{
    "disease_id": "DOID:0070737",
    "recommended_name": {
        "id": "DOID:0070737",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0070737",
        "name": "multiple mitochondrial dysfunctions syndrome 10",
        "description": "A multiple mitochondrial dysfunctions syndrome characterized by proximal and axial muscle weakness, fluctuating creatine kinase elevation, respiratory insufficiency and central nervous symptoms, including learning difficulties and neurobehavioral comorbidities, that has_material_basis_in compound heterozygous mutation in the CIAO1 gene on chromosome 2q11."
    },
    "synonyms": [
        {
            "id": "DOID:0070737",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070737",
            "name": "MMDS10",
            "description": ""
        },
        {
            "id": "MONDO:0975806",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0975806",
            "name": "multiple mitochondrial dysfunctions syndrome 10",
            "description": ""
        },
        {
            "id": "MIM:620960",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/620960",
            "name": "Multiple mitochondrial dysfunctions syndrome 10",
            "description": "Multiple mitochondrial dysfunctions syndrome 10"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070737"
    ],
    "unlinked_id_list": []
}