{
    "disease_id": "DOID:0060672", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011842", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011842", 
            "name": "frontotemporal dementia with Tdp43 inclusions, Grn-related"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011842", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011842", 
            "name": "frontotemporal lobar degeneration with Tdp43 inclusions, Grn-related"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011842", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011842", 
            "name": "frontotemporal dementia, ubiquitin-positive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011842", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011842", 
            "name": "frontotemporal lobar Degeneration with ubiquitin-positive inclusions"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011842", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011842", 
            "name": "aphasia, primary progressive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011842", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011842", 
            "name": "dementia, hereditary dysphasic disinhibition"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011842", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011842", 
            "name": "Ftld-TDP, Grn-related"
        }, 
        {
            "url": "https://www.omim.org/entry/607485", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:607485", 
            "name": "Ubiquitin-positive frontotemporal dementia"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060672", 
        "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060672", 
        "name": "Grn-related frontotemporal lobar degeneration with Tdp43 inclusions"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/607485", 
            "id": "607485", 
            "database": "MIM"
        }
    ]
}