{
    "disease_id": "DOID:0112094",
    "recommended_name": {
        "id": "DOID:0112094",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0112094",
        "name": "nuclear type mitochondrial complex I deficiency 14",
        "description": "A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in NDUFA11 on chromosome 19p13.3."
    },
    "synonyms": [
        {
            "id": "DOID:0112094",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0112094",
            "name": "MC1DN14",
            "description": ""
        },
        {
            "id": "MIM:618236",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/618236",
            "name": "Mitochondrial complex I deficiency, nuclear type 14",
            "description": "Mitochondrial complex I deficiency, nuclear type 14"
        }
    ]
}