{
    "disease_id": "DOID:0111945", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013956", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013956", 
            "name": "mendelian susceptibility to mycobacterial diseases due to partial STAT1 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013956", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013956", 
            "name": "immunodeficiency 31A; IMD31A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013956", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013956", 
            "name": "MSMD due to partial signal transducer and activator of transcription 1 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013956", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013956", 
            "name": "IMD31A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013956", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013956", 
            "name": "MSMD due to partial STAT1 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013956", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013956", 
            "name": "immunodeficiency 31A, Mycobacteriosis, autosomal dominant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013956", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013956", 
            "name": "autosomal dominant mendelian susceptibility to mycobacterial diseases due to a partial deficiency caused by mutation in STAT1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013956", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013956", 
            "name": "Mendelian susceptibility to mycobacterial diseases due to partial signal transducer and activator of transcription 1 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013956", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013956", 
            "name": "STAT1 autosomal dominant mendelian susceptibility to mycobacterial diseases due to a partial deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013956", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013956", 
            "name": "Stat1 deficiency, autosomal dominant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013956", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013956", 
            "name": "immunodeficiency type 31A"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111945", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111945", 
            "name": "Mendelian susceptibility to mycobacterial diseases due to partial STAT1 deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111945", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111945", 
            "name": "IMD31A"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111945", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111945", 
            "name": "MSMD due to partial signal transducer and activator of transcription 1 deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111945", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111945", 
            "name": "MSMD due to partial STAT1 deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111945", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111945", 
            "name": "autosomal dominant immunodeficiency 31A, mycobacteriosis"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111945", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111945", 
            "name": "Mendelian susceptibility to mycobacterial diseases due to partial signal transducer and activator of transcription 1 deficiency"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111945", 
        "description": "A primary immunodeficiency disease characterized by impaired response to IFNG but not to INFA or IFNB resulting in increased susceptibility to mycobacterial infection that has_material_basis_in heterozygous mutation in STAT1 on chromosome 2q32.2.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111945", 
        "name": "immunodeficiency 31A"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111945#disease-associations", 
            "id": "0111945", 
            "database": "Alliance of Genome Resources"
        }
    ]
}