internuclear ophthalmoplegia Gene Set

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

13 genes co-occuring with the disease internuclear ophthalmoplegia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
OMG oligodendrocyte myelin glycoprotein 1.10006
BMP2K BMP2 inducible kinase 1.09293
CXCR5 chemokine (C-X-C motif) receptor 5 0.854859
HCRT hypocretin (orexin) neuropeptide precursor 0.75412
MBP myelin basic protein 0.720461
HEXA hexosaminidase A (alpha polypeptide) 0.630027
PTCH1 patched 1 0.548971
AQP4 aquaporin 4 0.521117
PSEN1 presenilin 1 0.420641
IFNB1 interferon, beta 1, fibroblast 0.366301
NF1 neurofibromin 1 0.331391
BCHE butyrylcholinesterase 0.27794
F3 coagulation factor III (thromboplastin, tissue factor) 0.18151