{
    "disease_id": "DOID:0111978",
    "recommended_name": {
        "id": "DOID:0111978",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111978",
        "name": "immunodeficiency 65",
        "description": "A primary immunodeficiency disease characterized by onset in early infancy of recurrent and severe viral infections, impaired cellular type I interferon response, and poor outcomes after vaccination with live attenuated vaccines that has_material_basis_in homozygous or compound heterozygous mutation in the IRF9 gene on chromosome 14q12."
    },
    "synonyms": [
        {
            "id": "DOID:0111978",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111978",
            "name": "IMD65",
            "description": ""
        },
        {
            "id": "DOID:0111978",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111978",
            "name": "immunodeficiency 65, susceptibility to viral infections",
            "description": ""
        },
        {
            "id": "MONDO:0032848",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0032848",
            "name": "immunodeficiency 65, susceptibility to viral infections",
            "description": ""
        },
        {
            "id": "MONDO:0032848",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0032848",
            "name": "IMD65",
            "description": ""
        },
        {
            "id": "MIM:618648",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/618648",
            "name": "Immunodeficiency 65",
            "description": "Immunodeficiency 65"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111978"
    ],
    "unlinked_id_list": []
}