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
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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