{
    "disease_id": "DOID:0111989", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012682", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012682", 
            "name": "susceptibility to infection due to TYK2 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012682", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012682", 
            "name": "immunodeficiency type 35"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012682", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012682", 
            "name": "autosomal recessive mendelian susceptibility to mycobacterial diseases due to a partial deficiency caused by mutation in TYK2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012682", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012682", 
            "name": "hyper-IgE syndrome with atypical Mycobacteriosis, autosomal recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012682", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012682", 
            "name": "TYK2 autosomal recessive mendelian susceptibility to mycobacterial diseases due to a partial deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012682", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012682", 
            "name": "tyrosine kinase 2 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012682", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012682", 
            "name": "HIES with atypical Mycobacteriosis, autosomal recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012682", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012682", 
            "name": "immunodeficiency 35; IMD35"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012682", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012682", 
            "name": "TYK2 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012682", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012682", 
            "name": "autosomal recessive hyper-IgE syndrome due to TYK2 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012682", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012682", 
            "name": "IMD35"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111989", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111989", 
            "name": "IMD35"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111989", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111989", 
            "name": "TYK2 deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111989", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111989", 
            "name": "susceptibility to infection due to TYK2 deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111989", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111989", 
            "name": "tyrosine kinase 2 deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111989", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111989", 
            "name": "autosomal recessiv HIES with atypical mycobacteriosis"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111989", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111989", 
            "name": "autosomal recessive hyper-IgE syndrome with atypical mycobacteriosis"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111989", 
        "description": "A primary immunodeficiency disease characterized by increased susceptibility to mycobacterial infection after BCG vaccination and impaired cellular responses to IL-12, IFN-alpha/beta, IL-23, and IL-10 that has_material_basis_in homozygous or compound heterozygous mutation in TYK2 on chromosome 19p13.2.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111989", 
        "name": "immunodeficiency 35"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111989#disease-associations", 
            "id": "0111989", 
            "database": "Alliance of Genome Resources"
        }
    ]
}