obsolete_Waardenburg syndrome type 3 true Replaced with Mondo term. orphanet WS3 ICD10:E70.3 Waardenburg syndrome type 3 (WS3) is a very rare subtype of Waardenburg syndrome (WS; see this term) that is characterized by limb anomalies in association with congenital hearing loss, minor defects in structures arising from neural crest resulting in pigmentation anomalies of eyes, hair, and skin http://purl.obolibrary.org/obo/MONDO_0007862 Waardenburg syndrome with limb anomalies OMIM:148820 3.41.0 Klein-Waardenburg syndrome