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 )

Relationships
is a type of: autosomal recessive nonsyndromic deafness