Ex: C0006933 C0007102 C0007203 C3175196    or

CUI: C1279481   X-Linked Combined Immunodeficiency Diseases 
Forms of combined immunodeficiency caused by mutations in the gene for INTERLEUKIN RECEPTOR COMMON GAMMA SUBUNIT. Both severe and non-severe subtypes of the disease have been identified.

rdfs:seeAlso — C0022686 C0022688 C0427526 C2350463 C2709199 C2984255 C0000768 C0006111 C0015127 C0205269 C0231218 C1314792 C1331418 C1457887 C0012634 C0026538 C0178685 C0221423 C0231172 C0679215 C0683323 C0683324 C0683337 C0699749 C1514815 C2359469 C3540542 C0000769 C0427625 C0005804 C0005810 C0005844 C0797753 C1383165 C3869859 C0017262 C0017366 C1294197 C1708726 C0017337 C1517495 C0041625 C0181651 C0454530 C0564460 C0564461 C0730442 C1154975 C0085110 C0085112 C0392607 C0543687 C0039194 C0080202 C1155013 C1155065 C2362651 C0398686 C0021051 C0085393 C0398795 C0596032 C0597745 C1855771 C0085110 C0085112 C0017011 C2985557 C0206553 C1149183 C0004561 C0079004 C0312738 C1332133 C0039082 C0567439 C0599220 C0887892 C0241764 C0314614 C0678925 C0678928 C0815328 C1537071 C1883001 C0079249 C0935882 C1879714 C0022772 C0022340 C0027877 C0268279 C0751383 C2931673 C1166607 C3178867 C0007613 C0007634 C0010819 C0178539 C0243092 C1178969 C2734073 C2936218 C0085110 C0494261 C0596988 C0796357 C1512796 C0026882 C0034529 C0042333 C0544886 C0596611 C0678939 C1513776 C1515568 C1516517 C1564139 C1705285 C2985436 C2985439

skos:closeMatch —

skos:exactMatch — C1279481

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.