{
    "disease_id": "DOID:0060169", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011904", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011904", 
            "name": "seizures, benign familial infantile, 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011904", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011904", 
            "name": "convulsions, benign familial infantile, 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011904", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011904", 
            "name": "BFIS3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011904", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011904", 
            "name": "SCN2A benign familial infantile epilepsy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011904", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011904", 
            "name": "seizures, benign familial infantile, type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011904", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011904", 
            "name": "seizures, benign familial neonatal-infantile"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011904", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011904", 
            "name": "seizures, benign familial infantile, 3; BFIS3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011904", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011904", 
            "name": "benign familial infantile epilepsy caused by mutation in SCN2A"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060169", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060169", 
            "name": "BFIC"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060169", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060169", 
            "name": "BFIE"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060169", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060169", 
            "name": "benign familial infantile convulsion"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060169", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060169", 
            "name": "benign familial infantile seizures"
        }, 
        {
            "url": "https://www.omim.org/entry/607745", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:607745", 
            "name": "Seizures, benign familial infantile, 3"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060169", 
        "description": "An infancy electroclinical syndrome that is characterized by convulsions, with onset at age 3 to 12 months.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060169", 
        "name": "benign familial infantile epilepsy"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/607745", 
            "id": "607745", 
            "database": "MIM"
        }
    ]
}