"WAGR Syndrome" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
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.
| Descriptor ID |
D017624
|
| MeSH Number(s) |
C04.557.435.595.950 C04.588.945.947.535.585.950 C04.700.635.950 C10.597.606.643.969 C11.250.060.950 C11.270.060.950 C11.941.375.060.950 C12.706.316.096.875 C12.758.820.750.585.950 C12.777.419.473.585.950 C13.351.875.253.096.875 C13.351.937.820.535.585.950 C13.351.968.419.473.585.950 C16.131.260.940 C16.131.384.079.950 C16.131.939.316.096.875 C16.320.180.940 C16.320.290.078.950 C16.320.700.642.950 C19.391.119.096.875
|
| Concept/Terms |
WAGR Syndrome- WAGR Syndrome
- Syndrome, WAGR
- WAGR Syndromes
- Contiguous Gene Syndrome, WAGR
- WAGR Complex
- Complex, WAGR
- WAGR Complices
- WAGR Contiguous Gene Syndrome
- Wilms Tumor-Aniridia-Genital Anomalies-Retardation Syndrome
- Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation Syndrome
- Wilms Tumor-Aniridia-Genitourinary Anomalies-MR Syndrome
- Wilms Tumor-Aniridia-Gonadoblastoma-Mental Retardation Syndrome
- 11p Partial Monosomy Syndrome
- Chromosome 11p13 Deletion Syndrome
- Wilms Tumor, Aniridia, Genitourinary Anomalies, And Mental Retardation Syndrome
|
Below are MeSH descriptors whose meaning is more general than "WAGR Syndrome".
- Diseases [C]
- Neoplasms [C04]
- Neoplasms by Histologic Type [C04.557]
- Neoplasms, Complex and Mixed [C04.557.435]
- Wilms Tumor [C04.557.435.595]
- WAGR Syndrome [C04.557.435.595.950]
- Neoplasms by Site [C04.588]
- Urogenital Neoplasms [C04.588.945]
- Urologic Neoplasms [C04.588.945.947]
- Kidney Neoplasms [C04.588.945.947.535]
- Wilms Tumor [C04.588.945.947.535.585]
- WAGR Syndrome [C04.588.945.947.535.585.950]
- Neoplastic Syndromes, Hereditary [C04.700]
- Wilms Tumor [C04.700.635]
- WAGR Syndrome [C04.700.635.950]
- Nervous System Diseases [C10]
- Neurologic Manifestations [C10.597]
- Neurobehavioral Manifestations [C10.597.606]
- Intellectual Disability [C10.597.606.643]
- WAGR Syndrome [C10.597.606.643.969]
- Eye Diseases [C11]
- Eye Abnormalities [C11.250]
- Aniridia [C11.250.060]
- WAGR Syndrome [C11.250.060.950]
- Eye Diseases, Hereditary [C11.270]
- Aniridia [C11.270.060]
- WAGR Syndrome [C11.270.060.950]
- Uveal Diseases [C11.941]
- Iris Diseases [C11.941.375]
- Aniridia [C11.941.375.060]
- WAGR Syndrome [C11.941.375.060.950]
- Male Urogenital Diseases [C12]
- Urogenital Abnormalities [C12.706]
- Disorders of Sex Development [C12.706.316]
- 46, XY Disorders of Sex Development [C12.706.316.096]
- WAGR Syndrome [C12.706.316.096.875]
- Urogenital Neoplasms [C12.758]
- Urologic Neoplasms [C12.758.820]
- Kidney Neoplasms [C12.758.820.750]
- Wilms Tumor [C12.758.820.750.585]
- WAGR Syndrome [C12.758.820.750.585.950]
- Urologic Diseases [C12.777]
- Kidney Diseases [C12.777.419]
- Kidney Neoplasms [C12.777.419.473]
- Wilms Tumor [C12.777.419.473.585]
- WAGR Syndrome [C12.777.419.473.585.950]
- Female Urogenital Diseases and Pregnancy Complications [C13]
- Female Urogenital Diseases [C13.351]
- Urogenital Abnormalities [C13.351.875]
- Disorders of Sex Development [C13.351.875.253]
- 46, XY Disorders of Sex Development [C13.351.875.253.096]
- WAGR Syndrome [C13.351.875.253.096.875]
- Urogenital Neoplasms [C13.351.937]
