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