{
    "disease_id": "DOID:0111934", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014502", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014502", 
            "name": "mendelian susceptibility to mycobacterial diseases due to complete ISG15 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014502", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014502", 
            "name": "immunodeficiency 38, Mycobacteriosis, autosomal recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014502", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014502", 
            "name": "immunodeficiency 38 with basal ganglia calcification"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014502", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014502", 
            "name": "ISG15 autosomal recessive mendelian susceptibility to mycobacterial diseases due to a complete deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014502", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014502", 
            "name": "MSMD due to complete ISG15 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014502", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014502", 
            "name": "ISG15 deficiency, autosomal recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014502", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014502", 
            "name": "immunodeficiency 38 with basal ganglia calcification; IMD38"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014502", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014502", 
            "name": "autosomal recessive mendelian susceptibility to mycobacterial diseases due to a complete deficiency caused by mutation in ISG15"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014502", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014502", 
            "name": "IMD38"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111934", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111934", 
            "name": "Mendelian susceptibility to mycobacterial diseases due to complete ISG15 deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111934", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111934", 
            "name": "IMD38"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111934", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111934", 
            "name": "immunodeficiency 38 with basal ganglia calcification"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111934", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111934", 
            "name": "autosomal recessive ISG15 deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111934", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111934", 
            "name": "immunodeficiency 38, mycobacteriosis, autosomal recessive"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111934", 
        "description": "A primary immunodeficiency disease characterized by development of severe clinical disease upon infection with weakly virulent mycobacteria and intracranial calcification that has_material_basis_in homozygous or compound heterozygous mutation in ISG15 on chromosome 1p36.33.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111934", 
        "name": "immunodeficiency 38"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111934#disease-associations", 
            "id": "0111934", 
            "database": "Alliance of Genome Resources"
        }
    ]
}