MONDO_0008553 (platelet-type bleeding disorder 17) is 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, hereditary thrombasthenia-thrombocytopenia, inherited bleeding disorder, platelet-type caused by mutation in GFI1B.