{
    "disease_id": "DOID:0060708", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014054", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014054", 
            "name": "CD27 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014054", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014054", 
            "name": "lymphoproliferative syndrome type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014054", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014054", 
            "name": "lymphoproliferative syndrome caused by mutation in CD27"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014054", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014054", 
            "name": "CD27 lymphoproliferative syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014054", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014054", 
            "name": "lymphoproliferative syndrome 2; LPFS2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014054", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014054", 
            "name": "LPFS2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060708", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060708", 
            "name": "CD27 deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060708", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060708", 
            "name": "LPFS2"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060708", 
        "description": "A lymphoproliferative syndrome characterized by autosomal recessive inheritance, persistent symptomatic Epstein-Barr virus-associated viremia, hypogammaglobulinemia, and impairment in specific antibody function and that has_material_basis_in homozygous mutation in the CD27 gene on chromosome 12p13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060708", 
        "name": "lymphoproliferative syndrome 2"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060708#disease-associations", 
            "id": "0060708", 
            "database": "Alliance of Genome Resources"
        }
    ]
}