Structured Summary
Abstract
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.
MeSH Record
Classification
Related Concepts
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MeSH Record
See Also
MeSH Record
Synonyms
14 entry terms
- 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
- Complex, WAGR
- Syndrome, WAGR
- WAGR Complices
- WAGR Syndromes
MeSH Record
Aspects Covered
34 allowable subheadings
Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.
MeSH Record
History Note
1994
MeSH Record
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)
MeSH Hierarchy
Tree Numbers
- C04w.557.435w.595w.950w
- C04w.588.945w.947.535w.585w.950w
- C04w.700w.900w.950w
- C10w.597.606.360w.969w
- C11w.250.060w.950w
- C11w.270.060w.950w
- C11w.941.375.060w.950w
- C12.050.351.875w.253w.096w.875w
- C12.050.351.937w.820.535w.585w.950w
- C12.050.351.968w.419w.473w.585w.950w
- C12.200.706w.316w.096w.875w
- C12.200.758w.820.750w.585w.950w
- C12.200.777w.419w.473w.585w.950w
- C12.800w.316w.096w.875w
- C12.900w.820.535w.585w.950w
- C12.950w.419w.473w.585w.950w
- C12.950w.983.535w.585w.950w
- C16w.131w.260w.940w
- C16w.131w.384.079w.950w
- C16w.131w.939w.316w.096w.875w
- C16w.320w.180w.940w
- C16w.320w.290.078w.950w
- C16w.320w.700w.900w.950w
- C19w.391.119w.096w.875w
AMA Style
References
- National Library of Medicine. WAGR Syndrome. Medical Subject Headings (MeSH). 2026. Unique ID D017624. http://id.nlm.nih.gov/mesh/2026/D017624
- WAGR Syndrome. In: Wikipedia. https://en.wikipedia.org/wiki/WAGR_syndrome
- WAGR Syndrome. In: Wikidata. https://www.wikidata.org/wiki/Q1892153