{
    "disease_id": "DOID:0080416", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014607", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014607", 
            "name": "epileptic encephalopathy, early infantile, 32"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014607", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014607", 
            "name": "early infantile epileptic encephalopathy caused by mutation in KCNA2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014607", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014607", 
            "name": "epileptic encephalopathy, early infantile, type 32"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014607", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014607", 
            "name": "EIEE32"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014607", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014607", 
            "name": "epileptic encephalopathy, early infantile, 32; EIEE32"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014607", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014607", 
            "name": "KCNA2 early infantile epileptic encephalopathy"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080416", 
        "description": "An early infantile epileptic encephalopathy characterized by seizure onset between 5 and 17 months of age resulting in residual neurologic deficits; in some patients seizures may remit or respond to drug treatment, and that has_material_basis_in heterozygous mutation in the KCNA2 gene on chromosome 1p13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080416", 
        "name": "early infantile epileptic encephalopathy 32"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0080416#disease-associations", 
            "id": "0080416", 
            "database": "Alliance of Genome Resources"
        }
    ]
}