autosomal recessive neurosensory deafness 7 (DFNB7); autosomal recessive neurosensory deafness 11 (DFNB11)

Genetics

• autosomal recessive
• linked to TMC1

Clinical manifestations

• nonsyndromic, congenital & profound hearing loss

More general terms

• autosomal recessive neurosensory deafness

Additional terms

• transmembrane cochlear-expressed protein 1; transmembrane channel-like protein 1 (TMC1)

Database

• OMIM: https://mirror.omim.org/entry/600974