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 reference (FX) in Slovak
gény Wilmsovho nádoru
See also reference (FX) in English
Genes, Wilms Tumor
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subject heading
Number of the records: 1
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