{
    "disease_id": "DOID:0060685", 
    "synonyms": [
        {
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            "description": "", 
            "resource": "MONDO", 
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            "name": "autosomal dominant nocturnal frontal lobe epilepsy type 4"
        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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            "name": "nocturnal frontal lobe epilepsy 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012474", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012474", 
            "name": "seizures, benign familial infantile, 6"
        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012474", 
            "name": "ENFL4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012474", 
            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012474", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012474", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012474", 
            "name": "epilepsy, familial, with nocturnal wandering and Ictal fear"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012474", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012474", 
            "name": "autosomal dominant nocturnal frontal lobe epilepsy caused by mutation in CHRNA2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012474", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012474", 
            "name": "epilepsy, nocturnal frontal lobe, type 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012474", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012474", 
            "name": "convulsions, benign familial infantile, 6"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060685", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060685", 
            "name": "ENFL4"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060685", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060685", 
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        }, 
        {
            "url": "https://www.omim.org/entry/610353", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:610353", 
            "name": "Epilepsy, nocturnal frontal lobe, 4"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060685", 
        "description": "An autosomal dominant nocturnal frontal lobe epilepsy that has_material_basis_in heterozygous mutation in the CHRNA2 gene on chromosome 8p21.", 
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        "id": "DOID:0060685", 
        "name": "autosomal dominant nocturnal frontal lobe epilepsy 4"
    }, 
    "evidence": [
        {
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            "id": "610353", 
            "database": "MIM"
        }
    ]
}