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autosomal dominant nonsyndromic sensorineural deafness 22
Pathology:
- sensorineural deafness
Genetics:
1) autosomal dominant
2) associated with mutations in gene for myosin 6
Clinical manifestations:
- progressive & postlingual, with onset during childhood
- by the age of approximately 50 years, affected individuals invariably have profound sensorineural deafness
General
familial deafness
Database Correlations
OMIM 606346
References
OMIM :accession 606346