{
    "disease_id": "DOID:0111940", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014710", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014710", 
            "name": "autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014710", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014710", 
            "name": "RORC autosomal recessive mendelian susceptibility to mycobacterial diseases due to a complete deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014710", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014710", 
            "name": "IMD42"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014710", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014710", 
            "name": "immunodeficiency type 42"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014710", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014710", 
            "name": "immunodeficiency 42; IMD42"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014710", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014710", 
            "name": "autosomal recessive primary immunodeficiency due to RORC mutation"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014710", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014710", 
            "name": "autosomal recessive mendelian susceptibility to mycobacterial diseases due to a complete deficiency caused by mutation in RORC"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014710", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014710", 
            "name": "autosomal recessive MSMD due to complete RORgamma receptor defiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111940", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111940", 
            "name": "IMD42"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111940", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111940", 
            "name": "autosomal recessive primary immunodeficiency due to RORC mutation"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111940", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111940", 
            "name": "autosomal recessive MSMD due to complete RORgamma receptor defiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111940", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111940", 
            "name": "autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111940", 
        "description": "A primary immunodeficiency disease characterized by onset in infancy of increased susceptibility to mycobacterial and candidal infections that has_material_basis_in homozygous or compound heterozygous mutation in RORC on chromosome 1q21.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111940", 
        "name": "immunodeficiency 42"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111940#disease-associations", 
            "id": "0111940", 
            "database": "Alliance of Genome Resources"
        }
    ]
}