{
    "disease_id": "DOID:0111294",
    "recommended_name": {
        "id": "DOID:0111294",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111294",
        "name": "generalized epilepsy with febrile seizures plus 2",
        "description": "A generalized epilepsy with febrile seizures plus that has_material_basis_in heterozygous mutation in SCN1A on chromosome 2q24.3."
    },
    "synonyms": [
        {
            "id": "DOID:0111294",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111294",
            "name": "generalised epilepsy with febrile seizures plus type 2",
            "description": ""
        },
        {
            "id": "DOID:0111294",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111294",
            "name": "GEFS+2",
            "description": ""
        },
        {
            "id": "DOID:0111294",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111294",
            "name": "GEFSP2",
            "description": ""
        },
        {
            "id": "DOID:0111294",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111294",
            "name": "generalised epilepsy with febrile seizures plus 2",
            "description": ""
        },
        {
            "id": "DOID:0111294",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111294",
            "name": "generalized epilepsy with febrile seizures plus type 2",
            "description": ""
        },
        {
            "id": "MONDO:0011461",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011461",
            "name": "generalized epilepsy with febrile seizures plus, type 2",
            "description": "Any febrile seizures, familial in which the cause of the disease is a mutation in the SCN1A gene."
        },
        {
            "id": "MONDO:0011461",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011461",
            "name": "generalized epilepsy with febrile seizures plus, type 2",
            "description": ""
        },
        {
            "id": "MONDO:0011461",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011461",
            "name": "febrile seizures, familial caused by mutation in SCN1A",
            "description": ""
        },
        {
            "id": "MONDO:0011461",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011461",
            "name": "GEFSP2",
            "description": ""
        },
        {
            "id": "MONDO:0011461",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011461",
            "name": "SCN1A febrile seizures, familial",
            "description": ""
        },
        {
            "id": "MONDO:0011461",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011461",
            "name": "generalized epilepsy with febrile seizures plus, type 2; GEFSP2",
            "description": ""
        },
        {
            "id": "MONDO:0011461",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011461",
            "name": "Gefs+, type 2",
            "description": ""
        },
        {
            "id": "MONDO:0011461",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011461",
            "name": "febrile seizures, familial, 3A",
            "description": ""
        },
        {
            "id": "MIM:604403",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/604403",
            "name": "Febrile seizures, familial, 3A",
            "description": "Febrile seizures, familial, 3A"
        }
    ]
}
