Autosomal recessive nonsyndromic hearing loss 79

Definition

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

Also known as autosomal recessive nonsyndromic hearing loss 79 — per MONDO

Also identified as

• DOID 0110526 per MONDO
• MESH C567651 per MONDO
• OMIM 613307 per MONDO
• UMLS C2750082 per MONDO