{
    "disease_id": "DOID:0060672",
    "recommended_name": {
        "id": "DOID:0060672",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0060672",
        "name": "frontotemporal dementia 2",
        "description": "A frontotemporal dementia characterized by variable phenotypic expression typically including social, behavioral, or language deterioration, rather than memory or motor deficits and the presence of TARDBP-positive inclusions that has_material_basis_in mutation in the GRN gene on chromosome 17q21.31."
    },
    "synonyms": [
        {
            "id": "DOID:0060672",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060672",
            "name": "GRN-related frontotemporal lobar degeneration with Tdp43 inclusions",
            "description": ""
        },
        {
            "id": "MONDO:0011842",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011842",
            "name": "GRN-related frontotemporal lobar degeneration with Tdp43 inclusions",
            "description": "A frontotemporal dementia characterized by variable phenotypic expression typically including social, behavioral, or language deterioration, rather than memory or motor deficits and the presence of TARDBP-positive inclusions that has material basis in mutation in the GRN gene on chromosome 17q21.31."
        },
        {
            "id": "MIM:607485",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/607485",
            "name": "Frontotemporal dementia 2",
            "description": "Frontotemporal dementia 2"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0060672"
    ],
    "unlinked_id_list": []
}