(Q28024680)
English
autosomal dominant nonsyndromic deafness 22
autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with high frequency progressive hearing loss and has material basis in mutation in the MYO6 gene on chromosome 6q14
- DFNA22
- autosomal dominant deafness 22
- Progressive sensorineural deafness-hypertrophic cardiomyopathy syndrome
- Progressive neurosensory deafness-hypertrophic cardiomyopathy syndrome
- Progressive neurosensory hearing loss-hypertrophic cardiomyopathy syndrome
Statements
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Identifiers
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