这个词是什么意思？
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.
中文名称索引；定义为 MeSH 英文原文，尚未逐条译审。MESH:D017624 · MeSH 2026。
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