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Cogan syndrome

Disease Summary
Associated Targets ()

Mondo Description Cogan syndrome (CS) is a rare autoimmune disorder of unknown origin characterized by inflammatory ocular disease (mainly interstitial keratitis) and vestibulo-auditory manifestations (mainly acute onset hearing loss, tinnitus and vertigo), in the setting of a negative work-up for syphilis, with a variable risk of developing into a systemic disease. Systemic manifestations may occur in more than 70% of cases.
Mondo Term and Equivalent IDs
MONDO:0015453:  Cogan syndrome
GARD:0001421: 
MESH:D055952: 
Orphanet:1467: 
SCTID:405810005: 
UMLS:CN199560: