{
    "disease_id": "DOID:0060751",
    "recommended_name": {
        "id": "DOID:0060751",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0060751",
        "name": "familial temporal lobe epilepsy 7",
        "description": "A temporal lobe epilepsy characterized by autosomal dominant inheritance of focal seizures with prominent auditory symptoms and that has_material_basis_in heterozygous mutation in the RELN gene on chromosome 7q22."
    },
    "synonyms": [
        {
            "id": "DOID:0060751",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060751",
            "name": "ETL7",
            "description": ""
        },
        {
            "id": "MONDO:0014639",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014639",
            "name": "familial temporal lobe epilepsy 7",
            "description": "A temporal lobe epilepsy characterized by autosomal dominant inheritance of focal seizures with prominent auditory symptoms and that has material basis in heterozygous mutation in the RELN gene on chromosome 7q22."
        },
        {
            "id": "MONDO:0014639",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014639",
            "name": "ETL7",
            "description": ""
        },
        {
            "id": "MONDO:0014639",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014639",
            "name": "epilepsy, familial temporal lobe, type 7",
            "description": ""
        },
        {
            "id": "MONDO:0014639",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014639",
            "name": "familial temporal lobe epilepsy type 7",
            "description": ""
        },
        {
            "id": "MONDO:0014639",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014639",
            "name": "epilepsy, familial temporal lobe, 7",
            "description": ""
        },
        {
            "id": "MIM:616436",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/616436",
            "name": "Epilepsy, familial temporal lobe, 7",
            "description": "Epilepsy, familial temporal lobe, 7"
        }
    ]
}