non-syndromic deafness Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
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)
Similar Terms
Downloads & Tools

Genes

3 genes associated with the disease non-syndromic deafness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
GJA1 gap junction protein, alpha 1, 43kDa
GJB2 gap junction protein, beta 2, 26kDa
GJB6 gap junction protein, beta 6, 30kDa