{
    "disease_id": "DOID:0080117", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014364", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014364", 
            "name": "mitochondrial complex III deficiency, nuclear type 8"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014364", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014364", 
            "name": "LYRM7 mitochondrial complex III deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014364", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014364", 
            "name": "MC3DN8"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014364", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014364", 
            "name": "mitochondrial Complex 3 deficiency, nuclear type 8"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014364", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014364", 
            "name": "mitochondrial complex III deficiency, nuclear type 8; MC3DN8"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014364", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014364", 
            "name": "mitochondrial complex III deficiency caused by mutation in LYRM7"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080117", 
        "description": "A mitochondrial complex III deficiency characterized by childhood onset of progressive neurodegeneration that has_material_basis_in homozygous mutation in the LYRM7 gene on chromosome 5q23.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080117", 
        "name": "mitochondrial complex III deficiency nuclear type 8"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0080117#disease-associations", 
            "id": "0080117", 
            "database": "Alliance of Genome Resources"
        }
    ]
}