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Usher syndrome

Disease Summary
Associated Targets (16)
Tbio

15

Tchem

1


GARD Rare
Mondo Description Usher syndrome (US) is characterized by the association of sensorineural deafness (usually congenital) with retinitis pigmentosa and progressive vision loss.
Disease Ontology Description A syndrome characterized by a combination of hearing loss and visual impairment.
Mondo Term and Equivalent IDs
MONDO:0019501:  Usher syndrome
GARD:0007843: 
MESH:D052245: 
NCIT:C85217: 
OMIMPS:276900: 
Orphanet:886: 
UMLS:C0271097: