{
    "disease_id": "DOID:0060682",
    "recommended_name": {
        "id": "DOID:0060682",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0060682",
        "name": "autosomal dominant nocturnal frontal lobe epilepsy 1",
        "description": "An autosomal dominant nocturnal frontal lobe epilepsy that has_material_basis_in heterozygous mutation in the CHRNA4 gene on chromosome 20q13."
    },
    "synonyms": [
        {
            "id": "DOID:0060682",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060682",
            "name": "ENFL1",
            "description": ""
        },
        {
            "id": "DOID:0060682",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060682",
            "name": "nocturnal frontal lobe epilepsy 1",
            "description": ""
        },
        {
            "id": "MONDO:0010899",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010899",
            "name": "autosomal dominant nocturnal frontal lobe epilepsy 1",
            "description": "Any autosomal dominant nocturnal frontal lobe epilepsy in which the cause of the disease is a mutation in the CHRNA4 gene."
        },
        {
            "id": "MONDO:0010899",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010899",
            "name": "epilepsy, nocturnal frontal lobe, 1",
            "description": ""
        },
        {
            "id": "MONDO:0010899",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010899",
            "name": "ENFL1",
            "description": ""
        },
        {
            "id": "MONDO:0010899",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010899",
            "name": "epilepsy, nocturnal frontal lobe, 1; ENFL1",
            "description": ""
        },
        {
            "id": "MONDO:0010899",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010899",
            "name": "nocturnal frontal lobe epilepsy 1",
            "description": ""
        },
        {
            "id": "MONDO:0010899",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010899",
            "name": "epilepsy, nocturnal frontal lobe, type 1",
            "description": ""
        },
        {
            "id": "MONDO:0010899",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010899",
            "name": "autosomal dominant nocturnal frontal lobe epilepsy type 1",
            "description": ""
        },
        {
            "id": "MONDO:0010899",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010899",
            "name": "CHRNA4 autosomal dominant nocturnal frontal lobe epilepsy",
            "description": ""
        },
        {
            "id": "MONDO:0010899",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010899",
            "name": "autosomal dominant nocturnal frontal lobe epilepsy caused by mutation in CHRNA4",
            "description": ""
        },
        {
            "id": "MIM:600513",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/600513",
            "name": "Epilepsy, nocturnal frontal lobe, 1",
            "description": "Epilepsy, nocturnal frontal lobe, 1"
        }
    ]
}