To explore molecular mechanism of CAVD, ten hub genes (CXCL13, CCL19, CCL8, CXCL8, CXCL16, MMP9, CCL18, CXCL5, VCAM1, and PPBP) connected with CAVD occurrence were explored out based on the STRING and Cytoscape software. The gene discussed is MMP9; the disease is congenital bilateral aplasia of vas deferens from CFTR mutation.