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Source:http://linkedlifedata.com/resource/umls/id/C1832588

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Subject	Predicate	Object	Context
umls-concept:C1832588	rdf:type	umls-semnetwork:T047	lld:umls
umls-concept:C1832588	rdf:type	skos:Concept	lld:umls
umls-concept:C1832588	calbc:hasCorrelation	calbc-group:ANAT	lld:calbc
umls-concept:C1832588	calbc:hasCorrelation	calbc-group:DISO	lld:calbc
umls-concept:C1832588	skos:definition	NCI: A very rare genetic syndrome caused by deletions on the proximal short arm of chromosome 11. It is characterized by the presence of multiple exostoses and enlarged parietal foramina.	lld:umls
umls-concept:C1832588	skos:inScheme	lld:umls	lld:umls
umls-concept:C1832588	skos-xl:prefLabel	umls-label:A12107216	lld:umls
umls-concept:C1832588	skos-xl:altLabel	umls-label:A12028959	lld:umls
umls-concept:C1832588	skos-xl:altLabel	umls-label:A16756030	lld:umls
umls-concept:C1832588	skos-xl:altLabel	umls-label:A18465218	lld:umls
umls-concept:C1832588	skos-xl:altLabel	umls-label:A11943004	lld:umls
umls-concept:C1832588	skos-xl:altLabel	umls-label:A11986017	lld:umls
umls-concept:C1832588	skos-xl:altLabel	umls-label:A18449858	lld:umls
umls-concept:C1832588	skos-xl:altLabel	umls-label:A11986018	lld:umls
umls-concept:C1832588	skos-xl:altLabel	umls-label:A12000445	lld:umls
umls-concept:C1832588	skos-xl:altLabel	umls-label:A11979675	lld:umls
umls-concept:C0008626	skos:narrower	umls-concept:C1832588	lld:umls
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http://linkedlifedata.com/r...	umls:relatedConcept	umls-concept:C1832588	lld:umls
http://linkedlifedata.com/r...	umls:relatedConcept	umls-concept:C1832588	lld:umls
http://linkedlifedata.com/r...	umls:relatedConcept	umls-concept:C1832588	lld:umls

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