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

CUI: C0010324   Crigler Najjar syndrome, type 1 
A familial form of congenital hyperbilirubinemia transmitted as an autosomal recessive trait. It is characterized by icterus and brain damage caused by a glucuronyl transferase deficiency in the liver and faulty bilirubin conjugation.

rdfs:seeAlso —
http://dbpedia.org/resource/Bilirubin C0268306 C0005437 C0018937 C0201916 C0236556 C0301719 C0311468 C1881193
http://dbpedia.org/resource/Transmission_(medicine) C0242648 C0242781 C1519279 C1562835 C1642394 C1707758
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/Congenital_disorder C0265953 C0302142 C1704257 C0000768 C0000769 C0009677 C0220810 C0242354 C0243070 C0332907 C1275147 C1302790 C1457869 C1704258 C1705254 C1744681
http://dbpedia.org/resource/Heredity C0019266 C0265388 C0439660 C0678919 C0728826
http://dbpedia.org/resource/Glucuronosyltransferase C0041560 C0268306 C0537026 C0963309 C1422012 C1706403 C1823594 C3812292
http://dbpedia.org/resource/Diabetes_mellitus_type_1 C0011854 C0342302 C0441729
http://dbpedia.org/resource/Morphology_(biology) C0543482 C0586103
http://dbpedia.org/resource/Syndrome C1332133 C0039082 C0567439

skos:closeMatch —

skos:exactMatch —
http://dbpedia.org/resource/Crigler–Najjar_syndrome C0010324 C0017551 C2931132


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.