Disease Summary help help Associated Targets (1)Tbio1 Explore Associated Targets list Mondo Description Any non-syndromic synpolydactyly in which the cause of the disease is a mutation in the FBLN1 gene. Mondo Term and Equivalent IDs MONDO:0011984: synpolydactyly type 2 MESH:C564278: open_in_newOMIM:608180: SYNPOLYDACTYLY 2open_in_newOrphanet:295197: UMLS:C1842422: open_in_new