{
    "disease_id": "DOID:0112085",
    "recommended_name": {
        "id": "DOID:0112085",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0112085",
        "name": "nuclear type mitochondrial complex I deficiency 19",
        "description": "A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the FOXRED1 gene on chromosome 11q24.2."
    },
    "synonyms": [
        {
            "id": "DOID:0112085",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0112085",
            "name": "MC1DN19",
            "description": ""
        },
        {
            "id": "MONDO:0032624",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0032624",
            "name": "mitochondrial complex I deficiency, nuclear type 19",
            "description": ""
        },
        {
            "id": "MONDO:0032624",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0032624",
            "name": "MC1DN19",
            "description": ""
        },
        {
            "id": "MONDO:0032624",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0032624",
            "name": "MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 19",
            "description": ""
        },
        {
            "id": "MIM:618241",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/618241",
            "name": "Mitochondrial complex I deficiency, nuclear type 19",
            "description": "Mitochondrial complex I deficiency, nuclear type 19"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0112085"
    ],
    "unlinked_id_list": []
}