Ex: C0006933 C0007102 C0007203 C3175196    or

CUI: C0751587   CADASIL Syndrome 
A hereditary cerebrovascular disorder caused by mutations in the Notch 3 gene. It is characterized by alterations of the muscular wall of the small vessels in the brain, resulting in transient ischemic attacks. It may lead to cognitive problems and dementia.

rdfs:seeAlso — C0000768 C0006111 C0015127 C0205269 C0231218 C1314792 C1331418 C1457887 C0012634 C0026538 C0178685 C0221423 C0231172 C0679215 C0683323 C0683324 C0683337 C0699749 C1514815 C2359469 C3540542 C0002395 C0009241 C0011265 C0231337 C0234985 C0338656 C0392079 C0497327 C0860630 C4024935 C0596142 C0007820 C0241832 C1880018 C2733158 C0019266 C0265388 C0439660 C0678919 C0728826 C0270612 C0023524 C0017342 C0017361 C0178491 C0178492 C0441748 C0443147 C0678942 C0683222 C0683223 C1527180 C3899988 C3899989 C0007776 C0596129 C0815275 C0021308 C0333541 C1332133 C0039082 C0567439 C0439064 C0680948 C1880371 C0282495

skos:closeMatch —

skos:exactMatch — C0751587

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.