Autosomal recessive nonsyndromic hearing loss 21

Definition

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

Also known as autosomal recessive nonsyndromic hearing loss 21 — per MONDO

Also identified as

• DOID 0110479 per MONDO
• MESH C566353 per MONDO
• OMIM 603629 per MONDO
• UMLS C1863655 per MONDO