Human genes for nonsyndromic deafness
Nonsyndromic deafness [DOID:0050563]
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.
Synonyms: nonsyndromic deafness, DOID:0050563, nonsyndromic deafnesses, nonsyndromic hearing loss, nonsyndromic hereditary hearing loss ...
Linkouts: OMIM