{
    "disease_id": "DOID:0061081",
    "recommended_name": {
        "id": "DOID:0061081",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0061081",
        "name": "immunodeficiency 115",
        "description": "A primary immunodeficiency disease that is characterized by the onset of symptoms of immune dysregulation in early infancy and that has_material_basis_in homozygous or compound heterozygous mutation in the RNF31 gene on chromosome 14q11."
    },
    "synonyms": [
        {
            "id": "DOID:0061081",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0061081",
            "name": "immunodeficiency 115 with autoinflammation",
            "description": ""
        },
        {
            "id": "MONDO:0957981",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0957981",
            "name": "immunodeficiency 115 with autoinflammation",
            "description": ""
        },
        {
            "id": "MIM:620632",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/620632",
            "name": "Immunodeficiency 115 with autoinflammation",
            "description": "Immunodeficiency 115 with autoinflammation"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0061081"
    ],
    "unlinked_id_list": []
}