{
    "disease_id": "DOID:12583", 
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:12583", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:12583", 
            "name": "Shprintzen syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:12583", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:12583", 
            "name": "22q11 Deletion Syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:12583", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:12583", 
            "name": "VCF-Velocardiofacial syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:12583", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:12583", 
            "name": "deletion 22q11.2 syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008644", 
            "description": "A chromosomal disease that has_material_basis_in deletion polymorphisms at chromosome location 22q11 and is characterized by variable developmental problems and schizoid features.", 
            "resource": "MONDO", 
            "id": "MONDO:0008644", 
            "name": "velocardiofacial syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008644", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008644", 
            "name": "chromosome 22Q11.2 deletion syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008644", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008644", 
            "name": "Shprintzen syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008644", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008644", 
            "name": "22q11 deletion syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008644", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008644", 
            "name": "VCF-velocardiofacial syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008644", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008644", 
            "name": "Shprintzen Vcf syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008644", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008644", 
            "name": "Vcf syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008644", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008644", 
            "name": "velocardiofacial syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008644", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008644", 
            "name": "deletion 22q11.2 syndrome"
        }, 
        {
            "url": "https://www.omim.org/entry/192430", 
            "description": "Velocardiofacial syndrome", 
            "resource": "MIM", 
            "id": "MIM:192430", 
            "name": "Velocardiofacial syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:12583", 
        "description": "A chromosomal deletion disease that has_material_basis_in deletion polymorphisms at chromosome location 22q11 and that is characterized by variable developmental problems and schizoid features.", 
        "resource": "Disease Ontology", 
        "id": "DOID:12583", 
        "name": "velocardiofacial syndrome"
    }
}