ICD-10 block
D65–D69 Coagulation defects, purpura and other haemorrhagic conditions
The block D65–D69 of ICD-10 is titled “Coagulation defects, purpura and other haemorrhagic conditions”. It is part of Chapter III, Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism, and holds 5 groups.
Codes in D65–D69
- D68.0Von Willebrand disease
- D68.1Hereditary factor XI deficiency
- D68.2Hereditary deficiency of other clotting factors
- D68.3Haemorrhagic disorder due to circulating anticoagulants
- D68.4Acquired coagulation factor deficiency
- D68.5Primary thrombophilia
- D68.6Other thrombophilia
- D68.8Other specified coagulation defects
- D68.9Coagulation defect, unspecified
- D69.0Allergic purpura
- D69.1Qualitative platelet defects
- D69.2Other nonthrombocytopenic purpura
- D69.3Idiopathic thrombocytopenic purpura
- D69.4Other primary thrombocytopenia
- D69.5Secondary thrombocytopenia
- D69.6Thrombocytopenia, unspecified
- D69.8Other specified haemorrhagic conditions
- D69.9Haemorrhagic condition, unspecified
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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