Warning: The NCBI web site requires JavaScript to function. more...
An official website of the United States government
The .gov means it's official. Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you're on a federal government site.
The site is secure. The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.
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]
Filter your results:
Your browsing activity is empty.
Activity recording is turned off.
Turn recording back on