{
    "disease_id": "DOID:1415",
    "recommended_name": {
        "id": "DOID:1415",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:1415",
        "name": "gyrate atrophy",
        "description": ""
    },
    "synonyms": [
        {
            "id": "DOID:1415",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:1415",
            "name": "Gyrate atrophy of the choroid and/or retina",
            "description": ""
        },
        {
            "id": "DOID:1415",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:1415",
            "name": "Ornithinemia with gyrate atrophy",
            "description": ""
        },
        {
            "id": "DOID:1415",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:1415",
            "name": "gyrate atrophy of the retina",
            "description": ""
        },
        {
            "id": "MONDO:0009796",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009796",
            "name": "gyrate atrophy",
            "description": "Gyrate atrophy of the choroid and retina (GACR) is a very rare, inherited retinal dystrophy, characterized by progressive chorioretinal atrophy, myopia and early cataract."
        },
        {
            "id": "MONDO:0009796",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009796",
            "name": "gyrate atrophy of choroid and retina",
            "description": ""
        },
        {
            "id": "MONDO:0009796",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009796",
            "name": "Girate atrophy of the retina",
            "description": ""
        },
        {
            "id": "MONDO:0009796",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009796",
            "name": "hyperornithinemia",
            "description": ""
        },
        {
            "id": "MONDO:0009796",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009796",
            "name": "Oat deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0009796",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009796",
            "name": "hyperornithinemia with gyrate atrophy of choroid and retina",
            "description": ""
        },
        {
            "id": "MONDO:0009796",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009796",
            "name": "hoga",
            "description": ""
        },
        {
            "id": "MONDO:0009796",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009796",
            "name": "gyrate atrophy of the choroid and/or retina",
            "description": ""
        },
        {
            "id": "MONDO:0009796",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009796",
            "name": "ornithine Keto acid aminotransferase deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0009796",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009796",
            "name": "ornithine ketoacid aminotransferase deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0009796",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009796",
            "name": "Ornithinemia",
            "description": ""
        },
        {
            "id": "MONDO:0009796",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009796",
            "name": "gyrate atrophy",
            "description": ""
        },
        {
            "id": "MONDO:0009796",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009796",
            "name": "GACR",
            "description": ""
        },
        {
            "id": "MONDO:0009796",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009796",
            "name": "OKT deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0009796",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009796",
            "name": "Ornithinemia with gyrate atrophy",
            "description": ""
        },
        {
            "id": "MONDO:0009796",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009796",
            "name": "Fuchs gyrate atrophy",
            "description": ""
        },
        {
            "id": "MONDO:0009796",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009796",
            "name": "Okt deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0009796",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009796",
            "name": "Fuchs atrophia gyrata chorioideae et retinae",
            "description": ""
        },
        {
            "id": "MONDO:0009796",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009796",
            "name": "gyrate atrophy of the retina",
            "description": ""
        },
        {
            "id": "MONDO:0009796",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009796",
            "name": "Fuchs gyrate atrophy of the choroid and retina",
            "description": ""
        },
        {
            "id": "MONDO:0009796",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009796",
            "name": "gyrate atrophy of choroid and retina; GACR",
            "description": ""
        },
        {
            "id": "MONDO:0009796",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009796",
            "name": "ornithine-Delta-aminotransferase deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0009796",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009796",
            "name": "ornithine aminotransferase deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0009796",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009796",
            "name": "hyperornithinemia-gyrate atrophy of choroid and retina syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0009796",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009796",
            "name": "OAT deficiency",
            "description": ""
        },
        {
            "id": "MIM:258870",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/258870",
            "name": "Hyperornithinemia with gyrate atrophy of choroid and retina",
            "description": "Hyperornithinemia with gyrate atrophy of choroid and retina"
        }
    ]
}