Disease Summary help help Associated Targets (4)Tclin4 Explore Associated Targets list GARD Rare open_in_new Uniprot Description Part of a spectrum of Leber hereditary optic neuropathy. It is characterized by the association of optic atrophy and central vision loss with dystonia. Mondo Term and Equivalent IDs MONDO:0010772: Leber optic atrophy and dystonia DOID:0111755: open_in_newGARD:0008476: open_in_newMESH:C536024: open_in_newOMIM:500001: LEBER OPTIC ATROPHY AND DYSTONIAopen_in_newUMLS:C1839040: open_in_new