D69.1
Qualitative platelet defects
Coding guidance (WHO 2019)
Bernard-Soulier [giant platelet] syndrome Glanzmann disease Grey platelet syndrome Thromboasthenia (haemorrhagic)(hereditary) Thrombocytopathy Excl.: von Willebrand disease (D68.0)
Sibling codes
D69Purpura and other haemorrhagic conditionsD69.0Allergic purpuraD69.2Other nonthrombocytopenic purpuraD69.3Idiopathic thrombocytopenic purpuraD69.4Other primary thrombocytopeniaD69.5Secondary thrombocytopeniaD69.6Thrombocytopenia, unspecifiedD69.8Other specified haemorrhagic conditionsD69.9Haemorrhagic condition, unspecified