visual epilepsy Gene Set

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

12 genes co-occuring with the disease visual epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
CLN8 ceroid-lipofuscinosis, neuronal 8 (epilepsy, progressive with mental retardation) 2.24789
C14ORF1 chromosome 14 open reading frame 1 1.89499
MFSD8 major facilitator superfamily domain containing 8 1.89314
CLN6 ceroid-lipofuscinosis, neuronal 6, late infantile, variant 1.56889
CLN5 ceroid-lipofuscinosis, neuronal 5 1.55867
BNIP3L BCL2/adenovirus E1B 19kDa interacting protein 3-like 1.24037
STX8 syntaxin 8 1.16179
TPP1 tripeptidyl peptidase I 1.07404
PPT1 palmitoyl-protein thioesterase 1 1.06648
BNIP3 BCL2/adenovirus E1B 19kDa interacting protein 3 0.855677
CLN3 ceroid-lipofuscinosis, neuronal 3 0.835198
DNAH8 dynein, axonemal, heavy chain 8 0.199033