{
    "disease_id": "DOID:0060681", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010899", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010899", 
            "name": "autosomal dominant nocturnal frontal lobe epilepsy 1"
        }, 
        {
            "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:0060681", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060681", 
            "name": "ENFL"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060681", 
        "description": "A frontal lobe epilepsy that is characterized by autosomal dominant inheritance with childhood onset of clusters of brief nocturnal motor seizures with hyperkinetic or tonic manifestations.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060681", 
        "name": "autosomal dominant nocturnal frontal lobe epilepsy"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060681#disease-associations", 
            "id": "0060681", 
            "database": "Alliance of Genome Resources"
        }
    ]
}