Platelet-type bleeding disorder 17

An autosomal dominant condition caused by mutation(s) in the GFI1B gene, encoding zinc finger protein Gfi-1b. It is characterized by a tendency for increased bleeding due to abnormal platelet function.

Also known as: BDPLT17, GFI1B inherited bleeding disorder, platelet-type, bleeding disorder, platelet-type 17, inherited bleeding disorder, platelet-type caused by mutation in GFI1B, platelet-type bleeding disorder 17, bleeding disorder, platelet-type, 17, thrombasthenia-thrombocytopenia, hereditary

10 clinical trials for this condition and its sub-types, 0 tagged with Platelet-type bleeding disorder 17 itself.