Source: LHGDN

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3930
Gene Symbol: LBR
LBR
CUI: C0030779
Disease: Pelger-Huet Anomaly
Pelger-Huet Anomaly 		1.000 GeneticVariation LHGDN Mutations in the gene encoding the lamin B receptor produce an altered nuclear morphology in granulocytes (Pelger-Huët anomaly). 12118250

2002