{
    "disease_id": "DOID:3652", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009723", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009723", 
            "name": "Leigh syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009723", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009723", 
            "name": "Leigh syndrome due to mitochondrial Complex 2 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009723", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009723", 
            "name": "necrotizing encephalopathy, infantile Subacute, of Leigh"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009723", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009723", 
            "name": "Leigh syndrome due to mitochondrial Complex 3 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009723", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009723", 
            "name": "Leigh syndrome due to mitochondrial Complex 4 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009723", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009723", 
            "name": "Leigh syndrome due to mitochondrial Complex 5 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009723", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009723", 
            "name": "LS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009723", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009723", 
            "name": "Leigh syndrome; LS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009723", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009723", 
            "name": "Leigh syndrome due to mitochondrial Complex 1 deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:3652", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:3652", 
            "name": "Infantile necrotizing encephalomyelopathy"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:3652", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:3652", 
            "name": "Leigh syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:3652", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:3652", 
            "name": "juvenile subacute necrotizing encephalomyelopathy"
        }, 
        {
            "url": "https://www.omim.org/entry/256000", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:256000", 
            "name": "Leigh syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:3652", 
        "description": "A mitochondrial metabolism disease characterized by progressive loss of mental and movement abilities. Symptoms usually begin between ages of three months and two years and include loss of appetite, vomiting, irritability and seizure activity.", 
        "resource": "Disease Ontology", 
        "id": "DOID:3652", 
        "name": "Leigh disease"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/256000", 
            "id": "256000", 
            "database": "MIM"
        }
    ]
}