{
    "disease_id": "DOID:0060475", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014150", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014150", 
            "name": "CHD2 myoclonic encephalopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014150", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014150", 
            "name": "CHCHD10-related disorders"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014150", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014150", 
            "name": "EEOC"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014150", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014150", 
            "name": "epileptic encephalopathy, childhood-onset"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014150", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014150", 
            "name": "epileptic encephalopathy, childhood-onset; EEOC"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014150", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014150", 
            "name": "childhood-onset epileptic encephalopathy"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060475", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060475", 
            "name": "EEOC"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060475", 
        "description": "An idiopathic generalized epilepsy characterized by onset of multiple seizure types in the first few years of life and associated with poor prognosis. Affected individuals have cognitive regression and intellectual disability.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060475", 
        "name": "childhood onset epileptic encephalopathy"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060475#disease-associations", 
            "id": "0060475", 
            "database": "Alliance of Genome Resources"
        }
    ]
}