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Metadata
ID	DOID:0111644
Name	autosomal recessive nonsyndromic deafness 110
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. https://www.ncbi.nlm.nih.gov/pubmed/29449721
Xrefs	OMIM:618094
Synonyms	autosomal recessive deafness 110 [EXACT] DFNB110 [EXACT]
Parent Relationships	is_a autosomal recessive nonsyndromic deafness