HMG-CoA lyase deficiency

Download in:

Switch to

Named Graph Language Inference

Statements in which the resource exists as a subject.
Predicate	Object
rdf:type	umls-semnetwork:T047, skos:Concept
calbc:hasCorrelation	calbc-group:CHEM, calbc-group:CONC, calbc-group:DISO, calbc-group:GENE
skos:definition	NCI: A rare genetic inherited disorder characterized by inability of the body to process the amino acid leucine. Signs and symptoms include vomiting, dehydration, lethargy, convulsions, and coma.
skos:inScheme	lld:umls
skos:broader	umls-concept:C0002514
skos-xl:prefLabel	umls-label:A18474811
skos-xl:altLabel	umls-label:A17680491, umls-label:A17692108, umls-label:A18455969, umls-label:A18459079, umls-label:A18465213, umls-label:A18468244, umls-label:A18471365, umls-label:A20235919
umls:relation	http://linkedlifedata.com/resource/umls/relation/R115131608, http://linkedlifedata.com/resource/umls/relation/R128720320, http://linkedlifedata.com/resource/umls/relation/R128720321, http://linkedlifedata.com/resource/umls/relation/R129095150, http://linkedlifedata.com/resource/umls/relation/R62731167, http://linkedlifedata.com/resource/umls/relation/R44322304