|Dataset||ClinVar Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|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)|
|Downloads & Tools|
1 genes associated with the Nonsyndromic Deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
|COL11A2||collagen, type XI, alpha 2|