{
    "disease_id": "DOID:0060684",
    "recommended_name": {
        "id": "DOID:0060684",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0060684",
        "name": "autosomal dominant nocturnal frontal lobe epilepsy 3",
        "description": "An autosomal dominant nocturnal frontal lobe epilepsy that has_material_basis_in heterozygous mutation in the CHRNB2 gene on chromosome 1q21."
    },
    "synonyms": [
        {
            "id": "DOID:0060684",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060684",
            "name": "ENFL3",
            "description": ""
        },
        {
            "id": "DOID:0060684",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060684",
            "name": "nocturnal frontal lobe epilepsy 3",
            "description": ""
        },
        {
            "id": "MONDO:0011545",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011545",
            "name": "autosomal dominant nocturnal frontal lobe epilepsy 3",
            "description": "Any autosomal dominant nocturnal frontal lobe epilepsy in which the cause of the disease is a mutation in the CHRNB2 gene."
        },
        {
            "id": "MONDO:0011545",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011545",
            "name": "autosomal dominant nocturnal frontal lobe epilepsy caused by mutation in CHRNB2",
            "description": ""
        },
        {
            "id": "MONDO:0011545",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011545",
            "name": "epilepsy, nocturnal frontal lobe, 3",
            "description": ""
        },
        {
            "id": "MONDO:0011545",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011545",
            "name": "ENFL3",
            "description": ""
        },
        {
            "id": "MONDO:0011545",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011545",
            "name": "epilepsy, nocturnal frontal lobe, 3; ENFL3",
            "description": ""
        },
        {
            "id": "MONDO:0011545",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011545",
            "name": "autosomal dominant nocturnal frontal lobe epilepsy type 3",
            "description": ""
        },
        {
            "id": "MONDO:0011545",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011545",
            "name": "nocturnal frontal lobe epilepsy 3",
            "description": ""
        },
        {
            "id": "MONDO:0011545",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011545",
            "name": "CHRNB2 autosomal dominant nocturnal frontal lobe epilepsy",
            "description": ""
        },
        {
            "id": "MONDO:0011545",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011545",
            "name": "epilepsy, nocturnal frontal lobe, type 3",
            "description": ""
        },
        {
            "id": "MIM:605375",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/605375",
            "name": "Epilepsy, nocturnal frontal lobe, 3",
            "description": "Epilepsy, nocturnal frontal lobe, 3"
        }
    ]
}