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autosomal dominant nonsyndromic sensorineural deafness 48
Pathology:
- sensorineural hearing loss
Genetics:
1) autosomal dominant
2) associated with mutations in gene for myosin 1a
General
non-syndromic sensorineural hearing loss
familial deafness
Database Correlations
OMIM 607841
References
OMIM :accession 607841