{
    "disease_id": "DOID:0111301", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014517", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014517", 
            "name": "generalized epilepsy with febrile seizures plus, type 9"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014517", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014517", 
            "name": "STX1B generalized epilepsy with febrile seizures plus"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014517", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014517", 
            "name": "generalized epilepsy with febrile seizures plus, type 9; GEFSP9"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014517", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014517", 
            "name": "GEFSP9"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014517", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014517", 
            "name": "generalized epilepsy with febrile seizures plus caused by mutation in STX1B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014517", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014517", 
            "name": "Gefs+, type 9"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111301", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111301", 
            "name": "GEFS+9"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111301", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111301", 
            "name": "GEFSP9"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111301", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111301", 
            "name": "generalised epilepsy with febrile seizures plus 9"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111301", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111301", 
            "name": "generalized epilepsy with febrile seizures plus type 9"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111301", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111301", 
            "name": "generalised epilepsy with febrile seizures plus type 9"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111301", 
        "description": "A generalized epilepsy with febrile seizures plus that has_material_basis_in heterozygous mutation in STX1B on chromosome 16p11.2.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111301", 
        "name": "generalized epilepsy with febrile seizures plus 9"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111301#disease-associations", 
            "id": "0111301", 
            "database": "Alliance of Genome Resources"
        }
    ]
}