LBR, lamin B receptor, 3930

N. diseases: 307; N. variants: 17
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0011644
Disease: Scleroderma
Scleroderma
0.110 GeneticVariation disease BEFREE Altogether our results suggest that LMNA, ZMPSTE24, and LBR sequence variations are not major genetic determinants involved in scleroderma pathogenesis. 19645629 2009
CUI: C0011644
Disease: Scleroderma
Scleroderma
0.110 Biomarker disease HPO