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Summary Literature (0)
MIM:615629 - DEAFNESS, AUTOSOMAL DOMINANT 56; DFNA56

Xenbase Genes: tnc

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014283 - autosomal dominant nonsyndromic hearing loss 56
MONDO:0019587 - autosomal dominant nonsyndromic hearing loss

Disease Ontology (DO):
DOID:0110581 - autosomal dominant nonsyndromic deafness 56