{
    "disease_id": "DOID:0111941",
    "recommended_name": {
        "id": "DOID:0111941",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111941",
        "name": "immunodeficiency 20",
        "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 the FCGR3A gene on chromosome 1q23.3."
    },
    "synonyms": [
        {
            "id": "DOID:0111941",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111941",
            "name": "CD16 deficiency",
            "description": ""
        },
        {
            "id": "DOID:0111941",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111941",
            "name": "IMD20",
            "description": ""
        },
        {
            "id": "DOID:0111941",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111941",
            "name": "autosomal recessive primary immunodeficiency with defective spontaneous NK cell cytotoxicity",
            "description": ""
        },
        {
            "id": "DOID:0111941",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111941",
            "name": "autosomal recessive primary immunodeficiency with defective spontaneous natural killer cell cytotoxicity",
            "description": ""
        },
        {
            "id": "MONDO:0014313",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014313",
            "name": "autosomal recessive primary immunodeficiency with defective spontaneous natural killer cell cytotoxicity",
            "description": ""
        },
        {
            "id": "MONDO:0014313",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014313",
            "name": "CD16 deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0014313",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014313",
            "name": "autosomal recessive primary immunodeficiency with defective spontaneous NK cell cytotoxicity",
            "description": ""
        },
        {
            "id": "MONDO:0014313",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014313",
            "name": "immunodeficiency type 20",
            "description": ""
        },
        {
            "id": "MONDO:0014313",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014313",
            "name": "IMD20",
            "description": ""
        },
        {
            "id": "MONDO:0014313",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014313",
            "name": "immunodeficiency 20",
            "description": ""
        },
        {
            "id": "MIM:615707",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/615707",
            "name": "Immunodeficiency 20",
            "description": "Immunodeficiency 20"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111941"
    ],
    "unlinked_id_list": []
}