Niemann-Pick Disease, Type B

Source:http://linkedlifedata.com/resource/umls/id/C0268243

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Predicate	Object
rdf:type	umls-semnetwork:T047, skos:Concept
calbc:hasCorrelation	calbc-group:ANAT, calbc-group:CONC, calbc-group:DISO, calbc-group:PHEN, calbc-group:PROC
skos:exactMatch	pubmed-mesh:Niemann-Pick Disease, Type B
skos:definition	MSH: An allelic disorder of TYPE A NIEMANN-PICK DISEASE, a late-onset form. It is also caused by mutation in SPHINGOMYELIN PHOSPHODIESTERASE but clinical signs involve only visceral organs (non-neuropathic type).
skos:inScheme	lld:umls
skos:narrower	umls-concept:C0268248
skos-xl:prefLabel	umls-label:A10909181
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