LMNB2, lamin B2, 84823

N. diseases: 74; N. variants: 3
Disease: Partial lipodystrophy ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4316789
Disease: Partial lipodystrophy
Partial lipodystrophy 		0.030 GeneticVariation disease BEFREE A Chinese patient with acquired partial lipodystrophy caused by a novel mutation with LMNB2 gene. 22768673 2012
CUI: C4316789
Disease: Partial lipodystrophy
Partial lipodystrophy 		0.030 GeneticVariation disease BEFREE Duplication in LMNB1 encoding lamin B1 causes autosomal dominant leukodystrophy and mutations in LMNB2 encoding lamin B2 are associated with acquired partial lipodystrophy. 17467691 2007
CUI: C4316789
Disease: Partial lipodystrophy
Partial lipodystrophy 		0.030 GeneticVariation disease BEFREE Sequencing of the reannotated LMNB2 gene reveals novel mutations in patients with acquired partial lipodystrophy. 16826530 2006