{
    "disease_id": "DOID:0060686",
    "recommended_name": {
        "id": "DOID:0060686",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0060686",
        "name": "autosomal dominant nocturnal frontal lobe epilepsy 5",
        "description": "An autosomal dominant nocturnal frontal lobe epilepsy that has_material_basis_in heterozygous mutation in the KCNT1 gene on chromosome 9q34."
    },
    "synonyms": [
        {
            "id": "DOID:0060686",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060686",
            "name": "ENFL5",
            "description": ""
        },
        {
            "id": "DOID:0060686",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060686",
            "name": "nocturnal frontal lobe epilepsy 5",
            "description": ""
        },
        {
            "id": "MONDO:0014002",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014002",
            "name": "autosomal dominant nocturnal frontal lobe epilepsy 5",
            "description": "Any autosomal dominant nocturnal frontal lobe epilepsy in which the cause of the disease is a mutation in the KCNT1 gene."
        },
        {
            "id": "MONDO:0014002",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014002",
            "name": "ENFL5",
            "description": ""
        },
        {
            "id": "MONDO:0014002",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014002",
            "name": "KCNT1 autosomal dominant nocturnal frontal lobe epilepsy",
            "description": ""
        },
        {
            "id": "MONDO:0014002",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014002",
            "name": "autosomal dominant nocturnal frontal lobe epilepsy caused by mutation in KCNT1",
            "description": ""
        },
        {
            "id": "MONDO:0014002",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014002",
            "name": "autosomal dominant nocturnal frontal lobe epilepsy type 5",
            "description": ""
        },
        {
            "id": "MONDO:0014002",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014002",
            "name": "epilepsy nocturnal frontal lobe, 5",
            "description": ""
        },
        {
            "id": "MONDO:0014002",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014002",
            "name": "epilepsy, nocturnal frontal lobe, type 5",
            "description": ""
        },
        {
            "id": "MONDO:0014002",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014002",
            "name": "nocturnal frontal lobe epilepsy 5",
            "description": ""
        },
        {
            "id": "MONDO:0014002",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014002",
            "name": "epilepsy, nocturnal frontal lobe, 5",
            "description": ""
        },
        {
            "id": "MIM:615005",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/615005",
            "name": "Epilepsy, nocturnal frontal lobe, 5",
            "description": "Epilepsy, nocturnal frontal lobe, 5"
        }
    ]
}