Autosomal recessive nonsyndromic hearing loss 16

Definition

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

Also known as autosomal recessive nonsyndromic hearing loss 16 — per MONDO

Also identified as

• DOID 0110471 per MONDO
• MESH C566339 per MONDO
• OMIM 603720 per MONDO
• UMLS C1863561 per MONDO