{
    "disease_id": "DOID:0111955", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008856", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008856", 
            "name": "immunodeficiency type 27A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008856", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008856", 
            "name": "atypical mycobacterial infection, familial disseminated"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008856", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008856", 
            "name": "IFNGR1 deficiency, autosomal recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008856", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008856", 
            "name": "IMD27A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008856", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008856", 
            "name": "immunodeficiency 27A; IMD27A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008856", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008856", 
            "name": "atypical mycobacterial infection, disseminated"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008856", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008856", 
            "name": "immunodeficiency 27A, Mycobacteriosis, autosomal recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008856", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008856", 
            "name": "atypical mycobacteriosis, familial"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008856", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008856", 
            "name": "mycobacterial disease, Mendelian susceptibility to"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111955", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111955", 
            "name": "IMD27A"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111955", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111955", 
            "name": "autosomal recessive MSMD due to partial IFNgammaR1 deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111955", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111955", 
            "name": "autosomal recessive immunodeficiency 27A, mycobacteriosis"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111955", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111955", 
            "name": "autosomal recessive IFNGR1 deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111955", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111955", 
            "name": "autosomal recessive mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111955", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111955", 
            "name": "autosomal recessive mendelian susceptibility to mycobacterial diseases due to partial interferon gamma receptor 1 deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111955", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111955", 
            "name": "autosomal recessive MSMD due to partial interferon gamma receptor 1 deficiency"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111955", 
        "description": "A primary immunodeficiency disease characterized by high circulating levels of IFNG, failure of cellular responses to IFNG, and early and often fatal mycobacterial infections that has_material_basis_in homozygous or compound heterozygous mutation in IFNGR1 on chromosome 6q23.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111955", 
        "name": "immunodeficiency 27A"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111955#disease-associations", 
            "id": "0111955", 
            "database": "Alliance of Genome Resources"
        }
    ]
}