Switch to
Predicate | Object |
---|---|
rdf:type | |
calbc:hasCorrelation | |
skos:definition |
NCI: A genetic disorder characterized by deficiency of the enzyme long-chain acyl-coenzyme A dehydrogenase that metabolizes long-chain fatty acids. Signs and symptoms appear in infancy or childhood and may be triggered during fasting, illness or exercise. They include hypoglycemia, muscle weakness and lethargy.
|
skos:inScheme | |
skos:broader | |
skos-xl:prefLabel | |
skos-xl:altLabel | |
umls:relation |
http://linkedlifedata.com/resource/umls/relation/R115131626,
http://linkedlifedata.com/resource/umls/relation/R115131627,
http://linkedlifedata.com/resource/umls/relation/R128714686,
http://linkedlifedata.com/resource/umls/relation/R128714687,
http://linkedlifedata.com/resource/umls/relation/R129094439,
http://linkedlifedata.com/resource/umls/relation/R115203419,
http://linkedlifedata.com/resource/umls/relation/R116560696
|