{
    "disease_id": "DOID:0111950",
    "recommended_name": {
        "id": "DOID:0111950",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111950",
        "name": "immunodeficiency 29",
        "description": "A primary immunodeficiency disease characterized by undetectable IL12B secretion by leukocytes and increased susceptibility to intracellular bacterial infections that has_material_basis_in homozygous or compound heterozygous mutation in IL12B on chromosome 5q33.3."
    },
    "synonyms": [
        {
            "id": "DOID:0111950",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111950",
            "name": "Mendelian susceptibility to mycobacterial diseases due to complete IL12B deficiency",
            "description": ""
        },
        {
            "id": "DOID:0111950",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111950",
            "name": "IL12B deficiency",
            "description": ""
        },
        {
            "id": "DOID:0111950",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111950",
            "name": "IMD29",
            "description": ""
        },
        {
            "id": "DOID:0111950",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111950",
            "name": "MSMD due to complete IL12B deficiency",
            "description": ""
        },
        {
            "id": "DOID:0111950",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111950",
            "name": "MSMD due to complete interleukin 12B deficiency",
            "description": ""
        },
        {
            "id": "DOID:0111950",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111950",
            "name": "immunodeficiency 29, mycobacteriosis",
            "description": ""
        },
        {
            "id": "DOID:0111950",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111950",
            "name": "Mendelian susceptibility to mycobacterial diseases due to complete interleukin 12B deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0013954",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013954",
            "name": "mendelian susceptibility to mycobacterial diseases due to complete IL12B deficiency",
            "description": "Any autosomal recessive mendelian susceptibility to mycobacterial diseases due to a complete deficiency in which the cause of the disease is a mutation in the IL12B gene."
        },
        {
            "id": "MONDO:0013954",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013954",
            "name": "MSMD due to complete IL12B deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0013954",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013954",
            "name": "immunodeficiency type 29",
            "description": ""
        },
        {
            "id": "MONDO:0013954",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013954",
            "name": "IL12B deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0013954",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013954",
            "name": "immunodeficiency 29",
            "description": ""
        },
        {
            "id": "MONDO:0013954",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013954",
            "name": "MSMD due to complete interleukin 12B deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0013954",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013954",
            "name": "autosomal recessive mendelian susceptibility to mycobacterial diseases due to a complete deficiency caused by mutation in IL12B",
            "description": ""
        },
        {
            "id": "MONDO:0013954",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013954",
            "name": "immunodeficiency 29; IMD29",
            "description": ""
        },
        {
            "id": "MONDO:0013954",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013954",
            "name": "Mendelian susceptibility to mycobacterial diseases due to complete interleukin 12B deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0013954",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013954",
            "name": "IMD29",
            "description": ""
        },
        {
            "id": "MONDO:0013954",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013954",
            "name": "IL12B autosomal recessive mendelian susceptibility to mycobacterial diseases due to a complete deficiency",
            "description": ""
        },
        {
            "id": "MIM:614890",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/614890",
            "name": "Immunodeficiency 29",
            "description": "Immunodeficiency 29"
        }
    ]
}