{
    "disease_id": "DOID:0111691", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014167", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014167", 
            "name": "epilepsy, familial adult myoclonic, 5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014167", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014167", 
            "name": "epilepsy, familial ADULT myoclonic, 5; FAME5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014167", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014167", 
            "name": "FAME5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014167", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014167", 
            "name": "epilepsy, familial adult myoclonic, type 5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014167", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014167", 
            "name": "epilepsy, familial adult myoclonic caused by mutation in CNTN2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014167", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014167", 
            "name": "CNTN2 epilepsy, familial adult myoclonic"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014167", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014167", 
            "name": "cortical myoclonic tremor with epilepsy, familial, 5"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111691", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111691", 
            "name": "FAME5"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111691", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111691", 
            "name": "FCMTE5"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111691", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111691", 
            "name": "familial cortical myoclonic tremor and epilepsy 5"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111691", 
        "description": "A familial adult myoclonic epilepsy characterized by onset of seizures in adolescence, followed by the development of cortical myoclonic tremor that has_material_basis_in homozygous or compound heterozygous mutation in CNTN2 on chromosome 1q32.1.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111691", 
        "name": "familial adult myoclonic epilepsy 5"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111691#disease-associations", 
            "id": "0111691", 
            "database": "Alliance of Genome Resources"
        }
    ]
}