{
    "disease_id": "DOID:0061087",
    "recommended_name": {
        "id": "DOID:0061087",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0061087",
        "name": "immunodeficiency 121",
        "description": "A severe combined immunodeficiency that is characterized by T-, B-, NK+/- severe combined immunodeficiency associated with failure to thrive, erythrodermia, diarrhea, and alopecia and that has_material_basis_in heterozygous mutation in the PSMB10 gene on chromosome 16q22."
    },
    "synonyms": [
        {
            "id": "DOID:0061087",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0061087",
            "name": "immunodeficiency 121 with autoinflammation",
            "description": ""
        },
        {
            "id": "MONDO:0971001",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0971001",
            "name": "immunodeficiency 121 with autoinflammation",
            "description": ""
        },
        {
            "id": "MIM:620807",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/620807",
            "name": "Immunodeficiency 121 with autoinflammation",
            "description": "Immunodeficiency 121 with autoinflammation"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0061087"
    ],
    "unlinked_id_list": []
}