{
    "disease_id": "DOID:0111323", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011892", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011892", 
            "name": "epilepsy, idiopathic generalized, susceptibility to, 9"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011892", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011892", 
            "name": "EIG9"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011892", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011892", 
            "name": "epilepsy, idiopathic generalized, susceptibility to, type 9"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011892", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011892", 
            "name": "susceptibility to idiopathic generalized epilepsy 9"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011892", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011892", 
            "name": "epilepsy, idiopathic generalized, susceptibility to, 9; EIG9"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011892", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011892", 
            "name": "CACNB4 generalised epilepsy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011892", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011892", 
            "name": "epilepsy, juvenile myoclonic, susceptibility to, 6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011892", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011892", 
            "name": "generalised epilepsy caused by mutation in CACNB4"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111323", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111323", 
            "name": "EIG9"
        }, 
        {
            "url": "https://www.omim.org/entry/607682", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:607682", 
            "name": "Epilepsy, idiopathic generalized 9"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111323", 
        "description": "An idiopathic generalized epilepsy that has_material_basis_in heterozygous mutation in the CACNB4 on chromosome 2q23.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111323", 
        "name": "idiopathic generalized epilepsy 9"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/607682", 
            "id": "607682", 
            "database": "MIM"
        }
    ]
}