{
    "disease_id": "DOID:12583",
    "recommended_name": {
        "id": "DOID:12583",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:12583",
        "name": "velocardiofacial syndrome",
        "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."
    },
    "synonyms": [
        {
            "id": "DOID:12583",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:12583",
            "name": "22q11 Deletion Syndrome",
            "description": ""
        },
        {
            "id": "DOID:12583",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:12583",
            "name": "Shprintzen syndrome",
            "description": ""
        },
        {
            "id": "DOID:12583",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:12583",
            "name": "VCF-Velocardiofacial syndrome",
            "description": ""
        },
        {
            "id": "DOID:12583",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:12583",
            "name": "deletion 22q11.2 syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008644",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008644",
            "name": "velocardiofacial syndrome",
            "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."
        },
        {
            "id": "MONDO:0008644",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008644",
            "name": "chromosome 22Q11.2 deletion syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008644",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008644",
            "name": "Shprintzen Vcf syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008644",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008644",
            "name": "22q11 deletion syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008644",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008644",
            "name": "deletion 22q11.2 syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008644",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008644",
            "name": "Shprintzen syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008644",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008644",
            "name": "Vcf syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008644",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008644",
            "name": "VCF-velocardiofacial syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008644",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008644",
            "name": "velocardiofacial syndrome",
            "description": ""
        },
        {
            "id": "MIM:192430",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/192430",
            "name": "Velocardiofacial syndrome",
            "description": "Velocardiofacial syndrome"
        }
    ]
}