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WAGR Syndrome MeSH Descriptor Data 2023


MeSH Heading
WAGR Syndrome
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
Unique ID
D017624
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D017624
Scope Note
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.
Entry Term(s)
11p Partial Monosomy Syndrome
Chromosome 11p13 Deletion Syndrome
Contiguous Gene Syndrome, WAGR
WAGR Complex
WAGR Contiguous Gene Syndrome
Wilms Tumor, Aniridia, Genitourinary Anomalies, And Mental Retardation Syndrome
Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation Syndrome
Wilms Tumor-Aniridia-Genital Anomalies-Retardation Syndrome
Wilms Tumor-Aniridia-Genitourinary Anomalies-MR Syndrome
Wilms Tumor-Aniridia-Gonadoblastoma-Mental Retardation Syndrome
Previous Indexing
Chromosomes, Human, 6-12 (1980-1985)
Chromosomes, Human, Pair 11 (1986-1993)
Iris/abnormalities (1980-1993)
Mental Retardation (1984-1993)
Nephroblastoma (1980-1993)
Urogenital System/abnormalities (1984-1993)
See Also
Genes, Wilms Tumor
Public MeSH Note
1994
History Note
1994
Date Established
1994/01/01
Date of Entry
1993/06/03
Revision Date
2021/06/30
WAGR Syndrome Preferred
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