{
    "disease_id": "DOID:0111955",
    "recommended_name": {
        "id": "DOID:0111955",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111955",
        "name": "immunodeficiency 27A",
        "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 the IFNGR1 gene on chromosome 6q23.3."
    },
    "synonyms": [
        {
            "id": "DOID:0111955",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111955",
            "name": "autosomal recessive MSMD due to partial IFNgammaR1 deficiency",
            "description": ""
        },
        {
            "id": "DOID:0111955",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111955",
            "name": "IMD27A",
            "description": ""
        },
        {
            "id": "DOID:0111955",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111955",
            "name": "autosomal recessive immunodeficiency 27A, mycobacteriosis",
            "description": ""
        },
        {
            "id": "DOID:0111955",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111955",
            "name": "autosomal recessive IFNGR1 deficiency",
            "description": ""
        },
        {
            "id": "DOID:0111955",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111955",
            "name": "autosomal recessive mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency",
            "description": ""
        },
        {
            "id": "DOID:0111955",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111955",
            "name": "autosomal recessive mendelian susceptibility to mycobacterial diseases due to partial interferon gamma receptor 1 deficiency",
            "description": ""
        },
        {
            "id": "DOID:0111955",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111955",
            "name": "autosomal recessive MSMD due to partial interferon gamma receptor 1 deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0008856",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008856",
            "name": "immunodeficiency 27A",
            "description": ""
        },
        {
            "id": "MONDO:0008856",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008856",
            "name": "immunodeficiency 27A",
            "description": ""
        },
        {
            "id": "MONDO:0008856",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008856",
            "name": "immunodeficiency 27A, mycobacteriosis, AR",
            "description": ""
        },
        {
            "id": "MONDO:0008856",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008856",
            "name": "immunodeficiency type 27A",
            "description": ""
        },
        {
            "id": "MONDO:0008856",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008856",
            "name": "IFNGR1 deficiency, autosomal recessive",
            "description": ""
        },
        {
            "id": "MONDO:0008856",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008856",
            "name": "IMD27A",
            "description": ""
        },
        {
            "id": "MONDO:0008856",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008856",
            "name": "atypical mycobacterial infection, disseminated",
            "description": ""
        },
        {
            "id": "MONDO:0008856",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008856",
            "name": "atypical mycobacterial infection, familial disseminated",
            "description": ""
        },
        {
            "id": "MONDO:0008856",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008856",
            "name": "atypical mycobacteriosis, familial",
            "description": ""
        },
        {
            "id": "MONDO:0008856",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008856",
            "name": "immunodeficiency 27A, Mycobacteriosis, autosomal recessive",
            "description": ""
        },
        {
            "id": "MONDO:0008856",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008856",
            "name": "mycobacterial disease, Mendelian susceptibility to",
            "description": ""
        },
        {
            "id": "MIM:209950",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/209950",
            "name": "Immunodeficiency 27A",
            "description": "Immunodeficiency 27A"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111955"
    ],
    "unlinked_id_list": []
}