alpha) 0.995283
ERG v-ets avian erythroblastosis virus E26 oncogene homolog 0.956614
ROM1 retinal outer segment membrane protein 1 0.926279
TPT1 tumor protein, translationally-controlled 1 0.806488
FOXO4 forkhead box O4 0.793771
PNMA2 paraneoplastic Ma antigen 2 0.700722
C6ORF25 chromosome 6 open reading frame 25 0.535022
MTHFR methylenetetrahydrofolate reductase (NAD(P)H) 0.521117
F8 coagulation factor VIII, procoagulant component 0.433772
F3 coagulation factor III (thromboplastin, tissue factor) 0.392629
APOH apolipoprotein H (beta-2-glycoprotein I) 0.373328
F2 coagulation factor II (thrombin) 0.304142