{
    "disease_id": "DOID:0111690",
    "recommended_name": {
        "id": "DOID:0111690",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111690",
        "name": "familial adult myoclonic epilepsy 1",
        "description": "A familial adult myoclonic epilepsy that has_material_basis_in a heterozygous 5-bp repeat expansion in SAMD12 on chromosome 8q24.11-q24.12."
    },
    "synonyms": [
        {
            "id": "DOID:0111690",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111690",
            "name": "BAFME1",
            "description": ""
        },
        {
            "id": "DOID:0111690",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111690",
            "name": "FAME1",
            "description": ""
        },
        {
            "id": "DOID:0111690",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111690",
            "name": "FCMTE1",
            "description": ""
        },
        {
            "id": "DOID:0111690",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111690",
            "name": "benign adult familial myoclonic epilepsy 1",
            "description": ""
        },
        {
            "id": "DOID:0111690",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111690",
            "name": "familial cortical myoclonic tremor and epilepsy 1",
            "description": ""
        },
        {
            "id": "MONDO:0010985",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010985",
            "name": "FAME1",
            "description": ""
        },
        {
            "id": "MONDO:0010985",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010985",
            "name": "benign adult familial myoclonic epilepsy 1",
            "description": ""
        },
        {
            "id": "MONDO:0010985",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010985",
            "name": "epilepsy, familial ADULT myoclonic, 1",
            "description": ""
        },
        {
            "id": "MONDO:0010985",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010985",
            "name": "cortical myoclonic tremor with epilepsy, familial, 1",
            "description": ""
        },
        {
            "id": "MONDO:0010985",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010985",
            "name": "epilepsy, familial ADULT myoclonic, 1; FAME1",
            "description": ""
        },
        {
            "id": "MONDO:0010985",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010985",
            "name": "FAME1",
            "description": ""
        },
        {
            "id": "MIM:601068",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/601068",
            "name": "Epilepsy, familial adult myoclonic, 1",
            "description": "Epilepsy, familial adult myoclonic, 1"
        }
    ]
}