{
    "disease_id": "DOID:0111939",
    "recommended_name": {
        "id": "DOID:0111939",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111939",
        "name": "immunodeficiency 37",
        "description": "A combined T cell and B cell immunodeficiency characterized by hypogammaglobulinemia with profoundly reduced memory B cells and memory T cells and increased numbers of circulating naive lymphocytes that has_material_basis_in homozygous or compound heterozygous mutation in the BCL10 gene on chromosome 1p22.3."
    },
    "synonyms": [
        {
            "id": "DOID:0111939",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111939",
            "name": "IMD37",
            "description": ""
        },
        {
            "id": "MONDO:0014491",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014491",
            "name": "immunodeficiency 37",
            "description": "Any primary immunodeficiency disease in which the cause of the disease is a mutation in the BCL10 gene."
        },
        {
            "id": "MONDO:0014491",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014491",
            "name": "BCL10 primary immunodeficiency disease",
            "description": ""
        },
        {
            "id": "MONDO:0014491",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014491",
            "name": "combined immunodeficiency due to BCL10 deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0014491",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014491",
            "name": "immunodeficiency 37",
            "description": ""
        },
        {
            "id": "MONDO:0014491",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014491",
            "name": "immunodeficiency type 37",
            "description": ""
        },
        {
            "id": "MONDO:0014491",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014491",
            "name": "primary immunodeficiency disease caused by mutation in BCL10",
            "description": ""
        },
        {
            "id": "MONDO:0014491",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014491",
            "name": "IMD37",
            "description": ""
        },
        {
            "id": "MIM:616098",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/616098",
            "name": "Immunodeficiency 37",
            "description": "Immunodeficiency 37"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111939"
    ],
    "unlinked_id_list": []
}