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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.

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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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12/10/2024
MGI 6.24 		The Jackson Laboratory