{
    "disease_id": "DOID:0080118", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014496", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014496", 
            "name": "mitochondrial complex III deficiency caused by mutation in UQCC3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014496", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014496", 
            "name": "mitochondrial complex III deficiency, nuclear type 9"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014496", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014496", 
            "name": "mitochondrial complex III deficiency, nuclear type 9; MC3DN9"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014496", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014496", 
            "name": "MC3DN9"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014496", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014496", 
            "name": "mitochondrial Complex 3 deficiency, nuclear type 9"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014496", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014496", 
            "name": "UQCC3 mitochondrial complex III deficiency"
        }, 
        {
            "url": "https://www.omim.org/entry/616111", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:616111", 
            "name": "Mitochondrial complex III deficiency, nuclear 9"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080118", 
        "description": "A mitochondrial complex III deficiency that has_material_basis_in homozygous mutation in the UQCC3 gene on chromosome 11q12.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080118", 
        "name": "mitochondrial complex III deficiency nuclear type 9"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/616111", 
            "id": "616111", 
            "database": "MIM"
        }
    ]
}