A very rare inherited retinal dystrophy characterized by progressive chorioretinal atrophy, myopia and early cataract. The disease is MONDO_0009796 (ornithine aminotransferase deficiency). Also known as: GACR, HOGA, Ornithinemia with gyrate atrophy, gyrate atrophy, gyrate atrophy of choroid and retina with or without ornithinemia, gyrate atrophy of the choroid and/or retina, gyrate atrophy of the retina, hoga.