{
    "disease_id": "DOID:0080432",
    "recommended_name": {
        "id": "DOID:0080432",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0080432",
        "name": "early infantile epileptic encephalopathy 60",
        "description": "An early infantile epileptic encephalopathy that has_material_basis_in homozygous or compound heterozygous mutation in the CNPY3 gene on chromosome 6p."
    },
    "synonyms": [
        {
            "id": "MONDO:0033369",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0033369",
            "name": "epileptic encephalopathy, early infantile, 60",
            "description": ""
        },
        {
            "id": "MONDO:0033369",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0033369",
            "name": "epileptic encephalopathy, early infantile, 60; EIEE60",
            "description": ""
        },
        {
            "id": "MONDO:0033369",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0033369",
            "name": "EIEE60",
            "description": ""
        },
        {
            "id": "MIM:617929",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/617929",
            "name": "Developmental and epileptic encephalopathy 60",
            "description": "Developmental and epileptic encephalopathy 60"
        }
    ]
}