Autosomal recessive nonsyndromic hearing loss 91

Definition

Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the SERPINB6 gene.

Also known as autosomal recessive nonsyndromic hearing loss 91 — per MONDO

Also identified as

• DOID 0110536 per MONDO
• OMIM 613453 per MONDO
• UMLS C3150704 per MONDO