Ex: C0006933 C0007102 C0007203 C3175196    or

CUI: C3266898   Waardenburg Syndrome 
rare, autosomal dominant disease with variable penetrance and several known clinical subtypes; characteristics may include depigmentation of the hair and skin, congenital deafness, heterochromia iridis, medial eyebrow hyperplasia, hypertrophy of the nasal root, and especially dystopia canthorum; the underlying cause may be defective development of the neural crest (neurocristopathy); may be closely related to piebaldism; Klein-Waardenburg Syndrome refers to a disorder that also includes upper limb abnormalities.

rdfs:seeAlso — C0042321 C0017342 C0017361 C0178491 C0178492 C0441748 C0443147 C0678942 C0683222 C0683223 C1527180 C3899988 C3899989 C0678236 C0920627 C1332133 C0039082 C0567439

skos:closeMatch —

skos:exactMatch — C0079661 C1420317 C1421521 C1837203 C1838447 C1847722 C1847800 C1848519 C1860339 C2700265 C2750452 C2750457 C3266898

UMLS Concepts to DBPedia Link Discovery Browser

Enter an UMLS concept-unique-identifier (CUI) or DBPEDIA resource uri to show its rdfs:seeAlso, skos:closeMatch, and skos:exactMatch mapped relations to DBpedia. Alternatively, you can click on a CUI from the sample list to the right to compare our mapping to Wikidata.