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Summary Literature (0)
MIM:606346 - DEAFNESS, AUTOSOMAL DOMINANT 22; DFNA22

Xenbase Genes: myo6

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011660 - autosomal dominant nonsyndromic hearing loss 22
MONDO:0016424 - progressive sensorineural hearing loss-hypertrophic cardiomyopathy syndrome
MONDO:0019587 - autosomal dominant nonsyndromic hearing loss

Disease Ontology (DO):
DOID:0110552 - autosomal dominant nonsyndromic deafness 22