Autosomal recessive nonsyndromic hearing loss 8

Definition

An autosomal recessive nonsyndromic deafness that has material basis in mutation in the TMPRSS3 gene on chromosome 21q22.

Also known as autosomal recessive nonsyndromic hearing loss 8 — per MONDO

Also identified as

• DOID 0110527 per MONDO
• OMIM 601072 per MONDO
• UMLS C1832827 per MONDO