{
    "disease_id": "DOID:0060706",
    "recommended_name": {
        "id": "DOID:0060706",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0060706",
        "name": "X-linked lymphoproliferative syndrome 2",
        "description": "A lymphoproliferative syndrome characterized by X-linked inheritance, immune dysregulation after viral infect that may include lymphohystiocytosis, hypogammaglobulinemia and/or splenomegaly and that has_material_basis_in mutation in the XIAP gene on chromosome Xq25."
    },
    "synonyms": [
        {
            "id": "DOID:0060706",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060706",
            "name": "XIAP deficiency",
            "description": ""
        },
        {
            "id": "DOID:0060706",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060706",
            "name": "XLP2",
            "description": ""
        },
        {
            "id": "MONDO:0010385",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010385",
            "name": "X-linked lymphoproliferative syndrome 2",
            "description": "A condition of decreased or absent presence of baculoviral IAP repeat-containing protein 4. Deficiency of this protein is associated with X-linked lymphoproliferative syndrome 2."
        },
        {
            "id": "MONDO:0010385",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010385",
            "name": "lymphoproliferative syndrome, X-linked, 2",
            "description": ""
        },
        {
            "id": "MONDO:0010385",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010385",
            "name": "lymphoproliferative syndrome, X-linked, type 2",
            "description": ""
        },
        {
            "id": "MONDO:0010385",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010385",
            "name": "XLP2",
            "description": ""
        },
        {
            "id": "MONDO:0010385",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010385",
            "name": "X-linked lymphoproliferative syndrome type 2",
            "description": ""
        },
        {
            "id": "MONDO:0010385",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010385",
            "name": "XIAP deficiency/XLPs",
            "description": ""
        },
        {
            "id": "MONDO:0010385",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010385",
            "name": "XIAP-related lymphoproliferative disease, X-linked",
            "description": ""
        },
        {
            "id": "MONDO:0010385",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010385",
            "name": "XIAP deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0010385",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010385",
            "name": "lymphoproliferative syndrome, X-linked, 2; XLP2",
            "description": ""
        },
        {
            "id": "MONDO:0010385",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010385",
            "name": "Xiap deficiency",
            "description": ""
        },
        {
            "id": "MIM:300635",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/300635",
            "name": "Lymphoproliferative syndrome, X-linked, 2",
            "description": "Lymphoproliferative syndrome, X-linked, 2"
        }
    ]
}