{
    "disease_id": "DOID:0060706", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010385", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010385", 
            "name": "lymphoproliferative syndrome, X-linked, 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010385", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010385", 
            "name": "lymphoproliferative syndrome, X-linked, type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010385", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010385", 
            "name": "XLP2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010385", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010385", 
            "name": "X-linked lymphoproliferative syndrome type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010385", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010385", 
            "name": "XIAP deficiency/XLPs"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010385", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010385", 
            "name": "XIAP-related lymphoproliferative disease, X-linked"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010385", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010385", 
            "name": "XIAP deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010385", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010385", 
            "name": "lymphoproliferative syndrome, X-linked, 2; XLP2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060706", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060706", 
            "name": "XIAP deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060706", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060706", 
            "name": "XLP2"
        }, 
        {
            "url": "https://www.omim.org/entry/300635", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:300635", 
            "name": "Lymphoproliferative syndrome, X-linked, 2"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060706", 
        "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060706", 
        "name": "X-linked lymphoproliferative syndrome 2"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/300635", 
            "id": "300635", 
            "database": "MIM"
        }
    ]
}