Autosomal recessive nonsyndromic hearing loss 29

Definition

Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the CLDN14 gene.

Also known as autosomal recessive nonsyndromic hearing loss 29 — per MONDO

Also identified as

• DOID 0110487 per MONDO
• OMIM 614035 per MONDO
• UMLS C3279660 per MONDO