An inherited blood coagulation disease characterized by autosomal dominant inheritance of mildly increased bleeding, platelet aggregation defect, and impaired conversion of arachidonic acid to thromboxane A2 in platelets due to deficiency in PTGS1 activity.
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factor VII and Factor VIII, combined deficiency of
MONDO:0007595
gray platelet syndrome
MONDO:0007686
primary release disorder of platelets
MONDO:0008309
platelet-type von Willebrand disease
MONDO:0008332
platelet-type bleeding disorder 16
MONDO:0008552
platelet-type bleeding disorder 17
MONDO:0008553