{
    "disease_id": "DOID:0111995", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013953", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013953", 
            "name": "Ifngr2 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013953", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013953", 
            "name": "IFNGR2 primary immunodeficiency disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013953", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013953", 
            "name": "immunodeficiency 28; IMD28"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013953", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013953", 
            "name": "IMD28"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013953", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013953", 
            "name": "immunodeficiency 28, Mycobacteriosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013953", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013953", 
            "name": "immunodeficiency type 28"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013953", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013953", 
            "name": "primary immunodeficiency disease caused by mutation in IFNGR2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111995", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111995", 
            "name": "Mendelian susceptibility to mycobacterial diseases due to complete IFNgammaR2 deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111995", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111995", 
            "name": "IMD28"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111995", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111995", 
            "name": "MSMD due to complete interferon gamma receptor 2 deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111995", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111995", 
            "name": "IFNGR2 deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111995", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111995", 
            "name": "MSMD due to complete IFNgammaR2 deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111995", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111995", 
            "name": "immunodeficiency 28, mycobacteriosis"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111995", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111995", 
            "name": "Mendelian susceptibility to mycobacterial diseases due to complete interferon gamma receptor 2 deficiency"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111995", 
        "description": "A primary immunodeficiency disease characterized by increased susceptibility to mycobacterial disease, high levels of IFNG in the plasma, and absence of cellular response to IFNG that has_material_basis_in homozygous or compound heterozygous mutation in IFNGR2 on chromosome 21q22.11.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111995", 
        "name": "immunodeficiency 28"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111995#disease-associations", 
            "id": "0111995", 
            "database": "Alliance of Genome Resources"
        }
    ]
}