TMC1, another OMIM Morbid gene, whose variation associated with autosomal dominant deafness-36 (DFNA36; OMIM #606705) and autosomal recessive deafness-7 (DFNB7), also known as DFNB11 (OMIM #600974) (Kurima et al., 2002). Here, TMC1 is linked to autosomal dominant nonsyndromic hearing loss.