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Usher syndrome type 1

Disease Summary
Associated Targets (7)
Tbio

7


Mondo Description A syndrome characterized by congenital, bilateral, severe sensorineural hearing loss, abnormalities in the vestibular system, and adolescent-onset retinitis pigmentosa.
Mondo Term and Equivalent IDs
MONDO:0010168:  Usher syndrome type 1
GARD:0005435: 
GARD:0005436: 
NCIT:C126327: 
Orphanet:231169: 
SCTID:232057003: