WAGR Syndrome
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.
Year introduced: 1994
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Subheadings:
Tree Number(s): 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
MeSH Unique ID: D017624
Entry Terms:
- Syndrome, WAGR
- WAGR Syndromes
- Wilms Tumor-Aniridia-Genitourinary Anomalies-MR Syndrome
- WAGR Complex
- Complex, WAGR
- WAGR Complices
- WAGR Contiguous Gene Syndrome
- Wilms Tumor-Aniridia-Genital Anomalies-Retardation Syndrome
- Wilms Tumor-Aniridia-Gonadoblastoma-Mental Retardation Syndrome
- Wilms Tumor, Aniridia, Genitourinary Anomalies, And Mental Retardation Syndrome
- Chromosome 11p13 Deletion Syndrome
- 11p Partial Monosomy Syndrome
- Contiguous Gene Syndrome, WAGR
- Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation Syndrome
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