{
    "disease_id": "DOID:0061211",
    "recommended_name": {
        "id": "DOID:0061211",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0061211",
        "name": "Lafora disease 2",
        "description": "A Lafora disease that has_material_basis_in homozygous or compound heterozygous mutation in the NHLRC1 gene, which encodes malin, on chromosome 6p22."
    },
    "synonyms": [
        {
            "id": "DOID:0061211",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0061211",
            "name": "progressive myoclonic epilepsy 2B",
            "description": ""
        },
        {
            "id": "MONDO:0800306",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0800306",
            "name": "myoclonic epilepsy of Lafora 2",
            "description": "Any Lafora disease in which the cause of the disease is a variation in the NHLRC1 gene."
        },
        {
            "id": "MONDO:0800306",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0800306",
            "name": "EPM2B",
            "description": ""
        },
        {
            "id": "MONDO:0800306",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0800306",
            "name": "Lafora disease 2",
            "description": ""
        },
        {
            "id": "MONDO:0800306",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0800306",
            "name": "MELF2",
            "description": ""
        },
        {
            "id": "MONDO:0800306",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0800306",
            "name": "epilepsy, progressive myoclonic, 2B",
            "description": ""
        },
        {
            "id": "MONDO:0800306",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0800306",
            "name": "myoclonic epilepsy of Lafora 2",
            "description": ""
        },
        {
            "id": "MIM:620681",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/620681",
            "name": "Myoclonic epilepsy of Lafora 2",
            "description": "Myoclonic epilepsy of Lafora 2"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0061211"
    ],
    "unlinked_id_list": []
}