Autosomal recessive nonsyndromic hearing loss 2

Definition

Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the MYO7A gene.

Also identified as

• DOID 0110477 per MONDO
• MESH C564007 per MONDO
• OMIM 600060 per MONDO
• UMLS C1838701 per MONDO