|Dataset||DISEASES Text-mining Gene-Disease Assocation Evidence Scores|
|Category||disease or phenotype associations|
|Description||An agnosia that is a loss of the ability to perceive any auditory information but whose hearing is intact. (Human Disease Ontology, DOID_0060140)|
|Downloads & Tools|
1 genes co-occuring with the disease cortical deafness in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
|KCNT1||potassium channel, sodium activated subfamily T, member 1||1.92342|