{
    "disease_id": "DOID:0111143", 
    "synonyms": [], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111143", 
        "description": "A mitochondrial metabolism disease characterized by impaired function of one or more of the proteins making up the mitochondrial proton-transporting ATP synthase complex.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111143", 
        "name": "mitochondrial complex V (ATP synthase) deficiency"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111143#disease-associations", 
            "id": "0111143", 
            "database": "Alliance of Genome Resources"
        }
    ]
}