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WAGR Syndrome

More information in Books or onNLM PubMed
Definition: 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.     
See Also Genes, Wilms Tumor
Other names Wilms Tumor-Aniridia-Gonadoblastoma-Mental Retarda; Wilms Tumor-Aniridia-Genitourinary Anomalies-MR Sy; Wilms Tumor, Aniridia, Genitourinary Anomalies, Me; Contiguous Gene Syndrome, WAGR; WAGR Syndromes; WAGR Complices; Syndrome, WAGR; Complex, WAGR; WAGR Contiguous Gene Syndrome; WAGR Complex
 
SubstanceCAS Registry & nameCategoriesSource
Chromosome 11p Deletion Syndrome  0   *Chromosome Deletion *WAGR Syndrome Chromosomes, Human, Pair 11.

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Sources: NLM Medical Subject Headings, NIH UMLS, Drugs@FDA, FDA AERS original data copyright United States Government. No endorsement implied. Last modified 6/6/2012

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