Autosomal recessive nonsyndromic hearing loss 37

Definition

Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the MYO6 gene.

Also known as autosomal recessive nonsyndromic hearing loss 37 — per MONDO

Also identified as

• DOID 0110495 per MONDO
• MESH C564331 per MONDO
• OMIM 607821 per MONDO
• UMLS C1843028 per MONDO