has material basis in germline mutation in OAT optic choroid disorder ornithine aminotransferase deficiency https://github.com/monarch-initiative/mondo/issues/4521 https://rarediseases.info.nih.gov/diseases/6556/gyrate-atrophy-of-choroid-and-retina https://www.malacards.org/card/gyrate_atrophy_of_choroid_and_retina Fuchs gyrate atrophy hyperornithinemia-gyrate atrophy of choroid and retina syndrome MESH:D015799 gyrate atrophy hyperornithinemia with gyrate atrophy of choroid and retina NANDO:2200484 OMIM:258870 NANDO:2200486 GACR ornithine aminotransferase deficiency Fuchs gyrate atrophy of the choroid and retina MONDO:0009796 OKT deficiency Orphanet:414 GARD:0006556 gyrate atrophy of choroid and retina with or without ornithinemia ornithine ketoacid aminotransferase deficiency Girate atrophy of the retina hoga DOID:1415 UMLS:C0018425 HOGA MEDGEN:6695 OAT deficiency Ornithinemia NCIT:C84744 A very rare inherited retinal dystrophy characterized by progressive chorioretinal atrophy, myopia and early cataract. gyrate atrophy of choroid and retina hyperornithinemia Fuchs atrophia gyrata chorioideae et retinae inborn disorder of ornithine metabolism inherited retinal dystrophy hereditary peripheral neuropathy neurovascular disorder