{
    "disease_id": "DOID:0070367",
    "recommended_name": {
        "id": "DOID:0070367",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0070367",
        "name": "leukoencephalopathy with vanishing white matter 5",
        "description": "A leukoencephalopathy with vanishing white matter that has_material_basis_in homozygous or compound heterozygous mutation in the EIF2B5 gene on chromosome 3q27."
    },
    "synonyms": [
        {
            "id": "DOID:0070367",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070367",
            "name": "Cree leukoencephalopathy",
            "description": ""
        },
        {
            "id": "MONDO:0957873",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0957873",
            "name": "leukoencephalopathy with vanishing white matter 5",
            "description": ""
        },
        {
            "id": "MIM:620315",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/620315",
            "name": "Leukoencephalopathy with vanishing white matter 5",
            "description": "Leukoencephalopathy with vanishing white matter 5"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070367"
    ],
    "unlinked_id_list": []
}