| Term Name: | autosomal recessive nonsyndromic deafness 110 |
|---|---|
| Synonyms: | autosomal recessive deafness 110, DFNB110 |
| 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. |
| Ontology: | Human Disease [DOID:0111644] ( DOID:0111644 ) |