{
    "disease_id": "DOID:0060754",
    "recommended_name": {
        "id": "DOID:0060754",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0060754",
        "name": "familial temporal lobe epilepsy 8",
        "description": "A temporal lobe epilepsy characterized by autosomal dominant inheritance of complex partial seizures with occasional secondary generalization and that has_material_basis_in heterozygous mutation in the GAL gene on chromosome 11q13."
    },
    "synonyms": [
        {
            "id": "DOID:0060754",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060754",
            "name": "ETL8",
            "description": ""
        },
        {
            "id": "MONDO:0014650",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014650",
            "name": "familial temporal lobe epilepsy 8",
            "description": "A temporal lobe epilepsy characterized by autosomal dominant inheritance of complex partial seizures with occasional secondary generalization and that has_material_basis_in heterozygous mutation in the GAL gene on chromosome 11q13."
        },
        {
            "id": "MONDO:0014650",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014650",
            "name": "ETL8",
            "description": ""
        },
        {
            "id": "MONDO:0014650",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014650",
            "name": "familial temporal lobe epilepsy type 8",
            "description": ""
        },
        {
            "id": "MONDO:0014650",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014650",
            "name": "epilepsy, familial temporal lobe, 8; ETL8",
            "description": ""
        },
        {
            "id": "MONDO:0014650",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014650",
            "name": "epilepsy, familial temporal lobe, 8",
            "description": ""
        },
        {
            "id": "MONDO:0014650",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014650",
            "name": "epilepsy, familial temporal lobe, type 8",
            "description": ""
        },
        {
            "id": "MIM:616461",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/616461",
            "name": "Epilepsy, familial temporal lobe, 8",
            "description": "Epilepsy, familial temporal lobe, 8"
        }
    ]
}