tactile agnosia Gene Set

Dataset DISEASES Text-mining Gene-Disease Association Evidence Scores
Category disease or phenotype associations
Type disease
Description An agnosia that is a loss of the ability to recognize or identify objects by touch alone. (Human Disease Ontology, DOID_0060151)
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Genes

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

Symbol Name Standardized Value
COPS2 COP9 signalosome subunit 2 1.69678
NUMB numb homolog (Drosophila) 1.49043
SACS sacsin molecular chaperone 1.41972