{
    "disease_id": "DOID:0112101",
    "recommended_name": {
        "id": "DOID:0112101",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0112101",
        "name": "mitochondrial type mitochondrial complex I deficiency 1",
        "description": "A mitochondrial type mitochondrial complex I deficiency that has_material_basis_in mutation in MTND3 in the mitochondrial genome."
    },
    "synonyms": [
        {
            "id": "DOID:0112101",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0112101",
            "name": "MC1DM1",
            "description": ""
        },
        {
            "id": "MONDO:0027068",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0027068",
            "name": "mitochondrial complex I deficiency, mitochondrial type 1",
            "description": "Any mitochondrial complex I deficiency, mitochondrial type, in which the cause of the disease is a mutation in the MTND3 gene."
        },
        {
            "id": "MONDO:0027068",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0027068",
            "name": "MC1DM1",
            "description": ""
        },
        {
            "id": "MONDO:0027068",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0027068",
            "name": "mitochondrial complex I deficiency, mitochondrial type 1",
            "description": ""
        },
        {
            "id": "MIM:500014",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/500014",
            "name": "Mitochondrial complex I deficiency, mitochondrial type 1",
            "description": "Mitochondrial complex I deficiency, mitochondrial type 1"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0112101"
    ],
    "unlinked_id_list": []
}