Autosomal recessive nonsyndromic hearing loss 35

Definition

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

Also known as autosomal recessive nonsyndromic hearing loss 35 — per MONDO

Also identified as

• DOID 0110493 per MONDO
• MESH C563908 per MONDO
• OMIM 608565 per MONDO
• UMLS C1837857 per MONDO