CUI ⟾ or DBPEDIA ⟾
Ex: C0006933 C0007102 C0007203 C3175196    or    http://dbpedia.org/resource/Nosebleed    http://dbpedia.org/resource/Leg

CUI: C0031269   Peutz-Jeghers Syndrome 
A hereditary disease caused by autosomal dominant mutations involving CHROMOSOME 19. It is characterized by the presence of INTESTINAL POLYPS, consistently in the JEJUNUM, and mucocutaneous pigmentation with MELANIN spots of the lips, buccal MUCOSA, and digits.

rdfs:seeAlso —
http://dbpedia.org/resource/Hamartoma C0008519 C0018552 C0265315
http://dbpedia.org/resource/Mouth C0226896 C0442119 C0457008
http://dbpedia.org/resource/Dominance_(genetics) C0017342 C0017361 C0178491 C0178492 C0441748 C0443147 C0678942 C0683222 C0683223 C1527180 C3899988 C3899989
http://dbpedia.org/resource/Chromosome_19_(human) C0008661
http://dbpedia.org/resource/Genetic_disorder C1704258 C0019247 C0206530 C0262496 C0277558 C0683231 C0950123 C1704257 C2924406
http://dbpedia.org/resource/Thrombin C3274435 C0033706 C0040018 C0060008 C0200396 C0272317 C0723739 C1414504 C2256554 C2256560 C2256561 C3203356
http://dbpedia.org/resource/Mutation C0596988 C0796357 C1512796 C0026882 C0034529 C0042333 C0544886 C0596611 C0678939 C1513776 C1515568 C1516517 C1564139 C1705285 C2985436 C2985439
http://dbpedia.org/resource/Human_gastrointestinal_tract C0012238 C0017178 C0038351 C0012240 C0012242 C0017173 C0017189 C0017191 C0021831 C0021839 C0021853 C0030446 C0033151 C0226875 C0227435 C0516983 C0521362 C0545876 C0836213 C1185740 C1290944 C1304890 C3203348
http://dbpedia.org/resource/Lentiginosis C0023321
http://dbpedia.org/resource/Syndrome C1332133 C0039082 C0567439
http://dbpedia.org/resource/Polyp_(medicine) C0032584 C0206677 C0267573 C0334108
http://dbpedia.org/resource/Pigment C0031911 C0031916 C0682898 C1571592

skos:closeMatch —
http://dbpedia.org/resource/The_PJs C0031269

skos:exactMatch —
http://dbpedia.org/resource/Peutz–Jeghers_syndrome C0031269 C0456487


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.