Disease Summary help help Associated Targets (6)Tbio4Tclin1Tchem1 Explore Associated Targets list GARD Rare open_in_new Mondo Description Waardenburg syndrome type 2 (WS2) is an autosomal dominant subtype of Waardenburg syndrome (WS), characterized by varying degrees of deafness and pigmentation anomalies of eyes, hair and skin, but without dystopia canthorum. Mondo Term and Equivalent IDs MONDO:0019517: Waardenburg syndrome type 2 GARD:0005520: open_in_newMESH:C536463: open_in_newNCIT:C75009: open_in_newOrphanet:895: UMLS:C2700265: open_in_new