D69.1 is the ICD-10 code for Qualitative platelet defects. It is a four-character subcategory of D69 (Purpura and other haemorrhagic conditions), the most specific level in the WHO edition. It belongs to the block D65–D69 (Coagulation defects, purpura and other haemorrhagic conditions) in Chapter III, Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism.
- Code type
- Subcategory (4 characters)
- Chapter
- III · D50–D89
- Classification
- WHO ICD-10, 2019 version
What D69.1 includes
Conditions and terms that are coded here.
- Bernard-Soulier [giant platelet] syndrome
- Glanzmann disease
- Grey platelet syndrome
- Thromboasthenia (haemorrhagic)(hereditary)
- Thrombocytopathy
What D69.1 excludes
Conditions that look similar but belong under another code.
- von Willebrand disease D68.0
D69.1 in national editions
Countries report with their own edition of ICD-10. Most keep the WHO code and add more specific codes beneath it.
D69.1Kvalitativ blodplatedefekt
DD691Blodpladedefekter
- DD691ABernard-Soulier syndrom
- DD691BGlanzmanns trombasteni
- DD691CTrombasteni (hæmoragisk) (hereditær)
D69.1Trombosyyttien laadulliset vajavuudet
D69.1Qualitative Thrombozytendefekte
D69.1Modifications qualitatives des plaquettes
D69.1kwalitatieve trombocytenafwijkingen
D69.1Qualitative platelet defects
Based on the World Health Organization’s International Statistical Classification of Diseases and Related Health Problems, 10th revision (ICD-10), 2019 version, and the national editions published by each country’s health authority. This page is a reference, not coding advice; follow your national coding rules when you report.
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