{
    "disease_id": "DOID:0111949", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014453", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014453", 
            "name": "IMD36"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014453", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014453", 
            "name": "immunodeficiency type 36"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014453", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014453", 
            "name": "immunodeficiency 36; IMD36"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111949", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111949", 
            "name": "IMD36"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111949", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111949", 
            "name": "activated phosphoinositide 3-kinase delta syndrome 2"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111949", 
        "description": "A combined T cell and B cell immunodeficiency characterized by recurrent respiratory tract infections, lymphoproliferation, and antibody deficiency that has_material_basis_in heterozygous mutation in PIK3R1 on chromosome 5q13.1.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111949", 
        "name": "immunodeficiency 36"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111949#disease-associations", 
            "id": "0111949", 
            "database": "Alliance of Genome Resources"
        }
    ]
}