{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010857", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010857", 
            "name": "semantic dementia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010857", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010857", 
            "name": "frontotemporal lobar Degeneration with Tau inclusions"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010857", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010857", 
            "name": "Wilhelmsen-Lynch disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010857", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010857", 
            "name": "frontotemporal dementia with Parkinsonism"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010857", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010857", 
            "name": "frontotemporal lobe dementia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010857", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010857", 
            "name": "disinhibition-dementia-Parkinsonism-amyotrophy Complex"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010857", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010857", 
            "name": "semantic primary progressive aphasia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010857", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010857", 
            "name": "multiple system tauopathy with presenile dementia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010857", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010857", 
            "name": "dementia, frontotemporal, with Parkinsonism"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010857", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010857", 
            "name": "frontotemporal dementia; FTD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010857", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010857", 
            "name": "Pallidopontonigral Degeneration"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010857", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010857", 
            "name": "Pick Complex"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010857", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010857", 
            "name": "Ftdp17"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010857", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010857", 
            "name": "FTD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010857", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010857", 
            "name": "Ftld with Tau inclusions"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010857", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010857", 
            "name": "semantic variant PPA"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:9255", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:9255", 
            "name": "Wilhemsen-Lynch disease"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:9255", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:9255", 
            "name": "frontotemporal lobar degeneration"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:9255", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:9255", 
            "name": "multiple system tauopathy with presenile dementia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:9255", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:9255", 
            "name": "pallidopontonigral degeneration"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:9255", 
        "description": "A dementia characterized by progressive neuronal loss predominantly involving the frontal and/or temporal lobes of the brain resulting in a gradual and progressive decline in behavior or language.", 
        "resource": "Disease Ontology", 
        "id": "DOID:9255", 
        "name": "frontotemporal dementia"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/600274", 
            "id": "600274", 
            "database": "MIM"
        }
    ]
}