Autosomal recessive nonsyndromic hearing loss 36

Definition

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

Also known as autosomal recessive nonsyndromic hearing loss 36, deafness, neurosensory, without vestibular involvement, autosomal dominant — per MONDO

Also identified as

• DOID 0110494 per MONDO
• MESH C563815 per MONDO
• OMIM 609006 per MONDO
• UMLS C1837007 per MONDO