{
    "disease_id": "DOID:0111755", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010772", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010772", 
            "name": "Leber optic atrophy and dystonia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010772", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010772", 
            "name": "Leber's hereditary optic neuropathy with dystonia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010772", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010772", 
            "name": "LHON and dystonia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010772", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010772", 
            "name": "Leber hereditary optic neuropathy with dystonia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010772", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010772", 
            "name": "dystonia familial, with visual failure and striatal lucencies"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010772", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010772", 
            "name": "dystonia, familial, with visual failure and striatal lucencies"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010772", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010772", 
            "name": "LDYT"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010772", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010772", 
            "name": "Marsden syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111755", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111755", 
            "name": "LDYT"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111755", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111755", 
            "name": "Leber optic atrophy and dystonia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111755", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111755", 
            "name": "Marsden syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111755", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111755", 
            "name": "familial dystonia with visual failure and striatal lucencies"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111755", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111755", 
            "name": "Leber optic atrophy with dystonia"
        }, 
        {
            "url": "https://www.omim.org/entry/500001", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:500001", 
            "name": "Leber hereditary optic neuropathy with dystonia"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111755", 
        "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111755", 
        "name": "Leber hereditary optic neuropathy and dystonia"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/500001", 
            "id": "500001", 
            "database": "MIM"
        }
    ]
}