{
    "disease_id": "DOID:3534", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009697", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009697", 
            "name": "Lafora progressive myoclonic epilepsy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009697", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009697", 
            "name": "progressive myoclonic epilepsy type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009697", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009697", 
            "name": "myoclonic epilepsy of Lafora"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009697", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009697", 
            "name": "Lafora's disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009697", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009697", 
            "name": "Melf"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009697", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009697", 
            "name": "Lafora body disorder"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009697", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009697", 
            "name": "epilepsy, progressive myoclonic, 2B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009697", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009697", 
            "name": "Lafora body disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009697", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009697", 
            "name": "epilepsy, progressive myoclonic, 2A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009697", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009697", 
            "name": "Epm2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009697", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009697", 
            "name": "PME type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009697", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009697", 
            "name": "progressive myoclonus epilepsy type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009697", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009697", 
            "name": "epilepsy progressive myoclonic 2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:3534", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:3534", 
            "name": "Lafora Progressive Myoclonic Epilepsy"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:3534", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:3534", 
            "name": "Lafora's disease"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:3534", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:3534", 
            "name": "MYOCLONIC EPILEPSY OF LAFORA"
        }, 
        {
            "url": "https://www.omim.org/entry/254780", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:254780", 
            "name": "Epilepsy, progressive myoclonic 2"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:3534", 
        "description": "A progressive myoclonus epilepsy characterized by myoclonus and/or generalized seizures, visual hallucinations, and progressive neurological decline with onset between 8 and 18 years of age that has_material_basis_in homozygous or compound heterozygous mutation in either NHLRC1 on chromosome 6p22.3 or EPM2A on chromosome 6q24.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:3534", 
        "name": "Lafora disease"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/254780", 
            "id": "254780", 
            "database": "MIM"
        }
    ]
}