Platelet-type bleeding disorder 12
MONDO:0011588An 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
47 clinical trials for this condition and its sub-types.
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Disease
(618)
Hereditary disease
(172)
Hematologic disorder
(160)
Hemorrhagic disease
(100)
Blood coagulation disease
(51)
Blood platelet disease
(15)
Human disease
(14)
Inherited blood coagulation disorder
(7)
Inherited bleeding disorder, platelet-type
(6)
Disease of genetic or genomic mechanism
(2)