GJC2, gap junction protein gamma 2, 57165

N. diseases: 115; N. variants: 20
Disease: Lymphedema praecox ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0238261
Disease: Lymphedema praecox
Lymphedema praecox 		0.010 GeneticVariation disease BEFREE The identification of GJC2 mutations as a cause of primary lymphedema raises the possibility of novel gap-junction-modifying agents as potential therapy for some forms of lymphedema. 20537300 2010