Autosomal recessive nonsyndromic hearing loss 6

Definition

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

Also known as autosomal recessive nonsyndromic hearing loss 6 — per MONDO

Also identified as

• DOID 0110512 per MONDO
• MESH C563418 per MONDO
• OMIM 600971 per MONDO
• UMLS C1832992 per MONDO