{
    "disease_id": "DOID:0070660",
    "recommended_name": {
        "id": "DOID:0070660",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0070660",
        "name": "Lafora disease 1",
        "description": "A Lafora disease that has_material_basis_in homozygous or compound heterozygous mutation in the EPM2A gene on chromosome 6q24."
    },
    "synonyms": [
        {
            "id": "DOID:0070660",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070660",
            "name": "progressive myoclonic epilepsy 2A",
            "description": ""
        },
        {
            "id": "MONDO:0958199",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0958199",
            "name": "myoclonic epilepsy of Lafora 1",
            "description": "Any Lafora disease in which the cause of the disease is a variation in the EPM2A gene."
        },
        {
            "id": "MIM:254780",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/254780",
            "name": "Myoclonic epilepsy of lafora 1",
            "description": "Myoclonic epilepsy of lafora 1"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070660"
    ],
    "unlinked_id_list": []
}