- Urologic Neoplasms [C13.351.937.820]
- Kidney Neoplasms [C13.351.937.820.535]
- Wilms Tumor [C13.351.937.820.535.585]
- WAGR Syndrome [C13.351.937.820.535.585.950]
- Urologic Diseases [C13.351.968]
- Kidney Diseases [C13.351.968.419]
- Kidney Neoplasms [C13.351.968.419.473]
- Wilms Tumor [C13.351.968.419.473.585]
- WAGR Syndrome [C13.351.968.419.473.585.950]
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
- Congenital Abnormalities [C16.131]
- Chromosome Disorders [C16.131.260]
- WAGR Syndrome [C16.131.260.940]
- Eye Abnormalities [C16.131.384]
- Aniridia [C16.131.384.079]
- WAGR Syndrome [C16.131.384.079.950]
- Urogenital Abnormalities [C16.131.939]
- Disorders of Sex Development [C16.131.939.316]
- 46, XY Disorders of Sex Development [C16.131.939.316.096]
- WAGR Syndrome [C16.131.939.316.096.875]
- Genetic Diseases, Inborn [C16.320]
- Chromosome Disorders [C16.320.180]
- WAGR Syndrome [C16.320.180.940]
- Eye Diseases, Hereditary [C16.320.290]
- Aniridia [C16.320.290.078]
- WAGR Syndrome [C16.320.290.078.950]
- Neoplastic Syndromes, Hereditary [C16.320.700]
- Wilms Tumor [C16.320.700.642]
- WAGR Syndrome [C16.320.700.642.950]
- Endocrine System Diseases [C19]
- Gonadal Disorders [C19.391]
- Disorders of Sex Development [C19.391.119]
- 46, XY Disorders of Sex Development [C19.391.119.096]
- WAGR Syndrome [C19.391.119.096.875]
Below are MeSH descriptors whose meaning is more specific than "WAGR Syndrome".
This graph shows the total number of publications written about "WAGR Syndrome" by people in this website by year, and whether "WAGR Syndrome" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2000 | 1 | 0 | 1 |
| 2003 | 1 | 1 | 2 |
| 2005 | 1 | 0 | 1 |
| 2006 | 1 | 0 | 1 |
| 2017 | 1 | 0 | 1 |
| 2020 | 1 | 0 | 1 |
To return to the timeline,
click here.
Below are the most recent publications written about "WAGR Syndrome" by people in Profiles.
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Results of Treatment for Patients With Multicentric or Bilaterally Predisposed Unilateral Wilms Tumor (AREN0534): A report from the Children's Oncology Group. Cancer. 2020 08 01; 126(15):3516-3525.
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Sustained endocrine profiles of a girl with WAGR syndrome. BMC Med Genet. 2017 10 23; 18(1):117.
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WAGR(O?) syndrome and congenital ptosis caused by an unbalanced t(11;15)(p13;p11.2)dn demonstrating a 7 megabase deletion by FISH. Am J Med Genet A. 2006 Jun 01; 140(11):1214-8.
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Congenital diaphragmatic hernia in WAGR syndrome. Am J Med Genet A. 2005 May 01; 134(4):430-3.
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Characteristics and outcomes of children with the Wilms tumor-Aniridia syndrome: a report from the National Wilms Tumor Study Group. J Clin Oncol. 2003 Dec 15; 21(24):4579-85.
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Missense mutations in the DNA-binding region and termination codon in PAX6. Hum Mutat. 2003 Feb; 21(2):138-45.
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Renal failure in the Denys-Drash and Wilms' tumor-aniridia syndromes. Cancer Res. 2000 Aug 01; 60(15):4030-2.