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Summary Literature (0)
MIM:618094 - DEAFNESS, AUTOSOMAL RECESSIVE 110; DFNB110

Xenbase Genes: coch

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0054860 - hearing loss, autosomal recessive 110

Disease Ontology (DO):
DOID:0111644 - autosomal recessive nonsyndromic deafness 110