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GENATLAS PHENOTYPE
last update : 20/12/06
Symbol PVWD
Location 17p13.2
Name platelet-type von Willebrand disease
Other name(s) pseudo Von Willebrandt disease
Corresponding gene GP1BA
Main clinical features
  • bleeding disorder
  • abnormally enhanced binding of von Willebrand factor (vWF) by patient platelets
  • Genetic determination autosomal dominant
    Function/system disorder hematology
    Type disease
    Remark(s) allelic disorder: Bernard Souliť syndrome