Autosomal recessive nonsyndromic hearing loss 102

Definition

Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the EPS8 gene.

Also known as autosomal recessive nonsyndromic hearing loss 102 — per MONDO

Also identified as

• DOID 0110463 per MONDO
• OMIM 615974 per MONDO
• UMLS C3892050 per MONDO