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autosomal dominant neurosensory deafness 36 (DFNA36)
Genetics:
1) autosomal dominant
2) linked to TMC1
Clinical manifestations:
1) nonsyndromic, progressive sensorineural hearing loss
2) bilateral hearing loss
3) onset 5-10 years of age
4) progresses to profound deafness within 10-15 years
Related
transmembrane cochlear-expressed protein 1; transmembrane channel-like protein 1 (TMC1)
General
familial deafness
Database Correlations
OMIM 606705
References
OMIM :accession 606705