{
    "disease_id": "DOID:0111941", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014313", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014313", 
            "name": "autosomal recessive primary immunodeficiency with defective spontaneous natural killer cell cytotoxicity"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014313", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014313", 
            "name": "IMD20"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014313", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014313", 
            "name": "CD16 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014313", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014313", 
            "name": "immunodeficiency type 20"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014313", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014313", 
            "name": "autosomal recessive primary immunodeficiency with defective spontaneous NK cell cytotoxicity"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014313", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014313", 
            "name": "immunodeficiency 20; IMD20"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111941", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111941", 
            "name": "IMD20"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111941", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111941", 
            "name": "CD16 deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111941", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111941", 
            "name": "autosomal recessive primary immunodeficiency with defective spontaneous NK cell cytotoxicity"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111941", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111941", 
            "name": "autosomal recessive primary immunodeficiency with defective spontaneous natural killer cell cytotoxicity"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111941", 
        "description": "A primary immunodeficiency disease characterized by a defect in spontaneous NK cell cytotoxicity that has_material_basis_in homozygous or compound heterozygous mutation in FCGR3A on chromosome 1q23.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111941", 
        "name": "immunodeficiency 20"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111941#disease-associations", 
            "id": "0111941", 
            "database": "Alliance of Genome Resources"
        }
    ]
}