{
    "disease_id": "DOID:0112122", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010339", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010339", 
            "name": "X-linked epilepsy-learning disabilities-behavior disorders syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010339", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010339", 
            "name": "epilepsy, X-linked, with variable learning disabilities and behavior disorders"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0112122", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0112122", 
            "name": "X-linked epilepsy-learning disabilities-behavior disorders syndrome"
        }, 
        {
            "url": "https://www.omim.org/entry/300491", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:300491", 
            "name": "Epilepsy X-linked, with variable learning disabilities and behavior disorders"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0112122", 
        "description": "An epilepsy characterized by epilepsy with variable learning disabilities and behavioral disorders in some patients that has_material_basis_in heterozygous or hemizygous mutation in SYN1 on chromosome Xp11.3-p11.2.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0112122", 
        "name": "X-linked epilepsy with variable learning disabilities and behavior disorders"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/300491", 
            "id": "300491", 
            "database": "MIM"
        }
    ]
}