Autosomal recessive nonsyndromic hearing loss 1B

Definition

Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the GJB6 gene.

Also identified as

• DOID 0110476 per MONDO
• MESH C567213 per MONDO
• OMIM 612645 per MONDO
• UMLS C2675235 per MONDO