{
    "disease_id": "DOID:0060748",
    "recommended_name": {
        "id": "DOID:0060748",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0060748",
        "name": "familial temporal lobe epilepsy 1",
        "description": "A temporal lobe epilepsy characterized by autosomal dominant inheritance of partial seizures originating from the temporal lobe that are often accompanied by auditory symptoms and that has_material_basis_in heterozygous mutation in the LGI1 gene on chromosome 10q24."
    },
    "synonyms": [
        {
            "id": "DOID:0060748",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060748",
            "name": "ETL1",
            "description": ""
        },
        {
            "id": "DOID:0060748",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060748",
            "name": "partial epilepsy with auditory features",
            "description": ""
        },
        {
            "id": "MONDO:0010898",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010898",
            "name": "familial temporal lobe epilepsy 1",
            "description": "An autosomal dominant condition caused by mutation(s) in the LGI1 gene, encoding leucine-rich glioma-inactivated protein 1. It is characterized by partial seizures originating in the temporal lobe and often accompanied by auditory sensory manifestations."
        },
        {
            "id": "MONDO:0010898",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010898",
            "name": "autosomal dominant lateral temporal lobe epilepsy",
            "description": ""
        },
        {
            "id": "MONDO:0010898",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010898",
            "name": "epilepsy, partial, with auditory features",
            "description": ""
        },
        {
            "id": "MONDO:0010898",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010898",
            "name": "partial epilepsy with auditory aura",
            "description": ""
        },
        {
            "id": "MONDO:0010898",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010898",
            "name": "partial epilepsy with auditory features",
            "description": ""
        },
        {
            "id": "MONDO:0010898",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010898",
            "name": "familial temporal lobe epilepsy type 1",
            "description": ""
        },
        {
            "id": "MONDO:0010898",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010898",
            "name": "epilepsy, familial temporal lobe 1",
            "description": ""
        },
        {
            "id": "MONDO:0010898",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010898",
            "name": "ADPEAF",
            "description": ""
        },
        {
            "id": "MONDO:0010898",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010898",
            "name": "ADLTE",
            "description": ""
        },
        {
            "id": "MONDO:0010898",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010898",
            "name": "ETL1",
            "description": ""
        },
        {
            "id": "MONDO:0010898",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010898",
            "name": "epilepsy, familial temporal lobe, 1",
            "description": ""
        },
        {
            "id": "MONDO:0010898",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010898",
            "name": "autosomal dominant partial epilepsy with auditory features",
            "description": ""
        },
        {
            "id": "MONDO:0010898",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010898",
            "name": "ADEAF",
            "description": ""
        },
        {
            "id": "MONDO:0010898",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010898",
            "name": "autosomal dominant epilepsy with auditory features",
            "description": ""
        },
        {
            "id": "MONDO:0010898",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010898",
            "name": "epilepsy, familial temporal lobe, 1; ETL1",
            "description": ""
        },
        {
            "id": "MONDO:0010898",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010898",
            "name": "epilepsy, lateral temporal lobe, autosomal dominant",
            "description": ""
        },
        {
            "id": "MONDO:0010898",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010898",
            "name": "epilepsy, familial temporal lobe, type 1",
            "description": ""
        },
        {
            "id": "MIM:600512",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/600512",
            "name": "Epilepsy, familial temporal lobe, 1",
            "description": "Epilepsy, familial temporal lobe, 1"
        }
    ]
}