{
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:0080468", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0080468", 
            "name": "X-linked infantile spasm syndrome 1"
        }, 
        {
            "url": "https://www.omim.org/entry/308350", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:308350", 
            "name": "Epileptic encephalopathy, early infantile, 1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080468", 
        "description": "An early infantile epileptic encephalopathy characterized by X-linked recessive inheritance that has_material_basis_in mutation in the ARX gene on chromosome Xp21.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080468", 
        "name": "early infantile epileptic encephalopathy 1"
    }
}