Autosomal recessive nonsyndromic hearing loss 3

Definition

Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the MYO15A gene.

Also known as autosomal recessive nonsyndromic hearing loss 3 — per MONDO

Also identified as

• DOID 0110488 per MONDO
• MESH C563961 per MONDO
• OMIM 600316 per MONDO
• UMLS C1838263 per MONDO