{
    "disease_id": "DOID:0111972",
    "recommended_name": {
        "id": "DOID:0111972",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111972",
        "name": "immunodeficiency 19",
        "description": "A severe combined immunodeficiency characterized by onset in early infancy of recurrent bacterial, viral, and fungal infections with a T cell-negative, B cell-positive, natural killer cell-positive immune cell phenotype that has_material_basis_in homozygous or compound heterozygous mutation in the CD3D gene on chromosome 11q23.3."
    },
    "synonyms": [
        {
            "id": "DOID:0111972",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111972",
            "name": "SCID T cell-negative, B cell-positive, NK cell-positive",
            "description": ""
        },
        {
            "id": "DOID:0111972",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111972",
            "name": "CD3-delta deficiency",
            "description": ""
        },
        {
            "id": "DOID:0111972",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111972",
            "name": "IMD19",
            "description": ""
        },
        {
            "id": "DOID:0111972",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111972",
            "name": "severe combined immunodeficiency, T cell-negative, B cell-positive, NK cell-positive",
            "description": ""
        },
        {
            "id": "MONDO:0014280",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014280",
            "name": "immunodeficiency 19",
            "description": "Any severe combined immunodeficiency in which the cause of the disease is a mutation in the CD3D gene."
        },
        {
            "id": "MONDO:0014280",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014280",
            "name": "CD3D severe combined immunodeficiency (disease)",
            "description": ""
        },
        {
            "id": "MONDO:0014280",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014280",
            "name": "CD3delta deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0014280",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014280",
            "name": "immunodeficiency 19",
            "description": ""
        },
        {
            "id": "MONDO:0014280",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014280",
            "name": "immunodeficiency type 19",
            "description": ""
        },
        {
            "id": "MONDO:0014280",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014280",
            "name": "severe combined immunodeficiency (disease) caused by mutation in CD3D",
            "description": ""
        },
        {
            "id": "MONDO:0014280",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014280",
            "name": "IMD19",
            "description": ""
        },
        {
            "id": "MIM:615617",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/615617",
            "name": "Immunodeficiency 19, severe combined",
            "description": "Immunodeficiency 19, severe combined"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111972"
    ],
    "unlinked_id_list": []
}