{
    "disease_id": "DOID:0111295", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013470", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013470", 
            "name": "generalized epilepsy with febrile seizures plus, type 7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013470", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013470", 
            "name": "Gefs+, type 7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013470", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013470", 
            "name": "generalized epilepsy with febrile seizures plus caused by mutation in SCN9A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013470", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013470", 
            "name": "febrile seizures, familial, 3B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013470", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013470", 
            "name": "GEFSP7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013470", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013470", 
            "name": "generalized epilepsy with febrile seizures plus, type 7; GEFSP7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013470", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013470", 
            "name": "SCN9A generalized epilepsy with febrile seizures plus"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111295", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111295", 
            "name": "GEFS+7"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111295", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111295", 
            "name": "GEFSP7"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111295", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111295", 
            "name": "generalised epilepsy with febrile seizures plus 7"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111295", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111295", 
            "name": "generalized epilepsy with febrile seizures plus type 7"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111295", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111295", 
            "name": "generalised epilepsy with febrile seizures plus type 7"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111295", 
        "description": "A generalized epilepsy with febrile seizures plus that has_material_basis_in heterozygous mutation in SCN9A on chromosome 2q24.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111295", 
        "name": "generalized epilepsy with febrile seizures plus 7"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111295#disease-associations", 
            "id": "0111295", 
            "database": "Alliance of Genome Resources"
        }
    ]
}