visual agnosia Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description An agnosia that is a loss of the ability to visually recognize objects. (Human Disease Ontology, DOID_0060155)
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Genes

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

Symbol Name Standardized Value
LSR lipolysis stimulated lipoprotein receptor 1.27039
MRI1 methylthioribose-1-phosphate isomerase 1 1.13247
NOVA2 neuro-oncological ventral antigen 2 1.07362
ALLC allantoicase 0.855677
PSEN1 presenilin 1 0.505739
GAD2 glutamate decarboxylase 2 (pancreatic islets and brain, 65kDa) 0.474877
MB myoglobin 0.435651
SMUG1 single-strand-selective monofunctional uracil-DNA glycosylase 1 0.385565
SYP synaptophysin 0.377031
CYLD cylindromatosis (turban tumor syndrome) 0.351187