Disease Summary help help Associated Targets (1)Tbio1 Explore Associated Targets list GARD Rare open_in_new Mondo Description Any cone dystrophy in which the cause of the disease is a mutation in the CACNA2D4 gene. Uniprot Description Characterized by minimal symptoms except for slowly progressive reduction in visual acuity. Mondo Term and Equivalent IDs MONDO:0012507: retinal cone dystrophy 4 GARD:0010650: open_in_newMESH:C566470: open_in_newOMIM:610478: RETINAL CONE DYSTROPHY 4open_in_newUMLS:C1864849: open_in_new