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: C0036421
Disease: Systemic Scleroderma
Systemic 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: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma
0.110 Biomarker disease HPO