{
    "disease_id": "DOID:0061259",
    "recommended_name": {
        "id": "DOID:0061259",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0061259",
        "name": "congenital myopathy 28",
        "description": "A congenital myopathy characterized by exercise intolerance and early fatigue that has_material_basis_in homozygous or compound heterozygous mutation in the 3-hydroxy-3-methylglutaryl-CoA synthase 1 gene on chromosome 5p12."
    },
    "synonyms": [
        {
            "id": "DOID:0061259",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0061259",
            "name": "congenital myopathy 28 with rigid spine",
            "description": ""
        },
        {
            "id": "MONDO:0980756",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0980756",
            "name": "congenital myopathy 28 with rigid spine",
            "description": ""
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0061259"
    ],
    "unlinked_id_list": []
}