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autosomal recessive neurosensory deafness 7 (DFNB7); autosomal recessive neurosensory deafness 11 (DFNB11)
Genetics:
1) autosomal recessive
2) linked to TMC1
Clinical manifestations:
- nonsyndromic, congenital & profound hearing loss
Related
transmembrane cochlear-expressed protein 1; transmembrane channel-like protein 1 (TMC1)
General
autosomal recessive neurosensory deafness
Database Correlations
OMIM 600974
References
OMIM :accession 600974