HMG-CoA lyase deficiency

Source:http://linkedlifedata.com/resource/umls/id/C0268601

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Subject	Predicate	Object	Context
umls-concept:C0268601	rdf:type	umls-semnetwork:T047	lld:umls
umls-concept:C0268601	rdf:type	skos:Concept	lld:umls
umls-concept:C0268601	calbc:hasCorrelation	calbc-group:DISO	lld:calbc
umls-concept:C0268601	calbc:hasCorrelation	calbc-group:GENE	lld:calbc
umls-concept:C0268601	calbc:hasCorrelation	calbc-group:CONC	lld:calbc
umls-concept:C0268601	calbc:hasCorrelation	calbc-group:CHEM	lld:calbc
umls-concept:C0268601	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.	lld:umls
umls-concept:C0268601	skos:inScheme	lld:umls	lld:umls
umls-concept:C0268601	skos:broader	umls-concept:C0002514	lld:umls
umls-concept:C0268601	skos-xl:prefLabel	umls-label:A18474811	lld:umls
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umls-concept:C0268601	skos-xl:altLabel	umls-label:A18468244	lld:umls
umls-concept:C0268601	umls:relation	http://linkedlifedata.com/r...	lld:umls
umls-concept:C0268601	umls:relation	http://linkedlifedata.com/r...	lld:umls
umls-concept:C0268601	umls:relation	http://linkedlifedata.com/r...	lld:umls
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umls-concept:C0268601	umls:relation	http://linkedlifedata.com/r...	lld:umls
umls-concept:C0002514	skos:narrower	umls-concept:C0268601	lld:umls
pubmed-article:8798725	lifeskim:mentions	umls-concept:C0268601	lld:lifeskim
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http://linkedlifedata.com/r...	umls:relatedConcept	umls-concept:C0268601	lld:umls
http://linkedlifedata.com/r...	umls:relatedConcept	umls-concept:C0268601	lld:umls