platelet-type bleeding disorder 17

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Disease Overview

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.


Synonyms

  • BDPLT17
  • GFI1B inherited bleeding disorder, platelet-type
  • bleeding disorder, platelet-type 17
  • bleeding disorder, platelet-type, 17
  • hereditary thrombasthenia-thrombocytopenia
  • inherited bleeding disorder, platelet-type caused by mutation in GFI1B
  • platelet-type bleeding disorder 17
  • thrombasthenia-thrombocytopenia, hereditaryBDPLT17
  • GFI1B inherited bleeding disorder, platelet-type
  • bleeding disorder, platelet-type 17
  • bleeding disorder, platelet-type, 17
  • hereditary thrombasthenia-thrombocytopenia
  • inherited bleeding disorder, platelet-type caused by mutation in GFI1B
  • platelet-type bleeding disorder 17
  • thrombasthenia-thrombocytopenia, hereditary