Platelet-type bleeding disorder 11
MONDO:0013623Any inherited bleeding disorder, platelet-type in which the cause of the disease is a mutation in the GP6 gene.
Also known as: BDPLT11, GP6 inherited bleeding disorder, platelet-type, inherited bleeding disorder, platelet-type caused by mutation in GP6, platelet-type bleeding disorder 11, GP 6 deficiency, bleeding diathesis due to glycoprotein VI deficiency, bleeding disorder, platelet-type, 11, glycoprotein 6 deficiency
44 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsBroader categories
Disease
(618)
Hereditary disease
(172)
Hematologic disorder
(160)
Hemorrhagic disease
(100)
Blood platelet disease
(15)
Human disease
(14)
Inherited bleeding disorder, platelet-type
(6)
Disease of genetic or genomic mechanism
(2)
Disease by body system or component
(0)
Disease by etiologic mechanism
(0)