LMNB1, lamin B1, 4001

N. diseases: 128; N. variants: 1
Disease: Acquired partial lipodystrophy ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0220989
Disease: Acquired partial lipodystrophy
Acquired partial lipodystrophy 		0.010 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