| Disease Aliases (36) | Atrophy, gyrate Deficiency of ornithine-oxo-acid aminotransferase Deficiency, oat Deficiency, okt Deficiency, ornithine aminotransferase Deficiency, ornithine-delta-aminotransferase Fuchs atrophia gyrata chorioideae et retinae Fuchs gyrate atrophy Fuchs gyrate atrophy of the choroid and retina Gacr Gyrate atrophy Girate atrophy of the retina Gyrate atrophy of choroid and retina Gyrate atrophy of the choroid and retina Gyrate atrophy of the choroid and/or retina Hoga Hyperornithinemia with gyrate atrophy of choroid and retina High blood ornithine levels Hyperornithinemia Hyperornithinemia - gyrate atrophy of choroid and retina Hyperornithinemia-gyrate atrophy of choroid and retina syndrome Oat - ornithine oxo-acid aminotransferase deficiency Oat deficiency Okt deficiency Ornithine aminotransferase deficiency Ornithine keto acid aminotransferase deficiency Ornithine-delta-aminotransferase deficiency Ornithine delta aminotransferase deficiency Ornithine ketoacid aminotransferase deficiency Ornithine ketoacid transaminase deficiency Ornithine oxo-acid aminotransferase deficiency Ornithine-oxo-acid amino acid transferase deficiency Ornithinemia Ornithinemia with gyrate atrophy Gyrate atrophy of choroid and retina; gacr Gyrate atrophy of the retina |
Associated Genes (1) NCBI-RefSeq: OAT (Ornithine aminotransferase) External Links: gnomAD browser Ensembl GeneCards
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| Cross-references of Ornithine aminotransferase deficiency | OMIM | GARD | Orphanet | NCBI-GTR | NCBI-MedGen | MalaCards | MeSH | Annotations | |