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

CUI: C0018553   Hamartoma Syndrome, Multiple 
A hereditary disease characterized by multiple ectodermal, mesodermal, and endodermal nevoid and neoplastic anomalies. Facial trichilemmomas and papillomatous papules of the oral mucosa are the most characteristic lesions. Individuals with this syndrome have a high risk of BREAST CANCER; THYROID CANCER; and ENDOMETRIAL CANCER. This syndrome is associated with mutations in the gene for PTEN PHOSPHATASE.

rdfs:seeAlso —
http://dbpedia.org/resource/Hamartoma C0008519 C0018552 C0265315
http://dbpedia.org/resource/Disease C0000768 C0006111 C0015127 C0205269 C0231218 C1314792 C1331418 C1457887 C0012634 C0026538 C0178685 C0221423 C0231172 C0679215 C0683323 C0683324 C0683337 C0699749 C1514815 C2359469 C3540542
http://dbpedia.org/resource/Ectoderm C0013574
http://dbpedia.org/resource/Candela C0700300
http://dbpedia.org/resource/Multiple_sclerosis C0026769 C0751964 C0751967 C1095979
http://dbpedia.org/resource/Compact_Cassette C0450240 C0493659 C0681507 C1555029
http://dbpedia.org/resource/Genetic_disorder C1704258 C0019247 C0206530 C0262496 C0277558 C0683231 C0950123 C1704257 C2924406
http://dbpedia.org/resource/Syndrome C1332133 C0039082 C0567439
http://dbpedia.org/resource/PTEN_(gene) C0694888 C1430988

skos:closeMatch —

skos:exactMatch —
http://dbpedia.org/resource/Multiple_hamartoma_syndrome C0018553 C1959582
http://dbpedia.org/resource/Cowden_syndrome C0018553


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.