{
    "disease_id": "DOID:0060707", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013081", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013081", 
            "name": "lymphoproliferative syndrome 1; LPFS1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013081", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013081", 
            "name": "LPFS1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013081", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013081", 
            "name": "ITK lymphoproliferative syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013081", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013081", 
            "name": "ITK deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013081", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013081", 
            "name": "lymphoproliferative syndrome caused by mutation in ITK"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013081", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013081", 
            "name": "lymphoproliferative syndrome type 1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060707", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060707", 
            "name": "LPFS1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060707", 
        "description": "A lymphoproliferative syndrome characterized by autosomal recessive inheritance, early childhood onset of Epstein-Barr virus-associated immune dysregulation typically manifesting as lymphoma, lymphomatoid granulomatosis, hemophagocytic lymphohistiocytosis, Hodgkin disease, and-or hypogammaglobulinemia and that has_material_basis_in  homozygous mutation in the ITK gene on chromosome 5q32.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060707", 
        "name": "lymphoproliferative syndrome 1"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060707#disease-associations", 
            "id": "0060707", 
            "database": "Alliance of Genome Resources"
        }
    ]
}