{
    "disease_id": "DOID:0060748", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010898", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010898", 
            "name": "autosomal dominant lateral temporal lobe epilepsy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010898", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010898", 
            "name": "epilepsy, partial, with auditory features"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010898", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010898", 
            "name": "partial epilepsy with auditory aura"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010898", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010898", 
            "name": "partial epilepsy with auditory features"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010898", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010898", 
            "name": "familial temporal lobe epilepsy type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010898", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010898", 
            "name": "epilepsy, familial temporal lobe 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010898", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010898", 
            "name": "ADPEAF"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010898", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010898", 
            "name": "ADLTE"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010898", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010898", 
            "name": "ETL1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010898", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010898", 
            "name": "epilepsy, familial temporal lobe, 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010898", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010898", 
            "name": "autosomal dominant partial epilepsy with auditory features"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010898", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010898", 
            "name": "ADEAF"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010898", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010898", 
            "name": "autosomal dominant epilepsy with auditory features"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010898", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010898", 
            "name": "epilepsy, familial temporal lobe, 1; ETL1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010898", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010898", 
            "name": "epilepsy, lateral temporal lobe, autosomal dominant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010898", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010898", 
            "name": "epilepsy, familial temporal lobe, type 1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060748", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060748", 
            "name": "ETL1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060748", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060748", 
            "name": "partial epilepsy with auditory features"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060748", 
        "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060748", 
        "name": "familial temporal lobe epilepsy 1"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060748#disease-associations", 
            "id": "0060748", 
            "database": "Alliance of Genome Resources"
        }
    ]
}