{
    "disease_id": "DOID:0111935", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014268", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014268", 
            "name": "combined immunodeficiency due to OX40 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014268", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014268", 
            "name": "immunodeficiency 16; IMD16"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014268", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014268", 
            "name": "IMD16"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014268", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014268", 
            "name": "immunodeficiency type 16"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014268", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014268", 
            "name": "combined immunodeficiency with childhood-onset Kaposi sarcoma"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014268", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014268", 
            "name": "combined immunodeficiency with impaired immunity to human herpes virus 8"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014268", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014268", 
            "name": "OX40 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014268", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014268", 
            "name": "combined immunodeficiency with impaired immunity to HHV-8"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111935", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111935", 
            "name": "IMD16"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111935", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111935", 
            "name": "OX40 deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111935", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111935", 
            "name": "combined immunodeficiency with impaired immunity to HHV-8"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111935", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111935", 
            "name": "combined immunodeficiency with impaired immunity to human herpes virus 8"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111935", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111935", 
            "name": "combined immunodeficiency with childhood-onset Kaposi sarcoma"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111935", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111935", 
            "name": "combined immunodeficiency due to OX40 deficiency"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111935", 
        "description": "A combined T cell and B cell immunodeficiency characterized by classic Kaposi sarcoma of childhood, poor T-cell recall immune responses, and decrease in the proportion of circulating memory B cells that has_material_basis_in homozygous or compound heterozygous mutation in TNFRSF4 on chromosome 1p36.33.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111935", 
        "name": "immunodeficiency 16"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111935#disease-associations", 
            "id": "0111935", 
            "database": "Alliance of Genome Resources"
        }
    ]
}