obsolete_Waardenburg syndrome type 2 true WS2 OMIM:606662 OMIM:600193 MESH:C536463 OMIM:608890 OMIM:193510 ICD10:E70.3 OMIM:611584 orphanet http://purl.obolibrary.org/obo/MONDO_0019517 Waardenburg syndrome (WS2) is an autosomal dominant disorder characterized by varying degrees of deafness, minor defects in structures arising from neural crest and pigmentation anomalies of eyes, hair, and skin, but without dystopia cantorum Replaced with Mondo term. 3.41.0 UMLS:C2700265