nonsyndromic hearing impairment Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description a form of hearing impairment that is not associated with visible abnormalities of the external ear or other signs and symptoms; the vast majority of hereditary hearing loss is nonsyndromic and can be associated with abnormalities of the middle ear and/or inner ear (Mammalian Phenotype Ontology, MP_0006328)
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Genes

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

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