{
    "disease_id": "DOID:0111386",
    "recommended_name": {
        "id": "DOID:0111386",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111386",
        "name": "inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 3",
        "description": "An inclusion body myopathy with Paget disease of bone and frontotemporal dementia that has_material_basis_in heterozygous mutation in the HNRNPA1 gene on chromosome 12q13.13."
    },
    "synonyms": [
        {
            "id": "DOID:0111386",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111386",
            "name": "IBMPFD3",
            "description": ""
        },
        {
            "id": "DOID:0111386",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111386",
            "name": "MSP3",
            "description": ""
        },
        {
            "id": "DOID:0111386",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111386",
            "name": "multisystem proteinopathy 3",
            "description": ""
        },
        {
            "id": "MONDO:0014179",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014179",
            "name": "inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 3",
            "description": "Any inclusion body myopathy with Paget disease of bone and frontotemporal dementia in which the cause of the disease is a mutation in the HNRNPA1 gene."
        },
        {
            "id": "MONDO:0014179",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014179",
            "name": "HNRNPA1 inclusion body myopathy with Paget disease of bone and frontotemporal dementia",
            "description": ""
        },
        {
            "id": "MONDO:0014179",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014179",
            "name": "inclusion body myopathy with Paget disease of bone and frontotemporal dementia caused by mutation in HNRNPA1",
            "description": ""
        },
        {
            "id": "MONDO:0014179",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014179",
            "name": "inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 3",
            "description": ""
        },
        {
            "id": "MONDO:0014179",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014179",
            "name": "inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia type 3",
            "description": ""
        },
        {
            "id": "MONDO:0014179",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014179",
            "name": "inclusion body myopathy with early-onset paget disease without frontotemporal dementia 3",
            "description": ""
        },
        {
            "id": "MONDO:0014179",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014179",
            "name": "IBMPFD3",
            "description": ""
        },
        {
            "id": "MIM:615424",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/615424",
            "name": "Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 3",
            "description": "Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 3"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111386"
    ],
    "unlinked_id_list": []
}