{
    "disease_id": "DOID:0110069", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014641", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014641", 
            "name": "FTDALS4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014641", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014641", 
            "name": "frontotemporal dementia and/or amyotrophic lateral sclerosis 4; FTDALS4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014641", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014641", 
            "name": "frontotemporal dementia and/or amyotrophic lateral sclerosis 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014641", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014641", 
            "name": "frontotemporal dementia and/or amyotrophic lateral sclerosis type 4"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110069", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110069", 
            "name": "FTDALS4"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110069", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110069", 
            "name": "frontotemporal dementia and/or amyotrophic lateral sclerosis 4"
        }, 
        {
            "url": "https://www.omim.org/entry/616439", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:616439", 
            "name": "Frontotemporal dementia and/or amyotrophic lateral sclerosis 4"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110069", 
        "description": "An amyotrophic lateral sclerosis that has_material_basis_in mutation in the TBK1 gene on chromosome 12q14.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110069", 
        "name": "frontotemporal dementia and/or amyotrophic lateral sclerosis-4"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/616439", 
            "id": "616439", 
            "database": "MIM"
        }
    ]
}