{
    "disease_id": "DOID:0060201", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012790", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012790", 
            "name": "Ftld-TDP, Tardbp-related"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012790", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012790", 
            "name": "amyotrophic lateral sclerosis 10, with or without frontotemporal dementia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012790", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012790", 
            "name": "amyotrophic lateral sclerosis 10"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012790", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012790", 
            "name": "frontotemporal lobar Degeneration with Tdp43 inclusions, Tardbp-related"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012790", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012790", 
            "name": "TARDBP-related frontotemporal lobar degeneration with Tdp43 inclusions"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012790", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012790", 
            "name": "frontotemporal dementia with Tdp43 inclusions, Tardbp-related"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012790", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012790", 
            "name": "ALS10"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012790", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012790", 
            "name": "TARDBP amyotrophic lateral sclerosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012790", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012790", 
            "name": "amyotrophic lateral sclerosis 10 with or without frontotemporal dementia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012790", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012790", 
            "name": "amyotrophic lateral sclerosis 10 with or without frontotemporal dementia; ALS10"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012790", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012790", 
            "name": "amyotrophic lateral sclerosis caused by mutation in TARDBP"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060201", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060201", 
            "name": "TARDBP-related frontotemporal lobar degeneration with TDP43 inclusions"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060201", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060201", 
            "name": "ALS10"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060201", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060201", 
            "name": "amyotrophic lateral sclerosis 10"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060201", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060201", 
            "name": "amyotrophic lateral sclerosis 10, with or without frontotemporal dementia"
        }, 
        {
            "url": "https://www.omim.org/entry/612069", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:612069", 
            "name": "Amyotrophic lateral sclerosis 10"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060201", 
        "description": "An amyotrophic lateral sclerosis that has_material_basis_in mutation in the TARDBP gene on chromosome 1.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060201", 
        "name": "amyotrophic lateral sclerosis type 10"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/612069", 
            "id": "612069", 
            "database": "MIM"
        }
    ]
}
