{
    "disease_id": "DOID:14264",
    "recommended_name": {
        "id": "DOID:14264",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:14264",
        "name": "benign neonatal seizures",
        "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."
    },
    "synonyms": [
        {
            "id": "DOID:14264",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:14264",
            "name": "benign familial neonatal seizures",
            "description": ""
        },
        {
            "id": "DOID:14264",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:14264",
            "name": "benign neonatal convulsions",
            "description": ""
        },
        {
            "id": "MONDO:0007365",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007365",
            "name": "seizures, benign familial neonatal, 1",
            "description": "Any benign neonatal seizures in which the cause of the disease is a mutation in the KCNQ2 gene."
        },
        {
            "id": "MONDO:0007365",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007365",
            "name": "seizures, benign familial neonatal, 1, and/or myokymia",
            "description": ""
        },
        {
            "id": "MONDO:0007365",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007365",
            "name": "epilepsy, benign neonatal, 1, and/or myokymia",
            "description": ""
        },
        {
            "id": "MONDO:0007365",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007365",
            "name": "BFNS1",
            "description": ""
        },
        {
            "id": "MONDO:0007365",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007365",
            "name": "seizures, benign familial neonatal, type 1",
            "description": ""
        },
        {
            "id": "MONDO:0007365",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007365",
            "name": "seizures, benign familial neonatal, 1; BFNS1",
            "description": ""
        },
        {
            "id": "MONDO:0007365",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007365",
            "name": "KCNQ2 benign neonatal seizures",
            "description": ""
        },
        {
            "id": "MONDO:0007365",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007365",
            "name": "seizures, benign familial neonatal, 1",
            "description": ""
        },
        {
            "id": "MONDO:0007365",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007365",
            "name": "benign neonatal seizures caused by mutation in KCNQ2",
            "description": ""
        },
        {
            "id": "MONDO:0007366",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007366",
            "name": "seizures, benign familial neonatal, 2",
            "description": "Any benign neonatal seizures in which the cause of the disease is a mutation in the KCNQ3 gene."
        },
        {
            "id": "MONDO:0007366",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007366",
            "name": "seizures, benign familial neonatal, type 2",
            "description": ""
        },
        {
            "id": "MONDO:0007366",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007366",
            "name": "BFNS2",
            "description": ""
        },
        {
            "id": "MONDO:0007366",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007366",
            "name": "seizures, benign familial neonatal, 2; BFNS2",
            "description": ""
        },
        {
            "id": "MONDO:0007366",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007366",
            "name": "seizures, benign familial neonatal, 2",
            "description": ""
        },
        {
            "id": "MONDO:0007366",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007366",
            "name": "KCNQ3 benign neonatal seizures",
            "description": ""
        },
        {
            "id": "MONDO:0007366",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007366",
            "name": "benign neonatal seizures caused by mutation in KCNQ3",
            "description": ""
        },
        {
            "id": "MONDO:0007366",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007366",
            "name": "convulsions, benign familial neonatal, 2",
            "description": ""
        },
        {
            "id": "MONDO:0010021",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010021",
            "name": "seizures, benign familial neonatal, autosomal recessive",
            "description": ""
        },
        {
            "id": "MONDO:0010021",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010021",
            "name": "convulsions, benign familial neonatal, autosomal recessive",
            "description": ""
        },
        {
            "id": "MONDO:0010021",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010021",
            "name": "convulsions benign familial neonatal dominant form",
            "description": ""
        },
        {
            "id": "MONDO:0010021",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010021",
            "name": "seizures, benign familial neonatal, autosomal recessive",
            "description": ""
        },
        {
            "id": "MONDO:0010021",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010021",
            "name": "Bfns, autosomal recessive",
            "description": ""
        },
        {
            "id": "MONDO:0010021",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010021",
            "name": "autosomal dominant form of benign neonatal seizures",
            "description": ""
        },
        {
            "id": "MONDO:0010021",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010021",
            "name": "epilepsy, benign familial neonatal, autosomal recessive",
            "description": ""
        },
        {
            "id": "MIM:121200",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/121200",
            "name": "Seizures, benign familial neonatal 1",
            "description": "Seizures, benign familial neonatal 1"
        },
        {
            "id": "MIM:121201",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/121201",
            "name": "Seizures, benign familial neonatal 2",
            "description": "Seizures, benign familial neonatal 2"
        }
    ]
}