Usher syndrome type 1 https://www.malacards.org/card/usher_syndrome_type_i_2 icd11.foundation:237039059 USH1 MEDGEN:292820 NCIT:C126327 Usher syndrome, type 1 MONDO:0010168 UMLS:C1568247 NANDO:1200942 Usher syndrome, type Ia, formerly SCTID:232057003 Usher syndrome, type I, French variety, formerly Usher syndrome type 1 Usher syndrome, type Ia USHER syndrome, type I Usher syndrome, type 1B Usher syndrome, type 1A retinitis pigmentosa and congenital deafness Orphanet:231169 USH1A DOID:0110826 A syndrome characterized by congenital, bilateral, severe sensorineural hearing loss, abnormalities in the vestibular system, and adolescent-onset retinitis pigmentosa. Usher syndrome, type I, French variety GARD:0005435 Usher syndrome