{
    "disease_id": "DOID:0111322", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013032", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013032", 
            "name": "epilepsy, idiopathic generalized, susceptibility to, 8"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013032", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013032", 
            "name": "EIG8"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013032", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013032", 
            "name": "susceptibility to idiopathic generalized epilepsy 8"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013032", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013032", 
            "name": "epilepsy, idiopathic generalized, susceptibility to, type 8"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013032", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013032", 
            "name": "epilepsy, idiopathic generalized, susceptibility to, 8; EIG8"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013032", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013032", 
            "name": "CASR generalised epilepsy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013032", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013032", 
            "name": "generalised epilepsy caused by mutation in CASR"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111322", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111322", 
            "name": "EIG8"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111322", 
        "description": "An idiopathic generalized epilepsy that has_material_basis_in heterozygous mutation in the CASR on chromosome 3q13.3-q21.1.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111322", 
        "name": "idiopathic generalized epilepsy 8"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111322#disease-associations", 
            "id": "0111322", 
            "database": "Alliance of Genome Resources"
        }
    ]
}