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3B62 Qualitative platelet defects

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01

A disease caused by determinants arising after birth, during the antenatal period or genetically inherited factors. This disease is characterised by abnormalities in coagulation of the blood due to defective platelets. This condition may present with easy bruising, prolonged bleeding or bleeding gums. Confirmation is by identification of decreased platelets in a blood sample.

inclusions

• Thrombocytopathy

exclusions

• Von Willebrand disease  (3B12)

sections/codes in this section (3B62-3B62)

• Inherited qualitative platelet defects  (3B62.0)
• Bleeding diathesis due to thromboxane synthesis deficiency  (3B62.1)
• Isolated thrombocytopenia  (3B62.2)
• Dense granule disease  (3B62.3)
• Alpha-delta dense granule deficiency  (3B62.4)
• Haemophagocytic syndrome associated with infection  (3B62.5)
• Other specified qualitative platelet defects  (3B62.Y)
• Qualitative platelet defects, unspecified  (3B62.Z)

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