autosomal dominant disease syndromic disease multiple congenital anomalies/dysmorphic syndrome without intellectual disability obsolete neuro-ophthalmological disease Waardenburg syndrome https://github.com/monarch-initiative/mondo/issues/5682 https://www.malacards.org/card/waardenburg_syndrome OMIMPS:193500 DOID:9258 Waardenburg syndrome UMLS:C3266898 MONDO:0018094 MedDRA:10069203 Van der Hoeve Halbertsma Waardenburg Gualdi syndrome Mende syndrome MEDGEN:473809 GARD:0005525 NCIT:C85222 NORD:1832 A disorder characterized by varying degrees of deafness and minor defects in structures arising from neural crest, including pigmentation anomalies of eyes, hair, and skin. WS is classified into four clinical and genetic phenotypes. SCTID:715952000 MESH:D014849 Waardenburg's syndrome Orphanet:3440 icd11.foundation:304883627 hypopigmentation of the skin obsolete_Waardenburg syndrome