Ornithine aminotransferase deficiency

MONDO:0009796

A very rare inherited retinal dystrophy characterized by progressive chorioretinal atrophy, myopia and early cataract.

Also known as: GACR, HOGA, gyrate atrophy, gyrate atrophy of choroid and retina with or without ornithinemia, hoga, hyperornithinemia, hyperornithinemia-gyrate atrophy of choroid and retina syndrome, ornithine aminotransferase deficiency

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