{
    "disease_id": "DOID:0111968", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011664", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011664", 
            "name": "immunodeficiency due to CD25 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011664", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011664", 
            "name": "IL2RA deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011664", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011664", 
            "name": "Interleukin 2 receptor, alpha, deficiency of"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011664", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011664", 
            "name": "immunodeficiency 41 with lymphoproliferation and autoimmunity"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011664", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011664", 
            "name": "immunodeficiency 41 with lymphoproliferation and autoimmunity; IMD41"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011664", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011664", 
            "name": "IMD41"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011664", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011664", 
            "name": "Interleukin-2 receptor alpha chain deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011664", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011664", 
            "name": "CD25 deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111968", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111968", 
            "name": "CD25 deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111968", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111968", 
            "name": "IL2RA deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111968", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111968", 
            "name": "IMD41"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111968", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111968", 
            "name": "immunodeficiency due to CD25 deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111968", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111968", 
            "name": "interleukin-2 receptor alpha chain deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111968", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111968", 
            "name": "immunodeficiency 41 with lymphoproliferation and autoimmunity"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111968", 
        "description": "A combined immunodeficiency characterized by a defect in T cell regulation with proliferation of CD8+ T cells, impaired antibody specific responses, and elevated cytokines resulting in recurrent viral, fungal, and bacterial infections, lymphadenopathy, and variable autoimmune features that has_material_basis_in homozygous or compound heterozygous mutation in IL2RA on chromosome 10p15.1.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111968", 
        "name": "immunodeficiency 41"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111968#disease-associations", 
            "id": "0111968", 
            "database": "Alliance of Genome Resources"
        }
    ]
}