Human genes for autosomal recessive nonsyndromic deafness 113
Autosomal recessive nonsyndromic deafness 113 [DOID:0111636]
An autosomal recessive nonsyndromic deafness characterized by postlingual progressive hearing impairment that has_material_basis_in homozygous or compound heterozygous mutation in CEACAM16 on chromosome 19q13.
Synonyms: autosomal recessive nonsyndromic deafness 113, DOID:0111636, autosomal recessive deafness 113, DFNB113