{
    "disease_id": "DOID:0111972", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014280", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014280", 
            "name": "CD3D severe combined immunodeficiency (disease)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014280", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014280", 
            "name": "SCID, T cell-negative, B cell-positive, NK cell-positive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014280", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014280", 
            "name": "IMD19"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014280", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014280", 
            "name": "CD3delta deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014280", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014280", 
            "name": "immunodeficiency 19; IMD19"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014280", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014280", 
            "name": "severe combined immunodeficiency (disease) caused by mutation in CD3D"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014280", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014280", 
            "name": "immunodeficiency type 19"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014280", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014280", 
            "name": "CD3-Delta deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014280", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014280", 
            "name": "severe combined immunodeficiency, T cell-negative, B cell-positive, NK cell-positive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014280", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014280", 
            "name": "CD3D"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111972", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111972", 
            "name": "CD3-delta deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111972", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111972", 
            "name": "IMD19"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111972", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111972", 
            "name": "SCID T cell-negative, B cell-positive, NK cell-positive"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111972", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111972", 
            "name": "severe combined immunodeficiency, T cell-negative, B cell-positive, NK cell-positive"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111972", 
        "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 CD3D on chromosome 11q23.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111972", 
        "name": "immunodeficiency 19"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111972#disease-associations", 
            "id": "0111972", 
            "database": "Alliance of Genome Resources"
        }
    ]
}