{
    "disease_id": "DOID:0112108",
    "recommended_name": {
        "id": "DOID:0112108",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0112108",
        "name": "myofibrillar myopathy 10",
        "description": "A myofibrillar myopathy characterized by onset of muscle pain, cramping, and exercise fatigue in the first or second decades of life that has_material_basis_in homozygous or compound heterozygous mutation in the SVIL gene on chromosome 10p11.23."
    },
    "synonyms": [
        {
            "id": "DOID:0112108",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0112108",
            "name": "MFM10",
            "description": ""
        },
        {
            "id": "MONDO:0033620",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0033620",
            "name": "myofibrillar myopathy 10",
            "description": ""
        },
        {
            "id": "MONDO:0033620",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0033620",
            "name": "MFM10",
            "description": ""
        },
        {
            "id": "MIM:619040",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/619040",
            "name": "Myopathy, myofibrillar, 10",
            "description": "Myopathy, myofibrillar, 10"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0112108"
    ],
    "unlinked_id_list": []
}