DISEASES

Disease-gene associations mined from literature

Human genes for autosomal dominant nonsyndromic deafness 1

Autosomal dominant nonsyndromic deafness 1 [DOID:0110541]

An autosomal dominant nonsyndromic deafness that is characterized by low frequency progressive hearing loss and has_material_basis_in mutation in the DIAPH1 gene on chromosome 5q31.

Synonyms:  autosomal dominant nonsyndromic deafness 1,  DOID:0110541,  DFNA1,  Konigsmark syndrome,  LFHL1 ...