Autosomal recessive nonsyndromic hearing loss 22

Definition

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

Also known as autosomal recessive nonsyndromic hearing loss 22 — per MONDO

Also identified as

• DOID 0110480 per MONDO
• MESH C564633 per MONDO
• OMIM 607039 per MONDO
• UMLS C1846896 per MONDO