Usher syndrome type 1

Definition

A syndrome characterized by congenital, bilateral, severe sensorineural hearing loss, abnormalities in the vestibular system, and adolescent-onset retinitis pigmentosa.

Also known as retinitis pigmentosa and congenital deafness, USH1, Usher syndrome type 1, Usher syndrome, type 1 — per MONDO

Also identified as

• DOID 0110826 per MONDO
• NCIT C126327 per MONDO
• Orphanet 231169 per MONDO
• SCTID 232057003 per MONDO
• UMLS C1568247 per MONDO