Autosomal recessive nonsyndromic hearing loss 93

Definition

Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the CABP2 gene.

Also known as autosomal recessive nonsyndromic hearing loss 93 — per MONDO

Also identified as

• DOID 0110537 per MONDO
• OMIM 614899 per MONDO
• UMLS C3888355 per MONDO