{
    "disease_id": "DOID:0112005",
    "recommended_name": {
        "id": "DOID:0112005",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0112005",
        "name": "immunodeficiency 70",
        "description": "A combined T cell and B cell immunodeficiency characterized by decreased CD4+ T cells, decreased CD19+ B cells, recurrent bacterial infections, and severe cutaneous warts on the hands, feet, and face that has_material_basis_in heterozygous mutation in the IVNS1ABP gene on chromosome 1q25.3."
    },
    "synonyms": [
        {
            "id": "DOID:0112005",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0112005",
            "name": "IMD70",
            "description": ""
        },
        {
            "id": "MONDO:0033542",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0033542",
            "name": "immunodeficiency 70",
            "description": ""
        },
        {
            "id": "MONDO:0033542",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0033542",
            "name": "IMD70",
            "description": ""
        },
        {
            "id": "MIM:618969",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/618969",
            "name": "Immunodeficiency 70",
            "description": "Immunodeficiency 70"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0112005"
    ],
    "unlinked_id_list": []
}