{
    "disease_id": "DOID:0111944", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013427", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013427", 
            "name": "immunodeficiency 31B; IMD31B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013427", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013427", 
            "name": "susceptibility to viral and mycobacterial infections"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013427", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013427", 
            "name": "immunodeficiency type 31B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013427", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013427", 
            "name": "Stat1 deficiency, autosomal recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013427", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013427", 
            "name": "IMD31B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013427", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013427", 
            "name": "immunodeficiency 31B, mycobacterial and viral infections, autosomal recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013427", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013427", 
            "name": "STAT1 deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111944", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111944", 
            "name": "IMD31B"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111944", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111944", 
            "name": "susceptibility to viral and mycobacterial infections due to STAT1 deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111944", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111944", 
            "name": "autosomal recessive STAT1 deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111944", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111944", 
            "name": "autosomal recessive immunodeficiency 31B, mycobacterial and viral infections"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111944", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111944", 
            "name": "predisposition to severe viral infection due to STAT1 deficiency"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111944", 
        "description": "A primary immunodeficiency disease characterized by impaired cellular responses to interferons A, B, and G resulting increased susceptibility to mycobacteria, Salmonella, and viruses that has_material_basis_in homozygous or compound heterozygous mutation in STAT1 on chromosome 2q32.2.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111944", 
        "name": "immunodeficiency 31B"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111944#disease-associations", 
            "id": "0111944", 
            "database": "Alliance of Genome Resources"
        }
    ]
}