{
    "disease_id": "DOID:0111985", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009194", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009194", 
            "name": "chronic Epstein-Barr virus infection syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009194", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009194", 
            "name": "CAEBV syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009194", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009194", 
            "name": "IMD32B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009194", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009194", 
            "name": "CAEBV infection"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009194", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009194", 
            "name": "immunodeficiency 32B; IMD32B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009194", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009194", 
            "name": "chronic active Epstein-Barr virus infection"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009194", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009194", 
            "name": "chronic EBV infection syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009194", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009194", 
            "name": "Epstein-Barr VIRUS, susceptibility to chronic infection by"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009194", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009194", 
            "name": "chronic active Epstein-Barr disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009194", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009194", 
            "name": "CEBV"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009194", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009194", 
            "name": "immunodeficiency 32B, monocyte, Dendritic cell, and natural Killer cell deficiency, autosomal recessive"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111985", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111985", 
            "name": "IMD32B"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111985", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111985", 
            "name": "autosomal recessive IRF8 deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111985", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111985", 
            "name": "immunodeficiency 32B, monocyte and dendritic cell deficiency, autosomal recessive"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111985", 
        "description": "A monocyte, dendritic cell, and NK cell deficiency characterized by defects in monocyte, dendritic cell, and natural killer (NK) cell development or function resulting recurrent infections particularly viral nfections that has_material_basis_in homozygous or compound heterozygous mutation in IRF8 on chromosome 16q24.1.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111985", 
        "name": "immunodeficiency 32B"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111985#disease-associations", 
            "id": "0111985", 
            "database": "Alliance of Genome Resources"
        }
    ]
}