{
    "disease_id": "DOID:0060682",
    "recommended_name": {
        "id": "DOID:0060682",
        "resource": "Disease Ontology",
        "url": "https://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": "https://disease-ontology.org/term/DOID:0060682",
            "name": "ENFL1",
            "description": ""
        },
        {
            "id": "DOID:0060682",
            "resource": "Disease Ontology",
            "url": "https://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": "CHRNA4 autosomal dominant nocturnal frontal lobe epilepsy",
            "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": "autosomal dominant nocturnal frontal lobe epilepsy caused by mutation in CHRNA4",
            "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": "epilepsy, nocturnal frontal lobe, type 1",
            "description": ""
        },
        {
            "id": "MONDO:0010899",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010899",
            "name": "epilepsy, nocturnal frontal lobe, 1",
            "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"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0060682"
    ],
    "unlinked_id_list": [],
    "crossref": [
        {
            "id": "DOID:0060682",
            "database": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060682",
            "categories": []
        },
        {
            "id": "MONDO:0010899",
            "database": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010899",
            "categories": []
        },
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            "id": "MIM:600513",
            "database": "MIM",
            "url": "https://www.omim.org/entry/600513",
            "categories": []
        }
    ],
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                    "taxid": 10090,
                    "common_name": "Mouse",
                    "glygen_name": "Mouse",
                    "reference_species": "Mus musculus [10090]"
                }
            ],
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                    "type": "synonym"
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                {
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                    "name": "Homo sapiens",
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                    "type": "recommended"
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                    "name": "BFNC",
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                    "name": "EBN1",
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                    "name": "EBN",
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                    "name": "NACRA4",
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                    "id": "0060682",
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            ]
        },
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                    "name": "Rattus norvegicus",
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                    "common_name": "Rat",
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                {
                    "name": "neuronal acetylcholine receptor subunit alpha-4",
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                    "name": "Chrna4",
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                {
                    "name": "Acra4",
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                },
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                    "name": "Chrna4",
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                    "name": "NARAC",
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                    "name": "CG2302-PC",
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                    "name": "lincRNA.965",
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                    "id": "0060682",
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                    "name": "nAChR Dalpha2",
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                    "id": "0060682",
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                    "url": "https://www.alliancegenome.org/disease/DOID:0060682"
                }
            ]
        }
    ],
    "glycans": [],
    "biomarkers": [],
    "association_flag": "1000",
    "record_id": "doid.0060682"
}