{
    "disease_id": "DOID:0111227",
    "recommended_name": {
        "id": "DOID:0111227",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111227",
        "name": "chromosome 3-linked frontotemporal dementia",
        "description": "A frontotemporal dementia that has_material_basis_in heterozygous mutation in CHMP2B on 3p11.2."
    },
    "synonyms": [
        {
            "id": "DOID:0111227",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111227",
            "name": "amyotrophic lateral sclerosis type 17",
            "description": ""
        },
        {
            "id": "DOID:0111227",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111227",
            "name": "FTD3",
            "description": ""
        },
        {
            "id": "DOID:0111227",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111227",
            "name": "CHMP2B-related frontotemporal dementia",
            "description": ""
        },
        {
            "id": "MONDO:0010936",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010936",
            "name": "frontotemporal dementia and/or amyotrophic lateral sclerosis 7",
            "description": "Any amyotrophic lateral sclerosis in which the cause of the disease is a mutation in the CHMP2B gene."
        },
        {
            "id": "MONDO:0010936",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010936",
            "name": "CHMP2B amyotrophic lateral sclerosis",
            "description": ""
        },
        {
            "id": "MONDO:0010936",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010936",
            "name": "CHMP2B-related amyotrophic lateral sclerosis",
            "description": ""
        },
        {
            "id": "MONDO:0010936",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010936",
            "name": "FTD3",
            "description": ""
        },
        {
            "id": "MONDO:0010936",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010936",
            "name": "amyotrophic lateral sclerosis caused by mutation in CHMP2B",
            "description": ""
        },
        {
            "id": "MONDO:0010936",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010936",
            "name": "amyotrophic lateral sclerosis, Chmp2B-related",
            "description": ""
        },
        {
            "id": "MONDO:0010936",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010936",
            "name": "frontotemporal dementia, chromosome 3-linked",
            "description": ""
        },
        {
            "id": "MONDO:0010936",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010936",
            "name": "Dmt1",
            "description": ""
        },
        {
            "id": "MONDO:0010936",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010936",
            "name": "dementia, familial nonspecific",
            "description": ""
        },
        {
            "id": "MONDO:0010936",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010936",
            "name": "frontotemporal dementia and/or amyotrophic lateral sclerosis 7",
            "description": "Any amyotrophic lateral sclerosis in which the cause of the disease is a mutation in the CHMP2B gene."
        },
        {
            "id": "MONDO:0010936",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010936",
            "name": "CHMP2B amyotrophic lateral sclerosis",
            "description": ""
        },
        {
            "id": "MONDO:0010936",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010936",
            "name": "CHMP2B-related amyotrophic lateral sclerosis",
            "description": ""
        },
        {
            "id": "MONDO:0010936",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010936",
            "name": "FTD3",
            "description": ""
        },
        {
            "id": "MONDO:0010936",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010936",
            "name": "amyotrophic lateral sclerosis caused by mutation in CHMP2B",
            "description": ""
        },
        {
            "id": "MONDO:0010936",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010936",
            "name": "amyotrophic lateral sclerosis, Chmp2B-related",
            "description": ""
        },
        {
            "id": "MONDO:0010936",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010936",
            "name": "frontotemporal dementia, chromosome 3-linked",
            "description": ""
        },
        {
            "id": "MONDO:0010936",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010936",
            "name": "Dmt1",
            "description": ""
        },
        {
            "id": "MONDO:0010936",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010936",
            "name": "dementia, familial nonspecific",
            "description": ""
        },
        {
            "id": "MIM:600795",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/600795",
            "name": "Frontotemporal dementia and/or amyotrophic lateral sclerosis 7",
            "description": "Frontotemporal dementia and/or amyotrophic lateral sclerosis 7"
        }
    ]
}