Platelet-type bleeding disorder 17
Platelet-type bleeding disorder 17
Definition
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, bleeding disorder, platelet-type 17, GFI1B inherited bleeding disorder, platelet-type, inherited bleeding disorder, platelet-type caused by mutation in GFI1B, platelet-type bleeding disorder 17 — per MONDO