obsolete_Waardenburg syndrome true UMLS:C0043008 OMIM:611584 ICD10:E70.3 MedDRA:10069203 WS Replaced with Mondo term. 3.41.0 http://purl.obolibrary.org/obo/MONDO_0018094 OMIM:148820 OMIM:600193 OMIM:608890 MESH:D014849 Waardenburg syndrome (WS) 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. WS is classified into four clinical and genetic phenotypes. orphanet OMIM:606662 OMIM:193510 OMIM:193500