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Summary Literature (0)
MIM:603622 - DEAFNESS, AUTOSOMAL DOMINANT 17; DFNA17

Xenbase Genes: myh9

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011350 - autosomal dominant nonsyndromic hearing loss 17
MONDO:0019587 - autosomal dominant nonsyndromic hearing loss

Disease Ontology (DO):
DOID:0110548 - autosomal dominant nonsyndromic deafness 17