Disease-gene associations mined from literature

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 hearing loss,  nonsyndromic hereditary hearing loss,  nonsyndromic familial hearing loss

Linkouts:  OMIM