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Summary Literature (0)
OMIM:601543 - DEAFNESS, AUTOSOMAL DOMINANT 12; DFNA12

Xenbase Genes: tecta.2, tecta

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011102 - autosomal dominant nonsyndromic hearing loss 12
MONDO:0019587 - autosomal dominant nonsyndromic hearing loss

Disease Ontology (DO):
DOID:0110544 - autosomal dominant nonsyndromic deafness 12