{
    "disease_id": "DOID:14515",
    "recommended_name": {
        "id": "DOID:14515",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:14515",
        "name": "WAGR syndrome",
        "description": "A chromosomal deletion syndrome that is a nephroblastoma that results_in a rare genetic syndrome in which affected children are predisposed to develop Wilms tumor, Aniridia (absence of the colored part of the eye, the iris), genitourinary anomalies, and mental retardation. The condition results from a deletion on chromosome 11 resulting in the loss of several genes. As such, it is one of the best studied examples of a condition caused by loss of neighbouring (contiguous) genes."
    },
    "synonyms": [
        {
            "id": "DOID:14515",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:14515",
            "name": "Wilms tumor-Aniridia-Genitourinary Anomalies-Mental Retardation syndrome",
            "description": ""
        },
        {
            "id": "DOID:14515",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:14515",
            "name": "11p partial monosomy syndrome",
            "description": ""
        },
        {
            "id": "DOID:14515",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:14515",
            "name": "chromosome 11p13 deletion syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008681",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008681",
            "name": "WAGR syndrome",
            "description": "WAGR syndrome (Wilms tumor - aniridia - genitourinary anomalies - intellectual disability mental retardation) is a rare genetic disorder characterized by an unusual complex of congenital developmental abnormalities with intellectual disability, and an increased risk of developing Wilms tumor."
        },
        {
            "id": "MONDO:0008681",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008681",
            "name": "Del(11)(p13)",
            "description": ""
        },
        {
            "id": "MONDO:0008681",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008681",
            "name": "Wilms tumor, aniridia, genitourinary anomalies, and mental retardation syndrome; WAGR",
            "description": ""
        },
        {
            "id": "MONDO:0008681",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008681",
            "name": "11p partial monosomy syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008681",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008681",
            "name": "WAGR",
            "description": ""
        },
        {
            "id": "MONDO:0008681",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008681",
            "name": "Wilms tumor, aniridia, genitourinary anomalies, and mental retardation syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008681",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008681",
            "name": "11p deletion",
            "description": ""
        },
        {
            "id": "MONDO:0008681",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008681",
            "name": "WAGR syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008681",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008681",
            "name": "Wilms tumor-aniridia-gonadoblastoma-mental retardation syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008681",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008681",
            "name": "deletion 11p",
            "description": ""
        },
        {
            "id": "MONDO:0008681",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008681",
            "name": "deletion 11p13",
            "description": ""
        },
        {
            "id": "MONDO:0008681",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008681",
            "name": "chromosome 11P13 deletion syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008681",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008681",
            "name": "Wilms tumor, aniridia, genitourinary anomalies, mental retardation syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008681",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008681",
            "name": "11p monosomy",
            "description": ""
        },
        {
            "id": "MONDO:0008681",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008681",
            "name": "monosomy 11p",
            "description": ""
        },
        {
            "id": "MONDO:0008681",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008681",
            "name": "monosomy 11p13",
            "description": ""
        },
        {
            "id": "MONDO:0008681",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008681",
            "name": "partial monosomy 11p",
            "description": ""
        },
        {
            "id": "MONDO:0008681",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008681",
            "name": "chromosome 11p deletion syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008681",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008681",
            "name": "AGR triad",
            "description": ""
        },
        {
            "id": "MONDO:0008681",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008681",
            "name": "Wilms tumor-aniridia-genitourinary anomalies-mental retardation syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008681",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008681",
            "name": "chromosome 11p13 deletion syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008681",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008681",
            "name": "Wilms tumor, aniridia, genitourinary anomalies and developmental delay syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008681",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008681",
            "name": "chromosome 11p deletion",
            "description": ""
        },
        {
            "id": "MONDO:0008681",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008681",
            "name": "WAGR Complex",
            "description": ""
        },
        {
            "id": "MONDO:0008681",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008681",
            "name": "Wilms tumor-aniridia-genitourinary anomalies-intellectual disability syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008681",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008681",
            "name": "11p deletion syndrome",
            "description": ""
        }
    ]
}