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autosomal dominant nonsyndromic sensorineural deafness 23
Pathology:
- sensorineural deafness
- a conductive hearing loss component present in some but not all patients
Genetics:
1) autosomal dominant
2) associated with defects in SIX1
Clinical manifestations:
- prelingual, bilateral, symmetric hearing loss
General
familial deafness
Database Correlations
OMIM 605192
References
OMIM :accession 605192