{
    "disease_id": "DOID:0111950", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013954", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013954", 
            "name": "mendelian susceptibility to mycobacterial diseases due to complete IL12B deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013954", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013954", 
            "name": "MSMD due to complete IL12B deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013954", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013954", 
            "name": "immunodeficiency type 29"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013954", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013954", 
            "name": "IL12B deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013954", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013954", 
            "name": "MSMD due to complete interleukin 12B deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013954", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013954", 
            "name": "autosomal recessive mendelian susceptibility to mycobacterial diseases due to a complete deficiency caused by mutation in IL12B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013954", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013954", 
            "name": "immunodeficiency 29; IMD29"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013954", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013954", 
            "name": "Mendelian susceptibility to mycobacterial diseases due to complete interleukin 12B deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013954", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013954", 
            "name": "IMD29"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013954", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013954", 
            "name": "IL12B autosomal recessive mendelian susceptibility to mycobacterial diseases due to a complete deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111950", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111950", 
            "name": "Mendelian susceptibility to mycobacterial diseases due to complete IL12B deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111950", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111950", 
            "name": "IL12B deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111950", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111950", 
            "name": "IMD29"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111950", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111950", 
            "name": "MSMD due to complete IL12B deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111950", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111950", 
            "name": "MSMD due to complete interleukin 12B deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111950", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111950", 
            "name": "immunodeficiency 29, mycobacteriosis"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111950", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111950", 
            "name": "Mendelian susceptibility to mycobacterial diseases due to complete interleukin 12B deficiency"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111950", 
        "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111950", 
        "name": "immunodeficiency 29"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111950#disease-associations", 
            "id": "0111950", 
            "database": "Alliance of Genome Resources"
        }
    ]
}