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DOID:0111644 - autosomal recessive nonsyndromic deafness 110
Disease Ontology 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.
Synonyms: DFNB110, autosomal recessive deafness 110,
Xenbase Genes : coch
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee