Autosomal recessive nonsyndromic hearing loss 18B

Definition

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

Also known as autosomal recessive nonsyndromic hearing loss 18B — per MONDO

Also identified as

• DOID 0110474 per MONDO
• OMIM 614945 per MONDO
• UMLS C3554163 per MONDO