{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007366", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007366", 
            "name": "seizures, benign familial neonatal, 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007366", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007366", 
            "name": "seizures, benign familial neonatal, type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007366", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007366", 
            "name": "BFNS2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007366", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007366", 
            "name": "seizures, benign familial neonatal, 2; BFNS2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007366", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007366", 
            "name": "KCNQ3 benign neonatal seizures"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007366", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007366", 
            "name": "benign neonatal seizures caused by mutation in KCNQ3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007366", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007366", 
            "name": "convulsions, benign familial neonatal, 2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:14264", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:14264", 
            "name": "benign familial neonatal seizures"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:14264", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:14264", 
            "name": "benign neonatal convulsions"
        }, 
        {
            "url": "https://www.omim.org/entry/121201", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:121201", 
            "name": "Seizures, benign familial neonatal 2"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:14264", 
        "description": "A neonatal period electroclinical syndrome that is characterized by tonic-clonic seizures in newborns occurring within the first seven days of life and ceasing within the first 15 weeks of life and has_material_basis_in autosomal dominant inheritance of voltage-gated potassium channels or a chromosomal inversion.", 
        "resource": "Disease Ontology", 
        "id": "DOID:14264", 
        "name": "benign neonatal seizures"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/121201", 
            "id": "121201", 
            "database": "MIM"
        }
    ]
}