SEMA3D, semaphorin 3D, 223117

N. diseases: 44; N. variants: 6
Disease: Meniere Disease ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0025281
Disease: Meniere Disease
Meniere Disease 		0.010 GeneticVariation disease BEFREE Variable expressivity and genetic heterogeneity involving DPT and SEMA3D genes in autosomal dominant familial Meniere's disease. 27876815 2017