{
    "disease_id": "DOID:0050713",
    "recommended_name": {
        "id": "DOID:0050713",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0050713",
        "name": "COX deficiency, infantile mitochondrial myopathy",
        "description": "A cytochrome-c oxidase deficiency disease characterized by myotonia, abnormalities of the heart and kidneys, and lactic acidosis."
    },
    "synonyms": [
        {
            "id": "DOID:0050713",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0050713",
            "name": "fatal infantile COX deficiency",
            "description": ""
        },
        {
            "id": "DOID:0050713",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0050713",
            "name": "fatal infantile cytochrome C oxidase deficiency",
            "description": ""
        },
        {
            "id": "DOID:0050713",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0050713",
            "name": "fatal infantile encephalocardiomyopathy",
            "description": ""
        },
        {
            "id": "DOID:0050713",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0050713",
            "name": "cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency",
            "description": ""
        },
        {
            "id": "DOID:0050713",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0050713",
            "name": "fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency",
            "description": ""
        }
    ],
    "children": [
        {
            "id": "DOID:0080357",
            "label": "mitochondrial complex IV deficiency nuclear type 2",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0080358",
            "label": "mitochondrial complex IV deficiency nuclear type 6",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0080359",
            "label": "mitochondrial complex IV deficiency nuclear type 9",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0080360",
            "label": "mitochondrial complex IV deficiency nuclear type 13",
            "link_status": true,
            "children": []
        }
    ],
    "id_list": [
        "DOID:0080360",
        "DOID:0080357",
        "DOID:0080359",
        "DOID:0050713",
        "DOID:0080358"
    ],
    "unlinked_id_list": []
}