cortical deafness 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 perceive any auditory information but whose hearing is intact. (Human Disease Ontology, DOID_0060140)
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Genes

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.

Symbol Name Standardized Value
KCNT1 potassium channel, sodium activated subfamily T, member 1 1.92342