{
    "disease_id": "DOID:0111692",
    "recommended_name": {
        "id": "DOID:0111692",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111692",
        "name": "familial adult myoclonic epilepsy 2",
        "description": "A familial adult myoclonic epilepsy characterized by onset of tremor affecting the fingers, hand, and voice in adolescence or young adulthood with somewhat later onset of rhythmic myoclonic jerks and generalized tonic-clonic seizures that has_material_basis_in a heterozygous 5-bp repeat expansion in STARD7 on chromosome 2q11.2."
    },
    "synonyms": [
        {
            "id": "DOID:0111692",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111692",
            "name": "ADCME",
            "description": ""
        },
        {
            "id": "DOID:0111692",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111692",
            "name": "BAFME2",
            "description": ""
        },
        {
            "id": "DOID:0111692",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111692",
            "name": "FAME2",
            "description": ""
        },
        {
            "id": "DOID:0111692",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111692",
            "name": "FCMTE2",
            "description": ""
        },
        {
            "id": "DOID:0111692",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111692",
            "name": "autosomal dominant cortical myoclonus and epilepsy",
            "description": ""
        },
        {
            "id": "DOID:0111692",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111692",
            "name": "benign adult familial myoclonic epilepsy 2",
            "description": ""
        },
        {
            "id": "DOID:0111692",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111692",
            "name": "familial cortical myoclonic tremor and epilepsy 2",
            "description": ""
        },
        {
            "id": "MONDO:0011930",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011930",
            "name": "epilepsy, familial adult myoclonic, 2",
            "description": "Any epilepsy, familial adult myoclonic in which the cause of the disease is a mutation in the ADRA2B gene."
        },
        {
            "id": "MONDO:0011930",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011930",
            "name": "ADRA2B epilepsy, familial adult myoclonic",
            "description": ""
        },
        {
            "id": "MONDO:0011930",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011930",
            "name": "epilepsy, familial adult myoclonic caused by mutation in ADRA2B",
            "description": ""
        },
        {
            "id": "MONDO:0011930",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011930",
            "name": "epilepsy, familial adult myoclonic, 2",
            "description": ""
        },
        {
            "id": "MONDO:0011930",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011930",
            "name": "epilepsy, familial adult myoclonic, type 2",
            "description": ""
        },
        {
            "id": "MONDO:0011930",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011930",
            "name": "FAME2",
            "description": ""
        },
        {
            "id": "MIM:607876",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/607876",
            "name": "Epilepsy, familial adult myoclonic, 2",
            "description": "Epilepsy, familial adult myoclonic, 2"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111692"
    ],
    "unlinked_id_list": []
}