{
    "disease_id": "DOID:0060751", 
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:0060751", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060751", 
            "name": "ETL7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014639", 
            "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.", 
            "resource": "MONDO", 
            "id": "MONDO:0014639", 
            "name": "familial temporal lobe epilepsy 7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014639", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014639", 
            "name": "familial temporal lobe epilepsy type 7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014639", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014639", 
            "name": "epilepsy, familial temporal lobe, 7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014639", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014639", 
            "name": "ETL7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014639", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014639", 
            "name": "epilepsy, familial temporal lobe, type 7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014639", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014639", 
            "name": "epilepsy, familial temporal lobe, 7; ETL7"
        }, 
        {
            "url": "https://www.omim.org/entry/616436", 
            "description": "Epilepsy, familial temporal lobe, 7", 
            "resource": "MIM", 
            "id": "MIM:616436", 
            "name": "Epilepsy, familial temporal lobe, 7"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060751", 
        "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060751", 
        "name": "familial temporal lobe epilepsy 7"
    }
}