Autosomal recessive nonsyndromic hearing loss 53

Definition

Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the COL11A2 gene.

Also identified as

• DOID 0110509 per MONDO
• MESH C566453 per MONDO
• OMIM 609706 per MONDO
• UMLS C1864746 per MONDO