{
    "disease_id": "DOID:0060682", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010899", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010899", 
            "name": "epilepsy, nocturnal frontal lobe, 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010899", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010899", 
            "name": "ENFL1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010899", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010899", 
            "name": "epilepsy, nocturnal frontal lobe, 1; ENFL1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010899", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010899", 
            "name": "nocturnal frontal lobe epilepsy 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010899", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010899", 
            "name": "epilepsy, nocturnal frontal lobe, type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010899", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010899", 
            "name": "autosomal dominant nocturnal frontal lobe epilepsy type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010899", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010899", 
            "name": "CHRNA4 autosomal dominant nocturnal frontal lobe epilepsy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010899", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010899", 
            "name": "autosomal dominant nocturnal frontal lobe epilepsy caused by mutation in CHRNA4"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060682", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060682", 
            "name": "ENFL1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060682", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060682", 
            "name": "nocturnal frontal lobe epilepsy 1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060682", 
        "description": "An autosomal dominant nocturnal frontal lobe epilepsy that has_material_basis_in heterozygous mutation in the CHRNA4 gene on chromosome 20q13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060682", 
        "name": "autosomal dominant nocturnal frontal lobe epilepsy 1"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060682#disease-associations", 
            "id": "0060682", 
            "database": "Alliance of Genome Resources"
        }
    ]
}