Hearing impairment Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A decreased magnitude of the sensory perception of sound. (Human Phenotype Ontology, HP_0000365)
External Link http://www.ncbi.nlm.nih.gov/medgen/?term=CN000341
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Genes

1 genes associated with the Hearing impairment phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

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