Human genes for autosomal recessive nonsyndromic deafness 110
Autosomal recessive nonsyndromic deafness 110 [DOID:0111644]
An autosomal recessive nonsyndromic deafness characterized by prelingual, bilateral hearing loss that has_material_basis_in homozygous or compound heterozygous mutation in COCH on chromosome 14q12.
Synonyms: autosomal recessive nonsyndromic deafness 110, DOID:0111644, autosomal recessive deafness 110, DFNB110