{
    "disease_id": "DOID:0060204",
    "recommended_name": {
        "id": "DOID:0060204",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0060204",
        "name": "amyotrophic lateral sclerosis type 13",
        "description": "An amyotrophic lateral sclerosis where a mutation that has_material_basis_in the ATXN2 gene on chromosome 12 contributes to suscepitbility."
    },
    "synonyms": [
        {
            "id": "DOID:0060204",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060204",
            "name": "ALS13",
            "description": ""
        },
        {
            "id": "DOID:0060204",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060204",
            "name": "amyotrophic lateral sclerosis 13",
            "description": ""
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0060204"
    ],
    "unlinked_id_list": []
}