{
    "disease_id": "DOID:0112092", 
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:0112092", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0112092", 
            "name": "MC1DN7"
        }, 
        {
            "url": "https://www.omim.org/entry/618229", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:618229", 
            "name": "Mitochondrial complex I deficiency, nuclear type 7"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0112092", 
        "description": "A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in NDUFV2 on chromosome 18p11.22.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0112092", 
        "name": "nuclear type mitochondrial complex I deficiency 7"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/618229", 
            "id": "618229", 
            "database": "MIM"
        }
    ]
}