MeSH 搜索器

WAGR Syndrome

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.
推出的年份: 1994
副标题
树号:
MeSH 单一 ID: D017624
进入的组:
  • Syndrome, WAGR
  • WAGR Syndromes
  • Wilms Tumor-Aniridia-Genitourinary Anomalies-MR Syndrome
  • WAGR Complex
  • Complex, WAGR
  • WAGR Complices
  • WAGR Contiguous Gene Syndrome
  • Wilms Tumor-Aniridia-Genital Anomalies-Retardation Syndrome
  • Wilms Tumor-Aniridia-Gonadoblastoma-Mental Retardation Syndrome
  • Wilms Tumor, Aniridia, Genitourinary Anomalies, And Mental Retardation Syndrome
  • Chromosome 11p13 Deletion Syndrome
  • 11p Partial Monosomy Syndrome
  • Contiguous Gene Syndrome, WAGR
  • Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation Syndrome
早前的内容:
  • 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)

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