{
    "disease_id": "DOID:0070372",
    "recommended_name": {
        "id": "DOID:0070372",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0070372",
        "name": "leukoencephalopathy with vanishing white matter 3",
        "description": "A leukoencephalopathy with vanishing white matter that has_material_basis_in homozygous or compound heterozygous mutation in the EIF2B3 gene on chromosome 1p34."
    },
    "synonyms": [
        {
            "id": "MIM:620313",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/620313",
            "name": "Leukoencephalopathy with vanishing white matter 3",
            "description": "Leukoencephalopathy with vanishing white matter 3"
        }
    ]
}