nonsyndromic hearing loss 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)
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Genes

1 genes associated with the disease nonsyndromic hearing loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
GJB2 gap junction protein, beta 2, 26kDa