Autosomal recessive nonsyndromic hearing loss 30

Definition

Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the MYO3A gene.

Also known as autosomal recessive nonsyndromic hearing loss 30 — per MONDO

Also identified as

• DOID 0110489 per MONDO
• MESH C564624 per MONDO
• OMIM 607101 per MONDO
• UMLS C1846784 per MONDO