{
    "disease_id": "DOID:0111445", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014717", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014717", 
            "name": "early-onset Lafora body disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014717", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014717", 
            "name": "epilepsy, progressive myoclonic, 10"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014717", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014717", 
            "name": "epilepsy, progressive myoclonic, type 10"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014717", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014717", 
            "name": "epilepsy, progressive myoclonic, 10; EPM10"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014717", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014717", 
            "name": "EPM10"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111445", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111445", 
            "name": "EPM10"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111445", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111445", 
            "name": "early-onset Lafora body disease"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111445", 
        "description": "A progressive myoclonus epilepsy characterized by onset of progressive myoclonus, ataxia, spasticity, dysarthria, and cognitive decline in the first decade of life that has_material_basis_in homozygous or compoud heterozygous mutation in PRDM8 on chromosome 4q21.21.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111445", 
        "name": "progressive myoclonus epilepsy 10"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111445#disease-associations", 
            "id": "0111445", 
            "database": "Alliance of Genome Resources"
        }
    ]
}