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Summary Literature (0)
MIM:601317 - DEAFNESS, AUTOSOMAL DOMINANT 11; DFNA11

Xenbase Genes: myo7a

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011032 - autosomal dominant nonsyndromic hearing loss 11
MONDO:0019587 - autosomal dominant nonsyndromic hearing loss

Disease Ontology (DO):
DOID:0110543 - autosomal dominant nonsyndromic deafness 11