Platelet-type bleeding disorder 12

MONDO:0011588

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.

Also known as: BDPLT12, PGHS1 deficiency, platelet COX1 deficiency, platelet cyclooxygenase 1 deficiency, bleeding disorder, platelet-type, 12, prostaglandin-endoperoxide synthase 1 deficiency, platelet

13 clinical trials for this condition and its sub-types, 0 tagged with Platelet-type bleeding disorder 12 itself.

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↑ Inherited blood coagulation disorder (321) ↑ Inherited bleeding disorder, platelet-type (26)

Including sub-types (13) Tagged with Platelet-type bleeding disorder 12 (0)

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