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tmc1 in Homo sapiens | Mus musculus | Rattus norvegicus | All 586 Gene records
See tmc1 in MedGen (2)
Autosomal dominant nonsyndromic hearing loss 36
An autosomal dominant condition caused by mutations in the TMC1 gene, encoding transmembrane channel-like protein 1. It is characterized by bilateral progressive hearing loss. [from NCI]
Autosomal recessive nonsyndromic hearing loss 7
Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the TMC1 gene. [from MONDO]
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