{
    "disease_id": "DOID:0111936",
    "recommended_name": {
        "id": "DOID:0111936",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111936",
        "name": "immunodeficiency 14",
        "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."
    },
    "synonyms": [
        {
            "id": "DOID:0111936",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111936",
            "name": "APDS",
            "description": ""
        },
        {
            "id": "DOID:0111936",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111936",
            "name": "IMD14",
            "description": ""
        },
        {
            "id": "DOID:0111936",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111936",
            "name": "PASLI disease",
            "description": ""
        },
        {
            "id": "DOID:0111936",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111936",
            "name": "activated PI3K-delta syndrome",
            "description": ""
        },
        {
            "id": "DOID:0111936",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111936",
            "name": "senescent T-cells-lymphadenopathy-immunodeficiency syndrome due to p110delta-activating mutation",
            "description": ""
        },
        {
            "id": "MONDO:0014222",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014222",
            "name": "immunodeficiency 14",
            "description": ""
        },
        {
            "id": "MONDO:0014222",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014222",
            "name": "IMD14",
            "description": ""
        },
        {
            "id": "MONDO:0014222",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014222",
            "name": "immunodeficiency 14",
            "description": ""
        },
        {
            "id": "MONDO:0014222",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014222",
            "name": "immunodeficiency type 14",
            "description": ""
        },
        {
            "id": "MONDO:0014222",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014222",
            "name": "Activated PI3K-Delta syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0014222",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014222",
            "name": "p110-Delta-Activating mutation causing senescent T cells, lymphadenopathy, and immunodeficiency",
            "description": ""
        },
        {
            "id": "MONDO:0014222",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014222",
            "name": "immunodeficiency 14; IMD14",
            "description": ""
        },
        {
            "id": "MIM:615513",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/615513",
            "name": "Immunodeficiency 14A, autosomal dominant",
            "description": "Immunodeficiency 14A, autosomal dominant"
        }
    ]
}