{
    "disease_id": "DOID:14264", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010021", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010021", 
            "name": "seizures, benign familial neonatal, autosomal recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010021", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010021", 
            "name": "convulsions, benign familial neonatal, autosomal recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010021", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010021", 
            "name": "convulsions benign familial neonatal dominant form"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010021", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010021", 
            "name": "Bfns, autosomal recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010021", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010021", 
            "name": "autosomal dominant form of benign neonatal seizures"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010021", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010021", 
            "name": "epilepsy, benign familial neonatal, autosomal recessive"
        }, 
        {
            "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"
        }
    ], 
    "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.alliancegenome.org/gene/14264#disease-associations", 
            "id": "14264", 
            "database": "Alliance of Genome Resources"
        }
    ]
}