{
    "disease_id": "DOID:0111452", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009698", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009698", 
            "name": "Unverricht-Lundborg syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009698", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009698", 
            "name": "PME type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009698", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009698", 
            "name": "progressive myoclonic epilepsy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009698", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009698", 
            "name": "Unverricht's disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009698", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009698", 
            "name": "Unverricht - Lundborg disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009698", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009698", 
            "name": "progressive myoclonus epilepsy Baltic myoclonic epilepsy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009698", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009698", 
            "name": "Uld"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009698", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009698", 
            "name": "progressive myoclonus epilepsy type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009698", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009698", 
            "name": "epilepsy, progressive myoclonus 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009698", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009698", 
            "name": "myoclonic epilepsy of Unverricht and Lundborg"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009698", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009698", 
            "name": "Baltic myoclonic epilepsy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009698", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009698", 
            "name": "EPM1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009698", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009698", 
            "name": "Unverricht-Lundborg disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009698", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009698", 
            "name": "progressive myoclonic epilepsy type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009698", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009698", 
            "name": "epilepsy, progressive myoclonic type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009698", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009698", 
            "name": "epilepsy, progressive myoclonic, 1A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009698", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009698", 
            "name": "myoclonus progressive epilepsy of Unverricht and Lundborg"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009698", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009698", 
            "name": "epilepsy, progressive myoclonic, 1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111452", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111452", 
            "name": "EPM1A"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111452", 
        "description": "An Unverricht-Lundborg syndrome that has_material_basis_in homozygous or compound heterozygous in CSTB on chromosome 21q22.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111452", 
        "name": "progressive myoclonus epilepsy 1A"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111452#disease-associations", 
            "id": "0111452", 
            "database": "Alliance of Genome Resources"
        }
    ]
}