{
    "disease_id": "DOID:0111755",
    "recommended_name": {
        "id": "DOID:0111755",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111755",
        "name": "Leber hereditary optic neuropathy and dystonia",
        "description": "A Leber plus disease characterized by Leber hereditary optic neuropathy and dystonia that has_material_basis_in mutation in the mitochondrial genes MTND6, MTND4, MTND1 or MTND3 that make up the mitochondrial complex I."
    },
    "synonyms": [
        {
            "id": "DOID:0111755",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111755",
            "name": "familial dystonia with visual failure and striatal lucencies",
            "description": ""
        },
        {
            "id": "DOID:0111755",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111755",
            "name": "LDYT",
            "description": ""
        },
        {
            "id": "DOID:0111755",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111755",
            "name": "Leber optic atrophy and dystonia",
            "description": ""
        },
        {
            "id": "DOID:0111755",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111755",
            "name": "Leber optic atrophy with dystonia",
            "description": ""
        },
        {
            "id": "DOID:0111755",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111755",
            "name": "Marsden syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010772",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010772",
            "name": "Leber optic atrophy and dystonia",
            "description": ""
        },
        {
            "id": "MONDO:0010772",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010772",
            "name": "Leber optic atrophy and dystonia",
            "description": ""
        },
        {
            "id": "MONDO:0010772",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010772",
            "name": "LDYT",
            "description": ""
        },
        {
            "id": "MONDO:0010772",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010772",
            "name": "LHON and dystonia",
            "description": ""
        },
        {
            "id": "MONDO:0010772",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010772",
            "name": "Leber Hereditary optic neuropathy with dystonia",
            "description": ""
        },
        {
            "id": "MONDO:0010772",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010772",
            "name": "Leber's hereditary optic neuropathy with dystonia",
            "description": ""
        },
        {
            "id": "MONDO:0010772",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010772",
            "name": "dystonia familial, with visual failure and striatal lucencies",
            "description": ""
        },
        {
            "id": "MONDO:0010772",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010772",
            "name": "dystonia, familial, with visual failure and striatal lucencies",
            "description": ""
        },
        {
            "id": "MIM:500001",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/500001",
            "name": "Leber hereditary optic neuropathy with dystonia",
            "description": "Leber hereditary optic neuropathy with dystonia"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111755"
    ],
    "unlinked_id_list": []
}