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Summary Literature (2)
MIM:601544 - DEAFNESS, AUTOSOMAL DOMINANT 3A; DFNA3A

Xenbase Genes: gjb2

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011103 - autosomal dominant nonsyndromic hearing loss 3A
MONDO:0019587 - autosomal dominant nonsyndromic hearing loss

Disease Ontology (DO):
DOID:0110564 - autosomal dominant nonsyndromic deafness 3A