{
    "disease_id": "DOID:0060213",
    "recommended_name": {
        "id": "DOID:0060213",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0060213",
        "name": "frontotemporal dementia and/or amyotrophic lateral sclerosis 1",
        "description": "An amyotrophic lateral sclerosis that has_material_basis_in mutation in the C9ORF72 gene on chromosome 9. It is characterized by adult onset of either frontotemporal dementia and/or amyotrophic lateral sclerosis."
    },
    "synonyms": [
        {
            "id": "DOID:0060213",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060213",
            "name": "ALSFTD",
            "description": ""
        },
        {
            "id": "DOID:0060213",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060213",
            "name": "FTDMND",
            "description": ""
        },
        {
            "id": "DOID:0060213",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060213",
            "name": "amyotrophic lateral sclerosis and/or frontotemporal dementia",
            "description": ""
        },
        {
            "id": "DOID:0060213",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060213",
            "name": "frontotemporal dementia and/or motor neuron disease",
            "description": ""
        },
        {
            "id": "DOID:0060213",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060213",
            "name": "FTDALS1",
            "description": ""
        },
        {
            "id": "MONDO:0007105",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007105",
            "name": "frontotemporal dementia and/or amyotrophic lateral sclerosis 1",
            "description": "Any frontotemporal dementia with motor neuron disease in which the cause of the disease is a mutation in the C9orf72 gene."
        },
        {
            "id": "MONDO:0007105",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007105",
            "name": "ALSFTD",
            "description": ""
        },
        {
            "id": "MONDO:0007105",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007105",
            "name": "C9ORF72 frontotemporal dementia with motor neuron disease",
            "description": ""
        },
        {
            "id": "MONDO:0007105",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007105",
            "name": "C9orf72 frontotemporal dementia with motor neuron disease",
            "description": ""
        },
        {
            "id": "MONDO:0007105",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007105",
            "name": "FTDMND",
            "description": ""
        },
        {
            "id": "MONDO:0007105",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007105",
            "name": "amyotrophic lateral sclerosis and/or frontotemporal dementia",
            "description": ""
        },
        {
            "id": "MONDO:0007105",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007105",
            "name": "frontotemporal dementia and/or amyotrophic lateral sclerosis 1",
            "description": ""
        },
        {
            "id": "MONDO:0007105",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007105",
            "name": "frontotemporal dementia and/or amyotrophic lateral sclerosis type 1",
            "description": ""
        },
        {
            "id": "MONDO:0007105",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007105",
            "name": "frontotemporal dementia and/or motor neuron disease",
            "description": ""
        },
        {
            "id": "MONDO:0007105",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007105",
            "name": "frontotemporal dementia with motor neuron disease caused by mutation in C9ORF72",
            "description": ""
        },
        {
            "id": "MONDO:0007105",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007105",
            "name": "frontotemporal dementia with motor neuron disease caused by mutation in C9orf72",
            "description": ""
        },
        {
            "id": "MONDO:0007105",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007105",
            "name": "FTDALS1",
            "description": ""
        },
        {
            "id": "MONDO:0007105",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007105",
            "name": "frontotemporal dementia and/or amyotrophic lateral sclerosis",
            "description": ""
        },
        {
            "id": "MIM:105550",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/105550",
            "name": "Frontotemporal dementia and/or amyotrophic lateral sclerosis 1",
            "description": "Frontotemporal dementia and/or amyotrophic lateral sclerosis 1"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0060213"
    ],
    "unlinked_id_list": []
}