{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014276", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014276", 
            "name": "combined immunodeficiency due to CD3gamma deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014276", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014276", 
            "name": "CD3-gamma deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014276", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014276", 
            "name": "immunodeficiency type 17"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014276", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014276", 
            "name": "immunodeficiency 17"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014276", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014276", 
            "name": "CD3 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014276", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014276", 
            "name": "SCID-like immunodeficiency, T cell-partial, B cell-positive, NK cell-positive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014276", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014276", 
            "name": "immunodeficiency 17; IMD17"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014276", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014276", 
            "name": "IMD17"
        }, 
        {
            "url": "https://www.omim.org/entry/615607", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:615607", 
            "name": "Immunodeficiency 17"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060018", 
        "description": "A severe combined immunodeficiency that has_material_basis_in autosomal recessive mutations in the gene coding for T-cell surface glycoprotein CD3gamma chain precursors.  Patients with CD3gamma deficiency have a severe defect in the expression of the T-cell receptor CD3-complex. Affected patients have decreased T-cell numbers and function; B cells are variably affected.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060018", 
        "name": "CD3gamma deficiency"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/615607", 
            "id": "615607", 
            "database": "MIM"
        }
    ]
}