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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 Soulié syndrome