{
    "disease_id": "DOID:0111748", 
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:0111748", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111748", 
            "name": "MC5DM1"
        }, 
        {
            "url": "https://www.omim.org/entry/500015", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:500015", 
            "name": "Mitochondrial complex V deficiency, mitochondrial 1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111748", 
        "description": "A mitochondrial complex V (ATP synthase) deficiency characterized by lactic acidemia, hypotonia, and neurodegenerative disease that has_material_basis_in mutation in mitochondrial gene MTATP6.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111748", 
        "name": "mitochondrial complex V (ATP synthase) deficiency mitochondrial type 1"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/500015", 
            "id": "500015", 
            "database": "MIM"
        }
    ]
}