Ex: C0006933 C0007102 C0007203 C3175196    or

CUI: C0221757   alpha 1-Antitrypsin Deficiency 
autosomal recessive trait leading to destruction of lung tissue by neutrophil elastase and eventual emphysema; second only to cystic fibrosis as most common lethal genetic disorder among Caucasians of northern European ancestry.

rdfs:seeAlso — C0000768 C0006111 C0015127 C0205269 C0231218 C1314792 C1331418 C1457887 C0012634 C0026538 C0178685 C0221423 C0231172 C0679215 C0683323 C0683324 C0683337 C0699749 C1514815 C2359469 C3540542 C0017342 C0017361 C0178491 C0178492 C0441748 C0443147 C0678942 C0683222 C0683223 C1527180 C3899988 C3899989 C0040300 C0440744 C0457457 C0024119 C0024109 C0034071 C0038903 C0225730 C1261076 C1261077 C0064833 C1414369 C1261512 C1449772 C1552125 C0027950 C0229640 C0312861 C0682637 C0746885

skos:closeMatch —

skos:exactMatch — C0072348 C0002191 C0201856 C0221757 C1979844 C3501835

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.