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Summary Literature (0)
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
Parent(s): autosomal recessive nonsyndromic deafness (is_a)