|Dataset||GAD Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||An auditory system disease that is associated with permanent hearing loss caused by damage to structures in the inner ear and/or the middle ear, which is not associated with other signs and symptoms. (Human Disease Ontology, DOID_0050563)|
|Downloads & Tools|
3 genes associated with the disease non-syndromic deafness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.