Condition
WAGR Syndrome
Ophthalmology
Overview
A contiguous gene syndrome associated with hemizygous deletions of chromosome region 11p13. The condition is marked by the combination of WILMS TUMOR; ANIRIDIA; GENITOURINARY ABNORMALITIES; and INTELLECTUAL DISABILITY.
This information is general and should not be treated as medical advice. Always speak directly with a qualified healthcare professional before making decisions about treatment, diagnosis, procedures, medicines or care.
Quick facts about WAGR Syndrome
- Topic type
- Condition
- Category
- Ophthalmology
- MeSH classification
- C04.557.435.595.950|C04.588.945.947.535.585.950|C04.700.900.950|C10.597.606.360.969|C11.250.060.950|C11.270.060.950|C11.941.375.060.950|C12.050.351.875.253.096.875|C12.050.351.937.820.535.585.950|C12.050.351.968.419.473.585.950|C12.200.706.316.096.875|C12.200.758.820.750.585.950|C12.200.777.419.473.585.950|C12.800.316.096.875|C12.900.820.535.585.950|C12.950.419.473.585.950|C12.950.983.535.585.950|C16.131.260.940|C16.131.384.079.950|C16.131.939.316.096.875|C16.320.180.940|C16.320.290.078.950|C16.320.700.900.950|C19.391.119.096.875
Preparing for an appointment about WAGR Syndrome
If you are speaking with a healthcare professional about WAGR Syndrome, it can help to prepare a few details in advance.
- Write down your symptoms and when they started.
- Bring details of any medicines, supplements or previous treatments.
- Ask what tests or assessments may be needed.
- Ask what treatment or management options may be suitable.
- Ask when you should seek urgent medical help or follow-up care.
Finding care related to WAGR Syndrome
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Source: Medical Subject Headings (MeSH), produced by the U.S. National Library of Medicine. EuroCareFinder is not endorsed by the National Library of Medicine. MeSH version: 2026.