{
    "disease_id": "DOID:0080452",
    "recommended_name": {
        "id": "DOID:0080452",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0080452",
        "name": "early infantile epileptic encephalopathy 28",
        "description": "An early infantile epileptic encephalopathy that has_material_basis_in homozygous or compound heterozygous mutation in the WWOX gene on chromosome 16q23."
    },
    "synonyms": [
        {
            "id": "MONDO:0014533",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014533",
            "name": "epileptic encephalopathy, early infantile, 28",
            "description": "Any early infantile epileptic encephalopathy in which the cause of the disease is a mutation in the WWOX gene."
        },
        {
            "id": "MONDO:0014533",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014533",
            "name": "epileptic encephalopathy, early infantile, 28; EIEE28",
            "description": ""
        },
        {
            "id": "MONDO:0014533",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014533",
            "name": "epileptic encephalopathy, early infantile, 28",
            "description": ""
        },
        {
            "id": "MONDO:0014533",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014533",
            "name": "EIEE28",
            "description": ""
        },
        {
            "id": "MONDO:0014533",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014533",
            "name": "epileptic encephalopathy, early infantile, type 28",
            "description": ""
        },
        {
            "id": "MONDO:0014533",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014533",
            "name": "early infantile epileptic encephalopathy caused by mutation in WWOX",
            "description": ""
        },
        {
            "id": "MONDO:0014533",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014533",
            "name": "WWOX early infantile epileptic encephalopathy",
            "description": ""
        },
        {
            "id": "MIM:616211",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/616211",
            "name": "Developmental and epileptic encephalopathy 28",
            "description": "Developmental and epileptic encephalopathy 28"
        }
    ]
}