Ex: C0006933 C0007102 C0007203 C3175196    or

CUI: C0162809   Kallmann Syndrome 
A genetically heterogeneous disorder caused by hypothalamic GNRH deficiency and OLFACTORY NERVE defects. It is characterized by congenital HYPOGONADOTROPIC HYPOGONADISM and ANOSMIA, possibly with additional midline defects. It can be transmitted as an X-linked (GENETIC DISEASES, X-LINKED), an autosomal dominant, or an autosomal recessive trait.

rdfs:seeAlso — C0022735 C0020619 C0151721 C0271623 C0342384 C1295654 C1855333 C1856897 C0000768 C0006111 C0015127 C0205269 C0231218 C1314792 C1331418 C1457887 C0012634 C0026538 C0178685 C0221423 C0231172 C0679215 C0683323 C0683324 C0683337 C0699749 C1514815 C2359469 C3540542 C0016063 C0878500 C0156384 C0333910 C0333911 C0334044 C0346210 C1514392 C0009789 C0680204 C0683568 C1266852 C1517194 C1518469 C0019409 C1512426 C1881065 C3829671 C0019266 C0265388 C0439660 C0678919 C0728826 C0022735 C0271623 C1168263 C0042333 C0678919 C0017398 C0243064 C0314603 C0678922 C1705285 C2827447 C0003126 C0553757 C1332133 C0039082 C0567439 C0751437 C0020655 C0020656 C0020663 C0020664 C0228383

skos:closeMatch —

skos:exactMatch — C0162809 C0162809 C0338503

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.