Ex: C0006933 C0007102 C0007203 C3175196    or

CUI: C0341703   Adult Fanconi syndrome 
Probably related to a recessive gene, this is Fanconi Syndrome, characterised by adult onset. -- 2003

rdfs:seeAlso — C0035078 C0151746 C0812426 C1565489 C3279454 C0022674 C0022675 C0027713 C0332208 C0552639 C0736401 C1511528 C0017342 C0017361 C0178491 C0178492 C0441748 C0443147 C0678942 C0683222 C0683223 C1527180 C3899988 C3899989 C0015624 C0015625 C0022655 C0022675 C1510487 C1516697 C0022646 C0022658 C0035064 C0227611 C0266292 C0266304 C0553257 C0935623 C1285477 C0032702

skos:closeMatch —

skos:exactMatch —

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.