{
    "disease_id": "DOID:0111689", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010985", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010985", 
            "name": "FAME1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010985", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010985", 
            "name": "benign adult familial myoclonic epilepsy 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010985", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010985", 
            "name": "epilepsy, familial ADULT myoclonic, 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010985", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010985", 
            "name": "cortical myoclonic tremor with epilepsy, familial, 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010985", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010985", 
            "name": "epilepsy, familial ADULT myoclonic, 1; FAME1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111689", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111689", 
            "name": "BAFME"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111689", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111689", 
            "name": "FAME"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111689", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111689", 
            "name": "FCMTE"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111689", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111689", 
            "name": "benign adult familial myoclonic epilepsy"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111689", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111689", 
            "name": "benign adult familial myoclonus epilepsy"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111689", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111689", 
            "name": "familial cortical myoclonic tremor and epilepsy"
        }, 
        {
            "url": "https://www.omim.org/entry/601068", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:601068", 
            "name": "Epilepsy, familial adult myoclonic, 1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111689", 
        "description": "An adolescence-adult electroclinical syndrome characterized by adult-onset cortical myoclonus typically first seen as tremulous finger movements and myoclonus of the extremities.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111689", 
        "name": "familial adult myoclonic epilepsy"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/601068", 
            "id": "601068", 
            "database": "MIM"
        }
    ]
}