MLchartDataset catalogue

WAGR syndrome

Term · Oncology and biomedicine · MLC-T-ONC-009332

A rare, genetic disorder that is present at birth and has two or more of the following features: Wilms tumor (a type of kidney cancer), Aniridia (little or no iris, which is the colored part of the eye), defects in the Genitourinary tract (organs of the reproductive and urinary systems), and a Range of developmental delays. This syndrome occurs when part of chromosome 11 is missing.

Table 1. Record
IdentifierMLC-T-ONC-009332
FieldOncology and biomedicine
ReferencesNCI Dictionary of Cancer Terms
Record as JSON
{
  "id": "MLC-T-ONC-009332",
  "term": "WAGR syndrome",
  "field": "Oncology and biomedicine",
  "definition": "A rare, genetic disorder that is present at birth and has two or more of the following features: Wilms tumor (a type of kidney cancer), Aniridia (little or no iris, which is the colored part of the eye), defects in the Genitourinary tract (organs of the reproductive and urinary systems), and a Range of developmental delays. This syndrome occurs when part of chromosome 11 is missing.",
  "references": [
    "NCI Dictionary of Cancer Terms"
  ],
  "url": "https://mlchart.com/terminology/oncology/wagr-syndrome/"
}

Record 17,367 of 17,717 in Oncology and biomedicine terminology (MLC-0111). Request the full dataset.