{
    "disease_id": "DOID:0111694", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0054847", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0054847", 
            "name": "epilepsy, familial adult myoclonic, 7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0054847", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0054847", 
            "name": "benign Adult Familial myoclonic epilepsy 7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0054847", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0054847", 
            "name": "epilepsy, FAMILIAL ADULT myoclonic, 7; FAME7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0054847", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0054847", 
            "name": "cortical myoclonic tremor with epilepsy, Familial, 7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0054847", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0054847", 
            "name": "FAME7"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111694", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111694", 
            "name": "BAFME7"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111694", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111694", 
            "name": "FAME7"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111694", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111694", 
            "name": "FCMTE7"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111694", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111694", 
            "name": "benign adult familial myoclonic epilepsy 7"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111694", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111694", 
            "name": "familial cortical myoclonic tremor and epilepsy 7"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111694", 
        "description": "A familial adult myoclonic epilepsy that has_material_basis_in a heterozygous 5-bp repeat expansion in RAPGEF2 on chromosome 4q32.1.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111694", 
        "name": "familial adult myoclonic epilepsy 7"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111694#disease-associations", 
            "id": "0111694", 
            "database": "Alliance of Genome Resources"
        }
    ]
}