{
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    "synonyms": [
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            "description": "", 
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        }, 
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            "description": "", 
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        }, 
        {
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        }, 
        {
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        }, 
        {
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        }, 
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            "description": "", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013955", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013955", 
            "name": "IL12RB1 autosomal recessive mendelian susceptibility to mycobacterial diseases due to a complete deficiency"
        }, 
        {
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            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111990", 
            "name": "Mendelian susceptibility to mycobacterial diseases due to complete IL12RB1 deficiency"
        }, 
        {
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            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111990", 
            "name": "IMD30"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111990", 
            "description": "", 
            "resource": "Disease Ontology", 
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            "name": "Mendelian susceptibility to interleukin 12 receptor beta 1 deficiency"
        }, 
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            "description": "", 
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            "description": "", 
            "resource": "Disease Ontology", 
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        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111990", 
        "description": "A T cell and NK cell immunodeficiency characterized by absence of responses to IL12 and IL23 in T calls and NK cells that has_material_basis_in homozygous or compound heterozygous mutation in IL12RB1 on chromosome 19p13.11.", 
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        "id": "DOID:0111990", 
        "name": "immunodeficiency 30"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/614891", 
            "id": "614891", 
            "database": "MIM"
        }
    ]
}
