{
    "disease_id": "DOID:0111956", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014429", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014429", 
            "name": "autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014429", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014429", 
            "name": "immunodeficiency type 27B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014429", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014429", 
            "name": "autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial interferon gamma receptor 1 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014429", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014429", 
            "name": "IFNGR1 deficiency, autosomal dominant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014429", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014429", 
            "name": "autosomal dominant MSMD due to partial IFNgammaR1 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014429", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014429", 
            "name": "IMD27B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014429", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014429", 
            "name": "immunodeficiency 27B; IMD27B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014429", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014429", 
            "name": "IFNGR1 autosomal dominant mendelian susceptibility to mycobacterial diseases due to a partial deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014429", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014429", 
            "name": "autosomal dominant mendelian susceptibility to mycobacterial diseases due to a partial deficiency caused by mutation in IFNGR1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014429", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014429", 
            "name": "immunodeficiency 27B, Mycobacteriosis, autosomal dominant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014429", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014429", 
            "name": "autosomal dominant MSMD due to partial interferon gamma receptor 1 deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111956", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111956", 
            "name": "IMD27B"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111956", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111956", 
            "name": "autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial interferon gamma receptor 1 deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111956", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111956", 
            "name": "autosomal dominant IFNGR1 deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111956", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111956", 
            "name": "autosomal dominant MSMD due to partial IFNgammaR1 deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111956", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111956", 
            "name": "autosomal dominant immunodeficiency 27B, mycobacteriosis"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111956", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111956", 
            "name": "autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111956", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111956", 
            "name": "autosomal dominant MSMD due to partial interferon gamma receptor 1 deficiency"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111956", 
        "description": "A primary immunodeficiency disease characterized by residual cellular responses to IFNG in vitro, recurrent, moderately severe infections with environmental mycobacteria or bacillus Calmette-Guerin that has_material_basis_in heterozygous mutation in IFNGR1 on chromosome 6q23.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111956", 
        "name": "immunodeficiency 27B"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111956#disease-associations", 
            "id": "0111956", 
            "database": "Alliance of Genome Resources"
        }
    ]
}