Ex: C0006933 C0007102 C0007203 C3175196    or

CUI: C0268596   Multiple Acyl Coenzyme A Dehydrogenase Deficiency 
An autosomal recessive disorder of fatty acid oxidation, and branched chain amino acids (AMINO ACIDS, BRANCHED-CHAIN); LYSINE; and CHOLINE catabolism, that is due to defects in either subunit of ELECTRON TRANSFER FLAVOPROTEIN or its dehydrogenase, electron transfer flavoprotein-ubiquinone oxidoreductase (EC

rdfs:seeAlso — C0015540 C0044036 C0009140 C0009226 C0009228 C0000768 C0006111 C0015127 C0205269 C0231218 C1314792 C1331418 C1457887 C0012634 C0026538 C0178685 C0221423 C0231172 C0679215 C0683323 C0683324 C0683337 C0699749 C1514815 C2359469 C3540542 C0009235 C0178555 C0001374 C0539551 C2752255 C0059017 C1166888 C0017342 C0017361 C0178491 C0178492 C0441748 C0443147 C0678942 C0683222 C0683223 C1527180 C3899988 C3899989 C0268594 C0268595 C4025603 C0022192 C0002521 C1519946 C1414471 C0684263 C1158366 C2984153 C0042842 C0376286 C1510471 C0596038

skos:closeMatch —

skos:exactMatch — C1414471 C0268596 C1856401 C1856403 C1856405 C0241775 C0268594 C0268596 C0278026 C0342712 C1829844 C1865353

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.