{
    "disease_id": "DOID:0111298",
    "recommended_name": {
        "id": "DOID:0111298",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111298",
        "name": "familial febrile seizures 8",
        "description": "A familial febrile seizures that has_material_basis_in heterozygous mutation in GABRG2 on chromosome 5q34."
    },
    "synonyms": [
        {
            "id": "DOID:0111298",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111298",
            "name": "FEB8",
            "description": ""
        },
        {
            "id": "DOID:0111298",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111298",
            "name": "familial febrile convulsions 8",
            "description": ""
        },
        {
            "id": "MONDO:0011891",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011891",
            "name": "epilepsy, childhood absence, susceptibility to, 2",
            "description": "Any childhood absence epilepsy in which the cause of the disease is a mutation in the GABRG2 gene."
        },
        {
            "id": "MONDO:0011891",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011891",
            "name": "childhood absence epilepsy caused by mutation in GABRG2",
            "description": ""
        },
        {
            "id": "MONDO:0011891",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011891",
            "name": "GABRG2 childhood absence epilepsy",
            "description": ""
        },
        {
            "id": "MONDO:0011891",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011891",
            "name": "susceptibility to childhood absence epilepsy 2",
            "description": ""
        },
        {
            "id": "MONDO:0011891",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011891",
            "name": "ECA2",
            "description": ""
        },
        {
            "id": "MONDO:0011891",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011891",
            "name": "epilepsy, childhood absence, susceptibility to, 2; ECA2",
            "description": ""
        },
        {
            "id": "MONDO:0011891",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011891",
            "name": "epilepsy, childhood absence, susceptibility to, 2",
            "description": ""
        },
        {
            "id": "MONDO:0011891",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011891",
            "name": "epilepsy, childhood absence, susceptibility to, type 2",
            "description": ""
        },
        {
            "id": "MIM:607681",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/607681",
            "name": "Epilepsy, childhood absence 2",
            "description": "Epilepsy, childhood absence 2"
        }
    ]
}