{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008564", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008564", 
            "name": "pharyngeal pouch syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008564", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008564", 
            "name": "Di-George syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008564", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008564", 
            "name": "DiGeorge sequence"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008564", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008564", 
            "name": "DGS1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008564", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008564", 
            "name": "chromosome 22Q11.2 deletion syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008564", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008564", 
            "name": "DiGeorge syndrome; DGS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008564", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008564", 
            "name": "DiGeorge syndrome type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008564", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008564", 
            "name": "Takao VCF syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008564", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008564", 
            "name": "velocardiofacial syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008564", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008564", 
            "name": "third and fourth pharyngeal pouch syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008564", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008564", 
            "name": "Catch22"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008564", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008564", 
            "name": "Sphrintzen"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008564", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008564", 
            "name": "hypoplasia of thymus and parathyroids"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008564", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008564", 
            "name": "DGS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008564", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008564", 
            "name": "22q deletion syndrome(s)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008564", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008564", 
            "name": "DiGeorge syndrome chromosome region"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008564", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008564", 
            "name": "velo-cardio-facial syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008564", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008564", 
            "name": "VCF"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008564", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008564", 
            "name": "22q11.2 Deletion syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008564", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008564", 
            "name": "DiGeorge anomaly"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008564", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008564", 
            "name": "DiGeorge's syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008564", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008564", 
            "name": "Shprintzen syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:11198", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:11198", 
            "name": "22q11.2 deletion syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:11198", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:11198", 
            "name": "DiGeorge sequence"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:11198", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:11198", 
            "name": "DiGeorge's syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:11198", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:11198", 
            "name": "Pharyngeal pouch syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:11198", 
        "description": "A T cell deficiency disease that is the result of a large deletion of chromosome 22 which includes the DGS gene needed for development of the thymus and related glands with subsequent lack of T-cell production.", 
        "resource": "Disease Ontology", 
        "id": "DOID:11198", 
        "name": "DiGeorge syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/188400", 
            "id": "188400", 
            "database": "MIM"
        }
    ]
}