Nonsyndromic Deafness Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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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1 genes associated with the Nonsyndromic Deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
COL11A2 collagen, type XI, alpha 2