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Summary Literature (0)
MIM:601369 - DEAFNESS, AUTOSOMAL DOMINANT 9; DFNA9

Xenbase Genes: coch

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011058 - autosomal dominant nonsyndromic hearing loss 9
MONDO:0019587 - autosomal dominant nonsyndromic hearing loss

Disease Ontology (DO):
DOID:0110593 - autosomal dominant nonsyndromic deafness 9