Autosomal recessive nonsyndromic hearing loss 31

Definition

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

Also known as autosomal recessive nonsyndromic hearing loss 31 — per MONDO

Also identified as

• DOID 0110490 per MONDO
• MESH C564629 per MONDO
• OMIM 607084 per MONDO
• UMLS C1846839 per MONDO