"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".
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Below are the most recent publications written about "WAGR Syndrome" by people in Profiles.
MeSH information
