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Summary Literature (0)
MIM:612644 - DEAFNESS, AUTOSOMAL DOMINANT 2B; DFNA2B

Xenbase Genes: gjb3

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012976 - autosomal dominant nonsyndromic hearing loss 2B
MONDO:0019587 - autosomal dominant nonsyndromic hearing loss