{
    "disease_id": "DOID:0111180", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009069", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009069", 
            "name": "congenital lactic acidosis, Saguenay-Lac-Saint-Jean type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009069", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009069", 
            "name": "Cox deficiency, Saguenay Lac saint Jean type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009069", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009069", 
            "name": "Cox deficiency, French Canadian type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009069", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009069", 
            "name": "cytochrome C oxidase deficiency, French Canadian type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009069", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009069", 
            "name": "COX deficiency, French-Canadian type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009069", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009069", 
            "name": "Leigh syndrome, French Canadian type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009069", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009069", 
            "name": "cytochrome C oxidase deficiency, French-Canadian type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009069", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009069", 
            "name": "LSFC"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009069", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009069", 
            "name": "Leigh syndrome, French Canadian type; LSFC"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009069", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009069", 
            "name": "Leigh syndrome, Saguenay-Lac-Saint-Jean type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009069", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009069", 
            "name": "Cox deficiency, Saguenay-Lac-Saint-Jean type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009069", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009069", 
            "name": "Leigh syndrome, Saguenay Lac saint Jean type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009069", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009069", 
            "name": "cytochrome oxidase deficiency, Saguenay-Lac-Saint-Jean type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009069", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009069", 
            "name": "SLSJ-COX deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009069", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009069", 
            "name": "Leigh syndrome, French-Canadian type"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111180", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111180", 
            "name": "French Canadian type COX deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111180", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111180", 
            "name": "French Canadian type Leigh syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111180", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111180", 
            "name": "Saguenay Lac saint Jean type COX deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111180", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111180", 
            "name": "Saguenay Lac saint Jean type Leigh syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111180", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111180", 
            "name": "French Canadian type cytochrome c oxidase deficiency"
        }, 
        {
            "url": "https://www.omim.org/entry/220111", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:220111", 
            "name": "Leigh syndrome French-Canadian type"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111180", 
        "description": "A Leigh disease characterized by metabolic and/or neurological crises, chronic hyperlactataemia, hypotonia, ataxia, mild facial dysmorphism, delayed development and development of leasions in the brainstem and basal ganglia that has_material_basis_in homozygous or compound heterozygous mutations in LRPPRC on 2p21.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111180", 
        "name": "French Canadian Leigh disease"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/220111", 
            "id": "220111", 
            "database": "MIM"
        }
    ]
}