{
    "disease_id": "DOID:0111695", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013322", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013322", 
            "name": "FAME3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013322", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013322", 
            "name": "cortical myoclonic tremor with epilepsy, familial, 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013322", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013322", 
            "name": "epilepsy, familial ADULT myoclonic, 3; FAME3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013322", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013322", 
            "name": "epilepsy, familial ADULT myoclonic, 3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111695", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111695", 
            "name": "FAME3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111695", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111695", 
            "name": "FCMTE3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111695", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111695", 
            "name": "familial cortical myoclonic tremor and epilepsy 3"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111695", 
        "description": "A familial adult myoclonic epilepsy characterized by onset between 10 and 40 years of age of cortical tremor, mainly affecting the hands and voice that has_material_basis_in a heterozygous 5-bp repeat expansion in MARCHF6 on chromosome 5p15.2.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111695", 
        "name": "familial adult myoclonic epilepsy 3"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111695#disease-associations", 
            "id": "0111695", 
            "database": "Alliance of Genome Resources"
        }
    ]
}