Autosomal dominant nonsyndromic hearing loss 36

Your Results

Sign In

Description

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.

NCI

  • Mode of Inheritance

  • Autosomal dominant inheritance

Genes

External Links

© 2024 Biocodify. All rights reserved.