autosomal recessive nonsyndromic deafness 110 (DOID:0111644)
Alliance: disease page
Synonyms: autosomal recessive deafness 110; DFNB110
Alt IDs: OMIM:618094
Definition: An autosomal recessive nonsyndromic deafness characterized by prelingual, bilateral hearing loss that has_material_basis_in homozygous or compound heterozygous mutation in the COCH gene on chromosome 14q12.