{
    "disease_id": "DOID:0112003", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010386", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010386", 
            "name": "X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010386", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010386", 
            "name": "IMD33"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010386", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010386", 
            "name": "X-linked MSMD due to IKBKG deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010386", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010386", 
            "name": "IKBKG X-linked mendelian susceptibility to mycobacterial diseases"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010386", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010386", 
            "name": "atypical Mycobacteriosis, familial, X-linked 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010386", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010386", 
            "name": "immunodeficiency 33, Mycobacteriosis, X-linked"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010386", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010386", 
            "name": "immunodeficiency type 33"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010386", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010386", 
            "name": "NF-kappa B essential modulator deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010386", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010386", 
            "name": "X-linked mendelian susceptibility to mycobacterial diseases due to NEMO deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010386", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010386", 
            "name": "familial X-linked 1 atypical mycobacteriosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010386", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010386", 
            "name": "immunodeficiency 33; IMD33"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010386", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010386", 
            "name": "NEMO deficiency syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010386", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010386", 
            "name": "X-linked mendelian susceptibility to mycobacterial diseases caused by mutation in IKBKG"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010386", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010386", 
            "name": "X-linked MSMD due to NEMO deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0112003", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0112003", 
            "name": "X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0112003", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0112003", 
            "name": "IMD33"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0112003", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0112003", 
            "name": "X-linked MSMD due to IKBKG deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0112003", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0112003", 
            "name": "X-linked MSMD due to NEMO deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0112003", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0112003", 
            "name": "X-linked mendelian susceptibility to mycobacterial diseases due to NEMO deficiency"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0112003", 
        "description": "A combined immunodeficiency characterized by early-onset severe infection and variable immunological abnormalities that has_material_basis_in hemizygous mutation in IKBKG on chromosome Xq28.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0112003", 
        "name": "immunodeficiency 33"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0112003#disease-associations", 
            "id": "0112003", 
            "database": "Alliance of Genome Resources"
        }
    ]
}