{
    "disease_id": "DOID:705", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010788", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010788", 
            "name": "Lebers disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010788", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010788", 
            "name": "LHON"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010788", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010788", 
            "name": "Leber's hereditary optic neuropathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010788", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010788", 
            "name": "Leber's optic atrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010788", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010788", 
            "name": "Leber Hereditary optic atrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010788", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010788", 
            "name": "optic atrophy, Leber type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010788", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010788", 
            "name": "Leber optic atrophy"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:705", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:705", 
            "name": "Leber's hereditary optic neuropathy"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:705", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:705", 
            "name": "Leber's optic atrophy"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:705", 
        "description": "", 
        "resource": "Disease Ontology", 
        "id": "DOID:705", 
        "name": "Leber hereditary optic neuropathy"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/535000", 
            "id": "535000", 
            "database": "MIM"
        }
    ]
}