{
    "disease_id": "DOID:0111936", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014222", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014222", 
            "name": "IMD14"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014222", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014222", 
            "name": "immunodeficiency type 14"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014222", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014222", 
            "name": "Activated PI3K-Delta syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014222", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014222", 
            "name": "p110-Delta-Activating mutation causing senescent T cells, lymphadenopathy, and immunodeficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014222", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014222", 
            "name": "immunodeficiency 14; IMD14"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111936", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111936", 
            "name": "APDS"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111936", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111936", 
            "name": "IMD14"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111936", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111936", 
            "name": "PASLI disease"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111936", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111936", 
            "name": "activated PI3K-delta syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111936", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111936", 
            "name": "senescent T-cells-lymphadenopathy-immunodeficiency syndrome due to p110delta-activating mutation"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111936", 
        "description": "A combined T cell and B cell immunodeficiency characterized by  B- and T-cell abnormalities and onset of recurrent sinopulmonary and other infections in early childhood that has_material_basis_in heterozygous activating mutation in PIK3CD on chromosome 1p36.22.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111936", 
        "name": "immunodeficiency 14"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111936#disease-associations", 
            "id": "0111936", 
            "database": "Alliance of Genome Resources"
        }
    ]
}