DM2

Source:http://linkedlifedata.com/resource/umls/id/C2931689

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Subject	Predicate	Object	Context
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umls-concept:C2931689	calbc:hasCorrelation	calbc-group:CONC	lld:calbc
umls-concept:C2931689	skos:definition	NCI: A rare autosomal dominant disorder caused by mutations in the CNBP gene. It is characterized by muscle pain, fatigue, and weakness of the proximal muscles of the lower extremities.	lld:umls
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