{
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:0111296", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111296", 
            "name": "GEFS+10"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111296", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111296", 
            "name": "GEFSP10"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111296", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111296", 
            "name": "generalised epilepsy with febrile seizures plus 10"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111296", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111296", 
            "name": "generalised epilepsy with febrile seizures plus type 10"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111296", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111296", 
            "name": "generalized epilepsy with febrile seizures plus type 10"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111296", 
        "description": "A generalized epilepsy with febrile seizures plus that has_material_basis_in heterozygous mutation in HCN1 on chromosome 5p12.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111296", 
        "name": "generalized epilepsy with febrile seizures plus 10"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/618482", 
            "id": "618482", 
            "database": "MIM"
        }
    ]
}