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GENATLAS PHENOTYPE
last update : 26-01-2009
Symbol WATS
Location 17q11.2
Name Watson syndrome
Other name(s) cafe-au-lait spots with pulmonic stenosis
Corresponding gene NF1
Main clinical features
  • pulmonic stenosis, cafe-au-lait spots, and low normal or dull intelligence
  • absence of neurofibromas, Lisch nodules, lentigines, or deafness
  • Genetic determination
    Function/system disorder neurology
    dermatology
    Type disease
    Gene product
    Name neurofibromin
    Remark(s)