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GENATLAS PHENOTYPE
last update : 6/07/2006
Symbol GUD
Location 11p13
Name genitourinary dysplasia component of WAGR syndrome
Corresponding gene WT1
Main clinical features
  • overlapping Denys Drash syndrome (see DDS), associated with germline WT1 mutation
  • Genetic determination autosomal dominant
    Related entries including partial androgen resistance
    Function/system disorder congenital malformation
    kidney and urinary tract
    Type malignancy
    Gene product
    Name WT1 gene