CACH

Source:http://linkedlifedata.com/resource/umls/id/C1858991

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Subject	Predicate	Object	Context
umls-concept:C1858991	rdf:type	umls-semnetwork:T047	lld:umls
umls-concept:C1858991	rdf:type	skos:Concept	lld:umls
umls-concept:C1858991	calbc:hasCorrelation	calbc-group:DISO	lld:calbc
umls-concept:C1858991	calbc:hasCorrelation	calbc-group:GENE	lld:calbc
umls-concept:C1858991	calbc:hasCorrelation	calbc-group:CONC	lld:calbc
umls-concept:C1858991	skos:definition	MSH: Autosomal recessive disease characterized by the slow progress rarefaction of white matter with childhood-onset. More severe infancy-onset forms are also known.	lld:umls
umls-concept:C1858991	skos:inScheme	lld:umls	lld:umls
umls-concept:C1858991	skos-xl:prefLabel	umls-label:A18474759	lld:umls
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umls-concept:C1858991	skos-xl:altLabel	umls-label:A11955628	lld:umls
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umls-concept:C1858991	skos-xl:altLabel	umls-label:A12027115	lld:umls
umls-concept:C1858991	skos-xl:altLabel	umls-label:A11926808	lld:umls
umls-concept:C1858991	skos-xl:altLabel	umls-label:A11998679	lld:umls
umls-concept:C1858991	skos-xl:altLabel	umls-label:A18451115	lld:umls
umls-concept:C0270612	skos:narrower	umls-concept:C1858991	lld:umls
pubmed-article:11835386	lifeskim:mentions	umls-concept:C1858991	lld:lifeskim
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pubmed-article:21674432	lifeskim:mentions	umls-concept:C1858991	lld:lifeskim
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