Coagulation defects, purpura or other haemorrhagic or related conditions
International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01
A condition caused by determinants arising during the antenatal period, after birth or by genetically inherited factors, leading to coagulation defects. This condition is characterised by increased bruising and bleeding.
exclusions
sections/codes in this section (3B10-3B6Z)
- Coagulation defects (3B10-3B4Z)
- Fibrinolytic defects (3B50-3B51)
- Non-thrombocytopenic purpura (3B60)
- Thrombophilia (3B61)
- Qualitative platelet defects (3B62)
- Thrombocytosis (3B63)
- Thrombocytopenia (3B64)
- Thrombotic microangiopathy, not elsewhere classified (3B65)
- Other specified coagulation defects, purpura or other haemorrhagic or related conditions (3B6Y)
- Coagulation defects, purpura or other haemorrhagic or related conditions, unspecified (3B6Z)
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