Disease Summary help help Associated Targets (4)Tchem2Tclin1Tbio1 Explore Associated Targets list GARD Rare open_in_new Mondo Description An autosomal dominant hereditary condition characterized by optic atrophy and progressive visual loss. Mondo Term and Equivalent IDs MONDO:0020250: autosomal dominant optic atrophy GARD:0011972: open_in_newMESH:D029241: open_in_newNCIT:C84577: open_in_newOrphanet:98672: SCTID:2065009: open_in_newUMLS:C0338508: open_in_new